Consolidated CDA Release 2.2
2.2 - CI Build
Unknown state code 'US'
Consolidated CDA Release 2.2
2.2 - CI Build
Unknown state code 'US'
Consolidated CDA Release 2.2 - Local Development build (v2.2). See the Directory of published versions
The following resources are available to the C- CDA implementer community to support the growing use of this important information exchange standard for interoperability.
There are sample C-CDA files for a variety of Clinical Note types. Sample documents are posted in Github where they are incrementally improved by the CDA Examples Task Force. Reference the C-CDA Sample Document registry for the current version of these sample documents.^140
(^140) https://github.com/HL7/CDA-ccda-companion/tree/9832019cd7a324c445057e5f44c50897cb7e475b/examples/xml
| Type | C-CDA Sample File Name and brief description |
|---|---|
| Discharge Summary showing USCDI v2 Data Elements | DischargeSummary-USCDI-v2.xml This sample file represents new and revised templates necessary to convey USCDI V2 data elements. |
| CCD Patient Summary | CCD.xml This sample demonstrates sections relevant to creating a summary of essential clinical data to exchange from a patient’s health record. |
| Discharge Summary | DischargeSummary.xml This sample demonstrates sections relevant to creating a summary of information that supports a transfer of care following an inpatient discharge. |
| Referral Note | ReferralNote.xml This sample demonstrates sections relevant when initiating a referral to support a transfer of care to another care provider. |
| Progress Note | ProgressNote.xml This sample demonstrates sections relevant for documenting a patient’s progress during an ongoing episode of care. |
| Care Plan | CarePlan.xml This sample demonstrates the organization of care plan information for exchange. It shows the relationships between health concerns, goals, interventions and health assessment and outcome evaluation information are expressed. |
| Unstructured Document | UnstructuredDocument.xml This sample demonstrates use of the |
| Legal Authenticator-signed | LegalAuthenticator-signed.xml This sample demonstrates use of the HL7 Digital Signature standard for digitally signing a C-CDA document as the Legal Authenticator. |
Table 77: Sample Document Files
The HL7 Version 3 Clinical Document Architecture (CDA®) is a document markup standard that specifies the structure and semantics of “clinical documents” for the purpose of exchange between healthcare providers and patients. It defines a clinical document as having the following six characteristics: 1) Persistence, 2) Stewardship, 3) Potential for authentication, 4) Context, 5) Wholeness and 6) Human readability.
CDA R2.0 is the currently release normative version of the HL7 CDA standard. However, implementers are encouraged to begin educating themselves about the improvements offered by the new CDA R2.1. CDA R2.1 is a minor enhancement of the base Clinical Document Architecture standard that is backward compatible to the existing CDA R2.0 standard and provides optional improvements which natively support most previous extensions used in implementation guides world-wide.
Notable extensions have been added to the patient reference and classes in the clinical statement model used for machine process-ability. The documentation has been improved and updated to explain how CDA can be constrained using templating to support any number of use cases found in healthcare using a base schema just like CDA R2.0.
A CDA document can be used to represent any type of clinical content – a CDA document could be used to represent a Discharge Summary, Imaging Report, Admission & Physical, Pathology Report and more. The most popular use is for inter-enterprise information exchange, such as is envisioned for a US Health Information Exchange (HIE). The HL7 C-CDA Implementation Guide constrains the base CDA standard to meet the use cases for information exchange of common types of clinical notes.
As the demand for interoperable information exchange in healthcare grows, stakeholders across the C-CDA implementer community continue to develop and publish additional templating guidance to supplement the set of templates defined in C-CDA. Supplemental C-CDA implementation guides are balloted through the HL7 consensus process and published together with C-CDA on the HL7 Master Grid of Standards. Supplemental C-CDA implementation guides define additional templates and new versions of templates in C-CDA. All templates in Supplemental C-CDA implementation guides are considered for optional use.
Source: HL7 CDA® Release 2 Resource: https://www.hl7.org/implement/standards/product_brief.cfm?product_id=7 Description: This package includes additional publications such as Datatypes, HL7 Value Sets, and other detailed information required for proper implementation of CDA.
Source: CDA Management Group Listserv for HL7 CDA® Release 2.1 Resource: http://www.hl7.org/Special/committees/cdamg/index.cfm Description: At this time, there are no plans to migrate to the new version of CDA within the US. However, the CDA Management Group will begin an information gathering campaign in 2020 to allow the implementer community to explore and discuss the pros and cons of introducing CDA R2.1 into production.
