Literature DB >> 11281937

Reassurance through surveillance in the face of clinical uncertainty: the experience of women at risk of familial breast cancer.

Evelyn P. Parsons1, Valerie Beale, Helen Bennett, Jo Jones, Emma J Lycett.   

Abstract

OBJECTIVE: To identify the main issues raised by clinicians when they are counselling women at risk of breast cancer and explore the response of a group of women 1 year after counselling.
DESIGN: A qualitative study which involved the thematic analysis of a series of transcripts from clinical consultations, semi-structured interviews and focus groups. PARTICIPANTS: First, a series of clinical consultations (n=153), involving seven clinicians, were randomly selected during a Medical Research Council funded study of genetic assessment (TRACE). Second, a group of women (n=43), involved in the TRACE study, were interviewed, or joined a focus group, 1 year after their genetic assessment.
CONCLUSIONS: There was evidence that, although the clinical consultations were embedded with multiple messages of uncertainty, the women's accounts did not reflect this. The women talked about the reassurance they had found because they had met with an expert and become members of the surveillance society. The authors highlight the tension that exists because of the difference between lay expectations about on-going surveillance and the realities of collective service provision.

Entities:  

Year:  2000        PMID: 11281937      PMCID: PMC5060111          DOI: 10.1046/j.1369-6513.2000.00097.x

Source DB:  PubMed          Journal:  Health Expect        ISSN: 1369-6513            Impact factor:   3.377


  20 in total

1.  A model protocol evaluating the introduction of genetic assessment for women with a family history of breast cancer.

Authors:  J Gray; K Brain; P Norman; C Anglim; L France; G Barton; L Branston; E Parsons; A Clarke; J Sampson; E Roberts; R Newcombe; D Cohen; C Rogers; R Mansel; P Harper
Journal:  J Med Genet       Date:  2000-03       Impact factor: 6.318

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3.  The phenomenon of uncertainty in women with breast cancer.

Authors:  B A Hilton
Journal:  Issues Ment Health Nurs       Date:  1988       Impact factor: 1.835

4.  BRCA1--lots of mutations, lots of dilemmas.

Authors:  F S Collins
Journal:  N Engl J Med       Date:  1996-01-18       Impact factor: 91.245

5.  Measuring physicians' tolerance for ambiguity and its relationship to their reported practices regarding genetic testing.

Authors:  G Geller; E S Tambor; G A Chase; N A Holtzman
Journal:  Med Care       Date:  1993-11       Impact factor: 2.983

6.  The evolution of medical uncertainty.

Authors:  R C Fox
Journal:  Milbank Mem Fund Q Health Soc       Date:  1980

7.  Genetic counseling: provision and reception of information.

Authors:  A Lippman-Hand; F C Fraser
Journal:  Am J Med Genet       Date:  1979

8.  Genetic linkage analysis in familial breast and ovarian cancer: results from 214 families. The Breast Cancer Linkage Consortium.

Authors:  D F Easton; D T Bishop; D Ford; G P Crockford
Journal:  Am J Hum Genet       Date:  1993-04       Impact factor: 11.025

9.  BRCA1 5382insC mutation in sporadic and familial breast and ovarian carcinoma in Scotland.

Authors:  P Mullen; W R Miller; J Mackay; D R Fitzpatrick; S P Langdon; J P Warner
Journal:  Br J Cancer       Date:  1997       Impact factor: 7.640

10.  The impact of genetic counselling on risk perception in women with a family history of breast cancer.

Authors:  D G Evans; V Blair; R Greenhalgh; P Hopwood; A Howell
Journal:  Br J Cancer       Date:  1994-11       Impact factor: 7.640

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  6 in total

1.  Editorial.

Authors:  Angela Coulter
Journal:  Health Expect       Date:  2000-12       Impact factor: 3.377

2.  French women's breast self-examination practices with time after undergoing BRCA1/2 genetic testing.

Authors:  C Maheu; T Apostolidis; A Petri-Cal; E Mouret-Fourme; M Gauthier-Villars; C Lasset; P Berthet; J-P Fricker; O Caron; E Luporsi; L Gladieff; C Noguès; C Julian-Reynier
Journal:  Fam Cancer       Date:  2012-06       Impact factor: 2.375

Review 3.  How risk is perceived, constructed and interpreted by clients in clinical genetics, and the effects on decision making: systematic review.

Authors:  Stephanie Sivell; Glyn Elwyn; Clara L Gaff; Angus J Clarke; Rachel Iredale; Chris Shaw; Joanna Dundon; Hazel Thornton; Adrian Edwards
Journal:  J Genet Couns       Date:  2007-10-30       Impact factor: 2.537

4.  "I have always believed I was at high risk..." The role of expectation in emotional responses to the receipt of an average, moderate or high cancer genetic risk assessment result: a thematic analysis of free-text questionnaire comments.

Authors:  J Hilgart; C Phelps; P Bennett; K Hood; K Brain; A Murray
Journal:  Fam Cancer       Date:  2010-09       Impact factor: 2.375

5.  Living my family's story: identifying the lived experience in healthy women at risk for hereditary breast cancer.

Authors:  Meghan L Underhill; Robin M Lally; Marc T Kiviniemi; Christine Murekeyisoni; Suzanne S Dickerson
Journal:  Cancer Nurs       Date:  2012 Nov-Dec       Impact factor: 2.592

6.  Decision making with uncertain information: learning from women in a high risk breast cancer clinic.

Authors:  Caren J Frost; Vickie Venne; Dianne Cunningham; Ruth Gerritsen-McKane
Journal:  J Genet Couns       Date:  2004-06       Impact factor: 2.537

  6 in total

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