Breast Cancer Screening and Management (BCSM) Clinical Decision Support (CDS) Implementation Guide
1.0.0 - ci-build
Breast Cancer Screening and Management (BCSM) Clinical Decision Support (CDS) Implementation Guide - Local Development build (v1.0.0) built by the FHIR (HL7® FHIR® Standard) Build Tools. See the Directory of published versions
Generated Narrative: Bundle HighRiskExclusions_eve-geneticrisk_yes_eve-acsgeneticrisk_no_act-othergeneticrisk
Bundle HighRiskExclusions_eve-geneticrisk_yes_eve-acsgeneticrisk_no_act-othergeneticrisk of type collection
Entry 1 - fullUrl = http://cancerscreeningcds.github.io/bcsm-cds/CarePlan/431
Resource CarePlan:
Generated Narrative: CarePlan 431
instantiatesCanonical: High Risk Exclusions
status: Draft
intent: Proposal
subject: Jane Doe
created: 2024-12-10 00:00:00+0000
Activities
Reference Bundle: type = collection
Entry 2 - fullUrl = http://cancerscreeningcds.github.io/bcsm-cds/RequestGroup/432
Resource RequestGroup:
Generated Narrative: RequestGroup 432
instantiatesCanonical: High Risk Exclusions
status: Draft
intent: Proposal
subject: Jane Doe
action
id
SpecialtyReferralGeneticRisktitle: Refer to specialist recommendations
description: A number of other genetic variants are known to be associated with an increased risk of developing of breast cancer. For known personal history of these variants, refer to the consulting geneticist or to high risk breast specialist for guidance on routine screening. Variants may include ATM, BARD1, CDH1, CHEK2, NF1, PALB2, RAD51C, RAD51D, STK11.
code: Refer to specialist recommendations
resource: Bundle: type = collection
Entry 3 - fullUrl = http://cancerscreeningcds.github.io/bcsm-cds/ServiceRequest/433
Resource ServiceRequest:
Generated Narrative: ServiceRequest 433
basedOn: Breast Cancer Screening Service Request
status: option
intent: Proposal
code: Refer to specialist recommendations
subject: Jane Doe
reasonCode: Other genetic marker or syndrome associated with breast cancer