Enum V3ActCode
- All Implemented Interfaces:
Serializable
,Comparable<V3ActCode>
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Enum Constant Summary
Enum ConstantDescriptionConfirmed drug therapy appropriateProvided education or training to the patient on appropriate therapy useInstituted an additional therapy to mitigate potential negative effectsSuspended existing therapy that triggered interaction for the duration of this therapyAborted existing therapy that triggered interaction.Confirmed supply action appropriatePatient's existing supply was lost/wastedSupply date is due to patient vacationSupply date is intended to carry patient over weekendSupply is intended for use during a leave of absence from an institution.Consulted other supplier/pharmacy, therapy confirmedAssessed patient, therapy is appropriateDescription: Supply is different than expected as an additional quantity has been supplied in a separate dispense.Description: Indicates that the permissions have been externally verified and the request should be processed.Definition:Estimated age.Definition:Reported age.Description: The patient has the appropriate indication or diagnosis for the action to be taken.Description: It has been confirmed that the appropriate pre-requisite therapy has been tried.Definition:Calculated age.Patient gave adequate explanationDefinition:General specification of age with no implied method of determination.Definition:Age at onset of associated adverse event; no implied method of determination.Consulted other supply source, therapy still appropriate42 CFR Part 2 stipulates the right of an individual who has applied for or been given diagnosis or treatment for alcohol or drug abuse at a federally assisted program.Consulted prescriber, therapy confirmedConsulted prescriber and recommended change, prescriber declinedConcurrent therapy triggering alert is no longer on-going or plannedOrder is performed as issued, but other action taken to mitigate potential adverse effectsArranged to monitor patient for adverse effectsAn account represents a grouping of financial transactions that are tracked and reported together with a single balance.Includes coded responses that will occur as a result of the adjudication of an electronic invoice at a summary level and provides guidance on interpretation of the referenced adjudication results.Catagorization of grouping criteria for the associated transactions and/or summary (totals, subtotals).Actions to be carried out by the recipient of the Adjudication Result information.ActAdministrativeAuthorizationDetectedIssueCodeIdentifies types of detectyed issues for Act class "ALRT" for the administrative and patient administrative acts domains.Codes dealing with the management of Detected Issue observations for the administrative and patient administrative acts domains.ActAdministrativeRuleDetectedIssueCodeDefinition:An identifying modifier code for healthcare interventions or procedures.Definition: An identifying code for billable services, as opposed to codes for similar services used to identify them for functional purposes.The type of provision(s) made for reimbursing for the deliver of healthcare services and/or goods provided by a Provider, over a specified period.Type of bounded ROI.Description:The type and scope of responsibility taken-on by the performer of the Act for a specific subject of care.Description: Coded types of attachments included to support a healthcare claim.Specifies the type of agreement between one or more grantor and grantee in which rights and obligations related to one or more shared items of interest are allocated.Definition: The type of consent directive, e.g., to consent or dissent to collect, access, or use in specific ways within an EHRS or for health information exchange; or to disclose health information for purposes such as research.Constrains the ActCode to the domain of Container RegistrationAn observation form that determines parameters or attributes of an Act.Indication of authorization for healthcare service(s) and/or product(s).Response to an insurance coverage eligibility query or authorization request.Indication of eligibility coverage for healthcare service(s) and/or product(s).Criteria that are applicable to the authorized coverage.Maximum amount paid or maximum number of services/products covered; or maximum amount or number covered during a specified time period under the policy or program.Definition: Set of codes indicating the type of insurance policy or program that pays for the cost of benefits provided to covered parties.Codes representing the types of covered parties that may receive covered benefits under a policy or program.Description:The type and scope of legal and/or professional responsibility taken-on by the performer of the Act for a specific subject of care as described by a credentialing agency, i.e.Description:The type and scope of legal and/or professional responsibility taken-on by the performer of the Act for a specific subject of care as described by an agency for credentialing individuals.Description:The type and scope of legal and/or professional responsibility taken-on by the performer of the Act for a specific subject of care as described by an agency for credentialing programs within organizations.Codes dealing with the management of Detected Issue observationsAccommodation type.Domain provides codes that qualify the ActEncounterClass (ENC)Concepts that identify the type or nature of exposure interaction.ActFinancialTransactionCodeDefinition: Set of codes indicating the type of health insurance policy that covers health services provided to covered parties.Set of codes indicating the type of incident or accident.Description: The type of health information to which the subject of the information or the subject's delegate consents or dissents.Concepts conveying the context in which authorization given under jurisdictional law, by organizational policy, or by a patient consent directive permits the collection, access, use or disclosure of specified patient health information.Definition:Indicates the set of information types which may be manipulated or referenced, such as for recommending access restrictions.Types of sensitivity policies that apply to Acts.Set of codes indicating the type of insurance policy or other source of funds to cover healthcare costs.Definition: Set of codes indicating the type of insurance policy.Codes representing a grouping of invoice elements (totals, sub-totals), reported through a Payment Advice or a Statement of Financial Activity (SOFA).Codes representing adjustments to a Payment Advice such as retroactive, clawback, garnishee, etc.Codes representing a grouping of invoice elements (totals, sub-totals), reported through a Payment Advice or a Statement of Financial Activity (SOFA).An identifying data string for healthcare products.An identifying data string for healthcare procedures.Codes representing a service or product that is being invoiced (billed).An identifying data string for A substance used as a medication or in the preparation of medication.The billable item codes to identify adjudicator specified components to the total billing of a claim.The detail item codes to identify charges or changes to the total billing of a claim due to insurance rules and payments.The billable item codes to identify modifications to a billable item charge.The billable item codes to identify provider supplied charges or changes to the total billing of a claim.An identifying data string for medical facility accommodations.The billable item codes to identify modifications to a billable item charge by a tax factor applied to the amount.Type of invoice element that is used to assist in describing an Invoice that is either submitted for adjudication or for which is returned on adjudication results.Identifies the different types of summary information that can be reported by queries dealing with Statement of Financial Activity (SOFA).Type of invoice element that is used to assist in describing an Invoice that is either submitted for adjudication or for which is returned on adjudication results.Type of invoice element that is used to assist in describing an Invoice that is either submitted for adjudication or for which is returned on adjudication results.Includes coded responses that will occur as a result of the adjudication of an electronic invoice at a summary level and provides guidance on interpretation of the referenced adjudication results.Type of invoice element that is used to assist in describing an Invoice that is either submitted for adjudication or for which is returned on adjudication results.Provides codes associated with ActClass value of LIST (working list)General category of medical service provided to the patient during their encounter.Definition:A collection of concepts that identifies different types of 'duration-based' mediation working lists.Identifies types of monitoring programsDescription:Concepts representing indications (reasons for clinical action) other than diagnosis and symptoms.ActObservationListIdentifies the type of verification investigation being undertaken with respect to the subject of the verification activity.Description:Provides a categorization for annotations recorded directly against the patient .Definition: Characterizes how a patient was or will be transported to the site of a patient encounter.Code identifying the method or the movement of payment instructions.Identifies types of dispensing eventsDescription:Types of policies that further specify the ActClassPolicy value set.A jurisdictional mandate, regulation, obligation, requirement, rule, or expectation deeming certain information to be private to an individual or organization, which is imposed on: The activity of a governed party The behavior of a governed party The manner in which an act is executed by a governed partyA policy deeming certain information to be private to an individual or organization.An identifying code for healthcare interventions/procedures.The method that a product is obtained for use by the subject of the supply act (e.g.Definition: A set of codes used to indicate coverage under a program.Transportation of a specimen.Set of codes related to specimen treatmentsIdentifies the type of observation that is made about a specimen that may affect its processing, analysis or further result interpretationDescription: Describes the type of substance administration being performed.Identifies types of detected issues regarding the administration or supply of an item to a patient.Description: A task or action that a user may perform in a clinical information system (e.g., medication order entry, laboratory test results review, problem list entry).Codes used to identify different types of 'duration-based' working lists.Characterizes how a transportation act was or will be carried out.Definition: A jurisdictional mandate in the U.S.Administration of the proposed therapy may be inappropriate or contraindicated as proposedAnnotationTypeAppropriatenessDetectedIssueCodeAuthorization Issue Management CodeCode for the mechanism by which disease was acquired by the living subject involved in the public health case.ECGObservationSeriesTypeTypes of sensitivity policies that may apply to a sensitive attribute on an Entity.FDA label dataDescription: None providedDescription:Accommodation type.Domain provides the root for HL7-defined detailed or rich codes for the Act classes.Description: Observation codes which describe characteristics of the immunization material.A code that is used to indicate the type of case safety report received from sender.A mandate, obligation, requirement, rule, or expectation characterizing the value or importance of a resource and may include its vulnerability.InteractionDetectedIssueCodeTotal counts and total net amounts adjudicated for all Invoice Groupings that were adjudicated within a time period based on the adjudication date of the Invoice Grouping.Total counts and total net amounts paid for all Invoice Groupings that were paid within a time period based on the payment date.Total counts and total net amounts billed for all Invoice Groupings that were submitted within a time period.Definition:The set of LOINC codes for the act of determining the period of time that has elapsed since an entity was born or created.MedicationObservationTypeDistinguishes the kinds of coded observations that could be the trigger for clinical issue detection.Codes used to define various metadata aspects of a health quality measure.ObservationSequenceTypeObservationSeriesTypeIdentifies the kinds of observations that can be performedDescription: Reporting codes that are related to an immunization event.Observation types for specifying criteria used to assert that a subject is included in a particular population.Types of observations that can be made about Preferences.Shape of the region on the object being referencedTypes of sensitivity policies that apply to Roles.Supplying the product at this time may be inappropriate or indicate compliance issues with the associated therapyProposed therapy may be inappropriate or ineffective based on the proposed start or end time.The invoice element has been accepted for payment but one or more adjustment(s) have been made to one or more invoice element line items (component charges).Description:Scope of responsibility taken on by an organization for care of a patient as defined by the respective accreditation agency.Description:Scope of responsibility taken on by an organization for care of a patient as defined by the respective accreditation agency.Description:Scope of responsibility taken on by an organization for care of a patient as defined by the respective accreditation agency.Description:The proposed therapy is frequently misused or abused and therefore should be used with caution and/or monitoring.Description:Scope of responsibility taken on by an organization for care of a patient as defined by the respective accreditation agency.Description: Provide consent to collect, use, disclose, or access adverse drug reaction information for a patient.Description: Provide consent to collect, use, disclose, or access all information for a patient.Description: Provide consent to collect, use, disclose, or access allergy information for a patient.Description: Provide consent to collect, use, disclose, or access informational consent information for a patient.An account for collecting charges, reversals, adjustments and payments, including deductibles, copayments, coinsurance (financial transactions) credited or debited to the account receivable account for a patient's encounter.Description: Provide consent to collect, use, disclose, or access demographics information for a patient.Description: Provide consent to collect, use, disclose, or access diagnostic imaging information for a patient.Automated Clearing House (ACH).Description:Scope of responsibility taken on by an organization for care of a patient as defined by the respective accreditation agency.The lowering of specimen pH through the addition of an acidDescription: Provide consent to collect, use, disclose, or access immunization information for a patient.Description: Provide consent to collect, use, disclose, or access lab test result information for a patient.Description: Provide consent to collect, use, disclose, or access medical condition information for a patient.Definition: Provide consent to view or access medical condition information for a patient.Description:Provide consent to collect, use, disclose, or access mental health information for a patient.Description: Provide consent to collect, use, disclose, or access common observation information for a patient.Description: Provide consent to collect, use, disclose, or access coverage policy or program for a patient.Description: Provide consent to collect, use, disclose, or access provider information for a patient.Description: Provide consent to collect, use, disclose, or access professional service information for a patient.Description:Provide consent to collect, use, disclose, or access substance abuse information for a patient.A mandate, obligation, requirement, rule, or expectation conveyed as security metadata between senders and receivers required to establish the reliability, authenticity, and trustworthiness of their transactions.Definition:A list of medications which the patient is only expected to consume for the duration of the current order or limited set of orders and which is not expected to be renewed.An acute inpatient encounter.Proposed therapy is outside of the standard practice for an adult patient.Admitting diagnosis are the diagnoses documented for administrative purposes as the basis for a hospital admission.Identifies the total net amount of all Invoice Groupings that were adjudicated as payable prior to the specified time period (based on adjudication date), subsequently cancelled in the specified period and submitted electronically.Identifies the total number of all Invoice Groupings that were adjudicated as payable prior to the specified time period (based on adjudication date), subsequently cancelled in the specified period and submitted electronically.Identifies the total net amount of all Invoice Groupings that were adjudicated as payable prior to the specified time period (based on adjudication date), subsequently cancelled in the specified period and submitted manually.Identifies the total number of all Invoice Groupings that were adjudicated as payable prior to the specified time period (based on adjudication date), subsequently cancelled in the specified period and submitted manually.Identifies the total net amount of all Invoice Groupings that were adjudicated as payable during the specified time period (based on adjudication date), subsequently nullified in the specified period and submitted electronically.Identifies the total number of all Invoice Groupings that were adjudicated as payable during the specified time period (based on adjudication date), subsequently nullified in the specified period and submitted electronically.Identifies the total net amount of all Invoice Groupings that were adjudicated as payable during the specified time period (based on adjudication date), subsequently cancelled in the specified period and submitted manually.Identifies the total number of all Invoice Groupings that were adjudicated as payable during the specified time period (based on adjudication date), subsequently cancelled in the specified period and submitted manually.Identifies the total net amount of all Invoice Groupings that were adjudicated as payable prior to the specified time period (based on adjudication date) that do not match a specified payee (e.g.Identifies the total number of all Invoice Groupings that were adjudicated as payable prior to the specified time period (based on adjudication date) that do not match a specified payee (e.g.Identifies the total net amount of all Invoice Groupings that were adjudicated as payable prior to the specified time period (based on adjudication date) that do not match a specified payee (e.g.Identifies the total number of all Invoice Groupings that were adjudicated as payable prior to the specified time period (based on adjudication date) that do not match a specified payee (e.g.Identifies the total net amount of all Invoice Groupings that were adjudicated as payable during the specified time period (based on adjudication date) that do not match a specified payee (e.g.Identifies the total number of all Invoice Groupings that were adjudicated as payable during the specified time period (based on adjudication date) that do not match a specified payee (e.g.Identifies the total net amount of all Invoice Groupings that were adjudicated as payable during the specified time period (based on adjudication date) that do not match a specified payee (e.g.Identifies the total number of all Invoice Groupings that were adjudicated as payable during the specified time period (based on adjudication date) that do not match a specified payee (e.g.Policy for handling information related to an adolescent, which will be afforded heightened confidentiality per applicable organizational or jurisdictional policy.Identifies the total net amount of all Invoice Groupings that were adjudicated as payable prior to the specified time period (based on adjudication date) that match a specified payee (e.g.Identifies the total number of all Invoice Groupings that were adjudicated as payable prior to the specified time period (based on adjudication date) that match a specified payee (e.g.Identifies the total net amount of all Invoice Groupings that were adjudicated as payable prior to the specified time period (based on adjudication date) that match a specified payee (e.g.Identifies the total number of all Invoice Groupings that were adjudicated as payable prior to the specified time period (based on adjudication date) that match a specified payee (e.g.Identifies the total net amount of all Invoice Groupings that were adjudicated as payable during the specified time period (based on adjudication date) that match a specified payee (e.g.Identifies the total number of all Invoice Groupings that were adjudicated as payable during the specified time period (based on adjudication date) that match a specified payee (e.g.Identifies the total net amount of all Invoice Groupings that were adjudicated as payable during the specified time period (based on adjudication date) that match a specified payee (e.g.Identifies the total number of all Invoice Groupings that were adjudicated as payable during the specified time period (based on adjudication date) that match a specified payee (e.g.Identifies the total net amount of all Invoice Groupings that were adjudicated as refused prior to the specified time period (based on adjudication date) and submitted electronically.Identifies the total number of all Invoice Groupings that were adjudicated as refused prior to the specified time period (based on adjudication date) and submitted electronically.Identifies the total net amount of all Invoice Groupings that were adjudicated as refused prior to the specified time period (based on adjudication date) and submitted manually.Identifies the total number of all Invoice Groupings that were adjudicated as refused prior to the specified time period (based on adjudication date) and submitted manually.Identifies the total net amount of all Invoice Groupings that were adjudicated as refused during the specified time period (based on adjudication date) and submitted electronically.Identifies the total number of all Invoice Groupings that were adjudicated as refused during the specified time period (based on adjudication date) and submitted electronically.Identifies the total net amount of all Invoice Groupings that were adjudicated as refused during the specified time period (based on adjudication date) and submitted manually.Identifies the total number of all Invoice Groupings that were adjudicated as refused during the specified time period (based on adjudication date) and submitted manually.Indicates that the observation is of an unexpected negative occurrence in the subject suspected to result from the subject's exposure to one or more agents.American Expresspedestrian transportPremium paid on service fees in compensation for practicing outside of normal working hours.Proposed therapy may be inappropriate or contraindicated due to patient ageIndicates that the observation is carrying out an aggregation calculation, contained in the value element.Description:Scope of responsibility taken on by an organization for care of a patient as defined by the respective accreditation agency.Communication of an agent from a living subject or environmental source to a living subject through indirect contact via oral or nasal inhalation.Provision of Alternate Level of Care to a patient in an acute bed.Payment initiated by the payor as the result of adjudicating a submitted invoice that arrived to the payor from an electronic source that did not provide a conformant set of HL7 messages (e.g.Hypersensitivity to an agent caused by an immunologic response to an initial exposureProposed therapy may be inappropriate or contraindicated because of a recorded patient allergy to the proposed product.The act rendering alkaline by impregnating with an alkali; a conferring of alkaline qualities.Description: All patient information.Definition:The requested action has already been performed and so this request has no effectDescription: A person enters a known allergy for a given patient.Description: A person reviews a list of known allergies of a given patient.Definition:All information pertaining to a patient's allergy and intolerance records.Definition:Proposed therapy may be inappropriate or ineffective because the end of administration is too close to another planned therapy.Definition:Proposed therapy may be inappropriate or ineffective because the start of administration is too late after the onset of the condition.Description:Scope of responsibility taken on by an organization for care of a patient as defined by the respective accreditation agency.A comprehensive term for health care provided in a healthcare facility (e.g.fixed-wing ambulance transportground ambulance transporthelicopter ambulance transportambulance transportCommunication of an agent from one animal to another proximate animal.The invoice element has been accepted for payment but one or more adjustment(s) have been made to one or more invoice element line items (component charges) without changing the amount.Communication of an agent from an animal to a proximate person.Description:A note that is specific to a patient's diagnostic images, either historical, current or planned.Description:A general or uncategorized note.A note that is specific to a patient's immunizations, either historical, current or planned.Description:A note that is specific to a patient's laboratory results, either historical, current or planned.Description:A note that is specific to a patient's medications, either historical, current or planned.Definition: A policy that, after an initial premium or premiums, pays out a sum at pre-determined intervals.Custodian system must remove any information that could result in identifying the information subject.Custodian system must make available to an information subject upon request an accounting of certain disclosures of the individualâ??s protected health information over a period of time.Description:Scope of responsibility taken on by an organization for care of a patient as defined by the respective accreditation agency.The invoice element has passed through the adjudication process but payment is refused due to one or more reasons.Description: All information pertaining to a patient's adverse drug reactions.Describes the artificial blood identifier that is associated with the specimen.The invoice element was/will be paid exactly as submitted, without financial adjustment(s).Description:Refines classCode OBS to indicate an observation in which observation.value contains a finding or other nominalized statement, where the encoded information in Observation.value is not altered by Observation.code.Custodian system must monitor systems to ensure that all users are authorized to operate on information objects.Custodian system must monitor and maintain retrievable log for each user and operation on information.Authorization approved and funds have been set aside to pay for specified healthcare service(s) and/or product(s) within defined criteria for the authorization.Specifies whether or not automatic repeat testing is to be initiated on specimens.Description: Automobile Information AttachmentThe dilution of a sample performed by automated equipment.The dilution of a sample performed by automated equipment.Insurance policy for injuries sustained in an automobile accident.The available quantity of specimen.Policy for handling trade secrets such as financial information or intellectual property, which will be afforded heightened confidentiality.Communication of an agent from one living subject to another living subject through direct contact with any body fluid.Communication of an agent to a living subject through direct contact with blood or blood products whether the contact with blood is part of a therapeutic procedure or not.A billing arrangement where a Provider charges a lump sum to provide a prescribed group (volume) of services to a single patient which occur over a period of time.Bonus payments based on performance, volume, etc.An additional immunization administration within a series intended to bolster or enhance immunity.A diet exclusively composed of oatmeal, semolina, or rice, to be extremely easy to eat and digest.Description:A local business rule relating multiple elements has been violated.Description:Indicates that result data has been corrected.Description:Scope of responsibility taken on for specialty care as defined by the respective Specialty Board.Description:Scope of responsibility taken on by an organization for care of a patient as defined by the disease management certification agency.Description:Scope of responsibility taken on for specialty care as defined by the respective Specialty Board.Description:Scope of responsibility taken on for specialty care as defined by the respective Specialty Board.Description:Scope of responsibility taken on by an organization for care of a patient as defined by the disease management certification agency.Description:Scope of responsibility taken on for specialty care as defined by the respective Specialty Board.A charge to compensate the provider when a patient cancels an appointment with insufficient time for the provider to make another appointment with another patient.Definition: A program that provides low-income, uninsured, and underserved women access to timely, high-quality screening and diagnostic services, to detect breast and cervical cancer at the earliest stages.A billing arrangement where the payment made to a Provider is determined by analyzing one or more demographic attributes about the persons/patients who are enrolled with the Provider (in their practice).Description:Scope of responsibility taken on for specialty care as defined by the respective Specialty Board.Provision of diagnosis and treatment of diseases and disorders affecting the heartList of acts representing a care plan.Definition:An observation that provides a characterization of the level of harm to an investigation subject as a result of a reaction or event.CashDescription:Scope of responsibility taken on by an organization for care of a patient as defined by the disease management certification agency.Description:Scope of responsibility taken on by an organization for care of a patient as defined by the disease management certification agency.Description:Scope of responsibility taken on for specialty care as defined by the respective Specialty Board.Description: Types of advance payment to be made on a plastic card usually issued by a financial institution used of purchasing services and/or products.Description:Scope of responsibility taken on by an organization for care of a patient as defined by the disease management certification agency.Description:Scope of responsibility taken on by an organization for care of a patient as defined by the disease management certification agency.Description:Scope of responsibility taken on for specialty care as defined by the respective Specialty Board.Description:Scope of responsibility taken on for specialty care as defined by the respective Specialty Board.Description:Scope of responsibility taken on for specialty care as defined by the respective Specialty Board.Description:Scope of responsibility taken on for specialty care as defined by the respective Specialty Board.Description:Scope of responsibility taken on for specialty care as defined by the respective Specialty Board.Description:Scope of responsibility taken on by an organization for care of a patient as defined by the disease management certification agency.Description:Scope of responsibility taken on by an organization for care of a patient as defined by the disease management certification agency.Description:Scope of responsibility taken on by an organization for care of a patient as defined by the disease management certification agency.An observation that states whether the disease was likely acquired outside the jurisdiction of observation, and if so, the nature of the inter-jurisdictional relationship.Description:Scope of responsibility taken on for specialty care as defined by the respective Specialty Board.A person reviews a recommendation/assessment provided automatically by a clinical decision support application for a given patient.Policy for handling information related to a celebrity (people of public interest (VIP), which will be afforded heightened confidentiality.Description:Scope of responsibility taken on for specialty care as defined by the respective Specialty Board.Description:Scope of responsibility taken on by an organization for care of a patient as defined by the disease management certification agency.Description:Scope of responsibility taken on by an organization for care of a patient as defined by the disease management certification agency.Description:Scope of responsibility taken on for specialty care as defined by the respective Specialty Board.An amount still owing to the payor but the payment is 0$ and this cannot be settled until a future payment is made.Definition: A program that covers the cost of services provided directly to a beneficiary who typically has no other source of coverage without charge.Description:Scope of responsibility taken on by an organization for care of a patient as defined by the disease management certification agency.A written order to a bank to pay the amount specified from funds on deposit.Description: Exposure participants' interaction occurred in a child care settingProvision of recurring care for chronic illness.A type of transaction that represents a charge for a service or product.Description:Scope of responsibility taken on by an organization for care of a patient as defined by the disease management certification agency.Definition:A list of medications which are expected to be continued beyond the present order and which the patient should be assumed to be taking unless explicitly stopped.Description:Scope of responsibility taken on by an organization for care of a patient as defined by the disease management certification agency.Description:Scope of responsibility taken on for specialty care as defined by the respective Specialty Board.A circle defined by two (column,row) pairs.A clinician enters a clinical note about a given patientA person reviews a clinical note of a given patient.Description: The class room associated with the patient during the immunization event.Description:Scope of responsibility taken on for specialty care as defined by the respective Specialty Board.Description:.Indicates what method is used in a quality measure to combine the component measure results included in an composite measure.An attribute of a quality measure describing the weight this component measure score is to carry in determining the overall composite measure final score.Description:Scope of responsibility taken on by an organization for care of a patient as defined by the disease management certification agency.Description:Scope of responsibility taken on for specialty care as defined by the respective Specialty BoardDescription:Scope of responsibility taken on for specialty care as defined by the respective Specialty Board.Description:Scope of responsibility taken on for specialty care as defined by the respective Specialty Board.Description:Scope of responsibility taken on for specialty care as defined by the respective Specialty Board.Definition:All information pertaining to a patient's common observation records (height, weight, blood pressure, temperature, etc.).Description:The specified code has been deprecated and should no longer be used.Description:The specified code is not valid against the list of codes allowed for the element.Description:Scope of responsibility taken on for specialty care as defined by the respective Specialty Board.That portion of the eligible charges which a covered party must pay for each service and/or product.The covered party pays a percentage of the cost of covered services.Description:Scope of responsibility taken on by an organization for care of a patient as defined by the disease management certification agency.Definition: An automobile insurance policy under which the insurance company will cover the cost of damages to an automobile owned by the named insured that are caused by accident or intentionally by another party.Description:Scope of responsibility taken on for specialty care as defined by the respective Specialty Board.U.S.There may be an issue with the patient complying with the intentions of the proposed therapyThis is the healthcare analog to the US Intelligence Community's concept of a Special Access Program.Description:Scope of responsibility taken on by an organization for care of a patient as defined by the disease management certification agency.Proposed therapy may be inappropriate or contraindicated due to an existing/recent patient condition or diagnosisList of condition observations.The quantity of specimen that is used each time the equipment uses this substanceTransaction counts and value totals by Contract Identifier.A billing arrangement where a Provider charges a lump sum to provide a particular volume of one or more interventions/procedures or groups of interventions/procedures.Description: An interaction where the exposure participants traveled in/on the same vehicle (not necessarily concurrently, e.g.nullThat portion of the eligible charges which a covered party must pay for each service and/or product.Description:Scope of responsibility taken on for specialty care as defined by the respective Specialty Board.Description:Scope of responsibility taken on by an organization for care of a patient as defined by the disease management certification agency.Identifies the organization(s) who own the intellectual property represented by the eMeasure.Description:Scope of responsibility taken on by an organization for care of a patient as defined by the disease management certification agency.Description:Scope of responsibility taken on for specialty care as defined by the respective Specialty Board.Description:Scope of responsibility taken on for specialty care as defined by the respective Specialty Board.Insurance coverage problems have been encountered.Definition: Codes representing the maximum coverate or financial participation requirements.Description:A mandate, obligation, requirement, rule, or expectation unilaterally imposed on benefit coverage under a policy or program by a sponsor, underwriter or payor on: The activity of another party The behavior of another party The manner in which an act is executed Examples:A clinical protocol imposed by a payer to which a provider must adhere in order to be paid for providing the service.Codes representing the time period during which coverage is available; or financial participation requirements are in effect.Description:Scope of responsibility taken on by an organization for care of a patient as defined by the disease management certification agency.Description:Scope of responsibility taken on for specialty care as defined by the respective Specialty Board.Description:Scope of responsibility taken on for specialty care as defined by the respective Specialty Board.Description:Scope of responsibility taken on for specialty care as defined by the respective Specialty Board.Clinical product invoice where the Invoice Grouping contains one or more billable item and is supported by clinical product(s).Custodian security system must retrieve, evaluate, and comply with the information handling directions of the Confidentiality Code associated with an information target.Custodian security system must retrieve, evaluate, and comply with applicable information subject consent directives.Custodian security system must retrieve, evaluate, and comply with applicable jurisdictional privacy policies associated with the target information.Custodian security system must retrieve, evaluate, and comply with applicable organizational privacy policies associated with the target information.Custodian security system must retrieve, evaluate, and comply with the organizational security policies associated with the target information.Custodian security system must retrieve, evaluate, and comply with applicable policies associated with the target information.Description:Scope of responsibility taken on by an organization for care of a patient as defined by the disease management certification agency.A grouping of invoice element groups and details including the ones specifying the compound ingredients being invoiced.A grouping of invoice element details including the one specifying an ingredient drug being invoiced.A grouping of invoice element groups and details including the ones specifying the compound supplies being invoiced.Description:Scope of responsibility taken on for specialty care as defined by the respective Specialty Board.Description:Scope of responsibility taken on for specialty care as defined by the respective Specialty Board.Description:Scope of responsibility taken on by an organization for care of a patient as defined by the disease management certification agency.Description:CPT modifier codes are found in Appendix A of CPT 2000 Standard Edition.Description:Scope of responsibility taken on for specialty care as defined by the respective Specialty Board.Description:Proposed therapy may be inappropriate or contraindicated because of a common but non-patient specific reaction to the product.Definition: A program that covers the cost of services provided to crime victims for injuries or losses related to the occurrence of a crime.A clinical judgment as to the worst case result of a future exposure (including substance administration).Description:Scope of responsibility taken on for specialty care as defined by the respective Specialty Board.Description:Scope of responsibility taken on for specialty care as defined by the respective Specialty Board.Summary of relevant clinical guidelines or other clinical recommendations supporting this eMeasure.Description:Scope of responsibility taken on by an organization for care of a patient as defined by the disease management certification agency.Description:Scope of responsibility taken on by an organization for care of a patient as defined by the disease management certification agency.Clinical Services Invoice which can be used to describe a single service, multiple services or repeated services.Description:Scope of responsibility taken on by an organization for care of a patient as defined by the disease management certification agency.A clinical Invoice Grouping consisting of one or more services and one or more product.Description:Scope of responsibility taken on by an organization for care of a patient as defined by the disease management certification agency.Description:Scope of responsibility taken on for specialty care as defined by the respective Specialty Board.Description:Scope of responsibility taken on by an organization for care of a patient as defined by the disease management certification agency.A monitoring program that focuses on narcotics and/or commonly abused substances that are subject to legal restriction.An observation that states the mechanism by which disease was acquired by the living subject involved in the public health case.Description:Scope of responsibility taken on for specialty care as defined by the respective Specialty Board.Description:Scope of responsibility taken on for specialty care as defined by the respective Specialty Board.List of current medications.The current quantity of the specimen, i.e., initial quantity minus what has been actually used.Description:Scope of responsibility taken on by an organization for care of a patient as defined by the disease management certification agency.Description:Scope of responsibility taken on for specialty care as defined by the respective Specialty Board.Description:Scope of responsibility taken