This page is part of the HL7 Europe Laboratory Report (v0.1.0-ballot: STU 1 Ballot 1) based on FHIR R4. This is the current published version in its permanent home (it will always be available at this URL). For a full list of available versions, 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 Laboratory Guidelines
A - Laboratory Report |
Laboratory Report. eHN guideline model. |
A.1.3 - Health insurance and payment information |
Health insurance and payment information. Section A1.3 of the eHN guideline. |
A.1.4 - Information recipient |
Information recipient (intended recipient or recipients of the report, additional recipients might be identified by the ordering party, e.g. GP, other specialist), if applicable. Section A1.4 of the eHN guideline. |
A.1.5 - Author |
Author (by whom the Laboratory result report or a subset of its results was authored). Section A1.5 of the eHN guideline. |
A.1.6 - Legal authenticator |
Legal authenticator (The person taking responsibility for the medical content of the document). Section A1.6 of the eHN guideline. |
A.1.7 - Result validator |
Result validator. Section A1.7 of the eHN guideline. |
A.4 - Specimen information |
Specimen information. Section A4 of the eHN guideline. |
A.5 - Results data elements |
Results data elements. Section A5 of the eHN guideline. |
A1.1, A1.2 - Subject of care |
Patient or Subject of care. Sections A1.1 and A1.2 of the eHN guideline. |
A2, A3 - Order |
Order information and reason. Sections A2 and A3 of the eHN guideline. |
Concept Maps describing how the eHN Laboratory Guidelines are supposed to be implemented by using this guide
A - Laboratory Report model to this guide |
It shows how the Laboratory Report data set defined by the EU eHN guidelines is mapped into this guide. |
A.1.1, A.1.2 - Subject of care model to this guide |
It shows how the Subject data set defined by the EU eHN guidelines is mapped into this guide. |
A.1.3 - Health insurance and payment information model to this guide |
It shows how the A.1.3 - Health insurance and payment information data set defined by the EU eHN guidelines is mapped into this guide. |
A.1.4 - Information recipient model to this guide |
It shows how the A.1.4 - Information recipient data set defined by the EU eHN guidelines is mapped into this guide. |
A.1.5 - Author model to this guide |
It shows how the A.1.5 - Author data set defined by the EU eHN guidelines is mapped into this guide. |
A.1.6 - Legal authenticator model to this guide |
It shows how the A.1.6 - Legal authenticator data set defined by the EU eHN guidelines is mapped into this guide. |
A.1.7 - Result validator model to this guide |
It shows how the A.1.7 - Result validator data set defined by the EU eHN guidelines is mapped into this guide. |
A.2, A.3 - Order model to this guide |
It shows how the Order data set defined by the EU eHN guidelines is mapped into this guide. |
A.4 - Specimen information model to this guide |
It shows how the A.4 - Specimen information data set defined by the EU eHN guidelines is mapped into this guide. |
A.5 - Results data elements model to this guide |
It shows how the A.5 - Results data elements data set defined by the EU eHN guidelines is mapped into this guide. |
Actors and Obligations used to describe the Laboratory Report functional requirements for the specified data elements.
Actor Laboratory Report Consumer |
Laboratory Report Report Consumer: a system receiving/querying and using a Laboratory Report. |
Actor Laboratory Report Creator |
Laboratory Report Creator: a system generating and sending/providing a Laboratory Report to a Consumer or to a Repository for the report storage and sharing. |
Actor Laboratory Report Repository |
Laboratory Report Report Repository: a system maintaining a copy of the received Laboratory Report, to store and make it availaìble for the consumers. |
Human Name Obligations |
Specify the functional capabilities that the defined actors may, should or shall applied to the Human Name profile elements. |
Patient Obligations |
Specify the functional capabilities that the defined actors may, should or shall applied to the Patient EU Lab profile elements. |
These define constraints on FHIR resources for systems conforming to this implementation guide.
