Breast Cancer Screening and Management (BCSM) Clinical Decision Support (CDS) Implementation Guide
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: GeneticRiskReferral_eve-fhxgeneinherited_no_eve-brcageneancestry_no_eve-fhxbrcaovcatubalperit_yes_act-fhxrisktool_act-fhxriskassess - XML Representation

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<Bundle xmlns="http://hl7.org/fhir">
  <id
      value="GeneticRiskReferral_eve-fhxgeneinherited_no_eve-brcageneancestry_no_eve-fhxbrcaovcatubalperit_yes_act-fhxrisktool_act-fhxriskassess"/>
  <type value="collection"/>
  <entry>
    <fullUrl
             value="http://cancerscreeningcds.github.io/bcsm-cds/CarePlan/395"/>
    <resource>
      <CarePlan>
        <id value="395"/>
        <text>
          <status value="generated"/>
          <div xmlns="http://www.w3.org/1999/xhtml"><a name="CarePlan_395"> </a><p class="res-header-id"><b>Generated Narrative: CarePlan 395</b></p><a name="395"> </a><a name="hc395"> </a><a name="395-en-US"> </a><p><b>instantiatesCanonical</b>: <a href="PlanDefinition-flow-GeneticRiskReferral.html">Genetic Risk Referral</a></p><p><b>status</b>: Draft</p><p><b>intent</b>: Proposal</p><p><b>subject</b>: <a href="Bundle-eve-Age45to54_act-acsavgrecs45_act-uspstfavgrecs.html#Patient_defaultPatient">Jane Doe</a></p><p><b>created</b>: 2024-12-10 00:00:00+0000</p><h3>Activities</h3><table class="grid"><tr><td style="display: none">-</td><td><b>Reference</b></td></tr><tr><td style="display: none">*</td><td><a href="Bundle-GeneticRiskReferral_eve-fhxgeneinherited_no_eve-brcageneancestry_no_eve-fhxbrcaovcatubalperit_yes_act-fhxrisktool_act-fhxriskassess.html#RequestGroup_396">Bundle: type = collection</a></td></tr></table></div>
        </text>
        <instantiatesCanonical
                               value="http://cancerscreeningcds.github.io/bcsm-cds/PlanDefinition/flow-GeneticRiskReferral"/>
        <status value="draft"/>
        <intent value="proposal"/>
        <subject>
          <reference value="Patient/defaultPatient"/>
          <display value="Jane Doe"/>
        </subject>
        <created value="2024-12-10T00:00:00.0Z"/>
        <activity>
          <reference>
            <reference value="RequestGroup/396"/>
          </reference>
        </activity>
      </CarePlan>
    </resource>
  </entry>
  <entry>
    <fullUrl
             value="http://cancerscreeningcds.github.io/bcsm-cds/RequestGroup/396"/>
    <resource>
      <RequestGroup>
        <id value="396"/>
        <text>
          <status value="generated"/>
          <div xmlns="http://www.w3.org/1999/xhtml"><a name="RequestGroup_396"> </a><p class="res-header-id"><b>Generated Narrative: RequestGroup 396</b></p><a name="396"> </a><a name="hc396"> </a><a name="396-en-US"> </a><p><b>instantiatesCanonical</b>: <a href="PlanDefinition-flow-GeneticRiskReferral.html">Genetic Risk Referral</a></p><p><b>status</b>: Draft</p><p><b>intent</b>: Proposal</p><p><b>subject</b>: <a href="Bundle-eve-Age45to54_act-acsavgrecs45_act-uspstfavgrecs.html#Patient_defaultPatient">Jane Doe</a></p><blockquote><p><b>action</b></p><blockquote><p><b>id</b></p>GeneticRiskAssessment</blockquote><p><b>title</b>: Perform genetic risk assessment</p><p><b>description</b>: A genetic risk assessment, either informal or formal using a validated instrument, will help determine if the patient may benefit from referral for genetic risk counseling and testing.

