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Packagefhir.nwgenomics.nhs.uk
Resource TypeQuestionnaire
IdQuestionnaire-CancerTestAdditionalAskAtOrderQuestions.json
FHIR VersionR4
Sourcehttps://build.fhir.org/ig/nw-gmsa/nw-gmsa.github.com/Questionnaire-CancerTestAdditionalAskAtOrderQuestions.html
URLhttps://fhir.nwgenomics.nhs.uk/Questionnaire/CancerTestAdditionalAskAtOrderQuestions
Version2.2.0
Statusdraft
Date2026-09-27T08:17:18+00:00
TitleCancer Test Additional Ask At Order Entry Questions
Realmus
Authorityhl7
Description**This Questionnaire is a proposal, not an active or planned project.** **Test Specific Additional Ask At Order Entry Questions** for Cancer orders - used *alongside* the [common core order form](Questionnaire-GenomicTestOrder.html) **and** [Ask At Order Entry Questions Common](Questionnaire-GenomicGeneralAskAtOrderEntry.html), the same "Test Specific" tier pattern [WGS Test Additional Ask At Order Entry Questions](Questionnaire-WGSTestAdditionalAskAtOrderQuestions.html) already follows for WGS orders - see [Order Entry Questions](Questionnaire-GenomicTestOrder.html#order-entry-questions). Its content is **inferred**, not yet confirmed against a live order-entry screen the way `WGSTestAdditionalAskAtOrderQuestions` was: each item below is a concept that recurs independently across the two Cancer-category NW GLH paper forms - [HRD and Tumour BRCA](Questionnaire-HRDTumourBRCAAskAtOrderEntry.html) (GB-27189) and [GMS WGS Cancer](Questionnaire-GMSWGSCancerAskAtOrderEntry.html) (the national form) - see [NW GLH Paper Test Request Forms](Questionnaire-GenomicTestOrder.html#nw-glh-paper-test-request-forms). Neither of those two Questionnaires has been changed to actually use this one yet - both remain independent, standalone Questionnaires, each already carrying its own copy of the fields proposed here.

