| ARCHETYPE ID | openEHR-EHR-OBSERVATION.family_history_screening_questionnaire.v1 |
|---|---|
| Concept | Family history screening questionnaire |
| Description | Series of questions and associated answers used to screen for health-related problems found in genetic and non-genetic family members. |
| Use | Use to create a framework for recording answers to pre-defined screening questions about health-related problems found in both genetic and non-genetic family members. Traditionally the scope of family history has been focused on identifying factors or biomarkers in genetically related family members. Non-genetic family members may also be included, such as adopted or long term fostered children, those related by marriage, or other unrelated individuals who participate in the regular life and influence of the family. The intended scope of this archetype is to include the broadest range of problems or issues that might be found within families. It includes problems or diagnoses that are:
This archetype has two discrete approaches for screening for family history:
Common use cases include, but are not limited to:
Templates for specific use cases may be constrained to relationships with genetic family members if required. The semantics of this archetype are intentionally loose, and querying this archetype would normally only be useful or safe within the context of each specific template. In a template, each data element would usually be renamed to the specific question asked. Where value sets have been proposed for common use cases, these can be adapted for local use by using the DV_TEXT or the DV_BOOLEAN datatypes choice to match each specific use case. Use separate EVENTs to specify whether the questions relate to a point in time or an interval of time. For example: "Do any family members have COVID now?" as a point in time EVENT and "Have any family members had COVID during the past 4 weeks?" as an interval EVENT. The source of the information in a questionnaire response may vary in different contexts but can be specifically identified using the 'Information provider' element in the Reference Model. This archetype has been designed to be used as a screening tool or to record simple questionnaire-format data for use in situations such as a disease registry. If the screening questionnaire identifies the presence of a health concern in a family member, it is recommended that the clinical system record the specific details using the EVALUATION.family_history archetype or the CLUSTER.family_prevalence archetype. |
| Misuse | Not to be used to record details about the presence or absence of a family-related problem outside of a screening context. Use EVALUATION.family_history or EVALUATION.exclusion_specific for these purposes. Not to be used to record a Family Pedigree chart of health problems/diagnoses. Use the EVALUATION.family_history archetype for this purpose. |
| Purpose | To create a framework for recording answers to pre-defined screening questions about health-related problems found in both genetic and non-genetic family members. |
| References | |
| Copyright | © openEHR Foundation |
| Authors | Nom de l'autor: Marit Alice Venheim Organització: Helse Vest IKT AS Correu electrònic: marit.alice.venheim@helse-vest-ikt-no Data d'autor original: 2020-08-20 |
| Other Details Language | Nom de l'autor: Marit Alice Venheim Organització: Helse Vest IKT AS Correu electrònic: marit.alice.venheim@helse-vest-ikt-no Data d'autor original: 2020-08-20 |
| Other Details (Language Independent) |
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| Keywords | family, history, health, condition, problem, diagnosis, family history, relative, biological, relationship, background, genetic |
| Lifecycle | published |
| UID | ef2d55ec-d1f5-45d3-a123-472d91c327bc |
| Language used | en |
| Citeable Identifier | 1380.146.481 |
| Revision Number | 1.0.0 |
| Archetype Concept Comment | The answers may be self-reported. |
| data | |
| Screening purpose | Screening purpose: The context or reason for screening. This data element is intended to provide collection context for the question/answer groups when queried at a later date. It is not expected that this data element will be exposed to the individual, but only stored in data. For example: pre-admission screening or the name of the actual questionnaire. |
| Description | Description: Narrative description about the history of any problem or diagnosis in the family. |
| Any family member | Any family member: Presence of a specific problem or diagnosis in any family member. 'Problem/Diagnosis name' has been made mandatory as it is the sole focus of the question with no further details anticipated. For example: “Does anyone in the family have diabetes?”. |
| Problem/diagnosis name | Problem/diagnosis name: Identification of a specific problem or diagnosis, or a grouping of problems or diagnoses, in the family. For example: 'Colorectal cancer' or 'Cancer'; 'Angina' or 'Cardiovascular disease'. Coding of the 'Problem/diagnosis name' with a terminology is preferred, where possible. |
| Presence? | Presence?: Is there a history of a problem or diagnosis, or grouping of problems or diagnoses in the family? In a template, the data element would usually be renamed to the specific question asked. The proposed value set can be adapted for local use by using the DV_TEXT or the DV_BOOLEAN datatypes choice to match each specific use case. In cases where an individual is adopted and no information is available, it is recommended to record 'Unknown'. For example: Does any in your family have diabetes? Elecció de:
