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 PrimaryScreeningDecision_eve-geneticrisk_yes_eve-acsgeneticrisk_no_act-othergeneticrisk
Bundle PrimaryScreeningDecision_eve-geneticrisk_yes_eve-acsgeneticrisk_no_act-othergeneticrisk of type collection
Entry 1 - fullUrl = http://cancerscreeningcds.github.io/bcsm-cds/CarePlan/184
Resource CarePlan:
Generated Narrative: CarePlan 184
instantiatesCanonical: Primary Screening Decision
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/185
Resource RequestGroup:
Generated Narrative: RequestGroup 185
instantiatesCanonical: Primary Screening Decision
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/186
Resource ServiceRequest:
Generated Narrative: ServiceRequest 186
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