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Resource ValueSet/FHIR Server from package hl7.terminology#current (16 ms)

Package hl7.terminology
Type ValueSet
Id Id
FHIR Version R5
Source http://terminology.hl7.org/https://build.fhir.org/ig/HL7/UTG/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
Experimental False
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

ValueSet
v3-ClinicalResearchReason ClinicalResearchReason

Resources that this resource uses

CodeSystem
v3-ActReason ActReason
v3-ActReason v3 Code System ActReason


Narrative

Note: links and images are rebased to the (stated) source

Generated Narrative: ValueSet v3-ClinicalResearchObservationReason

Language: en

  • Include these codes as defined in http://terminology.hl7.org/CodeSystem/v3-ActReason
    CodeDisplayDefinition
    NPTnon-protocol**Definition:**The observation or test was neither defined or scheduled in the study protocol.
    PPTper 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.
    UPTper 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" : "<div xmlns=\"http://www.w3.org/1999/xhtml\" xml:lang=\"en\" lang=\"en\"><p class=\"res-header-id\"><b>Generated Narrative: ValueSet v3-ClinicalResearchObservationReason</b></p><a name=\"v3-ClinicalResearchObservationReason\"> </a><a name=\"hcv3-ClinicalResearchObservationReason\"> </a><a name=\"v3-ClinicalResearchObservationReason-en-US\"> </a><div style=\"display: inline-block; background-color: #d9e0e7; padding: 6px; margin: 4px; border: 1px solid #8da1b4; border-radius: 5px; line-height: 60%\"><p style=\"margin-bottom: 0px\">Language: en</p></div><ul><li>Include these codes as defined in <a href=\"CodeSystem-v3-ActReason.html\"><code>http://terminology.hl7.org/CodeSystem/v3-ActReason</code></a><table class=\"none\"><tr><td style=\"white-space:nowrap\"><b>Code</b></td><td><b>Display</b></td><td><b>Definition</b></td></tr><tr><td><a href=\"CodeSystem-v3-ActReason.html#v3-ActReason-NPT\">NPT</a></td><td style=\"color: #cccccc\">non-protocol</td><td>**Definition:**The observation or test was neither defined or scheduled in the study protocol.</td></tr><tr><td><a href=\"CodeSystem-v3-ActReason.html#v3-ActReason-PPT\">PPT</a></td><td style=\"color: #cccccc\">per protocol</td><td>**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.</td></tr><tr><td><a href=\"CodeSystem-v3-ActReason.html#v3-ActReason-UPT\">UPT</a></td><td style=\"color: #cccccc\">per definition</td><td>**:**The observation or test occurred as defined in the research protocol, but at a point in time not specified in the study protocol.</td></tr></table></li></ul></div>"
  },
  "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"
          }
        ]
      }
    ]
  }
}

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