on by an organization for care of a patient as defined by the disease management certification agency.Description:Scope of responsibility taken on by an organization for care of a patient as defined by the disease management certification agency.Description:Proposed therapy may be contraindicated or ineffective based on an existing or recent drug therapy.An allergy to a pharmaceutical product.Transaction counts and value totals for each calendar day within the date range specified.Electronic Funds Transfer (EFT) deposit into the payee's bank accountCustodian security system must declassify information assigned security labels by instantiating a new version of the classified information so as to break the binding of the classifying security label when assigning a new security label that marks the information as unclassified in accordance with applicable jurisdictional privacy policies associated with the target information.nullThat portion of the eligible charges which a covered party must pay in a particular period (e.g.Description of individual terms, provided as needed.The removal of fibrin from whole blood or plasma through physical or chemical meansCustodian system must strip information of data that would allow the identification of the source of the information or the information subject.Custodian system must remove target information from access after use.Policy for handling all demographic information about an information subject, which will be afforded heightened confidentiality.Definition:All information pertaining to a patient's demographics (such as name, date of birth, gender, address, etc).Criteria which specify subjects who should be removed from the eMeasure population and denominator before determining if numerator criteria are met.Criteria which specify the removal of a subject, procedure or unit of measurement from the denominator, only if the numerator criteria are not met.Criteria for specifying the entities to be evaluated by a specific quality measure, based on a shared common set of characteristics (within a specific measurement set to which a given measure belongs).Definition: A health insurance policy that that covers benefits for dental services.Definition: A public or government health program that administers and funds coverage for dental care to assist program eligible who meet financial and health status criteria.Communication of an agent from a living subject or environmental source to a living subject via agent migration through intact skin.A fill providing sufficient supply for one dayPolicy for handling information related to a diagnosis, health condition or health problem, which will be afforded heightened confidentiality.A clinician enters a diagnosis for a given patient.A person reviews a list of diagnoses of a given patient.Definition:All information pertaining to a patient's diagnostic image records (orders invalid input: '&' results).Code set to define specialized/allowed dietsAn observation that reports the dilution of a sample.Hypersensitivity resulting in an adverse reaction upon exposure to a drug.Definition: An insurance policy that provides a regular payment to compensate for income lost due to the covered party's inability to work because of illness or injury.Disclaimer information for the eMeasure.A person provides a discharge instruction to a patient.A clinician enters a discharge summary for a given patient.A person reviews a discharge summary of a given patient.List of discharge medications.Discharge diagnosis are the diagnoses documented for administrative purposes as the time of hospital discharge.Definition: A health insurance policy that covers benefits for healthcare services provided for named conditions under the policy, e.g., cancer, diabetes, or HIV-AIDS.Definition: A public or government health program that administers and funds coverage for health and social services to assist program eligible who meet financial and health status criteria related to a particular disease.The adjudication result associated is to be displayed to the receiver of the adjudication result.A diet that uses carbohydrates sparingly.Diner's ClubHypersensitivity to an agent caused by a mechanism other than an immunologic response to an initial exposureProvision of treatment for oral health and/or dental surgery.Policy for handling information related to an information subject's date of birth, which will be afforded heightened confidentiality.Policies may govern sensitivity of information related to an information subject's date of birth, the disclosure of which could impact the privacy, well-being, or safety of that subject.Description: Document AttachmentProposed dosage instructions for therapy differ from standard practice.Description:Proposed dosage is inappropriate due to patient's medical condition.Proposed length of therapy differs from standard practice.Proposed length of therapy is longer than standard practiceProposed length of therapy is longer than standard practice for the identified indication or diagnosisProposed length of therapy is shorter than that necessary for therapeutic effectProposed length of therapy is shorter than standard practice for the identified indication or diagnosisProposed dosage exceeds standard practiceHigh Dose for Indication AlertProposed dosage exceeds standard practice for the patient's ageProposed dosage exceeds standard practice for the patient's height or body surface areaProposed dosage exceeds standard practice for the patient's weightnullProposed dosage interval/timing differs from standard practiceProposed dosage interval/timing differs from standard practice for the identified indication or diagnosisProposed dosage is below suggested therapeutic levelsLow Dose for Indication AlertProposed dosage is below suggested therapeutic levels for the patient's ageProposed dosage is below suggested therapeutic levels for the patient's height or body surface areaProposed dosage is below suggested therapeutic levels for the patient's weightCustodian security system must downgrade information assigned security labels by instantiating a new version of the classified information so as to break the binding of the classifying security label when assigning a new security label that marks the information as classified at a less protected level in accordance with applicable jurisdictional privacy policies associated with the target information.Proposed therapy may interact with an existing or recent drug therapyPolicy for handling information related to a drug, which will be afforded heightened confidentiality.Provision of treatment for drug abuse.Custodian security system must assign and bind security labels derived from compilations of information by aggregation or disaggregation in order to classify information compiled in the information systems under its control for collection, access, use and disclosure in accordance with applicable jurisdictional privacy policies associated with the target information.The introduction of a drug into a subject with the intention of altering its biologic state with the intent of improving its health status.A grouping of invoice element details including the one specifying the drug being invoiced.Definition: A health insurance policy that covers benefits for prescription drugs, pharmaceuticals, and supplies.Definition: A public or government health program that administers and funds coverage for prescription drugs to assist program eligible who meet financial and health status criteria.A reduction in the amount charged as a percentage of the amount.Description:The proposed therapy appears to have the same intended therapeutic benefit as an existing therapy, though the specific mechanisms of action vary.Description:The proposed therapy appears to have the same intended therapeutic benefit as an existing therapy and uses the same mechanisms of action as the existing therapy.The proposed therapy appears to duplicate an existing therapyDiscover CardIncludes all codes defining types of indications such as diagnosis, symptom and other indications such as contrast agents for lab tests.An allergy to a substance other than a drug or a food.Definition: An employee assistance program is run by an employer or employee organization for the purpose of providing benefits and covering all or part of the cost for employees to receive counseling, referrals, and advice in dealing with stressful issues in their lives.Fees deducted on behalf of a payee for tuition and continuing education.Electronic form with supporting or additional information to follow.Private insurance policy that provides coverage in addition to other policies (e.g.Hypersensitivity resulting in an adverse reaction upon exposure to environmental conditions.Insurance coverage is in effect for healthcare service(s) and/or product(s).An ellipse defined by four (column,row) pairs, the first two points specifying the endpoints of the major axis and the second two points specifying the endpoints of the minor axis.A supply action where there is no 'valid' order for the supplied medication.Used to temporarily override normal authorization rules to gain access to data in a case of emergency.A patient encounter that takes place at a dedicated healthcare service delivery location where the patient receives immediate evaluation and treatment, provided until the patient can be discharged or responsibility for the patient's care is transferred elsewhere (for example, the patient could be admitted as an inpatient or transferred to another facility.)Policy for handling information related to an employee, which will be afforded heightened confidentiality.Policy for handling information related to an employer which is deemed classified to protect an employee who is the information subject, and which will be afforded heightened confidentiality.This general consent directive specifically limits disclosure of health information for purpose of emergency treatment.Hypersensitivity to an agent caused by a mechanism other than an immunologic response to an initial exposureCustodian system must render information unreadable by algorithmically transforming plaintext into ciphertext.Custodian system must render information unreadable and unusable by algorithmically transforming plaintext into ciphertext when "at rest" or in storage.Custodian system must render information unreadable and unusable by algorithmically transforming plaintext into ciphertext while "in transit" or being transported by any means.Custodian system must render information unreadable and unusable by algorithmically transforming plaintext into ciphertext while in use such that operations permitted on the target information are limited by the license granted to the end user.A baseline value for the measured test that is inherently contained in the diluent.Proposed therapy may be inappropriate or ineffective because the end of administration is too close to another planned therapyDefinition: A public or government program that administers publicly funded coverage of kidney dialysis and kidney transplant services.Communication of an agent from an environmental surface or source to a living subject by direct contact.Fees deducted on behalf of a payee for charges based on a shorter payment frequency (i.e.A premium on a service fee is requested because, due to extenuating circumstances, the service took an extraordinary amount of time or supplies.Policy for handling alcohol or drug-abuse information, which will be afforded heightened confidentiality.Domain provides codes that qualify the ActLabObsEnvfctsCode domain.Definition: An insurance policy under a benefit plan run by an employer or employee organization for the purpose of providing benefits other than pension-related to employees and their families.Description:Indicates that a result is complete.An allergy to a substance generally consumed for nutritional purposes.A person reviews a Falls Risk Assessment Instrument report of a given patient.No enteral intake of foot or liquids whatsoever, no smoking.Fax with supporting or additional information to follow.Description: The introduction of material into a subject with the intent of providing nutrition or other dietary supplements (e.g.FDA label coatingFDA label colorFDA label imprint codeFDA label logoFDA label scoringFDA label shapeFDA label sizeCommunication of an agent from a living subject or environmental source to a living subject through oral contact with material contaminated by person or animal fecal material.The initial fill against an order.A first fill where the quantity supplied is equal to one full repetition of the ordered amount.A first fill where the quantity supplied is equal to one full repetition of the ordered amount.A first fill where the quantity supplied is less than one full repetition of the ordered amount.A first fill where the quantity supplied is less than one full repetition of the ordered amount.A billing arrangement where a Provider charges a separate fee for each intervention/procedure/event or product.A first fill where the strength supplied is less than the ordered strength.Under agreement between the parties (payor and provider), a guaranteed level of income is established for the provider over a specific, pre-determined period of time.The Fibrin Index of the specimen.The passage of a liquid through a filter, accomplished by gravity, pressure or vacuum (suction).The timestamp when the eMeasure was last packaged in the Measure Authoring Tool.A billing arrangement where a Provider charges for non-clinical items.Invoice Grouping without clinical justification.Hypersensitivity resulting in an adverse reaction upon exposure to food.A patient encounter that takes place both outside a dedicated service delivery location and outside a patient's residence.Definition: An insurance policy that covers qualified benefits under a Flexible Benefit plan such as group medical insurance, long and short term disability income insurance, group term life insurance for employees only up to $50,000 face amount, specified disease coverage such as a cancer policy, dental and/or vision insurance, hospital indemnity insurance, accidental death and dismemberment insurance, a medical expense reimbursement plan and a dependent care reimbursement plan.Hypersensitivity to an agent caused by a mechanism other than an immunologic response to an initial exposureAnticipated or actual final fee associated with treating a patient.Communication of an agent from an non-living material to a living subject through direct contact.Proposed therapy may interact with certain foodsCommunication of an agent from a food source to a living subject via oral consumption.The adjudication result associated is to be printed on the specified form, which is then provided to the covered party.Description:The element does not follow the formatting or type rules defined for the field.A diet consisting of a formula feeding, either for an infant or an adult, to provide nutrition either orally or through the gastrointestinal tract via tube, catheter or stoma.A grouping of invoice element details including the ones specifying the frame fee and the frame dispensing cost that are being invoiced.Description:The request is suspected to have a fraudulent basis.Anticipated or actual initial fee associated with treating a patient.A supply action to restock a smaller more local dispensary.Federal tax on transactions such as the Goods and Services Tax (GST)Definition:The therapy being performed is in some way out of alignment with the requested therapy.Fees deducted on behalf of a payee for charges based on a per-transaction or time-period (e.g.Policy for handling genetic disease information, which will be afforded heightened confidentiality.Proposed therapy is outside of standard practice for a geriatric patient.Proposed therapy may be inappropriate or contraindicated due to patient genetic indicators.Proposed therapy may be inappropriate or contraindicated due to patient gender.Policy for handling information related to an information subject's gender and sexual orientation, which will be afforded heightened confidentiality.Description: A DNA segment that contributes to phenotype/function.General care performed by a general practitioner or family doctor as a responsible provider for a patient.Gluten free diet for celiac disease.The medical service was provided to a patient in good faith that they had medical coverage, although no evidence of coverage was available before service was rendered.Description: Accuracy determined as per the GIS tier code system.List of observations in goal mood.Definition: A set of codes used to indicate a government program that is an organized structure for administering and funding coverage of a benefit package for covered parties meeting eligibility criteria, typically related to employment, health and financial status.Description: The school grade or level the patient was in when immunized.A grantor's terms of agreement to which a grantee may assent or dissent, and which may include an opportunity for a grantee to request restrictions or extensions.Description:Global Trade Item Number is an identifier for trade items developed by GS1 (comprising the former EAN International and Uniform Code Council).Used to allow measure developers to provide additional guidance for implementers to understand greater specificity than could be provided in the logic for data criteria.Description:HCPCS Level II (HCFA-assigned) and Carrier-assigned (Level III) modifiers are reported in Appendix A of CPT 2000 Standard Edition and in the Medicare Bulletin.Description: Health Record AttachmentDefinition:There should be no actions taken in fulfillment of a request that has been held or suspended.An observation of the hemolysis index of the specimen in g/LnullHealthcare encounter that takes place in the residence of the patient or a designeeIndicates that the observation is of a person?s living situation in a household including the household composition and circumstances.Definition: A health insurance policy that covers healthcare benefits by protecting covered parties from medical expenses arising from health conditions, sickness, or accidental injury as well as preventive care.The U.S.The U.S.Section 13405(a) of the Health Information Technology for Economic and Clinical Health Act (HITECH) stipulates the right of an individual to have disclosures regarding certain health care items or services for which the individual pays out of pocket in full restricted from a health plan.Definition: A government program that provides health coverage to individuals who are considered medically uninsurable or high risk, and who have been denied health insurance due to a serious health condition.Historical list of medications.Description: While the record was accepted in the repository, there is a more recent version of a record of this type.Policy for handling HIV or AIDS information, which will be afforded heightened confidentiality.Definition: Government administered and funded HIV-AIDS program for beneficiaries meeting financial and health status criteria.Description: Exposure participants' interaction occurred during the course of health care delivery or in a health care delivery setting, but did not involve the direct provision of care (e.g.Definition: A policy for a health plan that provides coverage for health care only through contracted or employed physicians and hospitals located in particular geographic or service areas.Description: Exposure interaction occurred in context of one providing care for the other, i.e.Description: Exposure participants' interaction occurred when both were patients being treated in the same (acute) health care delivery facility.Description: Exposure participants' interaction occurred when one visited the other who was a patient being treated in a health care delivery facility.Description: Exposure interaction occurred in context of domestic interaction, i.e.A security category label field value, which indicates that access and use of an IT resource is restricted to members of human resources department or workflow.Insurance policy that provides for an allotment of funds replenished on a periodic (e.g.Joint Federal/Provincial Sales TaxCustodian system must require human review and approval for permission requested.Communication of an agent from a person to a proximate person.Accommodations used in the care of diseases that are transmitted through casual contact or respiratory transmission.Definition: Consent to have healthcare information collected in an electronic health record.An observation that describes the icterus index of the specimen.Used by one system to inform another that it has received a container.Definition: Consent to have collected healthcare information disclosed.Information on whether an increase or decrease in score is the preferred result (e.g., a higher score indicates better quality OR a lower score indicates better quality OR quality is within a range).Description:The request is missing elements or contains elements which cause it to not meet the legal standards for actioning.Description: Image AttachmentDescription: A person enters an immunization due or received for a given patient.Description: A person reviews a list of immunizations due or received for a given patient.Definition:All information pertaining to a patient's vaccination records.The introduction of an immunogen with the intent of stimulating an immune response, aimed at preventing subsequent infections by more viable agents.A patient encounter where a patient is admitted by a hospital or equivalent facility, assigned to a location where patients generally stay at least overnight and provided with room, board, and continuous nursing service.A grantor's presumed assent to the grantee's terms of agreement is based on the grantor's behavior, which may result from not expressly assenting to the consent directive offered, or from having no right to assent or dissent offered by the grantee.A grantor's presumed assent to the grantee's terms of agreement, which is based on the grantor's behavior, and includes a right to dissent to certain terms.Definition: Services provided directly and through contracted and operated indigenous peoples health programs.Description:Contrast agent required for imaging study.Description:Provision of prescription or direction to consume a product for purposes of bowel clearance in preparation for a colonoscopy.Description:Provision of medication as a preventative measure during a treatment or other period of increased risk.Description:Provision of medication during pre-operative phase; e.g., antibiotics before dental surgery or bowel prep before colon surgery.Description:Provision of medication for pregnancy --e.g., vitamins, antibiotic treatments for vaginal tract colonization, etc.Communication of an agent to a living subject via an undetermined route.Definition: Consent to access healthcare information.Definition: Consent to access or "read" only, which entails that the information is not to be copied, screen printed, saved, emailed, stored, re-disclosed or altered in any way.Definition: Consent to access and save only, which entails that access to the saved copy will remain locked.Authorization to collect, access, use, or disclose specified patient health information in accordance with jurisdictional law, organizational policy, or a patient's consent directive, which may be implied, deemed, opt-in, opt-out, or explicit.Authorization to collect, access, use, or disclose specified patient health information as explicitly consented to by the subject of the information or the subject's representative.Authorization to collect, access, use, or disclose specified patient health information in accordance with judicial system protocol, such as in the case of a subpoena or court order.Authorization to collect, access, use, or disclose specified patient health information where deemed necessary to avert potential danger to other persons in accordance with jurisdictional law, organizational policy, or standards of practice.Authorization to collect, access, use, or disclose specified patient health information in accordance with emergency information transfer protocol dictated by jurisdictional law, organization policy, or standards of practice.Authorization to collect, access, use, or disclose specified patient health information necessary to avert potential public welfare risk in accordance with jurisdictional law, organizational policy, or standards of practice.Authorization to collect, access, use, or disclose specified patient health information for public health, welfare, and safety purposes in accordance with jurisdictional law, organizational policy, or standards of practice.The initial quantity of the specimen in inventoryThe first immunization administration in a series intended to produce immunityDescription: Exposure participants' interaction occurred in the course of one or both participants being incarcerated at a correctional facilityProposed therapy may be inappropriate or contraindicated because of a recorded patient intolerance to the proposed product.Intermediate diagnoses are those diagnoses documented for administrative purposes during the course of a hospital stay.Definition:The therapy action is being performed outside the bounds of the time period requestedAn observation that relates to factors that may potentially cause interference with the observationDescription: Exposure interaction was intimate, i.e.List of intolerance observations.Definition:A monitoring program that focuses on a drug which is under investigation and has not received regulatory approval for the condition being investigatedPayment is based on a payment intent for a previously submitted Invoice, based on formal adjudication results..Transaction counts and value totals by invoice type (e.g.Used by one system to inform another that the container is in position for specimen transfer (e.g., container removal from track, pipetting, etc.).Criteria for specifying the entities to be evaluated by a specific quality measure, based on a shared common set of characteristics (within a specific measurement set to which a given measure belongs).Criteria for specifying the patients to be evaluated by a specific quality measure, based on a shared common set of characteristics (within a specific measurement set to which a given measure belongs).Definition: Information re-disclosed without the patient's consent.Premium paid on service fees in compensation for practicing in a remote location.There is a clinical issue for the therapy that makes continuation of the therapy inappropriate.Describes the items counted by the measure (e.g., patients, encounters, procedures, etc.)A significant word that aids in discoverability.The ID of the patient, order, etc., was not found.The ID of the patient, order, etc., already exists.Description: Metadata associated with the identification (e.g.Categorization of types of observation that capture the main clinical knowledge subject which may be a medication, a laboratory test, a disease.Categorization of types of observation that capture a knowledge subtopic which might be treatment, etiology, or prognosis.Used by one system to inform another that the container has been released from that system.Proposed therapy may be inappropriate or contraindicated due to recent lab test resultsDescription: All information pertaining to a patient's lab test records (orders invalid input: '&' results)Custodian security system must assign and bind security labels in order to classify information created in the information systems under its control for collection, access, use and disclosure in accordance with applicable jurisdictional privacy policies associated with the target information.A clinician creates a request for a laboratory test to be done for a given patient.Description: Lab Results AttachmentA person reviews a list of laboratory results of a given patient.Proposed therapy may be inappropriate or contraindicated when breast-feedingCommunication of an agent from one living subject to another living subject through direct contact with mammalian milk or colostrum.Knowingly over the payor's published time limit for this invoice possibly due to a previous payor's delays in processing.law enforcement transportLDL PrecipitationDescription:The length of the data specified is greater than the maximum length defined for the element.Description:The length of the data specified falls out of the range defined for the element.Description:The length of the data specified is less than the minimum length defined for the element.A grouping of invoice element details including the ones specifying the lens fee and the lens dispensing cost that are being invoiced.A diet low in fat, particularly to patients with hepatic diseases.Definition: Maximum amount paid by payer or covered party; or maximum number of services or products covered under the policy or program during a covered party's lifetime.Description:Scope of responsibility taken-on for physician care of a patient as defined by a governmental licensing agency.Definition: A policy under which the insurer agrees to pay a sum of money upon the occurrence of the covered partys death.An observation used to describe the Lipemia Index of the specimen.Policy for handling information related to an information subject's living arrangement, which will be afforded heightened confidentiality.Temporary supply of a product without transfer of ownership for the product.Transaction counts and value totals by service location (e.g clinic).Policy for handling information related to the location of the information subject, which will be afforded heightened confidentiality.A low protein diet for patients with renal failure.A strictly liquid diet, that can be fully absorbed in the intestine, and therefore may not contain fiber.A diet low in sodium for patients with congestive heart failure and/or renal failure.Definition: An insurance policy that covers benefits for long-term care services people need when they no longer can care for themselves.Description: Exposure participants' interaction occurred in the course of one or both participants being resident at a long term care facility (second participant may be a visitor, worker, resident or a physical place or object within the facility).Description:A drug that can be prescribed (and reimbursed) only if it meets certain criteria.Used by one system to inform another that the container did not arrive at its next expected location.mandatory health programManual review of the invoice is requested.An increase in the amount charged as a percentage of the amount.Policy for handling information related to an information subject's marital status, which will be afforded heightened confidentiality.A clinician reviews a work list of medications to be administered to a given patient.Custodian system must render information unreadable and unusable by algorithmically transforming plaintext into ciphertext.Description:The number of repeating elements is above the maximum number of repetitions allowed.Master CardDefinition: Government mandated program providing coverage, disability income, and vocational rehabilitation for injuries sustained in the work place or in the course of employment.Description:The maximum quantity of this drug allowed to be administered within a particular time-range (month, year, lifetime) has been reached or exceeded.Provision of diagnostic and/or therapeutic treatment.Definition:All information pertaining to a patient's medical condition records.List of medications.A clinician creates a request for the administration of one or more medications to a given patient.The end date of the measurement period.Description: All information pertaining to a patient's mental health records.Definition: A health insurance policy that covers benefits for mental health services and prescriptions.Definition: Government administered and funded mental health program for beneficiaries meeting financial and mental health status criteria.A person reviews organisms of microbiology results of a given patient.A person reviews a list of microbiology results of a given patient.A person reviews the sensitivity test of microbiology results of a given patient.Definition: A government program that provides coverage for health services to military personnel, retirees, and dependents.Custodian must limit access and disclosure to the minimum information required to support an authorized user's purpose of use.Definition:The therapy action is being performed too soon after the previous occurrence based on the requested frequencyDescription:The number of repeating elements is below the minimum number of repetitions allowed.A charge to compensate the provider when a patient does not show for an appointment.Description:The specified element must be specified with a non-null value under certain conditions.Description:The specified element is mandatory and was not included in the instance.A person reviews a list of medication orders submitted to a given patientDescription: Digital Model AttachmentTransaction counts and value totals for each calendar month within the date range specified.A supply of a manufacturer sampleThe start date of the measurement period.The method of adjusting for clinical severity and conditions present at the start of care that can influence patient outcomes for making valid comparisons of outcome measures across providers.Describes how to combine information calculated based on logic in each of several populations into one summarized result.Information on whether an increase or decrease in score is the preferred result.The list of jurisdiction(s) for which the measure applies.Criteria for specifying the measure population as a narrative description (e.g., all patients seen in the Emergency Department during the measurement period).Criteria for specifying subjects who should be removed from the eMeasure's Initial Population and Measure Population.Type of person or organization that is expected to report the issue.The maximum time that may elapse following completion of the measure until the measure report must be sent to the receiver.Indicates how the calculation is performed for the eMeasure (e.g., proportion, continuous variable, ratio)Location(s) in which care being measured is rendered Usage Note: MSRSET is used rather than RoleCode because the setting applies to what is being measured, as opposed to participating directly in the health quality measure documantion itself).health quality measure topic typeThe time period for which the eMeasure applies.Indicates whether the eMeasure is used to examine a process or an outcome over time (e.g., Structure, Process, Outcome).Incident or accident as the result of a motor vehicle accidentA normal diet, i.e.Hypersensitivity to an agent caused by a mechanism other than an immunologic response to an initial exposureThe requesting party has insufficient authorization to invoke the interaction.Authorization for specified healthcare service(s) and/or product(s) denied.Insurance coverage is not in effect for healthcare service(s) and/or product(s).Maximum net amount that will be covered for the product or service specified.The act or process by which an acid and a base are combined in such proportions that the resulting compound is neutral.A no fat diet for acute hepatic diseases.Proposed therapy may interact with existing or recent natural health product therapyProhibition on disclosure without information subject's authorization.Prohibition on collection or storage of the information.No notification or opportunity is provided for a grantor to assent or dissent to a grantee's terms of agreement.Prohibition on disclosure without organizational approved patient restriction.Prohibition on disclosure without a consent directive from the information subject.Description:More than one element with the same value exists in the set.The type of injury that the injury coding specifies.Prohibition on Integration into other records.Prohibition on disclosure except to entities on specific access list.Prohibition on disclosure without an interagency service agreement or memorandum of understanding (MOU).Non-Payment Data.Any category of inpatient encounter except 'acute'Proposed therapy may interact with a non-prescription drug (e.g.Prohibition on disclosure without organizational authorization.Prohibition on disclosing information to patient, family or caregivers without attending provider's authorization.Description: Element in submitted message will not persist in data storage based on detected issue.Prohibition on collection of the information beyond time necessary to accomplish authorized purpose of use is prohibited.Acknowledgement of custodian notice of privacy practices.Prohibition on redisclosure without patient consent directive.Prohibition on redisclosure without a consent directive from the information subject.Prohibition on disclosure without authorization under jurisdictional law.Prohibition on associating de-identified or pseudonymized information with other information in a manner that could or does result in disclosing information intended to be masked.Prohibition on use of the information beyond the purpose of use initially authorized.Communication of an agent from any entity to a living subject while the living subject is in the patient role in a healthcare facility.Definition:The status of the request being fulfilled has changed such that it is no longer actionable.Definition:The therapy being performed is not sufficiently equivalent to the therapy which was requested.Definition:The therapy being performed is not generically equivalent (having the identical biological action) to the therapy which was requested.Definition:The therapy being performed is not therapeutically equivalent (having the same overall patient effect) to the therapy which was requested.Prohibition on disclosure except to principals with access permission to specific VIP information.added to help the parsersCriteria for specifying the processes or outcomes expected for each patient, procedure, or other unit of measurement defined in the denominator for proportion measures, or related to (but not directly derived from) the denominator for ratio measures (e.g., a numerator listing the number of central line blood stream infections and a denominator indicating the days per thousand of central line usage in a specific time period).Criteria for specifying instances that should not be included in the numerator data.Used by one system to inform another that the specific container is being processed by the equipment.Conveys the mandated workflow action that an information custodian, receiver, or user must perform.Provision of care of women during pregnancy, childbirth and immediate postpartum period.Proposed therapy may be inappropriate or contraindicated due to conditions or characteristics of the patientDescription: Indicates the valid antigen count.Description: Indicates whether an antigen is valid or invalid.Description: One or more records in the query response have a status of 'obsolete'.A clinician creates a request for a service to be performed for a given patient.A clinical Invoice Grouping consisting of one or more oral health services.Hypersensitivity resulting in an adverse reaction upon exposure to an agent.Provision of treatment and/or diagnosis related to tumors and/or cancer.Definition:A list of medications which the patient is intended to be administered only once.The medical service and/or product was provided to a patient that has coverage in another jurisdiction.Premium paid on service fees in compensation for practicing at a location other than normal working location.A grantor's assent to the terms of an agreement offered by a grantee without an opportunity for to dissent to any terms.A grantor's assent to the grantee's terms of an agreement with an opportunity for to dissent to certain grantor or grantee selected terms.A grantor's dissent to the terms of agreement offered by a grantee without an opportunity for to assent to any terms.A grantor's dissent to the grantee's terms of agreement except for certain grantor or grantee selected terms.Prohibition on disclosure except as permitted by the information originator.A person reviews a list of orders submitted to a given patient.The service provided is required for orthodontic purposes.Medicines designated in this way may be supplied for patient use without a prescription.Accommodations in which there is only 1 bed.Phenylketonuria diet.HealthCare facility preferred accommodation invoice.Provision of care for patients who are living or dying from an advanced illness.Paper documentation (or other physical format) with supporting or additional information to follow.Patient is supplied with parenteral nutrition, typically described in terms of i.v.Communication of an agent from a living subject or environmental source to a living subject where the acquisition of the agent is not via the alimentary canal.Indicates that the ICSR is describing problems that a patient experienced after receiving a vaccine product.A person enters documentation about a given patient.A person provides a patient-specific education handout to a patient.A person (e.g., clinician, the patient herself) reviews patient information in the electronic medical record.Definition:The proposed therapy goes against preferences or consent constraints recorded in the patient's record.Definition:The proposed therapy goes against preferences or consent constraints recorded in the patient's record.A pathologist enters a report for a given patient.A person reviews a pathology report of a given patient.The guarantor, who may be the patient, pays the entire charge for a service.Transaction counts and value totals by each instance of an invoice payee.Transaction counts and value totals by each instance of an invoice payor.An account representing charges and credits (financial transactions) for a patient's encounter.Identifies the total net amount of all Invoice Groupings that were paid prior to the specified time period (based on payment date), subsequently nullified in the specified period and submitted electronically.Identifies the total number of all Invoice Groupings that were paid prior to the specified time period (based on payment date), subsequently nullified in the specified period and submitted electronically.Identifies the total net amount of all Invoice Groupings that were paid prior to the specified time period (based on payment date), subsequently nullified in the specified period and submitted manually.Identifies the total number of all Invoice Groupings that were paid prior to the specified time period (based on payment date), subsequently nullified in the specified period and submitted manually.Identifies the total net amount of all Invoice Groupings that were paid during the specified time period (based on payment date), subsequently nullified in the specified period and submitted electronically.Identifies the total number of all Invoice Groupings that were paid during the specified time period (based on payment date), subsequently cancelled in the specified period and submitted electronically.Identifies the total net amount of all Invoice Groupings that were paid during the specified time period (based on payment date), subsequently nullified in the specified period and submitted manually.Identifies the total number of all Invoice Groupings that were paid during the specified time period (based on payment date), subsequently nullified in the specified period and submitted manually.Identifies the total net amount of all Invoice Groupings that were paid prior to the specified time period (based on payment date) that do not match a specified payee (e.g.Identifies the total number of all Invoice Groupings that were paid prior to the specified time period (based on payment date) that do not match a specified payee (e.g.Identifies the total net amount of all Invoice Groupings that were paid prior to the specified time period (based on payment date) that do not match a specified payee (e.g.Identifies the total number of all Invoice Groupings that were paid prior to the specified time period (based on payment date) that do not match a specified payee (e.g.Identifies the total net amount of all Invoice Groupings that were paid during the specified time period (based on