|
297 | 297 | "resourceType": "ServiceRequest", |
298 | 298 | "id": "ServiceRequest-NonWGSTestOrderForm-FetalScenario-Example", |
299 | 299 | "extension": [ |
| 300 | + { |
| 301 | + "url": "https://fhir.nhs.uk/England/StructureDefinition/Extension-Genomic-Patient-Role", |
| 302 | + "valueCodeableConcept": { |
| 303 | + "coding": [ |
| 304 | + { |
| 305 | + "system": "https://fhir.nhs.uk/CodeSystem/patient-role-genomics", |
| 306 | + "code": "proband", |
| 307 | + "display": "Proband" |
| 308 | + } |
| 309 | + ] |
| 310 | + } |
| 311 | + }, |
300 | 312 | { |
301 | 313 | "url": "https://fhir.hl7.org.uk/StructureDefinition/Extension-UKCore-Coverage", |
302 | 314 | "valueCodeableConcept": { |
|
310 | 322 | } |
311 | 323 | } |
312 | 324 | ], |
| 325 | + "requisition": { |
| 326 | + "system": "https://fhir.kingstonandrichmond.nhs.uk/Id/grouptestId", |
| 327 | + "value": "RR-REQ20230925", |
| 328 | + "assigner": { |
| 329 | + "identifier": { |
| 330 | + "system": "https://fhir.nhs.uk/Id/ods-organization-code", |
| 331 | + "value": "RAX" |
| 332 | + } |
| 333 | + } |
| 334 | + }, |
313 | 335 | "status": "active", |
314 | 336 | "intent": "order", |
315 | 337 | "category": [ |
|
369 | 391 | ], |
370 | 392 | "supportingInfo": [ |
371 | 393 | { |
372 | | - "reference": "Observation/Observation-HistoryOfFetalLoss-Example" |
| 394 | + "reference": "Observation/Observation-NonConsanguinousUnion-Example" |
| 395 | + } |
| 396 | + ], |
| 397 | + "note": [ |
| 398 | + { |
| 399 | + "text": "No family history of relevant testing" |
373 | 400 | }, |
374 | 401 | { |
375 | | - "reference": "Observation/Observation-NonConsanguinousUnion-Example" |
| 402 | + "text": "Free text for diagnosis/reason for referral, relevant information including family history, phenotypic details/ HPO Terms/ E.g. large echogenic kidneys with normal bladder" |
| 403 | + } |
| 404 | + ] |
| 405 | + }, |
| 406 | + "request": { |
| 407 | + "method": "POST", |
| 408 | + "url": "ServiceRequest" |
| 409 | + } |
| 410 | + }, |
| 411 | + { |
| 412 | + "fullUrl": "http://example.org/fhir/ServiceRequest/ServiceRequest-NonWGSTestOrderForm-FetalScenarioMother-Example", |
| 413 | + "resource": { |
| 414 | + "resourceType": "ServiceRequest", |
| 415 | + "id": "ServiceRequest-NonWGSTestOrderForm-FetalScenarioMother-Example", |
| 416 | + "extension": [ |
| 417 | + { |
| 418 | + "url": "https://fhir.nhs.uk/England/StructureDefinition/Extension-Genomic-Patient-Role", |
| 419 | + "valueCodeableConcept": { |
| 420 | + "coding": [ |
| 421 | + { |
| 422 | + "system": "https://fhir.nhs.uk/CodeSystem/patient-role-genomics", |
| 423 | + "code": "consultand", |
| 424 | + "display": "Consultand" |
| 425 | + } |
| 426 | + ] |
| 427 | + } |
| 428 | + }, |
| 429 | + { |
| 430 | + "url": "https://fhir.hl7.org.uk/StructureDefinition/Extension-UKCore-Coverage", |
| 431 | + "valueCodeableConcept": { |
| 432 | + "coding": [ |
| 433 | + { |
| 434 | + "system": "https://fhir.hl7.org.uk/CodeSystem/UKCore-FundingCategory", |
| 435 | + "code": "nhs-england", |
| 436 | + "display": "NHS England" |
| 437 | + } |
| 438 | + ] |
| 439 | + } |
| 440 | + } |
| 441 | + ], |
| 442 | + "requisition": { |
| 443 | + "system": "https://fhir.kingstonandrichmond.nhs.uk/Id/grouptestId", |
| 444 | + "value": "RR-REQ20230925", |
| 445 | + "assigner": { |
| 446 | + "identifier": { |
| 447 | + "system": "https://fhir.nhs.uk/Id/ods-organization-code", |
| 448 | + "value": "RAX" |
| 449 | + } |
| 450 | + } |
| 451 | + }, |
| 452 | + "status": "active", |
| 453 | + "intent": "order", |
| 454 | + "category": [ |
| 455 | + { |
| 456 | + "coding": [ |
| 457 | + { |
| 458 | + "system": "https://fhir.hl7.org.uk/CodeSystem/UKCore-GenomeSequencingCategory", |
| 459 | + "code": "rare-disease-non-wgs", |
