TEMPLATE British Columbia Cancer agency Breast Cancer Synoptic Report (British Columbia Cancer agency Breast Cancer Synoptic Report)

TEMPLATE IDBritish Columbia Cancer agency Breast Cancer Synoptic Report
ConceptBritish Columbia Cancer agency Breast Cancer Synoptic Report
DescriptionThis template demonstrates representation of a NEHTA Synoptic report for Melanoma histopathology
PurposeThis template demonstrates representation of a NEHTA Synoptic report for Melanoma histopathology
References
Other Details (Language Independent)
  • MetaDataSet:Sample Set : Template metadata sample set
Language useden
Citeable Identifier1013.26.199
Root archetype idopenEHR-EHR-COMPOSITION.report.v1
British Columbia Cancer agency Breast Cancer Synoptic ReportBritish Columbia Cancer agency Breast Cancer Synoptic Report: Document to communicate information to others, commonly in response to a request from another party.
Other Context
Report IDReport ID: Identification information about the report.
StatusStatus: The status of the entire report. Note: This is not the status of any of the report components.
Patient IdentityPatient Identity: A generic section header which should be renamed in a template to suit a specific clinical context.

Annotations

  • Default: Basic patient identifier e.g. Name, address and ID are presumed to be held separately
Diagnostic SummaryDiagnostic Summary: A generic section header which should be renamed in a template to suit a specific clinical context.

