Common Data Models Harmonization
1.0.0 - STU 1 Publication

This page is part of the Common Data Models Harmonization FHIR IG (v1.0.0: STU 1) based on FHIR R4. This is the current published version in its permanent home (it will always be available at this URL). For a full list of available versions, see the Directory of published versions

: PCORNet Pro Type - JSON Representation

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{
  "resourceType" : "CodeSystem",
  "id" : "pcornet-pro-type",
  "text" : {
    "status" : "generated",
    "div" : "<div xmlns=\"http://www.w3.org/1999/xhtml\"><p>This code system http://hl7.org/fhir/us/cdmh/CodeSystem/pcornet-pro-type defines the following codes:</p><table class=\"codes\"><tr><td style=\"white-space:nowrap\"><b>Code</b></td><td><b>Display</b></td><td><b>Definition</b></td></tr><tr><td style=\"white-space:nowrap\">PM<a name=\"pcornet-pro-type-PM\"> </a></td><td>PROMIS</td><td>Self-reported and parent-reported measures of global, physical, mental, and social health for adults and children in the general population and those living with a chronic condition.</td></tr><tr><td style=\"white-space:nowrap\">NQ<a name=\"pcornet-pro-type-NQ\"> </a></td><td>Neuro-QoL</td><td>Self-reported and proxy-reported measures of physical, mental, and social health for adults and children living with a neurological condition.</td></tr><tr><td style=\"white-space:nowrap\">AM<a name=\"pcornet-pro-type-AM\"> </a></td><td>ASQC-Me</td><td>Self-reported measures of physical, mental, and social health for adults living with sickle cell disease.</td></tr><tr><td style=\"white-space:nowrap\">NT<a name=\"pcornet-pro-type-NT\"> </a></td><td>NIH Toolbox</td><td>Performance tests of cognitive, motor, and sensory function and self-reported measures of emotional function for adults and children in the general population and those living with a chronic condition.</td></tr><tr><td style=\"white-space:nowrap\">PC<a name=\"pcornet-pro-type-PC\"> </a></td><td>PRO_CTCAE</td><td>A patient-reported outcome measurement system developed by the National Cancer Institute to capture symptomatic adverse events in patients on cancer clinical trials.</td></tr><tr><td style=\"white-space:nowrap\">LC<a name=\"pcornet-pro-type-LC\"> </a></td><td>LOINC</td><td>Terminology / vocabulary used to describe the PRO item is LOINC.</td></tr><tr><td style=\"white-space:nowrap\">HC<a name=\"pcornet-pro-type-HC\"> </a></td><td>HCAHPS</td><td>HCAHPS initiative is to provide a standardized survey instrument and data collection methodology for measuring patients perspectives on hospital care.</td></tr><tr><td style=\"white-space:nowrap\">NI<a name=\"pcornet-pro-type-NI\"> </a></td><td>No information</td><td>Terminology / vocabulary used to describe the PRO item is No information.</td></tr><tr><td style=\"white-space:nowrap\">UN<a name=\"pcornet-pro-type-UN\"> </a></td><td>Unknown</td><td>Terminology / vocabulary used to describe the PRO item is Unknown.</td></tr><tr><td style=\"white-space:nowrap\">OT<a name=\"pcornet-pro-type-OT\"> </a></td><td>Other</td><td>Terminology / vocabulary used to describe the PRO item is Other.</td></tr></table></div>"
  },
  "url" : "http://hl7.org/fhir/us/cdmh/CodeSystem/pcornet-pro-type",
  "version" : "1.0.0",
  "name" : "PCORNetProType",
  "title" : "PCORNet Pro Type",
  "status" : "active",
  "date" : "2021-09-06",
  "publisher" : "HL7 International - Biomedical Research and Regulation Work Group",
  "contact" : [
    {
      "telecom" : [
        {
          "system" : "url",
          "value" : "http://hl7.org/Special/committees/rcrim"
        }
      ]
    }
  ],
  "description" : "The PCORNet Pro Type contains the codes to be used by PCORNet data marts.",
  "jurisdiction" : [
    {
      "coding" : [
        {
          "system" : "urn:iso:std:iso:3166",
          "code" : "US"
        }
      ]
    }
  ],
  "copyright" : "Used by permission of HL7, all rights reserved Creative Commons License",
  "caseSensitive" : true,
  "content" : "complete",
  "count" : 9,
  "concept" : [
    {
      "code" : "PM",
      "display" : "PROMIS",
      "definition" : "Self-reported and parent-reported measures of global, physical, mental, and social health for adults and children in the general population and those living with a chronic condition."
    },
    {
      "code" : "NQ",
      "display" : "Neuro-QoL",
      "definition" : "Self-reported and proxy-reported measures of physical, mental, and social health for adults and children living with a neurological condition."
    },
    {
      "code" : "AM",
      "display" : "ASQC-Me",
      "definition" : "Self-reported measures of physical, mental, and social health for adults living with sickle cell disease."
    },
    {
      "code" : "NT",
      "display" : "NIH Toolbox",
      "definition" : "Performance tests of cognitive, motor, and sensory function and self-reported measures of emotional function for adults and children in the general population and those living with a chronic condition."
    },
    {
      "code" : "PC",
      "display" : "PRO_CTCAE",
      "definition" : "A patient-reported outcome measurement system developed by the National Cancer Institute to capture symptomatic adverse events in patients on cancer clinical trials."
    },
    {
      "code" : "LC",
      "display" : "LOINC",
      "definition" : "Terminology / vocabulary used to describe the PRO item is LOINC."
    },
    {
      "code" : "HC",
      "display" : "HCAHPS",
      "definition" : "HCAHPS initiative is to provide a standardized survey instrument and data collection methodology for measuring patients perspectives on hospital care."
    },
    {
      "code" : "NI",
      "display" : "No information",
      "definition" : "Terminology / vocabulary used to describe the PRO item is No information."
    },
    {
      "code" : "UN",
      "display" : "Unknown",
      "definition" : "Terminology / vocabulary used to describe the PRO item is Unknown."
    },
    {
      "code" : "OT",
      "display" : "Other",
      "definition" : "Terminology / vocabulary used to describe the PRO item is Other."
    }
  ]
}