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 |
Keywords | family history, prevalence, affected, genetic |
Lifecycle | published |
UID | 28365b69-c6b7-4320-9329-c890dabd8b63 |
Language used | en |
Citeable Identifier | 1013.1.1975 |
Revision Number | 1.0.7 |
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=
, 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]], description=[], protocol=[], ism_transition=[], context=[], data=[], activities=[], relationships=[], credentials=[], target=[], source=[], state=[], content=[], contacts=[], capabilities=[]}, 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= , 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= , 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=
, 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] |