Source: C-CDA (HL7 CDA® R2 Implementation Guide: Consolidated CDA Templates for Clinical Notes - US Realm R2.1) Resource: http://www.hl7.org/implement/standards/product_brief.cfm?product_id=492 Description: The HL7 Consolidated CDA is an implementation guide which specifies a library of templates and prescribes their use for a set of specific document types. The Consolidated CDA (C-CDA) implementation guide contains a library of CDA templates, incorporating and harmonizing previous efforts from Health Level Seven (HL7), Integrating the Healthcare Enterprise (IHE), and Health Information Technology Standards Panel (HITSP). It represents harmonization of the HL7 Health Story guides, HITSP C32, related components of IHE Patient Care Coordination (IHE PCC), and Continuity of Care (CCD). C-CDA Release 1 included all required CDA templates in Final Rules for Stage 1 Meaningful Use and 45 CFR Part 170 – Health Information Technology: Initial Set of Standards, Implementation Specifications, and Certification Criteria for Electronic Health Record Technology; Final Rule. C-CDA R2.1 guide was developed and produced by the HL7 Structured Documents Workgroup. It updates the C-CDA R2 (2014) guide to support “on-the-wire” compatibility with R1.1 systems. The C-CDA Release 2.1 implementation guide, in conjunction with this Companion Guide, the published C-CDA R2.1 Supplemental Guides, and the HL7 CDA Release 2 (CDA R2) standard, are to be used for implementing the following CDA documents and header constraints for clinical notes: Care Plan including Home Health Plan of Care (HHPoC), Consultation Note, Continuity of Care Document (CCD), Diagnostic Imaging Reports (DIR), Discharge Summary, History and Physical (H&P), Operative Note, Procedure Note, Progress Note, Referral Note, Transfer Summary, as well as patient generated documents and all types of unstructured documents classified under the LOINC document ontology.
Source: C-CDA R2.1; Advance Directives Templates, Release 1 – US Realm Resource: https://www.hl7.org/implement/standards/product_brief.cfm?product_id=473 Description: Advance Directive Templates are important components of the C-CDA standard, yet to date, their usage in the standard has been optional. New focus within the industry on patient-centered care plans and value-based care has raised implementer interest in care planning and advance care planning. As implementers have started to include advance directive information, it became clear that additional guidance was needed and that the template designs required refinement. Also, the new standard was developed to represent personal advance care planning information have been developed to communicate health goals and treatment preferences expressed by the patient. The older Advance Directive templates needed revisions to take the newer work into consideration.
As advance care planning information began to be shared, concern increased about the possibility that clinicians might misinterpret patient wishes in a way that would result in errors that risk patient safety or that violate patient intent. Information context is crucial when it comes to interpreting advance directives. Directives should always be maintained in their original form - not chopped up and stored as structured data. There is a very high risk that the conversion from text to structure will lose critical information. Changes were needed to the templates to clarify that these observations DO NOT convert patient wishes into structured data that acts as a decision or an order. The structured data is used to document WHAT TYPE of CONTENT is present in the source document that describes the patient's wishes, health goals, and treatment preferences. Fixing this issue was a critical need.
For these reasons, the earlier versions of the Consolidated CDA Advance Directive Templates needed to be clarified and revised, and some additional templates needed to be added.
Source: HL7 CDA R2 Implementation Guide: C-CDA R2.1 Supplemental Templates for Nutrition, Release 1 – US Realm Resource: http://www.hl7.org/implement/standards/product_brief.cfm?product_id=478 Description: The Nutrition Care Process (NCP) is used by Registered Dietitians Nutritionists (RDN) and other nutrition and dietetics professionals as a systematic approach to providing high quality nutrition care. Templates in this guide are specific to the four steps of the Nutrition Care Process: Nutrition Assessment and Reassessment, Nutrition Diagnosis, Nutrition Intervention, and Nutrition Monitoring and Evaluation. These templates are intended to promote nutrition interoperability across care settings and will create information suitable for reuse in transitions of care, quality measurement, public health reporting, research and reimbursement.
Source: HL7 CDA R2 Implementation Guide: C-CDA R2.1 Supplemental Templates for Pregnancy Status, Release 1 – US Realm Resource: http://www.hl7.org/implement/standards/product_brief.cfm?product_id=494 Description: This implementation guide provides consistent guidance for capturing key pregnancy status information in healthcare information technology (HIT) products and contains optional supplemental pregnancy status templates for current C-CDA document types.
