FHIR Genomics Implementation Guide

Notice

Important: This guidance is under active development by NHS England and content may be added or updated on a regular basis.
This Implementation Guide is currently in Draft and SHOULD NOT be used for development or active implementation without express direction from the NHS England Genomics Unit.

ServiceRequest-SavedTestOrderUpdated-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

id : ServiceRequest-SavedTestOrderUpdated-Example

meta

versionId : 2

lastUpdated : 2023-08-10T11:10:00Z

extension

url : https://fhir.hl7.org.uk/StructureDefinition/Extension-UKCore-Coverage

value

coding

system : https://fhir.hl7.org.uk/CodeSystem/UKCore-FundingCategory

code : nhs

display : NHS

identifier

system : https://fhir.nhs.uk/Id/GMSOrder

value : ROA43728

status : active

intent : order

category

coding

system : https://fhir.hl7.org.uk/CodeSystem/UKCore-GenomeSequencingCategory

code : rare-disease-non-wgs

display : Rare Disease - Non-WGS

priority : routine

code

coding

system : https://fhir.nhs.uk/CodeSystem/England-GenomicTestDirectory

code : R67.1

display : Monogenic hearing loss

subject

reference : Patient/Patient-MeirLieberman-Example

identifier

system : https://fhir.nhs.uk/Id/nhs-number

value : 9449307873

authoredOn : 2023-08-05

requester

reference : PractitionerRole/PractitionerRole-GeneSmithENT-Example

identifier

system : https://fhir.nhs.uk/Id/sds-user-id

value : 9999999999

reasonCode

coding

system : http://snomed.info/sct

code : 103693007

display : Diagnostic procedure

supportingInfo

reference : Observation/Observation-GenomicEthnicity-Example

supportingInfo

reference : Observation/Observation-NoPregnancy-Example

supportingInfo

reference : Observation/Observation-DiseaseStatus-Example

supportingInfo

reference : FamilyMemberHistory/FamilyMemberHistory-NonConsanguinousUnion-Example

supportingInfo

reference : Observation/Observation-NoTransplant-Example

supportingInfo

reference : Observation/Observation-NoTransfusion-Example

supportingInfo

reference : Condition/Condition-HearingLoss-Example

note

text : No family history of genomic testing

note

text : Free text for diagnosis/reason for referral, relevant information including family history, phenotypic details/ HPO Terms/ Patient in need of test...example

relevantHistory

reference : Provenance/Provenance-ServiceRequestUpdate-Example

{
    "resourceType": "ServiceRequest",
    "id": "ServiceRequest-SavedTestOrderUpdated-Example",
    "meta": {
        "versionId": "2",
        "lastUpdated": "2023-08-10T11:10:00Z"
    },
    "extension":  [
        {
            "url": "https://fhir.hl7.org.uk/StructureDefinition/Extension-UKCore-Coverage",
            "valueCodeableConcept": {
                "coding":  [
                    {
                        "system": "https://fhir.hl7.org.uk/CodeSystem/UKCore-FundingCategory",
                        "code": "nhs",
                        "display": "NHS"
                    }
                ]
            }
        }
    ],
    "identifier":  [
        {
            "system": "https://fhir.nhs.uk/Id/GMSOrder",
            "value": "ROA43728"
        }
    ],
    "status": "active",
    "intent": "order",
    "category":  [
        {
            "coding":  [
                {
                    "system": "https://fhir.hl7.org.uk/CodeSystem/UKCore-GenomeSequencingCategory",
                    "code": "rare-disease-non-wgs",
                    "display": "Rare Disease - Non-WGS"
                }
            ]
        }
    ],
    "priority": "routine",
    "code": {
        "coding":  [
            {
                "system": "https://fhir.nhs.uk/CodeSystem/England-GenomicTestDirectory",
                "code": "R67.1",
                "display": "Monogenic hearing loss"
            }
        ]
    },
    "subject": {
        "reference": "Patient/Patient-MeirLieberman-Example",
        "identifier": {
            "system": "https://fhir.nhs.uk/Id/nhs-number",
            "value": "9449307873"
        }
    },
    "authoredOn": "2023-08-05",
    "requester": {
        "reference": "PractitionerRole/PractitionerRole-GeneSmithENT-Example",
        "identifier": {
            "system": "https://fhir.nhs.uk/Id/sds-user-id",
            "value": "9999999999"
        }
    },
    "reasonCode":  [
        {
            "coding":  [
                {
                    "system": "http://snomed.info/sct",
                    "code": "103693007",
                    "display": "Diagnostic procedure"
                }
            ]
        }
    ],
    "supportingInfo":  [
        {
            "reference": "Observation/Observation-GenomicEthnicity-Example"
        },
        {
            "reference": "Observation/Observation-NoPregnancy-Example"
        },
        {
            "reference": "Observation/Observation-DiseaseStatus-Example"
        },
        {
            "reference": "FamilyMemberHistory/FamilyMemberHistory-NonConsanguinousUnion-Example"
        },
        {
            "reference": "Observation/Observation-NoTransplant-Example"
        },
        {
            "reference": "Observation/Observation-NoTransfusion-Example"
        },
        {
            "reference": "Condition/Condition-HearingLoss-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/ Patient in need of test...example"
        }
    ],
    "relevantHistory":  [
        {
            "reference": "Provenance/Provenance-ServiceRequestUpdate-Example"
        }
    ]
}

