ARCHETYPE Family prevalence (openEHR-EHR-CLUSTER.family_prevalence.v1)

Name: Family prevalence
License: http://creativecommons.org/licenses/by-sa/4.0/

ARCHETYPE ID	openEHR-EHR-CLUSTER.family_prevalence.v1
Concept	Family prevalence
Description	Summary information about the prevalence of a risk factor, problem or diagnosis in all family members.
Use	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.
Misuse	Not to be used to record actual health information about problems or diagnoses in individual family members - use EVALUATION.family_history for this purpose.
Purpose	To record information about the prevalence of an identified risk factor, problem or diagnosis in genetic and non-genetic family members.
References	Risk of condition based on family history, rejected archetype, openEHR Clinical Knowledge Manager [Internet]. openEHR Foundation. Authored: 2006 04 23. Available at: http://www.openehr.org/ckm/#showArchetype_1013.1.125 (last accessed 2015 03 05).
Copyright	© openEHR Foundation
Authors	Author name: Heather Leslie Organisation: Atomica Informatics Email: heather.leslie@atomicainformatics.com Date originally authored: 2015-05-05
Other Details Language	Author name: Heather Leslie Organisation: Atomica Informatics Email: heather.leslie@atomicainformatics.com Date originally authored: 2015-05-05
OtherDetails Language Independent	{licence=This work is licensed under the Creative Commons Attribution-ShareAlike 4.0 International License. To view a copy of this license, visit http://creativecommons.org/licenses/by-sa/4.0/., custodian_organisation=openEHR Foundation, references=Risk of condition based on family history, rejected archetype, openEHR Clinical Knowledge Manager [Internet]. openEHR Foundation. Authored: 2006 04 23. Available at: http://www.openehr.org/ckm/#showArchetype_1013.1.125 (last accessed 2015 03 05)., current_contact=Heather Leslie, Atomica Informatics, original_namespace=org.openehr, original_publisher=openEHR Foundation, custodian_namespace=org.openehr, MD5-CAM-1.0.1=A76B97FA164830629EA15341E9229D7C, build_uid=252b7c71-387a-41d0-93ec-87cd7ee23cc8, revision=1.0.5}
Keywords	family history, prevalence, affected, genetic
Lifecycle	published
UID	28365b69-c6b7-4320-9329-c890dabd8b63
Language used	en
Citeable Identifier	1051.32.342
Revision Number	1.0.5
All	Archetype [runtimeNameConstraintForConceptName=null, archetypeConceptBinding=null, archetypeConceptDescription=Summary information about the prevalence of a risk factor, problem or diagnosis in all family members., archetypeConceptComment=null, otherContributors=Vebjoern Arntzen, Oslo university hospital, Norway Koray Atalag, University of Auckland, New Zealand Silje Ljosland Bakke, National ICT Norway, Norway (openEHR Editor) Lars Bitsch-Larsen, Haukeland University hospital, Norway Shahla Foozonkhah, Ocean Informatics, Australia Einar Fosse, National Centre for Integrated Care and Telemedicine, Norway Heather Grain, Llewelyn Grain Informatics, Australia Sam Heard, Ocean Informatics, Australia Lars Karlsen, DIPS ASA, Norway Shinji Kobayashi, Kyoto University, Japan Heather Leslie, Atomica Informatics, Australia (openEHR Editor) Hugh Leslie, Ocean Informatics, Australia Hallvard Lærum, Oslo University Hospital, Norway Ian McNicoll, freshEHR Clinical Informatics, United Kingdom (openEHR Editor) Andrej Orel, Marand d.o.o., Slovenia Jussara Rotzsch, UNB, Brazil, originalLanguage=en, translators= German: Sarah Ballout, ballout.sarah@mh-hannover.de Portuguese (Brazil): Osmeire Chamelette Sanzovo, Hospital Sírio Libanês - SP, osmeire.acsanzovo@hsl.org.br , subjectOfData=unconstrained, archetypeTranslationTree=null, topLevelToAshis={content=[], description=[], details=[], source=[], capabilities=[], other_participations=[], protocol=[], provider=[], activities=[], state=[], events=[], ism_transition=[], data=[], target=[], identities=[], items=[ResourceSimplifiedHierarchyItem [path=/items[at0030], code=at0030, itemType=ELEMENT, level=1, text=Description, description=Narrative description about occurrence in family members., comment=null, uncommonOntologyItems=null, occurencesFormal=0..1, occurencesText=Optional, cardinalityFormal=null, cardinalityText=null, subCardinalityFormal=null, subCardinalityText=null, dataType=DV_TEXT, bindings=null, values=, extendedValues=null], ResourceSimplifiedHierarchyItem [path=/items[at0055], code=at0055, itemType=ELEMENT, level=1, text=Genetic predisposition?, description=Is there a genetic basis for the identified risk factor, problem or diagnosis?, comment=Optional to record as True if there is a recognised genetic predisposition. In many cases, this may be inferred from the risk factor, problem or diagnosis and not need to be recorded explicitly., uncommonOntologyItems=null, occurencesFormal=0..1, occurencesText=Optional, cardinalityFormal=null, cardinalityText=null, subCardinalityFormal=null, subCardinalityText=null, dataType=DV_BOOLEAN, bindings=null, values=Allowed values: {true}, extendedValues=null], ResourceSimplifiedHierarchyItem [path=/items[at0056], code=at0056, itemType=ELEMENT, level=1, text=Inheritance type, description=Category of inheritance for the identified risk factor, problem or diagnosis., comment=For example: autosomal dominant, autosomal recessive, X-linked dominant, X-linked recessive, codominant, or mitochondrial., uncommonOntologyItems=null, occurencesFormal=0..1, occurencesText=Optional, cardinalityFormal=null, cardinalityText=null, subCardinalityFormal=null, subCardinalityText=null, dataType=DV_TEXT, bindings=null, values=, extendedValues=null], ResourceSimplifiedHierarchyItem [path=/items[at0031], code=at0031, itemType=CLUSTER, level=1, text=Affected family, description=Details about the numbers of family members affected., comment=This cluster will be repeated for each relationship, family line, sex value or combination of all three. For example, the cluster will be repeated for any or all of first degree relative (without sex specified), first degree relative from maternal line; first degree male relative or first degree female relative; or all males, all females., uncommonOntologyItems=null, occurencesFormal=0.., occurencesText=Optional, repeating, cardinalityFormal=1.., cardinalityText= (Cardinality: 1.., unordered), subCardinalityFormal=null, subCardinalityText=null, dataType=CLUSTER, bindings=null, values=, extendedValues=null], ResourceSimplifiedHierarchyItem [path=/items[at0031]/items[at0032], code=at0032, itemType=ELEMENT, level=2, text=Relationship, description=The degree of relationship between the subject of care and a selected group of family members., comment=null, uncommonOntologyItems=null, occurencesFormal=0..1, occurencesText=Optional, cardinalityFormal=null, cardinalityText=null, subCardinalityFormal=null, subCardinalityText=null, dataType=DV_CODED_TEXT, bindings=null, values= at0037::First degree relative [50% genetic share with the subject - for example, parent, sibling or child.] at0038::Second degree relative [25% genetic share with the subject - for example, grandparent, aunt, uncle, niece, nephew, grandchildren and half siblings.] at0039::Third degree relative [12.5% genetic share with the subject - for example, great grandparent, great aunt, great uncle, first cousin, children of nieces and nephews, and great grandchildren.] at0042::Genetic family [All genetically-related family members.] at0050::Non-genetic family [All non-genetic family members.] , extendedValues=null], ResourceSimplifiedHierarchyItem [path=/items[at0031]/items[at0051], code=at0051, itemType=ELEMENT, level=2, text=Family line, description=Identification of the maternal or paternal family line in the relationship., comment=Only for use with genetic family members., uncommonOntologyItems=null, occurencesFormal=0..1, occurencesText=Optional, cardinalityFormal=null, cardinalityText=null, subCardinalityFormal=null, subCardinalityText=null, dataType=DV_CODED_TEXT, bindings=null, values= at0040::Maternal line [Related through the subject's mother.] at0041::Paternal line [Related through the subject's father.] , extendedValues=null], ResourceSimplifiedHierarchyItem [path=/items[at0031]/items[at0033], code=at0033, itemType=ELEMENT, level=2, text=Biological sex, description=The biological sex of the family member/s., comment=null, uncommonOntologyItems=null, occurencesFormal=0..1, occurencesText=Optional, cardinalityFormal=null, cardinalityText=null, subCardinalityFormal=null, subCardinalityText=null, dataType=DV_CODED_TEXT, bindings=null, values= at0043::Male [Family member who