ID

23499

Descrição

Use to record information about the prevalence of an identified risk factor, problem or diagnosis in genetic and non-genetic family members. This archetype has specifically been designed to be used in the 'Detail' SLOT within the EVALUATION.health_risk archetype to support assessment of risk in the subject of care for the identified 'Risk factor' and the 'Family prevalence' SLOT in the EVALUATION.family_history archetype. It can also be used in the 'Specific details' SLOT within the EVALUATION.problem_diagnosis archetype ,or other EVALUATION or CLUSTER archetypes, where clinically appropriate.

Palavras-chave

Versões (3)
  1. 08/07/17 08/07/17 - Martin Dugas
  2. 08/07/17 08/07/17 - Martin Dugas
  3. 20/09/21 20/09/21 -
Transferido a

8 luglio 2017

DOI

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Licença

Creative Commons BY-NC 3.0
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Family prevalence

Inglês

openEHR-EHR-CLUSTER.family_prevalence.v1

1 Formulários  
  1. StudyEvent: openEHR-EHR-CLUSTER.family_prevalence.v1
    1. openEHR-EHR-CLUSTER.family_prevalence.v1
openEHR-EHR-CLUSTER.family_prevalence.v1.xml
Descrição

openEHR-EHR-CLUSTER.family_prevalence.v1.xml

Family prevalence
Descrição

Summary information about the prevalence of a risk factor, problem or diagnosis in all family members.

Tipo de dados

text

Description
Descrição

Narrative description about occurrence in family members.

Tipo de dados

text

Affected family
Descrição

Details about the numbers of family members affected.

Tipo de dados

text

Relationship
Descrição

The degree of relationship between the subject of care and a selected group of family members.

Tipo de dados

text

Biological sex
Descrição

The biological sex of the family member/s.

Tipo de dados

text

Number affected
Descrição

The number of family members known to be affected.

Tipo de dados

integer

Family line
Descrição

Identification of the maternal or paternal family line in the relationship.

Tipo de dados

text

Number eligible
Descrição

The number of eligible family members.

Tipo de dados

integer

Genetic predisposition?
Descrição

Is there a genetic basis for the identified risk factor, problem or diagnosis?

Tipo de dados

boolean

Inheritance type
Descrição

Category of inheritance for the identified identified risk factor, problem or diagnosis.

Tipo de dados

text

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Similar models

openEHR-EHR-CLUSTER.family_prevalence.v1

1 Formulários
  1. StudyEvent: openEHR-EHR-CLUSTER.family_prevalence.v1
    1. openEHR-EHR-CLUSTER.family_prevalence.v1
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
Alias
Family prevalence
Item
Family prevalence
text
Description
Item
Description
text
Affected family
Item
Affected family
text
Item
Relationship
text
Relationship
Code List
Relationship
CL Item
First degree relative (1)
CL Item
Second degree relative (2)
CL Item
Third degree relative (3)
CL Item
Genetic family (4)
CL Item
Non-genetic family (5)
Item
Biological sex
text
Biological sex
Code List
Biological sex
CL Item
Male (1)
CL Item
Female (2)
CL Item
Indeterminate/Intersex/Unspecified (3)
Number affected
Item
Number affected
integer
Item
Family line
text
Family line
Code List
Family line
CL Item
Maternal line (1)
CL Item
Paternal line (2)
Number eligible
Item
Number eligible
integer
Genetic predisposition?
Item
Genetic predisposition?
boolean
Inheritance type
Item
Inheritance type
text
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