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| Comment | Comment: Additional narrative about the specific problem or diagnosis in the family, not captured in other fields. |
| Specific relationship | Specific relationship: Details about an identified problem or diagnosis in a specific relationship or relationship degree. ‘Relationship’ is the focus of the question, and in order to answer the question both the 'Relationship' and the 'Problem/diagnosis name' need to be mandatory. For example: 'Does your father have diabetes?' or 'Have any of your first degree relations had colorectal cancer?' |
| Relationship | Relationship: The relationship of the family member to the individual. For example: First degree relative, mother, step-father, maternal grandmother, or paternal uncle. Coding of the relationship with a terminology is preferred, where possible and including specification of maternal and paternal as required. |
| Problem/diagnosis name | Problem/diagnosis name: Identification of a problem or diagnosis, or grouping of problems or diagnoses in the family. Coding of the 'Problem/diagnosis name' with a terminology is preferred, where possible. |
| Presence? | Presence?: Is there a history of a problem or diagnosis in family members? In a template, the data element would usually be renamed to the specific question asked. The proposed value set can be adapted for local use by using the DV_TEXT or the DV_BOOLEAN datatypes choice to match each specific use case. In cases where an individual is adopted and no information is available, it is recommended to record 'Unknown'. For example: Does your father have diabetes? Elecció de:
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| Timing | Timing: Indication of timing related to the problem or diagnosis. The 'Timing' data element has deliberately been loosely modelled to support the myriad of ways that it can be used in questionnaires to capture when an issue, problem or diagnosis occured. The specific and intended semantics can be further clarified in a template. For example: the actual date and/or time; the start and stop time for when the issue, problem or diagnosis occured; the interval of time during which the issue, problem or diagnosis occured; the duration of the issue, problem or diagnosis; the age of the individual at the time of the issue, problem or diagnosis; or the duration of time since it occurred. A partial date is valid, using the DV_DATE_TIME data type, to record only a year. Elecció de:
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| Additional details | Additional details: Structured details or questions about the specific problem or diagnosis. Incloure: Tots arquetips no exclosos explícitament |
| Comment | Comment: Additional narrative about the specific problem, diagnosis or family member, not captured in other fields. |
| Additional details | Additional details: Structured details or questions about screening for significant problems or diagnoses in family members. Incloure: Tots arquetips no exclosos explícitament |
| events | |
| Any event | Any event: Default, unspecified point in time or interval event which may be explicitly defined in a template or at run-time. |
| protocol | |
| Extension | Extension: Additional information required to capture local content or to align with other reference models/formalisms. For example: local information requirements or additional metadata to align with FHIR. Incloure: Tots arquetips no exclosos explícitament |
| Other contributors | Vebjørn Arntzen, Oslo University Hospital, Norway (openEHR Editor) Silje Ljosland Bakke, Helse Vest IKT AS, Norway (openEHR Editor) SB Bhattacharyya, Bhattacharyyas Clinical Records Research & Informatics LLP, India Hugo Claudio Briceño García, Catsalut, Spain Clara Calleja Vega, CatSalut. Servei Català de la Salut., Spain Christian Chevalley, ADOC, Thailand Giovanni Delussu, crs4, Italy Mona Didriksen, Helse Vest IKT, Norway Manuela Domingo, hospital general universitario dr. balmis, Spain Gunn Elin Blakkisrud, DIPS ASA, Norway Aleksander Furnes, Helse Nord IKT, Norway Ciprian Gerstenberger, HN IKT, Norway Rosane Gotardo, Systema Ltda., Brazil Heather Grain, Llewelyn Grain Informatics, Australia Atle Hansen, Universitetssykehuset Nord-Norge, Norway Evelyn Hovenga, EJSH Consulting, Australia Susanna Jönsson, Region Värmland, Sweden Mika Kiviaho, Tietoevry Care, Finland June Marie Nepstad Knappskog, Helse Nord IKT AS, Norway (openEHR Editor), Norway Martin Koch, Servei Català de la Salut, Spain Ronald Krawec, Alberta Health Services, Canada Lise Kristin Knutsen, Oslo universitetssykehus, Norway Anjali Kulkarni, Karkinos, India Kanika Kuwelker, Helse Vest IKT, Norway Jörgen Kuylenstierna, eWeave AB, Sweden Eli Larsen, UNN, Norway Liv Laugen, Oslo University Hospital, Norway, Norway (openEHR Editor) Darin Leonhardt, PLRI für medizinische Informatik/ Medizinische Hochschule, Germany Heather Leslie, Atomica Informatics, Australia (openEHR Editor) Ruth Lochan, Akademiska Sjukhuset Uppsala, Sweden Michael Lutz, BITsoft, Germany Hanne Marte Bårholm, Helse Vest IKT, Norway (openEHR Norway redaktør) Ian McNicoll, freshEHR Clinical Informatics, United Kingdom Arunakiry Natarajan, medondo, Germany Svenne Naumann, Finnmarkssykehuset, Norway Olha Nikolaieva, University Hospital Basel, Switzerland Terje Nordberg, Helse Bergen, Norway Mikael Nyström, Cambio Healthcare Systems AB, Sweden Marlene Pérez Colman, Digital Health and Care Wales, United Kingdom Benjamin Senst, Germany Andre Smitt-Ingebretsen, Sørlandet sykehus HF, Norway Norwegian Review Summary, Norwegian Public Hospitals, Norway John Tore Valand, Helse Vest IKT, Norway (openEHR Editor) Wouter Zanen, Eurotranplant, Netherlands |
| Translators |
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