payment date) that do not match a specified payee (e.g.Identifies the total number of all Invoice Groupings that were paid during the specified time period (based on payment date) that do not match a specified payee (e.g.Identifies the total net amount of all Invoice Groupings that were paid during the specified time period (based on payment date) that do not match a specified payee (e.g.Identifies the total number of all Invoice Groupings that were paid during the specified time period (based on payment date) that do not match a specified payee (e.g.Identifies the total net amount of all Invoice Groupings that were paid prior to the specified time period (based on payment date) that match a specified payee (e.g.Identifies the total number of all Invoice Groupings that were paid prior to the specified time period (based on payment date) that match a specified payee (e.g.Identifies the total net amount of all Invoice Groupings that were paid prior to the specified time period (based on payment date) that match a specified payee (e.g.Identifies the total number of all Invoice Groupings that were paid prior to the specified time period (based on payment date) that match a specified payee (e.g.Identifies the total net amount of all Invoice Groupings that were paid during the specified time period (based on payment date) that match a specified payee (e.g.Identifies the total number of all Invoice Groupings that were paid during the specified time period (based on payment date) that match a specified payee (e.g.Identifies the total net amount of all Invoice Groupings that were paid during the specified time period (based on payment date) that match a specified payee (e.g.Identifies the total number of all Invoice Groupings that were paid during the specified time period (based on payment date) that match a specified payee (e.g.Policy for handling information reported by the patient about another person, e.g., a family member, which will be afforded heightened confidentiality.Proposed therapy is outside of the standard practice for a pediatric patient.Provision of diagnosis and treatment of diseases and disorders affecting children.Anticipated or actual periodic fee associated with treating a patient.Transaction counts and value totals for the date range specified.The amount for a performance bonus that is being requested from a payor for the performance of certain services (childhood immunizations, influenza immunizations, mammograms, pap smears) on a sliding scale.Custodian security system must persist the binding of security labels to classify information received or imported by information systems under its control for collection, access, use and disclosure in accordance with applicable jurisdictional privacy policies associated with the target information.Pharmaceutical care performed by a pharmacist.Provision of treatment for physical injury.Public Insurance has been exhausted.Payment initiated by the payor as the result of adjudicating a paper (original, may have been faxed) invoice.Description: An interaction where the exposure participants were both present in the same location/place/space.Communication of an agent from a living subject to the progeny of that living subject via agent migration across the maternal-fetal placental membranes while in utero.A similar or identical therapy was recently ordered by a different practitioner.This patient was recently supplied a similar or identical therapy from a different pharmacy or supplier.Definition: A type of insurance that covers damage to or loss of the policyholderaTMs property by providing payments for damages to property damage or the injury or death of living subjects.A single point denoted by a single (column,row) pair, or multiple points each denoted by a (column,row) pair.A series of connected line segments with ordered vertices denoted by (column,row) pairs; if the first and last vertices are the same, it is a closed polygon.Definition: A policy for a health plan that has features of both an HMO and a FFS plan.Definition: A network-based, managed care plan that allows a covered party to choose any health care provider.An amount that was owed to the payor as indicated, by a carry forward adjusment, in a previous payment advicenullA grouping of invoice element details including the one specifying the product (good or supply) being invoiced.Definition: Maximum amount paid by payer or covered party; or maximum number of services/products covered under the policy or program by time period specified by the effective time on the act.The dilution of the specimen made prior to being loaded onto analytical equipmentAn observation about how important a preference is to the target of the preference.Proposed therapy may be inappropriate or contraindicated during pregnancyA patient encounter where patient is scheduled or planned to receive service delivery in the future, and the patient is given a pre-admission account number.Definition:The same or similar treatment has previously been attempted with the patient without achieving a positive effect.Custodian must create and/or maintain human readable security label tags as required by policy.Description:Indicates that a result is incomplete.Definition:A list of medications which the patient will consume intermittently based on the behavior of the condition for which the medication is indicated.Professional association fee that is collected by the payor from the practitioner/provider on behalf of the associationList of problem observations.A clinician enters a problem for a given patient.A person reviews a list of problems of a given patient.Transaction counts and value totals by Provider Identifier.For sensitive information relayed by or about a patient, which is deemed sensitive within the enterprise (i.e., by default regardless of whether the patient requested that the information be deemed sensitive.) If there is a jurisdictional mandate, then use the applicable ActPrivacyLaw code system, and specify the law rather than or in addition to this more generic code.private transportCustodian system must strip information of data that would allow the identification of the source of the information or the information subject.Tax levied by the provincial or state jurisdiction such as Provincial Sales TaxDefinition:All information pertaining to a patient's professional service records (such as smoking cessation, counseling, medication review, mental health).Policy for handling psychiatry information, which will be afforded heightened confidentiality.Provision of treatment of psychiatric disorder relating to mental illness.Description: Exposure participants' interaction occurred during the course of health care delivery by a provider (e.g.Insurance policy funded by a public health system such as a provincial or national health plan.public transportAllows provider to explain lateness of invoice to a subsequent payor.Status is used by one system to inform another that the processing has been completed, but the container has not been released from that system.Policy for handling information related to an information subject's race, which will be afforded heightened confidentiality.A radiologist enters a report for a given patient.A person reviews a radiology report of a given patient.Proposed therapy may be inappropriate or contraindicated because of a recorded patient allergy to a cross-sensitivity related product.Proposed therapy may be inappropriate or contraindicated because of a recorded prior adverse reaction to a cross-sensitivity related product.Succinct statement of the need for the measure.A diet that seeks to reduce body fat, typically low energy content (800-1600 kcal).Proposed therapy may be inappropriate or contraindicated based on the potential for a patient reaction to the proposed productThe addition of calcium back to a specimen after it was removed by chelating agentsRetroactive adjustment such as fee rate adjustment due to contract negotiations.Custodian system must remove information, which is not authorized to be access, used, or disclosed from records made available to otherwise authorized users.Identifies bibliographic citations or references to clinical practice guidelines, sources of evidence, or other relevant materials supporting the intent and rationale of the eMeasure.Specifies whether or not further testing may be automatically or manually initiated on specimens.Rules of practice do not require a physician's referral for the provider to perform a billable service.Conveys prohibited actions which an information custodian, receiver, or user is not permitted to perform unless otherwise authorized or permitted under specified circumstances.Definition: An agreement between two or more insurance companies by which the risk of loss is proportioned.Policy for handling information related to an information subject's religious affiliation, which will be afforded heightened confidentiality.Description: A person enters a health care reminder for a given patient.Description: A person reviews a list of health care reminders for a given patient.Temporary supply of a product with financial compensation, without transfer of ownership for the product.Description:This observation represents an 'average' or 'expected' half-life typical of the product.Description:The number of repeating elements falls outside the range of the allowed number of repetitions.This Observation Series type contains waveforms of a "representative beat" (a.k.a.The same service was delivered within a time period that would usually indicate a duplicate billing.The value of the dilution of a sample after it had been analyzed at a prior dilution valueA security category label field value, which indicates that access and use of an IT resource is restricted to members of a research project.Definition: Consent to have healthcare information in an electronic health record accessed for research purposes.A charge is requested because the patient failed to pick up the item and it took an amount of time to return it to stock for future use.Definition: A government mandated program with specific eligibility requirements based on premium contributions made during employment, length of employment, age, and employment status, e.g., being retired, disabled, or a dependent of a covered party under this program.Bonus payments based on performance, volume, etc.A type of transaction that represents a reversal of a previous charge for a service or product.A fill against an order that has already been filled (or partially filled) at least once.A refill where the quantity supplied is equal to one full repetition of the ordered amount.A refill where the quantity supplied is equal to one full repetition of the ordered amount.The first fill against an order that has already been filled at least once at another facility.The first fill against an order that has already been filled at least once at another facility and where the strength supplied is less than the ordered strength (e.g.A refill where the quantity supplied is less than one full repetition of the ordered amount.A refill where the quantity supplied is less than one full repetition of the ordered amount.A fill against an order that has already been filled (or partially filled) at least once and where the strength supplied is less than the ordered strength (e.g.This Observation type contains ECG "rhythm" waveforms.Proposed therapy may be inappropriate or contraindicated because of a recorded patient intolerance to a cross-sensitivity related product.A person reviews a Risk Assessment Instrument report of a given patient.List of risk factor observations.A security category label field value, which indicates that access and use of an IT resource is restricted to members of records management department or workflow.A fully specified bounded Region of Interest (ROI) delineates a ROI in which only those dimensions participate that are specified by boundary criteria, whereas all other dimensions are excluded.A partially specified bounded Region of Interest (ROI) specifies a ROI in which at least all values in the dimensions specified by the boundary criteria participate.A billing arrangement where funding is based on a list of individuals registered as patients of the Provider.Proposed therapy may be inappropriate or contraindicated because of a potential patient reaction to a cross-sensitivity related product.Definition: Consent to have de-identified healthcare information in an electronic health record that is accessed for research purposes, but without consent to re-identify the information under any circumstance.Definition: Consent to have de-identified healthcare information in an electronic health record that is accessed for research purposes re-identified under specific circumstances outlined in the consent.Some form of prescription is required before the related medicine can be supplied for a patient.Definition:All information pertaining to a patient's medication records (orders, dispenses and other active medications).Pharmacy dispense invoice for a compound.Pharmacy dispense invoice not involving a compoundUniquely designed and elegantly decorated accommodations with many amenities available for an additional charge.Definition:A drug that requires prior approval (to be reimbursed) before being dispensedDescription:A drug that requires special access permission to be prescribed and dispensed.Definition: Government administered and funded program to support provision of care to underserved populations through safety net clinics.Transfer of ownership for a product for financial compensation.Identifies the total net amount billed for all submitted Invoice Groupings within a time period and submitted electronically.Identifies the total number of submitted Invoice Groupings within a time period and submitted electronically.Clinical services invoice where the Invoice Group contains one billable item for multiple clinical services in one or more sessions.Identifies the total net amount billed for all submitted Invoice Groupings that were nullified within a time period and submitted electronically.Identifies the total number of submitted Invoice Groupings that were nullified within a time period and submitted electronically.Identifies the total net amount billed for all submitted Invoice Groupings that are pended or held by the payor, within a time period and submitted electronically.Identifies the total number of submitted Invoice Groupings that are pended or held by the payor, within a time period and submitted electronically.Policy for handling sickle cell disease information, which is afforded heightened confidentiality.A diet that avoids ingredients that might cause digestion problems, e.g., avoid excessive fat, avoid too much fiber (cabbage, peas, beans).Description: The school the patient attended when immunized.Description: The school division or district associated with the patient during the immunization event.Incident or accident is the result of a school place accident.Description: Exposure participants' interaction occurred in an academic setting (e.g., participants are fellow students, or student and teacher).Comparison of results across strata can be used to show where disparities exist or where there is a need to expose differences in results.Policy for handling sexual assault, abuse, or domestic violence information, which will be afforded heightened confidentiality.Type of security metadata observation made about the alteration integrity of an IT resource (data, information object, service, or system capability), which indicates the mechanism used for authorized transformations of the resource.Type of security metadata observation made about the category of an IT resource (data, information object, service, or system capability), which may be used to make access control decisions.Type of security metadata observation made about the classification of an IT resource (data, information object, service, or system capability), which may be used to make access control decisions.Type of security metadata observation made about the control of an IT resource (data, information object, service, or system capability), which may be used to make access control decisions.Type of security metadata observation made about the data integrity of an IT resource (data, information object, service, or system capability), which indicates the security mechanism used to preserve resource accuracy and consistency.Type of security metadata observation made about the integrity confidence of an IT resource (data, information object, service, or system capability), which may be used to make access control decisions.Type of security metadata observation made about the integrity of an IT resource (data, information object, service, or system capability), which may be used to make access control decisions.Type of security metadata observation made about the integrity provenance of an IT resource (data, information object, service, or system capability), which indicates the entity that made assertions about the resource.Type of security metadata observation made about the provenance integrity of an IT resource (data, information object, service, or system capability), which indicates the lifecycle completeness of an IT resource in terms of workflow status such as its creation, modification, suspension, and deletion; locations in which the resource has been collected or archived, from which it may be retrieved, and the history of its distribution and disclosure.Type of security metadata observation made about the integrity provenance of an IT resource (data, information object, service, or system capability), which indicates the entity that reported the existence of the resource.Type of security metadata observation made about the integrity status of an IT resource (data, information object, service, or system capability), which may be used to make access control decisions.An observation identifying security metadata about an IT resource (data, information object, service, or system capability), which may be used to make access control decisions.An observation identifying trust metadata about an IT resource (data, information object, service, or system capability), which may be used as a trust attribute to populate a computable trust policy, trust credential, trust assertion, or trust label field in a security label or trust policy, which are principally used for authentication, authorization, and access control decisions.Types of security policies that further specify the ActClassPolicy value set.Transaction counts and value totals by each instance of a messaging application on a single processor.A billing arrangement where a Provider charges a sum to provide a group (volume) of interventions/procedures to one or more patients within a defined period of time, typically on the same date.A subjective evaluation of the seriousness or intensity associated with another observation.Policy for handling sexuality and reproductive health information, which will be afforded heightened confidentiality.Communication of an agent from one living subject to another living subject through direct contact with genital or oral tissues as part of a sexual act.Types of sensitivity policies that apply to Acts.An emergency supply where the expectation is that a formal order authorizing the supply will be provided at a later date.Information about provision of social services.Definition: A social service program funded by a public or governmental entity.Description: An interaction where the exposure participants are social associates or members of the same extended familyAccommodations in which there are 2 beds.That total amount of the eligible charges which a covered party must periodically pay for services and/or products prior to the Medicaid program providing any coverage.Definition: A characteristic of an oral solid dosage form of a medicinal product, indicating whether it has one or more coatings such as sugar coating, film coating, or enteric coating.Definition: A characteristic of an oral solid dosage form of a medicinal product, specifying the color or colors that most predominantly define the appearance of the dose form.Description: A characteristic representing a single file reference that contains two or more views of the same dosage form of the product; in most cases this should represent front and back views of the dosage form, but occasionally additional views might be needed in order to capture all of the important physical characteristics of the dosage form.Definition: A characteristic of an oral solid dosage form of a medicinal product, specifying the alphanumeric text that appears on the solid dosage form, including text that is embossed, debossed, engraved or printed with ink.Definition: A characteristic of an oral solid dosage form of a medicinal product, specifying the number of equal pieces that the solid dosage form can be divided into using score line(s).Description: A characteristic of an oral solid dosage form of a medicinal product, specifying the two dimensional representation of the solid dose form, in terms of the outside perimeter of a solid dosage form when the dosage form, resting on a flat surface, is viewed from directly above, including slight rounding of corners.Definition: A characteristic of an oral solid dosage form of a medicinal product, specifying the longest single dimension of the solid dosage form as a physical quantity in the dimension of length (e.g., 3 mm).Definition: A characteristic of an oral solid dosage form of a medicinal product, to describe whether or not the medicinal product has a mark or symbol appearing on it for easy and definite recognition.Incident or accident is the result of a sporting accident.Description:Specimen has been received by the participating organization/department.An encounter where the patient is admitted to a health care facility for a predetermined length of time, usually less than 24 hours.Policy for handling information related to a provider of sensitive services, which will be afforded heightened confidentiality.Description:Specimen has been placed into storage at a participating location.Policy for handling sexually transmitted disease information, which will be afforded heightened confidentiality.The act of putting something away for safe keeping.Description:Specimen has been put in transit to a participating receiver.Describes the strata for which the measure is to be evaluated.Proposed therapy may be inappropriate or ineffective because the start of administration is too late after the onset of the conditionDefinition: A health insurance policy that covers benefits for substance use services.Definition: Government administered and funded substance use program for beneficiaries meeting financial, substance use behavior, and health status criteria.Definition: A government health program that provides coverage on a fee for service basis for health services to persons meeting eligibility criteria such as income, location of residence, access to other coverages, health condition, and age, the cost of which is to some extent subsidized by public funds.Definition: A government health program that provides coverage for health services to persons meeting eligibility criteria such as income, location of residence, access to other coverages, health condition, and age, the cost of which is to some extent subsidized by public funds.Definition: A government health program that provides coverage through managed care contracts for health services to persons meeting eligibility criteria such as income, location of residence, access to other coverages, health condition, and age, the cost of which is to some extent subsidized by public funds.Description: An interaction where the exposure participants shared or co-used a common substance (e.g.Definition: A government health program that provides coverage for health services to persons meeting eligibility criteria for a supplemental health policy or program such as income, location of residence, access to other coverages, health condition, and age, the cost of which is to some extent subsidized by public funds.A diet that is not intended to be complete but is added to other diets.Description: One or more records in the query response have been suppressed due to consent or privacy restrictions.Provision of surgical treatment.Definition: A risk or part of a risk for which there is no normal insurance market available.This is not really a diet, since it contains little nutritional value, but is essentially just water.A fill where the remainder of a 'complete' fill is provided after a trial fill has been provided.Policy for handling information not to be initially disclosed or discussed with patient except by a physician assigned to patient in this case.A fill where the remainder of a 'complete' fill is provided after a trial fill has been provided and where the strength supplied is less than the ordered strength (e.g.Description: The patient's teacher when immunized.A fill where a small portion is provided to allow for determination of the therapy effectiveness and patient tolerance.A fill where a small portion is provided to allow for determination of the therapy effectiveness and patient tolerance and also where the strength supplied is less than the ordered strength (e.g.Description:Proposed therapy may be inappropriate or ineffective based on the proposed start or end time.A sequence of values in the "absolute" time domain.A sequence of values in a "relative" time domain.Definition:The therapy is being performed at a time which diverges from the time the therapy was requestedTitle 38 Part 1-protected information may only be disclosed to a third party with the special written consent of the patient except where expressly authorized by 38 USC 7332.Definition: Life insurance under which the benefit is payable only if the insured dies during a specified period.The patient is receiving a subsequent fill significantly later than would be expected based on the amount previously supplied and the therapy dosage instructionsThe patient is receiving a subsequent fill significantly earlier than would be expected based on the amount previously supplied and the therapy dosage instructionsProposed therapy may interact with an existing or recent therapeutic productFees deducted on behalf of a payee for charges based on a per-transaction or time-period (e.g.Can be a URL or hyperlinks that link to the transmission formats that are specified for a particular reporting program.Transfer of ownership for a product.A charge to cover the cost of travel time and/or cost in conjuction with providing a service or product.Description: An interaction where the exposure participants traveled together in/on the same vehicle/trip (e.g.Communication of an agent from one living subject to another living subject through direct contact with blood or blood products where the contact with blood is part of a therapeutic procedure.Type of security metadata about the formal declaration by an authority or neutral third party that validates the technical, security, trust, and business practice conformance of Trust Agents to facilitate security, interoperability, and trust among participants within a security domain or trust framework.Type of security metadata observation made about the formal declaration by an authority or neutral third party that validates the technical, security, trust, and business practice conformance of Trust Agents to facilitate security, interoperability, and trust among participants within a security domain or trust framework.Type of security metadata about privacy and security requirements with which a security domain must comply.Type of security metadata observation made about privacy and security requirements with which a security domain must comply.Type of security metadata about the digital quality or reliability of a trust assertion, activity, capability, information exchange, mechanism, process, or protocol.Type of security metadata about a set of security-relevant data issued by a security authority or trusted third party, together with security information which is used to provide the integrity and data origin authentication services for an IT resource (data, information object, service, or system capability).Type of security metadata observation made about a set of security-relevant data issued by a security authority or trusted third party, together with security information which is used to provide the integrity and data origin authentication services for an IT resource (data, information object, service, or system capability).Type of security metadata about a complete set of contracts, regulations, or commitments that enable participating actors to rely on certain assertions by other actors to fulfill their information security requirements.Type of security metadata observation made about a complete set of contracts, regulations or commitments that enable participating actors to rely on certain assertions by other actors to fulfill their information security requirements.Type of security metadata observation made about the digital quality or reliability of a trust assertion, activity, capability, information exchange, mechanism, process, or protocol.Type of security metadata about a security architecture system component that supports enforcement of security policies.Type of security metadata observation made about a security architecture system component that supports enforcement of security policies.A supply action that provides sufficient material for a single dose.A supply action that provides sufficient material for a single dose via multiple products.The filtration of a colloidal substance through a semipermeable medium that allows only the passage of small molecules.Definition: Life insurance under which the benefit is payable upon the insuredaTMs death or diagnosis of a terminal illness.Definition: A form of insurance protection that provides additional liability coverage after the limits of your underlying policy are reached.Definition: An automobile insurance policy under which the insurance company will indemnify a loss for which another motorist is liable if that motorist is unable to pay because he or she is uninsured.Maximum unit price that will be covered for the authorized product or service.Maximum number of items that will be covered of the product or service specified.The service provided is not related to another billed service.Description:United Nations Standard Products and Services Classification, managed by Uniform Code Council (UCC): www.unspsc.orgDescription:Universal Product Code is one of a wide variety of bar code languages widely used in the United States and Canada for items in stores.Custodian security system must declassify information assigned security labels by instantiating a new version of the classified information so as to break the binding of the classifying security label when assigning a new security label that marks the information as classified at a more protected level in accordance with applicable jurisdictional privacy policies associated with the target information.Premium paid on service fees in compensation for providing an expedited response to an urgent situation.Usage notes.VisaIndicates that the ICSR is describing a problem with the actual vaccine product such as physical defects (cloudy, particulate matter) or inability to confer immunity.Description:The specified element did not pass business-rule validation.Communication of an agent from a living subject acting as a required intermediary in the agent transmission process to a recipient living subject via direct contact.The provider has received a verbal permission from an authoritative source to perform the service or supply the item being invoiced.Definition: Services provided directly and through contracted and operated veteran health programs.Definition:Indicates that the paper version of the record has, should be or is being verified against the electronic version.Definition: Set of codes for a policy that provides coverage for health care expenses arising from vision services.Diet with low content of the amino-acids valin, leucin, and isoleucin, for "maple syrup disease."An observation that reports the volume of a sample.A patient encounter where the patient and the practitioner(s) are not in the same physical location.Vision dispense invoice for up to 2 lens (left and right), frame and optional discount.Accommodations in which there are 3 or more beds.Communication of an agent from a contaminated water source to a living subject whether the water is ingested as a food or not.Insurance policy for injuries sustained in the work place or in the course of employment.Transaction counts and value totals for each calendar week within the date range specified.Description: A person enters a wellness or preventive care reminder for a given patient.Description: A person reviews a list of wellness or preventive care reminders for a given patient.nullDescription: Work Injury related additional Information AttachmentDescription: Exposure interaction occurred in a work setting, i.e.Incident or accident is the result of a work place accidentDefinition: Government mandated program providing coverage, disability income, and vocational rehabilitation for injuries sustained in the work place or in the course of employment.Used by one system to inform another that the container is no longer available within the scope of the system (e.g., tube broken or discarded).Description: Digital X-Ray AttachmentTransaction counts and value totals for each calendar year within the date range specified. -
Method Summary
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Enum Constant Details
-
_ACTACCOUNTCODE
An account represents a grouping of financial transactions that are tracked and reported together with a single balance. Examples of account codes (types) are Patient billing accounts (collection of charges), Cost centers; Cash. -
ACCTRECEIVABLE
An account for collecting charges, reversals, adjustments and payments, including deductibles, copayments, coinsurance (financial transactions) credited or debited to the account receivable account for a patient's encounter. -
CASH
Cash -
CC
Description: Types of advance payment to be made on a plastic card usually issued by a financial institution used of purchasing services and/or products. -
AE
American Express -
DN
Diner's Club -
DV
Discover Card -
MC
Master Card -
V
Visa -
PBILLACCT
An account representing charges and credits (financial transactions) for a patient's encounter. -
_ACTADJUDICATIONCODE
Includes coded responses that will occur as a result of the adjudication of an electronic invoice at a summary level and provides guidance on interpretation of the referenced adjudication results. -
_ACTADJUDICATIONGROUPCODE
Catagorization of grouping criteria for the associated transactions and/or summary (totals, subtotals). -
CONT
Transaction counts and value totals by Contract Identifier. -
DAY
Transaction counts and value totals for each calendar day within the date range specified. -
LOC
Transaction counts and value totals by service location (e.g clinic). -
MONTH
Transaction counts and value totals for each calendar month within the date range specified. -
PERIOD
Transaction counts and value totals for the date range specified. -
PROV
Transaction counts and value totals by Provider Identifier. -
WEEK
Transaction counts and value totals for each calendar week within the date range specified. -
YEAR
Transaction counts and value totals for each calendar year within the date range specified. -
AA
The invoice element has been accepted for payment but one or more adjustment(s) have been made to one or more invoice element line items (component charges). Also includes the concept 'Adjudicate as zero' and items not covered under a particular Policy. Invoice element can be reversed (nullified). Recommend that the invoice element is saved for DUR (Drug Utilization Reporting). -
ANF
The invoice element has been accepted for payment but one or more adjustment(s) have been made to one or more invoice element line items (component charges) without changing the amount. Invoice element can be reversed (nullified). Recommend that the invoice element is saved for DUR (Drug Utilization Reporting). -
AR
The invoice element has passed through the adjudication process but payment is refused due to one or more reasons. Includes items such as patient not covered, or invoice element is not constructed according to payer rules (e.g. 'invoice submitted too late'). If one invoice element line item in the invoice element structure is rejected, the remaining line items may not be adjudicated and the complete group is treated as rejected. A refused invoice element can be forwarded to the next payer (for Coordination of Benefits) or modified and resubmitted to refusing payer. Invoice element cannot be reversed (nullified) as there is nothing to reverse. Recommend that the invoice element is not saved for DUR (Drug Utilization Reporting). -
AS
The invoice element was/will be paid exactly as submitted, without financial adjustment(s). If the dollar amount stays the same, but the billing codes have been amended or financial adjustments have been applied through the adjudication process, the invoice element is treated as "Adjudicated with Adjustment". If information items are included in the adjudication results that do not affect the monetary amounts paid, then this is still Adjudicated as Submitted (e.g. 'reached Plan Maximum on this Claim'). Invoice element can be reversed (nullified). Recommend that the invoice element is saved for DUR (Drug Utilization Reporting). -
_ACTADJUDICATIONRESULTACTIONCODE
Actions to be carried out by the recipient of the Adjudication Result information. -
DISPLAY
The adjudication result associated is to be displayed to the receiver of the adjudication result. -
FORM
The adjudication result associated is to be printed on the specified form, which is then provided to the covered party. -
_ACTBILLABLEMODIFIERCODE
Definition:An identifying modifier code for healthcare interventions or procedures. -
CPTM
Description:CPT modifier codes are found in Appendix A of CPT 2000 Standard Edition. -
HCPCSA
Description:HCPCS Level II (HCFA-assigned) and Carrier-assigned (Level III) modifiers are reported in Appendix A of CPT 2000 Standard Edition and in the Medicare Bulletin. -
_ACTBILLINGARRANGEMENTCODE
The type of provision(s) made for reimbursing for the deliver of healthcare services and/or goods provided by a Provider, over a specified period. -
BLK
A billing arrangement where a Provider charges a lump sum to provide a prescribed group (volume) of services to a single patient which occur over a period of time. Services included in the block may vary. This billing arrangement is also known as Program of Care for some specific Payors and Program Fees for other Payors. -
CAP
A billing arrangement where the payment made to a Provider is determined by analyzing one or more demographic attributes about the persons/patients who are enrolled with the Provider (in their practice). -
CONTF
A billing arrangement where a Provider charges a lump sum to provide a particular volume of one or more interventions/procedures or groups of interventions/procedures. -
FINBILL
A billing arrangement where a Provider charges for non-clinical items. This includes interest in arrears, mileage, etc. Clinical content is not included in Invoices submitted with this type of billing arrangement. -
ROST
A billing arrangement where funding is based on a list of individuals registered as patients of the Provider. -
SESS
A billing arrangement where a Provider charges a sum to provide a group (volume) of interventions/procedures to one or more patients within a defined period of time, typically on the same date. Interventions/procedures included in the session may vary. -
FFS
A billing arrangement where a Provider charges a separate fee for each intervention/procedure/event or product. Fee for Service is used when an individual intervention/procedure/event is used for billing purposes. In other words, fees are associated with the intervention/procedure/event. For example, a specific CCI (Canadian Classification of Interventions) code has an associated fee and is used for billing purposes. -
FFPS
A first fill where the quantity supplied is less than one full repetition of the ordered amount. (e.g. If the order was 90 tablets, 3 refills, a partial fill might be for only 30 tablets.) and also where the strength supplied is less than the ordered strength (e.g. 10mg for an order of 50mg where a subsequent fill will dispense 40mg tablets) -
FFCS
A first fill where the quantity supplied is equal to one full repetition of the ordered amount. (e.g. If the order was 90 tablets, 3 refills, a complete fill would be for the full 90 tablets) and also where the strength supplied is less than the ordered strength (e.g. 10mg for an order of 50mg where a subsequent fill will dispense 40mg tablets). -
TFS
A fill where a small portion is provided to allow for determination of the therapy effectiveness and patient tolerance and also where the strength supplied is less than the ordered strength (e.g. 10mg for an order of 50mg where a subsequent fill will dispense 40mg tablets). -
_ACTBOUNDEDROICODE
Type of bounded ROI. -
ROIFS
A fully specified bounded Region of Interest (ROI) delineates a ROI in which only those dimensions participate that are specified by boundary criteria, whereas all other dimensions are excluded. For example a ROI to mark an episode of "ST elevation" in a subset of the EKG leads V2, V3, and V4 would include 4 boundaries, one each for time, V2, V3, and V4. -
ROIPS
A partially specified bounded Region of Interest (ROI) specifies a ROI in which at least all values in the dimensions specified by the boundary criteria participate. For example, if an episode of ventricular fibrillations (VFib) is observed, it usually doesn't make sense to exclude any EKG leads from the observation and the partially specified ROI would contain only one boundary for time indicating the time interval where VFib was observed. -
_ACTCAREPROVISIONCODE
Description:The type and scope of responsibility taken-on by the performer of the Act for a specific subject of care. -
_ACTCREDENTIALEDCARECODE
Description:The type and scope of legal and/or professional responsibility taken-on by the performer of the Act for a specific subject of care as described by a credentialing agency, i.e. government or non-government agency. Failure in executing this Act may result in loss of credential to the person or organization who participates as performer of the Act. Excludes employment agreements. Example:Hospital license; physician license; clinic accreditation. -
_ACTCREDENTIALEDCAREPROVISIONPERSONCODE
Description:The type and scope of legal and/or professional responsibility taken-on by the performer of the Act for a specific subject of care as described by an agency for credentialing individuals. -
CACC
Description:Scope of responsibility taken on for specialty care as defined by the respective Specialty Board. -
CAIC
Description:Scope of responsibility taken on for specialty care as defined by the respective Specialty Board. -
CAMC
Description:Scope of responsibility taken on for specialty care as defined by the respective Specialty Board. -
CANC
Description:Scope of responsibility taken on for specialty care as defined by the respective Specialty Board. -
CAPC
Description:Scope of responsibility taken on for specialty care as defined by the respective Specialty Board. -
CBGC
Description:Scope of responsibility taken on for specialty care as defined by the respective Specialty Board. -
CCCC
Description:Scope of responsibility taken on for specialty care as defined by the respective Specialty Board. -
CCGC
Description:Scope of responsibility taken on for specialty care as defined by the respective Specialty Board. -
CCPC
Description:Scope of responsibility taken on for specialty care as defined by the respective Specialty Board. -
CCSC
Description:Scope of responsibility taken on for specialty care as defined by the respective Specialty Board. -
CDEC
Description:Scope of responsibility taken on for specialty care as defined by the respective Specialty Board. -
CDRC
Description:Scope of responsibility taken on for specialty care as defined by the respective Specialty Board. -
