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The following sections provide the history of changes made to this document.
This document is now Released for Implementation.
This document has been updated to include the HITSP Security and Privacy constructs and has been updated to reflect the new template.
The following changes have been made to the construct:
Maintenance update to align this Component with the advancement of the IHE Laboratory Technical Framework Volume 3 (LAB TF-3) Specification; additional edits include typographical corrections and reformatting of text and tables to improve readability; significant changes are noted below.
Section 2.1.1 Component Constraints. The requirement for inclusion of machine processable entries (Level 3 entries) imposed by previous versions of this Component has been removed from Section 2.2.1 of this version as it is now imposed by the referenced specification
Section 2.2.1.1 Data Structure, Paragraph 5. The updated IHE specification has now adopted requirements previously imposed by HITSP in Section 2.2.1, most notably the requirement for inclusion of machine processable entries (Level 3 entries). The change of MAY to SHALL in paragraph 5 reflects that change
Section 2.3 List of Standards
- Updated the IHE Lab Technical Framework standard to reflect the inclusion of the previous supplement into the IHE Laboratory Technical Framework document
- Removed HIPAA and CLIA as these are guiding regulations, not standards
- Removed Health Level Seven (HL7) Version 3.0 Clinical Document Architecture (CDA/CDA R2) as it is indirectly referenced by the IHE Laboratory Technical Framework standard.
Upon approval by the HITSP Panel on March 27, 2008, this document is now Released for Implementation.
This document has been modified to reflect the updated HITSP approach to categorizing standards as Regulatory Guidance, Selected Standards, and Informative References.
The following standard has been added to the standards listing
- Health Level Seven (HL7) Clinical Document Architecture Release 2 (CDA R2)
The title of the document was updated by removing the reference to IHE XD* Lab. Please see previous Change History items for more informationon the standard list update that drove this change.
Upon approval by the HITSP Panel on August 27, 2008, this document is now Released for Implementation.
Minor editorial changes were made to this document. Removed boilerplate text for simplification. The term actor was replaced with interface.
Upon approval by the HITSP Panel on July 8, 2009, this document is now Released for Implementation.
[1] Adapted from HL7 CDA r2, 1.1 CDA Overview
[2] Although IHE discusses use in PHR applications, such use is outside the scope of the current AHIC Use Cases.
[3] IHE LAB TF-3 1.1 Scope
[4] HITSP has submitted comments to IHE to extend the LAB TF-3 Integration Profile to include: the CLIA requirement for Reference Laboratory Name and Address and Name of Medical Director, and the Intended Recipients of the document
[5] IHE LAB TF-3 4.1.1 Header Rendering
[6] IHE LAB TF-3 4.2 Level 2: Human-readable body of the report
[7] IHE LAB TF-3 4.4 Level 3 entries dedicated to multimedia rendering
[8] IHE LAB TF-3 4.4.1 Global model and general rules
[9] : In contrast to the above quotation regarding Level 3 entries, machine-readable observation entries are REQUIRED for all AHIC Use Cases
[10] A gap exists for a mapping from the HL7 V2.5.1[10] Laboratory Result message to a CDA-Lab document
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