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1.
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Clear description of the referenced document:
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Name:
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HL7 CDA-PHMR (2010)
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Title:
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HL7 Implementation Guide for CDA Release 2.0: Personal Healthcare Monitoring Report (PHMR), International Realm. Release 1.1.
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2.
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Status of approval:
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HL7 Draft Standard for Trial Use (DSTU) approved on 2010-10.
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3.
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Justification for the specific reference:
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The Continua Design Guidelines architecture uses HL7 Healthcare Monitoring Reports (PHMR). The purpose of HL7 CDA-PHMR is to describe constraints on the HL7 Clinical Document Architecture (CDA) Header and Body elements for Personal Healthcare Monitoring Report (PHMR) documents mostly containing analysed and raw information of data generated by personal healthcare monitoring devices such as glucometers, BP cuffs, thermometers, weight scales, etc.
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4.
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Current information, if any, about IPR issues:
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N/A
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5.
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Other useful information describing the "Quality" of the document:
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Second release (Release 1.1) of the Draft Standard for Trial Use (DSTU) for Personal Healthcare Monitoring Report in the HL7 Clinical Document Architecture (CDA) was issued in October 2010. After the comment period of 24 months, the document is expected to progress into a Standard phase based on comments received.
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6.
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The degree of stability or maturity of the document:
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See 5. above.
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7.
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Relationship with other existing or emerging documents:
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See 5. above.
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8.
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Any explicit references within that referenced document should also be listed:
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IETF RFC 2806 "URLs for Telephone Calls"/
Health Level Seven (2005-04), HL7 Clinical Document Architecture, Release 2.0/
IEEE 11073, /
SNOMED CT/
UCUM.
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9.
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Qualification of
HL7:
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Health Level 7 meets the qualifying criteria for normative referencing as per Recommendation ITU-T A.5.
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10.
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Other (for any supplementary information):
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N/A
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