CDA Implementation Guides

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1 CDA Overview

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2 Introduction to CDA Technical Artifacts

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3 CDA Document Exchange in HL7 Messages

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4 CDA Implementation Guides

The Clinical Document Architecture defines a single logical schema, which may be used to instantiate any clinical document for exchange. CDA can be used, by itself, to create such documents, which then can be shared and read by recipients with no problem. However the true utility of CDA to improve interoperability, is only realized when the base CDA standard is further constrained to define specific types of documents and their associated processable clinical statements.

4.1 Benefits of Constraining CDA

There are a number of benefits derived from constraining CDA documents:

1. Specific types of documents can be defined, instantiated, exchanged and used (E.g. Consult Note, Procedure Note, Continuity of Care Document, ...)
2. Required and optional sections of a clinical document can be identified (E.g. Reason for Visit, Family History, ...)
3. Realm specific constraints and conventions can be identified (E.g. US Realm Header, US Address and Patient Naming, ...)
4. Required and optional entries (machine processable content) can be identified (E.g. Medication Entries, Problem Entries, ...)

In addition to serving as a useful guides for implementers or creators of CDA documents, CDA Implementation Guides with their associated templates can:

1. Be used to create new document types, by using reusable sections and clinical statement models form previously defined IGs.
2. Be used to improve consistency across documents, by reusing sections and clinical statement models from previously IGs.
3. Be used to validate document instance conformance to constants and best practices (Machine Processable Conformance Testing)
4. Be used by receivers to aid in their processing of complex clinical content, there by improving semantic interoperability.

The Architecture of CDA is demonstrated in the system of reusable constraint models (templates) which have been created, used and reused in various CDA Implementation Guides. Implementation Guides define the constraints or expected additional conformance rules to be applied to document instances beyond those already defined within the CDA standard itself. As such every CDA document expressing conformance to a CDA Implementation Guides is still a CDA document, it simply asserts additional conformance to the constraints defined within an Implementation Guide.

4.2 Structure of CDA Implementation Guides

A CDA Implementation Guide is used package up the set of constraints defined for specific set of CDA document types. Some implementation Guides are for a single document types, while others are used to define sets of documents that share common features or use cases. Overtime, a structure has been established for CDA Implementation Guides.

CDA Implementation Guides generally contain:

1. Introduction
2. Additional background information
3. Shared Templates (Header)
4. Listing of Document Templates
5. Listing of Section Templates
6. Listing of Entry Templates
7. Shared Templates (Address, Name conventions, etc.)
8. Listing of all Templates
9. Listing of all Value Sets
10. Appendixes

There are generally four types of templates defined in a CDA Implementation Guide. Note that each element in the CDA Schema supports a templateId, therefore templates can be defined, as needed, anywhere they are required.

4.3 Templates on CDA

As can be seen, there are many kinds of templates that might be created. Among them, the most common are:

• Document-level templates: These templates constrain fields in the 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.
• Section-level templates: These 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 contains a Systolic Blood Pressure observation.
• Entry-level templates: These 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.
• Other templates: Templates that exist to establish a set of constraints that are reused in the CDA document. These other templates are only used within another template, rather than on their own as a complete clinical statement. For example, US Realm Date and Time (DTM.US.FIELDED) includes a set of common constraints for recording time. This template is referenced several times with other templates used in the implementation guide. They reduce the need to repeat constraints in templates that use the common set.

A CDA implementation guide includes references to those template versions that are applicable.

4.3.1 Template Identifiers

Each template specified in a CDA Implementation Guide will have an associated template identifier. Those identifiers can be placed in a CDA instance via the "templateId" to indicate where it wants to assert conformance to a given template version. On the receiving side, the recipient can then not only test the instance for conformance against the CDA Extensible Markup Language (XML) schema, but also test the instance for conformance against asserted templates.

4.3.2 Template Versioning

A new version of an existing implementation guide reuses templates from the previous version. During the ballot phase or update phase, templates carry the designation “Published” to indicate the template is unchanged from the previous version or “Draft” to indicate a new or revised template. Substantial revisions to previously published templates are indicated by the version number (V2, V3, etc.) in all phases: ballot, update, and published guides.

If there are no substantive changes to a template that has been successfully published, the template will carry the same templateId/@root (identifier oid) and templateId/@extension as in the previous implementation guide. (In the case of older templates, the @extension attribute will not be present.) During a new ballot or update phase, “Published” is appended to the main heading for the template to indicate that the template cannot be commented on in the ballot or update. The “Published” designation is removed in the final publication versions.

