This page is part of the Protocols for Clinical Registry Extraction and Data Submission (CREDS) IG (v1.0.0-ballot: STU1 Ballot 1) based on FHIR R4. . For a full list of available versions, see the Directory of published versions
Official URL: http://hl7.org/fhir/us/registry-protocols/ImplementationGuide/hl7.fhir.us.registry-protocols | Version: 1.0.0-ballot | |||
Draft as of 2023-03-29 | Computable Name: FHIRRegistryProtocolsIG |
The IG demonstrates a process and workflow to support the needs of clinical registries to define how registry submissions can be automatically extracted from multiple data sources and combined into a registry submission. It profiles the definitional resources needed to collect data and construct a registry submission using existing FHIR resource profiles.
This guide is organized into four main sections:
Click on any of the links above or refer to the table of contents, or if you are looking for a specific artifact, refer to the index.
You can also download:
The source code for this Implementation Guide can be found on https://github.com/HL7/fhir-registry-protocols-ig.
CREDS focuses on providing healthcare provider organizations information on how to collect the data needed to submit to registries. This may include but is not limited to data sources such as EHRs, HIEs and other sources using FHIR, HL7 CDA documents, and HL7 V3 messages that are not available via FHIR APIs.
The MedMorph Reference Architecture (RA) specifies the use of standard FHIR APIs to collect data from EHRs and potentially other systems and exchange with systems that can receive data in FHIR format. The RA can support multiple use cases through content IGs based on the MedMorph RA IG, including but not limited to case-based surveillance, registry reporting, national health care surveys, and research.
Use cases that can obtain all the needed data via FHIR APIs should consider the use of the MedMorph RA as the basis for their efforts. Use cases that need to obtain data not available via FHIR APIs should consider the use of CREDS. Once there is a CREDS FHIR bundle, the MedMorph RA could be used for transport.
While this implementation guide and the underlying FHIR are licensed as public domain under the FHIR license. The license page also describes rules for the use of the FHIR name and logo.
This guide includes examples making use of terminologies such as LOINC, SNOMED CT and RxNorm codes that have more restrictive licensing requirements. Implementers should make themselves familiar with licensing and any other constraints of terminologies, questionnaires, and other components used as part of their implementation process. In some cases, licensing requirements may limit the systems that data captured using certain Definitions may be shared with.
This publication includes IP covered under the following statements.
For information and exceptions regarding use of CDC material please see https://www.cdc.gov/other/agencymaterials.html.