<description value="Referral for genetic counseling if not previously evaluated for variant of concern based on known family history. Any blood relative with known BRCA1/BRCA2 variants, Li-Fraumeni syndrome (TP53 variant), Cowden or Bannayan-Riley-Ruvalcaba syndromes (PTEN variants), and other variants known to be associated with increased risk of development of breast cancer. Variants may include ATM, BARD1, CDH1, CHEK2, NF1, PALB2, RAD51C, RAD51D, STK11."/> <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> <resource> <reference value="ServiceRequest/409"/> </resource> </action> </RequestGroup> </resource> </entry> <entry> <fullUrl value="http://cancerscreeningcds.github.io/bcsm-cds/ServiceRequest/409"/> <resource> <ServiceRequest> <id value="409"/> <text> <status value="generated"/><div xmlns="http://www.w3.org/1999/xhtml"><a name="ServiceRequest_409"> </a>Generated Narrative: ServiceRequest 409<a name="409"> </a><a name="hc409"> </a><a name="409-en-US"> </a>basedOn: <a href="ActivityDefinition-GeneticCounselingReferralRequest.html">Genetic Counseling Referral Request</a>status: optionintent: Proposalcode: Genetic risk referralsubject: <a href="Bundle-eve-Age45to54_act-acsavgrecs45_act-uspstfavgrecs.html#Patient_defaultPatient">Jane Doe</a>reasonCode: Family history of inherited cancer susceptibility</div> </text> <basedOn> <reference value="http://cancerscreeningcds.github.io/bcsm-cds/ActivityDefinition/GeneticCounselingReferralRequest"/> </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="geneticriskreferral"/> <display value="Genetic risk referral"/> </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="fhxgenetic"/> <display value="Family history of inherited cancer susceptibility"/> </coding> </reasonCode> </ServiceRequest> </resource> </entry> </Bundle>

Generated Narrative: RequestGroup 408

instantiatesCanonical: Genetic Risk Referral

status: Draft

intent: Proposal

subject: Jane Doe

action
id
GeneticReferralVariant
title: Referral for genetic risk counseling
description: Referral for genetic counseling if not previously evaluated for variant of concern based on known family history. Any blood relative with known BRCA1/BRCA2 variants, Li-Fraumeni syndrome (TP53 variant), Cowden or Bannayan-Riley-Ruvalcaba syndromes (PTEN variants), and other variants known to be associated with increased risk of development of breast cancer. Variants may include ATM, BARD1, CDH1, CHEK2, NF1, PALB2, RAD51C, RAD51D, STK11.
Documentations
- Type Label Display Citation Url
* Citation USPSTF BRCA-Related Cancer: Risk Assessment, Genetic Counseling, and Genetic Testing
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.

https://www.uspreventiveservicestaskforce.org/uspstf/recommendation/brca-related-cancer-risk-assessment-genetic-counseling-and-genetic-testing
resource: Bundle: type = collection

Activities

Documentations