A revised version of a previously published template keeps the same templateId/@root as the previous version but is assigned a new templateId/@extension. The notation “(Vn)” (V2, V3, etc.) is also added to the template name. Versions are not necessarily forward or backward compatible. A versioning may be due to substantive changes in the template or because a contained template has changed. The “(Vn)” designation is persistent; it appears with that template when it is used in subsequent guides. During a new ballot or update phase, “Draft” is appended to the main heading for the template to indicate that it may be voted on in the ballot or commented on in the update; the “Draft” designation is removed in the final publication versions.

Structured Documents Working Group collaborated with Templates Working Group to establish template versioning recommendations, recently published in the following specification: HL7 Templates Standard: Specification and Use of Reusable Information Constraint Templates, Release 1. SDWG will leverage that specification to create guidance for template IDs and template versioning for future CDA implementation guides, including future versions of C-CDA, but that work is still in progress. The versioning approach used in this version of C-CDA is likely to be close to the final guidance, but has not been formally approved by SDWG for all implementation guides at this time.

Each version of a template has a status. For example, a template version can be draft, active, or deprecated, etc. The HL7 Templates DSTU describes the various status states that may apply to a template version over the course of its lifecycle. Each version of a template has an associated status. Thus, one version of a template may be deprecated, while a newer version of that template may be draft or active.

4.3.3 Open and Closed Templates

In open templates, all of the features of the CDA R2 base specification are allowed except as constrained by the templates. By contrast, a closed template specifies everything that is allowed and nothing further may be included.

Estimated Date of Delivery (templateId 2.16.840.1.113883.10.20.15.3.1) as defined in C-CDA R2.1 is an example of a closed template. Open templates allow HL7 implementers to develop additional structured content not constrained within this guide. HL7 encourages implementers to bring their use cases forward as candidate requirements to be formalized in a subsequent version of the standard to maximize the use of shared semantics.

4.4 Conformance Statements

Each template defined within a CDA Implementation Guide, will contain one or more conformance statements. Each conformance statement will have a conformance identifier, (CONF:####), identify a conformance verb, SHALL, SHOULD, MAY, etc.), identify the element or attribute that is the subject or context of the conformance constraint and define one or more constraint(s) to be imposed on that item. Constraints can specify cardinality, allowed use of nullFlavors, various types of attribute binding, inclusive of single code, value set and concept domain binding for code types and allowed specializations on data type usage. In general constrains can be defined as needed to ensure that implementers and receivers of CDA documents can semantically interpret and process the clinical content.

4.4.1 Conformance Verbs (Keywords)

The keywords SHALL, SHOULD, MAY, NEED NOT, SHOULD NOT, and SHALL NOT represent the set of conformance verbs that can be asserted on conformance statements. They are to be interpreted as described in the HL7 Version 3 Publishing Facilitator's Guide.

•  SHALL: an absolute requirement
•  SHALL NOT: an absolute prohibition against inclusion
•  SHOULD/SHOULD NOT: best practice or recommendation. There may be valid reasons to ignore an item, but the full implications must be understood and carefully weighed before choosing a different course
•  MAY/NEED NOT: truly optional; can be included or omitted as the author decides with no implications

The keyword "SHALL" allows the use of nullFlavor unless the requirement is on an attribute or the use of nullFlavor is explicitly precluded. When conformance statements are nested (or have subordinate clauses) the conformance statements are to be read and interpreted in hierarchical order. These hierarchical clauses can be interpreted as "if then, else" clauses. Thus...

a. This structuredBody SHOULD contain zero or one [0..1] component (CONF:1098-29066) such that it

  i. SHALL contain exactly one [1..1] Plan of Treatment Section (V2) 
(identifier: urn:hl7ii:2.16.840.1.113883.10.20.22.2.10:2014-06-09) (CONF:1098-29067).

...is understood as:

a. It is recommended (SHOULD) that the structureBody contains a component.

  i. If the component exists, then it must contain a Plan of Treatment Section (V2),

  ii. else the component does not exist, and the conformance statement about the Plan of Treatment Section (V2) 
should be skipped.

In the case where the higher level conformance statement is a SHALL, there is no conditional clause. Thus...

b. This structuredBody SHALL contain exactly one [1..1] component (CONF:1098-29086) such that it

  i. SHALL contain exactly one [1..1] Problem Section (entries required) (V2) 
(identifier: urn:hl7ii:2.16.840.1.113883.10.20.22.2.5.1:2014 -06-09) (CONF:1098-29087).

...means that the structuredBody is always required to have a component.

5 CDA R-MIM

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6 CDA Hierarchical Description

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7 CDA XML Implementation

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8 Appendix

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