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"may provide both synthetic anamnesis (e.g. description of phases of the pathology as
a chronological summary of clustered clinical information) and anecdotal evidence that clinicians can collect from the patient, and can read in a narrative form. See Section 2, Chapter III, Art 7, (c)." ( src
)
Code of Federal Regulation 21CFR§1271.290(c) ( src
)
HL7 Europe Patient Summary, published by HL7 Europe. This guide is not an authorized publication; it is the continuous build for version 1.0.0-ci-build built by the FHIR (HL7® FHIR® Standard) CI Build. This version is based on the current content of https://github.com/hl7-eu/eps/ and changes regularly. See the Directory of published versions ( src
)
There are examples where a medication request may include the option of an oral dose or an Intravenous or Intramuscular dose. For example, "Ondansetron 8mg orally or IV twice a day as needed for nausea" or "Compazine® (prochlorperazine) 5-10mg PO or 25mg PR bid prn nausea or vomiting". In these cases, two medication requests would be created that could be grouped together. The decision on which dose and route of administration to use is based on the patient's condition at the time the dose is needed. ( src
)
HL7 Europe Patient Summary, published by HL7 Europe. This guide is not an authorized publication; it is the continuous build for version 1.0.0-ci-build built by the FHIR (HL7® FHIR® Standard) CI Build. This version is based on the current content of https://github.com/hl7-eu/eps/
and changes regularly. See the Directory of published versions
For example codes, see
eHDSI Dose Form http://hl7.org/fhir/ValueSet/medication-form-codes|4.0.1
( example
to http://terminology.ehdsi.eu/ValueSet/eHDSIDoseForm
)
The UCUM codes, UCUM table (regardless of format), and UCUM Specification are copyright 1999-2009, Regenstrief Institute, Inc. and the Unified Codes for Units of Measures (UCUM) Organization. All rights reserved. https://ucum.org/trac/wiki/TermsOfUse
Specify a set of rules to be applied to HL7 FHIR to define how to represent a Patient Summary
in the European
Context, coherently with the European eHN Guidelines (see the European eHealth - Key documents
).
s
The Xt-EHR Joint Action
has developed a set of Logical data models (or information models) - see Xt-EHR EHDS Logical Information Models
Implementation Guide - that have been used as basis
for the future European Health Data Space (EHDS)
Implementing Act.
The Xt-EHR Joint Action
has developed a set of Logical data models (or information models) - see Xt-EHR EHDS Logical Information Models
Implementation Guide - that have been used as basis
for the future European Health Data Space (EHDS)
Implementing Act.
They represent evolving, refined interpretations
of the data sets described in the eHealth Network (eHN) Guidelines
, and are subject to further refinement.
