MedicalDevice-v3.1(2017EN): verschil tussen versies
(Copy of) |
|||
Regel 1: | Regel 1: | ||
− | ==General information== | + | <!-- Hieronder wordt een transclude page aangeroepen --> |
− | Name: '''nl.zorg.MedicalDevice''' [[Bestand:NL.png|link=MedischHulpmiddel-v3.1(2017NL)]]<BR> | + | {{Versions-2.16.840.1.113883.2.4.3.11.60.40.3.10.1(EN)|1|MedicalDevice-v3.1(2017EN)}} |
− | Version: '''3.1''' <br> | + | <!-- Tot hier de transclude page --> |
− | HCIM Status:Final<br> | + | ==General information<!--hdGeneralInformation-->== |
− | Release: '''2017''' <br> | + | Name<!--hdName-->: '''nl.zorg.MedicalDevice''' [[Bestand:NL.png|link=MedischHulpmiddel-v3.1(2017NL)]]<BR> |
− | Release status: Published<br> | + | Version<!--hdVersion-->: '''3.1''' <br> |
− | Release date: 31-12-2017 | + | HCIM Status<!--hdStatus-->:Final<br> |
+ | Release<!--hdPublication-->: '''2017''' <br> | ||
+ | Release status<!--hdPublicationStatus-->: Published<br> | ||
+ | Release date<!--hdPublicationDate-->: 31-12-2017 | ||
----- | ----- | ||
− | <div style="text-align: right; direction: ltr; margin-left: 1em;" >[[Bestand: Back 16.png| link= | + | <div style="text-align: right; direction: ltr; margin-left: 1em;" >[[Bestand: Back 16.png| link= HCIM_Release<!--wikiReleasePage-->_2017(EN)]] [[HCIM_Release<!--wikiReleasePage-->_2017(EN) |Back to HCIM list<!--hdBackToMainPage--> ]]</div> |
==Metadata== | ==Metadata== | ||
Regel 61: | Regel 64: | ||
==Revision History== | ==Revision History== | ||
<div class="mw-collapsible mw-collapsed"> | <div class="mw-collapsible mw-collapsed"> | ||
− | ''Only available in Dutch'' | + | ''Only available in Dutch<!--noTranslation-->'' |
<u>Publicatieversie 1.0</u> (15-02-2013) | <u>Publicatieversie 1.0</u> (15-02-2013) | ||
Regel 196: | Regel 199: | ||
<BR> | <BR> | ||
<imagemap> Bestand:MedicalDevice-v3.1Model(EN).png | center | <imagemap> Bestand:MedicalDevice-v3.1Model(EN).png | center | ||
− | rect | + | rect 509 358 623 428 [[#12921]] |
− | rect | + | rect 825 117 969 167 [[#HIBCProductIDCodelist]] |
− | rect | + | rect 52 465 273 515 [[#MedicalDeviceLateralityCodelist]] |
− | rect | + | rect 159 358 273 428 [[#12934]] |
− | rect | + | rect 331 465 551 515 [[#MedicalDeviceAnatomicalLocationCodelist]] |
− | rect | + | rect 825 185 969 235 [[#ProductIDCodelist]] |
− | rect | + | rect 825 261 969 311 [[#ProductTypeCodelist]] |
− | rect | + | rect 159 269 273 339 [[#12935]] |
− | rect | + | rect 508 91 622 161 [[HealthProfessional-v3.2(2017EN)]] |
− | rect | + | rect 334 91 458 161 [[HealthcareProvider-v3.1.1(2017EN)]] |
− | rect | + | rect 339 358 453 428 [[#12933]] |
− | rect | + | rect 159 180 273 250 [[Problem-v4.1(2017EN)]] |
− | rect | + | rect 694 254 784 324 [[#12928]] |
− | rect | + | rect 693 151 783 221 [[#12929]] |
− | rect | + | rect 508 203 622 273 [[#12932]] |
− | rect | + | rect 159 91 273 161 [[#12923]] |
− | rect | + | rect 344 198 448 278 [[#12931]] |
desc none | desc none | ||
</imagemap> | </imagemap> | ||
Regel 218: | Regel 221: | ||
{| border= "1" width="1500px" style = "font-size: 9.5pt; border: solid 1px silver; border-collapse:collapse;" cellpadding = "3px" cellspacing ="0px" | {| border= "1" width="1500px" style = "font-size: 9.5pt; border: solid 1px silver; border-collapse:collapse;" cellpadding = "3px" cellspacing ="0px" | ||
|-style="background-color: #1F497D; color: white; font-weight: bold; font-variant: small-caps; " | |-style="background-color: #1F497D; color: white; font-weight: bold; font-variant: small-caps; " | ||