Resources that use this resource

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Narrative

Note: links and images are rebased to the (stated) source

Generated Narrative: Questionnaire CancerTestAdditionalAskAtOrderQuestions

Profile: Questionnaire

Structure
LinkIDTextCardinalityTypeDescription & Constraintsdoco
.. **This Questionnaire is a proposal, not an active or planned project.** **Test Specific Additional Ask At Order Entry Questions** for Cancer orders - used *alongside* the [common core order form](Questionnaire-GenomicTestOrder.html) **and** [Ask At Order Entry Questions Common](Questionnaire-GenomicGeneralAskAtOrderEntry.html), the same "Test Specific" tier pattern [WGS Test Additional Ask At Order Entry Questions](Questionnaire-WGSTestAdditionalAskAtOrderQuestions.html) already follows for WGS orders - see [Order Entry Questions](Questionnaire-GenomicTestOrder.html#order-entry-questions). Its content is **inferred**, not yet confirmed against a live order-entry screen the way `WGSTestAdditionalAskAtOrderQuestions` was: each item below is a concept that recurs independently across the two Cancer-category NW GLH paper forms - [HRD and Tumour BRCA](Questionnaire-HRDTumourBRCAAskAtOrderEntry.html) (GB-27189) and [GMS WGS Cancer](Questionnaire-GMSWGSCancerAskAtOrderEntry.html) (the national form) - see [NW GLH Paper Test Request Forms](Questionnaire-GenomicTestOrder.html#nw-glh-paper-test-request-forms). Neither of those two Questionnaires has been changed to actually use this one yet - both remain independent, standalone Questionnaires, each already carrying its own copy of the fields proposed here.Questionnairehttps://fhir.nwgenomics.nhs.uk/Questionnaire/CancerTestAdditionalAskAtOrderQuestions#2.2.0
... AskAtOrderEntryAsk At Order Entry Questions0..1group
.... NOS/PresentationStatusPresentation status0..1choiceDefinition: Observation.valueCodeableConcept
Options: 3 options
..... NOS/PresentationStatus-designNoteInferred from [GMS WGS Cancer](Questionnaire-GMSWGSCancerAskAtOrderEntry.html)'s own `NOS/PresentationStatus` item. Generalises the same distinction [HRD and Tumour BRCA](Questionnaire-HRDTumourBRCAAskAtOrderEntry.html) makes via its own `Pathway` choice (HRD test = newly diagnosed, Tumour BRCA-only = relapsed) plus separate `NewlyDiagnosedAdvancedDiseaseConfirmation`/`RelapsedDiseaseConfirmation` booleans - that form conflates presentation status with test selection itself, since the pathway and the presentation are the same choice on that specific form; here they are kept separate, as GMS WGS Cancer already does.0..1display
.... NOS/NeoplasticCellContentNeoplastic/malignant cell content (%)0..1quantityDefinition: Observation.valueQuantity
..... NOS/NeoplasticCellContent-designNoteThe same underlying concept is independently modelled three times today, each under its own linkId despite sharing this same `NWGMSA` code: [HRD and Tumour BRCA](Questionnaire-HRDTumourBRCAAskAtOrderEntry.html)'s `NOS/NeoplasticCellContent` ("Approximate % neoplastic nuclei in tumour area highlighted"), [GMS WGS Cancer](Questionnaire-GMSWGSCancerAskAtOrderEntry.html)'s `NOS/NeoplasticCellContent-gms` ("% Malignant nuclei / blasts (or equivalent)"), and [WGS Local Test Order](Questionnaire-WGSLocalTestOrderAskAtOrderEntry.html)'s own `NOS/NeoplasticCellContent-wgs`. Proposed here as the single shared field this tier is for, rather than each Cancer-adjacent form continuing to reinvent its own suffixed linkId for the same value.0..1display
.... NOS/PathologistNamePathologist0..1stringDefinition: Observation.valueString
..... NOS/PathologistName-designNotePresent as its own named field on [HRD and Tumour BRCA](Questionnaire-HRDTumourBRCAAskAtOrderEntry.html). [GMS WGS Cancer](Questionnaire-GMSWGSCancerAskAtOrderEntry.html) doesn't ask for the pathologist by name, only a Histopathology Lab ID (see `Pathology hospital / laboratory` below) - proposed here as a genuinely Cancer-wide concept even though only one of the two source forms currently asks for it.0..1display
.... NOS/PathologyHospitalPathology hospital / laboratory0..1stringDefinition: Observation.valueString
..... NOS/PathologyHospital-designNoteGeneralises [HRD and Tumour BRCA](Questionnaire-HRDTumourBRCAAskAtOrderEntry.html)'s own `NOS/PathologyHospital` and [GMS WGS Cancer](Questionnaire-GMSWGSCancerAskAtOrderEntry.html)'s `NOS/HistopathologyLabID` ("Histopathology Lab ID", under that form's own Solid tumour sub-group) - both identify where the pathology specimen/report the order relies on came from, just at different granularity (a named hospital vs. a lab identifier). Kept as free text pending a decision on whether an [Organisation Code](StructureDefinition-OrganisationCode.html) reference would be more appropriate.0..1display
..... NOS/PathologyHospital-futureQueryAccessThis item, and Pathologist above, most directly relate to the [Cheshire and Merseyside Pathology](CheshireAndMerseysidePathology.html) reflex use case, where a genomic order follows on from a prior pathology order/report (`LAB-1`/`LAB-3`) rather than starting the clinical episode itself. That page's own [Current Process](CheshireAndMerseysidePathology.html#current-process) still models the pathology-to-genomics handoff entirely as HL7 v2/FHIR messaging (`LAB-1`/`LAB-35`/`LAB-3`/`LAB-36`), which is why today's answer is free text naming the pathologist/hospital rather than a machine-resolvable reference. A query-based alternative may remove the need to duplicate pathology content into the genomic order/message at all: some NW pathology LIMS deployments (e.g. Medicus) already support the Australian [AU eReq](https://hl7.org.au/fhir/ereq/index.html) FHIR IG for on-demand query access to pathology orders (and potentially reports), and MFT separately exposes pathology data through Epic's own [FHIR Query API](https://fhir.epic.com/). If a genomics laboratory can query pathology directly, these two free-text fields could be replaced by a **reference** instead - the Pathology Order Filler Number, Pathology Patient Identifier and/or Pathology Specimen Identifier - letting the genomic order carry a pointer for on-demand lookup rather than the pathology detail itself.0..1display

doco Documentation for this format

Options Sets

Answer options for NOS/PresentationStatus

  • https://fhir.nwgenomics.nhs.uk/CodeSystem/NWGMSA#PresentationFirstDiagnosis
  • https://fhir.nwgenomics.nhs.uk/CodeSystem/NWGMSA#PresentationRecurrenceRelapse
  • http://loinc.org#LA4489-6 ("Unknown")

