HL7 Europe Imaging Study Report, published by HL7 Europe. This guide is not an authorized publication; it is the continuous build for version 0.1.0 built by the FHIR (HL7® FHIR® Standard) CI Build. This version is based on the current content of https://github.com/hl7-eu/imaging/ and changes regularly. See the Directory of published versions
Contents:
This page provides a list of the FHIR artifacts defined as part of this implementation guide.
Logical models representing the eHN Imaging Studies and Reports Guidelines. This is informative material.
A Medical Imaging Report (eHN) |
Medical Imaging Report |
A.1 Report header data elements (eHN) |
A.1 Report header data elements (eHN) |
A.1.1 Identification of the patient/subject |
Identification of the patient/subject |
A.1.2 Patient/subject related contact information |
Patient/subject related contact information |
A.1.3 Health insurance and payment information |
Health insurance information is not always required, however, in some jurisdictions, the insurance number is also used as the patient identifier. It is necessary not just for identification but also forms access to funding for care. |
A.1.4 Information recipient |
Intended recipient or recipients of the report, e.g., GP, another specialist. Multiple recipients could be provided. |
A.1.5 Author |
Author (by whom the imaging report or a subset of its results was authored). Multiple authors could be provided. |
A.1.6 Legal authenticator |
The person taking responsibility for the medical content of the document. |
A.1.7 Result validator |
Result validator |
A.1.8 Document metadata |
Document metadata |
A.2 Order information |
Note: an imaging report could respond to multiple orders. |
A.3 Order Reason |
Note: an imaging report could respond to multiple reasons. |
A.4 Specimen information |
Note: a specimen (not attached to a body) can be used for diagnostic, forensic and medical research purposes. |
A.5 Examination Report |
Examination Report |
A.5.1 Imaging procedure description |
Note: this part records the technical details of the performed procedures and may include information about protocol, imaging phases, imaging device, anatomical location, performer, place, date and time of performance. |
A.5.2 Medication |
Medication section includes information about medication administered during the medical imaging examination (contrast, sedation, stress agents), etc. |
A.5.3 Adverse reaction |
Adverse reactions manifested during imaging investigation. |
A.5.4 Results |
Note: The results summarise the findings and observations by the health professional following the imaging study. Note: this part includes textual as well as structured results or findings of the imaging investigation. |
A.5.5 Conclusion |
A concise and clinically contextualised summary including interpretation/impression of the diagnostic report |
A.5.6 Recommendation |
Recommendation |
A.6 Key images associated with this report |
Key images associated with this report |
A.7 Comparison study |
Comparison study |
A.8 Presented form |
Presented form |
B Imaging study manifest data set (eHN) |
The data set defines the contents of the key information about the imaging study as conveyed by the imaging study manifest data set. The imaging study manifest contains key information about the imaging study that is referenced, including the “pointers” that allow access to the series of images. It is important to note that the metadata used in expressing the filters associated with the querying for a list of imaging studies and/or imaging reports are defined in Section 2 Article 10: Selection List and filtering Parameters. These parameters are expressed as coded values from standardised value sets to ensure a robust search for a list of relevant imaging studies. Such metadata filtering parameters are associated with imaging studies, but may not be present in the content of the imaging study manifest. |
The key resources representing the entry points for imaging study reports.
Imaging Composition |
Clinical document used to represent a Imaging Study Report for the scope of the HL7 Europe project. |
Imaging Diagnostic Report |
Diagnostic Report profile for Imaging Reports. This document represents the report of an imaging study. It is the anchor resource that refers to all structured data as well as the |
ImagingStudy |
This profile represents an imaging study instance. |
The following artifacts define the types of individuals and/or systems that will interact as part of the use cases covered by this implementation guide.
Imaging Study Reports Producer |
Producer profile for this IG |
These define constraints on FHIR resources for systems conforming to this implementation guide.
Adverse Event |
Adverse event during imaging procedure. |
Allergic Reaction |
This profile represents a suspected allergic reaction occurred during or due to an imaging study procedure. |
Bundle: Imaging Study Report |
Clinical document used to represent a Imaging Study Report for the scope of the HL7 Europe project. |
Coverage information |
Health Insurance and Payment Information. This resource represents the insurance coverage for a patient. |
Finding |
Finding during imaging procedure. |
Health Insurance Provider |
Health Insurance Provider profile for healthcare organizations, this resource contains all information related to a health insurance provider. |
ImBodyStructure | |
Imaging Authoring Device |
This profile represents the device used to author the Imaging Diagnostic Report. |
Imaging Device |
This profile on Device represents the imaging device. |
Imaging Key Image Document Reference |
A document containing key images for a patient. It can refer to a DICOM or non-DICOM image. When referring to a DICOM image, the DocumentReference.content.attachment.url should be a WADO-URI. When referring to a non-DICOM image, the DocumentReference.content.attachment.url should be a direct URL to the image. When the resource represents a DICOM instance it SHALL contain a the SOP Instance UID in the identifier element. When the resource represents a DICOM series it SHALL contain the Series Instance UID in the identifier element. |
Imaging Order |
This profile on ServiceRequest represents the order for the Imaging Study and report. |
Imaging Patient |
Human patient representing the subject of a medical imaging study for the scope of the HL7 Europe project. |
Imaging Procedure |
This profile on Procedure represents the imaging procedure. |
Imaging results from Procedure Phase |
Represents the part of an imaging study that relates to a procedure phase such as e.g., without contrast, arterial phase, venous phase, delayed phase. Only some types of studies have phases. |
Imaging study performer |
The healtcare professional who performed the study/procedure. |
Impression |
Impression of the imaging study. A conclusion drawn by the author based on the findings of the study. |
Information Recipient |
Information recipient (intended recipient or recipients of the report, e.g., GP, another specialist). |
Key images represented as an ImagingSelection | |
Legal Authenticator |
Legal authenticator (The person taking responsibility for the medical content of the document). |
Medication |
Based on EPD Medication profile. Reference it once it is published. |
Medication Administration |
Record of medication administration during imaging procedure. |
Order Placer |
The healthcare professional who placed the order for the study. |
Organization |
Organization profile for healthcare organizations, this resource contains all information related to healthcare organizations. |
Practitioner |
Practitioner profile for healthcare professionals, this resource contains all demographic information releted to healthcare professionals. |
Practitioner Role |
Practitioner Role profile for healthcare professionals, all references to healthcare professionals will be of this type. |
Radiation Dose Observation |
A record for the radiation dose the subject has been exposed to during an imaging procedure. This resource is a placeholder pending further refinement in this topic. E.g. based on information from https://dicom.nema.org/medical/dicom/current/output/html/part16.html. |
Recommended CarePlan |
Recommended care plan for the patient based on the imaging study. Contains the narrative containing the plan including proposals, goals, and order requests for monitoring, tracking, or improving the condition of the patient. In the future it is expected that the care plan could be provided in a structured and coded format. |
Report Author |
Author (by whom the imaging report or a subset of its results was authored). Multiple authors could be provided. |
Represents the part of an imaging study. | |
Result Validator |
Result validator. The healthcare professional who is responsible validating the diagnostic report. |
Viewer endpoint |
This profile defines a placeholder for an Endpoint for a viewer that can be used to access the study, serie it is present on. The application is based on IHE-IID. |
WADO endpoint |
This profile defines the WADO endpoint for accessing imaging study content. |
These define constraints on FHIR data types for systems conforming to this implementation guide.
Imaging Accession Number Identifier |
This profile on Identifier represents the Accession Number for the Imaging Order. |
Imaging Accession Number Reference |
This profile on Reference represents a reference to an Imaging Order. |
These define constraints on FHIR data types for systems conforming to this implementation guide.
Document DiagnosticReport Reference |
This extension provides a reference to the DiagnosticReport instance that is associated with this Composition. |
Imaging Adverse Event Criticality |
Replicates AllergyIntolerance.criticality to introduce functionality in AdverseEvent resource. |
These define sets of codes used by systems conforming to this implementation guide.
DiagnosticReport supportInfo codes |
Codes to be used in |
Imaging Report Types |
Imaging Report Types. This version includes only one code as suggested by the eHN guideline. To add specificity the https://loinc.org/kb/users-guide/loinc-rsna-radiology-playbook-user-guide/ could be incorporated as the source of imaging study/report types. |
Radiation Dose Observation Unit ValueSet |
Units for Radiation Dose Observations. |
These define new code systems used by systems conforming to this implementation guide.
CodeSystem for terminology for Endpoint resources used in the EU Imaging IG. |
This code system defines various codes used to define ValueSets for Endpoints within the HL7-EU imaging IG. |
Diagnostic Report Support Info Code System |
Code system for codes to be used in |
Missing DICOM Terminology |
Code system for codes that are defined in DICOM but for which no matching code system is available in FHIR. |
These define transformations to convert between codes by systems conforming with this implementation guide.
Mapping of A.1.1 Identification of the patient/subject |
This concept map defines the mapping between the A.1.1 Identification of the patient/subject section and the FHIR profiles. |
Mapping of A.1.2 Patient/subject related contact information |
This concept map defines the mapping between the A.1.2 Patient/subject related contact information section and the FHIR profiles. |
Mapping of A.1.3 Health Insurance and Payment Information |
This concept map defines the mapping between the A.1.3. Health Insurance and Payment Information section and the FHIR profiles. |
Mapping of A.1.4 Information Recipient |
This concept map defines the mapping between the A.1.4 Information Recipient section and the FHIR profiles. |
Mapping of A.1.5 Information Author |
This concept map defines the mapping between the A.1.5 Information Author section and the FHIR profiles. |
Mapping of A.1.6 Legal Authenticator |
This concept map defines the mapping between the A.1.6 Legal Authenticator section and the FHIR profiles. |
Mapping of A.1.7 Result Validator |
This concept map defines the mapping between the A.1.7 Result Validator section and the FHIR profiles. |
Mapping of A.1.8 Document Metadata |
This concept map defines the mapping between the A.1.8 Document Metadata section and the FHIR profiles. |
Mapping of A.2 Order Information to FHIR profiles |
This concept map defines the mapping between the A.2 Order Information section and the FHIR profiles. |
Mapping of A.3 Order Reason to FHIR profiles |
This concept map defines the mapping between the A.3 Order Reason section and the FHIR profiles. |
Mapping of A.4 Specimen |
This concept map defines the mapping between the A.3 Order Reason section and the FHIR profiles. The Specimen relates to a different type of information stored in a PACS: digital pathology. This has to analysed in more detail before inclusion in the IG. One of the things that might be impacted is the structure of the report. |
Mapping of A.5.1 Imaging Procedure Description |
The procedure information is expected to be part of the |
Mapping of A.5.2 Imaging Procedure Medication |
Maps on A.5.2-ImagingProcedureMedication section of the eHN Medical Imaging Report to the FHIR profiles. |
Mapping of A.5.3 Adverse reaction (Adverse reactions manifested during imaging investigation. |
Maps on A.5.2-ImagingProcedureMedication section of the eHN Medical Imaging Report to the FHIR profiles. |
Mapping of A.5.4 Results |
Maps the A.5.4 Results section of the eHN Medical Imaging Report to the FHIR profiles. |
Mapping of A.5.5 Conclusion |
Maps the A.5.5 Results section of the eHN Medical Imaging Report to the FHIR profiles. |
Mapping of A.5.6 Recommendation |
Maps the A.5.6 Results section of the eHN Medical Imaging Report to the FHIR profiles. |
Mapping of A.6 Key images associated with this report |
Maps the A.6 Key Images section of the eHN Medical Imaging Report to the FHIR profiles. |
Mapping of A.7 Comparison Study |
Maps the A.7 Key Images section of the eHN Medical Imaging Report to the FHIR profiles. |
Mapping of A.8 Presented Form |
Maps the A.8 Presented Form section of the eHN Medical Imaging Report to the FHIR profiles. |
Mapping of B Imaging study manifest data set |
Maps the B Imaging study manifest data set section of the eHN Medical Imaging Report to the FHIR profiles. |