{ "id": "ieee-11073-nomenclatuur", "url": "/fr/nomenclature-iso-ieee-11073-mdc/", "md_url": "/fr/nomenclature-iso-ieee-11073-mdc.md", "json_url": "/fr/nomenclature-iso-ieee-11073-mdc.json", "claims_url": "/fr/nomenclature-iso-ieee-11073-mdc/beweringen/", "type": { "code": "Terminology", "label": "Terminologie ou classification" }, "schema_type": "DefinedTermSet", "lang": "fr", "translation": { "lang": "fr", "source_url": "/ieee-11073-nomenclatuur/", "date": "2026-11-12", "stale": false, "fields": [ "in_het_kort", "lifecycle_note", "sectie:hoe-is-het-opgebouwd", "sectie:onzekerheden-en-tegenstrijdige-informatie", "sectie:planning", "sectie:waar-wordt-het-gebruikt", "sectie:wat-betekent-het-voor-een-ziekenhuis", "sectie:wat-is-het", "summary", "title", "version" ] }, "title": "Nomenclature ISO/IEEE 11073 des dispositifs médicaux (MDC)", "aliases": [ "IEEE 11073-10101", "ISO/IEEE 11073-10101", "MDC", "MDC-codes", "Medical Device Communications-nomenclatuur", "11073-nomenclatuur", "IDC-nomenclatuur (11073-10103)" ], "names": { "nl": "ISO/IEEE 11073-nomenclatuur voor medische toestellen (MDC)", "fr": "nomenclature ISO/IEEE 11073 des dispositifs médicaux (MDC)", "en": "ISO/IEEE 11073 Medical Device Communication nomenclature (MDC)", "de": "ISO/IEEE 11073-Nomenklatur für Medizingeräte (MDC)" }, "jurisdiction": [ { "code": "internationaal", "label": "International" } ], "themes": [ { "code": "terminologie", "label": "Terminologie et codage" }, { "code": "standaardisatie-en-governance", "label": "Normalisation et gouvernance" }, { "code": "telemonitoring", "label": "Télésurveillance et soins à distance" } ], "lifecycle": { "code": "productie", "label": "en production" }, "lifecycle_note_html": "En usage comme norme active : édition de base IEEE 11073-10101-2019 (ISO 2020) avec l'amendement 10101b-2023 ; les amendements 10101c et 10103b sont des projets en cours (IEEE SA et ISO/TC 215, novembre 2026).", "version": "IEEE 11073-10101-2019 / ISO/IEEE 11073-10101:2020, amendement 10101b-2023 (ISO Amd 1:2026) ; IEEE 11073-10103-2023 (ISO 2025)", "vendor": null, "sectors": [], "homologations": [], "links": [ { "kind": { "code": "documentatie", "label": "Documentation" }, "url": "https://standards.ieee.org/ieee/11073-10101/5034/", "label": "IEEE 11073-10101-2019 (IEEE SA)", "host": "standards.ieee.org", "lang": "en" }, { "kind": { "code": "documentatie", "label": "Documentation" }, "url": "https://standards.ieee.org/ieee/11073-10103/10855/", "label": "IEEE 11073-10103-2023 (IEEE SA)", "host": "standards.ieee.org", "lang": "en" }, { "kind": { "code": "register", "label": "Registre" }, "url": "https://terminology.hl7.org/en/MDC.html", "label": "MDC in HL7 Terminology", "host": "terminology.hl7.org", "lang": "en" }, { "kind": { "code": "portaal", "label": "Portail" }, "url": "https://rtmms.nist.gov/", "label": "RTMMS (NIST, aanmelden vereist)", "host": "rtmms.nist.gov", "lang": "en" }, { "kind": { "code": "website", "label": "Site web" }, "url": "https://sagroups.ieee.org/11073/pocd/", "label": "IEEE 11073 Point-of-Care Devices Working Group", "host": "sagroups.ieee.org", "lang": "en" } ], "summary_text": "La nomenclature ISO/IEEE 11073, en abrégé MDC (medical device communication), est le système de codes avec lequel les dispositifs médicaux tels que les moniteurs, les respirateurs, les pompes à perfusion et les dispositifs cardiaques implantables désignent leurs valeurs mesurées, unités, alarmes et sites corporels. Chaque terme possède un identifiant de référence lisible (comme MDC_PULS_RATE) et un code numérique de 32 bits, composé d'une partition et d'un code de terme. L'IEEE élabore les normes et l'ISO les reprend; les codes sont d'utilisation gratuite, le texte de la norme est payant. Les codes figurent dans les messages HL7 v2 des passerelles de dispositifs, dans les guides FHIR pour dispositifs et dans SDC; ils n'ont pas été trouvés dans les guides FHIR belges.", "summary_html": "

