Breast Cancer Screening and Management (BCSM) Clinical Decision Support (CDS) Implementation Guide
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"div" : "<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.\n\nWomen 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>\n</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>"
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