NHS North West Genomics
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: ServiceRequest ctDNA Example

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<ServiceRequest xmlns="http://hl7.org/fhir">
  <id value="ServiceRequest-ctDNA"/>
  <meta>
    <versionId value="1.0"/>
    <profile
             value="https://fhir.nwgenomics.nhs.uk/StructureDefinition/ServiceRequest"/>
  </meta>
  <language value="en"/>
  <text>
    <status value="generated"/>
    <div xmlns="http://www.w3.org/1999/xhtml"><p class="res-header-id"><b>Generated Narrative: ServiceRequest ServiceRequest-ctDNA</b></p><a name="ServiceRequest-ctDNA"> </a><a name="hcServiceRequest-ctDNA"> </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">version: 1.0</p><p style="margin-bottom: 0px">Profile: <a href="StructureDefinition-ServiceRequest.html">ServiceRequest</a></p></div><p><b>identifier</b>: Filler Identifier/T26-59XG</p><p><b>requisition</b>: Placer Group Number/R26-15AY</p><p><b>status</b>: Active</p><p><b>intent</b>: Order</p><p><b>category</b>: <span title="Codes:{http://snomed.info/sct 116148004}">Molecular genetics procedure</span></p><p><b>code</b>: <span title="Codes:{https://fhir.nhs.uk/CodeSystem/England-GenomicTestDirectory M4.14}">Non-Small Cell Lung Cancer, Multi-target ctDNA combined Multi-target NGS panel, small variant (EGFR, ALK, BRAF, KRAS, MET exon 14 skipping and copy number variations) and structural variant (ROS1, RET, ALK, NTRK1, NTRK2, NTRK3, MET exon</span></p><p><b>subject</b>: <a href="Bundle-FHIRDocumentGeneticReportBundle-ctDNA.html#urn-uuid-2160525b-0168-4f40-8ebf-9b053052a62c">Theon SHEFFIELD</a></p><p><b>requester</b>: Identifier: <a href="NamingSystem-ods-organization-code-namingsystem.html" title="The identifier system for an Organisation registered with the Organisation Data Service (ODS).">ODS Organisation Code</a>/RHQ</p><p><b>performer</b>: Identifier: <a href="NamingSystem-ods-organization-code-namingsystem.html" title="The identifier system for an Organisation registered with the Organisation Data Service (ODS).">ODS Organisation Code</a>/699X0</p><p><b>reasonCode</b>: <span title="Codes:{https://fhir.nwgenomics.nhs.uk/CodeSystem/GenomicClinicalIndication M4}">M4</span></p><p><b>specimen</b>: <a href="Bundle-FHIRDocumentGeneticReportBundle-ctDNA.html#urn-uuid-b930b4c4-327a-4728-8bb9-f90061914cc5">Specimen: identifier = Filler Identifier; status = available; type = Blood specimen</a></p></div>
  </text>
  <identifier>
    <type>
      <coding>
        <system value="http://terminology.hl7.org/CodeSystem/v2-0203"/>
        <code value="FILL"/>
      </coding>
    </type>
    <system value="https://fhir.nwgenomics.nhs.uk/iGene/ReportIdentifier"/>
    <value value="T26-59XG"/>
    <assigner>
      <identifier>
        <system value="https://fhir.nhs.uk/Id/ods-organization-code"/>
        <value value="699X0"/>
      </identifier>
    </assigner>
  </identifier>
  <requisition>
    <type>
      <coding>
        <system value="http://terminology.hl7.org/CodeSystem/v2-0203"/>
        <code value="PGN"/>
      </coding>
    </type>
    <system value="https://fhir.nwgenomics.nhs.uk/iGene/ReferralIdentifier"/>
    <value value="R26-15AY"/>
    <assigner>
      <identifier>
        <system value="https://fhir.nhs.uk/Id/ods-organization-code"/>
        <value value="699X0"/>
      </identifier>
    </assigner>
  </requisition>
  <status value="active"/>
  <intent value="order"/>
  <category>
    <coding>
      <system value="http://snomed.info/sct"/>
      <code value="116148004"/>
      <display value="Molecular genetics procedure"/>
    </coding>
  </category>
  <code>
    <coding>
      <system
              value="https://fhir.nhs.uk/CodeSystem/England-GenomicTestDirectory"/>
      <code value="M4.14"/>
    </coding>
  </code>
  <subject>
    <reference value="urn:uuid:2160525b-0168-4f40-8ebf-9b053052a62c"/>
    <identifier>
      <system value="https://fhir.nhs.uk/Id/nhs-number"/>
      <value value="9737873858"/>
    </identifier>
    <display value="Theon SHEFFIELD"/>
  </subject>
  <requester>
    <type value="Organization"/>
    <identifier>
      <system value="https://fhir.nhs.uk/Id/ods-organization-code"/>
      <value value="RHQ"/>
    </identifier>
  </requester>
  <performer>
    <type value="Organization"/>
    <identifier>
      <system value="https://fhir.nhs.uk/Id/ods-organization-code"/>
      <value value="699X0"/>
    </identifier>
  </performer>
  <reasonCode>
    <coding>
      <system
              value="https://fhir.nwgenomics.nhs.uk/CodeSystem/GenomicClinicalIndication"/>
      <code value="M4"/>
    </coding>
  </reasonCode>
  <specimen>
    <reference value="urn:uuid:b930b4c4-327a-4728-8bb9-f90061914cc5"/>
  </specimen>
</ServiceRequest>