ARCHETYPE Risk of condition based on family history (openEHR-EHR-EVALUATION.risk-family_history.v1)

ARCHETYPE IDopenEHR-EHR-EVALUATION.risk-family_history.v1
ConceptRisk of condition based on family history
DescriptionEvaluation to indicate that there is, or is not, a significant risk of this subject of care having, now or in the future, a condition due to prior occurrence in a family member.
UseFor recording information about the prevalence of the condition in relatives and quantifying risk to the subject of care.
MisuseNot for recording problems of individual relatives - use 'openEHR-EHR-EVALUATION.problem' and 'openEHR-EHR-EVALUATION.problem-diagnosis' and set the subject of data to the relative.
PurposeRecord the assessed risk of having or developing a condition due to prevalence in relatives.
References
Copyright© openEHR Foundation
AuthorsAuthor name: Sam Heard
Organisation: Ocean Informatics
Email: sam.heard@oceaninformatics.com
Date originally authored: 23/04/2006
Other Details LanguageAuthor name: Sam Heard
Organisation: Ocean Informatics
Email: sam.heard@oceaninformatics.com
Date originally authored: 23/04/2006
Other Details (Language Independent)
  • MD5-CAM-1.0.1: FD88DDB4CA8FED5B68B6F3F245C3B868
Keywords
LifecycleAuthorDraft
Language useden
Citeable Identifier1013.1.125
protocol
Risk calculationRisk calculation: The means of calculating the risk
data
Index conditionIndex condition: The condition on which the risk assessment is focussed
Genetic lociGenetic loci: *
Include:
All not explicitly excluded archetypes
PresencePresence: Presence of condition in at least one related party
Assessed riskAssessed risk: The degree of risk conferred on the subject by the presence of this condition amongst relatives
  • Not significant [The person is not assessed at being at higher risk than the general population]
  • Minimal significance [The person may be of somewhat greater risk of developing the condition ]
  • Significant [The person is considered to be more likely to develop the condition than the general population]
  • Highly significant [The person is considered to be likely to develop the condition]
Detailed risk resultsDetailed risk results: *
Analysis resultAnalysis result: *
ProbabilityProbability: *
Percentage riskPercentage risk: *
Relative riskRelative risk: *
Family historyFamily history: Relevant history in genetic relatives.
Genetic relativeGenetic relative: Relevant family genetic history.
Include:
openEHR-EHR-CLUSTER.genetic_relative.v1 and specialisations
Affected ratioAffected ratio: A ratio of the affected to non-affected relatives of a particular type
DegreeDegree: The proximity or line of the relatives
  • First degree relatives [Relatives with 50% genetic share - parent, sibling, child]
  • Second degree relatives [Relatives with 25% genetic share - grand parent, aunts and uncles, nieces and nephews, grand children]
  • Third degree relatives [Relatives with 12.5% genetic share, great grand parents, great aunts and uncles, first cousins, children of neices and nephews, great grand children]
  • Maternal relatives [Related through mother]
  • Paternal relatives [Related through father]
  • Family [Entire family]
GenderGender: The gender of the relatives included in the affected ratio
  • Male [Male gender]
  • Female [Female gender]
  • Male and female [Male and female relatives]
Number unaffectedNumber unaffected: The number of relatives in this group unaffected by the index condition
min: >=0; max: <=100

Number affectedNumber affected: The number affected by the index condition
min: >=0; max: <=100

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