CEMC
Description:Scope of responsibility taken on for specialty care as defined by the respective Specialty Board. -
CFPC
Description:Scope of responsibility taken on for specialty care as defined by the respective Specialty Board. -
CIMC
Description:Scope of responsibility taken on for specialty care as defined by the respective Specialty Board. -
CMGC
Description:Scope of responsibility taken on for specialty care as defined by the respective Specialty Board. -
CNEC
Description:Scope of responsibility taken on for specialty care as defined by the respective Specialty Board -
CNMC
Description:Scope of responsibility taken on for specialty care as defined by the respective Specialty Board. -
CNQC
Description:Scope of responsibility taken on for specialty care as defined by the respective Specialty Board. -
CNSC
Description:Scope of responsibility taken on for specialty care as defined by the respective Specialty Board. -
COGC
Description:Scope of responsibility taken on for specialty care as defined by the respective Specialty Board. -
COMC
Description:Scope of responsibility taken on for specialty care as defined by the respective Specialty Board. -
COPC
Description:Scope of responsibility taken on for specialty care as defined by the respective Specialty Board. -
COSC
Description:Scope of responsibility taken on for specialty care as defined by the respective Specialty Board. -
COTC
Description:Scope of responsibility taken on for specialty care as defined by the respective Specialty Board. -
CPEC
Description:Scope of responsibility taken on for specialty care as defined by the respective Specialty Board. -
CPGC
Description:Scope of responsibility taken on for specialty care as defined by the respective Specialty Board. -
CPHC
Description:Scope of responsibility taken on for specialty care as defined by the respective Specialty Board. -
CPRC
Description:Scope of responsibility taken on for specialty care as defined by the respective Specialty Board. -
CPSC
Description:Scope of responsibility taken on for specialty care as defined by the respective Specialty Board. -
CPYC
Description:Scope of responsibility taken on for specialty care as defined by the respective Specialty Board. -
CROC
Description:Scope of responsibility taken on for specialty care as defined by the respective Specialty Board. -
CRPC
Description:Scope of responsibility taken on for specialty care as defined by the respective Specialty Board. -
CSUC
Description:Scope of responsibility taken on for specialty care as defined by the respective Specialty Board. -
CTSC
Description:Scope of responsibility taken on for specialty care as defined by the respective Specialty Board. -
CURC
Description:Scope of responsibility taken on for specialty care as defined by the respective Specialty Board. -
CVSC
Description:Scope of responsibility taken on for specialty care as defined by the respective Specialty Board. -
LGPC
Description:Scope of responsibility taken-on for physician care of a patient as defined by a governmental licensing agency. -
_ACTCREDENTIALEDCAREPROVISIONPROGRAMCODE
Description:The type and scope of legal and/or professional responsibility taken-on by the performer of the Act for a specific subject of care as described by an agency for credentialing programs within organizations. -
AALC
Description:Scope of responsibility taken on by an organization for care of a patient as defined by the respective accreditation agency. -
AAMC
Description:Scope of responsibility taken on by an organization for care of a patient as defined by the respective accreditation agency. -
ABHC
Description:Scope of responsibility taken on by an organization for care of a patient as defined by the respective accreditation agency. -
ACAC
Description:Scope of responsibility taken on by an organization for care of a patient as defined by the respective accreditation agency. -
ACHC
Description:Scope of responsibility taken on by an organization for care of a patient as defined by the respective accreditation agency. -
AHOC
Description:Scope of responsibility taken on by an organization for care of a patient as defined by the respective accreditation agency. -
ALTC
Description:Scope of responsibility taken on by an organization for care of a patient as defined by the respective accreditation agency. -
AOSC
Description:Scope of responsibility taken on by an organization for care of a patient as defined by the respective accreditation agency. -
CACS
Description:Scope of responsibility taken on by an organization for care of a patient as defined by the disease management certification agency. -
CAMI
Description:Scope of responsibility taken on by an organization for care of a patient as defined by the disease management certification agency. -
CAST
Description:Scope of responsibility taken on by an organization for care of a patient as defined by the disease management certification agency. -
CBAR
Description:Scope of responsibility taken on by an organization for care of a patient as defined by the disease management certification agency. -
CCAD
Description:Scope of responsibility taken on by an organization for care of a patient as defined by the disease management certification agency. -
CCAR
Description:Scope of responsibility taken on by an organization for care of a patient as defined by the disease management certification agency. -
CDEP
Description:Scope of responsibility taken on by an organization for care of a patient as defined by the disease management certification agency. -
CDGD
Description:Scope of responsibility taken on by an organization for care of a patient as defined by the disease management certification agency. -
CDIA
Description:Scope of responsibility taken on by an organization for care of a patient as defined by the disease management certification agency. -
CEPI
Description:Scope of responsibility taken on by an organization for care of a patient as defined by the disease management certification agency. -
CFEL
Description:Scope of responsibility taken on by an organization for care of a patient as defined by the disease management certification agency. -
CHFC
Description:Scope of responsibility taken on by an organization for care of a patient as defined by the disease management certification agency. -
CHRO
Description:Scope of responsibility taken on by an organization for care of a patient as defined by the disease management certification agency. -
CHYP
Description:Scope of responsibility taken on by an organization for care of a patient as defined by the disease management certification agency. -
CMIH
Description:. -
CMSC
Description:Scope of responsibility taken on by an organization for care of a patient as defined by the disease management certification agency. -
COJR
Description:Scope of responsibility taken on by an organization for care of a patient as defined by the disease management certification agency. -
CONC
Description:Scope of responsibility taken on by an organization for care of a patient as defined by the disease management certification agency. -
COPD
Description:Scope of responsibility taken on by an organization for care of a patient as defined by the disease management certification agency. -
CORT
Description:Scope of responsibility taken on by an organization for care of a patient as defined by the disease management certification agency. -
CPAD
Description:Scope of responsibility taken on by an organization for care of a patient as defined by the disease management certification agency. -
CPND
Description:Scope of responsibility taken on by an organization for care of a patient as defined by the disease management certification agency. -
CPST
Description:Scope of responsibility taken on by an organization for care of a patient as defined by the disease management certification agency. -
CSDM
Description:Scope of responsibility taken on by an organization for care of a patient as defined by the disease management certification agency. -
CSIC
Description:Scope of responsibility taken on by an organization for care of a patient as defined by the disease management certification agency. -
CSLD
Description:Scope of responsibility taken on by an organization for care of a patient as defined by the disease management certification agency. -
CSPT
Description:Scope of responsibility taken on by an organization for care of a patient as defined by the disease management certification agency. -
CTBU
Description:Scope of responsibility taken on by an organization for care of a patient as defined by the disease management certification agency. -
CVDC
Description:Scope of responsibility taken on by an organization for care of a patient as defined by the disease management certification agency. -
CWMA
Description:Scope of responsibility taken on by an organization for care of a patient as defined by the disease management certification agency. -
CWOH
Description:Scope of responsibility taken on by an organization for care of a patient as defined by the disease management certification agency. -
_ACTENCOUNTERCODE
Domain provides codes that qualify the ActEncounterClass (ENC) -
AMB
A comprehensive term for health care provided in a healthcare facility (e.g. a practitioneraTMs office, clinic setting, or hospital) on a nonresident basis. The term ambulatory usually implies that the patient has come to the location and is not assigned to a bed. Sometimes referred to as an outpatient encounter. -
EMER
A patient encounter that takes place at a dedicated healthcare service delivery location where the patient receives immediate evaluation and treatment, provided until the patient can be discharged or responsibility for the patient's care is transferred elsewhere (for example, the patient could be admitted as an inpatient or transferred to another facility.) -
FLD
A patient encounter that takes place both outside a dedicated service delivery location and outside a patient's residence. Example locations might include an accident site and at a supermarket. -
HH
Healthcare encounter that takes place in the residence of the patient or a designee -
IMP
A patient encounter where a patient is admitted by a hospital or equivalent facility, assigned to a location where patients generally stay at least overnight and provided with room, board, and continuous nursing service. -
ACUTE
An acute inpatient encounter. -
NONAC
Any category of inpatient encounter except 'acute' -
PRENC
A patient encounter where patient is scheduled or planned to receive service delivery in the future, and the patient is given a pre-admission account number. When the patient comes back for subsequent service, the pre-admission encounter is selected and is encapsulated into the service registration, and a new account number is generated. Usage Note: This is intended to be used in advance of encounter types such as ambulatory, inpatient encounter, virtual, etc. -
SS
An encounter where the patient is admitted to a health care facility for a predetermined length of time, usually less than 24 hours. -
VR
A patient encounter where the patient and the practitioner(s) are not in the same physical location. Examples include telephone conference, email exchange, robotic surgery, and televideo conference. -
_ACTMEDICALSERVICECODE
General category of medical service provided to the patient during their encounter. -
ALC
Provision of Alternate Level of Care to a patient in an acute bed. Patient is waiting for placement in a long-term care facility and is unable to return home. -
CARD
Provision of diagnosis and treatment of diseases and disorders affecting the heart -
CHR
Provision of recurring care for chronic illness. -
DNTL
Provision of treatment for oral health and/or dental surgery. -
DRGRHB
Provision of treatment for drug abuse. -
GENRL
General care performed by a general practitioner or family doctor as a responsible provider for a patient. -
MED
Provision of diagnostic and/or therapeutic treatment. -
OBS
Provision of care of women during pregnancy, childbirth and immediate postpartum period. Also known as Maternity. -
ONC
Provision of treatment and/or diagnosis related to tumors and/or cancer. -
PALL
Provision of care for patients who are living or dying from an advanced illness. -
PED
Provision of diagnosis and treatment of diseases and disorders affecting children. -
PHAR
Pharmaceutical care performed by a pharmacist. -
PHYRHB
Provision of treatment for physical injury. -
PSYCH
Provision of treatment of psychiatric disorder relating to mental illness. -
SURG
Provision of surgical treatment. -
_ACTCLAIMATTACHMENTCATEGORYCODE
Description: Coded types of attachments included to support a healthcare claim. -
AUTOATTCH
Description: Automobile Information Attachment -
DOCUMENT
Description: Document Attachment -
HEALTHREC
Description: Health Record Attachment -
IMG
Description: Image Attachment -
LABRESULTS
Description: Lab Results Attachment -
MODEL
Description: Digital Model Attachment -
WIATTCH
Description: Work Injury related additional Information Attachment -
XRAY
Description: Digital X-Ray Attachment -
_ACTCONSENTTYPE
Definition: The type of consent directive, e.g., to consent or dissent to collect, access, or use in specific ways within an EHRS or for health information exchange; or to disclose health information for purposes such as research. -
ICOL
Definition: Consent to have healthcare information collected in an electronic health record. This entails that the information may be used in analysis, modified, updated. -
IDSCL
Definition: Consent to have collected healthcare information disclosed. -
INFA
Definition: Consent to access healthcare information. -
INFAO
Definition: Consent to access or "read" only, which entails that the information is not to be copied, screen printed, saved, emailed, stored, re-disclosed or altered in any way. This level ensures that data which is masked or to which access is restricted will not be. Example: Opened and then emailed or screen printed for use outside of the consent directive purpose. -
INFASO
Definition: Consent to access and save only, which entails that access to the saved copy will remain locked. -
IRDSCL
Definition: Information re-disclosed without the patient's consent. -
RESEARCH
Definition: Consent to have healthcare information in an electronic health record accessed for research purposes. -
RSDID
Definition: Consent to have de-identified healthcare information in an electronic health record that is accessed for research purposes, but without consent to re-identify the information under any circumstance. -
RSREID
Definition: Consent to have de-identified healthcare information in an electronic health record that is accessed for research purposes re-identified under specific circumstances outlined in the consent. Example:: Where there is a need to inform the subject of potential health issues. -
_ACTCONTAINERREGISTRATIONCODE
Constrains the ActCode to the domain of Container Registration -
ID
Used by one system to inform another that it has received a container. -
IP
Used by one system to inform another that the container is in position for specimen transfer (e.g., container removal from track, pipetting, etc.). -
L
Used by one system to inform another that the container has been released from that system. -
M
Used by one system to inform another that the container did not arrive at its next expected location. -
O
Used by one system to inform another that the specific container is being processed by the equipment. It is useful as a response to a query about Container Status, when the specific step of the process is not relevant. -
R
Status is used by one system to inform another that the processing has been completed, but the container has not been released from that system. -
X
Used by one system to inform another that the container is no longer available within the scope of the system (e.g., tube broken or discarded). -
_ACTCONTROLVARIABLE
An observation form that determines parameters or attributes of an Act. Examples are the settings of a ventilator machine as parameters of a ventilator treatment act; the controls on dillution factors of a chemical analyzer as a parameter of a laboratory observation act; the settings of a physiologic measurement assembly (e.g., time skew) or the position of the body while measuring blood pressure. Control variables are forms of observations because just as with clinical observations, the Observation.code determines the parameter and the Observation.value assigns the value. While control variables sometimes can be observed (by noting the control settings or an actually measured feedback loop) they are not primary observations, in the sense that a control variable without a primary act is of no use (e.g., it makes no sense to record a blood pressure position without recording a blood pressure, whereas it does make sense to record a systolic blood pressure without a diastolic blood pressure). -
AUTO
Specifies whether or not automatic repeat testing is to be initiated on specimens. -
ENDC
A baseline value for the measured test that is inherently contained in the diluent. In the calculation of the actual result for the measured test, this baseline value is normally considered. -
REFLEX
Specifies whether or not further testing may be automatically or manually initiated on specimens. -
_ACTCOVERAGECONFIRMATIONCODE
Response to an insurance coverage eligibility query or authorization request. -
_ACTCOVERAGEAUTHORIZATIONCONFIRMATIONCODE
Indication of authorization for healthcare service(s) and/or product(s). If authorization is approved, funds are set aside. -
AUTH
Authorization approved and funds have been set aside to pay for specified healthcare service(s) and/or product(s) within defined criteria for the authorization. -
NAUTH
Authorization for specified healthcare service(s) and/or product(s) denied. -
_ACTCOVERAGEELIGIBILITYCONFIRMATIONCODE
Indication of eligibility coverage for healthcare service(s) and/or product(s). -
ELG
Insurance coverage is in effect for healthcare service(s) and/or product(s). -
NELG
Insurance coverage is not in effect for healthcare service(s) and/or product(s). May optionally include reasons for the ineligibility. -
_ACTCOVERAGELIMITCODE
Criteria that are applicable to the authorized coverage. -
_ACTCOVERAGEQUANTITYLIMITCODE
Maximum amount paid or maximum number of services/products covered; or maximum amount or number covered during a specified time period under the policy or program. -
COVPRD
Codes representing the time period during which coverage is available; or financial participation requirements are in effect. -
LFEMX
Definition: Maximum amount paid by payer or covered party; or maximum number of services or products covered under the policy or program during a covered party's lifetime. -
NETAMT
Maximum net amount that will be covered for the product or service specified. -
PRDMX
Definition: Maximum amount paid by payer or covered party; or maximum number of services/products covered under the policy or program by time period specified by the effective time on the act. -
UNITPRICE
Maximum unit price that will be covered for the authorized product or service. -
UNITQTY
Maximum number of items that will be covered of the product or service specified. -
COVMX
Definition: Codes representing the maximum coverate or financial participation requirements. -
_ACTCOVEREDPARTYLIMITCODE
Codes representing the types of covered parties that may receive covered benefits under a policy or program. -
_ACTCOVERAGETYPECODE
Definition: Set of codes indicating the type of insurance policy or program that pays for the cost of benefits provided to covered parties. -
_ACTINSURANCEPOLICYCODE
Set of codes indicating the type of insurance policy or other source of funds to cover healthcare costs. -
EHCPOL
Private insurance policy that provides coverage in addition to other policies (e.g. in addition to a Public Healthcare insurance policy). -
HSAPOL
Insurance policy that provides for an allotment of funds replenished on a periodic (e.g. annual) basis. The use of the funds under this policy is at the discretion of the covered party. -
AUTOPOL
Insurance policy for injuries sustained in an automobile accident. Will also typically covered non-named parties to the policy, such as pedestrians and passengers. -
COL
Definition: An automobile insurance policy under which the insurance company will cover the cost of damages to an automobile owned by the named insured that are caused by accident or intentionally by another party. -
UNINSMOT
Definition: An automobile insurance policy under which the insurance company will indemnify a loss for which another motorist is liable if that motorist is unable to pay because he or she is uninsured. Coverage under the policy applies to bodily injury damages only. Injuries to the covered party caused by a hit-and-run driver are also covered. -
PUBLICPOL
Insurance policy funded by a public health system such as a provincial or national health plan. Examples include BC MSP (British Columbia Medical Services Plan) OHIP (Ontario Health Insurance Plan), NHS (National Health Service). -
DENTPRG
Definition: A public or government health program that administers and funds coverage for dental care to assist program eligible who meet financial and health status criteria. -
DISEASEPRG
Definition: A public or government health program that administers and funds coverage for health and social services to assist program eligible who meet financial and health status criteria related to a particular disease. Example: Reproductive health, sexually transmitted disease, and end renal disease programs. -
CANPRG
Definition: A program that provides low-income, uninsured, and underserved women access to timely, high-quality screening and diagnostic services, to detect breast and cervical cancer at the earliest stages. Example: To improve women's access to screening for breast and cervical cancers, Congress passed the Breast and Cervical Cancer Mortality Prevention Act of 1990, which guided CDC in creating the National Breast and Cervical Cancer Early Detection Program (NBCCEDP), which provides access to critical breast and cervical cancer screening services for underserved women in the United States. An estimated 7 to 10% of U.S. women of screening age are eligible to receive NBCCEDP services. Federal guidelines establish an eligibility baseline to direct services to uninsured and underinsured women at or below 250% of federal poverty level; ages 18 to 64 for cervical screening; ages 40 to 64 for breast screening. -
ENDRENAL
Definition: A public or government program that administers publicly funded coverage of kidney dialysis and kidney transplant services. Example: In the U.S., the Medicare End-stage Renal Disease program (ESRD), the National Kidney Foundation (NKF) American Kidney Fund (AKF) The Organ Transplant Fund. -
HIVAIDS
Definition: Government administered and funded HIV-AIDS program for beneficiaries meeting financial and health status criteria. Administration, funding levels, eligibility criteria, covered benefits, provider types, and financial participation are typically set by a regulatory process. Payer responsibilities for administering the program may be delegated to contractors. Example: In the U.S., the Ryan White program, which is administered by the Health Resources and Services Administration. -
MANDPOL
mandatory health program -
MENTPRG
Definition: Government administered and funded mental health program for beneficiaries meeting financial and mental health status criteria. Administration, funding levels, eligibility criteria, covered benefits, provider types, and financial participation are typically set by a regulatory process. Payer responsibilities for administering the program may be delegated to contractors. Example: In the U.S., states receive funding for substance use programs from the Substance Abuse Mental Health Administration (SAMHSA). -
SAFNET
Definition: Government administered and funded program to support provision of care to underserved populations through safety net clinics. Example: In the U.S., safety net providers such as federally qualified health centers (FQHC) receive funding under PHSA Section 330 grants administered by the Health Resources and Services Administration. -
SUBPRG
Definition: Government administered and funded substance use program for beneficiaries meeting financial, substance use behavior, and health status criteria. Beneficiaries may be required to enroll as a result of legal proceedings. Administration, funding levels, eligibility criteria, covered benefits, provider types, and financial participation are typically set by a regulatory process. Payer responsibilities for administering the program may be delegated to contractors. Example: In the U.S., states receive funding for substance use programs from the Substance Abuse Mental Health Administration (SAMHSA). -
SUBSIDIZ
Definition: A government health program that provides coverage for health services to persons meeting eligibility criteria such as income, location of residence, access to other coverages, health condition, and age, the cost of which is to some extent subsidized by public funds. -
SUBSIDMC
Definition: A government health program that provides coverage through managed care contracts for health services to persons meeting eligibility criteria such as income, location of residence, access to other coverages, health condition, and age, the cost of which is to some extent subsidized by public funds. Discussion: The structure and business processes for underwriting and administering a subsidized managed care program is further specified by the Underwriter and Payer Role.class and Role.code. -
SUBSUPP
Definition: A government health program that provides coverage for health services to persons meeting eligibility criteria for a supplemental health policy or program such as income, location of residence, access to other coverages, health condition, and age, the cost of which is to some extent subsidized by public funds. Example: Supplemental health coverage program may cover the cost of a health program or policy financial participations, such as the copays and the premiums, and may provide coverage for services in addition to those covered under the supplemented health program or policy. In the U.S., Medicaid programs may pay the premium for a covered party who is also covered under the Medicare program or a private health policy. Discussion: The structure and business processes for underwriting and administering a subsidized supplemental retiree health program is further specified by the Underwriter and Payer Role.class and Role.code. -
WCBPOL
Insurance policy for injuries sustained in the work place or in the course of employment. -
_ACTINSURANCETYPECODE
Definition: Set of codes indicating the type of insurance policy. Insurance, in law and economics, is a form of risk management primarily used to hedge against the risk of potential financial loss. Insurance is defined as the equitable transfer of the risk of a potential loss, from one entity to another, in exchange for a premium and duty of care. A policy holder is an individual or an organization enters into a contract with an underwriter which stipulates that, in exchange for payment of a sum of money (a premium), one or more covered parties (insureds) is guaranteed compensation for losses resulting from certain perils under specified conditions. The underwriter analyzes the risk of loss, makes a decision as to whether the risk is insurable, and prices the premium accordingly. A policy provides benefits that indemnify or cover the cost of a loss incurred by a covered party, and may include coverage for services required to remediate a loss. An insurance policy contains pertinent facts about the policy holder, the insurance coverage, the covered parties, and the insurer. A policy may include exemptions and provisions specifying the extent to which the indemnification clause cannot be enforced for intentional tortious conduct of a covered party, e.g., whether the covered parties are jointly or severably insured. Discussion: In contrast to programs, an insurance policy has one or more policy holders, who own the policy. The policy holder may be the covered party, a relative of the covered party, a partnership, or a corporation, e.g., an employer. A subscriber of a self-insured health insurance policy is a policy holder. A subscriber of an employer sponsored health insurance policy is holds a certificate of coverage, but is not a policy holder; the policy holder is the employer. See CoveredRoleType. -
_ACTHEALTHINSURANCETYPECODE
Definition: Set of codes indicating the type of health insurance policy that covers health services provided to covered parties. A health insurance policy is a written contract for insurance between the insurance company and the policyholder, and contains pertinent facts about the policy owner (the policy holder), the health insurance coverage, the insured subscribers and dependents, and the insurer. Health insurance is typically administered in accordance with a plan, which specifies (1) the type of health services and health conditions that will be covered under what circumstances (e.g., exclusion of a pre-existing condition, service must be deemed medically necessary; service must not be experimental; service must provided in accordance with a protocol; drug must be on a formulary; service must be prior authorized; or be a referral from a primary care provider); (2) the type and affiliation of providers (e.g., only allopathic physicians, only in network, only providers employed by an HMO); (3) financial participations required of covered parties (e.g., co-pays, coinsurance, deductibles, out-of-pocket); and (4) the manner in which services will be paid (e.g., under indemnity or fee-for-service health plans, the covered party typically pays out-of-pocket and then file a claim for reimbursement, while health plans that have contractual relationships with providers, i.e., network providers, typically do not allow the providers to bill the covered party for the cost of the service until after filing a claim with the payer and receiving reimbursement). -
DENTAL
Definition: A health insurance policy that that covers benefits for dental services. -
DISEASE
Definition: A health insurance policy that covers benefits for healthcare services provided for named conditions under the policy, e.g., cancer, diabetes, or HIV-AIDS. -
DRUGPOL
Definition: A health insurance policy that covers benefits for prescription drugs, pharmaceuticals, and supplies. -
HIP
Definition: A health insurance policy that covers healthcare benefits by protecting covered parties from medical expenses arising from health conditions, sickness, or accidental injury as well as preventive care. Health insurance policies explicitly exclude coverage for losses insured under a disability policy, workers' compensation program, liability insurance (including automobile insurance); or for medical expenses, coverage for on-site medical clinics or for limited dental or vision benefits when these are provided under a separate policy. Discussion: Health insurance policies are offered by health insurance plans that typically reimburse providers for covered services on a fee-for-service basis, that is, a fee that is the allowable amount that a provider may charge. This is in contrast to managed care plans, which typically prepay providers a per-member/per-month amount or capitation as reimbursement for all covered services rendered. Health insurance plans include indemnity and healthcare services plans. -
LTC
Definition: An insurance policy that covers benefits for long-term care services people need when they no longer can care for themselves. This may be due to an accident, disability, prolonged illness or the simple process of aging. Long-term care services assist with activities of daily living including: Help at home with day-to-day activities, such as cooking, cleaning, bathing and dressing Care in the community, such as in an adult day care facility Supervised care provided in an assisted living facility Skilled care provided in a nursing home -
MCPOL
Definition: Government mandated program providing coverage, disability income, and vocational rehabilitation for injuries sustained in the work place or in the course of employment. Employers may either self-fund the program, purchase commercial coverage, or pay a premium to a government entity that administers the program. Employees may be required to pay premiums toward the cost of coverage as well. Managed care policies specifically exclude coverage for losses insured under a disability policy, workers' compensation program, liability insurance (including automobile insurance); or for medical expenses, coverage for on-site medical clinics or for limited dental or vision benefits when these are provided under a separate policy. Discussion: Managed care policies are offered by managed care plans that contract with selected providers or health care organizations to provide comprehensive health care at a discount to covered parties and coordinate the financing and delivery of health care. Managed care uses medical protocols and procedures agreed on by the medical profession to be cost effective, also known as medical practice guidelines. Providers are typically reimbursed for covered services by a capitated amount on a per member per month basis that may reflect difference in the health status and level of services anticipated to be needed by the member. -
POS
Definition: A policy for a health plan that has features of both an HMO and a FFS plan. Like an HMO, a POS plan encourages the use its HMO network to maintain discounted fees with participating providers, but recognizes that sometimes covered parties want to choose their own provider. The POS plan allows a covered party to use providers who are not part of the HMO network (non-participating providers). However, there is a greater cost associated with choosing these non-network providers. A covered party will usually pay deductibles and coinsurances that are substantially higher than the payments when he or she uses a plan provider. Use of non-participating providers often requires the covered party to pay the provider directly and then to file a claim for reimbursement, like in an FFS plan. -
HMO
Definition: A policy for a health plan that provides coverage for health care only through contracted or employed physicians and hospitals located in particular geographic or service areas. HMOs emphasize prevention and early detection of illness. Eligibility to enroll in an HMO is determined by where a covered party lives or works. -
PPO
Definition: A network-based, managed care plan that allows a covered party to choose any health care provider. However, if care is received from a "preferred" (participating in-network) provider, there are generally higher benefit coverage and lower deductibles. -
MENTPOL
Definition: A health insurance policy that covers benefits for mental health services and prescriptions. -
SUBPOL
Definition: A health insurance policy that covers benefits for substance use services. -
VISPOL
Definition: Set of codes for a policy that provides coverage for health care expenses arising from vision services. A health insurance policy that covers benefits for vision care services, prescriptions, and products. -
DIS
Definition: An insurance policy that provides a regular payment to compensate for income lost due to the covered party's inability to work because of illness or injury. -
EWB
Definition: An insurance policy under a benefit plan run by an employer or employee organization for the purpose of providing benefits other than pension-related to employees and their families. Typically provides health-related benefits, benefits for disability, disease or unemployment, or day care and scholarship benefits, among others. An employer sponsored health policy includes coverage of health care expenses arising from sickness or accidental injury, coverage for on-site medical clinics or for dental or vision benefits, which are typically provided under a separate policy. Coverage excludes health care expenses covered by accident or disability, workers' compensation, liability or automobile insurance. -
FLEXP
Definition: An insurance policy that covers qualified benefits under a Flexible Benefit plan such as group medical insurance, long and short term disability income insurance, group term life insurance for employees only up to $50,000 face amount, specified disease coverage such as a cancer policy, dental and/or vision insurance, hospital indemnity insurance, accidental death and dismemberment insurance, a medical expense reimbursement plan and a dependent care reimbursement plan. Discussion: See UnderwriterRoleTypeCode flexible benefit plan which is defined as a benefit plan that allows employees to choose from several life, health, disability, dental, and other insurance plans according to their individual needs. Also known as cafeteria plans. Authorized under Section 125 of the Revenue Act of 1978. -
LIFE
Definition: A policy under which the insurer agrees to pay a sum of money upon the occurrence of the covered partys death. In return, the policyholder agrees to pay a stipulated amount called a premium at regular intervals. Life insurance indemnifies the beneficiary for the loss of the insurable interest that a beneficiary has in the life of a covered party. For persons related by blood, a substantial interest established through love and affection, and for all other persons, a lawful and substantial economic interest in having the life of the insured continue. An insurable interest is required when purchasing life insurance on another person. Specific exclusions are often written into the contract to limit the liability of the insurer; for example claims resulting from suicide or relating to war, riot and civil commotion. Discussion:A life insurance policy may be used by the covered party as a source of health care coverage in the case of a viatical settlement, which is the sale of a life insurance policy by the policy owner, before the policy matures. Such a sale, at a price discounted from the face amount of the policy but usually in excess of the premiums paid or current cash surrender value, provides the seller an immediate cash settlement. Generally, viatical settlements involve insured individuals with a life expectancy of less than two years. In countries without state-subsidized healthcare and high healthcare costs (e.g. United States), this is a practical way to pay extremely high health insurance premiums that severely ill people face. Some people are also familiar with life settlements, which are similar transactions but involve insureds with longer life expectancies (two to fifteen years). -
ANNU
Definition: A policy that, after an initial premium or premiums, pays out a sum at pre-determined intervals. For example, a policy holder may pay $10,000, and in return receive $150 each month until he dies; or $1,000 for each of 14 years or death benefits if he dies before the full term of the annuity has elapsed. -
TLIFE
Definition: Life insurance under which the benefit is payable only if the insured dies during a specified period. If an insured dies during that period, the beneficiary receives the death payments. If the insured survives, the policy ends and the beneficiary receives nothing. -
ULIFE
Definition: Life insurance under which the benefit is payable upon the insuredaTMs death or diagnosis of a terminal illness. If an insured dies during that period, the beneficiary receives the death payments. If the insured survives, the policy ends and the beneficiary receives nothing -
PNC
Definition: A type of insurance that covers damage to or loss of the policyholderaTMs property by providing payments for damages to property damage or the injury or death of living subjects. The terms "casualty" and "liability" insurance are often used interchangeably. Both cover the policyholder's legal liability for damages caused to other persons and/or their property. -
REI
Definition: An agreement between two or more insurance companies by which the risk of loss is proportioned. Thus the risk of loss is spread and a disproportionately large loss under a single policy does not fall on one insurance company. Acceptance by an insurer, called a reinsurer, of all or part of the risk of loss of another insurance company. Discussion: Reinsurance is a means by which an insurance company can protect itself against the risk of losses with other insurance companies. Individuals and corporations obtain insurance policies to provide protection for various risks (hurricanes, earthquakes, lawsuits, collisions, sickness and death, etc.). Reinsurers, in turn, provide insurance to insurance companies. For example, an HMO may purchase a reinsurance policy to protect itself from losing too much money from one insured's particularly expensive health care costs. An insurance company issuing an automobile liability policy, with a limit of $100,000 per accident may reinsure its liability in excess of $10,000. A fire insurance company which issues a large policy generally reinsures a portion of the risk with one or several other companies. Also called risk control insurance or stop-loss insurance. -
SURPL
Definition: A risk or part of a risk for which there is no normal insurance market available. Insurance written by unauthorized insurance companies. Surplus lines insurance is insurance placed with unauthorized insurance companies through licensed surplus lines agents or brokers. -
UMBRL
Definition: A form of insurance protection that provides additional liability coverage after the limits of your underlying policy are reached. An umbrella liability policy also protects you (the insured) in many situations not covered by the usual liability policies. -
_ACTPROGRAMTYPECODE
Definition: A set of codes used to indicate coverage under a program. A program is an organized structure for administering and funding coverage of a benefit package for covered parties meeting eligibility criteria, typically related to employment, health, financial, and demographic status. Programs are typically established or permitted by legislation with provisions for ongoing government oversight. Regulations may mandate the structure of the program, the manner in which it is funded and administered, covered benefits, provider types, eligibility criteria and financial participation. A government agency may be charged with implementing the program in accordance to the regulation. Risk of loss under a program in most cases would not meet what an underwriter would consider an insurable risk, i.e., the risk is not random in nature, not financially measurable, and likely requires subsidization with government funds. Discussion: Programs do not have policy holders or subscribers. Program eligibles are enrolled based on health status, statutory eligibility, financial status, or age. Program eligibles who are covered parties under the program may be referred to as members, beneficiaries, eligibles, or recipients. Programs risk are underwritten by not for profit organizations such as governmental entities, and the beneficiaries typically do not pay for any or some portion of the cost of coverage. See CoveredPartyRoleType. -
CHAR
Definition: A program that covers the cost of services provided directly to a beneficiary who typically has no other source of coverage without charge. -
CRIME
Definition: A program that covers the cost of services provided to crime victims for injuries or losses related to the occurrence of a crime. -
EAP
Definition: An employee assistance program is run by an employer or employee organization for the purpose of providing benefits and covering all or part of the cost for employees to receive counseling, referrals, and advice in dealing with stressful issues in their lives. These may include substance abuse, bereavement, marital problems, weight issues, or general wellness issues. The services are usually provided by a third-party, rather than the company itself, and the company receives only summary statistical data from the service provider. Employee's names and services received are kept confidential. -
GOVEMP
