HL7 FHIR Implementation Guide Laboratory Report, published by HL7 Italia. This guide is not an authorized publication; it is the continuous build for version 0.2.0 built by the FHIR (HL7® FHIR® Standard) CI Build. This version is based on the current content of https://github.com/hl7-it/lab-report/ and changes regularly. See the Directory of published versions
Plain Language Summary goes here
Home
Official URL: http://hl7.it/fhir/lab-report/ImplementationGuide/hl7.fhir.it.lab-report
L'obiettivo della seguente guida è quello di definire, secondo lo standard HL7 FHIR versione R4, le specifiche per l'implementazione dei profili che verranno utilizzati nel referto di medicina di laboratorio nel contesto italiano.
Definizione del Referto di Medicina di Laboratorio
Il referto di laboratorio appartiene al nucleo minimo dei documenti del Fascicolo Sanitario Elettronico.
Ai sensi dell'articolo 27, comma 1, lettera d), del decreto n. 178 del 29 settembre 2015, il referto di laboratorio e' il documento redatto dal medico di medicina di laboratorio.
Il contenuto informativo del Referto di Laboratorio è disciplinato all'art.2 dal Decreto del 18 maggio 2022 del Ministero della Salute (Decreto Contenuti).
Contesto
La guida intende fornire delle specifiche adeguate al contesto italiano secondo lo standard HL7 FHIR, per assicurare l’accuratezza dei risultati degli esami di laboratorio e la trasmissione degli stessi, al paziente o ad altra figura professionale, in modo chiaro e corretto.
Questa guida implementativa è stata creata per descrivere in modo più completo gli elementi standard necessari per supportare lo scambio sia semantico che sintattico di informazioni inerenti al referto di laboratorio e viene sviluppata considerando come soggetto la risorsa Patient.
La guida può essere utilizzata per descrivere i risultati di laboratorio nei settori chiave della diagnostica in vitro, come:
biochimica clinica
ematologia
medicina trasfusionale
microbiologia
immunologia.
Navigazione
Questa guida implementativa utilizza come metodo di pubblicazione i tool web-based offerti dallo standard FHIR. Ciò consente una facile navigazione tra le varie risorse, i data type, i set di valori e altri componenti offerti dallo standard FHIR.
Questo approccio consente inoltre agli implementatori di accedere facilmente alle informazioni necessarie per lo sviluppo di sistemi di interoperabilità.
This IG defines the global extensions - the ones defined for everyone. These extensions are always in scope wherever FHIR is being used (built Mon, Feb 10, 2025 21:45+1100+11:00)
Package hl7.fhir.uv.extensions.r4#1.0.0
This IG defines the global extensions - the ones defined for everyone. These extensions are always in scope wherever FHIR is being used (built Sun, Mar 26, 2023 08:46+1100+11:00)
Package hl7.fhir.uv.ips#1.1.0
International Patient Summary (IPS) FHIR Implementation Guide (built Tue, Nov 22, 2022 03:24+0000+00:00)
Package hl7.fhir.eu.extensions#0.1.0
This guide lists the extensions speciifed for the European REALM. (built Tue, Feb 20, 2024 08:56+0100+01:00)
Package hl7.fhir.eu.laboratory#0.1.0
This guide describes how the Laboratory Report can be represented in the European REALM. (built Mon, Feb 26, 2024 08:09+0100+01:00)
Package hl7.fhir.uv.tools.r4#0.8.0
This IG defines the extensions that the tools use internally. Some of these extensions are content that are being evaluated for elevation into the main spec, and others are tooling concerns (built Tue, Aug 5, 2025 20:09+1000+10:00)
The UCUM codes, UCUM table (regardless of format), and UCUM Specification are copyright 1999-2009, Regenstrief Institute, Inc. and the Unified Codes for Units of Measures (UCUM) Organization. All rights reserved. https://ucum.org/trac/wiki/TermsOfUse
The information in the various pages of the WHO web site is issued by the World Health Organization for general distribution. The information presented is protected under the Berne Convention for the Protection of Literature and Artistic works, under other international conventions and under national laws on copyright and neighbouring rights. Extracts of the information in the web site may be reviewed, reproduced or translated for research or private study but not for sale or for use in conjunction with commercial purposes. Any use of information in the web site should be accompanied by an acknowledgment of WHO as the source, citing the uniform resource locator (URL) of the article. Reproduction or translation of substantial portions of the web site, or any use other than for educational or other non-commercial purposes, require explicit, prior authorization in writing. Applications and enquiries should be addressed to the programme responsible for the page used. The designations employed and the presentation of the material in this publication do not imply the expression of any opinion whatsoever on the part of the World Health Organization concerning the legal status of any country, territory, city or area or of its authorities, or concerning the delimitation of its frontiers or boundaries. Dotted and dashed lines on maps represent approximate border lines for which there may not yet be full agreement. The mention of specific companies or of certain manufacturers' products does not imply that they are endorsed or recommended by the World Health Organization in preference to others of a similar nature that are not mentioned. Errors and omissions excepted, the names of proprietary products are distinguished by initial capital letters. The World Health Organization does not warrant that the information contained in the web site is complete and correct and shall not be liable whatsoever for any damages incurred as a result of its use.
This material contains content that is copyright of SNOMED International. Implementers of these specifications must have the appropriate SNOMED CT Affiliate license - for more information contact https://www.snomed.org/get-snomed or info@snomed.org.