Gebz:FHIR bc-DisorderOfChild
bc-DisorderOfChild
This is a generic profile for child conditions.
Each bc-DisorderOfChild must have:
- a code, specifying the condition
- a subject, the child patient
Profile
The entire profile can be found at: bc-DisorderOfChild
Pattern
This is a pattern for child Conditions in Birthcare. Note that the meta.profile element should preferably include bc-DisorderOfChild. Again, this may be the case for BGZ.
All FHIR instances which follow this pattern will be valid Child disorder. Other fields from the FHIR profile may be present: this description is a minimal representation.
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XML fragment
This is a recipe for postpartum disorders in Birthcare. Note that the meta.profile element should preferably be bc-DisorderOfChild.
<Condition xmlns="http://hl7.org/fhir">
<id value="[[a unique id]]"/>
<meta>
<profile value="http://nictiz.nl/fhir/StructureDefinition/bc-DisorderOfChild"/>
</meta>
[[# clinicalStatus is optional, only when known ]]
<clinicalStatus value="[[active | recurrence | inactive | remission | resolved]]"/>
[[/ clinicalStatus ]]
[[# category is optional ]]
<category>
<coding>
<system value="[[system | 2.16.840.1.113883.2.4.4.13]]" />
<code value="[[code | ProblematiekKind]]" />
<display value="[[display | Problematiek kind]]" />
</coding>
</category>
[[/ category ]]
<code>
<coding>
<system value="[[system, preferably from | http://snomed.info/sct]]"/>
<code value="[[code, to be taken from the relevant valuesets in ART-DECOR | 56110009"/>
<display value="[[display | Birth trauma of fetus (disorder)]]"/>
</coding>
</code>
<subject>
<reference value="[[reference to the Child Patient | Patient/XXX-KIND1VDWOUDEN" />
<display value="[[display of reference | Kind 1 van der Wouden]]" />
</subject>
<context>
<reference value="[[reference to the EpisodeOfCare | EpisodeOfCare/wouden-dossier-zwanger1]]"/>
</context>
</Condition>
Valuation table
PWD 2.3 to FHIR | ||||||||||||
Type | # | Concept | System | Code | Display | FHIR element | ValueSet | |||||
80997 | Congenitale afwijkingen? | http://snomed.info/sct | 276654001 443341004 | Congenital malformation (disorder) Congenital anomaly (disorder) | code | |||||||
80998 | Congenitale afwijkingen (groep) | http://snomed.info/sct | 276654001 443341004 | Congenital malformation (disorder) Congenital anomaly (disorder) | code | |||||||
81002 | Chromosomale afwijkingen? | http://snomed.info/sct | 74345006 | Congenital disorder due to abnormality of chromosome number OR structure (disorder) | code | |||||||
40080 | Congenitale afwijkingen? | http://snomed.info/sct | 276654001 443341004 | Congenital malformation (disorder) Congenital anomaly (disorder) | ||||||||
40081 | Congenitale afwijkingen (groep) | http://snomed.info/sct | 276654001 443341004 | Congenital malformation (disorder) Congenital anomaly (disorder) | ||||||||
40082 | Specificatie congenitale afwijking (groep) | http://snomed.info/sct | 276654001 443341004 | Congenital malformation (disorder) Congenital anomaly (disorder) | code | |||||||
40090 | Specificatie congenitale afwijking | code | Congenitale afwijking | |||||||||
40110 | Chromosomale afwijkingen? | http://snomed.info/sct | 74345006 | Congenital disorder due to abnormality of chromosome number OR structure (disorder) | code | |||||||
40111 | Specificatie chromosomale afwijking (groep) | http://snomed.info/sct | 74345006 | Congenital disorder due to abnormality of chromosome number OR structure (disorder) | code | |||||||
40120 | Specificatie chromosomale afwijking | code | ChromosomaleAfwijkingen | |||||||||
82334 | Problematiek kind? | urn:oid:2.16.840.1.113883.2.4.4.13 | ProblematiekKind | Problematiek kind | code | |||||||
80789 | Problematiek kind | code | Problematiek kind |