TEMPLATE Radiological findings - Hepatocellular carcinoma (Radiological findings - Hepatocellular carcinoma)

TEMPLATE IDRadiological findings - Hepatocellular carcinoma
ConceptRadiological findings - Hepatocellular carcinoma
DescriptionNot Specified
PurposeNot Specified
References
Authorsdate: 2019-09-10; name: Samer Abboud Alkarkoukly; organisation: Uniklinikum Köln; email: mabbouda@uni-koeln.de
Other Details Languagedate: 2019-09-10; name: Samer Abboud Alkarkoukly; organisation: Uniklinikum Köln; email: mabbouda@uni-koeln.de
Other Details (Language Independent)
  • Licence: This work is licensed under the Creative Commons Attribution-ShareAlike 3.0 License. To view a copy of this license, visit http://creativecommons.org/licenses/by-sa/3.0/.
  • Custodian Organisation: openEHR Foundation
  • Original Namespace: org.openehr
  • Original Publisher: openEHR Foundation
  • Custodian Namespace: org.openehr
  • MD5-CAM-1.0.1: 879bf80355e0b5633622772a3f01b0f3
  • PARENT:MD5-CAM-1.0.1: 005501C1FA493A4838F5F1121F2870EC
  • Build Uid: 5b4193bc-2b9b-43fb-9506-42f061ab3728
  • Original Language: ISO_639-1::en
  • Sem Ver: 49.0.0
Language useden
Citeable Identifier1246.169.3422
Root archetype idopenEHR-EHR-COMPOSITION.report.v1
Radiological findings - Hepatocellular carcinomaRadiological findings - Hepatocellular carcinoma: 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.
  • Vorläufig
  • Final
  • Korrigiert
Case identificationCase identification: To record case identification details for public health purposes.
Case identifierCase identifier: The identifier of this case.
Imaging examination resultImaging examination result: The result of an imaging examination performed on an individual, using radiological techniques.
Data
Any eventAny event: Default, unspecified point in time or interval event which may be explicitly defined in a template or at run-time.
Data
Study nameStudy name: The name of the imaging examination performed.
For example: 'CT abdomen'; 'Doppler ultrasound of renal artery' or 'Plain chest xray'. Coding with a terminology is strongly recommended, preferably a term specifying both modality and anatomical location, where possible. Examples of candidate terminologies are the LOINC Imaging Document Codes, RadLex Playbook or SNOMED-CT. Equivalent to DiagnosticReport.code in FHIR.
  • HCC Examination
ModalityModality: The type of imaging device, process or method that originally acquired or produced the data used to create the images in the study.
For example: 'XRay', 'CT scan', 'ultrasound', 'MRI', 'bone densitometry', 'tomography', 'mammography', 'nuclear medicine', 'PET', 'angiography', and 'fluoroscopy'. This data element may be redundant if the modality is clearly represented in the 'Study name'. Alternatively it may also be possible to autopopulate the 'Modality' from a coded 'Study name'. Coding of the 'Modality' with a value set is recommended, such as the DICOM CID 29 Acquisition Modality value set. Equivalent to ImagingStudy.modality in FHIR and Modality (0008, 0060) in DICOM.
  • CT
  • MR
Study dateStudy date: Date/time when the imaging started.
Equivalent to ImagingStudy.started in FHIR.
Treatment situationTreatment situation: Narrative description about the reason the examination was originally requested.
Also known as 'Clinical question' or 'Clinical query'.
  • Initial finding
  • After neoadjuvant therapy
  • After local therapy
  • Under systemic therapy
  • Follow-up without therapy
Imaging findingsImaging findings: Narrative description or overview of all clinical findings.
Imaging Examination of Target LesionsImaging Examination of Target Lesions: Findings observed in an imaging examination targeting the liver, using radiographic techniques.
Body structureBody structure: Identification of the body structure or region examined.
  • Liver 
Number of target lesionsNumber of target lesions: Narrative description of the imaging findings observed during this examination.
  • 0
  • 1
  • 2
  • 3
  • >3
To target lesionTo target lesion: A finding on radiological examination that deviates from what is standard, normal or expected within an identified body structure or region.
For example: a cyst or mass; a thrombosis; a polyp; a calculus or a foreign body.
Body structureBody structure: Identification of the body structure or region examined.
If the body structure has been fully identified in this 'Body structure' element, then the 'Body site' data element and 'Structured body site' SLOT becomes redundant.
  • Anomaly 
Target-lesion localizationTarget-lesion localization: Identification of the area of the body under examination.
For example: a lymph node group (body structure) which found in the 'Right axilla'. Coding of 'Body site' with a terminology, such as SNOMED CT, is desirable. If the body site has been fully identified in the 'Body structure' data element, this data element becomes redundant.
  • Liver segment 1
  • Liver segment 2
  • Liver segment 3
  • Liver segment 4
  • Liver segment 4a
  • Liver segment 4b
  • Liver segment 5
  • Liver segment 6
  • Liver segment 7
  • Liver segment 8
Description of the lesionDescription of the lesion: Narrative description of the imaging findings observed during this examination.
LI-RADSLI-RADS: The Liver Imaging Reporting and Data System (LI-RADS®) is a comprehensive system for standardizing the terminology, technique, interpretation, reporting, and data collection of liver observations in individuals at high risk for hepatocellular carcinoma (HCC).
LI-RADS algorithmLI-RADS algorithm: The algorithm used to assess and diagnose liver lesions in a patient at risk of HCC.
  • CT/MRI Diagnostic LI-RADS 
Report algorithm LI-RADSReport algorithm LI-RADS: The LI-RADS category is a score assigned to a focal lesion. The categories span the spectrum of benign to malignant observations occurring in patients with chronic liver disease at risk for cirrhosis.
  • LR-NC 
  • LR-TIV 
  • LR-1 
  • LR-2 
  • LR-3 
  • LR-4 
  • LR-5 
  • LR-M 
Therapy response categoryTherapy response category: The categories of therapy response (TR) are used to assess the tumor's response after a locoregional therapy.
  • LR-TR Not assessable 
  • LR-TR nonviable 
  • LR-TR not clear 
  • LR-TR vital 
LI-RADS commentsLI-RADS comments: Additional information about the report that has not yet been documented elsewhere.
Residual vitalityResidual vitality: A finding on radiological examination that deviates from what is standard, normal or expected within an identified body structure or region.
For example: a cyst or mass; a thrombosis; a polyp; a calculus or a foreign body.
Body structureBody structure: Identification of the body structure or region examined.
If the body structure has been fully identified in this 'Body structure' element, then the 'Body site' data element and 'Structured body site' SLOT becomes redundant.
  • Anomaly 
Residual vitalityResidual vitality: Narrative description of the imaging findings observed during this examination.
  • Yes
  • No
  • Unclear
Comment on the residual vitality of the lesionComment on the residual vitality of the lesion: Additional narrative about the imaging findings of the body structure, not captured in other fields.
Size of the vital part of the HCCSize of the vital part of the HCC: A measured dimension of the anomaly.
This data element has unlimited occurrences to allow for measurements in 2 or more axes. If there is no clear orientation of the anomaly, for example length vs width vs height, use multiple occurrences to allow recording of the length of 2 or more axes without any specific orientation, for example 3 x 4 x 5 mm.
>=0; >=0
Units:
  • mm
  • cm
Target-Lesion CommentTarget-Lesion Comment: Additional narrative about the imaging findings of the body structure, not captured in other fields.
Size of the lesionSize of the lesion: A measured dimension of the anomaly.
This data element has unlimited occurrences to allow for measurements in 2 or more axes. If there is no clear orientation of the anomaly, for example length vs width vs height, use multiple occurrences to allow recording of the length of 2 or more axes without any specific orientation, for example 3 x 4 x 5 mm.
>=0; >=0
Units:
  • mm
  • cm
Target Lesion CommentTarget Lesion Comment: Additional narrative about the imaging findings of the body structure, not captured in other fields.
Portal vein thrombosisPortal vein thrombosis: Findings on radiological examination of a specified body structure or region.
Body structureBody structure: Identification of the body structure or region examined.
For example: 'Liver', 'Right ankle' or 'Lymph node group'. Coding of the body structure with an appropriate terminology, such as SNOMED CT, is recommended. If the body structure has been fully identified in this 'Body structure' element, then the 'Body site' data element and 'Structured body site' SLOT become redundant.
Existing?Existing?: Narrative description of the imaging findings observed during this examination.
  • Yes
  • No
  • Unclear
Portal vein thrombosis commentPortal vein thrombosis comment: Additional narrative about the imaging findings of the body structure, not captured in other fields.
