Informe de alta en FHIR

Informe de alta es una categoría prioritaria del Espacio Europeo de Datos de Salud (artículo 14(1), letra (f) del Reglamento (UE) 2025/327). Se aplica desde el 26 de marzo de 2031. HL7 Europe la cubre con hdr 1.0.0.

Reglamento
Regulation (EU) 2025/327, Article 14(1)(f), Annex I
Se aplica desde
26 de marzo de 2031
Guías HL7 Europe
hl7.fhir.eu.hdr 1.0.0, publicada
Modelos lógicos Xt-EHR
EHDSDischargeReport
Tipo de documento
LOINC 18842-5 Discharge summaryLOINC 100719-4 Surgical oncology Discharge summary
Validador
Abrir el validador de perfiles EHDS

Qué dice el Reglamento

El anexo I del Reglamento describe las características principales de esta categoría. El texto es el original en inglés.

Discharge reports

Electronic health data related to a healthcare encounter or episode of care and including essential information about admission, treatment and discharge of a natural person.

Perfiles FHIR 33

Perfiles definidos por las guías anteriores. La columna de reglas cuenta los elementos en los que el perfil va más allá de FHIR base (obligatorios, prohibidos o limitados), que el validador comprueba; de los slices solo se comprueban los obligatorios que un valor fijo o el tipo de recurso permiten identificar.

PerfilRecursoGuía HL7 EuropeReglas comprobadasSlices comprobados / definidos
AllergyIntolerance: obligationshttp://hl7.eu/fhir/hdr/StructureDefinition/allergyIntolerance-obl-eu-hdr
AllergyIntolerancehdr10 / 7
Bundle (HDR)http://hl7.eu/fhir/hdr/StructureDefinition/bundle-eu-hdr
Bundlehdr103 / 31
Bundle: obligationshttp://hl7.eu/fhir/hdr/StructureDefinition/bundle-obl-eu-hdr
Bundlehdr103 / 31
CarePlan (HDR)http://hl7.eu/fhir/hdr/StructureDefinition/carePlan-eu-hdr
CarePlanhdr00 / 0
CarePlan: obligationshttp://hl7.eu/fhir/hdr/StructureDefinition/carePlan-obl-eu-hdr
CarePlanhdr00 / 0
Composition (HDR)http://hl7.eu/fhir/hdr/StructureDefinition/composition-eu-hdr
Compositionhdr60 / 61
Composition: obligationshttp://hl7.eu/fhir/hdr/StructureDefinition/composition-obl-eu-hdr
Compositionhdr60 / 61
Condition: obligationshttp://hl7.eu/fhir/hdr/StructureDefinition/condition-obl-eu-hdr
Conditionhdr10 / 5
Device (HDR)http://hl7.eu/fhir/hdr/StructureDefinition/device-eu-hdr
Devicehdr00 / 0
Device: obligationshttp://hl7.eu/fhir/hdr/StructureDefinition/device-obl-eu-hdr
Devicehdr00 / 0
DeviceUseStatement (HDR)http://hl7.eu/fhir/hdr/StructureDefinition/deviceUseStatement-eu-hdr
DeviceUseStatementhdr00 / 4
DeviceUseStatement: obligationshttp://hl7.eu/fhir/hdr/StructureDefinition/deviceUseStatement-obl-eu-hdr
DeviceUseStatementhdr00 / 4
Encounter (HDR)http://hl7.eu/fhir/hdr/StructureDefinition/encounter-eu-hdr
Encounterhdr10 / 7
Encounter: obligationshttp://hl7.eu/fhir/hdr/StructureDefinition/encounter-obl-eu-hdr
Encounterhdr10 / 7
Flag: obligationshttp://hl7.eu/fhir/hdr/StructureDefinition/flag-obl-eu-hdr
Flaghdr00 / 3
Goal (HDR)http://hl7.eu/fhir/hdr/StructureDefinition/goal-eu-hdr
Goalhdr00 / 2
Immunization: obligationshttp://hl7.eu/fhir/hdr/StructureDefinition/immunization-obl-eu-hdr
Immunizationhdr00 / 12
Medication: obligationshttp://hl7.eu/fhir/hdr/StructureDefinition/medication-obl-eu-hdr
Medicationhdr00 / 12
MedicationAdministration (HDR)http://hl7.eu/fhir/hdr/StructureDefinition/medicationAdministration-eu-hdr
MedicationAdministrationhdr00 / 0
MedicationAdministration: obligationshttp://hl7.eu/fhir/hdr/StructureDefinition/medicationAdministration-obl-eu-hdr
MedicationAdministrationhdr00 / 0
MedicationDispense (HDR)http://hl7.eu/fhir/hdr/StructureDefinition/medicationDispense-eu-hdr
MedicationDispensehdr20 / 0
MedicationDispense: obligationshttp://hl7.eu/fhir/hdr/StructureDefinition/medicationDispense-obl-eu-hdr
MedicationDispensehdr20 / 0
MedicationRequest: obligationshttp://hl7.eu/fhir/hdr/StructureDefinition/medicationRequest-obl-eu-hdr
MedicationRequesthdr00 / 6
MedicationStatement: obligationshttp://hl7.eu/fhir/hdr/StructureDefinition/medicationStatement-obl-eu-hdr
MedicationStatementhdr00 / 5
Observation (laboratory): obligationshttp://hl7.eu/fhir/hdr/StructureDefinition/laboratoryObservation-obl-eu-hdr
Observationhdr30 / 34
Observation: obligationshttp://hl7.eu/fhir/hdr/StructureDefinition/observation-obl-eu-hdr
Observationhdr00 / 26
Organization: obligationshttp://hl7.eu/fhir/hdr/StructureDefinition/organization-obl-eu-hdr
Organizationhdr10 / 0
Patient: obligationshttp://hl7.eu/fhir/hdr/StructureDefinition/patient-obl-eu-hdr
Patienthdr20 / 7
Practitioner: obligationshttp://hl7.eu/fhir/hdr/StructureDefinition/practitioner-obl-eu-hdr
Practitionerhdr10 / 0
PractitionerRole: obligationshttp://hl7.eu/fhir/hdr/StructureDefinition/practitionerRole-obl-eu-hdr
PractitionerRolehdr00 / 0
Procedure: obligationshttp://hl7.eu/fhir/hdr/StructureDefinition/procedure-obl-eu-hdr
Procedurehdr20 / 2
RelatedPerson: obligationshttp://hl7.eu/fhir/hdr/StructureDefinition/relatedPerson-obl-eu-hdr
RelatedPersonhdr00 / 0
Specimen: obligationshttp://hl7.eu/fhir/hdr/StructureDefinition/specimen-obl-eu-hdr
Specimenhdr00 / 0