− | |style="width:30px;"|Type||style="width:100px;"|Id||colspan="6 " style="width:140px;"|Concept||Card.||style="width: 600px;"|Definition||style="width:200px;"|DefinitionCode||style="width:200px;"|Reference | + | |style="width:30px;"|Type<!--imType-->||style="width:100px;"|Id<!--imId-->||colspan="6 " style="width:140px;"|Concept<!--imConcept-->||Card.<!--imCard-->||style="width: 600px;"|Definition<!--imDefinition-->||style="width:200px;"|DefinitionCode<!--imDefinitionCode-->||style="width:200px;"|Reference<!--imReference--> |
|-style="vertical-align:top; background-color: #E3E3E3; " | |-style="vertical-align:top; background-color: #E3E3E3; " | ||
|style = "text-align:center" |[[Bestand: block.png| 20px | link=]] | |style = "text-align:center" |[[Bestand: block.png| 20px | link=]] | ||
Regel 228: | Regel 231: | ||
{| | {| | ||
|- | |- | ||
− | |<span | + | |<span title = "Codesystem: SNOMED CT>[https://terminologie.nictiz.nl/art-decor/snomed-ct?conceptId=49062001 49062001] Device (physical object)</span> |
|} | |} | ||
| | | | ||
Regel 241: | Regel 244: | ||
{| | {| | ||
|- | |- | ||
− | |<span | + | |<span title = "Codesystem: SNOMED CT>[https://terminologie.nictiz.nl/art-decor/snomed-ct?conceptId=405815000 405815000] Procedure device</span> |
|} | |} | ||
| | | | ||
Regel 320: | Regel 323: | ||
{| | {| | ||
|- | |- | ||
− | |<span | + | |<span title = "Codesystem: LOINC>[https://terminologie.nictiz.nl/art-decor/loinc?conceptId=48767-8 48767-8] Annotation comment</span> |
|} | |} | ||
| | | | ||
Regel 333: | Regel 336: | ||
{| | {| | ||
|- | |- | ||
− | |<span | + | |<span title = "Codesystem: SNOMED CT>[https://terminologie.nictiz.nl/art-decor/snomed-ct?conceptId=363698007 363698007] Finding site</span> |
|} | |} | ||
| | | | ||
Regel 350: | Regel 353: | ||
{| | {| | ||
|- | |- | ||
− | |<span | + | |<span title = "Codesystem: SNOMED CT>[https://terminologie.nictiz.nl/art-decor/snomed-ct?conceptId=272741003 272741003] Laterality</span> |
|} | |} | ||
| | | | ||
Regel 384: | Regel 387: | ||
|} | |} | ||
|} | |} | ||
− | Columns Concept and DefinitionCode: hover over the values for more information<BR> | + | Columns Concept and DefinitionCode: hover over the values for more information<!--imHover--><BR> |
− | For explanation of the symbols, please see the legend page [[Bestand:list2.png|link=Legend]] | + | For explanation of the symbols, please see the legend page<!--imLegend--> [[Bestand:list2.png|link=Legend<!--wikiLegend-->]] |
==Example Instances== | ==Example Instances== | ||
− | ''Only available in Dutch'' | + | ''Only available in Dutch<!--noTranslation-->'' |
{|class="wikitable" width="1156px" style= "font-size: 9.5pt;" | {|class="wikitable" width="1156px" style= "font-size: 9.5pt;" | ||
Regel 513: | Regel 516: | ||
{| class="wikitable" width="60%" | {| class="wikitable" width="60%" | ||
|-style='vertical-align:top; background-color: #E8D7BE;' | |-style='vertical-align:top; background-color: #E8D7BE;' | ||
− | |Valueset OID 2.16.840.1.113883.2.4.3.11.60.40.2.10.1.5 | + | |Valueset OID<!--vsValuesetOID-->: 2.16.840.1.113883.2.4.3.11.60.40.2.10.1.5 |
+ | |Binding<!--vsBindingTag-->: | ||
|} | |} | ||
{| class="wikitable" width="60% " | {| class="wikitable" width="60% " | ||
|-style="background-color: #1F497D; color: white; font-weight: bold; " | |-style="background-color: #1F497D; color: white; font-weight: bold; " | ||
− | |Conceptname | + | |Conceptname<!--vsConceptName--> |
− | |Codesystem name||Codesystem OID | + | |Codesystem name<!--vsConceptSystemName-->||Codesystem OID<!--vsConceptSystemOID--> |
|-style="vertical-align:top; " | |-style="vertical-align:top; " | ||
|Alle waarden | |Alle waarden | ||
Regel 524: | Regel 528: | ||
|2.16.840.1.113883.6.40 | |2.16.840.1.113883.6.40 | ||
|} | |} | ||
− | |||
