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.
Bundle-WGSRoD-Example
Example of a consent resource with attached Record of Discussion form, as described in the Clinical Scenario: WGS Test Request - Rare Disease.
Bundle |
id : Bundle-WGSRoD-Example |
type : transaction |
entry |
fullUrl : http://example.org/fhir/Consent/Consent-RoDToFollow-Example |
resource |
id : Consent-RoDToFollow-Example |
status : active |
scope |
coding |
system : http://terminology.hl7.org/CodeSystem/consentscope |
code : research |
display : Research |
category |
coding |
system : http://terminology.hl7.org/CodeSystem/consentcategorycodes |
code : research |
display : Research Information Access |
source |
reference : QuestionnaireResponse/QuestionnaireResponse-RoD-Example |
policy |
authority : https://www.england.nhs.uk |
uri : https://www.england.nhs.uk/publication/nhs-genomic-medicine-service-record-of-discussion-form |
provision |
data |
meaning : instance |
reference |
reference : ServiceRequest/ServiceRequest-WGSTestOrderForm-Example |
request |
method : PUT |
url : Consent/Consent-RoDToFollow-Example |
entry |
fullUrl : http://example.org/fhir/QuestionnaireResponse/QuestionnaireResponse-RoD-Example |
resource |
id : QuestionnaireResponse-RoD-Example |
questionnaire : https://fhir.nhs.uk/Questionnaire/NHSDigital-Questionnaire-Genomics-Example |
status : completed |
subject |
reference : Patient/Patient-LindsaySorrell-Example |
identifier |
system : https://fhir.nhs.uk/Id/nhs-number |
value : 9449307946 |
authored : 2023-08-21 |
author |
identifier |
system : https://fhir.nhs.uk/Id/sds-role-profile-id |
value : 9999999996 |
display : Test AHP |
source |
reference : Patient/Patient-LindsaySorrell-Example |
identifier |
system : https://fhir.nhs.uk/Id/nhs-number |
value : 9449307946 |
item |
linkId : patientDetails |
text : Patient Details |
item |
linkId : givenName |
text : First Name |
answer |
value : Lindsay |
item |
linkId : familyName |
text : Last Name |
answer |
value : Sorrell |
item |
linkId : nhs_Number |
text : NHS number (or postcode if not not known) |
answer |
value : 944 9307 946 |
item |
linkId : birthDate |
text : Date of Birth |
answer |
value : 2011-04-12 |
item |
linkId : declaration4 |
text : Confirmation of Your Genomic Test and Research Choices |
item |
linkId : confirmation |
text : I confirm that I have had the opportunity to discuss information about genomic testing, I agree to the genomic test, and my research choice is indicated below. |
item |
linkId : researchConfirmation1 |
text : I have discussed taking part in the National Genomic Research Library. If your answer to A is NO then please ignore B and sign directly below |
answer |
value : True |
item |
linkId : researchConfirmation2 |
text : I agree that my data and remainder sample may contribute to the National Genomic Research Library |
answer |
value : True |
item |
linkId : isRespondentAttorney |
text : Are you completing this form on behalf of someone? |
answer |
value : False |
item |
linkId : patientValidation |
text : Patient Validation |
item |
linkId : patientNamecombined |
text : Patient Name |
answer |
value : Mr. Lindsay Sorrell |
item |
linkId : patientSignature |
text : Signature |
answer |
value : NA |
item |
linkId : datePatientCompletedForm |
text : Date |
answer |
value : 2023-08-21 |
item |
linkId : declaration5 |
text : Healthcare professional use only |
item |
linkId : healthcareProfessional |
text : To be completed by the healthcare professional recording the patient’s choices. |
item |
linkId : patientCategory |
text : Patient category |
answer |
value |
system : https://fhir.nhs.uk/CodeSystem/patient-choice-category-genomics |
code : adult-own-choice |
display : Adult(made their own choice) |
item |
linkId : testType |
text : Test type |
answer |
value |
system : https://fhir.nhs.uk/CodeSystem/test-type-genomics |
code : RID-WGS |
display : Rare and Inherited Diseases - WGS |
item |
linkId : remoteConsent |
text : Remote consent, recorded remotely by clinician, no patient signature |
answer |
value : True |
item |
linkId : responsibleClinician |
text : Responsible clinician |
answer |
value : Dr Hazel Smith |
item |
linkId : patientMRN |
text : Hospital number |
answer |
value : RWT14789 |
item |
linkId : healthcareProfessionalName |
text : Healthcare professional name |
answer |
value : Test AHP |
item |
linkId : healthcareProfessionalSignature |
text : Signature |
answer |
value : Dr. Hazel Smith |
item |
linkId : datehealthcareProfessionalCompletedForm |
text : Date |
answer |
value : 2023-08-21 |
request |
method : POST |
url : QuestionnaireResponse |
{
{
{
}
]
},
{
{
}
]
}
],
},
{
"uri": "https://www.england.nhs.uk/publication/nhs-genomic-medicine-service-record-of-discussion-form"
}
],
{
}
}
]
}
},
}
},
{
}
},
},
},
}
},
{
{
},
{
},
{
]
},
{
}
]
},
{
{
"text": "I confirm that I have had the opportunity to discuss information about genomic testing, I agree to the genomic test, and my research choice is indicated below.",
{
"text": "I have discussed taking part in the National Genomic Research Library. If your answer to A is NO then please ignore B and sign directly below",
]
},
{
"text": "I agree that my data and remainder sample may contribute to the National Genomic Research Library",
]
}
]
}
]
},
{
]
},
{
{
]
},
{
},
{
]
}
]
},
{
{
{
{
}
}
]
},
{
{
}
}
]
},
{
]
},
{
]
},
{
},
{
]
},
{
]
},
{
]
}
]
}
]
}
]
},
}
}
]
}
<Consent>
</coding>
</scope>
</coding>
</category>
</sourceReference>
<uri value="https://www.england.nhs.uk/publication/nhs-genomic-medicine-service-record-of-discussion-form" />
</policy>
</reference>
</data>
</provision>
</Consent>
</resource>
</request>
</entry>
<QuestionnaireResponse>
<questionnaire value="https://fhir.nhs.uk/Questionnaire/NHSDigital-Questionnaire-Genomics-Example" />
</identifier>
</subject>
</identifier>
</author>
</identifier>
</source>
</answer>
</item>
</answer>
</item>
</answer>
</item>
</answer>
</item>
</item>
<text value="I confirm that I have had the opportunity to discuss information about genomic testing, I agree to the genomic test, and my research choice is indicated below." />
<text value="I have discussed taking part in the National Genomic Research Library. If your answer to A is NO then please ignore B and sign directly below" />
</answer>
</item>
<text value="I agree that my data and remainder sample may contribute to the National Genomic Research Library" />
</answer>
</item>
</item>
</item>
</answer>
</item>
</answer>
</item>
</answer>
</item>
</answer>
</item>
</item>
</valueCoding>
</answer>
</item>
</valueCoding>
</answer>
</item>
</answer>
</item>
</answer>
</item>
</answer>
</item>
</answer>
</item>
</answer>
</item>
</answer>
</item>
</item>
</item>
</QuestionnaireResponse>
</resource>
</request>
</entry>
</Bundle>