Estructura del documento

Los perfiles de documento de esta categoría: las secciones que puede llevar una Composition y las entradas que puede contener un Bundle, tal como los perfiles las establecen. Los nombres son nombres de slice; el código de sección es el código LOINC que fija el perfil.

Bundle (HDR): entradas del Bundle 31

EntradaCard.Recurso FHIRPerfil
composition1..1CompositionCompositionEuHdr
patient1..*PatientPatientEuCore
encounter1..*EncounterEncounterEuHdr
allergyIntolerance0..*AllergyIntoleranceAllergyIntoleranceEuCore
bodyStructure0..*BodyStructureBodyStructureEuCore
condition0..*ConditionConditionEuCore
device0..*DeviceDeviceEuHdr
deviceUseStatement0..*DeviceUseStatementDeviceUseStatementEuHdr
diagnosticReport0..*DiagnosticReportDiagnosticReportEuCore
imagingStudy0..*ImagingStudy
immunization0..*ImmunizationImmunizationEuCore
media0..*Media
medication0..*MedicationMedicationEuCore
medicationRequest0..*MedicationRequestMedicationRequestEuCore
medicationStatement0..*MedicationStatementMedicationStatementEuCore
medicationDispense0..*MedicationDispenseMedicationDispenseEuHdr
medicationAdministration0..*MedicationAdministrationMedicationAdministrationEuHdr
practitioner0..*PractitionerPractitionerEuCore
practitionerRole0..*PractitionerRolePractitionerRoleEuCore
procedure0..*ProcedureProcedureEuCore
organization0..*OrganizationOrganizationEuCore
observation0..*Observation
specimen0..*Specimen
documentReference0..*DocumentReference
flag0..*FlagFlagPatientEuCore
location0..*LocationLocationEuCore
careplan0..*CarePlanCarePlanEuHdr
goal0..*GoalGoalEuHdr
relatedPerson0..*RelatedPerson
binary0..*Binary
serviceRequest0..*ServiceRequest

Composition (HDR): secciones 23

SecciónCard.Código de secciónDescripción
sectionAlert0..1LOINC 104605-1Substantial alerts and warnings
sectionAdmissionEvaluation0..1LOINC 67851-6Patient evaluation at hospital admission
sectionVitalSigns0..1LOINC 8716-3Vital signs during the encounter and at discharge
sectionPhysicalFindings0..1LOINC 29545-1Objective findings from physical examination
sectionFunctionalStatus0..1LOINC 47420-5Ability to perform activities of daily living
sectionDischargeSummary0..1LOINC 18842-5Complete narrative discharge summary
sectionHospitalCourse0..1LOINC 8648-8Significant information about course of hospital stay
sectionDiagnosticSummary0..1LOINC 11535-2Problems and diagnoses of the hospital stay
sectionSignificantProcedures0..1LOINC 10185-7Significant procedures performed during the stay
sectionMedicalDevices0..1LOINC 46264-8Devices used or implanted before this encounter
sectionProceduresHx0..1LOINC 47519-4Past procedures relevant to this encounter
sectionPharmacotherapy0..1LOINC 87232-5Drug treatment discontinued before discharge
sectionImplantedDevices0..1LOINC 57080-4Devices and implants during the hospital stay
sectionSignificantResults0..1LOINC 30954-2Significant medical test results of the stay
sectionSynthesis0..1LOINC 67781-5Clinical synthesis of the hospital stay
sectionPlanOfCare0..1LOINC 18776-5Plan of care and recommendations after discharge
sectionDischargeMedications0..1LOINC 75311-1Medication intended after discharge
sectionAllergies0..1LOINC 48765-2Relevant allergies and intolerances
sectionPatientHx0..1LOINC 11329-0Narrative patient health history (anamnesis)
sectionProblems0..1LOINC 11450-4Problems currently being monitored
sectionImmunizations0..1LOINC 11369-6Immunization status and vaccination history
sectionDischargeDetails0..1LOINC 8650-4Discharge status and disposition of the patient
sectionAttachments0..1LOINC 77599-9Library of attachments

Bindings de terminología 2

Value sets a los que los perfiles de esta categoría enlazan elementos con un binding required o extensible. Un binding required solo admite códigos del value set; uno extensible los espera salvo que ninguno encaje. Los value sets que definen los paquetes de HL7 Europe se listan con sus códigos en la referencia de value sets.

Los perfiles también declaran 4 bindings preferred y 1 example.

Value setBindingUsado porCódigos
Encounter Status Value Sethttp://hl7.eu/fhir/hdr/ValueSet/encounter-status-eu-hdr
required
EncounterEuHdr status
5 códigos
Encounter Class Value Sethttp://hl7.eu/fhir/hdr/ValueSet/encounter-class-eu-hdr
extensible
EncounterEuHdr class
5 códigos

Extensiones 2

Extensiones de HL7 Europe que llevan los perfiles de esta categoría, con el elemento que contiene cada una.

ExtensiónContextoValorUsada en
Encounter: Legal Statushttp://hl7.eu/fhir/StructureDefinition/encounter-legalStatus
Encounter
compleja
EncounterEuHdr extension:legalStatus 0..*
Composition: Information recipienthttp://hl7.eu/fhir/StructureDefinition/information-recipient
Composition
Reference
CompositionEuHdr extension:informationRecipient 0..*

Modelo lógico EHDSDischargeReport 65

Elementos del modelo lógico Xt-EHR con su cardinalidad y obligaciones. Las obligaciones indican a productores y consumidores de los datos qué DEBE o DEBERÍA hacer un sistema con cada elemento.

Obligaciones por actor

Cuántos elementos de EHDSDischargeReport llevan cada obligación para cada actor.

ObligaciónActorElementos
SHALL:able-to-populateproductor28
SHALL:displayconsumidor6
SHALL:processconsumidor43
SHOULD:able-to-populateproductor32
SHOULD:displayconsumidor2
SHOULD:processconsumidor1

Elementos 65

ElementoCard.ObligacionesDescripción
header1..1
SHALL:able-to-populate productor
A common document header is necessary to ensure that the document can be unambiguously identified, associated with a patient, and processed in an exchange context. Systems claiming conformance must be capable of populating this metadata for every document instance.
SHALL:process consumidor
EHR systems that consume discharge report SHALL process document header information.
Document header
subject1..1
SHALL:able-to-populate productor
EHR systems SHALL provide information about the subject of care.
SHALL:display consumidor
EHR system SHALL render information about the subject of care in such a way that unambiguous assignment to the care subject is preserved.
SHALL:process consumidor
Information about the subject of care SHALL be processed by the EHR system in such a way that the identity of the subject of care cannot be confused.
Patient/subject information
identifier1..*
SHALL:able-to-populate productorSHOULD:display consumidorSHALL:process consumidor
Unique identifier of the document
author[x]1..*
SHALL:able-to-populate productorSHALL:display consumidor
The author of the report.
date1..1
SHALL:able-to-populate productorSHALL:display consumidor
Date of finalising/issuing the document
status1..1
SHALL:able-to-populate productorSHALL:display consumidor
Status of the document
source0..0
Source of information (e.g. patient, patient's proxy). Used in case the patient has authored the information or the author has submitted patient-stated information.
language0..1
SHALL:able-to-populate productor
Language in which the resource is written. Language is expressed by the IETF language tag.
documentType1..1
SHALL:able-to-populate productor
Type of the document (e.g. '34105-7 Hospital discharge summary)
documentTitle1..1
SHALL:able-to-populate productor
Title of the document, possibly autogenerated from the structured fields (e.g. 'Hospital discharge report. Jane Green. 07.10.2025-10.10.2025')
period0..1
SHALL:able-to-populate productor
Time of service that is being documented (typically the same as the time/period of encounter)
version0..1
Business version of the document. The exact algorithm for versioning is decided by the producer/custodian
attestation0..*
SHALL:able-to-populate productorSHALL:display consumidor
Document attestation details
attester[x]1..1
SHALL:able-to-populate productorSHALL:display consumidor
Attester who validated the document
datetime1..1
SHALL:able-to-populate productor
Date and time of the approval of the document by Attester
legalAuthentication0..*
SHALL:able-to-populate productor
Document legal authentication details
legalAuthenticator[x]1..1
SHALL:able-to-populate productor
The person or organisation taking responsibility for the content of the document.
datetime1..1
SHALL:able-to-populate productor
Date and time when the document was authorised
eventType0..*
SHALL:able-to-populate productor
Categorisation of the event covered by the document (e.g. laboratory study types, imaging study types including modality, etc.). Selection of such tags or labels depends on the use case and agreement between data sharing parties. This meta-data element serves primarily for searching and filtering purposes.
serviceSpecialty0..*
SHALL:able-to-populate productorSHOULD:display consumidor
Additional details about where the content was created (e.g. clinical specialty)
custodian0..1
SHALL:able-to-populate productor
Organisation that is in charge of maintaining the document/report.
intendedRecipient[x]0..*
Intended recipient(s) of the information, i.e. a person or organisation that should be notified or be aware of the content. This element is used to indicate explicit communication intent and does not represent routine storage or passive availability of information (e.g. in portals). Listing an intended recipient does not create an assignment or responsibility.
presentedForm0..*
SHALL:able-to-populate productor
Systems claiming DR conformance shall demonstrate the capability to generate a human-readable representation of the document when required by the exchange context. This obligation applies to capability, not to population in every instance.
SHALL:process consumidor
EHR systems that consume DR report SHALL be able to process the human readable version of the report.
A narrative easy-to-read representation of the full data set, e.g. PDF-version of a document
body0..1
SHALL:able-to-populate productor
Each EHR system that is a producer of a discharge report SHALL be able to provide structured information about the report body. This obligation applies to capability, not to population in every instance.
SHALL:process consumidor
EHR systems that consume discharge report SHALL process structured body information.
Structured body of the discharge report document
alerts0..1
SHOULD:able-to-populate productor
Alerts may not be present in all encounters, but the document structure must support their representation. Systems must be capable of populating and processing this section when alerts are present; omission is acceptable where permanently out of scope and justified during conformance testing.
SHOULD:process consumidor
EHR systems that consume discharge report SHALL process the alerts section when it is present in the document.
Section: Alerts.
generatedNarrative0..1
SHOULD:able-to-populate productor
Narrative representation supports immediate clinical understanding of alerts. Systems must be capable of populating this narrative; omission is acceptable where permanently out of scope and justified during conformance testing.
SHALL:process consumidor
EHR systems that consume discharge report SHALL process the generatedNarrative element of the alerts section when it is present in the document.
Narrative, potentially formatted, content of the whole section.
medicalAlert0..*
SHOULD:able-to-populate productor