Source: HL7 CDA® R2 Implementation Guide: C-CDA R2.1 Supplemental Templates for Occupational Data for Health Release 1, STU Release 1.1 – US Realm Resource: https://www.hl7.org/implement/standards/product_brief.cfm?product_id=522 Description: This IG contains guidance, supporting material and new templates to implement support for Occupational Data for Health (ODH). ODH is primarily designed to facilitate clinical care, including population health; ODH also can be used to support public health reporting, population health, and similar value-based care. ODH is not designed to support billing activities. The scope of the work information includes:
- Employment Status - Retirement Date - Combat Zone Period - Past or Present Job for the patient or a household member - Usual Work of the patient or a household member
Source: HL7 CDA® R2 Implementation Guide: C-CDA R2.1 Supplemental Templates for Infectious Disease, Release 1 – US Realm Resource: https://www.hl7.org/implement/standards/product_brief.cfm?product_id=502 Description: This guide defines optional additions to the C-CDA R2.1 Continuity of Care Document (CCD), Transfer Summary, and Discharge Summary standards. These additional templates are available for use in any other CDA document-type where needed. They specify infectious disease data that should be included in the above-mentioned documents or any other relevant CDA document-type when patients are transferred between healthcare facilities, discharged home, or discharged to locations other than home (e.g. law enforcement).
Source: HL7 Implementation Guide: Data Segmentation for Privacy (DS4P), Release 1 Resource: http://www.hl7.org/implement/standards/product_brief.cfm?product_id=280 Description: This implementation guide defines constraints on the HL7 CDA standard to support Meaningful Use in provide data representation specifications that are consistent with federal and state privacy policies. The guidance enables the exchange of protected/sensitive personal health information. It supports secure exchange of health information and privacy annotations applied to documents, messages, or atomic data elementsHIT) products and contains optional supplemental pregnancy status templates for current C-CDA document types.
Source: HL7 CDA® R2 Implementation Guide: Privacy Consent Directives, Release 1 Resource: http://www.hl7.org/implement/standards/product_brief.cfm?product_id=354 Description: This implementation guide defines a CDA representation of privacy consents (e.g. authorization to disclose health information, consent for research) which enables the exchange of computable consents across EHRs. It supports the display of consents to end-users based on existing CDA infrastructure and applications. It also supports Data Use and Reciprocal Support Agreement (DURSA) opt-in and other opt-in consent agreements. This specification enhances IHE BPPC (Basic Patient Privacy Consent). his implementation guide defines constraints on the HL7 CDA standard to support Meaningful Use in provide data.
Below are brief descriptions of additional specifications relevant for C-CDA based information exchange.
The Joint Document Content Work Group was established in 2018 as a cooperative effort between Car e quality and CommonWell initiatives.^141 The outcome was the white paper “Concise Consolidated CDA: Deploying Encounter Summary CDA Documents with Clinical Notes ” which provides recommendations to improve content in C-CDA for document-based information exchange including the following topics: inclusion of Encounter Summary Documents, best practices for Clinical Notes, and document display guidance for Smart Senders and Resilient Receivers.
Source: Concise Consolidated CDA: Deploying Encounter Summary CDA Documents with Clinical Notes Resource: https://www.commonwellalliance.org/wp-content/uploads/2019/01/Improve-Joint-Document- Content-Whitepaper.pdf Description: Provides recommendations to improved content in C-CDA.
IHE is an initiative by healthcare professionals and industry to improve the way computer systems in healthcare share information. IHE promotes the coordinated use of established standards such as DICOM and HL7 to address specific clinical needs in support of optimal patient care.
Source: Integrating the Healthcare Enterprise (IHE) Patient Care Coordination Technical Framework Supplement: CDA Document Summary Sections (CDA-DSS) Resource: https://www.ihe.net/uploadedFiles/Documents/PCC/IHE_PCC_Suppl_CDA_DSS.pdf Description: Provides a method to summarize and communicate specific information to the reader ( e.g., provider and/or patient) in a concise and useful manner. This profile can be added to any CDA document that is an open template and allows a relevant and pertinent information in a section to be available to the reader while including the large amount of data in a CDA document.