=== MedicalDeviceAnatomicalLocationCodelist=== | === MedicalDeviceAnatomicalLocationCodelist=== | ||
{| class="wikitable" width="60%" | {| class="wikitable" width="60%" | ||
|-style='vertical-align:top; background-color: #E8D7BE;' | |-style='vertical-align:top; background-color: #E8D7BE;' | ||
− | |Valueset OID 2.16.840.1.113883.2.4.3.11.60.40.2.10.1.2 | + | |Valueset OID<!--vsValuesetOID-->: 2.16.840.1.113883.2.4.3.11.60.40.2.10.1.2 |
+ | |Binding<!--vsBindingTag-->: | ||
|} | |} | ||
{| class="wikitable" width="60% " | {| class="wikitable" width="60% " | ||
|-style="background-color: #1F497D; color: white; font-weight: bold; " | |-style="background-color: #1F497D; color: white; font-weight: bold; " | ||
− | |Conceptname | + | |Conceptname<!--vsConceptName--> |
− | |Codesystem name||Codesystem OID | + | |Codesystem name<!--vsConceptSystemName-->||Codesystem OID<!--vsConceptSystemOID--> |
|-style="vertical-align:top; " | |-style="vertical-align:top; " | ||
− | |SNOMED CT: < 442083009 <noWiki>|</noWiki>Anatomical or acquired body structure<noWiki>|</noWiki> | + | |SNOMED CT: < [https://terminologie.nictiz.nl/art-decor/snomed-ct?conceptId=442083009 442083009]<noWiki>|</noWiki>Anatomical or acquired body structure<noWiki>|</noWiki> |
|SNOMED CT | |SNOMED CT | ||
|2.16.840.1.113883.6.96 | |2.16.840.1.113883.6.96 | ||
|} | |} | ||
− | |||
=== MedicalDeviceLateralityCodelist=== | === MedicalDeviceLateralityCodelist=== | ||
{| class="wikitable" width="60%" | {| class="wikitable" width="60%" | ||
|-style='vertical-align:top; background-color: #E8D7BE;' | |-style='vertical-align:top; background-color: #E8D7BE;' | ||
− | |Valueset OID 2.16.840.1.113883.2.4.3.11.60.40.2.10.1.4 | + | |Valueset OID<!--vsValuesetOID-->: 2.16.840.1.113883.2.4.3.11.60.40.2.10.1.4 |
+ | |Binding<!--vsBindingTag-->: | ||
|} | |} | ||
{| class="wikitable" width="60% " | {| class="wikitable" width="60% " | ||
|-style="background-color: #1F497D; color: white; font-weight: bold; " | |-style="background-color: #1F497D; color: white; font-weight: bold; " | ||
− | |Conceptname | + | |Conceptname<!--vsConceptName--> |
− | |Conceptcode | + | |Conceptcode<!--vsConceptCode--> |
− | |Codesystem name||Codesystem OID | + | |Codesystem name<!--vsConceptSystemName-->||Codesystem OID<!--vsConceptSystemOID--> |
− | |Description | + | |Description<!--vsDescription--> |
|-style="vertical-align:top; " | |-style="vertical-align:top; " | ||
|Left | |Left | ||
− | |7771000 | + | |[https://terminologie.nictiz.nl/art-decor/snomed-ct?conceptId=7771000 7771000] |
|SNOMED CT | |SNOMED CT | ||
|2.16.840.1.113883.6.96 | |2.16.840.1.113883.6.96 | ||
Regel 559: | Regel 563: | ||
|-style="vertical-align:top; " | |-style="vertical-align:top; " | ||
|Right | |Right | ||
− | |24028007 | + | |[https://terminologie.nictiz.nl/art-decor/snomed-ct?conceptId=24028007 24028007] |
|SNOMED CT | |SNOMED CT | ||
|2.16.840.1.113883.6.96 | |2.16.840.1.113883.6.96 | ||
Regel 565: | Regel 569: | ||
|-style="vertical-align:top; " | |-style="vertical-align:top; " | ||
|Right and left | |Right and left | ||
− | |51440002 | + | |[https://terminologie.nictiz.nl/art-decor/snomed-ct?conceptId=51440002 51440002] |
|SNOMED CT | |SNOMED CT | ||
|2.16.840.1.113883.6.96 | |2.16.840.1.113883.6.96 | ||
|Rechts en links | |Rechts en links | ||
|} | |} | ||
− | |||
=== ProductIDCodelist=== | === ProductIDCodelist=== | ||
{| class="wikitable" width="60%" | {| class="wikitable" width="60%" | ||
|-style='vertical-align:top; background-color: #E8D7BE;' | |-style='vertical-align:top; background-color: #E8D7BE;' | ||
− | |Valueset OID 2.16.840.1.113883.2.4.3.11.60.40.2.10.1.3 | + | |Valueset OID<!--vsValuesetOID-->: 2.16.840.1.113883.2.4.3.11.60.40.2.10.1.3 |
+ | |Binding<!--vsBindingTag-->: | ||
|} | |} | ||
{| class="wikitable" width="60% " | {| class="wikitable" width="60% " | ||
|-style="background-color: #1F497D; color: white; font-weight: bold; " | |-style="background-color: #1F497D; color: white; font-weight: bold; " | ||
− | |Conceptname | + | |Conceptname<!--vsConceptName--> |
− | |Codesystem name||Codesystem OID | + | |Codesystem name<!--vsConceptSystemName-->||Codesystem OID<!--vsConceptSystemOID--> |
|-style="vertical-align:top; " | |-style="vertical-align:top; " | ||
|Alle waarden | |Alle waarden | ||
Regel 585: | Regel 589: | ||
|1.3.160 | |1.3.160 | ||
|} | |} | ||
− | |||
=== ProductTypeCodelist=== | === ProductTypeCodelist=== | ||
{| class="wikitable" width="60%" | {| class="wikitable" width="60%" | ||
|-style='vertical-align:top; background-color: #E8D7BE;' | |-style='vertical-align:top; background-color: #E8D7BE;' | ||
− | |Valueset OID 2.16.840.1.113883.2.4.3.11.60.40.2.10.1.1 | + | |Valueset OID<!--vsValuesetOID-->: 2.16.840.1.113883.2.4.3.11.60.40.2.10.1.1 |
+ | |Binding<!--vsBindingTag-->: | ||
|} | |} | ||
{| class="wikitable" width="60% " | {| class="wikitable" width="60% " | ||
|-style="background-color: #1F497D; color: white; font-weight: bold; " | |-style="background-color: #1F497D; color: white; font-weight: bold; " | ||
− | |Conceptname | + | |Conceptname<!--vsConceptName--> |
− | |Codesystem name||Codesystem OID | + | |Codesystem name<!--vsConceptSystemName-->||Codesystem OID<!--vsConceptSystemOID--> |
|-style="vertical-align:top; " | |-style="vertical-align:top; " | ||
|Alle waarden | |Alle waarden | ||
Regel 601: | Regel 605: | ||
|} | |} | ||
− | + | ==This information model in other releases<!--ftOtherReleases-->== | |
− | ==This information model in other releases== | + | <!-- Hieronder wordt een transclude page aangeroepen --> |
− | < | + | {{Versions-2.16.840.1.113883.2.4.3.11.60.40.3.10.1(EN)|2|2017}} |
− | < | + | <!-- Tot hier de transclude page --> |
− | + | ==Information model references<!--ftReferences-->== | |
− | + | ====This information model refers to<!--ftRefersTo-->==== | |
− | == | + | *[[HealthcareProvider-v3.1.1(2017EN)|HealthcareProvider-v3.1.1]] |
+ | *[[HealthProfessional-v3.2(2017EN)|HealthProfessional-v3.2]] | ||
+ | *[[Problem-v4.1(2017EN)|Problem-v4.1]] | ||
+ | ====This information model is used in<!--ftReferredBy-->==== | ||
+ | *[[AbilityToPerformMouthcareActivities-v3.1(2017EN)|AbilityToPerformMouthcareActivities-v3.1]] | ||
+ | *[[BladderFunction-v3.1(2017EN)|BladderFunction-v3.1]] | ||
+ | *[[BowelFunction-v3.1(2017EN)|BowelFunction-v3.1]] | ||
+ | *[[FeedingTubeSystem-v3.2(2017EN)|FeedingTubeSystem-v3.2]] | ||
+ | *[[FunctionalOrMentalStatus-v3.1(2017EN)|FunctionalOrMentalStatus-v3.1]] | ||
+ | *[[HearingFunction-v3.1(2017EN)|HearingFunction-v3.1]] | ||
+ | *[[Infusion-v3.2(2017EN)|Infusion-v3.2]] | ||
+ | *[[Mobility-v3.1(2017EN)|Mobility-v3.1]] | ||
+ | *[[NursingIntervention-v3.1(2017EN)|NursingIntervention-v3.1]] | ||
+ | *[[PlannedCareActivityForTransfer-v3.1(2017EN)|PlannedCareActivityForTransfer-v3.1]] | ||
+ | *[[Procedure-v4.1(2017EN)|Procedure-v4.1]] | ||
+ | *[[Respiration-v3.1(2017EN)|Respiration-v3.1]] | ||
+ | *[[Stoma-v3.2(2017EN)|Stoma-v3.2]] | ||
+ | *[[VisualFunction-v3.1(2017EN)|VisualFunction-v3.1]] | ||
+ | *[[Wound-v3.1(2017EN)|Wound-v3.1]] | ||
+ | ==Technical specifications in HL7v3 CDA and HL7 FHIR<!--ftHeader-->== | ||
To exchange information based on health and care information models, additional, more technical specifications are required.<BR> | To exchange information based on health and care information models, additional, more technical specifications are required.<BR> | ||
− | Not every environment can handle the same technical specifications. For this reason, there are several types of technical specifications: | + | Not every environment can handle the same technical specifications. For this reason, there are several types of technical specifications:<!--ftReferenceIntro--> |
<ul> | <ul> | ||
− | <li>HL7® version 3 CDA compatible specifications, available through the Nictiz ART-DECOR® environment [http://decor.nictiz.nl/art-decor/decor-scenarios--zib2017bbr-?id=2.16.840.1.113883.2.4.3.11.60.7.4.2.10.1&effectiveDate=2017-12-31T00:00:00&language=en-US&scenariotree=false [[File:artdecor.jpg|16px|link=]]]</li> | + | <li>HL7® version 3 CDA compatible specifications, available through the Nictiz ART-DECOR® environment<!--ftArtDecorReference--> [http://decor.nictiz.nl/art-decor/decor-scenarios--zib2017bbr-?id=2.16.840.1.113883.2.4.3.11.60.7.4.2.10.1&effectiveDate=2017-12-31T00:00:00&language=en-US&scenariotree=false [[File:artdecor.jpg|16px|link=]]]</li> |
− | <li>HL7® FHIR® compatible specifications, available through the Nictiz environment on the Simplifier FHIR | + | <li>HL7® FHIR® compatible specifications, available through the Nictiz environment on the Simplifier FHIR<!--ftSimplifierReference--> {{SimplefierLinks|2017}}</li> |
</ul> | </ul> | ||
− | This information model is also available as [[Media:nl.zorg.MedicalDevice-v3.1(2017EN).pdf|pdf file]] [[File:PDF.png|link=]] or as [[Media:nl.zorg.MedicalDevice-v3.1(2017EN).xlsx|spreadsheet]] [[File:xlsx.png|link=]] | + | ==Downloads<!--ftDownloadTitle-->== |
− | ==About this information== | + | This information model is also available as [[Media:nl.zorg.MedicalDevice-v3.1(2017EN).pdf|pdf file]] [[File:PDF.png|link=]] or as [[Media:nl.zorg.MedicalDevice-v3.1(2017EN).xlsx|spreadsheet]] [[File:xlsx.png|link=]]<!--ftDownloads--> |
− | The information in this wikipage is based on Release 2017 <BR> | + | ==About this information<!--ftHeader2-->== |
− | Conditions for use are located on the mainpage [[Bestand:list2.png|link=HCIM_Mainpage]]<BR> | + | The information in this wikipage is based on<!--ftInfoBase--> Release 2017 <BR> |
− | This page is generated on | + | Conditions for use are located on the mainpage<!--ftConditions--> [[Bestand:list2.png|link=HCIM_Mainpage<!--wikiMainpage-->]]<BR> |
+ | This page is generated on 19/12/2018 18:32:54 with ZibExtraction v. 3.0.6927.32850<!--ftDate--> <BR> | ||
----- | ----- | ||
− | <div style="text-align: right; direction: ltr; margin-left: 1em;" >[[Bestand: Back 16.png| link= | + | <div style="text-align: right; direction: ltr; margin-left: 1em;" >[[Bestand: Back 16.png| link= HCIM_Release<!--wikiReleasePage-->_2017(EN)]] [[HCIM_Release<!--wikiReleasePage-->_2017(EN) |Back to HCIM list<!--hdBackToMainPage--> ]]</div> |
Versie van 20 dec 2018 om 13:31
Inhoud
- 1 General information
- 2 Metadata
- 3 Revision History
- 4 Concept
- 5 Purpose
- 6 Evidence Base
- 7 Information Model
- 8 Example Instances
- 9 Issues
- 10 References
- 11 Valuesets
- 12 This information model in other releases
- 13 Information model references
- 14 Technical specifications in HL7v3 CDA and HL7 FHIR
- 15 Downloads
- 16 About this information
General information
Name: nl.zorg.MedicalDevice
Version: 3.1
HCIM Status:Final
Release: 2017
Release status: Published
Release date: 31-12-2017
Metadata
DCM::CoderList | Kerngroep Registratie aan de Bron |
DCM::ContactInformation.Address | * |
DCM::ContactInformation.Name | * |
DCM::ContactInformation.Telecom | * |
DCM::ContentAuthorList | Projectgroep Generieke Overdrachtsgegevens & Kerngroep Registratie aan de Bron |
DCM::CreationDate | 2-1-2013 |
DCM::DeprecatedDate | |
DCM::DescriptionLanguage | nl |
DCM::EndorsingAuthority.Address | |
DCM::EndorsingAuthority.Name | PM |
DCM::EndorsingAuthority.Telecom | |
DCM::Id | 2.16.840.1.113883.2.4.3.11.60.40.3.10.1 |
DCM::KeywordList | medisch hulpmiddel, implantaat |
DCM::LifecycleStatus | Final |
DCM::ModelerList | Kerngroep Registratie aan de Bron |
DCM::Name | nl.zorg.MedischHulpmiddel |
DCM::PublicationDate | 31-12-2017 |
DCM::PublicationStatus | Published |
DCM::ReviewerList | Projectgroep Generieke Overdrachtsgegevens & Kerngroep Registratie aan de Bron |
DCM::RevisionDate | 31-12-2017 |
DCM::Superseeds | nl.zorg.MedischHulpmiddel-v3.0 |
DCM::Version | 3.1 |
HCIM::PublicationLanguage | EN |
Revision History
Only available in Dutch
Publicatieversie 1.0 (15-02-2013) -
Publicatieversie 1.1 (01-07-2013)
ZIB-11 | Gebruik van de GS1 standaard |
Publicatieversie 1.2 (01-04-2015)
ZIB-83 | Wijzigingsvoorstel OverdrachtMedischHulpmiddel |
ZIB-88 | OverdrachtMedischHulpmiddel |
ZIB-110 | Example of the instrument van OverdrachtMedischHulpmiddel bevat kolom Zorgverlener, definities binnen deze kolom moeten duidelijker |
ZIB-249 | In de klinische bouwsteen OverdrachtMedischHulpmiddel DCM::ValueSet SNOMED CT aangepast van concept AnatomischeLocalisatie naar tagged value DCM::ContentExpression. |
ZIB-250 | In klinische bouwsteen OverdrachtMedischHulpmiddel de waarde van DCM::Name aanpassen van OverdrachtMedischHulpmiddel naar nl.nfu.OverdrachtMedischHulpmiddel. |
ZIB-251 | Tagged value DCM::ValueSet van concept ProductType aangepast naar DCM::CodeSystem. |
ZIB-252 | Tagged value DCM::ValueSet GTIN aangepast naar DCM::AssigningAuthority GTIN. |
ZIB-308 | Prefix Overdracht weggehaald bij de generieke bouwstenen |
ZIB-327 | AnatomischeLocalisatie wijzigen in AnatomischeLocatie |
ZIB-353 | Tagged values DCM::CodeSystem aanpassen naar DCM::ValueSet incl. gekoppelde codelijst. |
Incl. algemene wijzigingsverzoeken:
ZIB-94 | Aanpassen tekst van Disclaimer, Terms of Use & Copyrights |
ZIB-154 | Consequenties opsplitsing Medicatie bouwstenen voor overige bouwstenen. |
ZIB-200 | Naamgeving SNOMED CT in tagged values klinische bouwstenen gelijk getrokken. |
ZIB-201 | Naamgeving OID: in tagged value notes van klinische bouwstenen gelijk getrokken. |
ZIB-309 | EOI aangepast |
ZIB-324 | Codelijsten Name en Description beginnen met een Hoofdletter |
ZIB-326 | Tekstuele aanpassingen conform de kwaliteitsreview kerngroep 2015 |
Publicatieversie 3.0 (01-05-2016)
Publicatieversie 3.1 (04-09-2017)
ZIB-457 | Uitbreiding AnatomischeLocatieCodelijst met Snomed qualifiers |
ZIB-461 | Uitbreiding ProductIDCodelijst met HIBC |
ZIB-517 | Onduidelijk hoe ProductTypeCodelijst gebruikt moet worden. |
ZIB-522 | Codestelsel veranderen voor producttype |
ZIB-547 | Toevoegen SNOMED CT als mogelijk codestelsel voor het coderen van producttype |
ZIB-549 | De Engelse naam van de bouwsteen en het rootconcept zijn niet correct |
ZIB-564 | Aanpassing/harmonisatie Engelse conceptnamen |
ZIB-568 | Example Instances niet correct |
ZIB-573 | Toevoegen van de mogelijkheid om dimensies van het hulpmiddel aan te geven |
ZIB-574 | Alleen verwijzen naar het rootconcept van de ZIB. |
ZIB-578 | Aan het concept anatomische locatie moet een concept Laterariteit toegevoegd worden. |
ZIB-585 | Toevoegen concept Lateraliteit aan het concept Anatomische Locatie |
Concept
Medical devices are any internally implanted and external devices and/or aids used by the patient (in the past) to reduce the effects of functional limitations in organ systems or to facilitate the treatment of a disease.
Purpose
Data on medical devices is recorded for several reasons. Knowledge of the presence of these implants enables tracing and taking the aid or device into account in diagnostic or therapeutic procedures, care and transport.
Examples include:
- Consequences for transportation, toilet use, etc., in the case of a wheelchair;
- A pacemaker can be of medical importance, but also has consequences for planning radiological exams.
Evidence Base
Recording data on medically complex devices such as pacemakers is not yet common in EPD systems in the Netherlands, but is sometimes lacking: a letter from a specialist for example often does not include information on which type of pacemaker the patient has (and from which manufacturer).
The Dutch Ministry of Health, Welfare and Sport (VWS) will pass legislation for a national basic register of implants. Every healthcare center will have to supply a UDI (Unique Device Identification, with a link to GTIN) and a UPI (Unique Patient Identification) to the basic register. This will prevent situations in which a large group of patients have an aid or implant in which problems have been detected that cannot be traced.
Information Model
Type | Id | Concept | Card. | Definition | DefinitionCode | Reference | |||||||||
NL-CM:10.1.1 | MedicalDevice | Root concept of the MedicalDevice information model. This root concept contains all data elements of the MedicalDevice information model. |
|
||||||||||||
NL-CM:10.1.2 | Product | 1 | The medical aid used (internally or externally). |
|
|||||||||||
NL-CM:10.1.4 | ProductID | 0..1 | Unique identification of the product, such as the serial number.
Frequently used coding systems are HIBC and GTIN. If the law requires this to be registered on the basis of a UDI (Unique Device Identifier), the unique identification must consist of a UDI-DI (Device Identifier) and a UDI-PI (Production Identifier(s)). See http://www.gs1.org/healthcare/udi for more information. The UDI-DI must be recorded in reference to GS1 GTIN (01) encryptions, with which for example a firm is linked to the product type. The UDI-PI must consist of the following: application identifier (AI); expiration date (17) and serial number (21) and/or batch or lot number (10). |
| |||||||||||
NL-CM:10.1.3 | ProductType | 0..1 | The code of the type of product. |
| |||||||||||
NL-CM:10.1.13 | ProductDescription | 0..1 | Textual description of the product. | ||||||||||||
NL-CM:10.1.11 | StartDate | 0..1 | The start date of the first use or implant of the medical aid. A ‘vague’ date, such as only the year, is permitted. | ||||||||||||
NL-CM:10.1.7 | Indication::Problem | 0..* | The medical reason for use of the medical device. |
| |||||||||||
NL-CM:10.1.10 | Comment | 0..1 | Comment about use or information on the medical aid used. |
|
|||||||||||
NL-CM:10.1.6 | AnatomicalLocation | 0..1 | Patient’s anatomical location of the medical device used. |
|
| ||||||||||
NL-CM:10.1.12 | Laterality | 0..1 | Laterality adds information about body side to the anatomic location, e.g. left |
|
| ||||||||||
NL-CM:10.1.8 | Location::HealthcareProvider | 0..1 | The healthcare provider at which use of the medical aid was initiated or where the aid was implanted. |
| |||||||||||
NL-CM:10.1.9 | HealthProfessional | 0..1 | The healthcare provider involved in the indication for use of the medical aid implant. |
|
Columns Concept and DefinitionCode: hover over the values for more information
For explanation of the symbols, please see the legend page
Example Instances
Only available in Dutch
Begin Datum |
Product | Anatomische Locatie | Lateraliteit | Indicatie | Locatie | Toelichting | ||
ProductID | ProductType | ProbleemNaam | Organisatie Naam |
Afdeling Specialisme |
||||
08-03-2012 | GTIN/HIBC code | Rolstoel | Multiple sclerose | Kan korte afstanden lopen | ||||
Begin Datum |
Product | Anatomische Locatie | Lateraliteit | Lateraliteit | Locatie | Toelichting | ||
ProductID | ProductType | ProbleemNaam | Organisatie Naam |
Afdeling Specialisme |
||||
2007 | GTIN/HIBC code | Gehoorapparaat | Oor | Rechts | Presbyacusis | St. Franciscus Gasthuis | Audiologie | Apparaat niet zichtbaar (diep in de gehooringang) |
Begin Datum |
Product | Anatomische Locatie | Lateraliteit | Indicatie | Locatie | Toelichting | ||
ProductID | ProductType | ProbleemNaam | Organisatie Naam |
Afdeling Specialisme |
||||
10-02-2004 | GTIN/HIBC code | Pacemaker | Subclavian pouch | Links | Paroxymaal boezemfibrilleren | Academisch Medisch Centrum | Cardiologie | Laatst doorgemeten in 2011 |
Issues
The UNSPSC code system has a great many products (including non-medical products). That is why a Dutch set and/or subcollection of this code system is required to indicate the type of product. We have currently opted to consider all values in the UNPSPSC for documenting the type of medical aid product in the absence of such a set.
