HL7 Europe Laboratory Report
2.0.0-alpha - qa-preview 150

This page is part of the HL7 Europe Laboratory Report (v2.0.0-alpha: QA Preview) based on FHIR (HL7® FHIR® Standard) R4. This version is a pre-release. The current official version is 0.1.1. For a full list of available versions, see the Directory of published versions

Table of Contents

.. 0 Table of Contents
... 1 Home
... 2 Background
... 3 Laboratory Report scenarios
... 4 Managing Laboratory Report statuses
... 5 Design choices
... 6 Challenges
... 7 Implementation notes
... 8 Certified reference material
... 9 Downloads
... 10 eHN guideline data set
... 11 Authors and contributors
... 12 Obligations
... 13 Known Issues
... 14 Copyright
... 15 Cross-version Analysis
... 16 Dependencies
... 17 Mapping to Profiles
.... 17.1 EHDS Laboratory Report Mapping
.... 17.2 EHDS Laboratory Observation Mapping
.... 17.3 EHDS ServiceRequest Mapping
.... 17.4 EHDS Specimen Mapping
.... 17.5 EHDS MedicationAdministration Mapping
.... 17.6 EHDS Device Mapping
.... 17.7 EHDS Attachment Mapping
.... 17.8 EHDS RelatedPerson Mapping
... 18 Artifacts Summary
.... 18.1 Actor Laboratory Report Consumer
.... 18.2 Actor Laboratory Report Creator
.... 18.3 Actor Laboratory Report Repository
.... 18.4 Human Name Obligations
.... 18.5 Observation Obligations
.... 18.6 Patient Obligations
.... 18.7 ServiceRequest Obligations
.... 18.8 Specimen Obligations
.... 18.9 Bundle: Laboratory Report
.... 18.10 Composition: Laboratory Report
.... 18.11 DiagnosticReport: Laboratory Report
.... 18.12 Observation Results: laboratory
.... 18.13 Patient: Animal
.... 18.14 ServiceRequest: Laboratory Order
.... 18.15 Specimen: Laboratory
.... 18.16 Substance: Specimen Additive Substance
.... 18.17 Quantity (Eu Lab)
.... 18.18 Range (Eu Lab)
.... 18.19 Ratio (Eu Lab)
.... 18.20 Certified Reference Material: CodeableConcept
.... 18.21 Certified Reference Material: Identifier
.... 18.22 Device Laboratory Test Kit
.... 18.23 Document DiagnosticReport Reference
.... 18.24 Laboratory Certified Reference Material
.... 18.25 Laboratory Code
.... 18.26 Laboratory Code: LOINC
.... 18.27 Laboratory Code: NPU
.... 18.28 Laboratory Order
.... 18.29 Laboratory Report Types
.... 18.30 Laboratory Specialty
.... 18.31 Laboratory Study Types
.... 18.32 Laboratory Techniques
.... 18.33 Specimen Additive
.... 18.34 Specimen Container
.... 18.35 Specimen Types
.... 18.36 Types of species
.... 18.37 Laboratory Code: example
.... 18.38 Bundle: converted from CDA
.... 18.39 Bundle: Hepatitis Panel
.... 18.40 Bundle: Microbiology Culture + Susceptibility
.... 18.41 Bundle: MyHealth@EU Proof Of Concept
.... 18.42 Bundle: two sections
.... 18.43 Composition: example
.... 18.44 DiagnosticReport: example
.... 18.45 Observation: Aerobic Culture example
.... 18.46 Observation: Anaerobic Culture example
.... 18.47 Observation: certified reference material
.... 18.48 Observation: Gram Staining example
.... 18.49 Observation: Gram-positive cocci example
.... 18.50 Observation: Gram-positive cocci, observed quantity, example
.... 18.51 Observation: Leukocytes Presence example
.... 18.52 Observation: ratio example
.... 18.53 Observation: Staphylococcus aureus Cephalothin susceptibility example
.... 18.54 Observation: Staphylococcus aureus Growth example
.... 18.55 Observation: Staphylococcus aureus identified example
.... 18.56 Observation: Staphylococcus aureus levoFLOXacin susceptibility example
.... 18.57 Observation: Staphylococcus aureus Oxacillin susceptibility example
.... 18.58 Observation: Staphylococcus aureus susceptibility panel example
.... 18.59 Observation: Staphylococcus aureus Vancomycin susceptibility example
.... 18.60 Patient: animal example
.... 18.61 Patient: Dutch complete name
.... 18.62 Patient: example
.... 18.63 Practitioner: example
.... 18.64 PractitionerRole: example
.... 18.65 ServiceRequest: example
.... 18.66 Specimen: animal example