|
|
Line 176: |
Line 176: |
| * [[2.16.840.1.113883.10.21.4.4]] UV ClinicalStatement Encounter | | * [[2.16.840.1.113883.10.21.4.4]] UV ClinicalStatement Encounter |
| * [[2.16.840.1.113883.10.21.4.5]] UV Substitution Permission | | * [[2.16.840.1.113883.10.21.4.5]] UV Substitution Permission |
− | * [[2.16.840.1.113883.10.21.4.6]] Subordinate Substance Administration | + | * [[2.16.840.1.113883.10.21.4.6]] UV Subordinate Substance Administration |
| * [[2.16.840.1.113883.10.21.4.7]] UV Medication Statement | | * [[2.16.840.1.113883.10.21.4.7]] UV Medication Statement |
| * [[2.16.840.1.113883.10.21.4.8]] UV Medication Order Reference | | * [[2.16.840.1.113883.10.21.4.8]] UV Medication Order Reference |
| * [[2.16.840.1.113883.10.21.4.9]] UV Dispense Event Reference | | * [[2.16.840.1.113883.10.21.4.9]] UV Dispense Event Reference |
− | * [[2.16.840.1.113883.10.21.4.10]] Medication Information (simple) | + | * [[2.16.840.1.113883.10.21.4.10]] UV Medication Information (simple) |
− | * [[2.16.840.1.113883.10.21.4.11]] Medication Information (detail) | + | * [[2.16.840.1.113883.10.21.4.11]] UV Medication Information (detail) |
| * [[2.16.840.1.113883.10.21.9.1]] UV Use Period | | * [[2.16.840.1.113883.10.21.9.1]] UV Use Period |
| | | |
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Co-Chair, Primary Editor |
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Co-Chair, Primary Editor |
John Hatem jnhatem@hotmail.com
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Co-Chair |
Scott Robertson PharmD scott.m.robertson@kp.org
|
Co-Chair |
Jean Duteau jean@duteaudesign.com
|
Contributor |
Dr Kai U. Heitmann Heitmann Consulting and Services, ART-DECOR Open Tools GmbH, HL7 Germany info@kheitmann.de |
Contributor |
Giorgio Cangioli, PhD Consultant, HL7 Italy giorgio.cangioli@gmail.com
|
Contributor |
Tom de Jong VZVZ, HL7 The Netherlands tom@nova-pro.nl |
Contributor |
Dr Christof Geßner Gematik GmbH, HL7 Germany christof.gessner@gematik.de |
Introduction
This Implementation Guide provides templates for Medication Order and Medication Statement that can be used by HL7 standards developers and external projects to develop models for pharmacy related content. The implementation guide is intended to provide consistency of pharmacy related models across all uses regardless of the method of transport by:
- creating a library of Universal pharmacy templates that can be used by other Work Groups to derive constrained versions.
Purpose
Background
Historically multiple HL7 Work Groups have developed specifications for pharmacy related content and as a result, there is inconsistency in the models that exist in HL7 V2, V3, CDA and FHIR. The Pharmacy Work Group often receives questions as to how to model pharmacy related content but in some cases, the use case cannot be met with the existing models.
This Implementation Guide provides a library of pharmacy templates that can be used by HL7 Work Groups or external projects to derive constrained versions of models for pharmacy related content.
Scope
The scope of the Implementation Guide is limited to Medication Order and Medication Statement. The content was developed by aligning and harmonizing the existing specifications for Consolidated CDA (C-CDA Release 2.1).
Future releases of the Implementation Guide will include Medication Dispense and Medication Administration.
Ballot Status of the Document
The Implementation Guide is being balloted as Informative with the intention to go to Standard for Trial Use (STU) and then to Normative.
Audience
- Clinical and Public Health laboratories
- Immunization Registries
- Pharmaceutical Vendors
- EHR/PHR vendors
- Clinical Decision Support Systems
- HIS Vendors
- Emergency Services Providers
- Healthcare Institutions
- Pharmacists
- Physicians and other Clinicians
Relationships with other projects and guides
- Consolidated CDA (C-CDA)
- HL7 Version 3 Pharmacy Models
- HL7 FHIR® Pharmacy Resources
Principles and background
Please Note
Nothing in here yet. Do we want to report about
- the new method to represent normal, split and tapered dose information in CDA Substance Administrations?
- do we want to tell people that we reduced the richness of the original Pharmacy V3 templates drastically to ease implementation?
- do we want to mention FHIR profile work that influenced heavily the development of the CDA templates?
- And/or more general other design principles?
Technical Background
What is a CDA
CDA R2 is "… a document markup standard that specifies the structure and semantics of clinical documents for the purpose of exchange” [CDA R2, Section 1.1]. Clinical documents, according to CDA, have the following characteristics:
- Persistence
- Stewardship
- Potential for authentication
- Context
- Wholeness
- Human readability
CDA defines a header for classification and management and a document body that carries the clinical record. While the header metadata are prescriptive and designed for consistency across all instances, the body is highly generic, leaving the designation of semantic requirements to implementation.
Templated CDA
CDA R2 can be constrained by mechanisms defined in the “Refinement and Localization” section of the HL7 Version 3 Interoperability Standards. The mechanism most commonly used to constrain CDA is referred to as “templated CDA”. This specification created a set of artifacts containing modular CDA templates (and associated value sets) for the purpose of the International Patient Summary, and the templates can be reused across any number of CDA document types.
There are different kinds of templates that might be created. Among them, the most common ones are:
- CDA Document Level Templates constrain fields in the Clinical Document Architecture (CDA) header, and define containment relationships to CDA sections.
For example, a History-and-Physical document-level template might require that the patient’s name be present, and that the document contain a Physical Exam section.
- CDA Header Level Templates constrain fields for parts of the CDA header, like the patient (record target), the author, participations or the service event.
- CDA Section Level Templates constrain fields in the CDA section, and define containment relationships to CDA entries.
For example, a Physical-exam section-level template might require that the section/code be fixed to a particular LOINC code, and that the section contain a Systolic Blood Pressure observation.
- CDA Entry Level Templates constrain the CDA clinical statement model in accordance with real world observations and acts.
For example, a Systolic-blood-pressure entry-level template defines how the CDA Observation class is constrained (how to populate observation/code, how to populate observation/value, etc.) to represent the notion of a systolic blood pressure.
Open and Closed Templates
Open templates permit anything to be done in the underlying standard that is not explicitly prohibited. This allows templates to be built up over time that extend and go beyond the original use cases for which they were originally designed.
Closed templates only permit what has been defined in the template, and do not permit anything beyond that. There are good reasons to use closed templates, sometimes having to do with local policy. For example, in communicating information from a healthcare provider to an insurance company, some information may need to be omitted to ensure patient privacy laws are followed.
Most templates developed for CDA are of the open sort.
Template versioning
Template versioning is needed to enable template designs to evolve over time.
Template versioning enables template designers to control and shape the conformance statements that make up a template’s design over time tailoring the design to fit the template’s intended purpose.
Each template version is associated with a particular template. The template – as a whole – has a mandatory globally unique, non-semantic, identifier. The identifier serves as the identifier of the original intent of the template and as the identifier of the set of versions that represent the template over time.
Template versions have a mandatory timestamp (date and optional time), called the “effective date”. The date can be seen as the point in time when the template version “came into being”, i.e. was recognized as existent by the governance group. Use of the template prior to this date would be considered an invalid use of the template.
For further information on Templates, Template Versions and related topics refer to the HL7 Templates Standard[1].
Identifiers for Templates and Value Sets
This specification specifies CDA Entry Level Templates only. They can be re-used in any appropriate context, such as an Entry of a medication section.
Two "root" Entry Templates are provided as entry points for the two described use cases:
- UV Medication Order (2.16.840.1.113883.10.21.4.1)
- UV Medication Statement (2.16.840.1.113883.10.21.4.7)
These templates use other Entry Level Templates that are all listed in a subsequent section of this document.
This specification uses the following OIDs for the artefacts that are registered at the HL7 OID registry.
- The root OID for templates is 2.16.840.1.113883.10.21
- Entry Level templates are summarized under 2.16.840.1.113883.10.21.4, e.g. 2.16.840.1.113883.10.21.4.5 UV Substitution Permission
- “other” assistance templates are summarized under 2.16.840.1.113883.10.21.9, e.g. 2.16.840.1.113883.10.22.9.1 UV Use Period
- The root OID for Value Sets is 2.16.840.1.113883.11
The sub branches for templates follow the recommendations of HL7 International and ISO 13582[2]
How to read this document
All artifacts (templates, value sets etc.) listed with the status Draft or Pending are subject to ballot comments.
Artifacts with other status information, especially Final or Active are not (directly) part of the ballot and some artifacts actually even come from external sources. Reference artifacts are indicated by the symbol
ref
. These reference artifacts are also not subject to the ballot, as they might be balloted elsewhere already.