Definition: A set of codes used to indicate a government program that is an organized structure for administering and funding coverage of a benefit package for covered parties meeting eligibility criteria, typically related to employment, health and financial status. Government programs are established or permitted by legislation with provisions for ongoing government oversight. Regulation mandates the structure of the program, the manner in which it is funded and administered, covered benefits, provider types, eligibility criteria and financial participation. A government agency is charged with implementing the program in accordance to the regulation Example: Federal employee health benefit program in the U.S. -
HIRISK
Definition: A government program that provides health coverage to individuals who are considered medically uninsurable or high risk, and who have been denied health insurance due to a serious health condition. In certain cases, it also applies to those who have been quoted very high premiums a" again, due to a serious health condition. The pool charges premiums for coverage. Because the pool covers high-risk people, it incurs a higher level of claims than premiums can cover. The insurance industry pays into the pool to make up the difference and help it remain viable. -
IND
Definition: Services provided directly and through contracted and operated indigenous peoples health programs. Example: Indian Health Service in the U.S. -
MILITARY
Definition: A government program that provides coverage for health services to military personnel, retirees, and dependents. A covered party who is a subscriber can choose from among Fee-for-Service (FFS) plans, and their Preferred Provider Organizations (PPO), or Plans offering a Point of Service (POS) Product, or Health Maintenance Organizations. Example: In the U.S., TRICARE, CHAMPUS. -
RETIRE
Definition: A government mandated program with specific eligibility requirements based on premium contributions made during employment, length of employment, age, and employment status, e.g., being retired, disabled, or a dependent of a covered party under this program. Benefits typically include ambulatory, inpatient, and long-term care, such as hospice care, home health care and respite care. -
SOCIAL
Definition: A social service program funded by a public or governmental entity. Example: Programs providing habilitation, food, lodging, medicine, transportation, equipment, devices, products, education, training, counseling, alteration of living or work space, and other resources to persons meeting eligibility criteria. -
VET
Definition: Services provided directly and through contracted and operated veteran health programs. -
_ACTDETECTEDISSUEMANAGEMENTCODE
Codes dealing with the management of Detected Issue observations -
_ACTADMINISTRATIVEDETECTEDISSUEMANAGEMENTCODE
Codes dealing with the management of Detected Issue observations for the administrative and patient administrative acts domains. -
_AUTHORIZATIONISSUEMANAGEMENTCODE
Authorization Issue Management Code -
EMAUTH
Used to temporarily override normal authorization rules to gain access to data in a case of emergency. Use of this override code will typically be monitored, and a procedure to verify its proper use may be triggered when used. -
_21
Description: Indicates that the permissions have been externally verified and the request should be processed. -
_1
Confirmed drug therapy appropriate -
_19
Consulted other supplier/pharmacy, therapy confirmed -
_2
Assessed patient, therapy is appropriate -
_22
Description: The patient has the appropriate indication or diagnosis for the action to be taken. -
_23
Description: It has been confirmed that the appropriate pre-requisite therapy has been tried. -
_3
Patient gave adequate explanation -
_4
Consulted other supply source, therapy still appropriate -
_5
Consulted prescriber, therapy confirmed -
_6
Consulted prescriber and recommended change, prescriber declined -
_7
Concurrent therapy triggering alert is no longer on-going or planned -
_14
Confirmed supply action appropriate -
_15
Patient's existing supply was lost/wasted -
_16
Supply date is due to patient vacation -
_17
Supply date is intended to carry patient over weekend -
_18
Supply is intended for use during a leave of absence from an institution. -
_20
Description: Supply is different than expected as an additional quantity has been supplied in a separate dispense. -
_8
Order is performed as issued, but other action taken to mitigate potential adverse effects -
_10
Provided education or training to the patient on appropriate therapy use -
_11
Instituted an additional therapy to mitigate potential negative effects -
_12
Suspended existing therapy that triggered interaction for the duration of this therapy -
_13
Aborted existing therapy that triggered interaction. -
_9
Arranged to monitor patient for adverse effects -
_ACTEXPOSURECODE
Concepts that identify the type or nature of exposure interaction. Examples include "household", "care giver", "intimate partner", "common space", "common substance", etc. to further describe the nature of interaction. -
CHLDCARE
Description: Exposure participants' interaction occurred in a child care setting -
CONVEYNC
Description: An interaction where the exposure participants traveled in/on the same vehicle (not necessarily concurrently, e.g. both are passengers of the same plane, but on different flights of that plane). -
HLTHCARE
Description: Exposure participants' interaction occurred during the course of health care delivery or in a health care delivery setting, but did not involve the direct provision of care (e.g. a janitor cleaning a patient's hospital room). -
HOMECARE
Description: Exposure interaction occurred in context of one providing care for the other, i.e. a babysitter providing care for a child, a home-care aide providing assistance to a paraplegic. -
HOSPPTNT
Description: Exposure participants' interaction occurred when both were patients being treated in the same (acute) health care delivery facility. -
HOSPVSTR
Description: Exposure participants' interaction occurred when one visited the other who was a patient being treated in a health care delivery facility. -
HOUSEHLD
Description: Exposure interaction occurred in context of domestic interaction, i.e. both participants reside in the same household. -
INMATE
Description: Exposure participants' interaction occurred in the course of one or both participants being incarcerated at a correctional facility -
INTIMATE
Description: Exposure interaction was intimate, i.e. participants are intimate companions (e.g. spouses, domestic partners). -
LTRMCARE
Description: Exposure participants' interaction occurred in the course of one or both participants being resident at a long term care facility (second participant may be a visitor, worker, resident or a physical place or object within the facility). -
PLACE
Description: An interaction where the exposure participants were both present in the same location/place/space. -
PTNTCARE
Description: Exposure participants' interaction occurred during the course of health care delivery by a provider (e.g. a physician treating a patient in her office). -
SCHOOL2
Description: Exposure participants' interaction occurred in an academic setting (e.g., participants are fellow students, or student and teacher). -
SOCIAL2
Description: An interaction where the exposure participants are social associates or members of the same extended family -
SUBSTNCE
Description: An interaction where the exposure participants shared or co-used a common substance (e.g. drugs, needles, or common food item). -
TRAVINT
Description: An interaction where the exposure participants traveled together in/on the same vehicle/trip (e.g. concurrent co-passengers). -
WORK2
Description: Exposure interaction occurred in a work setting, i.e. participants are co-workers. -
_ACTFINANCIALTRANSACTIONCODE
ActFinancialTransactionCode -
CHRG
A type of transaction that represents a charge for a service or product. Expressed in monetary terms. -
REV
A type of transaction that represents a reversal of a previous charge for a service or product. Expressed in monetary terms. It has the opposite effect of a standard charge. -
_ACTINCIDENTCODE
Set of codes indicating the type of incident or accident. -
MVA
Incident or accident as the result of a motor vehicle accident -
SCHOOL
Incident or accident is the result of a school place accident. -
SPT
Incident or accident is the result of a sporting accident. -
WPA
Incident or accident is the result of a work place accident -
_ACTINFORMATIONACCESSCODE
Description: The type of health information to which the subject of the information or the subject's delegate consents or dissents. -
ACADR
Description: Provide consent to collect, use, disclose, or access adverse drug reaction information for a patient. -
ACALL
Description: Provide consent to collect, use, disclose, or access all information for a patient. -
ACALLG
Description: Provide consent to collect, use, disclose, or access allergy information for a patient. -
ACCONS
Description: Provide consent to collect, use, disclose, or access informational consent information for a patient. -
ACDEMO
Description: Provide consent to collect, use, disclose, or access demographics information for a patient. -
ACDI
Description: Provide consent to collect, use, disclose, or access diagnostic imaging information for a patient. -
ACIMMUN
Description: Provide consent to collect, use, disclose, or access immunization information for a patient. -
ACLAB
Description: Provide consent to collect, use, disclose, or access lab test result information for a patient. -
ACMED
Description: Provide consent to collect, use, disclose, or access medical condition information for a patient. -
ACMEDC
Definition: Provide consent to view or access medical condition information for a patient. -
ACMEN
Description:Provide consent to collect, use, disclose, or access mental health information for a patient. -
ACOBS
Description: Provide consent to collect, use, disclose, or access common observation information for a patient. -
ACPOLPRG
Description: Provide consent to collect, use, disclose, or access coverage policy or program for a patient. -
ACPROV
Description: Provide consent to collect, use, disclose, or access provider information for a patient. -
ACPSERV
Description: Provide consent to collect, use, disclose, or access professional service information for a patient. -
ACSUBSTAB
Description:Provide consent to collect, use, disclose, or access substance abuse information for a patient. -
_ACTINFORMATIONACCESSCONTEXTCODE
Concepts conveying the context in which authorization given under jurisdictional law, by organizational policy, or by a patient consent directive permits the collection, access, use or disclosure of specified patient health information. -
INFAUT
Authorization to collect, access, use, or disclose specified patient health information in accordance with jurisdictional law, organizational policy, or a patient's consent directive, which may be implied, deemed, opt-in, opt-out, or explicit. -
INFCON
Authorization to collect, access, use, or disclose specified patient health information as explicitly consented to by the subject of the information or the subject's representative. -
INFCRT
Authorization to collect, access, use, or disclose specified patient health information in accordance with judicial system protocol, such as in the case of a subpoena or court order. -
INFDNG
Authorization to collect, access, use, or disclose specified patient health information where deemed necessary to avert potential danger to other persons in accordance with jurisdictional law, organizational policy, or standards of practice. For example, disclosure about a person threatening violence. -
INFEMER
Authorization to collect, access, use, or disclose specified patient health information in accordance with emergency information transfer protocol dictated by jurisdictional law, organization policy, or standards of practice. For example, sharing of health information during disaster response. -
INFPWR
Authorization to collect, access, use, or disclose specified patient health information necessary to avert potential public welfare risk in accordance with jurisdictional law, organizational policy, or standards of practice. For example, reporting that a person is a victim of abuse or demonstrating suicidal tendencies. -
INFREG
Authorization to collect, access, use, or disclose specified patient health information for public health, welfare, and safety purposes in accordance with jurisdictional law, organizational policy, or standards of practice. For example, public health reporting of notifiable conditions. -
_ACTINFORMATIONCATEGORYCODE
Definition:Indicates the set of information types which may be manipulated or referenced, such as for recommending access restrictions. -
ALLCAT
Description: All patient information. -
ALLGCAT
Definition:All information pertaining to a patient's allergy and intolerance records. -
ARCAT
Description: All information pertaining to a patient's adverse drug reactions. -
COBSCAT
Definition:All information pertaining to a patient's common observation records (height, weight, blood pressure, temperature, etc.). -
DEMOCAT
Definition:All information pertaining to a patient's demographics (such as name, date of birth, gender, address, etc). -
DICAT
Definition:All information pertaining to a patient's diagnostic image records (orders invalid input: '&' results). -
IMMUCAT
Definition:All information pertaining to a patient's vaccination records. -
LABCAT
Description: All information pertaining to a patient's lab test records (orders invalid input: '&' results) -
MEDCCAT
Definition:All information pertaining to a patient's medical condition records. -
MENCAT
Description: All information pertaining to a patient's mental health records. -
PSVCCAT
Definition:All information pertaining to a patient's professional service records (such as smoking cessation, counseling, medication review, mental health). -
RXCAT
Definition:All information pertaining to a patient's medication records (orders, dispenses and other active medications). -
_ACTINVOICEELEMENTCODE
Type of invoice element that is used to assist in describing an Invoice that is either submitted for adjudication or for which is returned on adjudication results. -
_ACTINVOICEADJUDICATIONPAYMENTCODE
Codes representing a grouping of invoice elements (totals, sub-totals), reported through a Payment Advice or a Statement of Financial Activity (SOFA). The code can represent summaries by day, location, payee and other cost elements such as bonus, retroactive adjustment and transaction fees. -
_ACTINVOICEADJUDICATIONPAYMENTGROUPCODE
Codes representing adjustments to a Payment Advice such as retroactive, clawback, garnishee, etc. -
ALEC
Payment initiated by the payor as the result of adjudicating a submitted invoice that arrived to the payor from an electronic source that did not provide a conformant set of HL7 messages (e.g. web claim submission). -
BONUS
Bonus payments based on performance, volume, etc. as agreed to by the payor. -
CFWD
An amount still owing to the payor but the payment is 0$ and this cannot be settled until a future payment is made. -
EDU
Fees deducted on behalf of a payee for tuition and continuing education. -
EPYMT
Fees deducted on behalf of a payee for charges based on a shorter payment frequency (i.e. next day versus biweekly payments. -
GARN
Fees deducted on behalf of a payee for charges based on a per-transaction or time-period (e.g. monthly) fee. -
INVOICE
Payment is based on a payment intent for a previously submitted Invoice, based on formal adjudication results.. -
PINV
Payment initiated by the payor as the result of adjudicating a paper (original, may have been faxed) invoice. -
PPRD
An amount that was owed to the payor as indicated, by a carry forward adjusment, in a previous payment advice -
PROA
Professional association fee that is collected by the payor from the practitioner/provider on behalf of the association -
RECOV
Retroactive adjustment such as fee rate adjustment due to contract negotiations. -
RETRO
Bonus payments based on performance, volume, etc. as agreed to by the payor. -
TRAN
Fees deducted on behalf of a payee for charges based on a per-transaction or time-period (e.g. monthly) fee. -
_ACTINVOICEADJUDICATIONPAYMENTSUMMARYCODE
Codes representing a grouping of invoice elements (totals, sub-totals), reported through a Payment Advice or a Statement of Financial Activity (SOFA). The code can represent summaries by day, location, payee, etc. -
INVTYPE
Transaction counts and value totals by invoice type (e.g. RXDINV - Pharmacy Dispense) -
PAYEE
Transaction counts and value totals by each instance of an invoice payee. -
PAYOR
Transaction counts and value totals by each instance of an invoice payor. -
SENDAPP
Transaction counts and value totals by each instance of a messaging application on a single processor. It is a registered identifier known to the receivers. -
_ACTINVOICEDETAILCODE
Codes representing a service or product that is being invoiced (billed). The code can represent such concepts as "office visit", "drug X", "wheelchair" and other billable items such as taxes, service charges and discounts. -
_ACTINVOICEDETAILCLINICALPRODUCTCODE
An identifying data string for healthcare products. -
UNSPSC
Description:United Nations Standard Products and Services Classification, managed by Uniform Code Council (UCC): www.unspsc.org -
_ACTINVOICEDETAILDRUGPRODUCTCODE
An identifying data string for A substance used as a medication or in the preparation of medication. -
GTIN
Description:Global Trade Item Number is an identifier for trade items developed by GS1 (comprising the former EAN International and Uniform Code Council). -
UPC
Description:Universal Product Code is one of a wide variety of bar code languages widely used in the United States and Canada for items in stores. -
_ACTINVOICEDETAILGENERICCODE
The detail item codes to identify charges or changes to the total billing of a claim due to insurance rules and payments. -
_ACTINVOICEDETAILGENERICADJUDICATORCODE
The billable item codes to identify adjudicator specified components to the total billing of a claim. -
COIN
That portion of the eligible charges which a covered party must pay for each service and/or product. It is a percentage of the eligible amount for the service/product that is typically charged after the covered party has met the policy deductible. This amount represents the covered party's coinsurance that is applied to a particular adjudication result. It is expressed as a negative dollar amount in adjudication results. -
COPAYMENT
That portion of the eligible charges which a covered party must pay for each service and/or product. It is a defined amount per service/product of the eligible amount for the service/product. This amount represents the covered party's copayment that is applied to a particular adjudication result. It is expressed as a negative dollar amount in adjudication results. -
DEDUCTIBLE
That portion of the eligible charges which a covered party must pay in a particular period (e.g. annual) before the benefits are payable by the adjudicator. This amount represents the covered party's deductible that is applied to a particular adjudication result. It is expressed as a negative dollar amount in adjudication results. -
PAY
The guarantor, who may be the patient, pays the entire charge for a service. Reasons for such action may include: there is no insurance coverage for the service (e.g. cosmetic surgery); the patient wishes to self-pay for the service; or the insurer denies payment for the service due to contractual provisions such as the need for prior authorization. -
SPEND
That total amount of the eligible charges which a covered party must periodically pay for services and/or products prior to the Medicaid program providing any coverage. This amount represents the covered party's spend down that is applied to a particular adjudication result. It is expressed as a negative dollar amount in adjudication results -
COINS
The covered party pays a percentage of the cost of covered services. -
_ACTINVOICEDETAILGENERICMODIFIERCODE
The billable item codes to identify modifications to a billable item charge. As for example after hours increase in the office visit fee. -
AFTHRS
Premium paid on service fees in compensation for practicing outside of normal working hours. -
ISOL
Premium paid on service fees in compensation for practicing in a remote location. -
OOO
Premium paid on service fees in compensation for practicing at a location other than normal working location. -
_ACTINVOICEDETAILGENERICPROVIDERCODE
The billable item codes to identify provider supplied charges or changes to the total billing of a claim. -
CANCAPT
A charge to compensate the provider when a patient cancels an appointment with insufficient time for the provider to make another appointment with another patient. -
DSC
A reduction in the amount charged as a percentage of the amount. For example a 5% discount for volume purchase. -
ESA
A premium on a service fee is requested because, due to extenuating circumstances, the service took an extraordinary amount of time or supplies. -
FFSTOP
Under agreement between the parties (payor and provider), a guaranteed level of income is established for the provider over a specific, pre-determined period of time. The normal course of business for the provider is submission of fee-for-service claims. Should the fee-for-service income during the specified period of time be less than the agreed to amount, a top-up amount is paid to the provider equal to the difference between the fee-for-service total and the guaranteed income amount for that period of time. The details of the agreement may specify (or not) a requirement for repayment to the payor in the event that the fee-for-service income exceeds the guaranteed amount. -
FNLFEE
Anticipated or actual final fee associated with treating a patient. -
FRSTFEE
Anticipated or actual initial fee associated with treating a patient. -
MARKUP
An increase in the amount charged as a percentage of the amount. For example, 12% markup on product cost. -
MISSAPT
A charge to compensate the provider when a patient does not show for an appointment. -
PERFEE
Anticipated or actual periodic fee associated with treating a patient. For example, expected billing cycle such as monthly, quarterly. The actual period (e.g. monthly, quarterly) is specified in the unit quantity of the Invoice Element. -
PERMBNS
The amount for a performance bonus that is being requested from a payor for the performance of certain services (childhood immunizations, influenza immunizations, mammograms, pap smears) on a sliding scale. That is, for 90% of childhood immunizations to a maximum of $2200/yr. An invoice is created at the end of the service period (one year) and a code is submitted indicating the percentage achieved and the dollar amount claimed. -
RESTOCK
A charge is requested because the patient failed to pick up the item and it took an amount of time to return it to stock for future use. -
TRAVEL
A charge to cover the cost of travel time and/or cost in conjuction with providing a service or product. It may be charged per kilometer or per hour based on the effective agreement. -
URGENT
Premium paid on service fees in compensation for providing an expedited response to an urgent situation. -
_ACTINVOICEDETAILTAXCODE
The billable item codes to identify modifications to a billable item charge by a tax factor applied to the amount. As for example 7% provincial sales tax. -
FST
Federal tax on transactions such as the Goods and Services Tax (GST) -
HST
Joint Federal/Provincial Sales Tax -
PST
Tax levied by the provincial or state jurisdiction such as Provincial Sales Tax -
_ACTINVOICEDETAILPREFERREDACCOMMODATIONCODE
An identifying data string for medical facility accommodations. -
_ACTENCOUNTERACCOMMODATIONCODE
Accommodation type. In Intent mood, represents the accommodation type requested. In Event mood, represents accommodation assigned/used. In Definition mood, represents the available accommodation type. -
_HL7ACCOMMODATIONCODE
Description:Accommodation type. In Intent mood, represents the accommodation type requested. In Event mood, represents accommodation assigned/used. In Definition mood, represents the available accommodation type. -
I
Accommodations used in the care of diseases that are transmitted through casual contact or respiratory transmission. -
P
Accommodations in which there is only 1 bed. -
S
Uniquely designed and elegantly decorated accommodations with many amenities available for an additional charge. -
SP
Accommodations in which there are 2 beds. -
W
Accommodations in which there are 3 or more beds. -
_ACTINVOICEDETAILCLINICALSERVICECODE
An identifying data string for healthcare procedures. -
_ACTINVOICEGROUPCODE
Type of invoice element that is used to assist in describing an Invoice that is either submitted for adjudication or for which is returned on adjudication results. Invoice elements of this type signify a grouping of one or more children (detail) invoice elements. They do not have intrinsic costing associated with them, but merely reflect the sum of all costing for it's immediate children invoice elements. -
_ACTINVOICEINTERGROUPCODE
Type of invoice element that is used to assist in describing an Invoice that is either submitted for adjudication or for which is returned on adjudication results. Invoice elements of this type signify a grouping of one or more children (detail) invoice elements. They do not have intrinsic costing associated with them, but merely reflect the sum of all costing for it's immediate children invoice elements. The domain is only specified for an intermediate invoice element group (non-root or non-top level) for an Invoice. -
CPNDDRGING
A grouping of invoice element groups and details including the ones specifying the compound ingredients being invoiced. It may also contain generic detail items such as markup. -
CPNDINDING
A grouping of invoice element details including the one specifying an ingredient drug being invoiced. It may also contain generic detail items such as tax or markup. -
CPNDSUPING
A grouping of invoice element groups and details including the ones specifying the compound supplies being invoiced. It may also contain generic detail items such as markup. -
DRUGING
A grouping of invoice element details including the one specifying the drug being invoiced. It may also contain generic detail items such as markup. -
FRAMEING
A grouping of invoice element details including the ones specifying the frame fee and the frame dispensing cost that are being invoiced. -
LENSING
A grouping of invoice element details including the ones specifying the lens fee and the lens dispensing cost that are being invoiced. -
PRDING
A grouping of invoice element details including the one specifying the product (good or supply) being invoiced. It may also contain generic detail items such as tax or discount. -
_ACTINVOICEROOTGROUPCODE
Type of invoice element that is used to assist in describing an Invoice that is either submitted for adjudication or for which is returned on adjudication results. Invoice elements of this type signify a grouping of one or more children (detail) invoice elements. They do not have intrinsic costing associated with them, but merely reflect the sum of all costing for it's immediate children invoice elements. Codes from this domain reflect the type of Invoice such as Pharmacy Dispense, Clinical Service and Clinical Product. The domain is only specified for the root (top level) invoice element group for an Invoice. -
CPINV
Clinical product invoice where the Invoice Grouping contains one or more billable item and is supported by clinical product(s). For example, a crutch or a wheelchair. -
CSINV
Clinical Services Invoice which can be used to describe a single service, multiple services or repeated services. [1] Single Clinical services invoice where the Invoice Grouping contains one billable item and is supported by one clinical service. For example, a single service for an office visit or simple clinical procedure (e.g. knee mobilization). [2] Multiple Clinical services invoice where the Invoice Grouping contains more than one billable item, supported by one or more clinical services. The services can be distinct and over multiple dates, but for the same patient. This type of invoice includes a series of treatments which must be adjudicated together. For example, an adjustment and ultrasound for a chiropractic session where fees are associated for each of the services and adjudicated (invoiced) together. [3] Repeated Clinical services invoice where the Invoice Grouping contains one or more billable item, supported by the same clinical service repeated over a period of time. For example, the same Chiropractic adjustment (service or treatment) delivered on 3 separate occasions over a period of time at the discretion of the provider (e.g. month). -
CSPINV
A clinical Invoice Grouping consisting of one or more services and one or more product. Billing for these service(s) and product(s) are supported by multiple clinical billable events (acts). All items in the Invoice Grouping must be adjudicated together to be acceptable to the Adjudicator. For example , a brace (product) invoiced together with the fitting (service). -
FININV
Invoice Grouping without clinical justification. These will not require identification of participants and associations from a clinical context such as patient and provider. Examples are interest charges and mileage. -
OHSINV
A clinical Invoice Grouping consisting of one or more oral health services. Billing for these service(s) are supported by multiple clinical billable events (acts). All items in the Invoice Grouping must be adjudicated together to be acceptable to the Adjudicator. -
PAINV
HealthCare facility preferred accommodation invoice. -
RXCINV
Pharmacy dispense invoice for a compound. -
RXDINV
Pharmacy dispense invoice not involving a compound -
SBFINV
Clinical services invoice where the Invoice Group contains one billable item for multiple clinical services in one or more sessions. -
VRXINV
Vision dispense invoice for up to 2 lens (left and right), frame and optional discount. Eye exams are invoiced as a clinical service invoice. -
_ACTINVOICEELEMENTSUMMARYCODE
Identifies the different types of summary information that can be reported by queries dealing with Statement of Financial Activity (SOFA). The summary information is generally used to help resolve balance discrepancies between providers and payors. -
_INVOICEELEMENTADJUDICATED
Total counts and total net amounts adjudicated for all Invoice Groupings that were adjudicated within a time period based on the adjudication date of the Invoice Grouping. -
ADNFPPELAT
Identifies the total net amount of all Invoice Groupings that were adjudicated as payable prior to the specified time period (based on adjudication date), subsequently cancelled in the specified period and submitted electronically. -
ADNFPPELCT
Identifies the total number of all Invoice Groupings that were adjudicated as payable prior to the specified time period (based on adjudication date), subsequently cancelled in the specified period and submitted electronically. -
ADNFPPMNAT
Identifies the total net amount of all Invoice Groupings that were adjudicated as payable prior to the specified time period (based on adjudication date), subsequently cancelled in the specified period and submitted manually. -
ADNFPPMNCT
Identifies the total number of all Invoice Groupings that were adjudicated as payable prior to the specified time period (based on adjudication date), subsequently cancelled in the specified period and submitted manually. -
ADNFSPELAT
Identifies the total net amount of all Invoice Groupings that were adjudicated as payable during the specified time period (based on adjudication date), subsequently nullified in the specified period and submitted electronically. -
ADNFSPELCT
Identifies the total number of all Invoice Groupings that were adjudicated as payable during the specified time period (based on adjudication date), subsequently nullified in the specified period and submitted electronically. -
ADNFSPMNAT
Identifies the total net amount of all Invoice Groupings that were adjudicated as payable during the specified time period (based on adjudication date), subsequently cancelled in the specified period and submitted manually. -
ADNFSPMNCT
Identifies the total number of all Invoice Groupings that were adjudicated as payable during the specified time period (based on adjudication date), subsequently cancelled in the specified period and submitted manually. -
ADNPPPELAT
Identifies the total net amount of all Invoice Groupings that were adjudicated as payable prior to the specified time period (based on adjudication date) that do not match a specified payee (e.g. pay patient) and submitted electronically. -
ADNPPPELCT
Identifies the total number of all Invoice Groupings that were adjudicated as payable prior to the specified time period (based on adjudication date) that do not match a specified payee (e.g. pay patient) and submitted electronically. -
ADNPPPMNAT
Identifies the total net amount of all Invoice Groupings that were adjudicated as payable prior to the specified time period (based on adjudication date) that do not match a specified payee (e.g. pay patient) and submitted manually. -
ADNPPPMNCT
Identifies the total number of all Invoice Groupings that were adjudicated as payable prior to the specified time period (based on adjudication date) that do not match a specified payee (e.g. pay patient) and submitted manually. -
ADNPSPELAT
Identifies the total net amount of all Invoice Groupings that were adjudicated as payable during the specified time period (based on adjudication date) that do not match a specified payee (e.g. pay patient) and submitted electronically. -
ADNPSPELCT
Identifies the total number of all Invoice Groupings that were adjudicated as payable during the specified time period (based on adjudication date) that do not match a specified payee (e.g. pay patient) and submitted electronically. -
ADNPSPMNAT
Identifies the total net amount of all Invoice Groupings that were adjudicated as payable during the specified time period (based on adjudication date) that do not match a specified payee (e.g. pay patient) and submitted manually. -
ADNPSPMNCT
Identifies the total number of all Invoice Groupings that were adjudicated as payable during the specified time period (based on adjudication date) that do not match a specified payee (e.g. pay patient) and submitted manually. -
ADPPPPELAT
Identifies the total net amount of all Invoice Groupings that were adjudicated as payable prior to the specified time period (based on adjudication date) that match a specified payee (e.g. pay provider) and submitted electronically. -
ADPPPPELCT
Identifies the total number of all Invoice Groupings that were adjudicated as payable prior to the specified time period (based on adjudication date) that match a specified payee (e.g. pay provider) and submitted electronically. -
ADPPPPMNAT
Identifies the total net amount of all Invoice Groupings that were adjudicated as payable prior to the specified time period (based on adjudication date) that match a specified payee (e.g. pay provider) and submitted manually. -
ADPPPPMNCT
Identifies the total number of all Invoice Groupings that were adjudicated as payable prior to the specified time period (based on adjudication date) that match a specified payee (e.g. pay provider) and submitted manually. -
ADPPSPELAT
Identifies the total net amount of all Invoice Groupings that were adjudicated as payable during the specified time period (based on adjudication date) that match a specified payee (e.g. pay provider) and submitted electronically. -
ADPPSPELCT
Identifies the total number of all Invoice Groupings that were adjudicated as payable during the specified time period (based on adjudication date) that match a specified payee (e.g. pay provider) and submitted electronically. -
ADPPSPMNAT
Identifies the total net amount of all Invoice Groupings that were adjudicated as payable during the specified time period (based on adjudication date) that match a specified payee (e.g. pay provider) and submitted manually. -
ADPPSPMNCT
Identifies the total number of all Invoice Groupings that were adjudicated as payable during the specified time period (based on adjudication date) that match a specified payee (e.g. pay provider) and submitted manually. -
ADRFPPELAT
Identifies the total net amount of all Invoice Groupings that were adjudicated as refused prior to the specified time period (based on adjudication date) and submitted electronically. -
ADRFPPELCT
Identifies the total number of all Invoice Groupings that were adjudicated as refused prior to the specified time period (based on adjudication date) and submitted electronically. -
ADRFPPMNAT
Identifies the total net amount of all Invoice Groupings that were adjudicated as refused prior to the specified time period (based on adjudication date) and submitted manually. -
ADRFPPMNCT
Identifies the total number of all Invoice Groupings that were adjudicated as refused prior to the specified time period (based on adjudication date) and submitted manually. -
ADRFSPELAT
Identifies the total net amount of all Invoice Groupings that were adjudicated as refused during the specified time period (based on adjudication date) and submitted electronically. -
ADRFSPELCT
Identifies the total number of all Invoice Groupings that were adjudicated as refused during the specified time period (based on adjudication date) and submitted electronically. -
ADRFSPMNAT
Identifies the total net amount of all Invoice Groupings that were adjudicated as refused during the specified time period (based on adjudication date) and submitted manually. -
ADRFSPMNCT
Identifies the total number of all Invoice Groupings that were adjudicated as refused during the specified time period (based on adjudication date) and submitted manually. -
_INVOICEELEMENTPAID
Total counts and total net amounts paid for all Invoice Groupings that were paid within a time period based on the payment date. -
PDNFPPELAT
Identifies the total net amount of all Invoice Groupings that were paid prior to the specified time period (based on payment date), subsequently nullified in the specified period and submitted electronically. -
PDNFPPELCT
Identifies the total number of all Invoice Groupings that were paid prior to the specified time period (based on payment date), subsequently nullified in the specified period and submitted electronically. -
PDNFPPMNAT
Identifies the total net amount of all Invoice Groupings that were paid prior to the specified time period (based on payment date), subsequently nullified in the specified period and submitted manually. -
PDNFPPMNCT
Identifies the total number of all Invoice Groupings that were paid prior to the specified time period (based on payment date), subsequently nullified in the specified period and submitted manually. -
PDNFSPELAT
Identifies the total net amount of all Invoice Groupings that were paid during the specified time period (based on payment date), subsequently nullified in the specified period and submitted electronically. -
PDNFSPELCT
Identifies the total number of all Invoice Groupings that were paid during the specified time period (based on payment date), subsequently cancelled in the specified period and submitted electronically. -
PDNFSPMNAT
Identifies the total net amount of all Invoice Groupings that were paid during the specified time period (based on payment date), subsequently nullified in the specified period and submitted manually. -
PDNFSPMNCT
Identifies the total number of all Invoice Groupings that were paid during the specified time period (based on payment date), subsequently nullified in the specified period and submitted manually. -
PDNPPPELAT
Identifies the total net amount of all Invoice Groupings that were paid prior to the specified time period (based on payment date) that do not match a specified payee (e.g. pay patient) and submitted electronically. -
PDNPPPELCT
Identifies the total number of all Invoice Groupings that were paid prior to the specified time period (based on payment date) that do not match a specified payee (e.g. pay patient) and submitted electronically. -
PDNPPPMNAT
Identifies the total net amount of all Invoice Groupings that were paid prior to the specified time period (based on payment date) that do not match a specified payee (e.g. pay patient) and submitted manually. -
PDNPPPMNCT
Identifies the total number of all Invoice Groupings that were paid prior to the specified time period (based on payment date) that do not match a specified payee (e.g. pay patient) and submitted manually. -
PDNPSPELAT
Identifies the total net amount of all Invoice Groupings that were paid during the specified time period (based on payment date) that do not match a specified payee (e.g. pay patient) and submitted electronically. -
PDNPSPELCT
Identifies the total number of all Invoice Groupings that were paid during the specified time period (based on payment date) that do not match a specified payee (e.g. pay patient) and submitted electronically. -
PDNPSPMNAT
Identifies the total net amount of all Invoice Groupings that were paid during the specified time period (based on payment date) that do not match a specified payee (e.g. pay patient) and submitted manually. -
PDNPSPMNCT
Identifies the total number of all Invoice Groupings that were paid during the specified time period (based on payment date) that do not match a specified payee (e.g. pay patient) and submitted manually. -
PDPPPPELAT
Identifies the total net amount of all Invoice Groupings that were paid prior to the specified time period (based on payment date) that match a specified payee (e.g. pay provider) and submitted electronically. -
PDPPPPELCT
Identifies the total number of all Invoice Groupings that were paid prior to the specified time period (based on payment date) that match a specified payee (e.g. pay provider) and submitted electronically. -
PDPPPPMNAT
Identifies the total net amount of all Invoice Groupings that were paid prior to the specified time period (based on payment date) that match a specified payee (e.g. pay provider) and submitted manually. -
PDPPPPMNCT
Identifies the total number of all Invoice Groupings that were paid prior to the specified time period (based on payment date) that match a specified payee (e.g. pay provider) and submitted manually. -
PDPPSPELAT
Identifies the total net amount of all Invoice Groupings that were paid during the specified time period (based on payment date) that match a specified payee (e.g. pay provider) and submitted electronically. -
PDPPSPELCT
Identifies the total number of all Invoice Groupings that were paid during the specified time period (based on payment date) that match a specified payee (e.g. pay provider) and submitted electronically. -
PDPPSPMNAT
Identifies the total net amount of all Invoice Groupings that were paid during the specified time period (based on payment date) that match a specified payee (e.g. pay provider) and submitted manually. -
PDPPSPMNCT
Identifies the total number of all Invoice Groupings that were paid during the specified time period (based on payment date) that match a specified payee (e.g. pay provider) and submitted manually. -
_INVOICEELEMENTSUBMITTED
Total counts and total net amounts billed for all Invoice Groupings that were submitted within a time period. Adjudicated invoice elements are included. -
SBBLELAT
Identifies the total net amount billed for all submitted Invoice Groupings within a time period and submitted electronically. Adjudicated invoice elements are included. -
SBBLELCT
Identifies the total number of submitted Invoice Groupings within a time period and submitted electronically. Adjudicated invoice elements are included. -
SBNFELAT
Identifies the total net amount billed for all submitted Invoice Groupings that were nullified within a time period and submitted electronically. Adjudicated invoice elements are included. -
SBNFELCT
Identifies the total number of submitted Invoice Groupings that were nullified within a time period and submitted electronically. Adjudicated invoice elements are included. -
SBPDELAT
Identifies the total net amount billed for all submitted Invoice Groupings that are pended or held by the payor, within a time period and submitted electronically. Adjudicated invoice elements are not included. -