Source1

{
  "resourceType": "Questionnaire",
  "id": "CancerTestAdditionalAskAtOrderQuestions",
  "meta": {
    "profile": [
      "https://fhir.nwgenomics.nhs.uk/StructureDefinition/NWQuestionnaire"
    ]
  },
  "text": {
    "status": "extensions",
    "div": "<!-- snip (see above) -->"
  },
  "extension": [
    {
      "url": "http://hl7.org/fhir/StructureDefinition/artifact-versionAlgorithm",
      "valueCoding": {
        "system": "http://hl7.org/fhir/version-algorithm",
        "code": "semver"
      }
    }
  ],
  "url": "https://fhir.nwgenomics.nhs.uk/Questionnaire/CancerTestAdditionalAskAtOrderQuestions",
  "version": "2.2.0",
  "title": "Cancer Test Additional Ask At Order Entry Questions",
  "derivedFrom": [
    "https://fhir.nwgenomics.nhs.uk/Questionnaire/GenomicTestOrder"
  ],
  "_derivedFrom": [
    {
      "extension": [
        {
          "url": "http://hl7.org/fhir/StructureDefinition/questionnaire-derivationType",
          "valueCoding": {
            "system": "http://hl7.org/fhir/questionnaire-derivationType",
            "code": "extends"
          }
        }
      ]
    }
  ],
  "status": "draft",
  "date": "2026-09-27T08:17:18+00:00",
  "publisher": "NHS North West Genomics",
  "contact": [
    {
      "telecom": [
        {
          "system": "url",
          "value": "https://www.nwgenomics.nhs.uk/contact-us"
        }
      ]
    }
  ],
  "description": "**This Questionnaire is a proposal, not an active or planned project.**\n\n**Test Specific Additional Ask At Order Entry Questions** for Cancer\norders - used *alongside* the [common core order\nform](Questionnaire-GenomicTestOrder.html) **and** [Ask At Order Entry\nQuestions Common](Questionnaire-GenomicGeneralAskAtOrderEntry.html), the\nsame \"Test Specific\" tier pattern [WGS Test Additional Ask At Order Entry\nQuestions](Questionnaire-WGSTestAdditionalAskAtOrderQuestions.html) already\nfollows for WGS orders - see [Order Entry\nQuestions](Questionnaire-GenomicTestOrder.html#order-entry-questions).\n\nIts content is **inferred**, not yet confirmed against a live order-entry\nscreen the way `WGSTestAdditionalAskAtOrderQuestions` was: each item below\nis a concept that recurs independently across the two Cancer-category NW\nGLH paper forms - [HRD and Tumour\nBRCA](Questionnaire-HRDTumourBRCAAskAtOrderEntry.html) (GB-27189) and [GMS\nWGS Cancer](Questionnaire-GMSWGSCancerAskAtOrderEntry.html) (the national\nform) - see [NW GLH Paper Test Request\nForms](Questionnaire-GenomicTestOrder.html#nw-glh-paper-test-request-forms).\nNeither of those two Questionnaires has been changed to actually use this\none yet - both remain independent, standalone Questionnaires, each already\ncarrying its own copy of the fields proposed here.",
  "jurisdiction": [
    {
      "coding": [
        {
          "system": "urn:iso:std:iso:3166",
          "code": "GB",
          "display": "United Kingdom of Great Britain and Northern Ireland"
        }
      ]
    }
  ],
  "item": [
    {
      "linkId": "AskAtOrderEntry",
      "text": "Ask At Order Entry Questions",
      "type": "group",
      "item": [
        {
          "linkId": "NOS/PresentationStatus",
          "definition": "http://hl7.org/fhir/StructureDefinition/Observation#Observation.valueCodeableConcept",
          "text": "Presentation status",
          "type": "choice",
          "answerOption": [
            {
              "valueCoding": {
                "system": "https://fhir.nwgenomics.nhs.uk/CodeSystem/NWGMSA",
                "code": "PresentationFirstDiagnosis"
              }
            },
            {
              "valueCoding": {
                "system": "https://fhir.nwgenomics.nhs.uk/CodeSystem/NWGMSA",
                "code": "PresentationRecurrenceRelapse"
              }
            },
            {
              "valueCoding": {
                "system": "http://loinc.org",
                "code": "LA4489-6",
                "display": "Unknown"
              }
            }
          ],
          "item": [
            {
              "extension": [
                {
                  "url": "http://hl7.org/fhir/StructureDefinition/questionnaire-itemControl",
                  "valueCodeableConcept": {
