This page is part of the FHIR Specification (v1.2.0: STU 3 Draft). The current version which supercedes this version is 5.0.0. For a full list of available versions, see the Directory of published versions
Published by: HL7 Orders and Observations Workgroup
Primary Author/Editor: Eric M Haas, Health eData Inc.
The US Laboratory Report Implementation (USLabReport) consists of the guidance documentation, profiles, operations, value sets and conformance statements it defines. This implementation has been prepared as a U.S. Realm Specification on behalf of the HL7 Orders and Observation Workgroup.
Laboratory Test Reporting in the US Realm ambulatory care setting (USLab Report) - This use case is based upon upon existing regulatory requirements for Laboratories and Electronic Health Record Systems (EHR-S) for reporting clinical laboratory results to ordering providers. The content has been modeled after the joint HL7 and The Standards and Interoperability (S&I) Framework Laboratory Results Interface (LRI) Initiative and the HL7 V3 Lab Normative Standard . However, much of the content is likely to be usable outside the ambulatory space and in other jurisdictions.The USLabReport is built on top of the HL7 FHIR standard. Basic aspects of the FHIR protocol, including RESTful operations, data types, search, etc. apply.
Profiles -The current focus of implementing USLabReport is using a FHIR Bundle Resource to exchange a DiagnosticReport Profile and the Resource Profiles it references. This FHIR bundle completely defines the laboratory results report. The Resource Profiles that may be used in the bundle are outlined below: (This list is not meant to be exhaustive as additional resources may also to be used)
In addition to defining the the USLabReport bundle this implementation consists of the following components: