 0 Table of Contents |
  1 Home |
   1.1 Changes |
   1.2 Adapting Guidelines for Country use |
  2 Actors and Transactions |
   2.1 System Actors |
   2.2 Use Cases |
   2.3 Transactions |
  3 Domain Model |
  4 eHN Imaging Studies and Reports Guidelines |
  5 Design Considerations |
  6 Contributors |
  7 Open Topics |
  8 Artifacts Summary |
   8.1 A Medical Imaging Report (eHN) |
   8.2 A.1 Report header data elements (eHN) |
   8.3 A.1.1 Identification of the patient/subject |
   8.4 A.1.2 Patient/subject related contact information |
   8.5 A.1.3 Health insurance and payment information |
   8.6 A.1.4 Information recipient |
   8.7 A.1.5 Author |
   8.8 A.1.6 Legal authenticator |
   8.9 A.1.7 Result validator |
   8.10 A.1.8 Document metadata |
   8.11 A.2 Order information |
   8.12 A.3 Order Reason |
   8.13 A.4 Specimen information |
   8.14 A.5 Examination Report |
   8.15 A.5.1 Imaging procedure description |
   8.16 A.5.2 Medication |
   8.17 A.5.3 Adverse reaction |
   8.18 A.5.4 Results |
   8.19 A.5.5 Conclusion |
   8.20 A.5.6 Recommendation |
   8.21 A.6 Key images associated with this report |
   8.22 A.7 Comparison study |
   8.23 A.8 Presented form |
   8.24 B Imaging study manifest data set (eHN) |
   8.25 Imaging Composition |
   8.26 Imaging Diagnostic Report |
   8.27 ImagingStudy |
   8.28 Imaging Study Reports Producer |
   8.29 Adverse Event |
   8.30 Allergic Reaction |
   8.31 Bundle: Imaging Study Report |
   8.32 Coverage information |
   8.33 Finding |
   8.34 Health Insurance Provider |
   8.35 Imaging Authoring Device |
   8.36 Imaging Device |
   8.37 Imaging Key Image Document Reference |
   8.38 Imaging Order |
   8.39 Imaging Patient |
   8.40 Imaging Procedure |
   8.41 Imaging results from Procedure Phase |
   8.42 Imaging study performer |
   8.43 ImBodyStructure |
   8.44 Impression |
   8.45 Information Recipient |
   8.46 Key images represented as an ImagingSelection |
   8.47 Legal Authenticator |
   8.48 Medication |
   8.49 Medication Administration |
   8.50 Order Placer |
   8.51 Organization |
   8.52 Practitioner |
   8.53 Practitioner Role |
   8.54 Radiation Dose Observation |
   8.55 Recommended CarePlan |
   8.56 Report Author |
   8.57 Represents the part of an imaging study. |
   8.58 Result Validator |
   8.59 Viewer endpoint |
   8.60 WADO endpoint |
   8.61 Imaging Accession Number Identifier |
   8.62 Imaging Accession Number Reference |
   8.63 Document DiagnosticReport Reference |
   8.64 Imaging Adverse Event Criticality |
   8.65 DiagnosticReport supportInfo codes |
   8.66 Imaging Report Types |
   8.67 Radiation Dose Observation Unit ValueSet |
   8.68 CodeSystem for terminology for Endpoint resources used in the EU Imaging IG. |
   8.69 Diagnostic Report Support Info Code System |
   8.70 Missing DICOM Terminology |
   8.71 Mapping of A.1.1 Identification of the patient/subject |
   8.72 Mapping of A.1.2 Patient/subject related contact information |
   8.73 Mapping of A.1.3 Health Insurance and Payment Information |
   8.74 Mapping of A.1.4 Information Recipient |
   8.75 Mapping of A.1.5 Information Author |
   8.76 Mapping of A.1.6 Legal Authenticator |
   8.77 Mapping of A.1.7 Result Validator |
   8.78 Mapping of A.1.8 Document Metadata |
   8.79 Mapping of A.2 Order Information to FHIR profiles |
   8.80 Mapping of A.3 Order Reason to FHIR profiles |
   8.81 Mapping of A.4 Specimen |
   8.82 Mapping of A.5.1 Imaging Procedure Description |
   8.83 Mapping of A.5.2 Imaging Procedure Medication |
   8.84 Mapping of A.5.3 Adverse reaction (Adverse reactions manifested during imaging investigation. |
   8.85 Mapping of A.5.4 Results |
   8.86 Mapping of A.5.5 Conclusion |
   8.87 Mapping of A.5.6 Recommendation |
   8.88 Mapping of A.6 Key images associated with this report |
   8.89 Mapping of A.7 Comparison Study |
   8.90 Mapping of A.8 Presented Form |
   8.91 Mapping of B Imaging study manifest data set |