Women with a positive result on the risk assessment tool should receive genetic counseling and, if indicated after counseling, genetic testing.</p><h3>Documentations</h3><table class="grid"><tr><td style="display: none">-</td><td><b>Type</b></td><td><b>Label</b></td><td><b>Display</b></td><td><b>Citation</b></td><td><b>Url</b></td></tr><tr><td style="display: none">*</td><td>Citation</td><td>USPSTF</td><td>BRCA-Related Cancer: Risk Assessment, Genetic Counseling, and Genetic Testing</td><td><div><p>US Preventive Services Task Force. Risk Assessment, Genetic Counseling, and Genetic Testing for BRCA-Related Cancer: US Preventive Services Task Force Recommendation Statement. JAMA. 2019;322(7):652–665.</p>
</div></td><td><a href="https://www.uspreventiveservicestaskforce.org/uspstf/recommendation/brca-related-cancer-risk-assessment-genetic-counseling-and-genetic-testing">https://www.uspreventiveservicestaskforce.org/uspstf/recommendation/brca-related-cancer-risk-assessment-genetic-counseling-and-genetic-testing</a></td></tr></table><p><b>selectionBehavior</b>: Any</p><blockquote><p><b>action</b></p><blockquote><p><b>id</b></p>FhxGeneticRiskAssessment</blockquote><p><b>title</b>: Informal genetic risk assessment</p><p><b>description</b>: Perform assessment based on criteria in first- or second-degree blood relatives known to be associated with increased risk of inherited breast cancer susceptibility variant.</p><p><b>resource</b>: <a href="Bundle-GeneticRiskReferral_eve-fhxgeneinherited_no_eve-brcageneancestry_no_eve-fhxbrcaovcatubalperit_yes_act-fhxrisktool_act-fhxriskassess.html#ServiceRequest_397">Bundle: type = collection</a></p></blockquote><blockquote><p><b>action</b></p><blockquote><p><b>id</b></p>FhxGeneticRiskAssessmentTool</blockquote><p><b>title</b>: Genetic risk assessment instrument</p><p><b>description</b>: Tools evaluated by the USPSTF include the Ontario Family History Assessment Tool, Manchester Scoring System, Referral Screening Tool, Pedigree Assessment Tool, 7-Question Family History Screening Tool, International Breast Cancer Intervention Study instrument (Tyrer-Cuzick), and brief versions of BRCAPRO. </p><p><b>resource</b>: <a href="Bundle-GeneticRiskReferral_eve-fhxgeneinherited_no_eve-brcageneancestry_no_eve-fhxbrcaovcatubalperit_yes_act-fhxrisktool_act-fhxriskassess.html#ServiceRequest_398">Bundle: type = collection</a></p></blockquote></blockquote></div>
        </text>
        <instantiatesCanonical
                               value="http://cancerscreeningcds.github.io/bcsm-cds/PlanDefinition/flow-GeneticRiskReferral"/>
        <status value="draft"/>
        <intent value="proposal"/>
        <subject>
          <reference value="Patient/defaultPatient"/>
          <display value="Jane Doe"/>
        </subject>
        <action id="GeneticRiskAssessment">
          <title value="Perform genetic risk assessment"/>
          <description
                       value="A genetic risk assessment, either informal or formal using a validated instrument, will help determine if the patient may benefit from referral for genetic risk counseling and testing.

Women with a positive result on the risk assessment tool should receive genetic counseling and, if indicated after counseling, genetic testing."/>
          <documentation>
            <type value="citation"/>
            <label value="USPSTF"/>
            <display
                     value="BRCA-Related Cancer: Risk Assessment, Genetic Counseling, and Genetic Testing"/>
            <citation
                      value="US Preventive Services Task Force. Risk Assessment, Genetic Counseling, and Genetic Testing for BRCA-Related Cancer: US Preventive Services Task Force Recommendation Statement. JAMA. 2019;322(7):652–665."/>
            <url
                 value="https://www.uspreventiveservicestaskforce.org/uspstf/recommendation/brca-related-cancer-risk-assessment-genetic-counseling-and-genetic-testing"/>
          </documentation>
          <selectionBehavior value="any"/>
          <action id="FhxGeneticRiskAssessment">
            <title value="Informal genetic risk assessment"/>
            <description
                         value="Perform assessment based on criteria in first- or second-degree blood relatives known to be associated with increased risk of inherited breast cancer susceptibility variant."/>
            <resource>
              <reference value="ServiceRequest/397"/>
            </resource>
          </action>
          <action id="FhxGeneticRiskAssessmentTool">
            <title value="Genetic risk assessment instrument"/>
            <description
                         value="Tools evaluated by the USPSTF include the Ontario Family History Assessment Tool, Manchester Scoring System, Referral Screening Tool, Pedigree Assessment Tool, 7-Question Family History Screening Tool, International Breast Cancer Intervention Study instrument (Tyrer-Cuzick), and brief versions of BRCAPRO. "/>
            <resource>
              <reference value="ServiceRequest/398"/>
            </resource>
          </action>
        </action>
      </RequestGroup>
    </resource>
  </entry>
  <entry>
    <fullUrl
             value="http://cancerscreeningcds.github.io/bcsm-cds/ServiceRequest/397"/>
    <resource>
      <ServiceRequest>
        <id value="397"/>
        <text>
          <status value="generated"/>
          <div xmlns="http://www.w3.org/1999/xhtml"><a name="ServiceRequest_397"> </a><p class="res-header-id"><b>Generated Narrative: ServiceRequest 397</b></p><a name="397"> </a><a name="hc397"> </a><a name="397-en-US"> </a><p><b>basedOn</b>: <a href="ActivityDefinition-GeneticRiskAssessmentRequest.html">Genetic Risk Assessment Request</a></p><p><b>status</b>: option</p><p><b>intent</b>: Proposal</p><p><b>code</b>: <span title="Codes:{http://cancerscreeningcds.github.io/bcsm-cds/CodeSystem/plan-definition-action-code-system fhxriskassess}">Informal familial risk assessment</span></p><p><b>subject</b>: <a href="Bundle-eve-Age45to54_act-acsavgrecs45_act-uspstfavgrecs.html#Patient_defaultPatient">Jane Doe</a></p><p><b>reasonCode</b>: <span title="Codes:{http://cancerscreeningcds.github.io/bcsm-cds/CodeSystem/screening-observation-code-system fhxbrcaovcatubalperit}">Family history of breast, ovarian, tubal, or peritoneal cancer</span></p></div>
        </text>
        <basedOn>🔗 
          <reference
                     value="http://cancerscreeningcds.github.io/bcsm-cds/ActivityDefinition/GeneticRiskAssessmentRequest"/>
        </basedOn>
        <status value="option"/>
        <intent value="proposal"/>
        <code>
          <coding>
            <system
                    value="http://cancerscreeningcds.github.io/bcsm-cds/CodeSystem/plan-definition-action-code-system"/>
            <code value="fhxriskassess"/>
            <display value="Informal familial risk assessment"/>
          </coding>
        </code>
        <subject>
          <reference value="Patient/defaultPatient"/>
          <display value="Jane Doe"/>
        </subject>
        <reasonCode>
          <coding>
            <system
                    value="http://cancerscreeningcds.github.io/bcsm-cds/CodeSystem/screening-observation-code-system"/>
            <code value="fhxbrcaovcatubalperit"/>
            <display
                     value="Family history of breast, ovarian, tubal, or peritoneal cancer"/>
          </coding>
        </reasonCode>
      </ServiceRequest>
    </resource>
  </entry>
  <entry>
    <fullUrl
             value="http://cancerscreeningcds.github.io/bcsm-cds/ServiceRequest/398"/>
    <resource>
      <ServiceRequest>
        <id value="398"/>
        <text>
          <status value="generated"/>
          <div xmlns="http://www.w3.org/1999/xhtml"><a name="ServiceRequest_398"> </a><p class="res-header-id"><b>Generated Narrative: ServiceRequest 398</b></p><a name="398"> </a><a name="hc398"> </a><a name="398-en-US"> </a><p><b>basedOn</b>: <a href="ActivityDefinition-GeneticRiskAssessmentRequest.html">Genetic Risk Assessment Request</a></p><p><b>status</b>: option</p><p><b>intent</b>: Proposal</p><p><b>code</b>: <span title="Codes:{http://cancerscreeningcds.github.io/bcsm-cds/CodeSystem/plan-definition-action-code-system fhxrisktool}">Brief familial risk assessment tool</span></p><p><b>subject</b>: <a href="Bundle-eve-Age45to54_act-acsavgrecs45_act-uspstfavgrecs.html#Patient_defaultPatient">Jane Doe</a></p><p><b>reasonCode</b>: <span title="Codes:{http://cancerscreeningcds.github.io/bcsm-cds/CodeSystem/screening-observation-code-system fhxbrcaovcatubalperit}">Family history of breast, ovarian, tubal, or peritoneal cancer</span></p></div>
        </text>
        <basedOn>🔗 
          <reference
                     value="http://cancerscreeningcds.github.io/bcsm-cds/ActivityDefinition/GeneticRiskAssessmentRequest"/>
        </basedOn>
        <status value="option"/>
        <intent value="proposal"/>
        <code>
          <coding>
            <system
                    value="http://cancerscreeningcds.github.io/bcsm-cds/CodeSystem/plan-definition-action-code-system"/>
            <code value="fhxrisktool"/>
            <display value="Brief familial risk assessment tool"/>
          </coding>
        </code>
        <subject>
          <reference value="Patient/defaultPatient"/>
          <display value="Jane Doe"/>
        </subject>
        <reasonCode>
          <coding>
            <system
                    value="http://cancerscreeningcds.github.io/bcsm-cds/CodeSystem/screening-observation-code-system"/>
            <code value="fhxbrcaovcatubalperit"/>
            <display
                     value="Family history of breast, ovarian, tubal, or peritoneal cancer"/>
          </coding>
        </reasonCode>
      </ServiceRequest>
    </resource>
  </entry>
</Bundle>