                    "coding": [
                      {
                        "system": "http://hl7.org/fhir/questionnaire-item-control",
                        "code": "help"
                      }
                    ]
                  }
                }
              ],
              "linkId": "NOS/PresentationStatus-designNote",
              "text": "Inferred from [GMS WGS\nCancer](Questionnaire-GMSWGSCancerAskAtOrderEntry.html)'s own\n`NOS/PresentationStatus` item. Generalises the same distinction [HRD\nand Tumour BRCA](Questionnaire-HRDTumourBRCAAskAtOrderEntry.html)\nmakes via its own `Pathway` choice (HRD test = newly diagnosed,\nTumour BRCA-only = relapsed) plus separate\n`NewlyDiagnosedAdvancedDiseaseConfirmation`/`RelapsedDiseaseConfirmation`\nbooleans - that form conflates presentation status with test\nselection itself, since the pathway and the presentation are the same\nchoice on that specific form; here they are kept separate, as GMS WGS\nCancer already does.",
              "type": "display"
            }
          ]
        },
        {
          "extension": [
            {
              "url": "http://hl7.org/fhir/StructureDefinition/questionnaire-unit",
              "valueCoding": {
                "system": "http://unitsofmeasure.org",
                "code": "%",
                "display": "%"
              }
            }
          ],
          "linkId": "NOS/NeoplasticCellContent",
          "definition": "http://hl7.org/fhir/StructureDefinition/Observation#Observation.valueQuantity",
          "code": [
            {
              "system": "https://fhir.nwgenomics.nhs.uk/CodeSystem/NWGMSA",
              "code": "NeoplasticCellContent"
            }
          ],
          "text": "Neoplastic/malignant cell content (%)",
          "type": "quantity",
          "item": [
            {
              "extension": [
                {
                  "url": "http://hl7.org/fhir/StructureDefinition/questionnaire-itemControl",
                  "valueCodeableConcept": {
                    "coding": [
                      {
                        "system": "http://hl7.org/fhir/questionnaire-item-control",
                        "code": "help"
                      }
                    ]
                  }
                }
              ],
              "linkId": "NOS/NeoplasticCellContent-designNote",
              "text": "The same underlying concept is independently modelled three times\ntoday, each under its own linkId despite sharing this same\n`NWGMSA` code: [HRD and Tumour\nBRCA](Questionnaire-HRDTumourBRCAAskAtOrderEntry.html)'s\n`NOS/NeoplasticCellContent` (\"Approximate % neoplastic nuclei in\ntumour area highlighted\"), [GMS WGS\nCancer](Questionnaire-GMSWGSCancerAskAtOrderEntry.html)'s\n`NOS/NeoplasticCellContent-gms` (\"% Malignant nuclei / blasts (or\nequivalent)\"), and [WGS Local Test\nOrder](Questionnaire-WGSLocalTestOrderAskAtOrderEntry.html)'s own\n`NOS/NeoplasticCellContent-wgs`. Proposed here as the single shared\nfield this tier is for, rather than each Cancer-adjacent form\ncontinuing to reinvent its own suffixed linkId for the same value.",
              "type": "display"
            }
          ]
        },
        {
          "linkId": "NOS/PathologistName",
          "definition": "http://hl7.org/fhir/StructureDefinition/Observation#Observation.valueString",
          "code": [
            {
              "system": "https://fhir.nwgenomics.nhs.uk/CodeSystem/NWGMSA",
              "code": "PathologistName"
            }
          ],
          "text": "Pathologist",
          "type": "string",
          "item": [
            {
              "extension": [
                {
                  "url": "http://hl7.org/fhir/StructureDefinition/questionnaire-itemControl",
                  "valueCodeableConcept": {
                    "coding": [
                      {
                        "system": "http://hl7.org/fhir/questionnaire-item-control",
                        "code": "help"
                      }
                    ]
                  }
                }
              ],
              "linkId": "NOS/PathologistName-designNote",
