Literature DB >> 12477612

Women's views of consultations about familial risk of breast cancer in primary care.

Gunn E Grande1, Fawzia Hyland, Fiona M Walter, Ann Louise Kinmonth.   

Abstract

Developments within genetic testing may increase demands on general practitioners to advise about family history of breast cancer (FHBC). This descriptive, qualitative study, investigated women's views of GP consultations about FHBC and their context. Participants were women from the general population who had experienced a primary care consultation in which FHBC was mentioned, as reported by the practitioner. Information about women's views of consultation context was obtained from 72 telephone interviews. More in-depth information about context and women's evaluations of FHBC consultations were obtained from a sub-sample of 20 face to face interviews. FHBC was rarely the main focus of consultations. It featured as a part of an overall discussion of breast symptoms, treatment and cancer risk. Women's understanding of heredity and disease was often idiosyncratic and might differ from biomedical models. A main task for clinicians appeared to be appropriate reassurance. Failure to reassure was linked to a failure to provide explanations at the woman's level of understanding. Clinicians cannot assume that patients share their perceptions of the mechanisms of disease and heredity. Instead they need to ascertain the patient's understanding and provide explanations accordingly. GPs need to have, or access, enough knowledge to inform and reassure.

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Year:  2002        PMID: 12477612     DOI: 10.1016/s0738-3991(02)00035-6

Source DB:  PubMed          Journal:  Patient Educ Couns        ISSN: 0738-3991


  7 in total

Review 1.  Lay understanding of familial risk of common chronic diseases: a systematic review and synthesis of qualitative research.

Authors:  Fiona M Walter; Jon Emery; Dejana Braithwaite; Theresa M Marteau
Journal:  Ann Fam Med       Date:  2004 Nov-Dec       Impact factor: 5.166

2.  A primary care audit of familial risk in patients with a personal history of breast cancer.

Authors:  Paul Nathan; Aneeta Ahluwalia; Wendy Chorley
Journal:  Fam Cancer       Date:  2014-12       Impact factor: 2.375

3.  Missed opportunities: family history and behavioral risk factors in breast cancer risk assessment among a multiethnic group of women.

Authors:  Leah S Karliner; Anna Napoles-Springer; Karla Kerlikowske; Jennifer S Haas; Steven E Gregorich; Celia Patricia Kaplan
Journal:  J Gen Intern Med       Date:  2007-03       Impact factor: 5.128

4.  Educational needs about cancer family history and genetic counseling for cancer risk among frontline healthcare clinicians in New York City.

Authors:  Katarina M Sussner; Lina Jandorf; Heiddis B Valdimarsdottir
Journal:  Genet Med       Date:  2011-09       Impact factor: 8.822

5.  Psychological impact of family history risk assessment in primary care: a mixed methods study.

Authors:  Linda Birt; Jon D Emery; A Toby Prevost; Stephen Sutton; Fiona M Walter
Journal:  Fam Pract       Date:  2014-04-12       Impact factor: 2.267

6.  Patient satisfaction with two different models of cancer genetic services in south-east Scotland.

Authors:  S Holloway; M Porteous; R Cetnarskyj; E Anderson; R Rush; A Fry; D Gorman; M Steel; H Campbell
Journal:  Br J Cancer       Date:  2004-02-09       Impact factor: 7.640

7.  Improving the management of people with a family history of breast cancer in primary care: before and after study of audit-based education.

Authors:  Imran Rafi; Susmita Chowdhury; Tom Chan; Ibrahim Jubber; Mohammad Tahir; Simon de Lusignan
Journal:  BMC Fam Pract       Date:  2013-07-24       Impact factor: 2.497

  7 in total

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