The PDF version contains a ruler on the left side of the pages. A ruler has the page number on top of it and allows locating a line at the page by simply specifying the number at the scale tick. This is more precise and allows also commenting on graphics and pictures.
For example if you have a comment on page 29 because of a typo (see figure), you simply specify the error with its location p0029-04.
Of course you can also refer by classical chapter and section numbers. The use of the ruler has the ballot team's preference, though.
[Figure 1] To locate a typo on page 29 as a ballot comment, simply specify the location p0029-04.
Functional requirements and high-level use cases
The following use cases are relevant to the pharmacy domain for both community and institutional settings:
- Prescribing a medication (aka Prescription or Order or Request)
- Dispensing a medication
- Recording the administration of a medication
- Recording the use of a medication (in the past, current or future)
The following definitions are relevant to this Implementation Guide:
- “Prescribing” is an activity that can be performed by a variety of healthcare professionals and involves a variety of orderable items (see glossary entry). For the purposes of the following Implementation Guide, prescribing is defined as the act of prescribing a medication in either an ambulatory or an institutional setting. This could include initiating a new medication order or making all kinds of modifications to existing orders.
- “Dispensing” is an activity undertaken to fulfill the logistical requirements of a prescription. It supplies the materials needed to perform the prescribed actions by those who will perform them. Examples of dispensing include eyeglasses, contact lenses and medications. For the purposes of the following ballot material, dispensing is defined as supplying a medication in fulfillment of a prescription or medication order. While dispensing in these circumstances would usually be performed by a pharmacist, other health care providers such as nurses or physicians might also dispense medications.
- “Administration” is an activity undertaken to give medication to the patient. In the community, this process is usually not recorded, since the majority occurs in the patient's home; only administrations undertaken by a healthcare professional, such as vaccination, tend to be formally documented. Administration of medication in the institutional setting is usually recorded on a dose-by-dose basis, and may be messaged on that basis, or a summary of all the administrations occurring during an inpatient stay may be described.
Templates
Root Entry Level Templates
As mentioned before, this specification defines two "root" Entry Level Templates, one for each of the covered use cases.
UV Medication Order
The following graph gives an overview of the high-level template components of this template, followed by the actual definition.
-
Entry UV Medication Order (2.16.840.1.113883.10.21.4.1)
-
Entry UV Use Period (2.16.840.1.113883.10.21.9.1)
-
Entry CDA Subject (Body) (2.16.840.1.113883.10.12.320)
-
Entry UV Medication Information (simple) (2.16.840.1.113883.10.21.4.10)
-
* CDA Organization (2.16.840.1.113883.10.12.151)
-
Entry UV Medication Information (detail) (2.16.840.1.113883.10.21.4.11)
-
Entry UV Content (2.16.840.1.113883.10.21.4.17)
-
Entry UV Generalized Medicine Class (2.16.840.1.113883.10.21.4.19)
-
Entry UV Content (2.16.840.1.113883.10.21.4.17)
-
Entry UV Generalized Medicine Class (2.16.840.1.113883.10.21.4.19)
-
Entry UV Content (2.16.840.1.113883.10.21.4.17)
-
Entry UV Generalized Medicine Class (2.16.840.1.113883.10.21.4.19)
-
Entry UV Content (2.16.840.1.113883.10.21.4.17)
-
Entry UV Generalized Medicine Class (2.16.840.1.113883.10.21.4.19)
-
Entry UV Ingredient (2.16.840.1.113883.10.21.4.18)
-
Entry UV Ingredient (2.16.840.1.113883.10.21.4.18)
-
Entry UV Ingredient (2.16.840.1.113883.10.21.4.18)
-
Entry UV Ingredient (2.16.840.1.113883.10.21.4.18)
-
* CDA Organization (2.16.840.1.113883.10.12.151)
-
Entry CDA Author (Body) (2.16.840.1.113883.10.12.318)
-
* CDA Person (2.16.840.1.113883.10.12.152)
-
Entry CDA Device (2.16.840.1.113883.10.12.315)
-
* CDA Organization (2.16.840.1.113883.10.12.151)
-
Entry CDA Participant (Body) (2.16.840.1.113883.10.12.321)
-
Entry CDA Device (2.16.840.1.113883.10.12.315)
-
Entry CDA PlayingEntity (2.16.840.1.113883.10.12.313)
-
Entry CDA Participant (Body) (2.16.840.1.113883.10.12.321)
-
Entry CDA Device (2.16.840.1.113883.10.12.315)
-
Entry CDA PlayingEntity (2.16.840.1.113883.10.12.313)
-
Entry UV Subordinate Substance Administration (2.16.840.1.113883.10.21.4.6)
-
Entry UV Dispense Request (2.16.840.1.113883.10.21.4.2)
-
Entry CDA Subject (Body) (2.16.840.1.113883.10.12.320)
-
Entry CDA ManufacturedProduct (2.16.840.1.113883.10.12.312)
-
Entry CDA LabeledDrug (2.16.840.1.113883.10.12.310)
-
Entry CDA Material (2.16.840.1.113883.10.12.311)
-
* CDA Organization (2.16.840.1.113883.10.12.151)
-
Entry CDA Performer (Body) (2.16.840.1.113883.10.12.323)
-
* CDA AssignedEntity (2.16.840.1.113883.10.12.153)
-
* CDA Person (2.16.840.1.113883.10.12.152)
-
* CDA Organization (2.16.840.1.113883.10.12.151)
-
Entry CDA Participant (Body) (2.16.840.1.113883.10.12.321)
-
Entry CDA Device (2.16.840.1.113883.10.12.315)
-
Entry CDA PlayingEntity (2.16.840.1.113883.10.12.313)
-
Entry CDA Participant (Body) (2.16.840.1.113883.10.12.321)
-
Entry CDA Device (2.16.840.1.113883.10.12.315)
-
Entry CDA PlayingEntity (2.16.840.1.113883.10.12.313)
-
Entry CDA Participant (Body) (2.16.840.1.113883.10.12.321)
-
Entry CDA Device (2.16.840.1.113883.10.12.315)
-
Entry CDA PlayingEntity (2.16.840.1.113883.10.12.313)
-
Entry CDA Participant (Body) (2.16.840.1.113883.10.12.321)
-
Entry CDA Device (2.16.840.1.113883.10.12.315)
-
Entry CDA PlayingEntity (2.16.840.1.113883.10.12.313)
-
Entry UV ClinicalStatement Observation (2.16.840.1.113883.10.21.4.3)
-
Entry CDA Subject (Body) (2.16.840.1.113883.10.12.320)
-
Entry CDA Specimen (2.16.840.1.113883.10.12.322)
-
Entry CDA Performer (Body) (2.16.840.1.113883.10.12.323)
-
* CDA AssignedEntity (2.16.840.1.113883.10.12.153)
-
* CDA Person (2.16.840.1.113883.10.12.152)
-
* CDA Organization (2.16.840.1.113883.10.12.151)
-
Entry CDA Author (Body) (2.16.840.1.113883.10.12.318)
-
* CDA Person (2.16.840.1.113883.10.12.152)
-
Entry CDA Device (2.16.840.1.113883.10.12.315)
-
* CDA Organization (2.16.840.1.113883.10.12.151)
-
Entry CDA Informant (Body) (2.16.840.1.113883.10.12.319)
-
* CDA AssignedEntity (2.16.840.1.113883.10.12.153)
-
* CDA Person (2.16.840.1.113883.10.12.152)
-
* CDA Organization (2.16.840.1.113883.10.12.151)
-
Entry CDA RelatedEntity (2.16.840.1.113883.10.12.316)
-
* CDA Person (2.16.840.1.113883.10.12.152)
-
Entry CDA Participant (Body) (2.16.840.1.113883.10.12.321)
-
Entry CDA Device (2.16.840.1.113883.10.12.315)
-
Entry CDA PlayingEntity (2.16.840.1.113883.10.12.313)
-
Entry CDA Reference (2.16.840.1.113883.10.12.324)
-
Entry CDA ExternalAct (2.16.840.1.113883.10.12.325)
-
Entry CDA ExternalObservation (2.16.840.1.113883.10.12.326)
-
Entry CDA ExternalProcedure (2.16.840.1.113883.10.12.327)
-
Entry CDA ExternalDocument (2.16.840.1.113883.10.12.328)
-
Entry CDA Precondition (2.16.840.1.113883.10.12.329)
-
Entry IPS Internal Reference (2.16.840.1.113883.10.22.4.31)
-
Entry UV ClinicalStatement Observation (2.16.840.1.113883.10.21.4.3)
-
Entry CDA Subject (Body) (2.16.840.1.113883.10.12.320)
-
Entry CDA Specimen (2.16.840.1.113883.10.12.322)
-
Entry CDA Performer (Body) (2.16.840.1.113883.10.12.323)
-
* CDA AssignedEntity (2.16.840.1.113883.10.12.153)
-
* CDA Person (2.16.840.1.113883.10.12.152)
-
* CDA Organization (2.16.840.1.113883.10.12.151)
-
Entry CDA Author (Body) (2.16.840.1.113883.10.12.318)
-