SBPDELCT
Identifies the total number of submitted Invoice Groupings that are pended or held by the payor, within a time period and submitted electronically. Adjudicated invoice elements are not included. -
_ACTINVOICEOVERRIDECODE
Includes coded responses that will occur as a result of the adjudication of an electronic invoice at a summary level and provides guidance on interpretation of the referenced adjudication results. -
COVGE
Insurance coverage problems have been encountered. Additional explanation information to be supplied. -
EFORM
Electronic form with supporting or additional information to follow. -
FAX
Fax with supporting or additional information to follow. -
GFTH
The medical service was provided to a patient in good faith that they had medical coverage, although no evidence of coverage was available before service was rendered. -
LATE
Knowingly over the payor's published time limit for this invoice possibly due to a previous payor's delays in processing. Additional reason information will be supplied. -
MANUAL
Manual review of the invoice is requested. Additional information to be supplied. This may be used in the case of an appeal. -
OOJ
The medical service and/or product was provided to a patient that has coverage in another jurisdiction. -
ORTHO
The service provided is required for orthodontic purposes. If the covered party has orthodontic coverage, then the service may be paid. -
PAPER
Paper documentation (or other physical format) with supporting or additional information to follow. -
PIE
Public Insurance has been exhausted. Invoice has not been sent to Public Insuror and therefore no Explanation Of Benefits (EOB) is provided with this Invoice submission. -
PYRDELAY
Allows provider to explain lateness of invoice to a subsequent payor. -
REFNR
Rules of practice do not require a physician's referral for the provider to perform a billable service. -
REPSERV
The same service was delivered within a time period that would usually indicate a duplicate billing. However, the repeated service is a medical necessity and therefore not a duplicate. -
UNRELAT
The service provided is not related to another billed service. For example, 2 unrelated services provided on the same day to the same patient which may normally result in a refused payment for one of the items. -
VERBAUTH
The provider has received a verbal permission from an authoritative source to perform the service or supply the item being invoiced. -
_ACTLISTCODE
Provides codes associated with ActClass value of LIST (working list) -
_ACTOBSERVATIONLIST
ActObservationList -
CARELIST
List of acts representing a care plan. The acts can be in a varierty of moods including event (EVN) to record acts that have been carried out as part of the care plan. -
CONDLIST
List of condition observations. -
INTOLIST
List of intolerance observations. -
PROBLIST
List of problem observations. -
RISKLIST
List of risk factor observations. -
GOALLIST
List of observations in goal mood. -
_ACTTHERAPYDURATIONWORKINGLISTCODE
Codes used to identify different types of 'duration-based' working lists. Examples include "Continuous/Chronic", "Short-Term" and "As-Needed". -
_ACTMEDICATIONTHERAPYDURATIONWORKINGLISTCODE
Definition:A collection of concepts that identifies different types of 'duration-based' mediation working lists. Examples:"Continuous/Chronic" "Short-Term" and "As Needed" -
ACU
Definition:A list of medications which the patient is only expected to consume for the duration of the current order or limited set of orders and which is not expected to be renewed. -
CHRON
Definition:A list of medications which are expected to be continued beyond the present order and which the patient should be assumed to be taking unless explicitly stopped. -
ONET
Definition:A list of medications which the patient is intended to be administered only once. -
PRN
Definition:A list of medications which the patient will consume intermittently based on the behavior of the condition for which the medication is indicated. -
MEDLIST
List of medications. -
CURMEDLIST
List of current medications. -
DISCMEDLIST
List of discharge medications. -
HISTMEDLIST
Historical list of medications. -
_ACTMONITORINGPROTOCOLCODE
Identifies types of monitoring programs -
CTLSUB
A monitoring program that focuses on narcotics and/or commonly abused substances that are subject to legal restriction. -
INV
Definition:A monitoring program that focuses on a drug which is under investigation and has not received regulatory approval for the condition being investigated -
LU
Description:A drug that can be prescribed (and reimbursed) only if it meets certain criteria. -
OTC
Medicines designated in this way may be supplied for patient use without a prescription. The exact form of categorisation will vary in different realms. -
RX
Some form of prescription is required before the related medicine can be supplied for a patient. The exact form of regulation will vary in different realms. -
SA
Definition:A drug that requires prior approval (to be reimbursed) before being dispensed -
SAC
Description:A drug that requires special access permission to be prescribed and dispensed. -
_ACTNONOBSERVATIONINDICATIONCODE
Description:Concepts representing indications (reasons for clinical action) other than diagnosis and symptoms. -
IND01
Description:Contrast agent required for imaging study. -
IND02
Description:Provision of prescription or direction to consume a product for purposes of bowel clearance in preparation for a colonoscopy. -
IND03
Description:Provision of medication as a preventative measure during a treatment or other period of increased risk. -
IND04
Description:Provision of medication during pre-operative phase; e.g., antibiotics before dental surgery or bowel prep before colon surgery. -
IND05
Description:Provision of medication for pregnancy --e.g., vitamins, antibiotic treatments for vaginal tract colonization, etc. -
_ACTOBSERVATIONVERIFICATIONTYPE
Identifies the type of verification investigation being undertaken with respect to the subject of the verification activity. Examples: Verification of eligibility for coverage under a policy or program - aka enrolled/covered by a policy or program Verification of record - e.g., person has record in an immunization registry Verification of enumeration - e.g. NPI Verification of Board Certification - provider specific Verification of Certification - e.g. JAHCO, NCQA, URAC Verification of Conformance - e.g. entity use with HIPAA, conformant to the CCHIT EHR system criteria Verification of Provider Credentials Verification of no adverse findings - e.g. on National Provider Data Bank, Health Integrity Protection Data Base (HIPDB) -
VFPAPER
Definition:Indicates that the paper version of the record has, should be or is being verified against the electronic version. -
_ACTPAYMENTCODE
Code identifying the method or the movement of payment instructions. Codes are drawn from X12 data element 591 (PaymentMethodCode) -
ACH
Automated Clearing House (ACH). -
CHK
A written order to a bank to pay the amount specified from funds on deposit. -
DDP
Electronic Funds Transfer (EFT) deposit into the payee's bank account -
NON
Non-Payment Data. -
_ACTPHARMACYSUPPLYTYPE
Identifies types of dispensing events -
DF
A fill providing sufficient supply for one day -
EM
A supply action where there is no 'valid' order for the supplied medication. E.g. Emergency vacation supply, weekend supply (when prescriber is unavailable to provide a renewal prescription) -
SO
An emergency supply where the expectation is that a formal order authorizing the supply will be provided at a later date. -
FF
The initial fill against an order. (This includes initial fills against refill orders.) -
FFC
A first fill where the quantity supplied is equal to one full repetition of the ordered amount. (e.g. If the order was 90 tablets, 3 refills, a complete fill would be for the full 90 tablets). -
FFP
A first fill where the quantity supplied is less than one full repetition of the ordered amount. (e.g. If the order was 90 tablets, 3 refills, a partial fill might be for only 30 tablets.) -
FFSS
A first fill where the strength supplied is less than the ordered strength. (e.g. 10mg for an order of 50mg where a subsequent fill will dispense 40mg tablets). -
TF
A fill where a small portion is provided to allow for determination of the therapy effectiveness and patient tolerance. -
FS
A supply action to restock a smaller more local dispensary. -
MS
A supply of a manufacturer sample -
RF
A fill against an order that has already been filled (or partially filled) at least once. -
UD
A supply action that provides sufficient material for a single dose. -
RFC
A refill where the quantity supplied is equal to one full repetition of the ordered amount. (e.g. If the order was 90 tablets, 3 refills, a complete fill would be for the full 90 tablets.) -
RFCS
A refill where the quantity supplied is equal to one full repetition of the ordered amount. (e.g. If the order was 90 tablets, 3 refills, a complete fill would be for the full 90 tablets.) and where the strength supplied is less than the ordered strength (e.g. 10mg for an order of 50mg where a subsequent fill will dispense 40mg tablets). -
RFF
The first fill against an order that has already been filled at least once at another facility. -
RFFS
The first fill against an order that has already been filled at least once at another facility and where the strength supplied is less than the ordered strength (e.g. 10mg for an order of 50mg where a subsequent fill will dispense 40mg tablets). -
RFP
A refill where the quantity supplied is less than one full repetition of the ordered amount. (e.g. If the order was 90 tablets, 3 refills, a partial fill might be for only 30 tablets.) -
RFPS
A refill where the quantity supplied is less than one full repetition of the ordered amount. (e.g. If the order was 90 tablets, 3 refills, a partial fill might be for only 30 tablets.) and where the strength supplied is less than the ordered strength (e.g. 10mg for an order of 50mg where a subsequent fill will dispense 40mg tablets). -
RFS
A fill against an order that has already been filled (or partially filled) at least once and where the strength supplied is less than the ordered strength (e.g. 10mg for an order of 50mg where a subsequent fill will dispense 40mg tablets). -
TB
A fill where the remainder of a 'complete' fill is provided after a trial fill has been provided. -
TBS
A fill where the remainder of a 'complete' fill is provided after a trial fill has been provided and where the strength supplied is less than the ordered strength (e.g. 10mg for an order of 50mg where a subsequent fill will dispense 40mg tablets). -
UDE
A supply action that provides sufficient material for a single dose via multiple products. E.g. 2 50mg tablets for a 100mg unit dose. -
_ACTPOLICYTYPE
Description:Types of policies that further specify the ActClassPolicy value set. -
_ACTPRIVACYPOLICY
A policy deeming certain information to be private to an individual or organization. Definition: A mandate, obligation, requirement, rule, or expectation relating to privacy. Discussion: ActPrivacyPolicyType codes support the designation of the 1..* policies that are applicable to an Act such as a Consent Directive, a Role such as a VIP Patient, or an Entity such as a patient who is a minor. 1..* ActPrivacyPolicyType values may be associated with an Act or Role to indicate the policies that govern the assignment of an Act or Role confidentialityCode. Use of multiple ActPrivacyPolicyType values enables fine grain specification of applicable policies, but must be carefully assigned to ensure cogency and avoid creation of conflicting policy mandates. Usage Note: Statutory title may be named in the ActClassPolicy Act Act.title to specify which privacy policy is being referenced. -
_ACTCONSENTDIRECTIVE
Specifies the type of agreement between one or more grantor and grantee in which rights and obligations related to one or more shared items of interest are allocated. Usage Note: Such agreements may be considered "consent directives" or "contracts" depending on the context, and are considered closely related or synonymous from a legal perspective. Examples: Healthcare Privacy Consent Directive permitting or restricting in whole or part the collection, access, use, and disclosure of health information, and any associated handling caveats. Healthcare Medical Consent Directive to receive medical procedures after being informed of risks and benefits, thereby reducing the grantee's liability. Research Informed Consent for participation in clinical trials and disclosure of health information after being informed of risks and benefits, thereby reducing the grantee's liability. Substitute decision maker delegation in which the grantee assumes responsibility to act on behalf of the grantor. Contracts in which the agreement requires assent/dissent by the grantor of terms offered by a grantee, a consumer opts out of an "award" system for use of a retailer's marketing or credit card vendor's point collection cards in exchange for allowing purchase tracking and profiling. A mobile device or App privacy policy and terms of service to which a user must agree in whole or in part in order to utilize the service. Agreements between a client and an authorization server or between an authorization server and a resource operator and/or resource owner permitting or restricting e.g., collection, access, use, and disclosure of information, and any associated handling caveats. -
EMRGONLY
This general consent directive specifically limits disclosure of health information for purpose of emergency treatment. Additional parameters may further limit the disclosure to specific users, roles, duration, types of information, and impose uses obligations. Definition: Opt-in to disclosure of health information for emergency only consent directive. -
GRANTORCHOICE
A grantor's terms of agreement to which a grantee may assent or dissent, and which may include an opportunity for a grantee to request restrictions or extensions. Comment: A grantor typically is able to stipulate preferred terms of agreement when the grantor has control over the topic of the agreement, which a grantee must accept in full or may be offered an opportunity to extend or restrict certain terms. Usage Note: If the grantor's term of agreement must be accepted in full, then this is considered "basic consent". If a grantee is offered an opportunity to extend or restrict certain terms, then the agreement is considered "granular consent". Examples: Healthcare: A PHR account holder [grantor] may require any PHR user [grantee] to accept the terms of agreement in full, or may permit a PHR user to extend or restrict terms selected by the account holder or requested by the PHR user. Non-healthcare: The owner of a resource server [grantor] may require any authorization server [grantee] to meet authorization requirements stipulated in the grantor's terms of agreement. -
IMPLIED
A grantor's presumed assent to the grantee's terms of agreement is based on the grantor's behavior, which may result from not expressly assenting to the consent directive offered, or from having no right to assent or dissent offered by the grantee. Comment: Implied or "implicit" consent occurs when the behavior of the grantor is understood by a reasonable person to signal agreement to the grantee's terms. Usage Note: Implied consent with no opportunity to assent or dissent to certain terms is considered "basic consent". Examples: Healthcare: A patient schedules an appointment with a provider, and either does not take the opportunity to expressly assent or dissent to the provider's consent directive, does not have an opportunity to do so, as in the case where emergency care is required, or simply behaves as though the patient [grantor] agrees to the rights granted to the provider [grantee] in an implicit consent directive. An injured and unconscious patient is deemed to have assented to emergency treatment by those permitted to do so under jurisdictional laws, e.g., Good Samaritan laws. Non-healthcare: Upon receiving a driver's license, the driver is deemed to have assented without explicitly consenting to undergoing field sobriety tests. A corporation that does business in a foreign nation is deemed to have deemed to have assented without explicitly consenting to abide by that nation's laws. -
IMPLIEDD
A grantor's presumed assent to the grantee's terms of agreement, which is based on the grantor's behavior, and includes a right to dissent to certain terms. Comment: A grantor assenting to the grantee's terms of agreement may or may not exercise a right to dissent to grantor selected terms or to grantee's selected terms to which a grantor may dissent. Usage Note: Implied or "implicit" consent with an "opportunity to dissent" occurs when the grantor's behavior is understood by a reasonable person to signal assent to the grantee's terms of agreement whether the grantor requests or the grantee approves further restrictions, is considered "granular consent". Examples: Healthcare Examples: A healthcare provider deems a patient's assent to disclosure of health information to family members and friends, but offers an opportunity or permits the patient to dissent to such disclosures. A health information exchanges deems a patient to have assented to disclosure of health information for treatment purposes, but offers the patient an opportunity to dissents to disclosure to particular provider organizations. Non-healthcare Examples: A bank deems a banking customer's assent to specified collection, access, use, or disclosure of financial information as a requirement of holding a bank account, but provides the user an opportunity to limit third-party collection, access, use or disclosure of that information for marketing purposes. -
NOCONSENT
No notification or opportunity is provided for a grantor to assent or dissent to a grantee's terms of agreement. Comment: A "No Consent" policy scheme provides no opportunity for accommodation of an individual's preferences, and may not comply with Fair Information Practice Principles [FIPP] by enabling the data subject to object, access collected information, correct errors, or have accounting of disclosures. Usage Note: The grantee's terms of agreement, may be available to the grantor by reviewing the grantee's privacy policies, but there is no notice by which a grantor is apprised of the policy directly or able to acknowledge. Examples: Healthcare: Without notification or an opportunity to assent or dissent, a patient's health information is automatically included in and available (often according to certain rules) through a health information exchange. Note that this differs from implied consent, where the patient is assumed to have consented. Without notification or an opportunity to assent or dissent, a patient's health information is collected, accessed, used, or disclosed for research, public health, security, fraud prevention, court order, or law enforcement. Non-healthcare: Without notification or an opportunity to assent or dissent, a consumer's healthcare or non-healthcare internet searches are aggregated for secondary uses such as behavioral tracking and profiling. Without notification or an opportunity to assent or dissent, a consumer's location and activities in a shopping mall are tracked by RFID tags on purchased items. -
NOPP
Acknowledgement of custodian notice of privacy practices. Usage Notes: This type of consent directive acknowledges a custodian's notice of privacy practices including its permitted collection, access, use and disclosure of health information to users and for purposes of use specified. -
OPTIN
A grantor's assent to the terms of an agreement offered by a grantee without an opportunity for to dissent to any terms. Comment: Acceptance of a grantee's terms pertaining, for example, to permissible activities, purposes of use, handling caveats, expiry date, and revocation policies. Usage Note: Opt-in with no opportunity for a grantor to restrict certain permissions sought by the grantee is considered "basic consent". Examples: Healthcare: A patient [grantor] signs a provider's [grantee's] consent directive form, which lists permissible collection, access, use, or disclosure activities, purposes of use, handling caveats, and revocation policies. Non-healthcare: An employee [grantor] signs an employer's [grantee's] non-disclosure and non-compete agreement. -
OPTINR
A grantor's assent to the grantee's terms of an agreement with an opportunity for to dissent to certain grantor or grantee selected terms. Comment: A grantor dissenting to the grantee's terms of agreement may or may not exercise a right to assent to grantor's pre-approved restrictions or to grantee's selected terms to which a grantor may dissent. Usage Note: Opt-in with restrictions is considered "granular consent" because the grantor has an opportunity to narrow the permissions sought by the grantee. Examples: Healthcare: A patient assent to grantee's consent directive terms for collection, access, use, or disclosure of health information, and dissents to disclosure to certain recipients as allowed by the provider's pre-approved restriction list. Non-Healthcare: A cell phone user assents to the cell phone's privacy practices and terms of use, but dissents from location tracking by turning off the cell phone's tracking capability. -
OPTOUT
A grantor's dissent to the terms of agreement offered by a grantee without an opportunity for to assent to any terms. Comment: Rejection of a grantee's terms of agreement pertaining, for example, to permissible activities, purposes of use, handling caveats, expiry date, and revocation policies. Usage Note: Opt-out with no opportunity for a grantor to permit certain permissions sought by the grantee is considered "basic consent". Examples: Healthcare: A patient [grantor] declines to sign a provider's [grantee's] consent directive form, which lists permissible collection, access, use, or disclosure activities, purposes of use, handling caveats, revocation policies, and consequences of not assenting. Non-healthcare: An employee [grantor] refuses to sign an employer's [grantee's] agreement not to join unions or participate in a strike where state law protects employee's collective bargaining rights. A citizen [grantor] refuses to enroll in mandatory government [grantee] health insurance based on religious beliefs, which is an exemption. -
OPTOUTE
A grantor's dissent to the grantee's terms of agreement except for certain grantor or grantee selected terms. Comment: A rejection of a grantee's terms of agreement while assenting to certain permissions sought by the grantee or requesting approval of additional grantor terms. Usage Note: Opt-out with exceptions is considered a "granular consent" because the grantor has an opportunity to accept certain permissions sought by the grantee or request additional grantor terms, while rejecting other grantee terms. Examples: Healthcare: A patient [grantor] dissents to a health information exchange consent directive with the exception of disclosure based on a limited "time to live" shared secret [e.g., a token or password], which the patient can give to a provider when seeking care. Non-healthcare: A social media user [grantor] dissents from public access to their account, but assents to access to a circle of friends. -
_ACTPRIVACYLAW
A jurisdictional mandate, regulation, obligation, requirement, rule, or expectation deeming certain information to be private to an individual or organization, which is imposed on: The activity of a governed party The behavior of a governed party The manner in which an act is executed by a governed party -
_ACTUSPRIVACYLAW
Definition: A jurisdictional mandate in the U.S. relating to privacy. Usage Note: ActPrivacyLaw codes may be associated with an Act or a Role to indicate the legal provision to which the assignment of an Act.confidentialityCode or Role.confidentialtyCode complies. May be used to further specify rationale for assignment of other ActPrivacyPolicy codes in the US realm, e.g., ETH and 42CFRPart2 can be differentiated from ETH and Title38Part1. -
_42CFRPART2
42 CFR Part 2 stipulates the right of an individual who has applied for or been given diagnosis or treatment for alcohol or drug abuse at a federally assisted program. Definition: Non-disclosure of health information relating to health care paid for by a federally assisted substance abuse program without patient consent. Usage Note: May be associated with an Act or a Role to indicate the legal provision to which the assignment of an Act.confidentialityCode or Role.confidentialityCode complies. -
COMMONRULE
U.S. Federal regulations governing the protection of human subjects in research (codified at Subpart A of 45 CFR part 46) that has been adopted by 15 U.S. Federal departments and agencies in an effort to promote uniformity, understanding, and compliance with human subject protections. Existing regulations governing the protection of human subjects in Food and Drug Administration (FDA)-regulated research (21 CFR parts 50, 56, 312, and 812) are separate from the Common Rule but include similar requirements. Definition: U.S. federal laws governing research-related privacy policies. Usage Note: May be associated with an Act or a Role to indicate the legal provision to which the assignment of an Act.confidentialityCode or Role.confidentialtyCode complies. -
HIPAANOPP
The U.S. Public Law 104-191 Health Insurance Portability and Accountability Act (HIPAA) Privacy Rule (45 CFR Part 164 Subpart E) permits access, use and disclosure of certain personal health information (PHI as defined under the law) for purposes of Treatment, Payment, and Operations, and requires that the provider ask that patients acknowledge the Provider's Notice of Privacy Practices as permitted conduct under the law. Definition: Notification of HIPAA Privacy Practices. Usage Note: May be associated with an Act or a Role to indicate the legal provision to which the assignment of an Act.confidentialityCode or Role.confidentialtyCode complies. -
HIPAAPSYNOTES
The U.S. Public Law 104-191 Health Insurance Portability and Accountability Act (HIPAA) Privacy Rule (45 CFR Part 164 Section 164.508) requires authorization for certain uses and disclosure of psychotherapy notes. Definition: Authorization that must be obtained for disclosure of psychotherapy notes. Usage Note: May be associated with an Act or a Role to indicate the legal provision to which the assignment of an Act.confidentialityCode or Role.confidentialityCode complies. -
HIPAASELFPAY
Section 13405(a) of the Health Information Technology for Economic and Clinical Health Act (HITECH) stipulates the right of an individual to have disclosures regarding certain health care items or services for which the individual pays out of pocket in full restricted from a health plan. Definition: Non-disclosure of health information to a health plan relating to health care items or services for which an individual pays out of pocket in full. Usage Note: May be associated with an Act or a Role to indicate the legal provision to which the assignment of an Act.confidentialityCode or Role.confidentialityCode complies. -
TITLE38SECTION7332
Title 38 Part 1-protected information may only be disclosed to a third party with the special written consent of the patient except where expressly authorized by 38 USC 7332. VA may disclose this information for specific purposes to: VA employees on a need to know basis - more restrictive than Privacy Act need to know; contractors who need the information in order to perform or fulfil the duties of the contract; and researchers who provide assurances that the information will not be identified in any report. This information may also be disclosed without consent where patient lacks decision-making capacity; in a medical emergency for the purpose of treating a condition which poses an immediate threat to the health of any individual and which requires immediate medical intervention; for eye, tissue, or organ donation purposes; and disclosure of HIV information for public health purposes. Definition: Title 38 Part 1 - Section 1.462 Confidentiality restrictions. (a) General. The patient records to which Sections 1.460 through 1.499 of this part apply may be disclosed or used only as permitted by these regulations and may not otherwise be disclosed or used in any civil, criminal, administrative, or legislative proceedings conducted by any Federal, State, or local authority. Any disclosure made under these regulations must be limited to that information which is necessary to carry out the purpose of the disclosure. SUBCHAPTER III--PROTECTION OF PATIENT RIGHTS Sec. 7332. Confidentiality of certain medical records (a)(1) Records of the identity, diagnosis, prognosis, or treatment of any patient or subject which are maintained in connection with the performance of any program or activity (including education, training, treatment, rehabilitation, or research) relating to drug abuse, alcoholism or alcohol abuse, infection with the human immunodeficiency virus, or sickle cell anemia which is carried out by or for the Department under this title shall, except as provided in subsections (e) and (f), be confidential, and (section 5701 of this title to the contrary notwithstanding) such records may be disclosed only for the purposes and under the circumstances expressly authorized under subsection (b). Usage Note: May be associated with an Act or a Role to indicate the legal provision to which the assignment of an Act.confidentialityCode or Role.confidentialityCode complies. -
_INFORMATIONSENSITIVITYPOLICY
A mandate, obligation, requirement, rule, or expectation characterizing the value or importance of a resource and may include its vulnerability. (Based on ISO7498-2:1989. Note: The vulnerability of personally identifiable sensitive information may be based on concerns that the unauthorized disclosure may result in social stigmatization or discrimination.) Description: Types of Sensitivity policy that apply to Acts or Roles. A sensitivity policy is adopted by an enterprise or group of enterprises (a 'policy domain') through a formal data use agreement that stipulates the value, importance, and vulnerability of information. A sensitivity code representing a sensitivity policy may be associated with criteria such as categories of information or sets of information identifiers (e.g., a value set of clinical codes or branch in a code system hierarchy). These criteria may in turn be used for the Policy Decision Point in a Security Engine. A sensitivity code may be used to set the confidentiality code used on information about Acts and Roles to trigger the security mechanisms required to control how security principals (i.e., a person, a machine, a software application) may act on the information (e.g., collection, access, use, or disclosure). Sensitivity codes are never assigned to the transport or business envelope containing patient specific information being exchanged outside of a policy domain as this would disclose the information intended to be protected by the policy. When sensitive information is exchanged with others outside of a policy domain, the confidentiality code on the transport or business envelope conveys the receiver's responsibilities and indicates the how the information is to be safeguarded without unauthorized disclosure of the sensitive information. This ensures that sensitive information is treated by receivers as the sender intends, accomplishing interoperability without point to point negotiations. Usage Note: Sensitivity codes are not useful for interoperability outside of a policy domain because sensitivity policies are typically localized and vary drastically across policy domains even for the same information category because of differing organizational business rules, security policies, and jurisdictional requirements. For example, an employee's sensitivity code would make little sense for use outside of a policy domain. 'Taboo' would rarely be useful outside of a policy domain unless there are jurisdictional requirements requiring that a provider disclose sensitive information to a patient directly. Sensitivity codes may be more appropriate in a legacy system's Master Files in order to notify those who access a patient's orders and observations about the sensitivity policies that apply. Newer systems may have a security engine that uses a sensitivity policy's criteria directly. The specializable InformationSensitivityPolicy Act.code may be useful in some scenarios if used in combination with a sensitivity identifier and/or Act.title. -
_ACTINFORMATIONSENSITIVITYPOLICY
Types of sensitivity policies that apply to Acts. Act.confidentialityCode is defined in the RIM as "constraints around appropriate disclosure of information about this Act, regardless of mood." Usage Note: ActSensitivity codes are used to bind information to an Act.confidentialityCode according to local sensitivity policy so that those confidentiality codes can then govern its handling across enterprises. Internally to a policy domain, however, local policies guide the access control system on how end users in that policy domain are able to use information tagged with these sensitivity values. -
ETH
Policy for handling alcohol or drug-abuse information, which will be afforded heightened confidentiality. Information handling protocols based on organizational policies related to alcohol or drug-abuse information that is deemed sensitive. Usage Note: If there is a jurisdictional mandate, then use the applicable ActPrivacyLaw code system, and specify the law rather than or in addition to this more generic code. -
GDIS
Policy for handling genetic disease information, which will be afforded heightened confidentiality. Information handling protocols based on organizational policies related to genetic disease information that is deemed sensitive. Usage Note: If there is a jurisdictional mandate, then use the applicable ActPrivacyLaw code system, and specify the law rather than or in addition to this more generic code. -
HIV
Policy for handling HIV or AIDS information, which will be afforded heightened confidentiality. Information handling protocols based on organizational policies related to HIV or AIDS information that is deemed sensitive. Usage Note: If there is a jurisdictional mandate, then use the applicable ActPrivacyLaw code system, and specify the law rather than or in addition to this more generic code. -
PSY
Policy for handling psychiatry information, which will be afforded heightened confidentiality. Information handling protocols based on organizational policies related to psychiatry information that is deemed sensitive. Usage Note: If there is a jurisdictional mandate, then use the applicable ActPrivacyLaw code system, and specify the law rather than or in addition to this more generic code. -
SCA
Policy for handling sickle cell disease information, which is afforded heightened confidentiality. Information handling protocols are based on organizational policies related to sickle cell disease information, which is deemed sensitive. Usage Note: If there is a jurisdictional mandate, then the Act valued with this ActCode should be associated with an Act valued with any applicable laws from the ActPrivacyLaw code system. -
SOC
Information about provision of social services. Usage Note: This is a temporary addition to FHIR to be proposed in harmonization. -
SDV
Policy for handling sexual assault, abuse, or domestic violence information, which will be afforded heightened confidentiality. Information handling protocols based on organizational policies related to sexual assault, abuse, or domestic violence information that is deemed sensitive. Usage Note: If there is a jurisdictional mandate, then use the applicable ActPrivacyLaw code system, and specify the law rather than or in addition to this more generic code. -
SEX
Policy for handling sexuality and reproductive health information, which will be afforded heightened confidentiality. Information handling protocols based on organizational policies related to sexuality and reproductive health information that is deemed sensitive. Usage Note: If there is a jurisdictional mandate, then use the applicable ActPrivacyLaw code system, and specify the law rather than or in addition to this more generic code. -
STD
Policy for handling sexually transmitted disease information, which will be afforded heightened confidentiality. Information handling protocols based on organizational policies related to sexually transmitted disease information that is deemed sensitive. Usage Note: If there is a jurisdictional mandate, then use the applicable ActPrivacyLaw code system, and specify the law rather than or in addition to this more generic code. -
TBOO
Policy for handling information not to be initially disclosed or discussed with patient except by a physician assigned to patient in this case. Information handling protocols based on organizational policies related to sensitive patient information that must be initially discussed with the patient by an attending physician before being disclosed to the patient. Usage Note: If there is a jurisdictional mandate, then use the applicable ActPrivacyLaw code system, and specify the law rather than or in addition to this more generic code. Open Issue: This definition conflates a rule and a characteristic, and there may be a similar issue with ts sibling codes. -
SICKLE
Types of sensitivity policies that apply to Acts. Act.confidentialityCode is defined in the RIM as "constraints around appropriate disclosure of information about this Act, regardless of mood." Usage Note: ActSensitivity codes are used to bind information to an Act.confidentialityCode according to local sensitivity policy so that those confidentiality codes can then govern its handling across enterprises. Internally to a policy domain, however, local policies guide the access control system on how end users in that policy domain are able to use information tagged with these sensitivity values. -
_ENTITYSENSITIVITYPOLICYTYPE
Types of sensitivity policies that may apply to a sensitive attribute on an Entity. Usage Note: EntitySensitivity codes are used to convey a policy that is applicable to sensitive information conveyed by an entity attribute. May be used to bind a Role.confidentialityCode associated with an Entity per organizational policy. Role.confidentialityCode is defined in the RIM as "an indication of the appropriate disclosure of information about this Role with respect to the playing Entity." -
DEMO
Policy for handling all demographic information about an information subject, which will be afforded heightened confidentiality. Policies may govern sensitivity of information related to all demographic about an information subject, the disclosure of which could impact the privacy, well-being, or safety of that subject. Usage Note: If there is a jurisdictional mandate, then use the applicable ActPrivacyLaw code system, and specify the law rather than or in addition to this more generic code. -
DOB
Policy for handling information related to an information subject's date of birth, which will be afforded heightened confidentiality.Policies may govern sensitivity of information related to an information subject's date of birth, the disclosure of which could impact the privacy, well-being, or safety of that subject. Usage Note: If there is a jurisdictional mandate, then use the applicable ActPrivacyLaw code system, and specify the law rather than or in addition to this more generic code. -
GENDER
Policy for handling information related to an information subject's gender and sexual orientation, which will be afforded heightened confidentiality. Policies may govern sensitivity of information related to an information subject's gender and sexual orientation, the disclosure of which could impact the privacy, well-being, or safety of that subject. Usage Note: If there is a jurisdictional mandate, then use the applicable ActPrivacyLaw code system, and specify the law rather than or in addition to this more generic code. -
LIVARG
Policy for handling information related to an information subject's living arrangement, which will be afforded heightened confidentiality. Policies may govern sensitivity of information related to an information subject's living arrangement, the disclosure of which could impact the privacy, well-being, or safety of that subject. Usage Note: If there is a jurisdictional mandate, then use the applicable ActPrivacyLaw code system, and specify the law rather than or in addition to this more generic code. -
MARST
Policy for handling information related to an information subject's marital status, which will be afforded heightened confidentiality. Policies may govern sensitivity of information related to an information subject's marital status, the disclosure of which could impact the privacy, well-being, or safety of that subject. Usage Note: If there is a jurisdictional mandate, then use the applicable ActPrivacyLaw code system, and specify the law rather than or in addition to this more generic code. -
RACE
Policy for handling information related to an information subject's race, which will be afforded heightened confidentiality. Policies may govern sensitivity of information related to an information subject's race, the disclosure of which could impact the privacy, well-being, or safety of that subject. Usage Note: If there is a jurisdictional mandate, then use the applicable ActPrivacyLaw code system, and specify the law rather than or in addition to this more generic code. -
REL
Policy for handling information related to an information subject's religious affiliation, which will be afforded heightened confidentiality. Policies may govern sensitivity of information related to an information subject's religion, the disclosure of which could impact the privacy, well-being, or safety of that subject. Usage Notes: If there is a jurisdictional mandate, then use the applicable ActPrivacyLaw code system, and specify the law rather than or in addition to this more generic code. -
_ROLEINFORMATIONSENSITIVITYPOLICY
Types of sensitivity policies that apply to Roles. Usage Notes: RoleSensitivity codes are used to bind information to a Role.confidentialityCode per organizational policy. Role.confidentialityCode is defined in the RIM as "an indication of the appropriate disclosure of information about this Role with respect to the playing Entity." -
B
Policy for handling trade secrets such as financial information or intellectual property, which will be afforded heightened confidentiality. Description: Since the service class can represent knowledge structures that may be considered a trade or business secret, there is sometimes (though rarely) the need to flag those items as of business level confidentiality. Usage Notes: No patient related information may ever be of this confidentiality level. If there is a jurisdictional mandate, then use the applicable ActPrivacyLaw code system, and specify the law rather than or in addition to this more generic code. -
EMPL
Policy for handling information related to an employer which is deemed classified to protect an employee who is the information subject, and which will be afforded heightened confidentiality. Description: Policies may govern sensitivity of information related to an employer, such as law enforcement or national security, the identity of which could impact the privacy, well-being, or safety of an information subject who is an employee. Usage Notes: If there is a jurisdictional mandate, then use the applicable ActPrivacyLaw code system, and specify the law rather than or in addition to this more generic code. -
LOCIS
Policy for handling information related to the location of the information subject, which will be afforded heightened confidentiality. Description: Policies may govern sensitivity of information related to the location of the information subject, the disclosure of which could impact the privacy, well-being, or safety of that subject. Usage Notes: If there is a jurisdictional mandate, then use the applicable ActPrivacyLaw code system, and specify the law rather than or in addition to this more generic code. -
SSP
