This material contains content that is copyright of SNOMED International. Implementers of these specifications must have the appropriate SNOMED CT Affiliate license - for more information contact https://www.snomed.org/get-snomed
or info@snomed.org
.
Allergy intolerance codes value set. This value set includes codes from SNOMED Clinical Terms®: all descendants of 373873005 |Pharmaceutical / biologic product (product)|; all descendants of 105590001 |Substance (substance)|; all descendants of 418038007 |Propensity to adverse reactions to substance (finding)| plus codes for absent and unknown allergies. ( src
)
Allergy intolerance substances value set. This value set includes codes from SNOMED Clinical Terms®: all descendants of 373873005 |Pharmaceutical / biologic product (product)|; all descendants of 105590001 |Substance (substance)|; all descendants of 418038007 |Propensity to adverse reactions to substance (finding)| ( src
)
Code of Federal Regulation 21CFR§1271.290(c) ( src
)
HDR exposure agent value set. This value set includes codes from SNOMED Clinical Terms®: all descendants of 40733004 "Infectious disease (disorder)" and ICD-10 all descendants of chapter I: "Certain infectious and parasitic diseases" ( src
)
HL7 Europe Hospital Discharge Report, published by HL7 Europe. This guide is not an authorized publication; it is the continuous build for version 0.0.1-ci built by the FHIR (HL7® FHIR® Standard) CI Build. This version is based on the current content of https://github.com/hl7-eu/hdr/ 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
)
This value set includes codes from SNOMED Clinical Terms (SNOMED CT®) that are included in: all descendants of 49062001 |Device (physical object)|, plus IPS codes for absent/unknown devices. ( src
)
This value set includes codes from SNOMED Clinical Terms®: all descendants of 49062001 |Device (physical object)|. ( src
)
This value set includes codes from SNOMED Clinical Terms®: descendants of 71388002 |Procedure (procedure)|, excluding [all subtypes of 14734007 |Administrative procedure (procedure)|, all subtypes of 59524001 |Blood bank procedure (procedure)|, all subtypes of 389067005 |Community health procedure (procedure)|, all subtypes of 442006003 |Determination of information related to transfusion (procedure)|, all subtypes of 225288009 |Environmental care procedure (procedure)|, all subtypes of 308335008 |Patient encounter procedure (procedure)|, all subtypes of 710135002 |Promotion (procedure)|, all subtypes of 389084004 |Staff related procedure (procedure)|], plus IPS codes for absent/unknown procedures. ( src
)
This value set includes codes from SNOMED Clinical Terms®: descendants of 71388002 |Procedure (procedure)|, excluding [all subtypes of 14734007 |Administrative procedure (procedure)|, all subtypes of 59524001 |Blood bank procedure (procedure)|, all subtypes of 389067005 |Community health procedure (procedure)|, all subtypes of 442006003 |Determination of information related to transfusion (procedure)|, all subtypes of 225288009 |Environmental care procedure (procedure)|, all subtypes of 308335008 |Patient encounter procedure (procedure)|, all subtypes of 710135002 |Promotion (procedure)|, all subtypes of 389084004 |Staff related procedure (procedure)|]. ( src
)
HL7 Europe Hospital Discharge Report, published by HL7 Europe. This guide is not an authorized publication; it is the continuous build for version 0.0.1-ci built by the FHIR (HL7® FHIR® Standard) CI Build. This version is based on the current content of https://github.com/hl7-eu/hdr/
and changes regularly. See the Directory of published versions
This guide is part of the group of HL7 FHIR Implementation Guides published by HL7 Europe (see figure 1) to support the priority categories identified by the European Health Data Space Regulation
(EHDS).
empower individuals to take control of their health data and facilitate the exchange of data for the delivery of healthcare across the EU primary use of data
provide a consistent, trustworthy, and efficient system for reusing health data for research, innovation, policy-making, and regulatory activities secondary use of data
The EEHRxF will be defined by the European Commission through a set of Implementation Acts: a proposal for these Acts is being prepared by the Joint Action 09 (Xt-EHR)
Specify a set of rules to be applied to HL7 FHIR to define how to represent a Hospital Discharge Report
in the European
Context, coherently with the European eHN Guidelines (see the European eHealth - Key documents
).
This guide is part of the group of HL7 FHIR Implementation Guides published by HL7 Europe to support the priority categories identified by the European Health Data Space Regulation
(EHDS).