* CDA Person (2.16.840.1.113883.10.12.152)
-
Entry CDA Device (2.16.840.1.113883.10.12.315)
-
* CDA Organization (2.16.840.1.113883.10.12.151)
-
Entry CDA Informant (Body) (2.16.840.1.113883.10.12.319)
-
* CDA AssignedEntity (2.16.840.1.113883.10.12.153)
-
* CDA Person (2.16.840.1.113883.10.12.152)
-
* CDA Organization (2.16.840.1.113883.10.12.151)
-
Entry CDA RelatedEntity (2.16.840.1.113883.10.12.316)
-
* CDA Person (2.16.840.1.113883.10.12.152)
-
Entry CDA Participant (Body) (2.16.840.1.113883.10.12.321)
-
Entry CDA Device (2.16.840.1.113883.10.12.315)
-
Entry CDA PlayingEntity (2.16.840.1.113883.10.12.313)
-
Entry CDA Reference (2.16.840.1.113883.10.12.324)
-
Entry CDA ExternalAct (2.16.840.1.113883.10.12.325)
-
Entry CDA ExternalObservation (2.16.840.1.113883.10.12.326)
-
Entry CDA ExternalProcedure (2.16.840.1.113883.10.12.327)
-
Entry CDA ExternalDocument (2.16.840.1.113883.10.12.328)
-
Entry CDA Precondition (2.16.840.1.113883.10.12.329)
-
Entry UV Substitution Permission (2.16.840.1.113883.10.21.4.5)
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Entry UV ClinicalStatement Encounter (2.16.840.1.113883.10.21.4.4)
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Entry UV Comment Activity (2.16.840.1.113883.10.21.4.12)
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Entry CDA Author (Body) (2.16.840.1.113883.10.12.318)
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* CDA Person (2.16.840.1.113883.10.12.152)
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Entry CDA Device (2.16.840.1.113883.10.12.315)
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* CDA Organization (2.16.840.1.113883.10.12.151)
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Entry CDA Precondition (2.16.840.1.113883.10.12.329)
|
Id | 2.16.840.1.113883.10.21.4.1 | Effective Date | 2023‑01‑31 11:29:28 |
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Status | Draft | Version Label | 2023 |
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Name | UVSubstanceadministrationrequest | Display Name | UV Medication Order |
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Description | Universal Medication Order (Substance Administration Request) |
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Context | Parent nodes of template element with id 2.16.840.1.113883.10.21.4.1 |
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Label | MedicationOrder
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Classification | CDA Entry Level Template |
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Open/Closed | Open (other than defined elements are allowed) |
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Uses | Uses 14 templates | Uses | as | Name | Version |
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2.16.840.1.113883.10.21.9.1 | Include | UV Use Period (2023) | DYNAMIC | 2.16.840.1.113883.10.12.320 | Containment | CDA Subject (Body) | DYNAMIC | 2.16.840.1.113883.10.21.4.10 | Containment | UV Medication Information (simple) (R1-STU2-ballot) | DYNAMIC | 2.16.840.1.113883.10.21.4.11 | Containment | UV Medication Information (detail) (2023) | DYNAMIC | 2.16.840.1.113883.10.12.318 | Containment | CDA Author (Body) | DYNAMIC | 2.16.840.1.113883.10.12.321 | Containment | CDA Participant (Body) | DYNAMIC | 2.16.840.1.113883.10.21.4.6 | Containment | UV Subordinate Substance Administration (2023) | DYNAMIC | 2.16.840.1.113883.10.21.4.2 | Containment | UV Dispense Request (R1-STU2-ballot) | DYNAMIC | 2.16.840.1.113883.10.21.4.3 | Containment | UV ClinicalStatement Observation (R1-STU2-ballot) | DYNAMIC | 2.16.840.1.113883.10.22.4.31 | Containment | IPS Internal Reference (STU1) | DYNAMIC | 2.16.840.1.113883.10.21.4.5 | Containment | UV Substitution Permission (R1-STU2-ballot) | DYNAMIC | 2.16.840.1.113883.10.21.4.4 | Containment | UV ClinicalStatement Encounter (R1-STU2-ballot) | DYNAMIC | 2.16.840.1.113883.10.21.4.12 | Containment | UV Comment Activity (R1-STU2-ballot) | DYNAMIC | 2.16.840.1.113883.10.12.329 | Containment | CDA Precondition | DYNAMIC |
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Relationship | Version: template 2.16.840.1.113883.10.21.4.1 UV Medication Order (2015‑10‑07) Specialization: template 2.16.840.1.113883.10.12.308 CDA SubstanceAdministration (2005‑09‑07) ref ad1bbr- |
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Example | Example | <substanceAdministration classCode="SBADM" moodCode="RQO"> <templateId root="2.16.840.1.113883.10.21.4.1"/> <id root="1.2.3.99.99.99" extension="58768437489739"/> <code code="..." codeSystem="..."/> <text>...</text> <statusCode code="active"/> <effectiveTime value="..."/> <repeatNumber value="..."/> <routeCode code="IPINHL" codeSystem="2.16.840.1.113883.5.112" displayName="Inhalation, respiratory Inhalation, intrapulmonary Inhalation, oral"/> <approachSiteCode code="..." codeSystem="2.16.840.1.113883.5.1052"/> <administrationUnitCode code="PUFF" codeSystem="2.16.840.1.113883.5.85" displayName="Puff"/> <consumable typeCode="CSM"> <!-- Consumable --> </consumable> <participant typeCode="DEV"> <!-- Device --> </participant> <participant typeCode="LOC"> <!-- Location --> </participant> <entryRelationship typeCode="COMP"> <!-- Subordinate Substance Administrations --> </entryRelationship> <entryRelationship typeCode="COMP"> <!-- Annotations --> </entryRelationship> <precondition> <!-- Precondition --> </precondition></substanceAdministration> |
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Item | DT | Card | Conf | Description | Label |
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hl7:substanceAdministration
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| | | | | Medi...rder | | @classCode
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| cs | 1 … 1 | F | SBADM | | @moodCode
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| cs | 1 … 1 | F | RQO | | hl7:templateId
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| II | 1 … 1 | M | | Medi...rder | | | @root
|
| uid | 1 … 1 | F | 2.16.840.1.113883.10.21.4.1 | | hl7:id
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| II | 1 … * | R | | Medi...rder | | hl7:code
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| CD (extensible) | 0 … 1 | R | | Medi...rder | | CONF | The value of @code should be drawn from value set 2.16.840.1.113883.1.11.19708 ActSubstanceAdministrationCode (DYNAMIC) |
| | hl7:text
|
| ED | 0 … 1 | | | Medi...rder | | hl7:statusCode
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| CS (required) | 1 … 1 | M | | Medi...rder | | CONF | The value of @code shall be drawn from value set 2.16.840.1.113883.11.21.2 ActStatusActiveCompletedAbortedSuspended (DYNAMIC) |
| Included | | | from 2.16.840.1.113883.10.21.9.1 UV Use Period (DYNAMIC) | Choice | 1 … 1 | | The effectiveTime element encodes the use period of the medication, it is always expressed as an interval of time. It may be expressed using the low and high OR with the width element. The first is used to indicate a specified interval (e.g. from march 15th, 2017); the latter for indicating a 'floating' period (e.g. 2 weeks). Elements to choose from:- hl7:effectiveTime[hl7:low | hl7:high][not(hl7:width)]
- hl7:effectiveTime[hl7:width][not(hl7:low|hl7:high)]
- hl7:effectiveTime[hl7:low | hl7:width][not(hl7:high)]
| | | hl7:effectiveTime
|
| IVL_TS | 0 … 1 | C | Case 1: specified interval
The low and high values of the first effectiveTime element represent the start and stop times for the medication. The low value represents the start time, and the high value represents the stop time. If either the low or the high value is unknown, this shall be recorded by setting the nullFlavor attribute to UNK.
In case of unbounded period (continuous therapy) the high element will be valued with the nullFlavor attribute to NA.
