NPCR Anmälan FHIR Implementation Guide
This section provides a complete worked example of NPCR Anmälan reporting through 20 linked FHIR resource instances. Together they trace one fictional patient (Sven Svensson) from primary care referral through diagnosis to pathology report.
The example demonstrates how the profiles in this IG link via FHIR references to form a coherent record of a single Anmälan registration event.
Sven Svensson is a 70-year-old male (born 1953-08-15, personnummer 19530815-1212) living in Karlstad, Sweden. On 2024-03-10, a routine primary care visit found his serum PSA elevated at 18.5 µg/L (P-PSA, NPU08669), prompting his general practitioner to author a referral on 2024-03-15. The referral was received at the urology specialist clinic on 2024-03-22.
At his first specialist visit on 2024-04-08 (KVÅ VJ125, Kvalitetsregisterkod 484), the urologist measured the prostate by transrectal ultrasound (TRUS) at 47 ml and ordered a multiparametric MRI.
The MRI was performed on 2024-04-22 and showed prostate volume 45 ml with a PI-RADS 4 lesion (high likelihood of clinically significant cancer). Extraprostatic extension (EPE) was assessed as Sannolikt (likely, scale 4 of 5), while seminal vesicle invasion (SVI) was assessed as Sannolikt inte (unlikely, scale 2 of 5).
On 2024-05-06, the patient underwent a combined transrectal biopsy under povidone-iodine rectal preparation. Three MR-fusion targeted biopsies (technique: fusion MR/ultraljud) were taken from the PI-RADS 4 lesion, alongside 12 systematic biopsy cores. The diagnosis method was registered as histopathology from needle biopsy (NPCR D_Vavn = 1, KVÅ KEB00).
The pathology report (PAD number P24-12345, Patologi Centralsjukhuset Karlstad) was issued on 2024-05-22 with the following findings:
The patient-level Gleason summary was set to 4+3=7, taken from the targeted biopsy. This case illustrates the clinical value of MRI-targeted biopsy: the systematic 12-core sampling alone would have suggested a lower-grade tumor (Gleason 6, grade group 1), but MRI-fusion targeting of the PI-RADS 4 lesion revealed higher-grade cancer (Gleason 7, grade group 3) that determines management decisions. Prostate cancer was confirmed (ICD-10-SE C619, Malign tumör i prostata) and clinically staged as T2 N0 M0 per UICC TNM Edition 8 (NPCR simplified clinical T classification, no T2 sub-stages).
| Date | Event |
|---|---|
| 2024-03-10 | Primary care: PSA 18.5 µg/L |
| 2024-03-15 | General practitioner authors referral |
| 2024-03-22 | Specialist clinic receives referral |
| 2024-04-08 | First specialist visit (urology); prostate volume 47 ml (TRUS) |
| 2024-04-22 | Prostate MRI: PI-RADS 4, EPE Sannolikt, SVI Sannolikt inte, volume 45 ml |
| 2024-05-06 | Combined transrectal biopsy (3 targeted + 12 systematic cores) |
| 2024-05-22 | Pathology report; Gleason 4+3=7 (targeted) vs 3+3=6 (systematic); summary 4+3=7; T2 N0 M0 |
The 20 examples form a connected reference graph:
subjectbasedOnfocusderivedFrom to reference targeted and systematic Gleason observationsresult to aggregate 5 biopsy-derived observations and performer to reference the pathology OrganizationThis pattern demonstrates how NPCR Anmälan data, decomposed into discrete FHIR resources, can be reassembled into a clinically coherent registration record via standard FHIR references.
These 20 examples exercise 19 of the 24 profiles in this IG. The 5 profiles not exercised (NPCRCauseOfDeathObservation, NPCRWHOGradeObservation, NPCRGleasonScoreUnclearBiopsyObservation, NPCRGleasonScoreTURPCystoObservation, NPCRBiopsyResultsUnclearBiopsyObservation) are clinically inapplicable to this patient scenario:
Future iterations may add example sets for additional clinical scenarios (deceased patient, cytological diagnosis, TUR-P incidental finding) to exercise these profiles.