La nomenclature ISO/IEEE 11073, en abrégé MDC (medical device communication), est le système de codes avec lequel les dispositifs médicaux tels que les moniteurs, les respirateurs, les pompes à perfusion et les dispositifs cardiaques implantables désignent leurs valeurs mesurées, unités, alarmes et sites corporels. Chaque terme possède un identifiant de référence lisible (comme MDC_PULS_RATE) et un code numérique de 32 bits, composé d'une partition et d'un code de terme. L'IEEE élabore les normes et l'ISO les reprend ; les codes sont d'utilisation gratuite, le texte de la norme est payant. Les codes figurent dans les messages HL7 v2 des passerelles de dispositifs, dans les guides FHIR pour dispositifs et dans SDC ; ils n'ont pas été trouvés dans les guides FHIR belges.

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La nomenclature ISO/IEEE 11073 est la terminologie de la famille de normes ISO/IEEE 11073 pour la communication avec les dispositifs médicaux, tant les dispositifs au chevet du patient (point-of-care) que les dispositifs de santé personnels (PHD)[4]. Elle est spécialisée dans les paramètres vitaux et l'informatique des dispositifs, avec des concepts portant notamment sur l'ECG, l'hémodynamique, la respiration, les gaz du sang, l'urine, l'équilibre hydrique et la neurologie, ainsi que sur les unités, les événements des dispositifs, les alarmes et les sites corporels[1].

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La norme de base est IEEE 11073-10101 (Nomenclature)[1]. Une norme partielle distincte, IEEE 11073-10103, la nomenclature IDC (Implantable Device, Cardiac), définit les termes pour la lecture des stimulateurs cardiaques, des défibrillateurs, des dispositifs de resynchronisation cardiaque et des moniteurs cardiaques implantables, afin que ces données puissent passer des systèmes du fabricant vers le DPI ou un système de suivi des dispositifs[14]. IEEE 11073-10102 étend la nomenclature de base avec des termes pour les annotations d'ECG[15]. La nomenclature fournit les codes d'un modèle de données défini dans une autre norme partielle : IEEE 11073-10201, le modèle d'information du domaine (DIM) orienté objet qui fixe la structure des informations échangées[16].

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Attention à l'abréviation. MDC signifie ici medical device communication ; le préfixe des identifiants de référence est notamment utilisé dans HL7 pour désigner les termes de cette nomenclature[3]. Dans le financement hospitalier belge, la même abréviation figure dans l'AR BMF du 25 avril 2002 pour Major Diagnostic Category, les grands groupes de diagnostics qui concernent chacun un système ou un organe[17] ; cette notion est sans lien avec la présente nomenclature. Cette page ne traite pas non plus de l'EMDN européenne ni de la GMDN.

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Codes, partitions et identifiants de référence

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Les codes MDC sont des entiers de 32 bits : les 16 bits de poids fort indiquent la partition, un groupe de termes comme la partition « dimension » qui regroupe tous les codes d'unités, et les 16 bits de poids faible le code de terme[2]. Ce code de 16 bits dépend du contexte : il ne peut être utilisé que si la classe de l'information est déjà établie[3]. Certaines partitions ne sont en pratique utilisées que pour les dispositifs de santé personnels et d'autres que pour les dispositifs au chevet du patient, mais les normes 11073-10201, 11073-20601 et 11073-10101 ne limitent aucune partition à l'un des deux[2].

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Outre le code numérique, chaque terme possède un identifiant de référence textuel (reference identifier), comme MDC_PULS_RATE[3]. Dans un message HL7 v2 du domaine IHE Devices, le champ OBX-3 porte les deux ensemble avec le système de codes, par exemple 69641^MDC_DEV_ANALY_SAT_O2_MDS^MDC[6]. Dans FHIR, le système de codes est désigné par l'URI urn:iso:std:iso:11073:10101[2].

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Les unités figurent dans une partition propre : selon l'IHE Devices Technical Framework, les unités de base proviennent de la partition des unités de l'ISO/IEEE 11073-10101, même si certaines implémentations peuvent nécessiter un mapping vers d'autres systèmes terminologiques[3] ; le guide FHIR pour les dispositifs au chevet du patient exige UCUM pour la valeur elle-même[8].