The high value records the end of the medication regime according to the information provided in the prescription or order. For example, if the prescription is for enough medication to last 30 days, then the high value should contain a date that is 30 days later then the low value. The rationale is that a provider, seeing a prescription that has not been refilled would normally assume that the medication is no longer being taken, even if the intent of the treatment plan is to continue the medication indefinitely. | Medi...rder | where [hl7:low or [not(hl7:width)] | | | cs | 0 … 1 | | | | Example | Known Interval <effectiveTime type="IVL_TS"> <low value="20130321"/> <high value="20140321"/></effectiveTime> | | Example | Information not available about the period <effectiveTime type="IVL_TS" nullFlavor="NI"/> | | Example | Unknown end date <effectiveTime type="IVL_TS"> <low value="20130321"/> <high nullFlavor="UNK"/></effectiveTime> | | Example | continous therapy <effectiveTime type="IVL_TS"> <low value="20130321"/> <high nullFlavor="NA"/></effectiveTime> | | IVXB_TS | 1 … 1 | R | | Medi...rder | | IVXB_TS | 0 … 1 | R | | Medi...rder | | | hl7:effectiveTime
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| IVL_TS | 0 … 1 | C | Case 2: 'floating' period:
The width element is used to specify a period of (actual or intended) administration that is not anchored to any specific date (e.g. a two weeks therapy) | Medi...rder | where [hl7:width] [not(hl7:lowor hl7:high)] | | | Example | 2 week period <effectiveTime type="IVL_TS"> <width value="2" unit="w"/></effectiveTime> | | | | NP | | Medi...rder | | | | NP | | Medi...rder | | | | NP | | Medi...rder | | PQ | 1 … 1 | R | | Medi...rder | | cs | 1 … 1 | R | | | CONF | The value of @unit shall be drawn from value set 2.16.840.1.113883.11.21.1 Medication Time Units (UCUM) (DYNAMIC) |
| | | hl7:effectiveTime
|
| IVL_TS | 0 … 1 | C | Case 3: anchored period:
The width element is used to specify a period of (actual or intended) administration anchored to a specific date (e.g. a two weeks therapy starting today) | Medi...rder | where [hl7:low or [not(hl7:high)] | | | Example | 2 week period starting on 2013-03-21 <effectiveTime type="IVL_TS"> <low value="20130321"/> <width value="2" unit="w"/></effectiveTime> | | IVXB_TS | 0 … 1 | C | | Medi...rder | | PQ | 1 … 1 | R | | Medi...rder | | cs | 1 … 1 | R | | | CONF | The value of @unit shall be drawn from value set 2.16.840.1.113883.11.21.1 Medication Time Units (UCUM) (DYNAMIC) |
| | hl7:repeatNumber
|
| IVL_INT | 0 … 1 | | | Medi...rder | | hl7:routeCode
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| CE (example) | 0 … 1 | | | Medi...rder | | CONF | Examples of the value of @code are in the value set 2.16.840.1.113883.1.11.14581 RouteOfAdministration (DYNAMIC) |
| | hl7:approachSiteCode
|
| CD (example) | 0 … * | | | Medi...rder | | CONF | Examples of the value of @code are in the value set 2.16.840.1.113883.1.11.19724 HumanSubstanceAdministrationSite (DYNAMIC) |
| | hl7:doseQuantity
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| IVL_PQ | | NP | | Medi...rder | | hl7:rateQuantity
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| IVL_PQ | | NP | | Medi...rder | | hl7:maxDoseQuantity
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| RTO_PQ_PQ | 0 … 1 | | | Medi...rder | | hl7:administrationUnitCode
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| CE | | NP | | Medi...rder | | hl7:subject
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| | 0 … 1 | C | The patient, subject to requested dispenses or subject to substances being administered to. Contains 2.16.840.1.113883.10.12.320 CDA Subject (Body) (DYNAMIC) | Medi...rder | | Constraint | Condition: This can be omitted if the patient context that is provided in the CDA header is identical to the subject | Choice | 1 … 1 | | Elements to choose from:- hl7:consumable containing template 2.16.840.1.113883.10.21.4.10 UV Medication Information (simple) (DYNAMIC)
- hl7:consumable containing template 2.16.840.1.113883.10.21.4.11 UV Medication Information (detail) (DYNAMIC)
| | | hl7:consumable
|
| | 0 … 1 | R | Consumable: The medication that is administered (simple) Contains 2.16.840.1.113883.10.21.4.10 UV Medication Information (simple) (DYNAMIC) | Medi...rder | | cs | 1 … 1 | F | CSM | | | hl7:consumable
|
| | 0 … 1 | R | Consumable: The medication that is administered (detail) Contains 2.16.840.1.113883.10.21.4.11 UV Medication Information (detail) (DYNAMIC) | Medi...rder | | cs | 1 … 1 | F | CSM | | hl7:author
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| | 0 … * | | Prescriber: A party that originates the order and therefore has responsibility for the information given in the order. Contains 2.16.840.1.113883.10.12.318 CDA Author (Body) (DYNAMIC) | Medi...rder | | hl7:participant
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| | 0 … 1 | | Record Target: indicates the person who's medical record holds the documentation of this medication statement. This element is only populated when the document is placed in a medical record of someone other than the patient (subject). Contains 2.16.840.1.113883.10.12.321 CDA Participant (Body) (DYNAMIC) | Medi...rder | where [@typeCode='RCT'] | | | | @typeCode
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| cs | 1 … 1 | F | RCT | | hl7:participant
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| | 0 … 1 | | Verifier: The person or organization that has primary responsibility for the order. The responsible party is not necessarily present in an action, but is accountable for the action through the power to delegate. Contains 2.16.840.1.113883.10.12.321 CDA Participant (Body) (DYNAMIC) | Medi...rder | where [@typeCode='VRF'] | | | | @typeCode
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| cs | 1 … 1 | F | VRF | | hl7:entryRelationship
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| | 0 … * | C | Subordinate Substance Administration Request as a component of the overall order. At least one subordinated Substance Administration should be present to convey information about dosages (dose, frequency of intakes,..) unless dosage is unknown. Subordinated Substance Administration elements can be also used either to handle split dosing, or to support combination medications. Contains 2.16.840.1.113883.10.21.4.6 UV Subordinate Substance Administration (DYNAMIC) | Medi...rder | where [hl7:substanceAdministration] | | | | @typeCode
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| cs | 1 … 1 | F | COMP | | Constraint | At least one subordinate element SHALL be present. | | Example | <entryRelationship typeCode="COMP"> <!-- component: Subordinate Substance Administration Request. --> <substanceAdministration classCode="SBADM" moodCode="RQO"> <templateId root="2.16.840.1.113883.10.21.4.6"/> <!-- .. --> </substanceAdministration></entryRelationship> | | | hl7:sequenceNumber
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| INT | 0 … 1 | | Sequence number of the Subordinate Substance Administration. | Medi...rder | | hl7:entryRelationship
|
| | 0 … 1 | R | Dispense Request as a component of the overall order. This element is used in the medication order when the dispense request information contains additional information to support a fully specified medication prescription. For example, to include the validity period of the dispense or the organization to dispense the medication. Contains 2.16.840.1.113883.10.21.4.2 UV Dispense Request (DYNAMIC) | Medi...rder | where [hl7:supply] | | | | @typeCode
|
| cs | 1 … 1 | F | COMP | | Example | <entryRelationship typeCode="COMP"> <!-- component: The Dispense Request is a component of the overall order. --> <supply classCode="SPLY" moodCode="RQO"> <templateId root="2.16.840.1.113883.10.21.4.2"/> <!-- .. --> </supply></entryRelationship> | Choice | 0 … * | | Elements to choose from:- hl7:entryRelationship containing template 2.16.840.1.113883.10.21.4.3 UV ClinicalStatement Observation (DYNAMIC)
- hl7:entryRelationship containing template 2.16.840.1.113883.10.22.4.31 IPS Internal Reference (DYNAMIC)
| | | hl7:entryRelationship
|
| | 0 … * | R | Reason: Specifies the reason (indication) for authoring the order. Contains 2.16.840.1.113883.10.21.4.3 UV ClinicalStatement Observation (DYNAMIC) | Medi...rder | | cs | 1 … 1 | F | RSON | | Example | <hl7:entryRelationship typeCode="RSON"> <priorityNumber value="1"/> <!-- template 2.16.840.1.113883.10.21.4.3 'UV ClinicalStatement Observation' (2016-05-01T00:00:00) --> </hl7:entryRelationship> | | INT.NONNEG | 0 … 1 | R | Indicates the priority of this reason for the order in relation to its sibling reasons. | Medi...rder | | | hl7:entryRelationship
|
| | 0 … * | R | Reason: Specifies the reason (indication) for authoring the order. Contains 2.16.840.1.113883.10.22.4.31 IPS Internal Reference (DYNAMIC) | Medi...rder | | cs | 1 … 1 | F | RSON | | Example | <entryRelationship typeCode="RSON"> <priorityNumber value="1"/> <act> <!-- Clinical Statement Minimal --> </act></entryRelationship> | | INT.NONNEG | 0 … 1 | R | Indicates the priority of this reason for the order in relation to its sibling reasons. | Medi...rder | | hl7:entryRelationship
|
| | 0 … * | R | Pertinent Information: Specifies any pertinent information (observation) relevant to the order. Contains 2.16.840.1.113883.10.21.4.3 UV ClinicalStatement Observation (DYNAMIC) | Medi...rder | | | @typeCode
|
| cs | 1 … 1 | F | PERT | | Example | <entryRelationship typeCode="PERT"> <observation> <!-- Clinical Statement Observation --> </observation></entryRelationship> | | hl7:entryRelationship
|
| | 0 … 1 | R | Permission: The order can be the subject of the permissions related to substitution. Contains 2.16.840.1.113883.10.21.4.5 UV Substitution Permission (DYNAMIC) | Medi...rder | where [hl7:act] | | | | @typeCode
|
| cs | 1 … 1 | F | COMP | | hl7:entryRelationship
|
| | 0 … 1 | R | Encounter: Used to link an order to a specific encounter. Contains 2.16.840.1.113883.10.21.4.4 UV ClinicalStatement Encounter (DYNAMIC) | Medi...rder | where [hl7:encounter] | | | | @typeCode
|
| cs | 1 … 1 | F | COMP | | Example | <encounter classCode="ENC" moodCode="EVN"> <id/> <code code="..."/></encounter> | | hl7:entryRelationship
|
| | 0 … * | | Annotations: The Medication Order can be the subject of annotations. Contains 2.16.840.1.113883.10.21.4.12 UV Comment Activity (DYNAMIC) | Medi...rder | | | @typeCode
|
| cs | 1 … 1 | F | COMP | | hl7:precondition
|
| | 0 … * | | Precondition: A requirement to be true before the SubstanceAdministration is performed. Contains 2.16.840.1.113883.10.12.329 CDA Precondition (DYNAMIC) | Medi...rder |
|
UV Medication Statement
The following graph gives an overview of the high-level template components of this template, followed by the actual definition.