| 460 | + "display": "Rare Disease - Non-WGS" |
| 461 | + } |
| 462 | + ] |
| 463 | + }, |
| 464 | + { |
| 465 | + "coding": [ |
| 466 | + { |
| 467 | + "system": "https://fhir.nhs.uk/CodeSystem/rare-diseaseTesting-genomics", |
| 468 | + "code": "prenatal-diagnosis", |
| 469 | + "display": "Prenatal diagnosis" |
| 470 | + } |
| 471 | + ] |
| 472 | + } |
| 473 | + ], |
| 474 | + "priority": "urgent", |
| 475 | + "subject": { |
| 476 | + "reference": "Patient/Patient-RyanneBoulder-Example", |
| 477 | + "identifier": { |
| 478 | + "system": "https://fhir.nhs.uk/Id/nhs-number", |
| 479 | + "value": "9449307687" |
| 480 | + } |
| 481 | + }, |
| 482 | + "authoredOn": "2023-09-25", |
| 483 | + "requester": { |
| 484 | + "reference": "PractitionerRole/PractitionerRole-LoisLaneKingstonClinicalGenetics-Example" |
| 485 | + }, |
| 486 | + "reasonCode": [ |
| 487 | + { |
| 488 | + "coding": [ |
| 489 | + { |
| 490 | + "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestService", |
| 491 | + "code": "TP289", |
| 492 | + "display": "Common aneuploidy testing - prenatal", |
| 493 | + "extension": [ |
| 494 | + { |
| 495 | + "url": "https://fhir.nhs.uk/England/StructureDefinition/Extension-GenomicTestCode-Version", |
| 496 | + "valueDecimal": 1.0 |
| 497 | + } |
| 498 | + ] |
| 499 | + } |
| 500 | + ] |
| 501 | + } |
| 502 | + ], |
| 503 | + "supportingInfo": [ |
| 504 | + { |
| 505 | + "reference": "Observation/Observation-HistoryOfFetalLoss-Example" |
376 | 506 | }, |
377 | 507 | { |
378 | 508 | "reference": "Observation/Observation-GenomicEthnicity-Example" |
|
394 | 524 | }, |
395 | 525 | { |
396 | 526 | "reference": "RelatedPerson/RelatedPerson-RyanneBoulder-Example" |
| 527 | + } |
| 528 | + ], |
| 529 | + "note": [ |
| 530 | + { |
| 531 | + "text": "No family history of relevant testing" |
397 | 532 | }, |
398 | 533 | { |
399 | | - "reference": "Patient/Patient-RyanneBoulder-Example", |
400 | | - "identifier": { |
401 | | - "system": "https://fhir.nhs.uk/Id/nhs-number", |
402 | | - "value": "9449307687" |
| 534 | + "text": "Free text for diagnosis/reason for referral, relevant information including family history, phenotypic details/ HPO Terms/ E.g. large echogenic kidneys with normal bladder" |
| 535 | + } |
| 536 | + ] |
| 537 | + }, |
| 538 | + "request": { |
| 539 | + "method": "POST", |
| 540 | + "url": "ServiceRequest" |
| 541 | + } |
| 542 | + }, |
| 543 | + { |
| 544 | + "fullUrl": "http://example.org/fhir/ServiceRequest/ServiceRequest-NonWGSTestOrderForm-FetalScenarioFather-Example", |
| 545 | + "resource": { |
| 546 | + "resourceType": "ServiceRequest", |
| 547 | + "id": "ServiceRequest-NonWGSTestOrderForm-FetalScenarioFather-Example", |
| 548 | + "extension": [ |
| 549 | + { |
| 550 | + "url": "https://fhir.nhs.uk/England/StructureDefinition/Extension-Genomic-Patient-Role", |
| 551 | + "valueCodeableConcept": { |
| 552 | + "coding": [ |
| 553 | + { |
| 554 | + "system": "https://fhir.nhs.uk/CodeSystem/patient-role-genomics", |
| 555 | + "code": "consultand", |
| 556 | + "display": "Consultand" |
| 557 | + } |
| 558 | + ] |
403 | 559 | } |
404 | 560 | }, |
405 | 561 | { |
406 | | - "reference": "RelatedPerson/RelatedPerson-RyanneBoulderPartner-Example" |
| 562 | + "url": "https://fhir.hl7.org.uk/StructureDefinition/Extension-UKCore-Coverage", |
| 563 | + "valueCodeableConcept": { |
| 564 | + "coding": [ |
| 565 | + { |
| 566 | + "system": "https://fhir.hl7.org.uk/CodeSystem/UKCore-FundingCategory", |
| 567 | + "code": "nhs-england", |
| 568 | + "display": "NHS England" |
| 569 | + } |
| 570 | + ] |
| 571 | + } |
| 572 | + } |
| 573 | + ], |
| 574 | + "requisition": { |
| 575 | + "system": "https://fhir.kingstonandrichmond.nhs.uk/Id/grouptestId", |