Policy for handling information related to a provider of sensitive services, which will be afforded heightened confidentiality. Description: Policies may govern sensitivity of information related to providers who deliver sensitive healthcare services in order to protect the privacy, well-being, and safety of the provider and of patients receiving sensitive services. Usage Notes: If there is a jurisdictional mandate, then use the applicable ActPrivacyLaw code system, and specify the law rather than or in addition to this more generic code. -
ADOL
Policy for handling information related to an adolescent, which will be afforded heightened confidentiality per applicable organizational or jurisdictional policy. An enterprise may have a policy that requires that adolescent patient information be provided heightened confidentiality. Information deemed sensitive typically includes health information and patient role information including patient status, demographics, next of kin, and location. Usage Note: For use within an enterprise in which an adolescent is the information subject. If there is a jurisdictional mandate, then use the applicable ActPrivacyLaw code system, and specify the law rather than or in addition to this more generic code. -
CEL
Policy for handling information related to a celebrity (people of public interest (VIP), which will be afforded heightened confidentiality. Celebrities are people of public interest (VIP) about whose information an enterprise may have a policy that requires heightened confidentiality. Information deemed sensitive may include health information and patient role information including patient status, demographics, next of kin, and location. Usage Note: For use within an enterprise in which the information subject is deemed a celebrity or very important person. If there is a jurisdictional mandate, then use the applicable ActPrivacyLaw code system, and specify the law rather than or in addition to this more generic code. -
DIA
Policy for handling information related to a diagnosis, health condition or health problem, which will be afforded heightened confidentiality. Diagnostic, health condition or health problem related information may be deemed sensitive by organizational policy, and require heightened confidentiality. Usage Note: For use within an enterprise that provides heightened confidentiality to diagnostic, health condition or health problem related information deemed sensitive. If there is a jurisdictional mandate, then use the applicable ActPrivacyLaw code system, and specify the law rather than or in addition to this more generic code. -
DRGIS
Policy for handling information related to a drug, which will be afforded heightened confidentiality. Drug information may be deemed sensitive by organizational policy, and require heightened confidentiality. Usage Note: For use within an enterprise that provides heightened confidentiality to drug information deemed sensitive. If there is a jurisdictional mandate, then use the applicable ActPrivacyLaw code system, and specify the law rather than or in addition to this more generic code. -
EMP
Policy for handling information related to an employee, which will be afforded heightened confidentiality. When a patient is an employee, an enterprise may have a policy that requires heightened confidentiality. Information deemed sensitive typically includes health information and patient role information including patient status, demographics, next of kin, and location. Usage Note: Policy for handling information related to an employee, which will be afforded heightened confidentiality. Description: When a patient is an employee, an enterprise may have a policy that requires heightened confidentiality. Information deemed sensitive typically includes health information and patient role information including patient status, demographics, next of kin, and location. -
PDS
Policy for handling information reported by the patient about another person, e.g., a family member, which will be afforded heightened confidentiality. Sensitive information reported by the patient about another person, e.g., family members may be deemed sensitive by default. The flag may be set or cleared on patient's request. Usage Note: For sensitive information relayed by or about a patient, which is deemed sensitive within the enterprise (i.e., by default regardless of whether the patient requested that the information be deemed sensitive.) If there is a jurisdictional mandate, then use the applicable ActPrivacyLaw code system, and specify the law rather than or in addition to this more generic code. -
PRS
For sensitive information relayed by or about a patient, which is deemed sensitive within the enterprise (i.e., by default regardless of whether the patient requested that the information be deemed sensitive.) If there is a jurisdictional mandate, then use the applicable ActPrivacyLaw code system, and specify the law rather than or in addition to this more generic code. Usage Note: For use within an enterprise that provides heightened confidentiality to certain types of information designated by a patient as sensitive. If there is a jurisdictional mandate, then use the applicable ActPrivacyLaw code system, and specify the law rather than or in addition to this more generic code. -
COMPT
This is the healthcare analog to the US Intelligence Community's concept of a Special Access Program. Compartment codes may be used in as a field value in an initiator's clearance to indicate permission to access and use an IT Resource with a security label having the same compartment value in security category label field. Map: Aligns with ISO 2382-8 definition of Compartment - "A division of data into isolated blocks with separate security controls for the purpose of reducing risk." -
HRCOMPT
A security category label field value, which indicates that access and use of an IT resource is restricted to members of human resources department or workflow. -
RESCOMPT
A security category label field value, which indicates that access and use of an IT resource is restricted to members of a research project. -
RMGTCOMPT
A security category label field value, which indicates that access and use of an IT resource is restricted to members of records management department or workflow. -
ACTTRUSTPOLICYTYPE
A mandate, obligation, requirement, rule, or expectation conveyed as security metadata between senders and receivers required to establish the reliability, authenticity, and trustworthiness of their transactions. Trust security metadata are observation made about aspects of trust applicable to an IT resource (data, information object, service, or system capability). Trust applicable to IT resources is established and maintained in and among security domains, and may be comprised of observations about the domain's trust authority, trust framework, trust policy, trust interaction rules, means for assessing and monitoring adherence to trust policies, mechanisms that enforce trust, and quality and reliability measures of assurance in those mechanisms. [Based on ISO IEC 10181-1 and NIST SP 800-63-2] For example, identity proofing , level of assurance, and Trust Framework. -
TRSTACCRD
Type of security metadata about the formal declaration by an authority or neutral third party that validates the technical, security, trust, and business practice conformance of Trust Agents to facilitate security, interoperability, and trust among participants within a security domain or trust framework. -
TRSTAGRE
Type of security metadata about privacy and security requirements with which a security domain must comply. [ISO IEC 10181-1] -
TRSTASSUR
Type of security metadata about the digital quality or reliability of a trust assertion, activity, capability, information exchange, mechanism, process, or protocol. -
TRSTCERT
Type of security metadata about a set of security-relevant data issued by a security authority or trusted third party, together with security information which is used to provide the integrity and data origin authentication services for an IT resource (data, information object, service, or system capability). [Based on ISO IEC 10181-1] -
TRSTFWK
Type of security metadata about a complete set of contracts, regulations, or commitments that enable participating actors to rely on certain assertions by other actors to fulfill their information security requirements. [Kantara Initiative] -
TRSTMEC
Type of security metadata about a security architecture system component that supports enforcement of security policies. -
COVPOL
Description:A mandate, obligation, requirement, rule, or expectation unilaterally imposed on benefit coverage under a policy or program by a sponsor, underwriter or payor on: The activity of another party The behavior of another party The manner in which an act is executed Examples:A clinical protocol imposed by a payer to which a provider must adhere in order to be paid for providing the service. A formulary from which a provider must select prescribed drugs in order for the patient to incur a lower copay. -
SECURITYPOLICY
Types of security policies that further specify the ActClassPolicy value set. Examples: obligation to encrypt refrain from redisclosure without consent -
OBLIGATIONPOLICY
Conveys the mandated workflow action that an information custodian, receiver, or user must perform. Usage Notes: Per ISO 22600-2, ObligationPolicy instances 'are event-triggered and define actions to be performed by manager agent'. Per HL7 Composite Security and Privacy Domain Analysis Model: This value set refers to the action required to receive the permission specified in the privacy rule. Per OASIS XACML, an obligation is an operation specified in a policy or policy that is performed in conjunction with the enforcement of an access control decision. -
ANONY
Custodian system must remove any information that could result in identifying the information subject. -
AOD
Custodian system must make available to an information subject upon request an accounting of certain disclosures of the individualâ??s protected health information over a period of time. Policy may dictate that the accounting include information about the information disclosed, the date of disclosure, the identification of the receiver, the purpose of the disclosure, the time in which the disclosing entity must provide a response and the time period for which accountings of disclosure can be requested. -
AUDIT
Custodian system must monitor systems to ensure that all users are authorized to operate on information objects. -
AUDTR
Custodian system must monitor and maintain retrievable log for each user and operation on information. -
CPLYCC
Custodian security system must retrieve, evaluate, and comply with the information handling directions of the Confidentiality Code associated with an information target. -
CPLYCD
Custodian security system must retrieve, evaluate, and comply with applicable information subject consent directives. -
CPLYJPP
Custodian security system must retrieve, evaluate, and comply with applicable jurisdictional privacy policies associated with the target information. -
CPLYOPP
Custodian security system must retrieve, evaluate, and comply with applicable organizational privacy policies associated with the target information. -
CPLYOSP
Custodian security system must retrieve, evaluate, and comply with the organizational security policies associated with the target information. -
CPLYPOL
Custodian security system must retrieve, evaluate, and comply with applicable policies associated with the target information. -
DECLASSIFYLABEL
Custodian security system must declassify information assigned security labels by instantiating a new version of the classified information so as to break the binding of the classifying security label when assigning a new security label that marks the information as unclassified in accordance with applicable jurisdictional privacy policies associated with the target information. The system must retain an immutable record of the previous assignment and binding. -
DEID
Custodian system must strip information of data that would allow the identification of the source of the information or the information subject. -
DELAU
Custodian system must remove target information from access after use. -
DOWNGRDLABEL
Custodian security system must downgrade information assigned security labels by instantiating a new version of the classified information so as to break the binding of the classifying security label when assigning a new security label that marks the information as classified at a less protected level in accordance with applicable jurisdictional privacy policies associated with the target information. The system must retain an immutable record of the previous assignment and binding. -
DRIVLABEL
Custodian security system must assign and bind security labels derived from compilations of information by aggregation or disaggregation in order to classify information compiled in the information systems under its control for collection, access, use and disclosure in accordance with applicable jurisdictional privacy policies associated with the target information. The system must retain an immutable record of the previous assignment and binding. -
ENCRYPT
Custodian system must render information unreadable by algorithmically transforming plaintext into ciphertext. Usage Notes: A mathematical transposition of a file or data stream so that it cannot be deciphered at the receiving end without the proper key. Encryption is a security feature that assures that only the parties who are supposed to be participating in a videoconference or data transfer are able to do so. It can include a password, public and private keys, or a complex combination of all. (Per Infoway.) -
ENCRYPTR
Custodian system must render information unreadable and unusable by algorithmically transforming plaintext into ciphertext when "at rest" or in storage. -
ENCRYPTT
Custodian system must render information unreadable and unusable by algorithmically transforming plaintext into ciphertext while "in transit" or being transported by any means. -
ENCRYPTU
Custodian system must render information unreadable and unusable by algorithmically transforming plaintext into ciphertext while in use such that operations permitted on the target information are limited by the license granted to the end user. -
HUAPRV
Custodian system must require human review and approval for permission requested. -
LABEL
Custodian security system must assign and bind security labels in order to classify information created in the information systems under its control for collection, access, use and disclosure in accordance with applicable jurisdictional privacy policies associated with the target information. The system must retain an immutable record of the assignment and binding. Usage Note: In security systems, security policy label assignments do not change, they may supersede prior assignments, and such reassignments are always tracked for auditing and other purposes. -
MASK
Custodian system must render information unreadable and unusable by algorithmically transforming plaintext into ciphertext. User may be provided a key to decrypt per license or "shared secret". -
MINEC
Custodian must limit access and disclosure to the minimum information required to support an authorized user's purpose of use. Usage Note: Limiting the information available for access and disclosure to that an authorized user or receiver "needs to know" in order to perform permitted workflow or purpose of use. -
PERSISTLABEL
Custodian security system must persist the binding of security labels to classify information received or imported by information systems under its control for collection, access, use and disclosure in accordance with applicable jurisdictional privacy policies associated with the target information. The system must retain an immutable record of the assignment and binding. -
PRIVMARK
Custodian must create and/or maintain human readable security label tags as required by policy. Map: Aligns with ISO 22600-3 Section A.3.4.3 description of privacy mark: "If present, the privacy-mark is not used for access control. The content of the privacy-mark may be defined by the security policy in force (identified by the security-policy-identifier) which may define a list of values to be used. Alternately, the value may be determined by the originator of the security-label." -
PSEUD
Custodian system must strip information of data that would allow the identification of the source of the information or the information subject. Custodian may retain a key to relink data necessary to reidentify the information subject. -
REDACT
Custodian system must remove information, which is not authorized to be access, used, or disclosed from records made available to otherwise authorized users. -
UPGRDLABEL
Custodian security system must declassify information assigned security labels by instantiating a new version of the classified information so as to break the binding of the classifying security label when assigning a new security label that marks the information as classified at a more protected level in accordance with applicable jurisdictional privacy policies associated with the target information. The system must retain an immutable record of the previous assignment and binding. -
REFRAINPOLICY
Conveys prohibited actions which an information custodian, receiver, or user is not permitted to perform unless otherwise authorized or permitted under specified circumstances. Usage Notes: ISO 22600-2 species that a Refrain Policy "defines actions the subjects must refrain from performing". Per HL7 Composite Security and Privacy Domain Analysis Model: May be used to indicate that a specific action is prohibited based on specific access control attributes e.g., purpose of use, information type, user role, etc. -
NOAUTH
Prohibition on disclosure without information subject's authorization. -
NOCOLLECT
Prohibition on collection or storage of the information. -
NODSCLCD
Prohibition on disclosure without organizational approved patient restriction. -
NODSCLCDS
Prohibition on disclosure without a consent directive from the information subject. -
NOINTEGRATE
Prohibition on Integration into other records. -
NOLIST
Prohibition on disclosure except to entities on specific access list. -
NOMOU
Prohibition on disclosure without an interagency service agreement or memorandum of understanding (MOU). -
NOORGPOL
Prohibition on disclosure without organizational authorization. -
NOPAT
Prohibition on disclosing information to patient, family or caregivers without attending provider's authorization. Usage Note: The information may be labeled with the ActInformationSensitivity TBOO code, triggering application of this RefrainPolicy code as a handling caveat controlling access. Maps to FHIR NOPAT: Typically, this is used on an Alert resource, when the alert records information on patient abuse or non-compliance. FHIR print name is "keep information from patient". Maps to the French realm - code: INVISIBLE_PATIENT. displayName: Document non visible par le patient codingScheme: 1.2.250.1.213.1.1.4.13 French use case: A label for documents that the author chose to hide from the patient until the content can be disclose to the patient in a face to face meeting between a healthcare professional and the patient (in French law some results like cancer diagnosis or AIDS diagnosis must be announced to the patient by a healthcare professional and should not be find out by the patient alone). -
NOPERSISTP
Prohibition on collection of the information beyond time necessary to accomplish authorized purpose of use is prohibited. -
NORDSCLCD
Prohibition on redisclosure without patient consent directive. -
NORDSCLCDS
Prohibition on redisclosure without a consent directive from the information subject. -
NORDSCLW
Prohibition on disclosure without authorization under jurisdictional law. -
NORELINK
Prohibition on associating de-identified or pseudonymized information with other information in a manner that could or does result in disclosing information intended to be masked. -
NOREUSE
Prohibition on use of the information beyond the purpose of use initially authorized. -
NOVIP
Prohibition on disclosure except to principals with access permission to specific VIP information. -
ORCON
Prohibition on disclosure except as permitted by the information originator. -
_ACTPRODUCTACQUISITIONCODE
The method that a product is obtained for use by the subject of the supply act (e.g. patient). Product examples are consumable or durable goods. -
LOAN
Temporary supply of a product without transfer of ownership for the product. -
RENT
Temporary supply of a product with financial compensation, without transfer of ownership for the product. -
TRANSFER
Transfer of ownership for a product. -
SALE
Transfer of ownership for a product for financial compensation. -
_ACTSPECIMENTRANSPORTCODE
Transportation of a specimen. -
SREC
Description:Specimen has been received by the participating organization/department. -
SSTOR
Description:Specimen has been placed into storage at a participating location. -
STRAN
Description:Specimen has been put in transit to a participating receiver. -
_ACTSPECIMENTREATMENTCODE
Set of codes related to specimen treatments -
ACID
The lowering of specimen pH through the addition of an acid -
ALK
The act rendering alkaline by impregnating with an alkali; a conferring of alkaline qualities. -
DEFB
The removal of fibrin from whole blood or plasma through physical or chemical means -
FILT
The passage of a liquid through a filter, accomplished by gravity, pressure or vacuum (suction). -
LDLP
LDL Precipitation -
NEUT
The act or process by which an acid and a base are combined in such proportions that the resulting compound is neutral. -
RECA
The addition of calcium back to a specimen after it was removed by chelating agents -
UFIL
The filtration of a colloidal substance through a semipermeable medium that allows only the passage of small molecules. -
_ACTSUBSTANCEADMINISTRATIONCODE
Description: Describes the type of substance administration being performed. This should not be used to carry codes for identification of products. Use an associated role or entity to carry such information. -
DRUG
The introduction of a drug into a subject with the intention of altering its biologic state with the intent of improving its health status. -
FD
Description: The introduction of material into a subject with the intent of providing nutrition or other dietary supplements (e.g. minerals or vitamins). -
IMMUNIZ
The introduction of an immunogen with the intent of stimulating an immune response, aimed at preventing subsequent infections by more viable agents. -
BOOSTER
An additional immunization administration within a series intended to bolster or enhance immunity. -
INITIMMUNIZ
The first immunization administration in a series intended to produce immunity -
_ACTTASKCODE
Description: A task or action that a user may perform in a clinical information system (e.g., medication order entry, laboratory test results review, problem list entry). -
OE
A clinician creates a request for a service to be performed for a given patient. -
LABOE
A clinician creates a request for a laboratory test to be done for a given patient. -
MEDOE
A clinician creates a request for the administration of one or more medications to a given patient. -
PATDOC
A person enters documentation about a given patient. -
ALLERLREV
Description: A person reviews a list of known allergies of a given patient. -
CLINNOTEE
A clinician enters a clinical note about a given patient -
DIAGLISTE
A clinician enters a diagnosis for a given patient. -
DISCHINSTE
A person provides a discharge instruction to a patient. -
DISCHSUME
A clinician enters a discharge summary for a given patient. -
PATEDUE
A person provides a patient-specific education handout to a patient. -
PATREPE
A pathologist enters a report for a given patient. -
PROBLISTE
A clinician enters a problem for a given patient. -
RADREPE
A radiologist enters a report for a given patient. -
IMMLREV
Description: A person reviews a list of immunizations due or received for a given patient. -
REMLREV
Description: A person reviews a list of health care reminders for a given patient. -
WELLREMLREV
Description: A person reviews a list of wellness or preventive care reminders for a given patient. -
PATINFO
A person (e.g., clinician, the patient herself) reviews patient information in the electronic medical record. -
ALLERLE
Description: A person enters a known allergy for a given patient. -
CDSREV
A person reviews a recommendation/assessment provided automatically by a clinical decision support application for a given patient. -
CLINNOTEREV
A person reviews a clinical note of a given patient. -
DISCHSUMREV
A person reviews a discharge summary of a given patient. -
DIAGLISTREV
A person reviews a list of diagnoses of a given patient. -
IMMLE
Description: A person enters an immunization due or received for a given patient. -
LABRREV
A person reviews a list of laboratory results of a given patient. -
MICRORREV
A person reviews a list of microbiology results of a given patient. -
MICROORGRREV
A person reviews organisms of microbiology results of a given patient. -
MICROSENSRREV
A person reviews the sensitivity test of microbiology results of a given patient. -
MLREV
A person reviews a list of medication orders submitted to a given patient -
MARWLREV
A clinician reviews a work list of medications to be administered to a given patient. -
OREV
A person reviews a list of orders submitted to a given patient. -
PATREPREV
A person reviews a pathology report of a given patient. -
PROBLISTREV
A person reviews a list of problems of a given patient. -
RADREPREV
A person reviews a radiology report of a given patient. -
REMLE
Description: A person enters a health care reminder for a given patient. -
WELLREMLE
Description: A person enters a wellness or preventive care reminder for a given patient. -
RISKASSESS
A person reviews a Risk Assessment Instrument report of a given patient. -
FALLRISK
A person reviews a Falls Risk Assessment Instrument report of a given patient. -
_ACTTRANSPORTATIONMODECODE
Characterizes how a transportation act was or will be carried out. Examples: Via private transport, via public transit, via courier. -
_ACTPATIENTTRANSPORTATIONMODECODE
Definition: Characterizes how a patient was or will be transported to the site of a patient encounter. Examples: Via ambulance, via public transit, on foot. -
AFOOT
pedestrian transport -
AMBT
ambulance transport -
AMBAIR
fixed-wing ambulance transport -
AMBGRND
ground ambulance transport -
AMBHELO
helicopter ambulance transport -
LAWENF
law enforcement transport -
PRVTRN
private transport -
PUBTRN
public transport -
_OBSERVATIONTYPE
Identifies the kinds of observations that can be performed -
_ACTSPECOBSCODE
Identifies the type of observation that is made about a specimen that may affect its processing, analysis or further result interpretation -
ARTBLD
Describes the artificial blood identifier that is associated with the specimen. -
DILUTION
An observation that reports the dilution of a sample. -
AUTOHIGH
The dilution of a sample performed by automated equipment. The value is specified by the equipment -
AUTOLOW
The dilution of a sample performed by automated equipment. The value is specified by the equipment -
PRE
The dilution of the specimen made prior to being loaded onto analytical equipment -
RERUN
The value of the dilution of a sample after it had been analyzed at a prior dilution value -
EVNFCTS
Domain provides codes that qualify the ActLabObsEnvfctsCode domain. (Environmental Factors) -
INTFR
An observation that relates to factors that may potentially cause interference with the observation -
FIBRIN
The Fibrin Index of the specimen. In the case of only differentiating between Absent and Present, recommend using 0 and 1 -
HEMOLYSIS
An observation of the hemolysis index of the specimen in g/L -
ICTERUS
An observation that describes the icterus index of the specimen. It is recommended to use mMol/L of bilirubin -
LIPEMIA
An observation used to describe the Lipemia Index of the specimen. It is recommended to use the optical turbidity at 600 nm (in absorbance units). -
VOLUME
An observation that reports the volume of a sample. -
AVAILABLE
The available quantity of specimen. This is the current quantity minus any planned consumption (e.g., tests that are planned) -
CONSUMPTION
The quantity of specimen that is used each time the equipment uses this substance -
CURRENT
The current quantity of the specimen, i.e., initial quantity minus what has been actually used. -
INITIAL
The initial quantity of the specimen in inventory -
_ANNOTATIONTYPE
AnnotationType -
_ACTPATIENTANNOTATIONTYPE
Description:Provides a categorization for annotations recorded directly against the patient . -
ANNDI
Description:A note that is specific to a patient's diagnostic images, either historical, current or planned. -
ANNGEN
Description:A general or uncategorized note. -
ANNIMM
A note that is specific to a patient's immunizations, either historical, current or planned. -
ANNLAB
Description:A note that is specific to a patient's laboratory results, either historical, current or planned. -
ANNMED
Description:A note that is specific to a patient's medications, either historical, current or planned. -
_GENETICOBSERVATIONTYPE
Description: None provided -
GENE
Description: A DNA segment that contributes to phenotype/function. In the absence of demonstrated function a gene may be characterized by sequence, transcription or homology -
_IMMUNIZATIONOBSERVATIONTYPE
Description: Observation codes which describe characteristics of the immunization material. -
OBSANTC
Description: Indicates the valid antigen count. -
OBSANTV
Description: Indicates whether an antigen is valid or invalid. -
_INDIVIDUALCASESAFETYREPORTTYPE
A code that is used to indicate the type of case safety report received from sender. The current code example reference is from the International Conference on Harmonisation (ICH) Expert Workgroup guideline on Clinical Safety Data Management: Data Elements for Transmission of Individual Case Safety Reports. The unknown/unavailable option allows the transmission of information from a secondary sender where the initial sender did not specify the type of report. Example concepts include: Spontaneous, Report from study, Other. -
PATADVEVNT
Indicates that the ICSR is describing problems that a patient experienced after receiving a vaccine product. -
VACPROBLEM
Indicates that the ICSR is describing a problem with the actual vaccine product such as physical defects (cloudy, particulate matter) or inability to confer immunity. -
_LOINCOBSERVATIONACTCONTEXTAGETYPE
Definition:The set of LOINC codes for the act of determining the period of time that has elapsed since an entity was born or created. -
_216119
Definition:Estimated age. -
_216127
Definition:Reported age. -
_295535
Definition:Calculated age. -
_305250
Definition:General specification of age with no implied method of determination. -
_309724
Definition:Age at onset of associated adverse event; no implied method of determination. -
_MEDICATIONOBSERVATIONTYPE
MedicationObservationType -
REPHALFLIFE
Description:This observation represents an 'average' or 'expected' half-life typical of the product. -
SPLCOATING
Definition: A characteristic of an oral solid dosage form of a medicinal product, indicating whether it has one or more coatings such as sugar coating, film coating, or enteric coating. Only coatings to the external surface or the dosage form should be considered (for example, coatings to individual pellets or granules inside a capsule or tablet are excluded from consideration). Constraints: The Observation.value must be a Boolean (BL) with true for the presence or false for the absence of one or more coatings on a solid dosage form. -
SPLCOLOR
Definition: A characteristic of an oral solid dosage form of a medicinal product, specifying the color or colors that most predominantly define the appearance of the dose form. SPLCOLOR is not an FDA specification for the actual color of solid dosage forms or the names of colors that can appear in labeling. Constraints: The Observation.value must be a single coded value or a list of multiple coded values, specifying one or more distinct colors that approximate of the color(s) of distinct areas of the solid dosage form, such as the different sides of a tablet or one-part capsule, or the different halves of a two-part capsule. Bands on banded capsules, regardless of the color, are not considered when assigning an SPLCOLOR. Imprints on the dosage form, regardless of their color are not considered when assigning an SPLCOLOR. If more than one color exists on a particular side or half, then the most predominant color on that side or half is recorded. If the gelatin capsule shell is colorless and transparent, use the predominant color of the contents that appears through the colorless and transparent capsule shell. Colors can include: Black;Gray;White;Red;Pink;Purple;Green;Yellow;Orange;Brown;Blue;Turquoise. -
SPLIMAGE
Description: A characteristic representing a single file reference that contains two or more views of the same dosage form of the product; in most cases this should represent front and back views of the dosage form, but occasionally additional views might be needed in order to capture all of the important physical characteristics of the dosage form. Any imprint and/or symbol should be clearly identifiable, and the viewer should not normally need to rotate the image in order to read it. Images that are submitted with SPL should be included in the same directory as the SPL file. -
SPLIMPRINT
Definition: A characteristic of an oral solid dosage form of a medicinal product, specifying the alphanumeric text that appears on the solid dosage form, including text that is embossed, debossed, engraved or printed with ink. The presence of other non-textual distinguishing marks or symbols is recorded by SPLSYMBOL. Examples: Included in SPLIMPRINT are alphanumeric text that appears on the bands of banded capsules and logos and other symbols that can be interpreted as letters or numbers. Constraints: The Observation.value must be of type Character String (ST). Excluded from SPLIMPRINT are internal and external cut-outs in the form of alphanumeric text and the letter 'R' with a circle around it (when referring to a registered trademark) and the letters 'TM' (when referring to a 'trade mark'). To record text, begin on either side or part of the dosage form. Start at the top left and progress as one would normally read a book. Enter a semicolon to show separation between words or line divisions. -
SPLSCORING
Definition: A characteristic of an oral solid dosage form of a medicinal product, specifying the number of equal pieces that the solid dosage form can be divided into using score line(s). Example: One score line creating two equal pieces is given a value of 2, two parallel score lines creating three equal pieces is given a value of 3. Constraints: Whether three parallel score lines create four equal pieces or two intersecting score lines create two equal pieces using one score line and four equal pieces using both score lines, both have the scoring value of 4. Solid dosage forms that are not scored are given a value of 1. Solid dosage forms that can only be divided into unequal pieces are given a null-value with nullFlavor other (OTH). -
SPLSHAPE
Description: A characteristic of an oral solid dosage form of a medicinal product, specifying the two dimensional representation of the solid dose form, in terms of the outside perimeter of a solid dosage form when the dosage form, resting on a flat surface, is viewed from directly above, including slight rounding of corners. SPLSHAPE does not include embossing, scoring, debossing, or internal cut-outs. SPLSHAPE is independent of the orientation of the imprint and logo. Shapes can include: Triangle (3 sided); Square; Round; Semicircle; Pentagon (5 sided); Diamond; Double circle; Bullet; Hexagon (6 sided); Rectangle; Gear; Capsule; Heptagon (7 sided); Trapezoid; Oval; Clover; Octagon (8 sided); Tear; Freeform. -
SPLSIZE
Definition: A characteristic of an oral solid dosage form of a medicinal product, specifying the longest single dimension of the solid dosage form as a physical quantity in the dimension of length (e.g., 3 mm). The length is should be specified in millimeters and should be rounded to the nearest whole millimeter. Example: SPLSIZE for a rectangular shaped tablet is the length and SPLSIZE for a round shaped tablet is the diameter. -
SPLSYMBOL
Definition: A characteristic of an oral solid dosage form of a medicinal product, to describe whether or not the medicinal product has a mark or symbol appearing on it for easy and definite recognition. Score lines, letters, numbers, and internal and external cut-outs are not considered marks or symbols. See SPLSCORING and SPLIMPRINT for these characteristics. Constraints: The Observation.value must be a Boolean (BL) with true indicating the presence and false for the absence of marks or symbols. Example: -
_OBSERVATIONISSUETRIGGERCODEDOBSERVATIONTYPE
Distinguishes the kinds of coded observations that could be the trigger for clinical issue detection. These are observations that are not measurable, but instead can be defined with codes. Coded observation types include: Allergy, Intolerance, Medical Condition, Pregnancy status, etc. -
_CASETRANSMISSIONMODE
Code for the mechanism by which disease was acquired by the living subject involved in the public health case. Includes sexually transmitted, airborne, bloodborne, vectorborne, foodborne, zoonotic, nosocomial, mechanical, dermal, congenital, environmental exposure, indeterminate. -
AIRTRNS
Communication of an agent from a living subject or environmental source to a living subject through indirect contact via oral or nasal inhalation. -
ANANTRNS
Communication of an agent from one animal to another proximate animal. -
ANHUMTRNS
Communication of an agent from an animal to a proximate person. -
BDYFLDTRNS
Communication of an agent from one living subject to another living subject through direct contact with any body fluid. -
BLDTRNS
Communication of an agent to a living subject through direct contact with blood or blood products whether the contact with blood is part of a therapeutic procedure or not. -
DERMTRNS
Communication of an agent from a living subject or environmental source to a living subject via agent migration through intact skin. -
ENVTRNS
Communication of an agent from an environmental surface or source to a living subject by direct contact. -
FECTRNS
Communication of an agent from a living subject or environmental source to a living subject through oral contact with material contaminated by person or animal fecal material. -
FOMTRNS
Communication of an agent from an non-living material to a living subject through direct contact. -
FOODTRNS
Communication of an agent from a food source to a living subject via oral consumption. -
HUMHUMTRNS
Communication of an agent from a person to a proximate person. -
INDTRNS
Communication of an agent to a living subject via an undetermined route. -
LACTTRNS
Communication of an agent from one living subject to another living subject through direct contact with mammalian milk or colostrum. -
NOSTRNS
Communication of an agent from any entity to a living subject while the living subject is in the patient role in a healthcare facility. -
PARTRNS
Communication of an agent from a living subject or environmental source to a living subject where the acquisition of the agent is not via the alimentary canal. -
PLACTRNS
Communication of an agent from a living subject to the progeny of that living subject via agent migration across the maternal-fetal placental membranes while in utero. -
SEXTRNS
Communication of an agent from one living subject to another living subject through direct contact with genital or oral tissues as part of a sexual act. -
TRNSFTRNS
Communication of an agent from one living subject to another living subject through direct contact with blood or blood products where the contact with blood is part of a therapeutic procedure. -
VECTRNS
Communication of an agent from a living subject acting as a required intermediary in the agent transmission process to a recipient living subject via direct contact. -
WATTRNS
Communication of an agent from a contaminated water source to a living subject whether the water is ingested as a food or not. The route of entry of the water may be through any bodily orifice. -
_OBSERVATIONQUALITYMEASUREATTRIBUTE
Codes used to define various metadata aspects of a health quality measure. -
AGGREGATE
Indicates that the observation is carrying out an aggregation calculation, contained in the value element. -
CMPMSRMTH
Indicates what method is used in a quality measure to combine the component measure results included in an composite measure. -
CMPMSRSCRWGHT
An attribute of a quality measure describing the weight this component measure score is to carry in determining the overall composite measure final score. The value is real value greater than 0 and less than 1.0. Each component measure score will be multiplied by its CMPMSRSCRWGHT and then summed with the other component measures to determine the final overall composite measure score. The sum across all CMPMSRSCRWGHT values within a single composite measure SHALL be 1.0. The value assigned is scoped to the composite measure referencing this component measure only. -
COPY
Identifies the organization(s) who own the intellectual property represented by the eMeasure. -
CRS
Summary of relevant clinical guidelines or other clinical recommendations supporting this eMeasure. -
DEF
Description of individual terms, provided as needed. -
DISC
Disclaimer information for the eMeasure. -
FINALDT
The timestamp when the eMeasure was last packaged in the Measure Authoring Tool. -
GUIDE
Used to allow measure developers to provide additional guidance for implementers to understand greater specificity than could be provided in the logic for data criteria. -
IDUR
Information on whether an increase or decrease in score is the preferred result (e.g., a higher score indicates better quality OR a lower score indicates better quality OR quality is within a range). -
ITMCNT
Describes the items counted by the measure (e.g., patients, encounters, procedures, etc.) -
KEY
A significant word that aids in discoverability. -
MEDT
The end date of the measurement period. -
MSD
The start date of the measurement period. -
MSRADJ
The method of adjusting for clinical severity and conditions present at the start of care that can influence patient outcomes for making valid comparisons of outcome measures across providers. Indicates whether an eMeasure is subject to the statistical process for reducing, removing, or clarifying the influences of confounding factors to allow more useful comparisons. -
MSRAGG
Describes how to combine information calculated based on logic in each of several populations into one summarized result. It can also be used to describe how to risk adjust the data based on supplemental data elements described in the eMeasure. (e.g., pneumonia hospital measures antibiotic selection in the ICU versus non-ICU and then the roll-up of the two). Open Issue: The description does NOT align well with the definition used in the HQMF specfication; correct the MSGAGG definition, and the possible distinction of MSRAGG as a child of AGGREGATE. -
MSRIMPROV
Information on whether an increase or decrease in score is the preferred result. This should reflect information on which way is better, an increase or decrease in score. -
MSRJUR
The list of jurisdiction(s) for which the measure applies. -
MSRRPTR
Type of person or organization that is expected to report the issue. -
MSRRPTTIME
The maximum time that may elapse following completion of the measure until the measure report must be sent to the receiver. -
MSRSCORE
Indicates how the calculation is performed for the eMeasure (e.g., proportion, continuous variable, ratio) -
MSRSET
Location(s) in which care being measured is rendered Usage Note: MSRSET is used rather than RoleCode because the setting applies to what is being measured, as opposed to participating directly in the health quality measure documantion itself). -
MSRTOPIC