Source: Integrating the Healthcare Enterprise (IHE) Patient Care Coordination Technical Framework Supplement: Multiple Content Views (MCV) Resource: https://www.ihe.net/uploadedFiles/Documents/PCC/IHE_PCC_Suppl_MCV.pdf Description: Provides guidance on how to tag text in CDA documents for rendering of the narrative for different Document Consumers and their specific viewing requirements.
(^141) https://www.commonwellalliance.org/wp-content/uploads/2019/01/Improve-Joint-Document-Content-Whitepaper.pdf
Source: Integrating the Healthcare Enterprise (IHE) Patient Care Coordination Technical Framework Supplement: Reconciliation of Clinical Content and Care Providers (RECON) Resource: http://ihe.net/uploadedFiles/Documents/PCC/IHE_PCC_Suppl_RECON.pdf Description: This profile enables Health Information Systems and Exchanges to support automation of reconciliation of tasks and clinical workflows and the ability to communicate lists of reconciled clinical data, when they were reconciled and who did the reconciliation using CDA constructs and FHIR Resource attributes.
A joint effort of the HL7 Attachments Work Group, the HL7 Structured Documents Work Group, the Centers for Medicare & Medicaid Services (CMS), and the Office of the National Coordinator (ONC) Standards and Interoperability (S&I) Framework Electronic Submission of Medical Documentation (esMD) Initiative that addresses the need for additional documentation to support data required for processing claims.
Source: HL7 CDA® Release 2 Implementation Guide: Additional CDA R2 Templates – Clinical Documents for Payers Set 1, Release 1 – US Realm Resource: http://www.hl7.org/implement/standards/product_brief.cfm?product_id=410 Description: Provides guidance on structured documentation templates to exchange clinical and administrative information to support bi-lateral communication between providers and payers to expedite processing of claims.
The Quality Reporting Document Architecture (QRDA) project is developing a standard for communicating health care quality measurement information. It continues to be co-sponsored by the HL7 Structured Documents and Child Health Work Groups and is supported by the Centers for Medicare & Medicaid Services (CMS).
The Phase IV effort was launched in Summer 2014 to develop and ballot QRDA Category I, Release 3. It is co- sponsored by the HL7 Clinical Quality Information (CQI) WG and Structured Documents Work Groups and continues to be supported by CMS. The scope of this effort will include the following:
Source: QRDA I Release 1, STU Release 5.1, Supports QDM v5.4 Resource: http://www.hl7.org/implement/standards/product_brief.cfm?product_id=35 Description: Defines the requirements for sending and receiving standards-based electronic attachments. Defines the set of attachment documents as those that contain the minimum standard metadata to support basic document management functions including identification of patients and providers, the type of document, date of creation, encounter information, and a globally unique document identifier.
Source: HL7 Clinical Quality Information Workgroup Resource: https://confluence.hl7.org/display/CQIWC/Clinical+Quality+Information+WG+%28CQI%29+Home Description: The Clinical Quality Information (CQI) Work Group creates and maintains HL7 standards supporting quality measuring, evaluating, and reporting of quality data. Specific areas of interest include the measurement and reporting of quality and its dimensions including: safe, effective, patient-centered, timely, efficient, and equitable as defined by the Institute of Medicine (now the US Academy of Medicine).
Below are brief descriptions of tools available to support C-CDA development.
HL7 makes available resources that support implementers with their use of the CDA base standard and published implementation guides. The resources are currently housed in the HL7 gForge repository.
Source: CDA R2 Schema File Resource: https://hl7.org/permalink/?CDAR2.0schema Description: This folder contains the CDA R2 Schema file with updates that contain approved extensions.
Source: C-CDA Schematron Validation Files Resource: https://github.com/HL7/cda-ccda-2.1/blob/master/schematron/Consolidation.sch Description: This folder contains Schematron validation files for C-CDA templates and any C-CDA supplemental templates. Note: Schematron is an optional quality criteria at this time.
Source: CDA Sample Stylesheet Resource: https://hl7.org/permalink/?CDAStyleSheet Description: This folder contains a sample stylesheet developed to expose the structured header elements and attestable content (the section.text Narrative Block in each section) for a CDA document.
The Standards Implementation & Testing Environment (SITE) is a centralized collection of testing tools and resources designed to assist health IT developers and health IT users fully evaluate specific technical standards and maximize the potential of their health IT implementations. SITE is organized in a collection of sandboxes that provide test tools, sample data, collaboration resources, and useful links.
