FHIR CI-Build

This is the Continuous Integration Build of FHIR (will be incorrect/inconsistent at times).
See the Directory of published versions

Example RiskAssessment/breastcancer-risk (XML)

Clinical Decision Support Work GroupMaturity Level: N/AStandards Status: InformativeCompartments: Device, Patient, Practitioner

Raw XML (canonical form + also see XML Format Specification)

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Breast cancer risk assessment (id = "breastcancer-risk")

<?xml version="1.0" encoding="UTF-8"?>

<RiskAssessment xmlns="http://hl7.org/fhir">
  <id value="breastcancer-risk"/> 
  <text> 
    <status value="additional"/> <div xmlns="http://www.w3.org/1999/xhtml">
      <table> 
        <tr> 
          <td colspan="2">
            <h1> Information about your risk score:</h1> 
          </td> 
        </tr> 
        <tr> 
          <td> 
            <strong> Birthdate:</strong> 
          </td> 
          <td> 1981-01-01</td> 
        </tr> 
        <tr> 
          <td> 
            <strong> Gender:</strong> 
          </td> 
          <td> female</td> 
        </tr> 
        <tr> 
          <td> 
            <strong> Ethnicity:</strong> 
          </td> 
          <td> Unknown / Not Reported</td> 
        </tr> 
      </table> 
    </div> 
  </text> 
  <identifier> 
    <use value="official"/> 
    <system value="http://example.org"/> 
    <value value="risk-assessment-breastcancer1"/> 
  </identifier> 
  <status value="final"/> 
  <code> 
    <coding> 
      <system value="http://browser.ihtsdotools.org/"/> 
      <code value="709510001"/> 
      <display value="Assessment of risk for disease (procedure)"/> 
    </coding> 
  </code> 
  <subject> 
    <reference value="Patient/example"/> 
  </subject> 
  <performer> 
    <reference value="Practitioner/example"/> 
  </performer> 
  <basis> 
    <reference value="Observation/example-genetics-brcapat"/> 
  </basis> 
  <prediction> 
    <outcome> 
      <text value="Unknown risk of developing breast cancer"/> 
    </outcome> 
  </prediction> 
  <note> 
    <text value="This risk assessment is based on BRCA1 and BRCA2 genetic mutation test"/> 
  </note> 
</RiskAssessment> 

Usage note: every effort has been made to ensure that the examples are correct and useful, but they are not a normative part of the specification.