LOINC – IVD Test Code (LIVD) Mapping, published by HL7 International / Orders and Observations. This guide is not an authorized publication; it is the continuous build for version 1.0.0-ballot built by the FHIR (HL7® FHIR® Standard) CI Build. This version is based on the current content of https://github.com/HL7/livd/ and changes regularly. See the Directory of published versions
Official URL: http://hl7.org/fhir/uv/livd/ImplementationGuide/hl7.fhir.uv.livd | Version: 1.0.0-ballot | |||
Active as of 2024-12-19 | Computable Name: LoincIvdTestCodeMapping |
This specification represents the updates from the first ballot (September 2019) and subsequent addition enabling documentation of Result Value mapping guidance. It furthermore reflects updates in the "LIVD - Digital Format for Publication of LOINC to Vendor IVD Test Results" specification that is undergoing further updates to reflect Result Value mapping as well. A draft is available here. This is the second STU ballot with the intent to publish LIVD STU R1 version upon completing ballot reconciliaton.
Feedback is welcome and may be submitted through the FHIR Jira tracker
The objective of this implementation guide is to define an In Vitro Diagnostic (IVD) industry format to facilitate the publication and exchange of suggested LOINC codes for vendor IVD test assays, based on either vendor IVD test transmission codes or manual test identification, for use by laboratory personnel or laboratory applications. It is not intended to cover information for other related activities, such as purchasing tests from a vendor. Expected systems using the format include Laboratory Information Systems (LIS), clinical middleware applications, databases, and terminology servers.
This implementation guide defines a digital format that can be easily:
Both vendor-defined IVD test by a vendor IVD instrument and vendor-defined manual IVD test are in scope.
By voluntarily adopting the format described here as an industry convention, IVD vendors will understand what data and in what format they should provide when publishing suggested LOINC codes for their IVD tests. By doing so, this work will significantly reduce the variability of the content and format of the multiple publications received by laboratory environments, further reducing the time and effort required by laboratories to review and integrate this information into their laboratory software systems. The format includes additional vendor information, such as a description of the result, used to easily discriminate between multiple LOINC codes for the same IVD test.
Ideally it is envisioned that the LOINC codes selected by manufacturers would be reviewed by a common party (e.g. Regenstrief) for correctness and consistency across vendors, and also that the industry would establish conventions for the storage and access of the IVD vendor LOINC publications. The effort required for these objectives will also be reduced by having this standard publication format and associated content.
The implementation guide has an initial scope that does not address: