 0 Table of Contents |
  1 Home |
   1.1 Changes |
   1.2 Adapting Guidelines for Country use |
   1.3 Contributors |
  2 Actors and Transactions |
  3 XtEHR |
   3.1 XtEHR Logical Model |
   3.2 Mapping to XtEHR Logical Model |
  4 Deployment profiles |
   4.1 Imaging Manifest |
   4.2 Imaging Report |
  5 Design Considerations |
  6 Artifacts |
   6.1 Structural artifacts |
  7 Artifacts Summary |
   7.1 Imaging Manifest Reports Provider/Creator |
   7.2 Imaging Study Report Provider/Creator |
   7.3 Address model |
   7.4 Alert flag model |
   7.5 Allergy intolerance model |
   7.6 Appointment model |
   7.7 Attachment model |
   7.8 Attachments |
   7.9 Care plan model |
   7.10 Clinical impression model |
   7.11 Condition model |
   7.12 Coverage model |
   7.13 Device model |
   7.14 Device use model |
   7.15 Dispense decline |
   7.16 Document header model |
   7.17 Dosaging model |
   7.18 Encounter model |
   7.19 Endpoint model |
   7.20 Episode of care model |
   7.21 Functional status |
   7.22 Goal model |
   7.23 Group model |
   7.24 Health professional model |
   7.25 Hospital Discharge Report |
   7.26 Hospital Discharge Report header model |
   7.27 Human name model |
   7.28 Imaging report body model |
   7.29 Imaging report header model |
   7.30 Imaging report model |
   7.31 Imaging study model |
   7.32 Immunization model |
   7.33 Inpatient encounter model |
   7.34 Laboratory observation model |
   7.35 Laboratory order |
   7.36 Laboratory order body model |
   7.37 Laboratory order header model |
   7.38 Laboratory report body model |
   7.39 Laboratory report header model |
   7.40 Laboratory report model |
   7.41 Location model |
   7.42 Media model |
   7.43 Medication administration model |
   7.44 Medication dispensation model |
   7.45 Medication dispense header |
   7.46 Medication prescription header model |
   7.47 Medication prescription model |
   7.48 Medicinal product model |
   7.49 Observation model |
   7.50 Organization model |
   7.51 Patient model |
   7.52 Patient summary body model |
   7.53 Patient summary header model |
   7.54 Patient summary model |
   7.55 Procedure model |
   7.56 Related person model |
   7.57 Report header model |
   7.58 Resource header model |
   7.59 Service request model |
   7.60 Slot model |
   7.61 Specimen model |
   7.62 Substance model |
   7.63 Task model |
   7.64 Telecom model |
   7.65 Document Bundle for Imaging Report |
   7.66 DocumentReferenceEu |
   7.67 EU AllergyIntolerance |
   7.68 EU BodyStructure |
   7.69 EU CarePlan |
   7.70 EU Composition |
   7.71 EU Condition |
   7.72 EU Encounter |
   7.73 EU Endpoint |
   7.74 EU Medication |
   7.75 EU Observation |
   7.76 EU Procedure |
   7.77 Finding |
   7.78 Gestational Age Observation |
   7.79 IM Image Viewer Endpoint |
   7.80 Im Imaging Device |
   7.81 IM Imaging Order |
   7.82 IM Imaging Patient |
   7.83 IM Imaging Procedure |
   7.84 IM Imaging Study |
   7.85 IM ImagingStudy Manifest |
   7.86 IM WADO Endpoint |
   7.87 Imaging Adverse Event |
   7.88 Imaging Composition |
   7.89 Imaging Diagnostic Report |
   7.90 Imaging Key Image Document Reference |
   7.91 Imaging Selection profile for R4 |
   7.92 Imaging Selection referring to a DICOM SR instance for R4 |
   7.93 Key images represented as an ImagingSelection for R4 |
   7.94 Manifest DocumentReference for MHD deployments |
   7.95 Patient: Animal |
   7.96 r4 DocumentReference for MHD deployments |
   7.97 Radiation Dose Observation |
   7.98 RelatedPerson Eu |
   7.99 Report DocumentReference for MHD deployments |
   7.100 Specimen: Laboratory |
   7.101 EU Quantity |
   7.102 EU Range |
   7.103 EU SimpleQuantity |
   7.104 Imaging Accession Number Identifier |
   7.105 Imaging SOP Class UID Identifier |
   7.106 Placeholder for IHE MHD Entry UUID Identifier in FHIR R5. |
   7.107 Study Instance UID Identifier |
   7.108 Cross-version Extension for R5.Composition.event.detail for use in FHIR R4 |
   7.109 Cross-version Extension for R5.Composition.identifier for use in FHIR R4 |
   7.110 Cross-version Extension for R5.Device.category for use in FHIR R4 |
   7.111 Cross-version Extension for R5.DiagnosticReport.composition for use in FHIR R4 |
   7.112 Cross-version Extension for R5.DiagnosticReport.supportingInfo for use in FHIR R4 |
   7.113 Cross-version Extension for R5.DocumentReference.basedOn for use in FHIR R4 |
   7.114 Cross-version Extension for R5.DocumentReference.basedOn for use in FHIR R4 |
   7.115 Cross-version Extension for R5.DocumentReference.bodySite for use in FHIR R4 |
   7.116 Cross-version Extension for R5.DocumentReference.content.profile for use in FHIR R4 |
   7.117 Cross-version Extension for R5.DocumentReference.modality for use in FHIR R4 |
   7.118 Cross-version Extension for R5.Endpoint.connectionType for use in FHIR R4 |
   7.119 Cross-version Extension for R5.Endpoint.payload for use in FHIR R4 |
   7.120 Cross-version Extension for R5.ImagingSelection for use in FHIR R4 |
   7.121 Document DiagnosticReport Reference |
   7.122 Imaging Adverse Event Subject Research Subject |
   7.123 Instance Description |
   7.124 Media.view extension |
   7.125 Periods of Life Extension |
   7.126 ServiceRequest.reason extension for R4 |
   7.127 SupportingInfo CodeableConcept extension for R4 |
   7.128 Cross-version VS for R5.ImagingSelection2DGraphicType for use in FHIR R4 |
   7.129 Cross-version VS for R5.ImagingSelection3DGraphicType for use in FHIR R4 |
   7.130 Cross-version VS for R5.ImagingSelectionStatus for use in FHIR R4 |
   7.131 DiagnosticReport supportInfo codes |
   7.132 Dose Length Units |
   7.133 Effective Dose Units |
   7.134 FHIR Device Category |
   7.135 Gray Square Units |
   7.136 HL7 EU Imaging Manifest Types |
   7.137 HL7 EU Imaging Report Types |
   7.138 Imaging Device Type |
   7.139 Imaging Procedure Type |
   7.140 Imaging Study Performer Type Value Set |
   7.141 Media View types - placeholder for cross-version extension |
   7.142 Periods of Life |
   7.143 Reasons a section in an imaging report is empty. |
   7.144 CodeSystem for terminology used in Endpoint resources in the EU Imaging IG. |
   7.145 Diagnostic Report Support Info Code System |
   7.146 HL7 EU Document Types |
   7.147 Missing DICOM Terminology |