is biologically male.] at0044::Female [Family member who is biologically female.] at0052::Indeterminate/Intersex/Unspecified [Family member who either has the biological attributes of both sexes or lacks some of the biological attributes considered necessary to be defined as one or the other sex.] , extendedValues=null], ResourceSimplifiedHierarchyItem [path=/items[at0031]/items[at0034], code=at0034, itemType=ELEMENT, level=2, text=Number affected, description=The number of family members known to be affected., comment=This is the number of family members who are affected AND who also fit selected relationship, family line and sex criteria. Effectively this number is the numerator for calculation of an 'Affected ratio'., uncommonOntologyItems=null, occurencesFormal=0..1, occurencesText=Optional, cardinalityFormal=null, cardinalityText=null, subCardinalityFormal=null, subCardinalityText=null, dataType=DV_COUNT, bindings=null, values=min: >=0 , extendedValues=null], ResourceSimplifiedHierarchyItem [path=/items[at0031]/items[at0054], code=at0054, itemType=ELEMENT, level=2, text=Number eligible, description=The number of eligible family members., comment=This is the number of family members who potentially could be affected AND who also fit selected relationship, family line and sex criteria. Effectively this number is the denominator for calculation of an 'Affected ratio'., uncommonOntologyItems=null, occurencesFormal=0..1, occurencesText=Optional, cardinalityFormal=null, cardinalityText=null, subCardinalityFormal=null, subCardinalityText=null, dataType=DV_COUNT, bindings=null, values=min: >=0 , extendedValues=null]], relationships=[], credentials=[], context=[], contacts=[]}, topLevelItems={items=ResourceSimplifiedHierarchyItem [path=ROOT_/, code=at0000, itemType=CLUSTER, level=0, text=null, description=null, comment=null, uncommonOntologyItems=null, occurencesFormal=1..1, occurencesText=Mandatory, cardinalityFormal=1.., cardinalityText= (Cardinality: 1.., unordered), subCardinalityFormal=null, subCardinalityText=null, dataType=CLUSTER, bindings=null, values=null, extendedValues=null]}, addHierarchyItemsTo=items, currentHierarchyItemsForAdding=[ResourceSimplifiedHierarchyItem [path=/items[at0030], code=at0030, itemType=ELEMENT, level=1, text=Description, description=Narrative description about occurrence in family members., comment=null, uncommonOntologyItems=null, occurencesFormal=0..1, occurencesText=Optional, cardinalityFormal=null, cardinalityText=null, subCardinalityFormal=null, subCardinalityText=null, dataType=DV_TEXT, bindings=null, values=, extendedValues=null], ResourceSimplifiedHierarchyItem [path=/items[at0055], code=at0055, itemType=ELEMENT, level=1, text=Genetic predisposition?, description=Is there a genetic basis for the identified risk factor, problem or diagnosis?, comment=Optional to record as True if there is a recognised genetic predisposition. In many cases, this may be inferred from the risk factor, problem or diagnosis and not need to be recorded explicitly., uncommonOntologyItems=null, occurencesFormal=0..1, occurencesText=Optional, cardinalityFormal=null, cardinalityText=null, subCardinalityFormal=null, subCardinalityText=null, dataType=DV_BOOLEAN, bindings=null, values=Allowed values: {true}, extendedValues=null], ResourceSimplifiedHierarchyItem [path=/items[at0056], code=at0056, itemType=ELEMENT, level=1, text=Inheritance type, description=Category of inheritance for the identified risk factor, problem or diagnosis., comment=For example: autosomal dominant, autosomal recessive, X-linked dominant, X-linked recessive, codominant, or mitochondrial., uncommonOntologyItems=null, occurencesFormal=0..1, occurencesText=Optional, cardinalityFormal=null, cardinalityText=null, subCardinalityFormal=null, subCardinalityText=null, dataType=DV_TEXT, bindings=null, values=, extendedValues=null], ResourceSimplifiedHierarchyItem [path=/items[at0031], code=at0031, itemType=CLUSTER, level=1, text=Affected family, description=Details about the numbers of family members affected., comment=This cluster will be repeated for each relationship, family line, sex value or combination of all three. For example, the cluster will be repeated for any or all of first degree relative (without sex