| 576 | + "value": "RR-REQ20230925", |
| 577 | + "assigner": { |
| 578 | + "identifier": { |
| 579 | + "system": "https://fhir.nhs.uk/Id/ods-organization-code", |
| 580 | + "value": "RAX" |
| 581 | + } |
| 582 | + } |
| 583 | + }, |
| 584 | + "status": "active", |
| 585 | + "intent": "order", |
| 586 | + "category": [ |
| 587 | + { |
| 588 | + "coding": [ |
| 589 | + { |
| 590 | + "system": "https://fhir.hl7.org.uk/CodeSystem/UKCore-GenomeSequencingCategory", |
| 591 | + "code": "rare-disease-non-wgs", |
| 592 | + "display": "Rare Disease - Non-WGS" |
| 593 | + } |
| 594 | + ] |
407 | 595 | }, |
408 | 596 | { |
409 | | - "reference": "Patient/Patient-RyanneBoulderPartner-Example", |
410 | | - "identifier": { |
411 | | - "system": "urn:oid:2.16.840.1.113883.2.1.3.2.4.18.24", |
412 | | - "value": "P-RWT13521", |
413 | | - "assigner": { |
414 | | - "identifier": { |
415 | | - "system": "https://fhir.nhs.uk/Id/ods-organization-code", |
416 | | - "value": "RAX" |
417 | | - } |
| 597 | + "coding": [ |
| 598 | + { |
| 599 | + "system": "https://fhir.nhs.uk/CodeSystem/rare-diseaseTesting-genomics", |
| 600 | + "code": "prenatal-diagnosis", |
| 601 | + "display": "Prenatal diagnosis" |
| 602 | + } |
| 603 | + ] |
| 604 | + } |
| 605 | + ], |
| 606 | + "priority": "urgent", |
| 607 | + "subject": { |
| 608 | + "reference": "Patient/Patient-RyanneBoulderPartner-Example", |
| 609 | + "identifier": { |
| 610 | + "system": "urn:oid:2.16.840.1.113883.2.1.3.2.4.18.24", |
| 611 | + "value": "P-RWT13521", |
| 612 | + "assigner": { |
| 613 | + "identifier": { |
| 614 | + "system": "https://fhir.nhs.uk/Id/ods-organization-code", |
| 615 | + "value": "RAX" |
418 | 616 | } |
419 | 617 | } |
420 | | - }, |
| 618 | + } |
| 619 | + }, |
| 620 | + "authoredOn": "2023-09-25", |
| 621 | + "requester": { |
| 622 | + "reference": "PractitionerRole/PractitionerRole-LoisLaneKingstonClinicalGenetics-Example" |
| 623 | + }, |
| 624 | + "reasonCode": [ |
421 | 625 | { |
422 | | - "reference": "Specimen/Specimen-BloodEDTA-Example" |
423 | | - }, |
| 626 | + "coding": [ |
| 627 | + { |
| 628 | + "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestService", |
| 629 | + "code": "TP289", |
| 630 | + "display": "Common aneuploidy testing - prenatal", |
| 631 | + "extension": [ |
| 632 | + { |
| 633 | + "url": "https://fhir.nhs.uk/England/StructureDefinition/Extension-GenomicTestCode-Version", |
| 634 | + "valueDecimal": 1.0 |
| 635 | + } |
| 636 | + ] |
| 637 | + } |
| 638 | + ] |
| 639 | + } |
| 640 | + ], |
| 641 | + "supportingInfo": [ |
424 | 642 | { |
425 | | - "reference": "Specimen/Specimen-RyanneBoulderSaliva-Example" |
| 643 | + "reference": "RelatedPerson/RelatedPerson-RyanneBoulderPartner-Example" |
426 | 644 | } |
427 | 645 | ], |
428 | 646 | "note": [ |
|
722 | 940 | ] |
723 | 941 | }, |
724 | 942 | "subject": { |
| 943 | + "reference": "Patient/Patient-RyanneBoulder-Example", |
725 | 944 | "identifier": { |
726 | 945 | "system": "https://fhir.nhs.uk/Id/nhs-number", |
727 | 946 | "value": "9449307687" |
|
769 | 988 | }, |
770 | 989 | "request": [ |
771 | 990 | { |
772 | | - "reference": "ServiceRequest/ServiceRequest-NonWGSTestOrderForm-FetalScenario-Example" |
| 991 | + "reference": "ServiceRequest/ServiceRequest-NonWGSTestOrderForm-FetalScenarioMother-Example" |
773 | 992 | } |
774 | 993 | ], |
775 | 994 | "container": [ |
|
826 | 1045 | ], |
827 | 1046 | "request": [ |
828 | 1047 | { |
829 | | - "reference": "ServiceRequest/ServiceRequest-NonWGSTestOrderForm-FetalScenario-Example" |
| 1048 | + "reference": "ServiceRequest/ServiceRequest-NonWGSTestOrderForm-FetalScenarioMother-Example" |
830 | 1049 | } |
831 | 1050 | ] |
832 | 1051 | }, |
|
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