Annotations

  • Default: From the generic framework recommendation
DiagnosisDiagnosis: A diagnosis defined by a clinician which is coded in an accepted terminology and may include the stage of the condition and the diagnostic criteria
DiagnosisDiagnosis: The index diagnosis
Value set: ac0.1
Clinical descriptionClinical description: Description of the clinical aspects of the problem
Date clinically recognisedDate clinically recognised: Date the problem was recognised by clinicians
2. Current biopsy findings2. Current biopsy findings: A generic section header which should be renamed in a template to suit a specific clinical context.
Breast cancer biopsy resultBreast cancer biopsy result: Simple histopathology lab test result.
Data
Any eventAny event: *
Data
Test nameTest name: Specific identifier for this lab test. e.g. Full blood count , blood glucose, urine microbiology. May equate to the result name for a single value result. Commonly a coded term e.g from LOINC or SNOMED-CT.
  • Breast Biopsy
Default value: Breast Biopsy
Diagnostic serviceDiagnostic service: The type of high-level diagnostic service e.g. biochemistry, haematology.
MacroscopicMacroscopic: Macroscopic findings - more than one set of findings may be recorded.
Macroscopic findingMacroscopic finding: A single set of macroscopic pathology findings.
Tissue presentTissue present: Confirmation, or otherwise, that the tissue or structure referred to by this macroscopic finding is present in the specimen for analysis.
  • Present 
  • Absent 
DescriptionDescription: Narrative text recorded at the time of specimen macroscopic dissection.
Overall macroscopic descriptionOverall macroscopic description: General comment or description about macroscopy findings.
MicroscopicMicroscopic: Microscopic findings - more than one set of findings may be recorded.
Histopathological resultHistopathological result: A conclusion or 'pathological diagnosis' for this individual microscopic finding.
SpecimenSpecimen: To record details of a laboratory specimen.
Specimen typeSpecimen type: The type of specimen to be collected e.g venous blood, prostatic biopsy.
Optional[{fhir_mapping=Specimen.type}]
Datetime collectedDatetime collected: The date and time that collection has been ordered to take place or has taken place.
Sampling conditionsSampling conditions: Any conditions to be met before the sample should be taken.
e.g. fasting, 'full bladder', 'sterile field' or any special instructions on the handling or immediate processing of the sample e.g. centrifuge on receipt. Can also be used to document any known deviations from collection or handling instructions e.g patient was not fasted.
Collection methodCollection method: The method of collection to be used eg Venepuncture, biopsy, resection.
Optional[{fhir_mapping=Specimen.collection.method}]
Collection method descriptionCollection method description: Additional detailed description of method of sample collection.
Potential riskPotential risk: Any risk or biohazard associated with collecting or handling the specimen.
Collection settingCollection setting: Identification of the setting at which the specimen was collected from a subject of care. The specimen is often collected by a healthcare provider, but may be collected directly by the patient or carer at home.
This specifies the specimen collection location within the healthcare environment. It enables the laboratory to ask questions about the collection of the specimen, if required. The specimen collection setting may provide additional information relevant to the analysis of the result.
Specimen collector identifierSpecimen collector identifier: Identifier of the person or agency responsible for collecting the specimen.
Optional[{fhir_mapping=Specimen.collection.collector}]
Number of containersNumber of containers: The total number of containers holding this specimen.
>=0
Specimen qualitySpecimen quality: Problems with the received specimen.
Specimen received issuesSpecimen received issues: Specific issue with a received specimen.
  •  Coded Text
    • Haemolysed 
    • Lipaemic 
    • Incorrect transport medium 
    • Insufficient sample 
  •  Text
Laboratory handling issuesLaboratory handling issues: Issue arising with handling or processing of the specimen within the laboratory.
  •  Coded Text
    • Handling error 
    • Age 
    • Laboratory accident 
    • Technical failure 
  •  Text
Adequacy for testingAdequacy for testing: Is the specimen adequate for testing?
  •  Coded Text
    • Satisfactory 
    • Unsatisfactory - processed 
    • Unsatisfactory - not processed 
  •  Text
CommentComment: An additional text comment on the quality of the received specimen.
Related specimenRelated specimen: Details of a related specimen.
Parent specimen identifierParent specimen identifier: Unique identifier of the parent specimen, where the specimen is split into sub-samples.
Microscopic findings - Breast cancerMicroscopic findings - Breast cancer: Microscopic anatomic pathology findings related to breast cancer.
Histologic gradingHistologic grading: Histologic grading of breast cancer.
Bloom and Richardson GradeBloom and Richardson Grade: Bloom and Richardson Histology Grade ( with modification by Elston and Ellis) is composed of three components which are combined to produce a calculated Histology Grade.
Mitosis countMitosis count: Mitotic frequency is calculated from the number of mitoses per 10 high-power fields.
Mitotic frequency scoreMitotic frequency score: Mitotic frequency score calculated from the mitosis count and the microscopy field diameter via a lookup table.
  • 1: Score 1 
  • 2: Score 2 
  • 3: Score 3 
Nuclear scoreNuclear score: Nuclear score.
  • 1: Score 1 
  • 2: Score 2 
  • 3: Score 3 
Tubular formation scoreTubular formation score: Tubular formation score, representing the extent of tubular formation within invasive carcinoma cells.
  • 1: Tubular formation score 1 
  • 2: Tubular formation score 2 
  • 3: Tubular formation score 3 
Histologic gradeHistologic grade: Bloom and Richardson Grade of breast cancer, derived from the total score of its components: Mitotic frequency score, Nuclear score and Tubular formation score.