Regional lymph node metastasesRegional lymph node metastases: Findings on radiological examination of a specified body structure or region.
Body structureBody structure: Identification of the body structure or region examined.
For example: 'Liver', 'Right ankle' or 'Lymph node group'. Coding of the body structure with an appropriate terminology, such as SNOMED CT, is recommended. If the body structure has been fully identified in this 'Body structure' element, then the 'Body site' data element and 'Structured body site' SLOT become redundant.
Existing?Existing?: Narrative description of the imaging findings observed during this examination.
  • Yes
  • No
  • Unclear
Regional lymph node metastases CommentRegional lymph node metastases Comment: Additional narrative about the imaging findings of the body structure, not captured in other fields.
Distant metastasesDistant metastases: Findings on radiological examination of a specified body structure or region.
Body structureBody structure: Identification of the body structure or region examined.
For example: 'Liver', 'Right ankle' or 'Lymph node group'. Coding of the body structure with an appropriate terminology, such as SNOMED CT, is recommended. If the body structure has been fully identified in this 'Body structure' element, then the 'Body site' data element and 'Structured body site' SLOT become redundant.
  • Distant metastases
Metastasis siteMetastasis site: A physical site on or within the human body.
Metastasis siteMetastasis site: Identification of a single physical site either on, or within, the human body.
This data element is the only mandated data point in this archetype and should be used as the primary data point to record an anatomical location with a commonly used name. It is strongly recommended that 'Body site name' be recorded as specifically as is anatomically possible. For example: record 'upper eyelid' rather than recording 'eyelid' with 'upper' as a qualifier; 'fifth rib' rather than 'rib' with a numeric qualifier. Use the other data elements for laterality, aspect, region and anatomical line to provide more detail. This data element should be coded with a terminology capable of triggering decision support, where possible - an appropriate termset for use here could comprise individual concepts or a list of precoordinated terms. Free text should be used only if there is no appropriate terminology available. If body site name is already identified in the parent archetype, then this data element may be redundant. Alternatively, a use case has been identified where the value may be duplicated into this element to support semantic querying using this archetype, rather than the data element within the parent.
Terminology: local_terms
  • Lung 
  • Bone 
  • Liver 
  • Brain 
  • Lymph node 
  • Bone marrow 
  • Pleura 
  • Peritoneum 
  • Adrenal gland 
  • Kidney 
  • Skin 
  • Other organs 
  • Generalized metastasis 
Distant metastases present?Distant metastases present?: Narrative description of the imaging findings observed during this examination.
  • Yes
  • No
  • Unclear
Distant Metastases CommentDistant Metastases Comment: Additional narrative about the imaging findings of the body structure, not captured in other fields.
mRECISTmRECIST: Evaluation of the response of a disease to therapy. This helps to assess the success of treatment, e.g. radiation or chemotherapy for a tumor.
Overall responseOverall response: Term that describes the response to treatment of a disease.
This is an already coded terminology of response to, for example, oncological therapy. Symptoms can be, for example, CR (complete remission of the disease), PR (partial remission), SD (stable disease) or PD (progression of the disease).
  • PR (partial response)
  • SD (stable disease)
  • PD (progressive disease)
  • CR (complete response)
  • U (assesment impossible)
  • X (missing information)
Assessment of the overall findingsAssessment of the overall findings: Narrative description about the comparison of this examination with previous similar studies.
Also use this data element to indicate if no comparison images and/or reports are available. Details about the images used for comparison can be recorded using the 'Comparison study details' CLUSTER, within Protocol.
  • Consistency of findings
  • Improvement of findings
  • Deterioration of findings
  • Divergent behavior
  • Assessment is not possible
  • Not applicable (initial findings)
Diagnostic qualityDiagnostic quality: Assessment about the quality of the examination.
Coding of the imaging quality with a value set is recommended. For example: 'excellent, good, fair, poor, and non-diagnostic'; or 'adequate, suboptimal and inadequate'.
  • Sufficient quality
  • Quality limited
  • Non-diagnostic
Overall impressionOverall impression: Narrative concise, clinically relevant interpretation of all imaging findings, and include a comparison with previous studies where appropriate.
Also referred to as 'Opinion' or 'Conclusion'. Equivalent to DiagnosticReport.conclusion in FHIR.
Protocol
DICOM study instance UIDDICOM study instance UID: Unique identifier for the imaging study assigned by the imaging device.
Equivalent to Study Instance UID (0020,000D) in DICOM and ImagingStudy.identifier in FHIR.
  •  Identifier
  •  Text
Report identifierReport identifier: Unique identifier for the imaging report assigned by the radiology service.
As one instance of this archetype is used per study, this identifier can be used to connect more than one imaging study within a single combined report. Equivalent to DiagnosticReport.identifier in FHIR.
  •  Identifier
  •  Text
CT Imaging ProcedureCT Imaging Procedure: To present the technical specifications of an imaging examination carried out.
Name of the technical processName of the technical process: To document the type of imaging procedure performed.
e.g. B. Diffusion weighting in MRI, the type or route of contrast medium administration, radiopharmaceuticals and/or treatment applied.
  • CT
Default value: CT
Native PhaseNative Phase: To document the subtype of imaging procedure performed.
e.g. B. Native phase, late arterial phase for CT, or T1 GRE fat suppressed late venous axial, T2 coronal for MRI
  • Native phase - Yes
  • Native phase - No
Late arterial phaseLate arterial phase: To document the subtype of imaging procedure performed.
e.g. B. Native phase, late arterial phase for CT, or T1 GRE fat suppressed late venous axial, T2 coronal for MRI
  • Late arterial phase - Yes
  • Late Arterial Phase - No
Venous phaseVenous phase: To document the subtype of imaging procedure performed.
e.g. B. Native phase, late arterial phase for CT, or T1 GRE fat suppressed late venous axial, T2 coronal for MRI
  • Portal Venous Phase - Yes
  • Portal Venous Phase - No
Late venous phaseLate venous phase: To document the subtype of imaging procedure performed.
e.g. B. Native phase, late arterial phase for CT, or T1 GRE fat suppressed late venous axial, T2 coronal for MRI
  • Late venous phase - Yes
  • Late venous phase - No
MR ProcedureMR Procedure: To present the technical specifications of an imaging examination carried out.
Name of the technical processName of the technical process: To document the type of imaging procedure performed.
e.g. B. Diffusion weighting in MRI, the type or route of contrast medium administration, radiopharmaceuticals and/or treatment applied.
  • MR
Default value: MR
T1 with chemical shift imaging (in-opp phase /Dixon) axialT1 with chemical shift imaging (in-opp phase /Dixon) axial: To document the subtype of imaging procedure performed.
e.g. B. Native phase, late arterial phase for CT, or T1 GRE fat suppressed late venous axial, T2 coronal for MRI
  • T1 with chemical shift imaging (in-opp phase /Dixon) axial - Yes
  • T1 with chemical shift imaging (in-opp phase /Dixon) axial - No
T1 GRE grease suppressed native axialT1 GRE grease suppressed native axial: To document the subtype of imaging procedure performed.
e.g. B. Native phase, late arterial phase for CT, or T1 GRE fat suppressed late venous axial, T2 coronal for MRI
  • T1 GRE Fat Suppressed Native Axial - Yes
  • T1 GRE Grease Suppressed Native Axial - No
T1 GRE fat suppressed late arterial axialT1 GRE fat suppressed late arterial axial: To document the subtype of imaging procedure performed.
e.g. B. Native phase, late arterial phase for CT, or T1 GRE fat suppressed late venous axial, T2 coronal for MRI
  • T1 GRE fat suppressed late arterial axial - Yes
  • T1 GRE fat suppressed late arterial axial - No
T1 GRE fat suppressed venous axialT1 GRE fat suppressed venous axial: To document the subtype of imaging procedure performed.
e.g. B. Native phase, late arterial phase for CT, or T1 GRE fat suppressed late venous axial, T2 coronal for MRI
  • T1 GRE fat suppressed venous axial - Yes
  • T1 GRE fat suppressed venous axial - No
T1 GRE fat-suppressed late venous axialT1 GRE fat-suppressed late venous axial: To document the subtype of imaging procedure performed.
e.g. B. Native phase, late arterial phase for CT, or T1 GRE fat suppressed late venous axial, T2 coronal for MRI
  • T1 GRE fat-suppressed late venous axial - Yes
  • T1 GRE fat-suppressed late venous axial - No
T1 GRE fat-suppressed hepatobiliary axialT1 GRE fat-suppressed hepatobiliary axial: To document the subtype of imaging procedure performed.