Bundle: Laboratory Report |
Clinical document used to represent a Laboratory Report for the scope of the HL7 Europe project. |
Composition: Laboratory Report |
Clinical document used to represent a Laboratory Report for the scope of the HL7 Europe project. |
DiagnosticReport: Laboratory Report |
DiagnosticReport used to represent an entry of a Laboratory Report, including its context, for the scope of the HL7 Europe project. |
Observation Results: laboratory |
This profile constrains the Observation resource to represent results produced by laboratory tests or panels/studies for the HL7 Europe project. This observation may represent the result of a simple laboratory test such as hematocrit or it may group the set of results produced by a multi-test study or panel such as a complete blood count, a dynamic function test, a urine specimen study. In the latter case, the observation carries the overall conclusion of the study and or a global interpretation by the producer of the study, in the comment element; and references the atomic results of the study as “has-member” child observations. |
Patient: Animal |
This profile defines how to represent an Animal as subject of care in FHIR for the purpose of this guide. This is used to identify the species when a specimen is collected from an animal |
Patient: Person |
This profile defines how to represent a human Patient in FHIR for the purpose of this guide. When the ips-pat-1 invariant is satified (Patient.name.given, Patient.name.family or Patient.name.text SHALL be present) then this proifle complies with the IPS patient profile. |
Practitioner: Laboratory Report |
This profile defines how to represent Practitioners in FHIR for the purpose of the HL7 Europe project. |
PractitionerRole: Laboratory Report |
This profile defines how to represent Practitioners (with their roles) in FHIR for the purpose of the HL7 Europe project. |
ServiceRequest: Laboratory Order |
This profile defines how to represent an laboratory orders using the HL7 FHIR ServiceRequest for the purpose of this guide. |
Specimen: Laboratory |
This profile defines how to represent Specimens in HL7 FHIR for the purpose of this guide. |
Substance: Specimen Additive Substance |
This profile defines how to represent Specimen Additive Substances in HL7 FHIR for the purpose of this guide. |
These define constraints on FHIR data types for systems conforming to this implementation guide.
Address (EU) |
European profile on Address. It includes extensions to support seperate streetname, housenumber and postal box It is RECOMMENDED to give these elements seperately. |
HumanName (Eu) |
European profile on HumanName data type. It includes extensions to support multiple family names. |
Quantity (Eu) for lab observations |
Data type Quantity constrained to use UCUM as the code system for units and optionally share measurement uncertainty |
Ratio (Eu) for lab observations |
Data type Ratio constrained to use UCUM as the code system for units and optionally share measurement uncertainty |
These define constraints on FHIR data types for systems conforming to this implementation guide.
Document Based On Order |
This extension provides a link to the order [(Reference(ServiceRequest)] or requisition [ServiceRequest.requisition (i.e., ‘Request.groupIdentifier’)] that this report document is based on and fulfills. |
Information recipient |
This extension applies to the Composition resource and is used to represent an intended recipient of the composition. |
These define sets of codes used by systems conforming to this implementation guide.
Lab Specimen Additive |
Laboratory specimen additives. |
Lab Specimen Container |
Laboratory specimen containers. |
Laboratory Order [LOINC] |
Laboratory order codes for use in HL7 Europe. |
Laboratory Report Types |
Laboratory Report Types. This version includes only one code as suggested by the eHN guideline. Catgegory can be used for filtering per study type or specialty. |
Laboratory Specialty |
Laboratory Specialties. Notes: Note 1: This value set is based on analysis of national coding practices in 8 european countries (AT, CZ, DE, FR, IE, IT, PT, SE) and agreed by involved lab experts as a common lab specialty value set. Note 2: Many european countries are usign additional laboratory specialty types, which should be mapped towards this value set. Note 3: In case of documented need, this value set could be extended. |
Laboratory Specimen Types |
Laboratory Specimen Types |
Laboratory Study Types |
Laboratory Study Types Notes: Note 1:26436-6 (Laboratory studies) enables issuing a report putting together observations from multiple specialties (disciplines) in the same text block, allowing delivery of a global interpretation comment at the end of the text block that will be rendered at the end of the report. Note 2:Mycology and parasitology, as well as bacteriology, are part of the 18725-2 (Microbiology studies (set)) studies. Note 3:Virology MAY be included in 18725-2 (MICROBIOLOGY STUDIES) or 18727-8 (SEROLOGY STUDIES) or split between both study types, depending upon the Content Creator Actor’s choice. |
Laboratory Techniques |
Laboratory Technique [SNOMED CT] |
NPU Laboratory Codes VS |
NPU laboratory codes Value Set |
Standard Laboratory Codes |
Standard laboratory codes |
These define new code systems used by systems conforming to this implementation guide.
