Literature DB >> 20423577

Family history in primary care: understanding GPs' resistance to clinical genetics--qualitative study.

Jonathan Mathers1, Sheila Greenfield, Alison Metcalfe, Trevor Cole, Sarah Flanagan, Sue Wilson.   

Abstract

BACKGROUND: National and local evaluations of clinical genetics service pilots have experienced difficulty in engaging with GPs. AIM: To understand GPs' reluctance to engage with clinical genetics service developments, via an examination of the role of family history in general practice. DESIGN OF STUDY: Qualitative study using semi-structured one-to-one interviews.
SETTING: The West Midlands, UK.
METHOD: Interviews with 21 GPs working in 15 practices, based on a stratified random sample from the Midlands Research Practices Consortium database. Thematic analysis proceeded alongside data generation. Framework grids were constructed for comparative analytical questioning. Interpretation was framed by two explanatory models: a knowledge deficit model, and practice and professional identity model.
RESULTS: There is a clear distinction between the routine use and function of family history in GPs' clinical decision making, and contrasting conceptualisations of genetics and 'genetic conditions'. Although genetics is clearly a part of current GP practice, with acknowledgement of genetic components to multifactorial disease, this is distinguished from 'genetic conditions' which are seen as rare, complex single-gene disorders. Importantly, family history takes its place within a broader notion of the 'family doctor' that interviewees identified as a key aspect of their role. In contrast, clinical genetics was not identified as a core component of generalist practice.
CONCLUSION: The likely effectiveness of educational policy interventions aimed at GPs that focus solely on knowledge deficit models, is questionable. There is a need to acknowledge how appropriate practice is constructed by GPs, within the context of accepted generalist roles and related identities.

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Year:  2010        PMID: 20423577      PMCID: PMC2858554          DOI: 10.3399/bjgp10X501868

Source DB:  PubMed          Journal:  Br J Gen Pract        ISSN: 0960-1643            Impact factor:   5.386


  23 in total

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Authors:  J Emery; S Hayflick
Journal:  BMJ       Date:  2001-04-28

2.  Resisting revolution: generalism and the new genetics.

Authors:  S Kumar
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3.  General practitioners' views on genetic screening for common diseases.

Authors:  M A Suchard; P Yudkin; J S Sinsheimer; G H Fowler
Journal:  Br J Gen Pract       Date:  1999-01       Impact factor: 5.386

Review 4.  Reconsidering the family history in primary care.

Authors:  Eugene C Rich; Wylie Burke; Caryl J Heaton; Susanne Haga; Linda Pinsky; M Priscilla Short; Louise Acheson
Journal:  J Gen Intern Med       Date:  2004-03       Impact factor: 5.128

5.  Reactions of GPs to a triage-controlled referral system for cancer genetics.

Authors:  Glyn Elwyn; Rachel Iredale; Jonathon Gray
Journal:  Fam Pract       Date:  2002-02       Impact factor: 2.267

Review 6.  The new genetics. Implications for clinical services in Britain and the United States.

Authors:  A L Kinmonth; J Reinhard; M Bobrow; S Pauker
Journal:  BMJ       Date:  1998-03-07

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Authors:  P Fugelli; I Heath
Journal:  BMJ       Date:  1996-02-24

8.  The family history in family practice: a questionnaire study.

Authors:  N Summerton; P V Garrood
Journal:  Fam Pract       Date:  1997-08       Impact factor: 2.267

9.  Experiences and expectations of the new genetics in relation to familial risk of breast cancer: a comparison of the views of GPs and practice nurses.

Authors:  F M Walter; A L Kinmonth; F Hyland; P Murrell; T M Marteau; C Todd
Journal:  Fam Pract       Date:  2001-10       Impact factor: 2.267

10.  Integrating genetics as practices of primary care.

Authors:  Rosemary Robins; Sylvia Metcalfe
Journal:  Soc Sci Med       Date:  2004-07       Impact factor: 4.634

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  18 in total

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Review 3.  A review of consanguinity in Ireland--estimation of frequency and approaches to mitigate risks.

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4.  Discussions about predictive genetic testing for Lynch syndrome: the role of health professionals and families in decisions to decline.

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6.  Introducing genetic testing with case finding for familial hypercholesterolaemia in primary care: qualitative study of patient and health professional experience.

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7.  A primary care specialist genetics service: a cluster-randomised factorial trial.

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Journal:  Br J Gen Pract       Date:  2012-03       Impact factor: 5.386

8.  Is patient-centered care the same as person-focused care?

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Journal:  Perm J       Date:  2011

Review 9.  Primary-care providers' perceived barriers to integration of genetics services: a systematic review of the literature.

Authors:  Natalie A Mikat-Stevens; Ingrid A Larson; Beth A Tarini
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10.  Development and evaluation of a brief self-completed family history screening tool for common chronic disease prevention in primary care.

Authors:  Fiona M Walter; A Toby Prevost; Linda Birt; Nicola Grehan; Kathy Restarick; Helen C Morris; Stephen Sutton; Peter Rose; Sarah Downing; Jon D Emery
Journal:  Br J Gen Pract       Date:  2013-06       Impact factor: 5.386

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