FHIR IG Statistics: ValueSet/v3-ClinicalResearchObservationReason
| Package | hl7.terminology.r4b |
| Type | ValueSet |
| Id | v3-ClinicalResearchObservationReason |
| FHIR Version | R4B |
| Source | http://terminology.hl7.org/http://terminology.hl7.org/6.0.2/ValueSet-v3-ClinicalResearchObservationReason.html |
| URL | http://terminology.hl7.org/ValueSet/v3-ClinicalResearchObservationReason |
| Version | 3.0.0 |
| Status | active |
| Date | 2014-03-26 |
| Name | ClinicalResearchObservationReason |
| Title | ClinicalResearchObservationReason |
| Realm | uv |
| Authority | hl7 |
| Description | **Definition:**SSpecifies the reason that a test was performed or observation collected in a clinical research study.
**Note:**This set of codes are not strictly reasons, but are used in the currently Normative standard. Future revisions of the specification will model these as ActRelationships and thes codes may subsequently be retired. Thus, these codes should not be used for new specifications. |
| Copyright | This material derives from the HL7 Terminology THO. THO is copyright ©1989+ Health Level Seven International and is made available under the CC0 designation. For more licensing information see: https://terminology.hl7.org/license.html |
Resources that use this resource
Resources that this resource uses
Narrative
Note: links and images are rebased to the (stated) source
- Include these codes as defined in
http://terminology.hl7.org/CodeSystem/v3-ActReason| Code | Display | Definition |
| NPT | non-protocol | **Definition:**The observation or test was neither defined or scheduled in the study protocol. |
| PPT | per protocol | **Definition:**The observation or test occurred due to it being defined in the research protocol, and during an activity or event that was scheduled in the protocol. |
| UPT | per definition | **:**The observation or test occurred as defined in the research protocol, but at a point in time not specified in the study protocol. |
Source
{
"resourceType": "ValueSet",
"id": "v3-ClinicalResearchObservationReason",
"language": "en",
"text": {
"status": "extensions",
"div": "<!-- snip (see above) -->"
},
"url": "http://terminology.hl7.org/ValueSet/v3-ClinicalResearchObservationReason",
"identifier": [
{
"system": "urn:ietf:rfc:3986",
"value": "urn:oid:2.16.840.1.113883.1.11.19756"
}
],
"version": "3.0.0",
"name": "ClinicalResearchObservationReason",
"title": "ClinicalResearchObservationReason",
"status": "active",
"experimental": false,
"date": "2014-03-26",
"publisher": "Health Level Seven International",
"contact": [
{
"telecom": [
{
"system": "url",
"value": "http://hl7.org"
},
{
"system": "email",
"value": "hq@HL7.org"
}
]
}
],
"description": "**Definition:**SSpecifies the reason that a test was performed or observation collected in a clinical research study.\r\n\r\n**Note:**This set of codes are not strictly reasons, but are used in the currently Normative standard. Future revisions of the specification will model these as ActRelationships and thes codes may subsequently be retired. Thus, these codes should not be used for new specifications.",
"copyright": "This material derives from the HL7 Terminology THO. THO is copyright ©1989+ Health Level Seven International and is made available under the CC0 designation. For more licensing information see: https://terminology.hl7.org/license.html",
"compose": {
"include": [
{
"system": "http://terminology.hl7.org/CodeSystem/v3-ActReason",
"concept": [
{
"code": "NPT"
},
{
"code": "PPT"
},
{
"code": "UPT"
}
]
}
]
}
}
FHIR