ServiceRequest-WGSTestOrderFormUpdated-DirectToLab-Example

Example of a ServiceRequest which has been modified. After modification, the ServiceRequest SHALL include a meta.lastUpdated element and a relevantHitory element referencing the provenance resource detailing the change.

ServiceRequest
{
    "resourceType": "ServiceRequest",
    "id": "ServiceRequest-WGSTestOrderFormUpdated-DirectToLab-Example",
    "meta": {
        "versionId": "2",
        "lastUpdated": "2023-10-10T16:00:00Z"
    },
    "extension":  [
        {
            "url": "https://fhir.hl7.org.uk/StructureDefinition/Extension-UKCore-Coverage",
            "valueCodeableConcept": {
                "coding":  [
                    {
                        "system": "https://fhir.hl7.org.uk/CodeSystem/UKCore-FundingCategory",
                        "code": "nhs-england",
                        "display": "NHS England"
                    }
                ]
            }
        }
    ],
    "status": "active",
    "intent": "order",
    "category":  [
        {
            "coding":  [
                {
                    "system": "https://fhir.hl7.org.uk/CodeSystem/UKCore-GenomeSequencingCategory",
                    "code": "rare-disease-wgs",
                    "display": "Rare Disease - WGS"
                }
            ]
        }
    ],
    "priority": "urgent",
    "code": {
        "coding":  [
            {
                "system": "https://fhir.nhs.uk/CodeSystem/England-GenomicTestDirectory",
                "code": "R14",
                "display": "Acutely unwell children with a likely monogenic disorder",
                "version": "7"
            }
        ]
    },
    "subject": {
        "reference": "Patient/Patient-JamesMetcalfe-Example",
        "identifier": {
            "system": "https://fhir.nhs.uk/Id/nhs-number",
            "value": "7449306524"
        }
    },
    "authoredOn": "2023-10-10T11:00:00Z",
    "requester": {
        "reference": "PractitionerRole/PractitionerRole-EugeneSmith-Example"
    },
    "reasonCode":  [
        {
            "coding":  [
                {
                    "system": "https://fhir.nhs.uk/CodeSystem/reasonfortesting-genomics",
                    "code": "diagnostic",
                    "display": "Diagnostic"
                }
            ]
        }
    ],
    "performer":  [
        {
            "identifier": {
                "system": "https://fhir.nhs.uk/Id/ods-organization-code",
                "value": "RH8"
            }
        }
    ],
    "supportingInfo":  [
        {
            "reference": "Observation/Observation-GenomicEthnicity-Example"
        },
        {
            "reference": "Observation/Observation-NoPregnancy-Example"
        },
        {
            "reference": "Observation/Observation-DiseaseStatus-Example"
        },
        {
            "reference": "Observation/Observation-DiseasePenetrance-Example"
        },
        {
            "reference": "Observation/Observation-NonConsanguinousUnion-Example"
        },
        {
            "reference": "Observation/Observation-NoBoneMarrowTransplant-Example"
        },
        {
            "reference": "Observation/Observation-Immunodefficiency-Example"
        },
        {
            "reference": "Observation/Observation-NoTransfusion-Example"
        },
        {
            "reference": "Consent/Consent-RoDYoungPersonAssentFormAvailable-Example"
        }
    ],
    "specimen":  [
        {
            "reference": "Specimen/Specimen-JamesMetcalfeBloodEDTA-Example"
        }
    ],
    "note":  [
        {
            "text": "No family history of genomic testing"
        },
        {
            "text": "Free text for diagnosis/reason for referral, relevant information including family history, phenotypic details/ HPO Terms"
        },
        {
            "text": "E.g.  non genetic investigations are pathognomonic of a single gene disorder, R26 previously ordered on the child  and molecular testing needed to guide management"
        }
    ]
}
<ServiceRequest xmlns="http://hl7.org/fhir">
    <id value="ServiceRequest-WGSTestOrderFormUpdated-DirectToLab-Example" />
    <meta>
        <versionId value="2" />
        <lastUpdated value="2023-10-10T16:00:00Z" />
    </meta>
    <extension url="https://fhir.hl7.org.uk/StructureDefinition/Extension-UKCore-Coverage">
        <valueCodeableConcept>
            <coding>
                <system value="https://fhir.hl7.org.uk/CodeSystem/UKCore-FundingCategory" />
                <code value="nhs-england" />
                <display value="NHS England" />
            </coding>
        </valueCodeableConcept>
    </extension>
    <status value="active" />
    <intent value="order" />
    <category>
        <coding>
            <system value="https://fhir.hl7.org.uk/CodeSystem/UKCore-GenomeSequencingCategory" />
            <code value="rare-disease-wgs" />
            <display value="Rare Disease - WGS" />
        </coding>
    </category>
    <priority value="urgent" />
    <code>
        <coding>
            <system value="https://fhir.nhs.uk/CodeSystem/England-GenomicTestDirectory" />
            <version value="7" />
            <code value="R14" />
            <display value="Acutely unwell children with a likely monogenic disorder" />
        </coding>
    </code>
    <subject>
        <reference value="Patient/Patient-JamesMetcalfe-Example" />
        <identifier>
            <system value="https://fhir.nhs.uk/Id/nhs-number" />
            <value value="7449306524" />
        </identifier>
    </subject>
    <authoredOn value="2023-10-10T11:00:00Z" />
    <requester>
        <reference value="PractitionerRole/PractitionerRole-EugeneSmith-Example" />
    </requester>
    <performer>
        <identifier>
            <system value="https://fhir.nhs.uk/Id/ods-organization-code" />
            <value value="RH8" />
        </identifier>
    </performer>
    <reasonCode>
        <coding>
            <system value="https://fhir.nhs.uk/CodeSystem/reasonfortesting-genomics" />
            <code value="diagnostic" />
            <display value="Diagnostic" />
        </coding>
    </reasonCode>
    <supportingInfo>
        <reference value="Observation/Observation-GenomicEthnicity-Example" />
    </supportingInfo>
    <supportingInfo>
        <reference value="Observation/Observation-NoPregnancy-Example" />
    </supportingInfo>
    <supportingInfo>
        <reference value="Observation/Observation-DiseaseStatus-Example" />
    </supportingInfo>
    <supportingInfo>
        <reference value="Observation/Observation-DiseasePenetrance-Example" />
    </supportingInfo>
    <supportingInfo>
        <reference value="Observation/Observation-NonConsanguinousUnion-Example" />
    </supportingInfo>
    <supportingInfo>
        <reference value="Observation/Observation-NoBoneMarrowTransplant-Example" />
    </supportingInfo>
    <supportingInfo>
        <reference value="Observation/Observation-Immunodefficiency-Example" />
    </supportingInfo>
    <supportingInfo>
        <reference value="Observation/Observation-NoTransfusion-Example" />
    </supportingInfo>
    <supportingInfo>
        <reference value="Consent/Consent-RoDYoungPersonAssentFormAvailable-Example" />
    </supportingInfo>
    <specimen>
        <reference value="Specimen/Specimen-JamesMetcalfeBloodEDTA-Example" />
    </specimen>
    <note>
        <text value="No family history of genomic testing" />
    </note>
    <note>
        <text value="Free text for diagnosis/reason for referral, relevant information including family history, phenotypic details/ HPO Terms" />
    </note>
    <note>
        <text value="E.g.&#160; non genetic investigations are pathognomonic of a single gene disorder, R26 previously ordered on the child&#160; and molecular testing needed to guide management" />
    </note>
</ServiceRequest>