Task-FollowupRecommendationReport-Example

Example of a Task represented a recommneded action to be taken as a consequence of a genomic test, created by a filler organization upon completion of a test, attached to a diagnostic report.

Task
{
    "resourceType": "Task",
    "id": "Task-FollowupRecommendationReport-Example",
    "meta": {
        "profile":  [
            "http://hl7.org/fhir/uv/genomics-reporting/StructureDefinition/followup-recommendation"
        ]
    },
    "status": "requested",
    "intent": "proposal",
    "code": {
        "coding":  [
            {
                "system": "http://loinc.org",
                "code": "LA14021-2",
                "display": "Confirmatory testing recommended"
            }
        ]
    },
    "description": "Testing of Pheobe's parents is recommended (via referral to the clinical genetics service) in order to confirm that both are heterozygous carriers of the missense variant.",
    "for": {
        "reference": "Patient/Patient-PheobeSmitham-Example"
    },
    "reasonReference": {
        "reference": "Observation/Observation-GenomicImplication-Therapeutic"
    },
    "input":  [
        {
            "type": {
                "coding":  [
                    {
                        "system": "http://terminology.hl7.org/CodeSystem/v3-RoleCode",
                        "code": "NFTH",
                        "display": "natural father"
                    }
                ]
            },
            "valueReference": {
                "reference": "Patient/Patient-PheobeSmithamFather-Example"
            }
        },
        {
            "type": {
                "coding":  [
                    {
                        "system": "http://terminology.hl7.org/CodeSystem/v3-RoleCode",
                        "code": "NMTH",
                        "display": "natural mother"
                    }
                ]
            },
            "valueReference": {
                "reference": "Patient/Patient-PheobeSmithamMother-Example"
            }
        }
    ]
}
<Task xmlns="http://hl7.org/fhir">
    <id value="Task-FollowupRecommendationReport-Example" />
    <meta>
        <profile value="http://hl7.org/fhir/uv/genomics-reporting/StructureDefinition/followup-recommendation" />
    </meta>
    <status value="requested" />
    <intent value="proposal" />
    <code>
        <coding>
            <system value="http://loinc.org" />
            <code value="LA14021-2" />
            <display value="Confirmatory testing recommended" />
        </coding>
    </code>
    <description value="Testing of Pheobe&#39;s parents is recommended (via referral to the clinical genetics service) in order to confirm that both are heterozygous carriers of the missense variant." />
    <for>
        <reference value="Patient/Patient-PheobeSmitham-Example" />
    </for>
    <reasonReference>
        <reference value="Observation/Observation-GenomicImplication-Therapeutic" />
    </reasonReference>
    <input>
        <type>
            <coding>
                <system value="http://terminology.hl7.org/CodeSystem/v3-RoleCode" />
                <code value="NFTH" />
                <display value="natural father" />
            </coding>
        </type>
        <valueReference>
            <reference value="Patient/Patient-PheobeSmithamFather-Example" />
        </valueReference>
    </input>
    <input>
        <type>
            <coding>
                <system value="http://terminology.hl7.org/CodeSystem/v3-RoleCode" />
                <code value="NMTH" />
                <display value="natural mother" />
            </coding>
        </type>
        <valueReference>
            <reference value="Patient/Patient-PheobeSmithamMother-Example" />
        </valueReference>
    </input>
</Task>