<ServiceRequest xmlns="http://hl7.org/fhir">
    <id value="ServiceRequest-SavedTestOrderUpdated-Example" />
    <meta>
        <versionId value="2" />
        <lastUpdated value="2023-08-10T11:10:00Z" />
    </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" />
                <display value="NHS" />
            </coding>
        </valueCodeableConcept>
    </extension>
    <identifier>
        <system value="https://fhir.nhs.uk/Id/GMSOrder" />
        <value value="ROA43728" />
    </identifier>
    <status value="active" />
    <intent value="order" />
    <category>
        <coding>
            <system value="https://fhir.hl7.org.uk/CodeSystem/UKCore-GenomeSequencingCategory" />
            <code value="rare-disease-non-wgs" />
            <display value="Rare Disease - Non-WGS" />
        </coding>
    </category>
    <priority value="routine" />
    <code>
        <coding>
            <system value="https://fhir.nhs.uk/CodeSystem/England-GenomicTestDirectory" />
            <code value="R67.1" />
            <display value="Monogenic hearing loss" />
        </coding>
    </code>
    <subject>
        <reference value="Patient/Patient-MeirLieberman-Example" />
        <identifier>
            <system value="https://fhir.nhs.uk/Id/nhs-number" />
            <value value="9449307873" />
        </identifier>
    </subject>
    <authoredOn value="2023-08-05" />
    <requester>
        <reference value="PractitionerRole/PractitionerRole-GeneSmithENT-Example" />
        <identifier>
            <system value="https://fhir.nhs.uk/Id/sds-user-id" />
            <value value="9999999999" />
        </identifier>
    </requester>
    <reasonCode>
        <coding>
            <system value="http://snomed.info/sct" />
            <code value="103693007" />
            <display value="Diagnostic procedure" />
        </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="FamilyMemberHistory/FamilyMemberHistory-NonConsanguinousUnion-Example" />
    </supportingInfo>
    <supportingInfo>
        <reference value="Observation/Observation-NoTransplant-Example" />
    </supportingInfo>
    <supportingInfo>
        <reference value="Observation/Observation-NoTransfusion-Example" />
    </supportingInfo>
    <supportingInfo>
        <reference value="Condition/Condition-HearingLoss-Example" />
    </supportingInfo>
    <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/ Patient in need of test...example" />
    </note>
    <relevantHistory>
        <reference value="Provenance/Provenance-ServiceRequestUpdate-Example" />
    </relevantHistory>
</ServiceRequest>

Notice

ServiceRequest-SavedTestOrderUpdated-Example

Propose a change to ServiceRequest/ServiceRequest-SavedTestOrderUpdated-Example