e.g. B. Native phase, late arterial phase for CT, or T1 GRE fat suppressed late venous axial, T2 coronal for MRI
  • T1 GRE fat-suppressed hepatobiliary axial - Yes
  • T1 GRE fat-suppressed hepatobiliary axial - No
T2 axialT2 axial: To document the subtype of imaging procedure performed.
e.g. B. Native phase, late arterial phase for CT, or T1 GRE fat suppressed late venous axial, T2 coronal for MRI
  • T2 axial - Ja
  • T2 axial - Nein
T2 coronaryT2 coronary: To document the subtype of imaging procedure performed.
e.g. B. Native phase, late arterial phase for CT, or T1 GRE fat suppressed late venous axial, T2 coronal for MRI
  • T2 koronar - Ja
  • T2 koronar - Nein
Diffusion-weighting b=0-100 s/mm2Diffusion-weighting b=0-100 s/mm2: To document the subtype of imaging procedure performed.
e.g. B. Native phase, late arterial phase for CT, or T1 GRE fat suppressed late venous axial, T2 coronal for MRI
  • Diffusion-weighting b=0-100 s/mm2 - Yes
  • Diffusion-weighting b=0-100 s/mm² - No
Diffusion-weighting b=500-1000 s/mm2Diffusion-weighting b=500-1000 s/mm2: To document the subtype of imaging procedure performed.
e.g. B. Native phase, late arterial phase for CT, or T1 GRE fat suppressed late venous axial, T2 coronal for MRI
  • Diffusion weighting b=500-1000 s/mm² - Yes
  • Diffusion weighting b=500-1000 s/mm² - No
Contrast mediumContrast medium: To present the technical specifications of an imaging examination carried out.
Name of the technical processName of the technical process: To document the type of imaging procedure performed.
e.g. B. Diffusion weighting in MRI, the type or route of contrast medium administration, radiopharmaceuticals and/or treatment applied.
  • Contrast medium
CM Applied ParametersCM Applied Parameters: To document the subtype of imaging procedure performed.
e.g. B. Native phase, late arterial phase for CT, or T1 GRE fat suppressed late venous axial, T2 coronal for MRI
  • Native
  • Extracellular CM
  • Liver-specific CM
CommentComment: Additional information about the imaging procedure performed.
may contain a text comment such as "the patient refused the use of a contrast agent" or "MRI could not be performed due to...".
DICOM module series metadataDICOM module series metadata: DICOM compliant representation of metadata referring to the module series of DICOM.
DICOM series instance UID (series ID)DICOM series instance UID (series ID): Referes to DICOM Tag (0020,000E).
Tumor diagnosis sectionTumor diagnosis section: Framework for consistent modelling of content within a template for a Problem list.
Intended to be used within the COMPOSITION.problem_list.
Tumor diagnosisTumor diagnosis: Details about a single identified health condition, injury, disability or any other issue which impacts on the physical, mental and/or social well-being of an individual.
Clear delineation between the scope of a problem versus a diagnosis is not easy to achieve in practice. For the purposes of clinical documentation with this archetype, problem and diagnosis are regarded as a continuum, with increasing levels of detail and supportive evidence usually providing weight towards the label of 'diagnosis'.
Data
Diagnosis name (ICD-10)Diagnosis name (ICD-10): Identification of the problem or diagnosis, by name.
Coding of the name of the problem or diagnosis with a terminology is preferred, where possible.
VariantVariant: Specific variant or subtype of the Diagnosis, if relevant.
For example: 'acute motor axonal neuropathy' as a variant of Guillain-Barre Syndrome. Coding of the name of the variant with a terminology is preferred, where possible.
Clinical descriptionClinical description: Narrative description about the problem or diagnosis.
Use to provide background and context, including evolution, episodes or exacerbations, progress and any other relevant details, about the problem or diagnosis.
Protocol
Tumor IDTumor ID: To display the ID of the tumor.
Tumor IDTumor ID: The ID/identifier of the tumor.
Other contributorsAurelie Tomczak, Institute of Pathology, University Hospital Heidelberg; Nina Bougatf, University Hospital Heidelberg; Natalia Strauch, Medizinische Hochschule Hannover; Antje Wulff, Medizinische Hochschule Hannover