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Codes privés et termes provisoires. MDC prévoit des plages de codes privés dans lesquelles les fabricants définissent leurs propres codes pour des concepts sans code standard ; le profil IHE SDPi les déconseille autant que possible parce qu'ils compromettent l'interopérabilité[9]. Si un concept manque dans la norme de base, l'IHE Devices Technical Framework demande d'introduire une demande auprès de l'organisation de normalisation compétente, et des codes de termes provisoires sont attribués au besoin[3]. Dans RTMMS, ces termes provisoires peuvent être utilisés pour le développement et les tests d'interopérabilité, mais pas dans des dispositifs en production[2]. Chaque terme dans RTMMS porte aussi une propriété « harmonized » qui indique si le code a été convenu dans le processus ouvert d'harmonisation Rosetta[2] ; voir IHE Rosetta Terminology Mapping (RTM).

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Éditions et parties apparentées

\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n
NormeContenuStatutDateSource
ISO/IEEE 11073-10101:2004première édition de la nomenclatureannulée à l'ISO (95.99), remplacée par l'édition 2019première édition 2004-12-15[18][19][1]
IEEE 11073-10101a-2015 (ISO Amd 1:2017)extension pour l'hémodynamique, la respiration, la ventilation et l'anesthésie, les gaz du sang, l'urine, l'équilibre hydrique, la neurologie, les unités et les sites de mesureremplacée à l'IEEE ; amendement ISO annulé (95.99)publiée 2015-12-09[20][20][19]
IEEE 11073-10101-2019édition de baseactiveapprouvée 2019-06-13, publiée 2019-10-09[1]
ISO/IEEE 11073-10101:2020reprise par l'ISO de l'édition 2019active, confirmée à l'ISO (90.93)publiée 2020-08-28[4][19]
IEEE 11073-10101b-2023termes pour les pompes à perfusion, la ventilation et la dialyse, identificateurs d'événements et d'alarmes pour les soins aigusactiveapprouvée 2023-11-08, publiée 2024-01-12[5][5]
ISO/IEEE 11073-10101:2020/Amd 1:2026« Définitions supplémentaires »publiée (60.60)2026[19]
IEEE P11073-10101ctermes pour l'endoscopie, la chirurgie à haute fréquence et les participants d'un système SDCprojet (Active PAR)PAR 2020-12-03 ; publication absente de la source[21][21]
IEEE 11073-10102-2012 (ISO 10102:2014)ECG annotéinactive à l'IEEE (« Inactive-Reserved ») ; confirmée à l'ISO (90.93)publiée 2013-02-15, inactive depuis 2023-03-30[15][15][19]
IEEE 11073-10103-2012édition précédente de la nomenclature IDCremplacée, inactive depuis 2023-03-30publiée 2012-08-27[22]
IEEE 11073-10103-2023nomenclature IDC pour les dispositifs cardiaques implantablesactiveapprouvée 2023-11-08, publiée 2024-05-30[14]
ISO/IEEE 11073-10103:2025reprise par l'ISO de l'édition 2023publiée (60.60)2025-10-14[23][19]
IEEE P11073-10103btermes pour les dispositifs cardiaques implantables, comme la version du firmware, « brady mode off », le type de session et la localisation des sondesprojet (Active PAR)PAR 2025-09-10[24][24]
IEEE 11073-10201-2018modèle d'information du domaine (DIM)activeapprouvée 2018-12-05, publiée 2019-06-10[16][16]
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Gestion

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Au sein du groupe de travail IEEE 11073 Point-of-Care Devices, le sous-groupe RTM (Terminology) élabore et maintient la nomenclature pour les dispositifs au chevet du patient et les dispositifs de santé personnels[25]. Le sous-groupe IDCO du même groupe de travail élabore la nomenclature pour les dispositifs cardiaques implantables, comme 11073-10103[25]. L'IEEE publie les normes[1] ; l'ISO les reprend sous forme de norme ISO/IEEE à double logo dans le catalogue de l'ISO/TC 215[19]. La première édition a été publiée conjointement par l'ISO et l'IEEE[18].

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Ce qui ne figure pas encore dans une édition publiée passe par la table Rosetta de l'IHE RTM : celle-ci sert de dépôt temporaire pour les nouveaux termes qui ne figurent pas encore dans l'ISO/IEEE 11073-10101[26]. RTMMS, le système de gestion de ces données, est maintenu par le NIST et contient aussi de nouveaux codes encore en cours de publication[2]. Une gestion belge, comme un National Release Center pour SNOMED CT, n'a pas été trouvée pour MDC.

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Licence et accès

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Le texte de la norme 11073-10101 doit être acheté ; qui n'a besoin que des codes, des identifiants de référence et des descriptions les trouve gratuitement dans l'outil RTMMS du NIST[2]. L'IEEE met les termes à disposition via la base de données RTMMS et un accord libre de redevances avec le NIST pour le développement de produits conformes à l'IEEE 11073 et la documentation qui s'y rapporte[2]. Le NIST rend ainsi la terminologie des dispositifs librement et publiquement disponible sur la base d'un memorandum of understanding avec l'IEEE[27]. L'ensemble complet des codes MDC peut être téléchargé depuis RTMMS sous forme de fichier Excel ou de FHIR CodeSystem[8] ; RTMMS fonctionne avec une page de connexion[28] ; voir IHE Rosetta Terminology Mapping (RTM).

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Mappings

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ContexteCe que la spécification demandeÉtatSource
IHE Devices Technical Framework (volume sémantique)profils de contenu pour dispositifs de soins fondés sur l'ISO/IEEE 11073-10101Final Text, rev. 10.0[3][29]
HL7 v2, profils IHE Devicesl'OBX-3 porte le code MDC numérique, l'identifiant de référence et le système de codes « MDC » ; pour les transactions IHE PCD, codes tirés de la Harmonized Rosetta actuelleFinal Text, rev. 10.0[6][6]
IHE IDCO (lecture des dispositifs cardiaques implantables)message ORU HL7 v2.6 codé avec la nomenclature IDC IEEE 11073-10103Final Text, rev. 10.0[6]
HL7 Point-of-Care Device FHIR IG (PoCD)MDC est le système de codes préféré ; codage MDC obligatoire dans Observation.code (et, pour les mesures composées, dans Observation.component.code)uniquement la version de ballot 1.0.0-ballot3, pas encore de version officielle[8][8][8]
HL7 Personal Health Device FHIR IG (PHD)code MDC obligatoire dans Observation.code ; des traductions vers d'autres systèmes de codes peuvent y être ajoutéesversion 1.1.0 (STU 1), publication actuelle[7][7]
IEEE 11073 SDC (BICEPS, IEEE 11073-10207)10207 utilise la nomenclature IEEE 11073-10101 et prend en charge d'autres systèmes de codesnorme 2017, révision en cours[30]
IHE SDPiMDC est le système de codes standard dans SDC ; éviter autant que possible les codes privésprofil IHE[9][9]
\n

Les profils IHE Devices fixent aussi, via RTM, quels codes, unités et valeurs énumérées sont autorisés par paramètre[26]. Pour SDC, une extension de la nomenclature avec des commandes pour le pilotage externe des dispositifs est en développement (IEEE P11073-10107)[31].

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En Belgique

\n\n

Non trouvé dans les spécifications belges. La page de terminologie du guide d'implémentation belge Patient Monitoring (en développement) désigne SNOMED CT comme premier choix en Belgique et ne mentionne pas MDC[11]. Dans l'aperçu BMUC du 14 janvier 2026, la menu-fonctionnalité 11 compte les patients bénéficiant d'une surveillance à domicile dont les paramètres vitaux sont enregistrés en tant que données discrètes dans le DPI, sans citer de système de codes[34] ; les Belgian Meaningful Use Criteria de 2016 permettaient déjà d'enregistrer automatiquement les paramètres vitaux via des dispositifs connectés (historique)[35]. Les bonnes pratiques mHealth du Comité de sécurité de l'information demandent des standards ouverts, de préférence ceux de la Plate-forme eHealth, mais ne citent aucune nomenclature de dispositifs[36]. Une recherche de code dans les dépôts GitHub de HL7 Belgium sur « 11073 » et « MDC » n'a donné aucun résultat le 9 novembre 2026. Non trouvé ne signifie pas que MDC n'est utilisé nulle part dans des projets belges.

