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HITSP C37 Lab Report Document Component


Type:Data Agreement
Scope:This section describes the contents of this specification and provides a high level definition of this Component and background information about the underlying standards that the Component is based on.
The purpose of this Component is to describe the specification for an electronic document as required by the AHIC EHR and Biosurveillance Use Cases. This is based upon the standard Health Level Seven (HL7) Clinical Document Architecture Release 2 (CDA R2), as in the HL7 V3 2006 normative edition. The goals supported by this Component specification are stated in the EHR and Biosurveillance Use Cases:
- Transmission of complete, preliminary, final and updated laboratory results to the EHR system (local or remote) of the ordering clinician
- Transmission of complete, preliminary, final and updated (or notification) laboratory results to the EHR system (local or remote) or other clinical data system of designated providers of care (with respect to a specific patient)
- Transmit laboratory result data from electronically enabled healthcare delivery and public health systems in standardized and anonymized format to authorized Public Health Agencies with less than one day lag time
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Relationship Organization Item
references HITSP Result   

There are no Value Domains linked to HITSP C37 Lab Report Document Component.

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