              "text": "Present as its own named field on [HRD and Tumour\nBRCA](Questionnaire-HRDTumourBRCAAskAtOrderEntry.html). [GMS WGS\nCancer](Questionnaire-GMSWGSCancerAskAtOrderEntry.html) doesn't ask\nfor the pathologist by name, only a Histopathology Lab ID (see\n`Pathology hospital / laboratory` below) - proposed here as a\ngenuinely Cancer-wide concept even though only one of the two source\nforms currently asks for it.",
              "type": "display"
            }
          ]
        },
        {
          "linkId": "NOS/PathologyHospital",
          "definition": "http://hl7.org/fhir/StructureDefinition/Observation#Observation.valueString",
          "code": [
            {
              "system": "https://fhir.nwgenomics.nhs.uk/CodeSystem/NWGMSA",
              "code": "PathologyHospital"
            }
          ],
          "text": "Pathology hospital / laboratory",
          "type": "string",
          "item": [
            {
              "extension": [
                {
                  "url": "http://hl7.org/fhir/StructureDefinition/questionnaire-itemControl",
                  "valueCodeableConcept": {
                    "coding": [
                      {
                        "system": "http://hl7.org/fhir/questionnaire-item-control",
                        "code": "help"
                      }
                    ]
                  }
                }
              ],
              "linkId": "NOS/PathologyHospital-designNote",
              "text": "Generalises [HRD and Tumour\nBRCA](Questionnaire-HRDTumourBRCAAskAtOrderEntry.html)'s own\n`NOS/PathologyHospital` and [GMS WGS\nCancer](Questionnaire-GMSWGSCancerAskAtOrderEntry.html)'s\n`NOS/HistopathologyLabID` (\"Histopathology Lab ID\", under that form's\nown Solid tumour sub-group) - both identify where the pathology\nspecimen/report the order relies on came from, just at different\ngranularity (a named hospital vs. a lab identifier). Kept as free\ntext pending a decision on whether an\n[Organisation Code](StructureDefinition-OrganisationCode.html)\nreference would be more appropriate.",
              "type": "display"
            },
            {
              "extension": [
                {
                  "url": "http://hl7.org/fhir/StructureDefinition/questionnaire-itemControl",
                  "valueCodeableConcept": {
                    "coding": [
                      {
                        "system": "http://hl7.org/fhir/questionnaire-item-control",
                        "code": "help"
                      }
                    ]
                  }
                }
              ],
              "linkId": "NOS/PathologyHospital-futureQueryAccess",
              "text": "This item, and Pathologist above, most directly relate to the\n[Cheshire and Merseyside\nPathology](CheshireAndMerseysidePathology.html) reflex use case, where\na genomic order follows on from a prior pathology order/report\n(`LAB-1`/`LAB-3`) rather than starting the clinical episode itself.\nThat page's own [Current\nProcess](CheshireAndMerseysidePathology.html#current-process) still\nmodels the pathology-to-genomics handoff entirely as HL7 v2/FHIR\nmessaging (`LAB-1`/`LAB-35`/`LAB-3`/`LAB-36`), which is why today's\nanswer is free text naming the pathologist/hospital rather than a\nmachine-resolvable reference.\n\nA query-based alternative may remove the need to duplicate pathology\ncontent into the genomic order/message at all: some NW pathology LIMS\ndeployments (e.g. Medicus) already support the Australian [AU\neReq](https://hl7.org.au/fhir/ereq/index.html) FHIR IG for on-demand\nquery access to pathology orders (and potentially reports), and MFT\nseparately exposes pathology data through Epic's own [FHIR Query\nAPI](https://fhir.epic.com/). If a genomics laboratory can query\npathology directly, these two free-text fields could be replaced by a\n**reference** instead - the Pathology Order Filler Number, Pathology\nPatient Identifier and/or Pathology Specimen Identifier - letting the\ngenomic order carry a pointer for on-demand lookup rather than the\npathology detail itself.",
              "type": "display"
            }
          ]
        }
      ]
    }
  ]
}