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Entry UV Medication Statement (2.16.840.1.113883.10.21.4.7)
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Entry UV Use Period (2.16.840.1.113883.10.21.9.1)
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Entry CDA Subject (Body) (2.16.840.1.113883.10.12.320)
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Entry UV Medication Information (simple) (2.16.840.1.113883.10.21.4.10)
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* CDA Organization (2.16.840.1.113883.10.12.151)
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Entry UV Medication Information (detail) (2.16.840.1.113883.10.21.4.11)
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Entry UV Content (2.16.840.1.113883.10.21.4.17)
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Entry UV Generalized Medicine Class (2.16.840.1.113883.10.21.4.19)
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Entry UV Content (2.16.840.1.113883.10.21.4.17)
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Entry UV Generalized Medicine Class (2.16.840.1.113883.10.21.4.19)
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Entry UV Content (2.16.840.1.113883.10.21.4.17)
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Entry UV Generalized Medicine Class (2.16.840.1.113883.10.21.4.19)
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Entry UV Content (2.16.840.1.113883.10.21.4.17)
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Entry UV Generalized Medicine Class (2.16.840.1.113883.10.21.4.19)
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Entry UV Ingredient (2.16.840.1.113883.10.21.4.18)
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Entry UV Ingredient (2.16.840.1.113883.10.21.4.18)
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Entry UV Ingredient (2.16.840.1.113883.10.21.4.18)
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Entry UV Ingredient (2.16.840.1.113883.10.21.4.18)
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* CDA Organization (2.16.840.1.113883.10.12.151)
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Entry CDA Author (Body) (2.16.840.1.113883.10.12.318)
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* CDA Person (2.16.840.1.113883.10.12.152)
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Entry CDA Device (2.16.840.1.113883.10.12.315)
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* CDA Organization (2.16.840.1.113883.10.12.151)
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* CDA AssignedEntity (2.16.840.1.113883.10.12.153)
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* CDA Person (2.16.840.1.113883.10.12.152)
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* CDA Organization (2.16.840.1.113883.10.12.151)
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Entry CDA RelatedEntity (2.16.840.1.113883.10.12.316)
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* CDA Person (2.16.840.1.113883.10.12.152)
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Entry CDA Participant (Body) (2.16.840.1.113883.10.12.321)
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Entry CDA Device (2.16.840.1.113883.10.12.315)
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Entry CDA PlayingEntity (2.16.840.1.113883.10.12.313)
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Entry CDA Participant (Body) (2.16.840.1.113883.10.12.321)
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Entry CDA Device (2.16.840.1.113883.10.12.315)
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Entry CDA PlayingEntity (2.16.840.1.113883.10.12.313)
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Entry UV Subordinate Substance Administration (2.16.840.1.113883.10.21.4.6)
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Entry UV Medication Order Reference (2.16.840.1.113883.10.21.4.8)
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Entry CDA Author (Body) (2.16.840.1.113883.10.12.318)
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* CDA Person (2.16.840.1.113883.10.12.152)
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Entry CDA Device (2.16.840.1.113883.10.12.315)
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* CDA Organization (2.16.840.1.113883.10.12.151)
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Entry UV Dispense Event Reference (2.16.840.1.113883.10.21.4.9)
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Entry UV ClinicalStatement Observation (2.16.840.1.113883.10.21.4.3)
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Entry CDA Subject (Body) (2.16.840.1.113883.10.12.320)
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Entry CDA Specimen (2.16.840.1.113883.10.12.322)
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Entry CDA Performer (Body) (2.16.840.1.113883.10.12.323)
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* CDA AssignedEntity (2.16.840.1.113883.10.12.153)
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* CDA Person (2.16.840.1.113883.10.12.152)
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* CDA Organization (2.16.840.1.113883.10.12.151)
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Entry CDA Author (Body) (2.16.840.1.113883.10.12.318)
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* CDA Person (2.16.840.1.113883.10.12.152)
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Entry CDA Device (2.16.840.1.113883.10.12.315)
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* CDA Organization (2.16.840.1.113883.10.12.151)
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Entry CDA Informant (Body) (2.16.840.1.113883.10.12.319)
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* CDA AssignedEntity (2.16.840.1.113883.10.12.153)
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* CDA Person (2.16.840.1.113883.10.12.152)
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* CDA Organization (2.16.840.1.113883.10.12.151)
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Entry CDA RelatedEntity (2.16.840.1.113883.10.12.316)
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* CDA Person (2.16.840.1.113883.10.12.152)
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Entry CDA Participant (Body) (2.16.840.1.113883.10.12.321)
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Entry CDA Device (2.16.840.1.113883.10.12.315)
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Entry CDA PlayingEntity (2.16.840.1.113883.10.12.313)
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Entry CDA Reference (2.16.840.1.113883.10.12.324)
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Entry CDA ExternalAct (2.16.840.1.113883.10.12.325)
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Entry CDA ExternalObservation (2.16.840.1.113883.10.12.326)
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Entry CDA ExternalProcedure (2.16.840.1.113883.10.12.327)
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Entry CDA ExternalDocument (2.16.840.1.113883.10.12.328)
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Entry CDA Precondition (2.16.840.1.113883.10.12.329)
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Entry IPS Internal Reference (2.16.840.1.113883.10.22.4.31)
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Id | 2.16.840.1.113883.10.21.4.7 | Effective Date | 2023‑01‑30 08:32:34Other versions this id: - UVMedicationstatement as of 2021‑08‑04 14:09:15
- UVMedicationstatement as of 2017‑05‑01
|
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Status | Draft | Version Label | 2023 |
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Name | UVMedicationstatement | Display Name | UV Medication Statement |
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Description | Universal Medication Statement: Recording a "medication statement" is an activity that can be performed by a variety of healthcare professionals, or the patient, or non-healthcare professionals. Examples of recording medication statements include taking a patient's medication history, recording reported use of medications where the source of the patient
information is from a third party and not the patient e.g. a family member when the patient is unable to communicate their medication history. |
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Context | Parent nodes of template element with id 2.16.840.1.113883.10.21.4.7 |
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Label | MedicationStatement