specified), first degree relative from maternal line; first degree male relative or first degree female relative; or all males, all females., uncommonOntologyItems=null, occurencesFormal=0.., occurencesText=Optional, repeating, cardinalityFormal=1.., cardinalityText= (Cardinality: 1.., unordered), subCardinalityFormal=null, subCardinalityText=null, dataType=CLUSTER, bindings=null, values=, extendedValues=null], ResourceSimplifiedHierarchyItem [path=/items[at0031]/items[at0032], code=at0032, itemType=ELEMENT, level=2, text=Relationship, description=The degree of relationship between the subject of care and a selected group of family members., comment=null, uncommonOntologyItems=null, occurencesFormal=0..1, occurencesText=Optional, cardinalityFormal=null, cardinalityText=null, subCardinalityFormal=null, subCardinalityText=null, dataType=DV_CODED_TEXT, bindings=null, values= at0037::First degree relative [50% genetic share with the subject - for example, parent, sibling or child.] at0038::Second degree relative [25% genetic share with the subject - for example, grandparent, aunt, uncle, niece, nephew, grandchildren and half siblings.] at0039::Third degree relative [12.5% genetic share with the subject - for example, great grandparent, great aunt, great uncle, first cousin, children of nieces and nephews, and great grandchildren.] at0042::Genetic family [All genetically-related family members.] at0050::Non-genetic family [All non-genetic family members.] , extendedValues=null], ResourceSimplifiedHierarchyItem [path=/items[at0031]/items[at0051], code=at0051, itemType=ELEMENT, level=2, text=Family line, description=Identification of the maternal or paternal family line in the relationship., comment=Only for use with genetic family members., uncommonOntologyItems=null, occurencesFormal=0..1, occurencesText=Optional, cardinalityFormal=null, cardinalityText=null, subCardinalityFormal=null, subCardinalityText=null, dataType=DV_CODED_TEXT, bindings=null, values= at0040::Maternal line [Related through the subject's mother.] at0041::Paternal line [Related through the subject's father.] , extendedValues=null], ResourceSimplifiedHierarchyItem [path=/items[at0031]/items[at0033], code=at0033, itemType=ELEMENT, level=2, text=Biological sex, description=The biological sex of the family member/s., comment=null, uncommonOntologyItems=null, occurencesFormal=0..1, occurencesText=Optional, cardinalityFormal=null, cardinalityText=null, subCardinalityFormal=null, subCardinalityText=null, dataType=DV_CODED_TEXT, bindings=null, values= at0043::Male [Family member who is biologically male.] at0044::Female [Family member who is biologically female.] at0052::Indeterminate/Intersex/Unspecified [Family member who either has the biological attributes of both sexes or lacks some of the biological attributes considered necessary to be defined as one or the other sex.] , extendedValues=null], ResourceSimplifiedHierarchyItem [path=/items[at0031]/items[at0034], code=at0034, itemType=ELEMENT, level=2, text=Number affected, description=The number of family members known to be affected., comment=This is the number of family members who are affected AND who also fit selected relationship, family line and sex criteria. Effectively this number is the numerator for calculation of an 'Affected ratio'., uncommonOntologyItems=null, occurencesFormal=0..1, occurencesText=Optional, cardinalityFormal=null, cardinalityText=null, subCardinalityFormal=null, subCardinalityText=null, dataType=DV_COUNT, bindings=null, values=min: >=0 , extendedValues=null], ResourceSimplifiedHierarchyItem [path=/items[at0031]/items[at0054], code=at0054, itemType=ELEMENT, level=2, text=Number eligible, description=The number of eligible family members., comment=This is the number of family members who potentially could be affected AND who also fit selected relationship, family line and sex criteria. Effectively this number is the denominator for calculation of an 'Affected ratio'., uncommonOntologyItems=null, occurencesFormal=0..1, occurencesText=Optional, cardinalityFormal=null, cardinalityText=null, subCardinalityFormal=null, subCardinalityText=null, dataType=DV_COUNT, bindings=null, values=min: >=0 , extendedValues=null]], minIndents={}, termBindingRetrievalErrorMessage=null]