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How is family health history discussed in routine primary healthcare? A qualitative study of archived family doctor consultations
OBJECTIVES: Family health history underpins genetic medicine. Our study aimed to explore language and patterns of communication relating to family health history observed in interactions between general practitioners (GPs) and their patients within routine primary care consultations. DESIGN: Seconda...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BMJ Publishing Group
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8493894/ https://www.ncbi.nlm.nih.gov/pubmed/34610935 http://dx.doi.org/10.1136/bmjopen-2021-049058 |
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author | Filoche, Sara Stubbe, Maria H Grainger, Rebecca Robson, Bridget Paringatai, Karyn Wilcox, Phil Jefferies, Regina Dowell, Anthony |
author_facet | Filoche, Sara Stubbe, Maria H Grainger, Rebecca Robson, Bridget Paringatai, Karyn Wilcox, Phil Jefferies, Regina Dowell, Anthony |
author_sort | Filoche, Sara |
collection | PubMed |
description | OBJECTIVES: Family health history underpins genetic medicine. Our study aimed to explore language and patterns of communication relating to family health history observed in interactions between general practitioners (GPs) and their patients within routine primary care consultations. DESIGN: Secondary analysis of patient and GP routine consultation data (n=252). PARTICIPANTS: Consultations that included ‘family health history’ were eligible for inclusion (n=58). PRIMARY OUTCOMES: A qualitative inductive analysis of the interactions from consultation transcripts. RESULTS: 46/58 conversations about family health history were initiated by the GP. Most discussions around family history lasted for between approximately 1 to 2 min. Patients were invited to share family health history through one of two ways: non-specific enquiry (eg, by asking the patient about ‘anything that runs in the family’); or specific enquiry where they were asked if they had a ‘strong family history’ in relation to a particular condition, for example, breast cancer. Patients often responded to either approach with a simple no, but fuller negative responses also occurred regularly and typically included an account of some kind (eg, explaining family relationships/dynamics which impeded or prevented the accessibility of information). CONCLUSIONS: Family health history is regarded as a genetic test and is embedded in the sociocultural norms of the patient from whom information is being sought. Our findings highlight that it is more complex than asking simply if ‘anything’ runs in the family. As the collection of family health history is expected to be more routine, it will be important to also consider it from sociocultural perspectives in order to help mitigate any inequities in how family history is collected, and therefore used (or not) in a person’s healthcare. Orientating an enquiry away from ‘anything’ and asking more specific details about particular conditions may help facilitate the dialogue. |
format | Online Article Text |
id | pubmed-8493894 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BMJ Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-84938942021-10-14 How is family health history discussed in routine primary healthcare? A qualitative study of archived family doctor consultations Filoche, Sara Stubbe, Maria H Grainger, Rebecca Robson, Bridget Paringatai, Karyn Wilcox, Phil Jefferies, Regina Dowell, Anthony BMJ Open Genetics and Genomics OBJECTIVES: Family health history underpins genetic medicine. Our study aimed to explore language and patterns of communication relating to family health history observed in interactions between general practitioners (GPs) and their patients within routine primary care consultations. DESIGN: Secondary analysis of patient and GP routine consultation data (n=252). PARTICIPANTS: Consultations that included ‘family health history’ were eligible for inclusion (n=58). PRIMARY OUTCOMES: A qualitative inductive analysis of the interactions from consultation transcripts. RESULTS: 46/58 conversations about family health history were initiated by the GP. Most discussions around family history lasted for between approximately 1 to 2 min. Patients were invited to share family health history through one of two ways: non-specific enquiry (eg, by asking the patient about ‘anything that runs in the family’); or specific enquiry where they were asked if they had a ‘strong family history’ in relation to a particular condition, for example, breast cancer. Patients often responded to either approach with a simple no, but fuller negative responses also occurred regularly and typically included an account of some kind (eg, explaining family relationships/dynamics which impeded or prevented the accessibility of information). CONCLUSIONS: Family health history is regarded as a genetic test and is embedded in the sociocultural norms of the patient from whom information is being sought. Our findings highlight that it is more complex than asking simply if ‘anything’ runs in the family. As the collection of family health history is expected to be more routine, it will be important to also consider it from sociocultural perspectives in order to help mitigate any inequities in how family history is collected, and therefore used (or not) in a person’s healthcare. Orientating an enquiry away from ‘anything’ and asking more specific details about particular conditions may help facilitate the dialogue. BMJ Publishing Group 2021-10-05 /pmc/articles/PMC8493894/ /pubmed/34610935 http://dx.doi.org/10.1136/bmjopen-2021-049058 Text en © Author(s) (or their employer(s)) 2021. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) . |
spellingShingle | Genetics and Genomics Filoche, Sara Stubbe, Maria H Grainger, Rebecca Robson, Bridget Paringatai, Karyn Wilcox, Phil Jefferies, Regina Dowell, Anthony How is family health history discussed in routine primary healthcare? A qualitative study of archived family doctor consultations |
title | How is family health history discussed in routine primary healthcare? A qualitative study of archived family doctor consultations |
title_full | How is family health history discussed in routine primary healthcare? A qualitative study of archived family doctor consultations |
title_fullStr | How is family health history discussed in routine primary healthcare? A qualitative study of archived family doctor consultations |
title_full_unstemmed | How is family health history discussed in routine primary healthcare? A qualitative study of archived family doctor consultations |
title_short | How is family health history discussed in routine primary healthcare? A qualitative study of archived family doctor consultations |
title_sort | how is family health history discussed in routine primary healthcare? a qualitative study of archived family doctor consultations |
topic | Genetics and Genomics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8493894/ https://www.ncbi.nlm.nih.gov/pubmed/34610935 http://dx.doi.org/10.1136/bmjopen-2021-049058 |
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