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Classification | CDA Entry Level Template |
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Open/Closed | Open (other than defined elements are allowed) |
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Uses | Uses 13 templates | Uses | as | Name | Version |
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2.16.840.1.113883.10.21.9.1 | Include | UV Use Period (2023) | DYNAMIC | 2.16.840.1.113883.10.12.320 | Containment | CDA Subject (Body) | DYNAMIC | 2.16.840.1.113883.10.21.4.10 | Containment | UV Medication Information (simple) (R1-STU2-ballot) | DYNAMIC | 2.16.840.1.113883.10.21.4.11 | Containment | UV Medication Information (detail) (2023) | DYNAMIC | 2.16.840.1.113883.10.12.318 | Containment | CDA Author (Body) | DYNAMIC | 2.16.840.1.113883.10.12.153 | Containment | CDA AssignedEntity | DYNAMIC | 2.16.840.1.113883.10.12.316 | Containment | CDA RelatedEntity | DYNAMIC | 2.16.840.1.113883.10.12.321 | Containment | CDA Participant (Body) | DYNAMIC | 2.16.840.1.113883.10.21.4.6 | Containment | UV Subordinate Substance Administration (2023) | DYNAMIC | 2.16.840.1.113883.10.21.4.8 | Containment | UV Medication Order Reference (R1-STU2-ballot) | DYNAMIC | 2.16.840.1.113883.10.21.4.9 | Containment | UV Dispense Event Reference (R1-STU2-ballot) | DYNAMIC | 2.16.840.1.113883.10.21.4.3 | Containment | UV ClinicalStatement Observation (R1-STU2-ballot) | DYNAMIC | 2.16.840.1.113883.10.22.4.31 | Containment | IPS Internal Reference (STU1) | DYNAMIC |
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Relationship | Version: template 2.16.840.1.113883.10.21.4.7 UV Medication Statement (2021‑08‑04 14:09:15) Version: template 2.16.840.1.113883.10.21.4.7 UV Medication Statement (2017‑05‑01) Specialization: template 2.16.840.1.113883.10.12.308 CDA SubstanceAdministration (2005‑09‑07) ref ad1bbr- |
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Example | Example | <substanceAdministration classCode="SBADM" moodCode="EVN"> <templateId root="2.16.840.1.113883.10.21.4.7"/> <id root="1.2.3.99.99.99" extension="988437489739"/> <code code="..." codeSystem="..."/> <text>...</text> <statusCode code="active"/> <effectiveTime value="..."/> <repeatNumber value="..."/> <routeCode code="SOAK" codeSystem="2.16.840.1.113883.5.112" displayName="Immersion (soak)"/> <approachSiteCode code="..." codeSystem="2.16.840.1.113883.5.1052"/> <administrationUnitCode code="PUFF" displayName="Puff" codeSystem="2.16.840.1.113883.5.85"/> <consumable typeCode="CSM"> <!-- Consumable --> </consumable> <participant typeCode="DEV"> <!-- Device --> </participant> <participant typeCode="LOC"> <!-- Location --> </participant> <entryRelationship typeCode="COMP"> <!-- Subordinate Substance Administrations --> </entryRelationship> <entryRelationship typeCode="COMP"> <!-- Annotations --> </entryRelationship> <precondition> <!-- Precondition --> </precondition></substanceAdministration> |
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Example | Example | <substanceAdministration classCode="SBADM" moodCode="EVN"> <templateId root="2.16.840.1.113883.10.21.4.7"/> <id root="1.2.3.999" extension="--example only--"/> <code code="DRUG" displayName="Drug therapy" codeSystem="2.16.840.1.113883.5.4"/> <text/> <statusCode code="active"/> <!-- include template 'UV Use Period' (dynamic) .. O --> <repeatNumber/> <routeCode code="SOAK" displayName="Immersion (soak)" codeSystem="2.16.840.1.113883.5.112"/> <approachSiteCode code="--code--" codeSystem="2.16.840.1.113883.5.1052"/> <administrationUnitCode code="APPFUL" displayName="Applicatorful" codeSystem="2.16.840.1.113883.5.85"/> <subject> <!-- template 'CDA Subject (Body)' (dynamic) --> </subject> <consumable typeCode="CSM"> <!-- template 2.16.840.1.113883.10.12.312 'CDA ManufacturedProduct' (dynamic) --> </consumable> <!-- choice: 1..1 element hl7:author element hl7:participant[@typeCode='AUT'] --> <!-- choice: 0..1 element hl7:informant[exists(hl7:assignedEntity)] element hl7:participant[@typeCode='INF'] element hl7:informant[exists(hl7:relatedEntity)] --> <participant typeCode="RCT"> <!-- template 2.16.840.1.113883.10.12.321 'CDA Participant (Body)' (dynamic) --> </participant> <participant typeCode="VRF"> <!-- template 2.16.840.1.113883.10.12.321 'CDA Participant (Body)' (dynamic) --> </participant> <entryRelationship typeCode="COMP"> <sequenceNumber value="1"/> <!-- template 2.16.840.1.113883.10.21.4.6 'Subordinate Substance Administration' (dynamic) --> </entryRelationship> <entryRelationship typeCode="REFR"> <!-- template 2.16.840.1.113883.10.21.4.8 'UV Medication Order Reference' (dynamic) --> </entryRelationship> <entryRelationship typeCode="REFR"> <!-- template 2.16.840.1.113883.10.21.4.9 'UV Dispense Event Reference' (dynamic) --> </entryRelationship></substanceAdministration> |
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Example | Example | <substanceAdministration classCode="SBADM" moodCode="EVN"> <templateId root="2.16.840.1.113883.10.21.4.7"/> <id root="1.2.3.99.99.99" extension="988437489739"/> <code code="..." codeSystem="..."/> <text>...</text> <statusCode code="active"/> <effectiveTime value="..."/> <repeatNumber value="..."/> <routeCode code="SOAK" codeSystem="2.16.840.1.113883.5.112" displayName="Immersion (soak)"/> <approachSiteCode code="..." codeSystem="2.16.840.1.113883.5.1052"/> <administrationUnitCode code="PUFF" displayName="Puff" codeSystem="2.16.840.1.113883.5.85"/> <consumable typeCode="CSM"> <!-- Consumable --> </consumable> <participant typeCode="DEV"> <!-- Device --> </participant> <participant typeCode="LOC"> <!-- Location --> </participant> <entryRelationship typeCode="COMP"> <!-- Subordinate Substance Administrations --> </entryRelationship> <entryRelationship typeCode="COMP"> <!-- Annotations --> </entryRelationship> <precondition> <!-- Precondition --> </precondition></substanceAdministration> |
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Item | DT | Card | Conf | Description | Label |
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hl7:substanceAdministration
|
| | | | | Medi...ment | | @classCode
|
| cs | 1 … 1 | F | SBADM | | @moodCode
|
| cs | 1 … 1 | R | EVN will be used to record a medication statement where the patient is currently taking or has taken the medication in the past. INT will be used to record a medication statement where the patient plans to take the medication or be administered the medication in the future. | | CONF | @moodCode shall be "EVN" | or | @moodCode shall be "INT" |
| | hl7:templateId
|
| II | 1 … 1 | M | | Medi...ment | | | @root
|
| uid | 1 … 1 | F | 2.16.840.1.113883.10.21.4.7 | | hl7:id
|
| II | 0 … * | R | | Medi...ment | | hl7:code
|
| CD (preferred) | 0 … 1 | R | The code element is valorized with the ACT code DRUG; FD or IMMUNIZ unless it is used for asserting the known absence of medication treatments or no information about them. | Medi...ment | | CONF | The value of @code comes preferably from value set 2.16.840.1.113883.1.11.19708 ActSubstanceAdministrationCode (DYNAMIC) | or | The value of @code comes preferably from value set 2.16.840.1.113883.11.21.5 Unknown or absent medication (DYNAMIC) |
| | hl7:text
|
| ED | 0 … 1 | | | Medi...ment | | hl7:statusCode
|
| CS (required) | 1 … 1 | M | | Medi...ment | | CONF | The value of @code shall be drawn from value set 2.16.840.1.113883.1.11.15933 ActStatus (DYNAMIC) |
| Included | | | from 2.16.840.1.113883.10.21.9.1 UV Use Period (DYNAMIC) | Choice | 1 … 1 | | The effectiveTime element encodes the use period of the medication, it is always expressed as an interval of time. It may be expressed using the low and high OR with the width element. The first is used to indicate a specified interval (e.g. from march 15th, 2017); the latter for indicating a 'floating' period (e.g. 2 weeks). Elements to choose from:- hl7:effectiveTime[hl7:low | hl7:high][not(hl7:width)]
- hl7:effectiveTime[hl7:width][not(hl7:low|hl7:high)]
- hl7:effectiveTime[hl7:low | hl7:width][not(hl7:high)]
| | | hl7:effectiveTime
|
| IVL_TS | 0 … 1 | C | Case 1: specified interval
The low and high values of the first effectiveTime element represent the start and stop times for the medication. The low value represents the start time, and the high value represents the stop time. If either the low or the high value is unknown, this shall be recorded by setting the nullFlavor attribute to UNK.
In case of unbounded period (continuous therapy) the high element will be valued with the nullFlavor attribute to NA.