Laboratory local codes Code System |
Laboratory local codes Code System |
These define transformations to convert between codes by systems conforming with this implementation guide.
DiagnosticReport to Composition status |
Proposed relationship between the statuses used in the DiagnosticReport resource and that used for the Composition. |
These are example instances that show what data produced and consumed by systems conforming with this implementation guide might look like.
Bundle Converted from CDA |
Example of FHIR bundle converted from a CDA Lab report |
Bundle Hepatitis Panel |
Hepatitis Panel |
Bundle Laboratory Result Report for POC |
Bundle Laboratory Result Report for POC |
Bundle Microbiology Culture + Susceptibility Lab Result |
Microbiology Culture + Susceptibility Lab Result |
Composition: example |
Example of Composition conforming this guide. |
DiagnosticReport: example |
Example of DiagnosticReport conforming this guide. |
Laboratory Result Report |
Laboratory Result Report Example includes one section with single study type:
|
Observation with ratio result type |
Observation with ratio result type example |
Observation: Aerobic Culture example |
Example of Aerobic Culture Observation conforming this guide. |
Observation: Anaerobic Culture example |
Example of Anaerobic Culture Observation conforming this guide. |
Observation: Gram-positive cocci example |
Example of Gram-positive cocci in clusters by gram staining Observation conforming this guide. |
Observation: Gram-positive cocci, observed quantity, example |
Example of Gram-positive cocci in clusters by gram staining, observed quantity, Observation conforming this guide. |
Observation: Leukocytes Presence example |
Example of Leukocytes Presence by gram staining Observation conforming this guide. |
Observation: Staphylococcus aureus Cephalothin susceptibility example |
Example of Staphylococcus aureus Cephalothin susceptibility Observation conforming this guide. |
Observation: Staphylococcus aureus Growth example |
Example of Staphylococcus aureus Growth Observation conforming this guide. |
Observation: Staphylococcus aureus Oxacillin susceptibility example |
Example of Staphylococcus aureus Oxacillin susceptibility Observation conforming this guide. |
Observation: Staphylococcus aureus Vancomycin susceptibility example |
Example of Staphylococcus aureus Vancomycin susceptibility Observation conforming this guide. |
Observation: Staphylococcus aureus identified example |
Example of Staphylococcus aureus identified by Aerobe culture Observation conforming this guide. |
Observation: Staphylococcus aureus levoFLOXacin susceptibility example |
Example of Staphylococcus aureus levoFLOXacin susceptibility Observation conforming this guide. |
Observation: Staphylococcus aureus susceptibility panel example |
Example of Staphylococcus aureus susceptibility panel Observation conforming this guide. |
Observation: gram staining example |
Example of gram staining result Observation conforming this guide. |
Patient: animal example |
Example of Patient resource used for indicating an animal (cat) conforming this guide. |
Patient: example |
Example of Patient conforming this guide. |
Practitioner: example |
Example of Practitioner conforming this guide. |
PractitionerRole: example |
Example of PractitionerRole conforming this guide. |
ServiceRequest: example |
Example of ServiceRequest conforming this guide. |
Specimen: animal example |
Example of specimen collected from an animal. |