Structured or textual alert entries represent clinically critical information when present. Systems must be capable of populating these entries; omission is acceptable where permanently out of scope and justified during conformance testing.
SHALL:process consumidor
EHR systems that consume discharge report SHALL process the medicalAlert element of the alerts section when it is present in the document.
Description of medical alerts in textual format: any clinical information that is imperative to know so that the life or health of the patient does not come under threat.
encounterInformation1..1
SHALL:able-to-populate productor
Encounter context is essential for interpreting all clinical content in the document. Systems claiming conformance must be capable of populating this section for every document instance.
SHALL:process consumidor
EHR systems that consume discharge report SHALL process structured information about the encounter.
Section: Encounter information.
generatedNarrative0..1
SHALL:able-to-populate productor
A narrative description of the encounter context is necessary to ensure human interpretability. Systems must be capable of populating this narrative in every document instance.
SHALL:process consumidor
EHR systems that consume discharge report SHALL process the generatedNarrative element of the encounterInformation section.
Narrative, potentially formatted, content of the whole section.
encounter0..1
SHALL:able-to-populate productor
A structured encounter reference supports linkage and reuse where available. Systems must be capable of populating this reference; omission is acceptable where permanently out of scope and justified during conformance testing.
SHALL:process consumidor
EHR systems that consume discharge report SHALL process the encounter element of the encounterInformation section.
Encounter information
note0..1
SHOULD:able-to-populate productorSHALL:process consumidor
Free text notes by the health professional
admissionEvaluation0..1
SHALL:able-to-populate productor
Admission evaluation does not occur in all encounters but must be representable where applicable. Systems must be capable of populating this section; omission is acceptable where permanently out of scope and justified during conformance testing.
SHALL:process consumidor
EHR systems that consume discharge report SHALL process structured information about the admission evaluation.
Section: Admission evaluation. Admission evaluation section should be reported only if it is relevant to ensure continuity of care.
generatedNarrative0..1
SHOULD:able-to-populate productor
Narrative summarisation supports clinical understanding of admission findings. Systems must be capable of populating this narrative; omission is acceptable where permanently out of scope and justified during conformance testing.
SHALL:process consumidor
EHR systems that consume discharge report SHALL process the generatedNarrative element of the admissionEvaluation section.
Narrative, potentially formatted, content of the whole section.
objectiveFindings0..*
SHOULD:able-to-populate productor
Objective findings are part of structured clinical assessment when performed. Systems must be capable of populating this container; omission is acceptable where permanently out of scope and justified during conformance testing.
SHALL:process consumidor
EHR systems that consume discharge report SHALL process the objectiveFindings element of the admissionEvaluation section when it is present in the document.
Objective findings, such as anthropometric measurements, vital signs, or objective anatomical findings of physical examination
functionalStatus[x]0..*
SHOULD:able-to-populate productor
Functional status assessment is context-dependent but relevant for continuity of care. Systems must be capable of populating this section; omission is acceptable where permanently out of scope and justified during conformance testing.
SHALL:process consumidor
EHR systems that consume discharge report SHALL process the functionalStatus element of the admissionEvaluation section when it is present in the document.
An individual's ability to perform normal daily activities required to meet basic needs, fulfil usual roles and maintain health and well-being
note0..1
SHOULD:able-to-populate productorSHALL:process consumidor
Free text notes by the evaluation performer
patientHistory0..1
SHOULD:able-to-populate productor
Patient history may not be available or relevant in all care contexts, but systems must be capable of representing this section when such information exists. Omission is acceptable where the capability is permanently out of scope and justified during conformance testing.
SHALL:process consumidor
EHR systems that consume discharge report SHALL process structured information about patient history.
Section: Patient health history (anamnesis) containing only information that is highly relevant for this specific episode of care. The model is designed with the expectation that patient summary is available.
generatedNarrative0..1
SHOULD:able-to-populate productor
A narrative overview supports human understanding of the patient’s history when structured data is incomplete or heterogeneous. Systems must be capable of populating and processing narrative content; omission is acceptable where justified during conformance testing.
SHALL:process consumidor
EHR systems that consume discharge report SHALL process the generatedNarrative element of the patientHistory section.
Narrative, potentially formatted, content of the whole section. In case the section includes structured information, it should also be included in generatedNarrative.
pastProblems0..*
SHOULD:able-to-populate productor
Past problems relevant to the current episode of care should be representable in a structured format. Systems must be capable of populating this section when such information is available; omission is acceptable where permanently out of scope and justified during conformance testing.
SHALL:process consumidor
EHR systems that consume discharge report SHALL process the pastProblems element of the patientHistory section when it is present in the document.
A list of conditions of a patient that the patient suffered in the past or still suffers. Unlike diagnostic summary, medical history is not only a list of problems, but could contain broader description of the condition and its progress, details about treatment including medication and patient response to treatment. Past problem section (unlike the same section of the patient summary) should include only conditions that are important for continuity of care. This section, if provided, complements the diagnostic summary section of the discharge report.
devicesAndImplants0..*
SHOULD:able-to-populate productor
Information about devices and implants in patient history may be relevant for continuity of care. Systems must be capable of populating this section when such information is available; omission is acceptable where permanently out of scope and justified during conformance testing.
SHALL:process consumidor
EHR systems that consume discharge report SHALL process the devicesAndImplants element of the patientHistory section when it is present in the document.
Devices and implants in patient anamnesis.
procedures0..*
SHOULD:able-to-populate productor
Historical procedures relevant to the current episode of care should be representable in a structured format. Systems must be capable of populating this section when such information is available; omission is acceptable where permanently out of scope and justified during conformance testing.
SHALL:process consumidor
EHR systems that consume discharge report SHALL process the procedures element of the patientHistory section when it is present in the document.
Procedures in patient anamnesis.
note0..1
SHOULD:able-to-populate productorSHALL:process consumidor
Free text notes by the health professional
courseOfEncounter1..1
SHALL:able-to-populate productor
Course of encounter is a core component of the discharge report. Systems claiming conformance must be capable of populating this section for every document instance.
SHALL:process consumidor
EHR systems that consume discharge report SHALL process structured information about the course of encounter.
Course of inpatient or outpatient encounter.
generatedNarrative0..1
SHOULD:able-to-populate productor
A narrative summary of the course of encounter supports human understanding of the clinical course. Systems must be capable of populating this narrative when such information is available.
SHALL:process consumidor
EHR systems that consume discharge report SHALL process the generatedNarrative element of the courseOfEncounter section.
Narrative, potentially formatted, content of the whole section.
diagnosticSummary0..*
SHOULD:able-to-populate productor
A diagnostic summary is essential for continuity of care. Systems claiming conformance must be capable of populating this section when such information is available.
SHALL:process consumidor
EHR systems that consume discharge report SHALL process the diagnosticSummary element of the courseOfEncounter section.
Problems that were treated or affected provisioning of care (diagnostics, therapy, nursing, monitoring) during the encounter. At least one treated problem should be marked. Other problems are recorded only if they are important for continuity of care (after discharge).
procedures0..*
SHOULD:able-to-populate productor
Procedures performed during the encounter are important for continuity of care. Systems must be capable of populating this section when such information is available.
SHALL:process consumidor
EHR systems that consume discharge report SHALL process the procedures element of the courseOfEncounter section when it is present in the document.
Procedures performed during encounter which are significant for continuity of care, e.g. surgeries and other instrumental interventions (endoscopic, intravascular), chemotherapy, radiotherapy, purification methods (dialysis, hemoperfusion), circulation support methods (counterpulsation, etc.), administration of blood derivatives or others. Diagnostic procedures are typically captured as observation results and not repeated here.
medicalDevicesAndImplants0..*
SHOULD:able-to-populate productor
Devices and implants are clinically significant historical data and must be representable when medical history is present. Systems must be capable of populating and processing these entries.
SHALL:process consumidor
EHR systems that consume discharge report SHALL process the medicalDevicesAndImplants element of the courseOfEncounter section when it is present in the document.
Medical devices (including implants) whose use was started, stopped, or otherwise modified during the encounter.
pharmacotherapy0..*
SHOULD:able-to-populate productor
Medication treatments during the encounter are important for continuity of care. Systems must be capable of populating this section when such information is available.
SHALL:process consumidor
EHR systems that consume discharge report SHALL process the medications element of the courseOfEncounter section when it is present in the document.
Significant medication treatments during encounter. The content of this section may be repeated in the medication summary for full overview of patient's medications.
testResults[x]0..*
SHOULD:able-to-populate productor
Test results of functional, diagnostic, and imaging examinations are important for continuity of care. Systems must be capable of populating this section when such information is available.
SHALL:process consumidor
EHR systems that consume discharge report SHALL process the testResults element of the courseOfEncounter section when it is present in the document.
Significant medical test results of functional, diagnostic (including laboratory), and imaging examinations performed during encounter. This may include orders for which the results have not yet arrived.
note0..1
SHOULD:able-to-populate productorSHALL:process consumidor
Free text notes by the health professional
dischargeDetails0..1
SHOULD:able-to-populate productor
Discharge details are essential to ensure safe transition of care and continuity after discharge. Systems claiming conformance must be capable of populating this section.
SHALL:process consumidor
EHR systems that consume discharge report SHALL process structured information about discharge details.
Discharge details
generatedNarrative0..1
SHOULD:able-to-populate productor
Narrative discharge summaries support human understanding of discharge context. Systems must be capable of populating this narrative; omission is acceptable where justified during conformance testing.
SHALL:process consumidor
EHR systems that consume discharge report SHALL process the generatedNarrative element of the dischargeDetails section.
Narrative, potentially formatted, content of the whole section.
objectiveFindings0..*
SHOULD:able-to-populate productor
Objective findings at discharge may not always be collected but must be representable when available. Systems must be capable of populating this section; omission is acceptable where justified during conformance testing.
SHALL:process consumidor
EHR systems that consume discharge report SHALL process the objectiveFindings element of the dischargeDetails section when it is present in the document.
Objective findings, such as anthropometric measurements, vital signs, or objective anatomical findings of physical examination
functionalStatus[x]0..*
SHOULD:able-to-populate productor
Functional status at discharge may influence care planning but is context-dependent. Systems must be capable of representing this section; omission is acceptable where justified during conformance testing.
SHALL:process consumidor
EHR systems that consume discharge report SHALL process the functionalStatus element of the dischargeDetails section when it is present in the document.
An individual's ability to perform normal daily activities required to meet basic needs, fulfil usual roles and maintain health and well-being
note0..1
SHOULD:able-to-populate productorSHALL:process consumidor
Free text notes by the health professional
medicationSummary0..1
SHALL:able-to-populate productor
Medication summary at discharge may vary by encounter but must be representable when applicable. Systems must be capable of populating this section; omission is acceptable where justified during conformance testing.
SHALL:process consumidor
EHR systems that consume discharge report SHALL process structured information about medication summary.
Summary information on the medication recommended for the period after discharge, indicating whether the medication is changed or newly started. Compared to previous practices, the overview is supplemented with medication that has been discontinued.
generatedNarrative0..1
SHOULD:able-to-populate productor
Narrative summarisation supports understanding of medication changes after discharge. Systems must be capable of populating this narrative; omission is acceptable where justified during conformance testing.
SHALL:process consumidor
EHR systems that consume discharge report SHALL process the generatedNarrative element of the medicationSummary section.
Narrative, potentially formatted, content of the whole section.
medicationUse0..*
SHALL:able-to-populate productor
Medication and dosing details are essential for safe post-discharge therapy. Systems must be capable of populating this information whenever a medication entry is present.
SHALL:process consumidor
EHR systems that consume discharge report SHALL process the medicationUse element of the medicationSummary section when it is present in the document.
Details about medication and dosage
note0..1
SHOULD:able-to-populate productorSHALL:process consumidor
Free text notes by the health professional
carePlan0..1
SHOULD:able-to-populate productor
Post-discharge care plans and recommendations may vary by encounter. Systems must be capable of representing this section; omission is acceptable where justified during conformance testing.
SHALL:process consumidor
EHR systems that consume discharge report SHALL process structured information about care plan and recommendations after discharge.
Care plan and other recommendations after discharge.
generatedNarrative0..1
SHOULD:able-to-populate productor
Narrative recommendations support human interpretation of post-discharge care. Systems must be capable of populating this narrative; omission is acceptable where justified during conformance testing.
SHALL:process consumidor
EHR systems that consume discharge report SHALL process the generatedNarrative element of the carePlan section.
Narrative, potentially formatted, content of the whole section.
carePlan0..*
Structured care plan after discharge. Multiple care plans could be provided.
otherRecommendations0..1
SHOULD:able-to-populate productor
Additional advice may be clinically relevant but is context-dependent. Systems must be capable of representing this information; omission is acceptable where justified during conformance testing.
SHALL:process consumidor
EHR systems that consume discharge report SHALL process the otherRecommendations element of the carePlan section when it is present in the document.
Other recommendations (advice) after discharge. E.g., recommendation to suggest hip replacement, reduce number of cigarettes, stop smoking, increase physical exercises, etc.
synthesis0..1
SHOULD:able-to-populate productorSHALL:process consumidor
Clinical synthesis (e.g. description of reasons and course of encounter) clustered by managed conditions. Clinical synthesis may include clinical reasoning (differential diagnostics, explanation of clinical context) in clinically complex conditions.
attachments0..*
Report attachments. Implementations may define what kind of attachments are allowed and may ignore unexpected attachments for security reasons.

Mapeo de EHDSDischargeReport a FHIR 50

Cómo aterriza cada elemento lógico en FHIR, según lo publicado en la guía de HL7 Europe. Mapeado a: BundleEuHdr, CompositionEuHdr.

ElementoRelaciónRecurso FHIRElemento FHIRNotas
headerrelacionado conComposition.CompositionEuHdr constrains header elements for HDR.
author[x]equivalenteCompositionauthorReference to Practitioner/PractitionerRole/Organization/Device per profile.
statusequivalenteCompositionstatus
documentTypeequivalenteCompositiontypeFixed to LOINC 34105-7 in CompositionEuHdr.
documentTitleequivalenteCompositiontitle
periodrelacionado conCompositionevent.periodMap to the primary Composition.event entry.
intendedRecipient[x]relacionado conCompositionextension:information-recipientUses the information-recipient extension in CompositionEuHdr.
encounterInformationrelacionado conCompositionencounterUse EncounterEuHdr.
generatedNarrativerelacionado conEncountertext
encounterequivalenteCompositionencounter
noterelacionado conCompositionextension:note
alertsequivalenteCompositionsection:sectionAlertUse LOINC 104605-1.
generatedNarrativeequivalenteCompositionsection:sectionAlert.text
medicalAlertequivalenteCompositionsection:sectionAlertReference to Flag (EHDSAlert).
admissionEvaluationequivalenteCompositionsection:sectionAdmissionEvaluationReported only if relevant.
generatedNarrativeequivalenteCompositionsection:sectionAdmissionEvaluation.text
objectiveFindingsrelacionado conCompositionsection:sectionVitalSignsUse Observation where appropriate.
objectiveFindingsrelacionado conCompositionsection:sectionAnthropometryUse Observation where appropriate.
objectiveFindingsrelacionado conCompositionsection:sectionPhysicalFindingsUse Observation where appropriate.
functionalStatus[x]relacionado conCompositionsection:sectionFunctionalStatusCondition/Observation/ClinicalImpression as allowed.
noterelacionado conCompositionsection:sectionAdmissionEvaluation.text
patientHistoryequivalenteCompositionsection:sectionPatientHx
generatedNarrativeequivalenteCompositionsection:sectionPatientHx.text
noterelacionado conCompositionsection:sectionPatientHx.extension:note
courseOfEncounterequivalenteCompositionsection:sectionHospitalCourse
generatedNarrativeequivalenteCompositionsection:sectionHospitalCourse.text
diagnosticSummaryequivalenteCompositionsection:sectionDiagnosticSummaryReference to ConditionEuCore.
proceduresequivalenteCompositionsection:sectionSignificantProceduresReference to ProcedureEuCore.
medicalDevicesAndImplantsequivalenteCompositionsection:sectionMedicalDevicesReference to DeviceUseStatementEuHdr.
pharmacotherapyequivalenteCompositionsection:sectionPharmacotherapyMedicationStatement/Request/Dispense/Administration.
objectiveFindingsrelacionado conCompositionsection:sectionVitalSignsUse Observation where appropriate.
objectiveFindingsrelacionado conCompositionsection:sectionAnthropometryUse Observation where appropriate.
objectiveFindingsrelacionado conCompositionsection:sectionPhysicalFindingsUse Observation where appropriate.
testResultsequivalenteCompositionsection:sectionSignificantResultsObservation/DiagnosticReport/DocumentReference.
noterelacionado conCompositionsection:sectionHospitalCourse.text
dischargeDetailsequivalenteCompositionsection:sectionDischargeDetails
generatedNarrativeequivalenteCompositionsection:sectionDischargeDetails.text
objectiveFindingsrelacionado conCompositionsection:sectionPhysicalFindings / section:sectionVitalSignsUse Observation where appropriate.
functionalStatus[x]relacionado conCompositionsection:sectionFunctionalStatus
noterelacionado conCompositionsection:sectionDischargeDetails.text
medicationSummaryrelacionado conCompositionsection:sectionDischargeMedicationsPost-discharge medications summary.
generatedNarrativeequivalenteCompositionsection:sectionDischargeMedications.text
medicationUseequivalenteCompositionsection:sectionDischargeMedicationsMedicationRequest/MedicationDispense/MedicationStatement.
noterelacionado conCompositionsection:sectionDischargeMedications.text
carePlanequivalenteCompositionsection:sectionPlanOfCare
generatedNarrativeequivalenteCompositionsection:sectionPlanOfCare.text
carePlanequivalenteCompositionsection:sectionPlanOfCareReference to CarePlanEuHdr.
otherRecommendationsrelacionado conCompositionsection:sectionPlanOfCare.textMay also be represented in Discharge Instructions narrative.
synthesisequivalenteCompositionsection:sectionSynthesis.text
attachmentsequivalenteCompositionsection:sectionAttachmentsDocumentReference/Binary in CompositionEuHdr.

Documentos CDA (eHDSI)

La misma categoría se transporta en CDA con estas plantillas de documento eHDSI. Su estructura, sus conjuntos de valores y un validador de documentos CDA están en la guía CDA.

Fuentes

Reglamento (UE) 2025/327, Diario Oficial de la Unión Europea; guías de implementación FHIR de HL7 Europe; modelos lógicos Xt-EHR (xtehr.eu.ehds.models). Las guías en ballot aún pueden cambiar. Esta guía es informativa: no es asesoramiento jurídico ni una certificación de conformidad.