The high value records the end of the medication regime according to the information provided in the prescription or order. For example, if the prescription is for enough medication to last 30 days, then the high value should contain a date that is 30 days later then the low value. The rationale is that a provider, seeing a prescription that has not been refilled would normally assume that the medication is no longer being taken, even if the intent of the treatment plan is to continue the medication indefinitely. | Medi...ment | where [hl7:low or [not(hl7:width)] | | | cs | 0 … 1 | | | | Example | Known Interval <effectiveTime type="IVL_TS"> <low value="20130321"/> <high value="20140321"/></effectiveTime> | | Example | Information not available about the period <effectiveTime type="IVL_TS" nullFlavor="NI"/> | | Example | Unknown end date <effectiveTime type="IVL_TS"> <low value="20130321"/> <high nullFlavor="UNK"/></effectiveTime> | | Example | continous therapy <effectiveTime type="IVL_TS"> <low value="20130321"/> <high nullFlavor="NA"/></effectiveTime> | | IVXB_TS | 1 … 1 | R | | Medi...ment | | IVXB_TS | 0 … 1 | R | | Medi...ment | | | hl7:effectiveTime
|
| IVL_TS | 0 … 1 | C | Case 2: 'floating' period:
The width element is used to specify a period of (actual or intended) administration that is not anchored to any specific date (e.g. a two weeks therapy) | Medi...ment | where [hl7:width] [not(hl7:lowor hl7:high)] | | | Example | 2 week period <effectiveTime type="IVL_TS"> <width value="2" unit="w"/></effectiveTime> | | | | NP | | Medi...ment | | | | NP | | Medi...ment | | | | NP | | Medi...ment | | PQ | 1 … 1 | R | | Medi...ment | | cs | 1 … 1 | R | | | CONF | The value of @unit shall be drawn from value set 2.16.840.1.113883.11.21.1 Medication Time Units (UCUM) (DYNAMIC) |
| | | hl7:effectiveTime
|
| IVL_TS | 0 … 1 | C | Case 3: anchored period:
The width element is used to specify a period of (actual or intended) administration anchored to a specific date (e.g. a two weeks therapy starting today) | Medi...ment | where [hl7:low or [not(hl7:high)] | | | Example | 2 week period starting on 2013-03-21 <effectiveTime type="IVL_TS"> <low value="20130321"/> <width value="2" unit="w"/></effectiveTime> | | IVXB_TS | 0 … 1 | C | | Medi...ment | | PQ | 1 … 1 | R | | Medi...ment | | cs | 1 … 1 | R | | | CONF | The value of @unit shall be drawn from value set 2.16.840.1.113883.11.21.1 Medication Time Units (UCUM) (DYNAMIC) |
| | hl7:repeatNumber
|
| IVL_INT | 0 … 1 | | | Medi...ment | | hl7:routeCode
|
| CE (example) | 0 … 1 | | | Medi...ment | | CONF | Examples of the value of @code are in the value set 2.16.840.1.113883.1.11.14581 RouteOfAdministration (DYNAMIC) |
| | hl7:approachSiteCode
|
| CD (example) | 0 … * | | | Medi...ment | | CONF | Examples of the value of @code are in the value set 2.16.840.1.113883.1.11.19724 HumanSubstanceAdministrationSite (DYNAMIC) |
| | hl7:doseQuantity
|
| IVL_PQ | | NP | | Medi...ment | | hl7:rateQuantity
|
| IVL_PQ | | NP | | Medi...ment | | hl7:maxDoseQuantity
|
| RTO_PQ_PQ | 0 … 1 | | | Medi...ment | | hl7:administrationUnitCode
|
| CE | | NP | | Medi...ment | | hl7:subject
|
| | 0 … 1 | C | Patient: The patient that takes the medicine. Contains 2.16.840.1.113883.10.12.320 CDA Subject (Body) (DYNAMIC) | Medi...ment | | Constraint | Condition: This can be omitted if the patient context that is provided in the CDA header is identical to the subject | Choice | | | Elements to choose from:- hl7:consumable containing template 2.16.840.1.113883.10.21.4.10 UV Medication Information (simple) (DYNAMIC)
- hl7:consumable containing template 2.16.840.1.113883.10.21.4.11 UV Medication Information (detail) (DYNAMIC)
| | | hl7:consumable
|
| | 0 … 1 | R | Consumable: The medication that is administered (simple) Contains 2.16.840.1.113883.10.21.4.10 UV Medication Information (simple) (DYNAMIC) | Medi...ment | | cs | 1 … 1 | F | CSM | | | hl7:consumable
|
| | 0 … 1 | R | Consumable: The medication that is administered (detail) Contains 2.16.840.1.113883.10.21.4.11 UV Medication Information (detail) (DYNAMIC) | Medi...ment | | cs | 1 … 1 | F | CSM | Choice | | | Required author of the medication statement: healthcare professional or patient Elements to choose from:- hl7:author containing template 2.16.840.1.113883.10.12.318 CDA Author (Body) (DYNAMIC)
- hl7:participant[@typeCode='AUT']
| | | hl7:author
|
| | | | Use this if the author of the medication statement is a healthcare professional Contains 2.16.840.1.113883.10.12.318 CDA Author (Body) (DYNAMIC) | Medi...ment | | Example | Author of the medication statement is a healthcare professional <author> <time value="20170221"/> <assignedAuthor> <id root="1.2.3.99.99.99" extension="75487435893498"/> <assignedPerson> <name> <given qualifier="IN">Ampu</given> <prefix qualifier="VV">L.</prefix> <family>Lee</family> </name> </assignedPerson> </assignedAuthor></author> | | | hl7:participant
|
| | | | Use this if the author of the medication statement is the patient | Medi...ment | where [@typeCode='AUT'] | | | cs | 1 … 1 | F | AUT | | Example | Author of the medication statement is the patient <participant typeCode="AUT"> <time value="20170121091548"/> <participantRole classCode="PAT"/></participant> | | TS | 1 … 1 | R | | Medi...ment | | | 1 … 1 | M | | Medi...ment | | cs | 1 … 1 | F | PAT | Choice | | | Optional informants of the medication statement: healthcare professional or patient contact party (related party) Elements to choose from:- hl7:informant[exists(hl7:assignedEntity)]
- hl7:participant[@typeCode='INF']
- hl7:informant[exists(hl7:relatedEntity)]
| | | hl7:informant
|
| | | | Use this if the informant of the medication statement is a healthcare professional | Medi...ment | where [exists(hl7:assignedEntity)] | | | cs | 0 … 1 | F | INF | | cs | 0 … 1 | F | OP | | Example | Informant of the medication statement is a healthcare professional <informant> <assignedEntity> <id root="1.2.3.99.99.99" extension="75487435893498"/> <assignedPerson> <name> <given qualifier="IN">Ampu</given> <prefix qualifier="VV">L.</prefix> <family>Lee</family> </name> </assignedPerson> </assignedEntity></informant> | | | 1 … 1 | | Contains 2.16.840.1.113883.10.12.153 CDA AssignedEntity (DYNAMIC) | Medi...ment | | | hl7:participant
|
| | | | Use this if the informant of the medication statement is the patient | Medi...ment | where [@typeCode='INF'] | | | cs | 1 … 1 | F | INF | | Example | Informant of the medication statement is the patient <participant typeCode="INF"> <time value="20170121091548"/> <participantRole classCode="PAT"/></participant> | | TS | 1 … 1 | R | | Medi...ment | | | 1 … 1 | M | | Medi...ment | | cs | 1 … 1 | F | PAT | | | hl7:informant
|
| | | | Use this if the informant of the medication statement is a contact party (related party) | Medi...ment | where [exists(hl7:relatedEntity)] | | | cs | 0 … 1 | F | INF | | cs | 0 … 1 | F | OP | | Example | Informant of the medication statement is a contact party (related party) <informant> <relatedEntity classCode="AGNT"> <relatedPerson classCode="PSN" determinerCode="INSTANCE"> <name> <!-- .. --> </name> </relatedPerson> </relatedEntity></informant> | | | 1 … 1 | | Contains 2.16.840.1.113883.10.12.316 CDA RelatedEntity (DYNAMIC) | Medi...ment | | hl7:participant
|
| | 0 … 1 | | Record Target: indicates the person who's medical record holds the documentation of this medication statement. This element is only populated when the document is placed in a medical record of someone other than the patient (subject). Contains 2.16.840.1.113883.10.12.321 CDA Participant (Body) (DYNAMIC) | Medi...ment | where [@typeCode='RCT'] | | | | @typeCode
|
| cs | 1 … 1 | F | RCT | | hl7:participant
|
| | 0 … 1 | | Verifier: The person or organization that has primary responsibility for the medication statement. The responsible party is not necessarily present in an action, but is accountable for the action through the power to delegate. Contains 2.16.840.1.113883.10.12.321 CDA Participant (Body) (DYNAMIC) | Medi...ment | where [@typeCode='VRF'] | | | | @typeCode
|
| cs | 1 … 1 | F | VRF | | hl7:entryRelationship
|
| | 0 … * | C | Subordinate Substance Administration Statament as a component of the overall medication statement. At least one subordinated <substanceAdministration> has to be present to convey information about dosages (dose, frequency of intakes,..) unless medications are unknown or known absent. Subordinated <substanceAdministration> elements can be also used either to handle split dosing, or to support combination medications. Contains 2.16.840.1.113883.10.21.4.6 UV Subordinate Substance Administration (DYNAMIC) | Medi...ment | where [exists(hl7:substanceAdministration)] | | | | @typeCode