health quality measure topic type -
MSRTP
The time period for which the eMeasure applies. -
MSRTYPE
Indicates whether the eMeasure is used to examine a process or an outcome over time (e.g., Structure, Process, Outcome). -
RAT
Succinct statement of the need for the measure. Usually includes statements pertaining to Importance criterion: impact, gap in care and evidence. -
REF
Identifies bibliographic citations or references to clinical practice guidelines, sources of evidence, or other relevant materials supporting the intent and rationale of the eMeasure. -
SDE
Comparison of results across strata can be used to show where disparities exist or where there is a need to expose differences in results. For example, Centers for Medicare invalid input: '&' Medicaid Services (CMS) in the U.S. defines four required Supplemental Data Elements (payer, ethnicity, race, and gender), which are variables used to aggregate data into various subgroups. Additional supplemental data elements required for risk adjustment or other purposes of data aggregation can be included in the Supplemental Data Element section. -
STRAT
Describes the strata for which the measure is to be evaluated. There are three examples of reasons for stratification based on existing work. These include: (1) evaluate the measure based on different age groupings within the population described in the measure (e.g., evaluate the whole [age 14-25] and each sub-stratum [14-19] and [20-25]); (2) evaluate the eMeasure based on either a specific condition, a specific discharge location, or both; (3) evaluate the eMeasure based on different locations within a facility (e.g., evaluate the overall rate for all intensive care units and also some strata include additional findings [specific birth weights for neonatal intensive care units]). -
TRANF
Can be a URL or hyperlinks that link to the transmission formats that are specified for a particular reporting program. -
USE
Usage notes. -
_OBSERVATIONSEQUENCETYPE
ObservationSequenceType -
TIMEABSOLUTE
A sequence of values in the "absolute" time domain. This is the same time domain that all HL7 timestamps use. It is time as measured by the Gregorian calendar -
TIMERELATIVE
A sequence of values in a "relative" time domain. The time is measured relative to the earliest effective time in the Observation Series containing this sequence. -
_OBSERVATIONSERIESTYPE
ObservationSeriesType -
_ECGOBSERVATIONSERIESTYPE
ECGObservationSeriesType -
REPRESENTATIVEBEAT
This Observation Series type contains waveforms of a "representative beat" (a.k.a. "median beat" or "average beat"). The waveform samples are measured in relative time, relative to the beginning of the beat as defined by the Observation Series effective time. The waveforms are not directly acquired from the subject, but rather algorithmically derived from the "rhythm" waveforms. -
RHYTHM
This Observation type contains ECG "rhythm" waveforms. The waveform samples are measured in absolute time (a.k.a. "subject time" or "effective time"). These waveforms are usually "raw" with some minimal amount of noise reduction and baseline filtering applied. -
_PATIENTIMMUNIZATIONRELATEDOBSERVATIONTYPE
Description: Reporting codes that are related to an immunization event. -
CLSSRM
Description: The class room associated with the patient during the immunization event. -
GRADE
Description: The school grade or level the patient was in when immunized. -
SCHL
Description: The school the patient attended when immunized. -
SCHLDIV
Description: The school division or district associated with the patient during the immunization event. -
TEACHER
Description: The patient's teacher when immunized. -
_POPULATIONINCLUSIONOBSERVATIONTYPE
Observation types for specifying criteria used to assert that a subject is included in a particular population. -
DENEX
Criteria which specify subjects who should be removed from the eMeasure population and denominator before determining if numerator criteria are met. Denominator exclusions are used in proportion and ratio measures to help narrow the denominator. -
DENEXCEP
Criteria which specify the removal of a subject, procedure or unit of measurement from the denominator, only if the numerator criteria are not met. Denominator exceptions allow for adjustment of the calculated score for those providers with higher risk populations. Denominator exceptions are used only in proportion eMeasures. They are not appropriate for ratio or continuous variable eMeasures. Denominator exceptions allow for the exercise of clinical judgment and should be specifically defined where capturing the information in a structured manner fits the clinical workflow. Generic denominator exception reasons used in proportion eMeasures fall into three general categories: Medical reasons Patient (or subject) reasons System reasons -
DENOM
Criteria for specifying the entities to be evaluated by a specific quality measure, based on a shared common set of characteristics (within a specific measurement set to which a given measure belongs). The denominator can be the same as the initial population, or it may be a subset of the initial population to further constrain it for the purpose of the eMeasure. Different measures within an eMeasure set may have different denominators. Continuous Variable eMeasures do not have a denominator, but instead define a measure population. -
IPOP
Criteria for specifying the entities to be evaluated by a specific quality measure, based on a shared common set of characteristics (within a specific measurement set to which a given measure belongs). -
IPPOP
Criteria for specifying the patients to be evaluated by a specific quality measure, based on a shared common set of characteristics (within a specific measurement set to which a given measure belongs). Details often include information based upon specific age groups, diagnoses, diagnostic and procedure codes, and enrollment periods. -
MSRPOPL
Criteria for specifying the measure population as a narrative description (e.g., all patients seen in the Emergency Department during the measurement period). This is used only in continuous variable eMeasures. -
MSRPOPLEX
Criteria for specifying subjects who should be removed from the eMeasure's Initial Population and Measure Population. Measure Population Exclusions are used in Continuous Variable measures to help narrow the Measure Population before determining the value(s) of the continuous variable(s). -
NUMER
Criteria for specifying the processes or outcomes expected for each patient, procedure, or other unit of measurement defined in the denominator for proportion measures, or related to (but not directly derived from) the denominator for ratio measures (e.g., a numerator listing the number of central line blood stream infections and a denominator indicating the days per thousand of central line usage in a specific time period). -
NUMEX
Criteria for specifying instances that should not be included in the numerator data. (e.g., if the number of central line blood stream infections per 1000 catheter days were to exclude infections with a specific bacterium, that bacterium would be listed as a numerator exclusion). Numerator Exclusions are used only in ratio eMeasures. -
_PREFERENCEOBSERVATIONTYPE
Types of observations that can be made about Preferences. -
PREFSTRENGTH
An observation about how important a preference is to the target of the preference. -
ADVERSEREACTION
Indicates that the observation is of an unexpected negative occurrence in the subject suspected to result from the subject's exposure to one or more agents. Observation values would be the symptom resulting from the reaction. -
ASSERTION
Description:Refines classCode OBS to indicate an observation in which observation.value contains a finding or other nominalized statement, where the encoded information in Observation.value is not altered by Observation.code. For instance, observation.code="ASSERTION" and observation.value="fracture of femur present" is an assertion of a clinical finding of femur fracture. -
CASESER
Definition:An observation that provides a characterization of the level of harm to an investigation subject as a result of a reaction or event. -
CDIO
An observation that states whether the disease was likely acquired outside the jurisdiction of observation, and if so, the nature of the inter-jurisdictional relationship. OpenIssue: This code could be moved to LOINC if it can be done before there are significant implemenations using it. -
CRIT
A clinical judgment as to the worst case result of a future exposure (including substance administration). When the worst case result is assessed to have a life-threatening or organ system threatening potential, it is considered to be of high criticality. -
CTMO
An observation that states the mechanism by which disease was acquired by the living subject involved in the public health case. OpenIssue: This code could be moved to LOINC if it can be done before there are significant implemenations using it. -
DX
Includes all codes defining types of indications such as diagnosis, symptom and other indications such as contrast agents for lab tests. -
ADMDX
Admitting diagnosis are the diagnoses documented for administrative purposes as the basis for a hospital admission. -
DISDX
Discharge diagnosis are the diagnoses documented for administrative purposes as the time of hospital discharge. -
INTDX
Intermediate diagnoses are those diagnoses documented for administrative purposes during the course of a hospital stay. -
NOI
The type of injury that the injury coding specifies. -
GISTIER
Description: Accuracy determined as per the GIS tier code system. -
HHOBS
Indicates that the observation is of a person?s living situation in a household including the household composition and circumstances. -
ISSUE
There is a clinical issue for the therapy that makes continuation of the therapy inappropriate. Open Issue: The definition of this code does not correctly represent the concept space of its specializations (children) -
_ACTADMINISTRATIVEDETECTEDISSUECODE
Identifies types of detectyed issues for Act class "ALRT" for the administrative and patient administrative acts domains. -
_ACTADMINISTRATIVEAUTHORIZATIONDETECTEDISSUECODE
ActAdministrativeAuthorizationDetectedIssueCode -
NAT
The requesting party has insufficient authorization to invoke the interaction. -
SUPPRESSED
Description: One or more records in the query response have been suppressed due to consent or privacy restrictions. -
VALIDAT
Description:The specified element did not pass business-rule validation. -
KEY204
The ID of the patient, order, etc., was not found. Used for transactions other than additions, e.g. transfer of a non-existent patient. -
KEY205
The ID of the patient, order, etc., already exists. Used in response to addition transactions (Admit, New Order, etc.). -
COMPLY
There may be an issue with the patient complying with the intentions of the proposed therapy -
DUPTHPY
The proposed therapy appears to duplicate an existing therapy -
DUPTHPCLS
Description:The proposed therapy appears to have the same intended therapeutic benefit as an existing therapy, though the specific mechanisms of action vary. -
DUPTHPGEN
Description:The proposed therapy appears to have the same intended therapeutic benefit as an existing therapy and uses the same mechanisms of action as the existing therapy. -
ABUSE
Description:The proposed therapy is frequently misused or abused and therefore should be used with caution and/or monitoring. -
FRAUD
Description:The request is suspected to have a fraudulent basis. -
PLYDOC
A similar or identical therapy was recently ordered by a different practitioner. -
PLYPHRM
This patient was recently supplied a similar or identical therapy from a different pharmacy or supplier. -
DOSE
Proposed dosage instructions for therapy differ from standard practice. -
DOSECOND
Description:Proposed dosage is inappropriate due to patient's medical condition. -
DOSEDUR
Proposed length of therapy differs from standard practice. -
DOSEDURH
Proposed length of therapy is longer than standard practice -
DOSEDURHIND
Proposed length of therapy is longer than standard practice for the identified indication or diagnosis -
DOSEDURL
Proposed length of therapy is shorter than that necessary for therapeutic effect -
DOSEDURLIND
Proposed length of therapy is shorter than standard practice for the identified indication or diagnosis -
DOSEH
Proposed dosage exceeds standard practice -
DOSEHINDA
Proposed dosage exceeds standard practice for the patient's age -
DOSEHIND
High Dose for Indication Alert -
DOSEHINDSA
Proposed dosage exceeds standard practice for the patient's height or body surface area -
DOSEHINDW
Proposed dosage exceeds standard practice for the patient's weight -
DOSEIVL
Proposed dosage interval/timing differs from standard practice -
DOSEIVLIND
Proposed dosage interval/timing differs from standard practice for the identified indication or diagnosis -
DOSEL
Proposed dosage is below suggested therapeutic levels -
DOSELINDA
Proposed dosage is below suggested therapeutic levels for the patient's age -
DOSELIND
Low Dose for Indication Alert -
DOSELINDSA
Proposed dosage is below suggested therapeutic levels for the patient's height or body surface area -
DOSELINDW
Proposed dosage is below suggested therapeutic levels for the patient's weight -
MDOSE
Description:The maximum quantity of this drug allowed to be administered within a particular time-range (month, year, lifetime) has been reached or exceeded. -
OBSA
Proposed therapy may be inappropriate or contraindicated due to conditions or characteristics of the patient -
AGE
Proposed therapy may be inappropriate or contraindicated due to patient age -
ADALRT
Proposed therapy is outside of the standard practice for an adult patient. -
GEALRT
Proposed therapy is outside of standard practice for a geriatric patient. -
PEALRT
Proposed therapy is outside of the standard practice for a pediatric patient. -
COND
Proposed therapy may be inappropriate or contraindicated due to an existing/recent patient condition or diagnosis -
HGHT
null -
LACT
Proposed therapy may be inappropriate or contraindicated when breast-feeding -
PREG
Proposed therapy may be inappropriate or contraindicated during pregnancy -
WGHT
null -
CREACT
Description:Proposed therapy may be inappropriate or contraindicated because of a common but non-patient specific reaction to the product. Example:There is no record of a specific sensitivity for the patient, but the presence of the sensitivity is common and therefore caution is warranted. -
GEN
Proposed therapy may be inappropriate or contraindicated due to patient genetic indicators. -
GEND
Proposed therapy may be inappropriate or contraindicated due to patient gender. -
LAB
Proposed therapy may be inappropriate or contraindicated due to recent lab test results -
REACT
Proposed therapy may be inappropriate or contraindicated based on the potential for a patient reaction to the proposed product -
ALGY
Proposed therapy may be inappropriate or contraindicated because of a recorded patient allergy to the proposed product. (Allergies are immune based reactions.) -
INT
Proposed therapy may be inappropriate or contraindicated because of a recorded patient intolerance to the proposed product. (Intolerances are non-immune based sensitivities.) -
RREACT
Proposed therapy may be inappropriate or contraindicated because of a potential patient reaction to a cross-sensitivity related product. -
RALG
Proposed therapy may be inappropriate or contraindicated because of a recorded patient allergy to a cross-sensitivity related product. (Allergies are immune based reactions.) -
RAR
Proposed therapy may be inappropriate or contraindicated because of a recorded prior adverse reaction to a cross-sensitivity related product. -
RINT
Proposed therapy may be inappropriate or contraindicated because of a recorded patient intolerance to a cross-sensitivity related product. (Intolerances are non-immune based sensitivities.) -
BUS
Description:A local business rule relating multiple elements has been violated. -
CODEINVAL
Description:The specified code is not valid against the list of codes allowed for the element. -
CODEDEPREC
Description:The specified code has been deprecated and should no longer be used. Select another code from the code system. -
FORMAT
Description:The element does not follow the formatting or type rules defined for the field. -
ILLEGAL
Description:The request is missing elements or contains elements which cause it to not meet the legal standards for actioning. -
LENRANGE
Description:The length of the data specified falls out of the range defined for the element. -
LENLONG
Description:The length of the data specified is greater than the maximum length defined for the element. -
LENSHORT
Description:The length of the data specified is less than the minimum length defined for the element. -
MISSCOND
Description:The specified element must be specified with a non-null value under certain conditions. In this case, the conditions are true but the element is still missing or null. -
MISSMAND
Description:The specified element is mandatory and was not included in the instance. -
NODUPS
Description:More than one element with the same value exists in the set. Duplicates not permission in this set in a set. -
NOPERSIST
Description: Element in submitted message will not persist in data storage based on detected issue. -
REPRANGE
Description:The number of repeating elements falls outside the range of the allowed number of repetitions. -
MAXOCCURS
Description:The number of repeating elements is above the maximum number of repetitions allowed. -
MINOCCURS
Description:The number of repeating elements is below the minimum number of repetitions allowed. -
_ACTADMINISTRATIVERULEDETECTEDISSUECODE
ActAdministrativeRuleDetectedIssueCode -
KEY206
Description: Metadata associated with the identification (e.g. name or gender) does not match the identification being verified. -
OBSOLETE
Description: One or more records in the query response have a status of 'obsolete'. -
_ACTSUPPLIEDITEMDETECTEDISSUECODE
Identifies types of detected issues regarding the administration or supply of an item to a patient. -
_ADMINISTRATIONDETECTEDISSUECODE
Administration of the proposed therapy may be inappropriate or contraindicated as proposed -
_APPROPRIATENESSDETECTEDISSUECODE
AppropriatenessDetectedIssueCode -
_INTERACTIONDETECTEDISSUECODE
InteractionDetectedIssueCode -
FOOD
Proposed therapy may interact with certain foods -
TPROD
Proposed therapy may interact with an existing or recent therapeutic product -
DRG
Proposed therapy may interact with an existing or recent drug therapy -
NHP
Proposed therapy may interact with existing or recent natural health product therapy -
NONRX
Proposed therapy may interact with a non-prescription drug (e.g. alcohol, tobacco, Aspirin) -
PREVINEF
Definition:The same or similar treatment has previously been attempted with the patient without achieving a positive effect. -
DACT
Description:Proposed therapy may be contraindicated or ineffective based on an existing or recent drug therapy. -
TIME
Description:Proposed therapy may be inappropriate or ineffective based on the proposed start or end time. -
ALRTENDLATE
Definition:Proposed therapy may be inappropriate or ineffective because the end of administration is too close to another planned therapy. -
ALRTSTRTLATE
Definition:Proposed therapy may be inappropriate or ineffective because the start of administration is too late after the onset of the condition. -
_TIMINGDETECTEDISSUECODE
Proposed therapy may be inappropriate or ineffective based on the proposed start or end time. -
ENDLATE
Proposed therapy may be inappropriate or ineffective because the end of administration is too close to another planned therapy -
STRTLATE
Proposed therapy may be inappropriate or ineffective because the start of administration is too late after the onset of the condition -
_SUPPLYDETECTEDISSUECODE
Supplying the product at this time may be inappropriate or indicate compliance issues with the associated therapy -
ALLDONE
Definition:The requested action has already been performed and so this request has no effect -
FULFIL
Definition:The therapy being performed is in some way out of alignment with the requested therapy. -
NOTACTN
Definition:The status of the request being fulfilled has changed such that it is no longer actionable. This may be because the request has expired, has already been completely fulfilled or has been otherwise stopped or disabled. (Not used for 'suspended' orders.) -
NOTEQUIV
Definition:The therapy being performed is not sufficiently equivalent to the therapy which was requested. -
NOTEQUIVGEN
Definition:The therapy being performed is not generically equivalent (having the identical biological action) to the therapy which was requested. -
NOTEQUIVTHER
Definition:The therapy being performed is not therapeutically equivalent (having the same overall patient effect) to the therapy which was requested. -
TIMING
Definition:The therapy is being performed at a time which diverges from the time the therapy was requested -
INTERVAL
Definition:The therapy action is being performed outside the bounds of the time period requested -
MINFREQ
Definition:The therapy action is being performed too soon after the previous occurrence based on the requested frequency -
HELD
Definition:There should be no actions taken in fulfillment of a request that has been held or suspended. -
TOOLATE
The patient is receiving a subsequent fill significantly later than would be expected based on the amount previously supplied and the therapy dosage instructions -
TOOSOON
The patient is receiving a subsequent fill significantly earlier than would be expected based on the amount previously supplied and the therapy dosage instructions -
HISTORIC
Description: While the record was accepted in the repository, there is a more recent version of a record of this type. -
PATPREF
Definition:The proposed therapy goes against preferences or consent constraints recorded in the patient's record. -
PATPREFALT
Definition:The proposed therapy goes against preferences or consent constraints recorded in the patient's record. An alternate therapy meeting those constraints is available. -
KSUBJ
Categorization of types of observation that capture the main clinical knowledge subject which may be a medication, a laboratory test, a disease. -
KSUBT
Categorization of types of observation that capture a knowledge subtopic which might be treatment, etiology, or prognosis. -
OINT
Hypersensitivity resulting in an adverse reaction upon exposure to an agent. -
ALG
Hypersensitivity to an agent caused by an immunologic response to an initial exposure -
DALG
An allergy to a pharmaceutical product. -
EALG
An allergy to a substance other than a drug or a food. E.g. Latex, pollen, etc. -
FALG
An allergy to a substance generally consumed for nutritional purposes. -
DINT
Hypersensitivity resulting in an adverse reaction upon exposure to a drug. -
DNAINT
Hypersensitivity to an agent caused by a mechanism other than an immunologic response to an initial exposure -
EINT
Hypersensitivity resulting in an adverse reaction upon exposure to environmental conditions. -
ENAINT
Hypersensitivity to an agent caused by a mechanism other than an immunologic response to an initial exposure -
FINT
Hypersensitivity resulting in an adverse reaction upon exposure to food. -
FNAINT
Hypersensitivity to an agent caused by a mechanism other than an immunologic response to an initial exposure -
NAINT
Hypersensitivity to an agent caused by a mechanism other than an immunologic response to an initial exposure -
SEV
A subjective evaluation of the seriousness or intensity associated with another observation. -
_FDALABELDATA
FDA label data -
FDACOATING
FDA label coating -
FDACOLOR
FDA label color -
FDAIMPRINTCD
FDA label imprint code -
FDALOGO
FDA label logo -
FDASCORING
FDA label scoring -
FDASHAPE
FDA label shape -
FDASIZE
FDA label size -
_ROIOVERLAYSHAPE
Shape of the region on the object being referenced -
CIRCLE
A circle defined by two (column,row) pairs. The first point is the center of the circle and the second point is a point on the perimeter of the circle. -
ELLIPSE
An ellipse defined by four (column,row) pairs, the first two points specifying the endpoints of the major axis and the second two points specifying the endpoints of the minor axis. -
POINT
A single point denoted by a single (column,row) pair, or multiple points each denoted by a (column,row) pair. -
POLY
A series of connected line segments with ordered vertices denoted by (column,row) pairs; if the first and last vertices are the same, it is a closed polygon. -
C
Description:Indicates that result data has been corrected. -
DIET
Code set to define specialized/allowed diets -
BR
A diet exclusively composed of oatmeal, semolina, or rice, to be extremely easy to eat and digest. -
DM
A diet that uses carbohydrates sparingly. Typically with a restriction in daily energy content (e.g. 1600-2000 kcal). -
FAST
No enteral intake of foot or liquids whatsoever, no smoking. Typically 6 to 8 hours before anesthesia. -
FORMULA
A diet consisting of a formula feeding, either for an infant or an adult, to provide nutrition either orally or through the gastrointestinal tract via tube, catheter or stoma. -
GF
Gluten free diet for celiac disease. -
LF
A diet low in fat, particularly to patients with hepatic diseases. -
LP
A low protein diet for patients with renal failure. -
LQ
A strictly liquid diet, that can be fully absorbed in the intestine, and therefore may not contain fiber. Used before enteral surgeries. -
LS
A diet low in sodium for patients with congestive heart failure and/or renal failure. -
N
A normal diet, i.e. no special preparations or restrictions for medical reasons. This is notwithstanding any preferences the patient might have regarding special foods, such as vegetarian, kosher, etc. -
NF
A no fat diet for acute hepatic diseases. -
PAF
Phenylketonuria diet. -
PAR
Patient is supplied with parenteral nutrition, typically described in terms of i.v. medications. -
RD
A diet that seeks to reduce body fat, typically low energy content (800-1600 kcal). -
SCH
A diet that avoids ingredients that might cause digestion problems, e.g., avoid excessive fat, avoid too much fiber (cabbage, peas, beans). -
SUPPLEMENT
A diet that is not intended to be complete but is added to other diets. -
T
This is not really a diet, since it contains little nutritional value, but is essentially just water. Used before coloscopy examinations. -
VLI
Diet with low content of the amino-acids valin, leucin, and isoleucin, for "maple syrup disease." -
DRUGPRG
Definition: A public or government health program that administers and funds coverage for prescription drugs to assist program eligible who meet financial and health status criteria. -
F
Description:Indicates that a result is complete. No further results are to come. This maps to the 'complete' state in the observation result status code. -
PRLMN
Description:Indicates that a result is incomplete. There are further results to come. This maps to the 'active' state in the observation result status code. -
SECOBS
An observation identifying security metadata about an IT resource (data, information object, service, or system capability), which may be used to make access control decisions. Security metadata are used to name security labels. Rationale: According to ISO/TS 22600-3:2009(E) A.9.1.7 SECURITY LABEL MATCHING, Security label matching compares the initiator's clearance to the target's security label. All of the following must be true for authorization to be granted: The security policy identifiers shall be identical The classification level of the initiator shall be greater than or equal to that of the target (that is, there shall be at least one value in the classification list of the clearance greater than or equal to the classification of the target), and For each security category in the target label, there shall be a security category of the same type in the initiator's clearance and the initiator's classification level shall dominate that of the target. Examples: SecurityObservationType security label fields include: Confidentiality classification Compartment category Sensitivity category Security mechanisms used to ensure data integrity or to perform authorized data transformation Indicators of an IT resource completeness, veracity, reliability, trustworthiness, or provenance. Usage Note: SecurityObservationType codes designate security label field types, which are valued with an applicable SecurityObservationValue code as the "security label tag". -
SECCATOBS
Type of security metadata observation made about the category of an IT resource (data, information object, service, or system capability), which may be used to make access control decisions. Security category metadata is defined by ISO/IEC 2382-8:1998(E/F)/ T-REC-X.812-1995 as: "A nonhierarchical grouping of sensitive information used to control access to data more finely than with hierarchical security classification alone." Rationale: A security category observation supports requirement to specify the type of IT resource to facilitate application of appropriate levels of information security according to a range of levels of impact or consequences that might result from the unauthorized disclosure, modification, or use of the information or information system. A resource is assigned to a specific category of information (e.g., privacy, medical, proprietary, financial, investigative, contractor sensitive, security management) defined by an organization or in some instances, by a specific law, Executive Order, directive, policy, or regulation. [FIPS 199] Examples: Types of security categories include: Compartment: A division of data into isolated blocks with separate security controls for the purpose of reducing risk. (ISO 2382-8). A security label tag that "segments" an IT resource by indicating that access and use is restricted to members of a defined community or project. (HL7 Healthcare Classification System) Sensitivity: The characteristic of an IT resource which implies its value or importance and may include its vulnerability. (ISO 7492-2) Privacy metadata for information perceived as undesirable to share. (HL7 Healthcare Classification System) -
SECCLASSOBS
Type of security metadata observation made about the classification of an IT resource (data, information object, service, or system capability), which may be used to make access control decisions. Security classification is defined by ISO/IEC 2382-8:1998(E/F)/ T-REC-X.812-1995 as: "The determination of which specific degree of protection against access the data or information requires, together with a designation of that degree of protection." Security classification metadata is based on an analysis of applicable policies and the risk of financial, reputational, or other harm that could result from unauthorized disclosure. Rationale: A security classification observation may indicate that the confidentiality level indicated by an Act or Role confidentiality attribute has been overridden by the entity responsible for ascribing the SecurityClassificationObservationValue. This supports the business requirement for increasing or decreasing the level of confidentiality (classification or declassification) based on parameters beyond the original assignment of an Act or Role confidentiality. Examples: Types of security classification include: HL7 Confidentiality Codes such as very restricted, unrestricted, and normal. Intelligence community examples include top secret, secret, and confidential. Usage Note: Security classification observation type codes designate security label field types, which are valued with an applicable SecurityClassificationObservationValue code as the "security label tag". -
SECCONOBS
Type of security metadata observation made about the control of an IT resource (data, information object, service, or system capability), which may be used to make access control decisions. Security control metadata convey instructions to users and receivers for secure distribution, transmission, and storage; dictate obligations or mandated actions; specify any action prohibited by refrain policy such as dissemination controls; and stipulate the permissible purpose of use of an IT resource. Rationale: A security control observation supports requirement to specify applicable management, operational, and technical controls (i.e., safeguards or countermeasures) prescribed for an information system to protect the confidentiality, integrity, and availability of the system and its information. [FIPS 199] Examples: Types of security control metadata include: handling caveats dissemination controls obligations refrain policies purpose of use constraints -
SECINTOBS
Type of security metadata observation made about the integrity of an IT resource (data, information object, service, or system capability), which may be used to make access control decisions. Rationale: A security integrity observation supports the requirement to guard against improper information modification or destruction, and includes ensuring information non-repudiation and authenticity. (44 U.S.C., SEC. 3542) Examples: Types of security integrity metadata include: Integrity status, which indicates the completeness or workflow status of an IT resource (data, information object, service, or system capability) Integrity confidence, which indicates the reliability and trustworthiness of an IT resource Integrity control, which indicates pertinent handling caveats, obligations, refrain policies, and purpose of use for the resource Data integrity, which indicate the security mechanisms used to ensure that the accuracy and consistency are preserved regardless of changes made (ISO/IEC DIS 2382-8) Alteration integrity, which indicate the security mechanisms used for authorized transformations of the resource Integrity provenance, which indicates the entity responsible for a report or assertion relayed "second-hand" about an IT resource -
SECALTINTOBS
Type of security metadata observation made about the alteration integrity of an IT resource (data, information object, service, or system capability), which indicates the mechanism used for authorized transformations of the resource. Examples: Types of security alteration integrity observation metadata, which may value the observation with a code used to indicate the mechanism used for authorized transformation of an IT resource, including: translation syntactic transformation semantic mapping redaction masking pseudonymization anonymization -
SECDATINTOBS
Type of security metadata observation made about the data integrity of an IT resource (data, information object, service, or system capability), which indicates the security mechanism used to preserve resource accuracy and consistency. Data integrity is defined by ISO 22600-23.3.21 as: "The property that data has not been altered or destroyed in an unauthorized manner", and by ISO/IEC 2382-8: The property of data whose accuracy and consistency are preserved regardless of changes made." Examples: Types of security data integrity observation metadata, which may value the observation, include cryptographic hash function and digital signature. -
SECINTCONOBS
Type of security metadata observation made about the integrity confidence of an IT resource (data, information object, service, or system capability), which may be used to make access control decisions. Examples: Types of security integrity confidence observation metadata, which may value the observation, include highly reliable, uncertain reliability, and not reliable. Usage Note: A security integrity confidence observation on an Act may indicate that a valued Act.uncertaintycode attribute has been overridden by the entity responsible for ascribing the SecurityIntegrityConfidenceObservationValue. This supports the business requirements for increasing or decreasing the assessment of the reliability or trustworthiness of an IT resource based on parameters beyond the original assignment of an Act statement level of uncertainty. -
SECINTPRVOBS
Type of security metadata observation made about the provenance integrity of an IT resource (data, information object, service, or system capability), which indicates the lifecycle completeness of an IT resource in terms of workflow status such as its creation, modification, suspension, and deletion; locations in which the resource has been collected or archived, from which it may be retrieved, and the history of its distribution and disclosure. Integrity provenance metadata about an IT resource may be used to assess its veracity, reliability, and trustworthiness. Examples: Types of security integrity provenance observation metadata, which may value the observation about an IT resource, include: completeness or workflow status, such as authentication the entity responsible for original authoring or informing about an IT resource the entity responsible for a report or assertion about an IT resource relayed â??second-handâ?? the entity responsible for excerpting, transforming, or compiling an IT resource -
SECINTPRVABOBS
Type of security metadata observation made about the integrity provenance of an IT resource (data, information object, service, or system capability), which indicates the entity that made assertions about the resource. The asserting entity may not be the original informant about the resource. Examples: Types of security integrity provenance asserted by observation metadata, which may value the observation, including: assertions about an IT resource by a patient assertions about an IT resource by a clinician assertions about an IT resource by a device -
SECINTPRVRBOBS
Type of security metadata observation made about the integrity provenance of an IT resource (data, information object, service, or system capability), which indicates the entity that reported the existence of the resource. The reporting entity may not be the original author of the resource. Examples: Types of security integrity provenance reported by observation metadata, which may value the observation, include: reports about an IT resource by a patient reports about an IT resource by a clinician reports about an IT resource by a device -
SECINTSTOBS
Type of security metadata observation made about the integrity status of an IT resource (data, information object, service, or system capability), which may be used to make access control decisions. Indicates the completeness of an IT resource in terms of workflow status, which may impact users that are authorized to access and use the resource. Examples: Types of security integrity status observation metadata, which may value the observation, include codes from the HL7 DocumentCompletion code system such as legally authenticated, in progress, and incomplete. -
SECTRSTOBS
An observation identifying trust metadata about an IT resource (data, information object, service, or system capability), which may be used as a trust attribute to populate a computable trust policy, trust credential, trust assertion, or trust label field in a security label or trust policy, which are principally used for authentication, authorization, and access control decisions. -
TRSTACCRDOBS
Type of security metadata observation made about the formal declaration by an authority or neutral third party that validates the technical, security, trust, and business practice conformance of Trust Agents to facilitate security, interoperability, and trust among participants within a security domain or trust framework. -
TRSTAGREOBS
Type of security metadata observation made about privacy and security requirements with which a security domain must comply. [ISO IEC 10181-1] -
TRSTCERTOBS
Type of security metadata observation made about a set of security-relevant data issued by a security authority or trusted third party, together with security information which is used to provide the integrity and data origin authentication services for an IT resource (data, information object, service, or system capability). [Based on ISO IEC 10181-1] For example, A Certificate Policy (CP), which is a named set of rules that indicates the applicability of a certificate to a particular community and/or class of application with common security requirements. For example, a particular Certificate Policy might indicate the applicability of a type of certificate to the authentication of electronic data interchange transactions for the trading of goods within a given price range. [Trust Service Principles and Criteria for Certification Authorities Version 2.0 March 2011 Copyright 2011 by Canadian Institute of Chartered Accountants. A Certificate Practice Statement (CSP), which is a statement of the practices which an Authority employs in issuing and managing certificates. [Trust Service Principles and Criteria for Certification Authorities Version 2.0 March 2011 Copyright 2011 by Canadian Institute of Chartered Accountants.] -
TRSTFWKOBS
Type of security metadata observation made about a complete set of contracts, regulations or commitments that enable participating actors to rely on certain assertions by other actors to fulfill their information security requirements. [Kantara Initiative] -
TRSTLOAOBS
Type of security metadata observation made about the digital quality or reliability of a trust assertion, activity, capability, information exchange, mechanism, process, or protocol. -
TRSTMECOBS
Type of security metadata observation made about a security architecture system component that supports enforcement of security policies. -
SUBSIDFFS
Definition: A government health program that provides coverage on a fee for service basis for health services to persons meeting eligibility criteria such as income, location of residence, access to other coverages, health condition, and age, the cost of which is to some extent subsidized by public funds. Discussion: The structure and business processes for underwriting and administering a subsidized fee for service program is further specified by the Underwriter and Payer Role.class and Role.code. -
WRKCOMP
Definition: Government mandated program providing coverage, disability income, and vocational rehabilitation for injuries sustained in the work place or in the course of employment. Employers may either self-fund the program, purchase commercial coverage, or pay a premium to a government entity that administers the program. Employees may be required to pay premiums toward the cost of coverage as well. -
_ACTPROCEDURECODE
An identifying code for healthcare interventions/procedures. -
_ACTBILLABLESERVICECODE
Definition: An identifying code for billable services, as opposed to codes for similar services used to identify them for functional purposes. -
_HL7DEFINEDACTCODES
Domain provides the root for HL7-defined detailed or rich codes for the Act classes. -
COPAY
null -
DEDUCT
null -
DOSEIND
null -
PRA
null -
STORE
The act of putting something away for safe keeping. The "something" may be physical object such as a specimen, or information, such as observations regarding a specimen. -
NULL
added to help the parsers
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Method Details
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values
Returns an array containing the constants of this enum type, in the order they are declared.- Returns:
- an array containing the constants of this enum type, in the order they are declared
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valueOf
Returns the enum constant of this type with the specified name. The string must match exactly an identifier used to declare an enum constant in this type. (Extraneous whitespace characters are not permitted.)- Parameters:
name
- the name of the enum constant to be returned.- Returns:
- the enum constant with the specified name
- Throws:
IllegalArgumentException
- if this enum type has no constant with the specified nameNullPointerException
- if the argument is null
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fromCode
- Throws:
org.hl7.fhir.exceptions.FHIRException
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toCode
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getSystem
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getDefinition
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getDisplay
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