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wanneer volgt een editie die 10101b en 10101c integreert?", "Wanneer worden P11073-10101c (endoscopie, hoogfrequente chirurgie, SDC) en P11073-10103b (implanteerbare hartapparaten) gepubliceerd?", "Welke editie of RTMMS-stand weerspiegelt MDC-versie 2024-12-05 op de terminologieserver dte-tx van het eHealth-platform, en biedt ook de FOD-terminologieserver MDC aan?", "Bestaat er een officiële mapping tussen MDC en SNOMED CT (zoals de LOINC/IEEE-tabel), of enkel de mappingvoorziening in RTMMS?", "Nemen Belgische specificaties voor telemonitoring of de Patient Monitoring-IG MDC-codes op naast SNOMED CT en LOINC, bijvoorbeeld voor gegevens van toestelgateways?", "Waarom staat 11073-10102 (geannoteerd ECG) bij IEEE als inactief terwijl de ISO-versie 10102:2014 bevestigd is?" ], "open_questions": [ { "id": "oq-24a735", "html": "Is ISO/IEEE 11073-10101:2020/Amd 1:2026 de ISO-overname van IEEE 11073-10101b-2023, en wanneer volgt een editie die 10101b en 10101c integreert?", "text": "Is ISO/IEEE 11073-10101:2020/Amd 1:2026 de ISO-overname van IEEE 11073-10101b-2023, en wanneer volgt een editie die 10101b en 10101c integreert?" }, { "id": "oq-2d4e19", "html": "Wanneer worden P11073-10101c (endoscopie, hoogfrequente chirurgie, SDC) en P11073-10103b (implanteerbare hartapparaten) gepubliceerd?", "text": "Wanneer worden P11073-10101c (endoscopie, hoogfrequente chirurgie, SDC) en P11073-10103b (implanteerbare hartapparaten) gepubliceerd?" }, { "id": "oq-346f65", "html": "Welke editie of RTMMS-stand weerspiegelt MDC-versie 2024-12-05 op de terminologieserver dte-tx van het eHealth-platform, en biedt ook de FOD-terminologieserver MDC aan?", "text": "Welke editie of RTMMS-stand weerspiegelt MDC-versie 2024-12-05 op de terminologieserver dte-tx van het eHealth-platform, en biedt ook de FOD-terminologieserver MDC aan?" }, { "id": "oq-080cf7", "html": "Bestaat er een officiële mapping tussen MDC en SNOMED CT (zoals de LOINC/IEEE-tabel), of enkel de mappingvoorziening in RTMMS?", "text": "Bestaat er een officiële mapping tussen MDC en SNOMED CT (zoals de LOINC/IEEE-tabel), of enkel de mappingvoorziening in RTMMS?" }, { "id": "oq-a9b3ad", "html": "Nemen Belgische specificaties voor telemonitoring of de Patient Monitoring-IG MDC-codes op naast SNOMED CT en LOINC, bijvoorbeeld voor gegevens van toestelgateways?", "text": "Nemen Belgische specificaties voor telemonitoring of de Patient Monitoring-IG MDC-codes op naast SNOMED CT en LOINC, bijvoorbeeld voor gegevens van toestelgateways?" }, { "id": "oq-0978f9", "html": "Waarom staat 11073-10102 (geannoteerd ECG) bij IEEE als inactief terwijl de ISO-versie 10102:2014 bevestigd is?", "text": "Waarom staat 11073-10102 (geannoteerd ECG) bij IEEE als inactief terwijl de ISO-versie 10102:2014 bevestigd is?" } ], "exchanges": [], "sources": [ { "n": 1, "id": "SRC-e8042c9010", "title": "IEEE 11073-10101-2019 - Health informatics--Point-of-care medical device communication - Part 10101: Nomenclature", "publisher": "IEEE 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null, "figuur": null, "in_text": true, "on_page": true }, { "id": "CLM-8b91514e", "statement": "De terminologiepagina van de Belgische Patient Monitoring-IG (in ontwikkeling) noemt SNOMED CT de eerste keuze in België; MDC wordt op die pagina niet genoemd.", "kind": "fact", "kind_label": "fait", "locator": "terminology.md (branch main)", "as_of": "2026-11-09", "source": { "id": "SRC-b4d61e3fd7", "title": "Patient Monitoring Outcome FHIR IG - terminology (bronpagina, branch main)", "publisher": "HL7 Belgium", "url": "https://raw.githubusercontent.com/hl7-be/patient-monitoring/main/input/pagecontent/terminology.md", "published": null }, "citaat": null, "figuur": null, "in_text": true, "on_page": true }, { "id": "CLM-21f656a2", "statement": "Het overzicht van de NIST-legacywebsite vermeldt RTMMS (er gespeld als 'RTMSS') als 'Transitioning to IEEE', met tijdlijn en gegevensoverdracht nog te bepalen.", "kind": "fact", "kind_label": "fait", "locator": "tabel Web Application Tools, rij RTMSS", "as_of": "2026-11-09", "source": { "id": "SRC-2e4e8ba853", "title": "NIST Health IT Program Legacy Website", "publisher": "NIST", "url": "https://www.nist.gov/itl/products-and-services/healthcare-standards-testing", "published": "2026-04-10" }, "citaat": null, "figuur": null, "in_text": true, "on_page": true }, { "id": "CLM-3a6b8856", "statement": "De informatiefiche van RTMMS op dezelfde NIST-legacywebsite geeft als bestemming 'Transition to IHE (In discussion)', met toegang en tijdlijn nog te bepalen.", "kind": "fact", "kind_label": "fait", "locator": "Information Sheet, Disposition", "as_of": "2026-11-09", "source": { "id": "SRC-cc24cc4af0", "title": "RTMMS - Information Sheet (NIST Health IT Program Legacy Website)", "publisher": "NIST", "url": "https://www.nist.gov/itl/nist-health-it-program-legacy-website/rtmss", "published": "2026-06-15" }, "citaat": null, "figuur": null, "in_text": true, "on_page": true }, { "id": "CLM-94c44562", "statement": "De nomenclatuur IEEE 11073-10101 dient zowel point-of-care-toestellen als persoonlijke gezondheidstoestellen (PHD) binnen de ISO/IEEE 11073-familie.", "kind": "fact", "kind_label": "fait", "locator": "abstract en statusblok", "as_of": "2026-11-09", "source": { "id": "SRC-8e040d9d00", "title": "IEEE/ISO 11073-10101-2020 - Nomenclature", "publisher": "IEEE Standards Association", "url": "https://standards.ieee.org/ieee/11073-10101/10343/", "published": "2020-08-28" }, "citaat": null, "figuur": null, "in_text": true, "on_page": true }, { "id": "CLM-ced49b73", "statement": "IEEE 11073-10103 (Implantable Device, Cardiac, IDC-nomenclatuur) definieert terminologie voor de samenvatting van een uitlezing van pacemakers, defibrillatoren, CRT-toestellen en implanteerbare hartmonitoren, om gegevens uit de systemen van de fabrikanten naar het EPD of een toestelopvolgsysteem te brengen.", "kind": "fact", "kind_label": "fait", "locator": "abstract", "as_of": "2026-11-09", "source": { "id": "SRC-0a36987423", "title": "IEEE 11073-10103-2023 - Nomenclature - Implantable Device, Cardiac", "publisher": "IEEE Standards Association", "url": "https://standards.ieee.org/ieee/11073-10103/10855/", "published": "2024-05-30" }, "citaat": null, "figuur": null, "in_text": true, "on_page": true }, { "id": "CLM-e9fc375a", "statement": "IEEE 11073-10102 breidt de basisnomenclatuur 11073-10101 uit met terminologie voor ECG-annotaties.", "kind": "fact", "kind_label": "fait", "locator": "abstract", "as_of": "2026-11-09", "source": { "id": "SRC-28435b77b5", "title": "IEEE 11073-10102-2012 - Nomenclature - Annotated ECG", "publisher": "IEEE Standards Association", "url": "https://standards.ieee.org/ieee/11073-10102/3698/", "published": "2013-02-15" }, "citaat": null, "figuur": null, "in_text": true, "on_page": true }, { "id": "CLM-4fbb28f6", "statement": "IEEE 11073-10201 levert het abstracte, objectgeoriënteerde domeininformatiemodel (DIM) dat de structuur van de uitgewisselde informatie en de gebeurtenissen en diensten per objecttype vastlegt.", "kind": "fact", "kind_label": "fait", "locator": "abstract", "as_of": "2026-11-09", "source": { "id": "SRC-300d7624d9", "title": "IEEE 11073-10201-2018 - Domain Information Model", "publisher": "IEEE Standards Association", "url": "https://standards.ieee.org/ieee/11073-10201/6847/", "published": "2019-06-10" }, "citaat": null, "figuur": null, "in_text": true, "on_page": true }, { "id": "CLM-4451ffb7", "statement": "In het KB van 25 april 2002 over de financiering van ziekenhuizen (BFM-KB) staat MDC voor Major Diagnostic Category: grote diagnosegroepen die elk een systeem of een orgaan omvatten.", "kind": "fact", "kind_label": "fait", "locator": "definities, MDC", "as_of": "2026-11-09", "source": { "id": "SRC-219631bfbe", "title": "Koninklijk besluit van 25 april 2002 betreffende de vaststelling en de vereffening van het budget van financiële middelen van de ziekenhuizen (Justel, geconsolideerd)", "publisher": "FOD Justitie (Justel)", "url": "https://www.ejustice.just.fgov.be/eli/besluit/2002/04/25/2002022335/justel", "published": "2002-05-30" }, "citaat": null, "figuur": null, "in_text": true, "on_page": true }, { "id": "CLM-04b51251", "statement": "De 16-bitcode is contextgevoelig: ze mag enkel gebruikt worden wanneer de klasse van de informatie (bijvoorbeeld eenheden) al vastligt.", "kind": "fact", "kind_label": "fait", "locator": "p. 10, 3.1.3", "as_of": "2026-11-09", "source": { "id": "SRC-530c82a901", "title": "IHE Devices Technical Framework, Volume 3 (DEV TF-3): Semantic Content, Revision 10.0 - Final Text", "publisher": "IHE International", "url": "https://www.ihe.net/uploadedFiles/Documents/DEV/IHE_DEV_TF_Vol3.pdf", "published": "2024-11-04" }, "citaat": null, "figuur": null, "in_text": true, "on_page": true }, { "id": "CLM-f4eaf5df", "statement": "Sommige partities worden enkel voor persoonlijke gezondheidstoestellen (PHD) gebruikt en andere enkel voor point-of-care-toestellen, maar de normen 11073-10201, 11073-20601 en 11073-10101 beperken geen enkele partitie tot één van beide.", "kind": "fact", "kind_label": "fait", "locator": "sectie over partities", "as_of": "2026-11-09", "source": { "id": "SRC-359ddd5d7a", "title": "HL7 Terminology (THO) 7.5.0 - MDC", "publisher": "HL7 International", "url": "https://terminology.hl7.org/en/MDC.html", "published": null }, "citaat": null, "figuur": null, "in_text": true, "on_page": true }, { "id": "CLM-bda8c76d", "statement": "In FHIR wordt het MDC-codesysteem geïdentificeerd met de URI urn:iso:std:iso:11073:10101.", "kind": "fact", "kind_label": "fait", "locator": "tabel 'System'", "as_of": "2026-11-09", "source": { "id": "SRC-359ddd5d7a", "title": "HL7 Terminology (THO) 7.5.0 - MDC", "publisher": "HL7 International", "url": "https://terminology.hl7.org/en/MDC.html", "published": null }, "citaat": null, "figuur": null, "in_text": true, "on_page": true }, { "id": "CLM-c63b813b", "statement": "Volgens het IHE Devices Technical Framework komen de basiseenheden uit de eenhedenpartitie van ISO/IEEE 11073-10101, maar kunnen sommige implementaties een mapping naar andere terminologiesystemen nodig hebben.", "kind": "fact", "kind_label": "fait", "locator": "p. 13, 3.1.7 Alternative units of measurement mapping", "as_of": "2026-11-09", "source": { "id": "SRC-530c82a901", "title": "IHE Devices Technical Framework, Volume 3 (DEV TF-3): Semantic Content, Revision 10.0 - Final Text", "publisher": "IHE International", "url": "https://www.ihe.net/uploadedFiles/Documents/DEV/IHE_DEV_TF_Vol3.pdf", "published": "2024-11-04" }, "citaat": null, "figuur": null, "in_text": true, "on_page": true }, { "id": "CLM-64042848", "statement": "Voor de eenheid in de waarde van een observatie vereisen de PoCD-profielen UCUM voor alle numerieke waarden (waar beschikbaar).", "kind": "fact", "kind_label": "fait", "locator": "regels voor terminologiegebruik", "as_of": "2026-11-09", "source": { "id": "SRC-ad2b28228c", "title": "Point-of-care Device FHIR IG 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"locator": "sectie RTMMS", "as_of": "2026-11-09", "source": { "id": "SRC-ad2b28228c", "title": "Point-of-care Device FHIR IG 1.0.0-ballot3 - Terminology", "publisher": "HL7 International", "url": "https://hl7.org/fhir/uv/pocd/1.0.0-202609-ballot3/en/terminology.html", "published": null }, "citaat": null, "figuur": null, "in_text": true, "on_page": true }, { "id": "CLM-23179b0d", "statement": "De aanmeldpagina van RTMMS waarschuwt dat het systeem geen vervanging is voor de gepubliceerde IEEE-normen, maar een hulpmiddel bij hun implementatie.", "kind": "fact", "kind_label": "fait", "locator": "welkomsttekst", "as_of": "2026-11-09", "source": { "id": "SRC-53c173d6c2", "title": "Rosetta Terminology Mapping Management System (aanmeldpagina)", "publisher": "NIST", "url": "https://rtmms.nist.gov/gb_users/login", "published": null }, "citaat": null, "figuur": null, "in_text": true, "on_page": true }, { "id": "CLM-dfbd96a2", "statement": "HL7 Terminology (THO) vermeldt dat de fysiologische 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"published": null }, "citaat": null, "figuur": null, "in_text": true, "on_page": true }, { "id": "CLM-13889ecf", "statement": "Dezelfde PHD-IG verwijst Amerikaanse implementatoren naar een gratis te gebruiken mappingtabel van MDC naar LOINC.", "kind": "fact", "kind_label": "fait", "locator": "Obtaining the Observation.code", "as_of": "2026-11-09", "source": { "id": "SRC-6d1b402875", "title": "Personal Health Device FHIR IG 1.1.0 - Obtaining the Observation.code", "publisher": "HL7 International", "url": "https://hl7.org/fhir/uv/phd/ObtainObservationCode.html", "published": null }, "citaat": null, "figuur": null, "in_text": true, "on_page": true }, { "id": "CLM-22b6d569", "statement": "RTMMS voorziet het vastleggen van equivalentiemappings van toestelterminologie naar andere vocabularia, waaronder LOINC en SNOMED CT.", "kind": "fact", "kind_label": "fait", "locator": "opsomming vocabulairediensten", "as_of": "2026-11-09", "source": { "id": "SRC-dd54d25908", "title": "Medical Device 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"Point-of-care Device FHIR IG 1.0.0-ballot3 - Terminology", "publisher": "HL7 International", "url": "https://hl7.org/fhir/uv/pocd/1.0.0-202609-ballot3/en/terminology.html", "published": null }, "citaat": null, "figuur": null, "in_text": true, "on_page": true }, { "id": "CLM-7f5ac1ab", "statement": "De PHD-IG die dit voorschrijft is versie 1.1.0 (STU 1), de huidige gepubliceerde versie.", "kind": "fact", "kind_label": "fait", "locator": "kopregel van de pagina", "as_of": "2026-11-09", "source": { "id": "SRC-6d1b402875", "title": "Personal Health Device FHIR IG 1.1.0 - Obtaining the Observation.code", "publisher": "HL7 International", "url": "https://hl7.org/fhir/uv/phd/ObtainObservationCode.html", "published": null }, "citaat": null, "figuur": null, "in_text": true, "on_page": true }, { "id": "CLM-a9ee37ff", "statement": "Volgens de scope van de revisie gebruikt IEEE 11073-10207 de nomenclatuur IEEE 11073-10101 en ondersteunt het andere codesystemen; netwerktransport valt buiten de 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Gebruik en onderhoud van CIED software", "publisher": "Publicatiebureau van de Europese Unie (TED)", "url": "https://ted.europa.eu/en/notice/674691-2026/pdf", "published": "2026-10-01" }, "citaat": null, "figuur": null, "in_text": true, "on_page": true }, { "id": "CLM-518e6638", "statement": "Volgens dezelfde aanbesteding toonde een voorstudie dat de CIED-fabrikanten de IEEE 11073-10103-standaard nog niet uniform toepassen.", "kind": "fact", "kind_label": "fait", "locator": "p. 1, 2.1 Procedure, Description", "as_of": "2026-11-09", "source": { "id": "SRC-f1e50b9e9d", "title": "TED 674691-2026 - Gebruik en onderhoud van CIED software", "publisher": "Publicatiebureau van de Europese Unie (TED)", "url": "https://ted.europa.eu/en/notice/674691-2026/pdf", "published": "2026-10-01" }, "citaat": null, "figuur": null, "in_text": true, "on_page": true }, { "id": "CLM-3f19decd", "statement": "In het BMUC-overzicht van 14 januari 2026 telt menufunctionaliteit 11 de patiënten met thuismonitoring van wie klinische waarden zoals vitale parameters als discrete gegevens in het EPD worden geregistreerd; een codesysteem wordt daar niet genoemd.", "kind": "fact", "kind_label": "fait", "locator": "Menu 11, teller", "as_of": "2026-11-09", "source": { "id": "SRC-94b0514e73", "title": "BMUC_Functionaliteiten_Fonctionnalités_14012026 (overzicht kern- en menufunctionaliteiten met teller/noemer en FAQ)", "publisher": "FOD Volksgezondheid", "url": "https://www.health.belgium.be/sites/default/files/media/files/2026-01/bmuc_functionaliteiten_fonctionnalites_14012026.xlsx", "published": "2026-01-14" }, "citaat": null, "figuur": null, "in_text": true, "on_page": true }, { "id": "CLM-6c2573c6", "statement": "De Belgische Meaningful Use Criteria van 2016 lieten de registratie van vitale parameters manueel of automatisch via gekoppelde toestellen toe, met de mogelijkheid om automatisch geregistreerde gegevens te valideren (historisch).", "kind": "fact", "kind_label": "fait", "locator": "p. 16, 11. 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