Birth And Fetal Death (BFDR) FHIR Implementation Guide, published by HL7 International / Public Health. This guide is not an authorized publication; it is the continuous build for version 2.0.0 built by the FHIR (HL7® FHIR® Standard) CI Build. This version is based on the current content of https://github.com/HL7/fhir-bfdr/ and changes regularly. See the Directory of published versions
The Centers for Disease Control (CDC) National Center for Health Statistics (NCHS) Division of Vital Statics (DVS) is currently modernizing the submission of vital records to the National Vital Statistics System (NVSS). CDC/NCHS/DVS funds the development of the FHIR IGs for submission submission of death records – Vital Records Death Reporting (VRDR) – and birth and fetal death records – Birth and Fetal Death Reporting (BFDR), manages the NVSS Community of Practice (CoP), and holds quarterly testing events. Vital records offices (VROs) participate in these testing events with some on the path to pre-certification as a milestone for moving into production submission via FHIR to NVSS.
NCHS has begin the transition of submission of death records by VROs to NCHS based on VRDR STU2.2. The next vital records process planned for FHIR-based modernization is the submission of birth records. To support submission of birth records from VROs to NCHS requires extension of the BFDR and VRCL FHIR IGs. Both VRCL STU2 and BFDR STU2 are being balloted in the January 2024 ballot cycle with the goal of enabling initial testing of birth record submission during 2024. This page describes the structural and content changes to BFDR and VRCL as they move from STU1.1 to STU2, and the motivation for making these changes.
FHIR Implementation Collaborative led by the CDC Foundation is working with CDC/NCHS’s Collaborating Office for Medical Examiners and Coroners (COMEC) to test and pilot FHIR-based Application Programming Interface (API) enabled data exchange for medicolegal death investigation workflows. This effort is a collaboration with MDI offices and identified partners: state vital records offices, toxicology labs and/or other entities. It funds development of the Medicolegal Death Investigation (MDI) FHIR IG as well as collaborative testing events with MDI sites.
The goals of FHIR IG development and harmonization are:
To achieve the goals for harmonization listed above involves modification to the content of the current IGs, development of new content, and transition of content between the IGs. This will reduce the proliferation of content across the set of IGs due to redundancy and near-redundancy, simplify implementation of the IGs, and simplify adoption.
Figure 1 shows the current dependencies among published vital reocrds FHIR IGs. Figure 2 shows the dependencies after harmonization. Harmonization will result in significant simplification of the MDI IG, and consolidation of all general Vital Records specific content within the VRCL.
Although it has not yet been balloted, the design of the VRCL STU1 was driven by consideration of a future Birth Defects FHIR IG. The dependencies of this not-yet-balloted IG would change as a result of the harmonization effort, since much birth-related content has been consolidated within The BFDR STU2 IG. This change should not impact the ability of the Birth Defects IG to leverage vital records content, but would change the precise dependencies. Figure 3 shows the current dependencies of a potential Birth Defects FHIR IG. Figure 4 shows the dependencies following the proposed harmonization.
To implement the goals of harmonization described above, we are proposing the following content changes. The VRCL and BFDR changes are implemented in the January 2024 ballot cycle with STU2 ballots: