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FHIR IG Statistics: StructureDefinition/be-patientwill

Packageehealthplatform.be.r4.federalprofiles
TypeStructureDefinition
Idbe-patientwill
FHIR VersionR4
Sourcehttps://www.ehealth.fgov.be/standards/fhir/https://simplifier.net/resolve?scope=ehealthplatform.be.r4.federalprofiles@1.3.3-beta&canonical=https://www.ehealth.fgov.be/standards/fhir/StructureDefinition/be-patientwill
URLhttps://www.ehealth.fgov.be/standards/fhir/StructureDefinition/be-patientwill
Version1.0.0
Statusactive
Date2021-01-10T10:59:49+00:00
NameBePatientWill
TitleBePatientWill
Authorityhl7
DescriptionBelgian federal profile for a patient will ONLY in the context of the patient will in the context of limitations to treatment, DNR etc. Initially based on the functional description of the NIHDI. This profile will in the future be also used to record agreement to participate in clinical trials etc. Any usecase around informed consent is out of scope for this profile.
TypeConsent
Kindresource

Resources that use this resource

No resources found


Resources that this resource uses

StructureDefinition
be-organizationBeOrganization
be-patientBePatient
be-practitionerBePractitioner
be-practitionerroleBePractitionerRole
ValueSet
be-vs-patientwill-categoryPatient Will Category
be-vs-patientwill-codePatient Will code Value Set

Narrative

Note: links and images are rebased to the (stated) source

NameFlagsCard.TypeDescription & Constraintsdoco
..Consent0..*ConsentA healthcare consumer's choices to permit or deny recipients or roles to perform actions for specific purposes and periods of time
...identifierS0..*IdentifierIdentifier for this record (external references)
...statusS1..1codedraft | proposed | active | rejected | inactive | entered-in-error
...scopeS1..1CodeableConceptWhich of the four areas this resource covers (extensible)
...categoryS1..*CodeableConceptThe category or the patient will directive
Binding: Patient Will Category (required)
...patientS1..1Reference(BePatient)The subject of the patient will.
...dateTimeS1..1dateTimeThe dateTime when the patient will has been recorded
...performerS1..*Reference(https://www.ehealth.fgov.be/standards/fhir/StructureDefinition/be-organization | BePatient | BePractitioner | BePractitionerRole | RelatedPerson)Who is agreeing to the policy and rules
...source[x]S0..1Attachment, Reference(Consent | DocumentReference | Contract | QuestionnaireResponse)The evidence used to support the patient will.
...policyRuleS1..1CodeableConceptRegulation that this consents to
....textS0..1stringPlain text representation of the concept
Fixed Value: Belgian policy
...provisionS1..1BackboneElementConstraints to the base Consent.policyRule
....typeS0..1codedeny | permit
....periodS1..1PeriodTimeframe for this rule
....securityLabel0..0
....purpose0..0
....class0..0
....codeS0..*CodeableConceptThe actual directive in the will
Binding: Patient Will directives Value Set (required)
....data0..0

doco Documentation for this format

Source

{
  "resourceType": "StructureDefinition",
  "id": "be-patientwill",
  "text": {
    "status": "extensions",
    "div": "<!-- snip (see above) -->"
  },
  "url": "https://www.ehealth.fgov.be/standards/fhir/StructureDefinition/be-patientwill",
  "version": "1.0.0",
  "name": "BePatientWill",
  "title": "BePatientWill",
  "status": "active",
  "date": "2021-01-10T10:59:49+00:00",
  "publisher": "eHealth Platform",
  "contact": [
    {
      "name": "eHealth Platform",
      "telecom": [
        {
          "system": "url",
          "value": "https://www.ehealth.fgov.be"
        }
      ]
    },
    {
      "name": "Message structure",
      "telecom": [
        {
          "system": "email",
          "value": "message-structure@ehealth.fgov.be"
        }
      ]
    }
  ],
  "description": "Belgian federal profile for a patient will ONLY in the context of the patient will in the context of limitations to treatment, DNR etc. Initially based on the functional description of the NIHDI. This profile will in the future be also used to record agreement to participate in clinical trials etc. Any usecase around informed consent is out of scope for this profile.",
  "jurisdiction": [
    {
      "coding": [
        {
          "system": "http://unstats.un.org/unsd/methods/m49/m49.htm",
          "code": "056"
        },
        {
          "system": "urn:iso:std:iso:3166",
          "code": "BE"
        }
      ]
    }
  ],
  "fhirVersion": "4.0.1",
  "mapping": [
    {
      "identity": "workflow",
      "uri": "http://hl7.org/fhir/workflow",
      "name": "Workflow Pattern"
    },
    {
      "identity": "v2",
      "uri": "http://hl7.org/v2",
      "name": "HL7 v2 Mapping"
    },
    {
      "identity": "rim",
      "uri": "http://hl7.org/v3",
      "name": "RIM Mapping"
    },
    {
      "identity": "w5",
      "uri": "http://hl7.org/fhir/fivews",
      "name": "FiveWs Pattern Mapping"
    }
  ],
  "kind": "resource",
  "abstract": false,
  "type": "Consent",
  "baseDefinition": "http://hl7.org/fhir/StructureDefinition/Consent",
  "derivation": "constraint",
  "differential": {
    "element": [
      {
        "id": "Consent.identifier",
        "path": "Consent.identifier",
        "mustSupport": true
      },
      {
        "id": "Consent.status",
        "path": "Consent.status",
        "mustSupport": true
      },
      {
        "id": "Consent.scope",
        "path": "Consent.scope",
        "mustSupport": true
      },
      {
        "id": "Consent.category",
        "path": "Consent.category",
        "mustSupport": true,
        "binding": {
          "strength": "required",
          "valueSet": "https://www.ehealth.fgov.be/standards/fhir/ValueSet/be-vs-patientwill-category"
        }
      },
      {
        "id": "Consent.patient",
        "path": "Consent.patient",
        "short": "The subject of the patient will.",
        "definition": "The subject of the patient will.",
        "min": 1,
        "type": [
          {
            "code": "Reference",
            "targetProfile": [
              "https://www.ehealth.fgov.be/standards/fhir/StructureDefinition/be-patient"
            ]
          }
        ],
        "mustSupport": true
      },
      {
        "id": "Consent.dateTime",
        "path": "Consent.dateTime",
        "short": "The dateTime when the patient will has been recorded",
        "definition": "The date and/or time when the patient will has been recorded",
        "comment": "This is not the time the patient expressed their will, but the time that this patient was recorded.&#xD;&#xA;",
        "min": 1,
        "mustSupport": true
      },
      {
        "id": "Consent.performer",
        "path": "Consent.performer",
        "comment": "Commonly, the patient will is expressed by the patient, but for some cases it may be some other person.&#xD;&#xA;",
        "min": 1,
        "type": [
          {
            "code": "Reference",
            "targetProfile": [
              "https://www.ehealth.fgov.be/standards/fhir/StructureDefinition/be-organization",
              "https://www.ehealth.fgov.be/standards/fhir/StructureDefinition/be-patient",
              "https://www.ehealth.fgov.be/standards/fhir/StructureDefinition/be-practitioner",
              "https://www.ehealth.fgov.be/standards/fhir/StructureDefinition/be-practitionerrole",
              "http://hl7.org/fhir/StructureDefinition/RelatedPerson"
            ]
          }
        ],
        "mustSupport": true
      },
      {
        "id": "Consent.source[x]",
        "path": "Consent.source[x]",
        "short": "The evidence used to support the patient will.",
        "definition": "Supporting evidence for the patient will (e.g. a paper signed by the patient to refuse a specific treatment)",
        "comment": "The source can be contained inline (Attachment), referenced directly (Consent), referenced in a consent repository (DocumentReference), or simply by an identifier (Identifier), e.g. a CDA document id.&#xD;&#xA;It is at the discretion of the practitioner whether to include this when available. A consumer SHALL NOT ignore it when available.",
        "mustSupport": true
      },
      {
        "id": "Consent.policyRule",
        "path": "Consent.policyRule",
        "min": 1,
        "mustSupport": true
      },
      {
        "id": "Consent.policyRule.text",
        "path": "Consent.policyRule.text",
        "comment": "This field is added as a fixed value because in FHIR 4.0.1 this is technically required. It has no functional purpose in Belgium.",
        "fixedString": "Belgian policy",
        "mustSupport": true
      },
      {
        "id": "Consent.provision",
        "path": "Consent.provision",
        "min": 1,
        "mustSupport": true
      },
      {
        "id": "Consent.provision.type",
        "path": "Consent.provision.type",
        "mustSupport": true
      },
      {
        "id": "Consent.provision.period",
        "path": "Consent.provision.period",
        "min": 1,
        "mustSupport": true
      },
      {
        "id": "Consent.provision.securityLabel",
        "path": "Consent.provision.securityLabel",
        "max": "0"
      },
      {
        "id": "Consent.provision.purpose",
        "path": "Consent.provision.purpose",
        "max": "0"
      },
      {
        "id": "Consent.provision.class",
        "path": "Consent.provision.class",
        "max": "0"
      },
      {
        "id": "Consent.provision.code",
        "path": "Consent.provision.code",
        "short": "The actual directive in the will",
        "definition": "The detailed patient will directive (e.g. no hospitalization, bloodtransfusion refusal) (Valueset will be delivered by a working group of NIHDI)",
        "mustSupport": true,
        "binding": {
          "strength": "required",
          "valueSet": "https://www.ehealth.fgov.be/standards/fhir/ValueSet/be-vs-patientwill-code"
        }
      },
      {
        "id": "Consent.provision.data",
        "path": "Consent.provision.data",
        "max": "0"
      }
    ]
  }
}