References
1. Kamerbrief over het voorstel voor een register van implantaten. [Online] Beschikbaar op: http://www.rijksoverheid.nl/documenten-en-publicaties/kamerstukken/2012/11/20/kamerbrief-over-het-voorstel-voor-een-register-van-implantaten.html [Geraadpleegd: 15 september 2014].
Valuesets
HIBCProductIDCodelist
Valueset OID: 2.16.840.1.113883.2.4.3.11.60.40.2.10.1.5 | Binding: |
Conceptname | Codesystem name | Codesystem OID |
Alle waarden | Health Industry Bar Code (HIBC) | 2.16.840.1.113883.6.40 |
MedicalDeviceAnatomicalLocationCodelist
Valueset OID: 2.16.840.1.113883.2.4.3.11.60.40.2.10.1.2 | Binding: |
Conceptname | Codesystem name | Codesystem OID |
SNOMED CT: < 442083009|Anatomical or acquired body structure| | SNOMED CT | 2.16.840.1.113883.6.96 |
MedicalDeviceLateralityCodelist
Valueset OID: 2.16.840.1.113883.2.4.3.11.60.40.2.10.1.4 | Binding: |
Conceptname | Conceptcode | Codesystem name | Codesystem OID | Description |
Left | 7771000 | SNOMED CT | 2.16.840.1.113883.6.96 | Links |
Right | 24028007 | SNOMED CT | 2.16.840.1.113883.6.96 | Rechts |
Right and left | 51440002 | SNOMED CT | 2.16.840.1.113883.6.96 | Rechts en links |
ProductIDCodelist
Valueset OID: 2.16.840.1.113883.2.4.3.11.60.40.2.10.1.3 | Binding: |
Conceptname | Codesystem name | Codesystem OID |
Alle waarden | Global Trade Item Number (GTIN) | 1.3.160 |
ProductTypeCodelist
Valueset OID: 2.16.840.1.113883.2.4.3.11.60.40.2.10.1.1 | Binding: |
Conceptname | Codesystem name | Codesystem OID |
Alle waarden | SNOMED CT | 2.16.840.1.113883.6.96 |
This information model in other releases
- Release 2015, (Version 1.2)
- Release 2016, (Version 3.0)
- Prerelease 2018-2, (Version 3.2)
- Prerelease 2019-2, (Version 3.3)
- Release 2020, (Version 3.3.1)
- Prerelease 2021-2, (Version 3.4)
- Prerelease 2022-1, (Version 3.5)
- Prerelease 2023-1, (Version 4.0)
- Prerelease 2024-1, (Version 4.0)
Information model references
This information model refers to
This information model is used in
- AbilityToPerformMouthcareActivities-v3.1
- BladderFunction-v3.1
- BowelFunction-v3.1
- FeedingTubeSystem-v3.2
- FunctionalOrMentalStatus-v3.1
- HearingFunction-v3.1
- Infusion-v3.2
- Mobility-v3.1
- NursingIntervention-v3.1
- PlannedCareActivityForTransfer-v3.1
- Procedure-v4.1
- Respiration-v3.1
- Stoma-v3.2
- VisualFunction-v3.1
- Wound-v3.1
Technical specifications in HL7v3 CDA and HL7 FHIR
To exchange information based on health and care information models, additional, more technical specifications are required.
Not every environment can handle the same technical specifications. For this reason, there are several types of technical specifications:
- HL7® version 3 CDA compatible specifications, available through the Nictiz ART-DECOR® environment
- HL7® FHIR® compatible specifications, available through the Nictiz environment on the Simplifier FHIR
Downloads
This information model is also available as pdf file or as spreadsheet
About this information
The information in this wikipage is based on Release 2017
Conditions for use are located on the mainpage
This page is generated on 19/12/2018 18:32:54 with ZibExtraction v. 3.0.6927.32850