  • 1: Grade 1 
  • 2: Grade 2 
  • 3: Grade 3 
Confounding issuesConfounding issues: A text description of any assessment issues which may confound the accuracy of the Bloom and Richardson histologic grade.
Non-neoplastic cellular changesNon-neoplastic cellular changes: Findings of non-neoplastic cellular changes.
Non-neoplastic cellular changeNon-neoplastic cellular change: Finding of non-neoplastic cellular change.
Lobular neoplasiaLobular neoplasia: Findings of lobular neoplasia and variants.
Lobular neoplasiaLobular neoplasia: Finding of lobular neoplasia.
  •  Coded Text
    • Present - classical 
    • Present - pleomorphic 
    • Absent 
    • Indeterminate 
  •  Text
Atypical lobular hyperplasiaAtypical lobular hyperplasia: Finding of atypical lobular hyperplasia.
  •  Coded Text
    • Present - classical 
    • Present - pleomorphic 
    • Absent 
    • Indeterminate 
  •  Text
Lobular carcinoma-in-situLobular carcinoma-in-situ: Finding of lobular carcinoma-in-situ.
  •  Coded Text
    • Present - classical 
    • Present - pleomorphic 
    • Absent 
    • Indeterminate 
  •  Text
DescriptionDescription: A text description of finding of lobular neoplasia.
Paget's disease of nipplePaget's disease of nipple: Findings related to Paget's disease of the nipple.
Paget's disease of nipplePaget's disease of nipple: Finding of Paget's disease of the nipple.
  • Present 
  • Absent 
  • Indeterminate 
MicrocalcificationMicrocalcification: Findings related to microcalcification.
MicrocalcificationMicrocalcification: Findings of microcalcification.
  • Present 
  • Absent 
  • Indeterminate 
  • Present - no evidence of necrosis 
  • Present - with evidence of necrosis 
Associated pathologyAssociated pathology: A text description of pathology associated with microcalcification.
DCIS featuresDCIS features: Findings related to Ductal carcinoma-in-situ (DCIS).
CalcificationCalcification: Finding of calcification in DCIS tissue.
  • Present with necrosis 
  • Present without necrosis 
  • Absent 
  • Indeterminate 
Histologic gradeHistologic grade: Histologic grading of DCIS.
NecrosisNecrosis: Findings of tumour necrosis.
  • Present (non-comedo type) 
  • Present (Comedo type) 
  • Absent or minimal 
Nuclear scoreNuclear score: Nuclear score, using the Elston and Ellis modification of the Bloom and Richardson system for grading invasive carcinoma.
  • 1: Score 1 
  • 2: Score 2 
  • 3: Score 3 
Van Nuys Prognostic IndexVan Nuys Prognostic Index: The Van Nuys Prognostic Index (VNPI).
  • 1: Van Nuys Group 1 
  • 2: Van Nuys Group 2 
  • 3: Van Nuys Group 3 
CommentComment: Comment on estimation of the histologic grade.
DCIS ArchitectureDCIS Architecture: Findings related to architecture of the ductal carcinoma-in-situ.
Dominant patternDominant pattern: Findingof the dominant DCIS architectural pattern.
  •  Coded Text
    • Solid 
    • Cribriform 
    • Micropapillary 
    • Apocrine 
    • Papillary 
    • Indeterminate 
  •  Text
DescriptionDescription: A text description of the architectural pattern.
Hormone Receptor assaysHormone Receptor assays: Immunohistochemical assays of oestrogen receptor (ER) and progesterone receptor (PR).
Oestrogen receptor assay (ER)Oestrogen receptor assay (ER): Oestrogen Receptor assay (ER).
ER resultER result: Oestrogen Receptor assay result.
  • Positive 
  • Negative 
  • Equivocal 
Proportion of nuclei stainedProportion of nuclei stained: An estimate of the percentage of nuclei stained.
Predominant staining intensityPredominant staining intensity: Predominant intensity of staining.
  • Low 
  • Intermediate 
  • High 
Progesterone receptor assay (PR)Progesterone receptor assay (PR): Progesterone Receptor (PR) assay.
PR resultPR result: Progesterone Receptor assay result.
  • Positive 
  • Negative 
  • Equivocal 
Proportion of nuclei stainedProportion of nuclei stained: An estimate of the percentage of nuclei stained.
Predominant staining intensityPredominant staining intensity: Predominant intensity of staining.
  • Low 
  • Intermediate 
  • High 
Human Oestrogen receptor 2 assay (HER2)Human Oestrogen receptor 2 assay (HER2): Human Oestrogen receptor 2 (HER2) assay.
ImmunohistochemistryImmunohistochemistry: HER2 Immunohistochemistry result.
Immunohistochemistry scoreImmunohistochemistry score: HER2 immunohistochemistry score.
>=0
Immunohistochemistry resultImmunohistochemistry result: HER2 Immunohistochemistry result.
  • Positive 
  • Negative 
  • Equivocal 
In situ hybridisation (ISH)In situ hybridisation (ISH): HER2 In situ hybridisation (ISH).
ISH resultISH result: HER2 In situ hybridisation (ISH) result.
  • Positive 
  • Negative 
  • Equivocal 
CommentComment: A text comment on HER2 In situ hybridisation (ISH) result.
Non-neoplastic changesNon-neoplastic changes: Findings of non-neoplastic change.
Non-neoplastic changeNon-neoplastic change: Finding of non-neoplastic change.
  • Columnar cell changes 
  • Intraductal papilloma 
  • Radial scars 
  • Atypical ductal hyperplasia (ADH) 
  • Absent 
  • Indeterminate 
CommentsComments: Narrative text recorded at the time of specimen microscopic examination.
Overall microscopic descriptionOverall microscopic description: General comment or description about microscopy findings as a whole.
Histopathological resultHistopathological result: Conclusions or 'pathological diagnoses' for the whole test.
Histopathological subtypeHistopathological subtype: A subtype of the histopthological result.
Overall interpretationOverall interpretation: An overall interpretative comment on this test.
Test identificationTest identification: Unique identifiers used in delivery of the care process.
Placer order identifierPlacer order identifier: The ID assigned to the order by the order requester. Equivalent to the NEHTA Requester Order Identifier.
Filler order IdentifierFiller order Identifier: The ID assigned to the test order by the order filler, usually by the (LIS) Laboratory Information System. Equivalent to the DICOM Accession Number and NEHTA Laboratory Request Identifier.
Laboratory test result identifierLaboratory test result identifier: The identifier given to the laboratory test result of a pathology investigation.