Source: SITE Validation Resource: https://site.healthit.gov/sandbox-ccda Description: The C-CDA Sandbox contains resources and tools for the HL7 Consolidated Clinical Document Architecture (C-CDA) implementation guides. These tools will help in testing of C-CDA documents for conformance to the C-CDA IG, the ONC 2014 Edition and ONC 2015 Edition C-CDA objectives and also help with quantitative assessment of the data quality using the Scorecard.
Source: C-CDA Scorecard Resource: https://ccda.healthit.gov/scorecard/ Description: The ONC Scorecard tool is used to compare a C-CDA R2.1 document against a rubric of best practice guidance developed by the HL7 C-CDA implementer community and vetted through the HL7 ballot process. The C- CDA Scorecard does not retain your submitted C-CDA file as the file is deleted from the server immediately after processing. However, we strongly suggest that you do not include any Protected Health Information (PHI) or Personally Identifiable Information (PII) in your C-CDA file submissions to the Scorecard.
MDHT allows the creation of computable models of the templates in UML. These models can be used to produce template specifications (DITA, XHTML, PDF, Other), validation tools, and model driven code generation. Thus far, the project has built models from the specifications including Consolidated CDA, HITSP C83, and IHE Patient Care Coordination Technical Framework.
Source: Java Runtime MDHT Resource: https://github.com/mdht/mdht-models Description: All MDHT projects supporting the various CDA based implementation guides including Consolidate CDA.
Source: ECLIPSE MDHT Resource: https://projects.eclipse.org/projects/modeling.mdht Description: Eclipse MDHT delivers a standard object-oriented alternative to proprietary development methodologies and tooling used to specify and implement most healthcare industry standards. The tool generates domain-specific Java classes for templates/profiles/archetypes.
HL7 and the C-CDA implementer community offer educational and support resources to help build essential implementer skills and production capacity for the use of C-CDA. Information on the HL7 Confluence sites for the SDWG and CDA Management group keeps the community informed about all aspects of the management and methodology associated with the CDA standard and its associated product families such as C-CDA.
Source: HL7 Training Resource: http://www.hl7.org/implement/training.cfm?ref=nav Description: HL7 training programs provide knowledge and support to guide the healthcare industry through successful implementation of HL7 standards. Certification testing is available for specific HL7 standards including CDA.
Source: The CDA Book Resource: http://www.amazon.com/The-CDA-book-Keith- Boone/dp/0857293354/ref=sr_1_1?ie=UTF8&qid=1337020821&sr=8-1 Description: Written by Keith W. Boone, The CDA Book provides clear and simplified guidance for the HL7 CDA standard, the foundation of Consolidated CDA. The book is available for purchase through retailers and is highly recommended to assist in understanding core concepts of the standard.
Source: HL7 CDA Management Group Confluence Space Resource: https://confluence.hl7.org/display/CDA/CDA+Management+Group Description: The HL7 CDA Management Group (CMG) is responsible for the management of the CDA standard and its derivative product families. This website is the primary repository for their projects and meetings.
Source: HL7 SDWG Confluence Space Resource: https://confluence.hl7.org/display/SD/Structured+Documents Description: The HL7 Structured Documents Work Group (SDWG) is responsible for the methodology used to develop and sustain the CDA standard and its derivative product families. This website is the primary repository for their projects and meetings.
Source: HL7 Listserv registration Resource: http://www.hl7.org/myhl7/managelistservs.cfm Description: Stakeholders within the CDA and C-CDA implementer community are encouraged to sign up for the Structured Documents and CDA Management Group listservs to stay apprised of topics relevant to the management and maintenance of these HL7 standards.
Source: HL7 CDA Example Search Resource: https://cdasearch.hl7.org/ Description: The CDA Examples Task Force has created a large number of examples showing how to convey information accurately in a C- CDA document. The CDA Example search tool allows users to find examples based on keywords.
Reference : See the file named CDAR2_IG_CCDA_COMPANION_R4_D1_AppxA included in this Companion Guide package for Templates that are defined in this Companion Guide.
Reference: See the file named CDAR2_IG_CCDA_COMPANION_R4_D1_AppxB included in this Companion Guide package for the UDI Organizer template defined in HL7 CDA® R2 Implementation Guide: C-CDA Supplemental
IG © 2019+ Health Level Seven. Package hl7.cda.us.ccdar2dot2#2.2 based on FHIR 4.0.1. Generated 2023-05-30
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