|
| cs | 1 … 1 | F | COMP | | Constraint | At least one subordinate <substanceAdministration> element SHALL be present unless medications are unknown or known absent.</substanceAdministration>
| | Example | <entryRelationship typeCode="COMP"> <!-- component: Subordinate Substance Administration Statement. --> <substanceAdministration classCode="SBADM" moodCode="EVN"> <templateId root="2.16.840.1.113883.10.21.4.6"/> <!-- .. --> </substanceAdministration></entryRelationship> | | | hl7:sequenceNumber
|
| INT | 0 … 1 | | Sequence number of the Subordinate Substance Administration. | Medi...ment | | hl7:entryRelationship
|
| | 0 … * | R | Medication Order Reference. Contains 2.16.840.1.113883.10.21.4.8 UV Medication Order Reference (DYNAMIC) | Medi...ment | where [@typeCode='REFR' and exists(hl7:substanceAdministration)] | | | | @typeCode
|
| cs | 1 … 1 | F | REFR | | Example | <entryRelationship typeCode="REFR"> <substanceAdministration classCode="SBADM" moodCode="RQO"> <templateId root="2.16.840.1.113883.10.21.4.8"/> <!-- .. --> </substanceAdministration></entryRelationship> | | hl7:entryRelationship
|
| | 0 … * | R | Dispense Event Reference. Contains 2.16.840.1.113883.10.21.4.9 UV Dispense Event Reference (DYNAMIC) | Medi...ment | where [@typeCode='REFR' and exists(hl7:supply)] | | | | @typeCode
|
| cs | 1 … 1 | F | REFR | | Example | <entryRelationship typeCode="REFR"> <supply classCode="SPLY" moodCode="EVN"> <templateId root="2.16.840.1.113883.10.21.4.9"/> <!-- .. --> </supply></entryRelationship> | Choice | | | Elements to choose from:- hl7:entryRelationship[@typeCode='RSON' and exists(hl7:observation)] containing template 2.16.840.1.113883.10.21.4.3 UV ClinicalStatement Observation (DYNAMIC)
- hl7:entryRelationship[@typeCode='RSON' and exists(hl7:act)] containing template 2.16.840.1.113883.10.22.4.31 IPS Internal Reference (DYNAMIC)
| | | hl7:entryRelationship
|
| | 0 … * | R | Reason: Specifies the reason (indication) for authoring the order. Contains 2.16.840.1.113883.10.21.4.3 UV ClinicalStatement Observation (DYNAMIC) | Medi...ment | where [@typeCode='RSON' and exists(hl7:observation)] | | | cs | 1 … 1 | F | RSON | | Example | <cda:entryRelationship typeCode="RSON"> <priorityNumber value="1"/> <!-- template 2.16.840.1.113883.10.21.4.3 'UV ClinicalStatement Observation' (2016-05-01T00:00:00) --> </cda:entryRelationship> | | INT.NONNEG | 0 … 1 | R | Indicates the priority of this reason for the order in relation to its sibling reasons. | Medi...ment | | | hl7:entryRelationship
|
| | 0 … * | R | Reason: Specifies the reason (indication) for authoring the order. Contains 2.16.840.1.113883.10.22.4.31 IPS Internal Reference (DYNAMIC) | Medi...ment | where [@typeCode='RSON' and exists(hl7:act)] | | | cs | 1 … 1 | F | RSON | | Example | <entryRelationship typeCode="RSON"> <priorityNumber value="1"/> <act> <!-- Clinical Statement Minimal --> </act></entryRelationship> | | INT.NONNEG | 0 … 1 | R | Indicates the priority of this reason for the order in relation to its sibling reasons. | Medi...ment |
|
Entry Level Templates
Appendix (Informative)
Acronyms and abbreviations
C-CDA | Consolidated CDA |
CDA | Clinical Document Architecture |
DSTU | Draft Standard for Trial Use |
EDQM | European Directorate for the Quality of Medicines & Healthcare |
EHR | Electronic Healthcare Record |
HL7 | Health Level Seven |
HP | Healthcare Professional |
IDMP | IDentification of Medicinal Products (ISO Standard) |
IHE | Integrating the Healthcare Enterprise |
ISO | International Organization for Standardization |
JIC | Joint Initiative Council on SDO Global Health Informatics Standardization |
LOINC | Logical Observation Identifiers Names & Codes |
MPID | Medicinal Product Identifier |
PCID | Medicinal Product Package Identifier |
PhPID(s) | Pharmaceutical Product Identifier(s) |
SDO | Standard Developing Organization |
STU | Standard for Trial Use |
UCUM | Unified Code for Units of Measure |
Glossary
- Prescribing is an activity that can be performed by a variety of healthcare professionals and involves a variety of orderable items (see glossary entry). For the purposes of the following Implementation Guide, prescribing is defined as the act of prescribing a medication in either an ambulatory or an institutional setting. This could include initiating a new medication order or making all kinds of modifications to existing orders.
- Dispensing is an activity undertaken to fulfill the logistical requirements of a prescription. It supplies the materials needed to perform the prescribed actions by those who will perform them. Examples of dispensing include eyeglasses, contact lenses and medications. For the purposes of the following ballot material, dispensing is defined as supplying a medication in fulfillment of a prescription or medication order. While dispensing in these circumstances would usually be performed by a pharmacist, other health care providers such as nurses or physicians might also dispense medications.
- Administration is an activity undertaken to give medication to the patient. In the community, this process is usually not recorded, since the majority occurs in the patient's home; only administrations undertaken by a healthcare professional, such as vaccination, tend to be formally documented. Administration of medication in the institutional setting is usually recorded on a dose-by-dose basis, and may be messaged on that basis, or a summary of all the administrations occurring during an inpatient stay may be described.
Integrated examples
The Medication on CDA specification releases are published at Project Publication Page. The actual release has a link to the XML materials as which the W3C schemas are part of; it also includes example CDA document instances. A set of use cases have been defined and represented in Medication on CDA format.
It is likely that the publication site will move to hl7.org permanently, we will inform about that process.
Validation artifacts
You can test your implementation (instances) against the Medication on CDA specification. To download materials to your computer for local testing and validation consider...
- ...the W3C schemas (actually valid for any CDA specification) located at the Project Publication Page. The actual release has a link to the XML materials as which the W3C schemas are part of; it also includes example CDA document instances.
- ..the ISO schematron, automatically generated by the tool. These are files to do validation locally by associating IPS CDA instances with the main schematron using an XML editor or to use the derived XSLT conversions and apply the according XSLT derivation to your local IPS CDA instance.
For further information you can follow the documentation.
Operational information
- The original specification is hosted on the logical ART-DECOR main server art-decor.org under the Governance Group HL7 International, the project is reachable at the Live Project Landing Page.
- Any Medication on CDA specification release in HTML format resides at Project Publication Page. It is likely that the publication site will move to hl7.org permanently, we will inform about that process.
Licenses
Following is a non-exhaustive list of third-party terminologies that may require a separate license:
- SNOMED CT: SNOMED International (formerly know as International Healthcare Terminology Standards Development Organization IHTSDO)[3] or info@ihtsdo.org
- Logical Observation Identifiers Names & Codes (LOINC): The Regenstrief Institute, Inc.
- Unified Code for Units of Measure (UCUM) : Regenstrief Institute, Inc. and the UCUM Organization
- EDQM Standard Terms : European Directorate for the Quality of Medicines & Healthcare (EDQM) [4]
List of all artifacts used in this guide
CDA Templates
References (re-used) from current C-CDA
Unconstrained Templates from the original CDA specification
Value Sets
System OIDs / IDs
Code systems
Datatypes
References
Literature
- Keith W. Boone: The CDA TM Book. Springer 2011, ISBN 978-0-85729-336-7
Links
- ↑ Cite error: Invalid
<ref>
tag;
no text was provided for refs named teits
- ↑ ISO/TS 13582:2013 Health informatics -- Sharing of OID registry information
- ↑ Get SNOMED CT http://www.ihtsdo.org/snomed-ct/get-snomed-ct
- ↑ EDQM Standard Terms https://standardterms.edqm.eu
Figures
- ↑ Locating ballot comments