Literature DB >> 24848747

Accuracy of recall of information about a cancer-predisposing BRCA1/2 gene mutation among patients and relatives.

Chris Jacobs1, Caroline Dancyger2, Jonathan A Smith3, Susan Michie4.   

Abstract

This observational study aimed to (i) compare the accuracy of information recalled by patients and relatives following genetic counselling about a newly identified BRCA1/2 mutation, (ii) identify differences in accuracy of information about genetics and hereditary cancer and (iii) investigate whether accuracy among relatives improved when information was provided directly by genetics health professionals. Semistructured interviews following results from consultations with 10 breast/ovarian cancer patients and 22 relatives were audio-recorded and transcribed. Information provided by the genetics health professional was tracked through the families and coded for accuracy. Accuracy was analysed using the Wilcoxon Signed-Ranks test. Sources of information were tested using Spearman's rank-order correlation coefficient. Fifty-three percent of the information recalled by patients was accurate. Accuracy of recall among relatives was significantly lower than that among patients (P=0.017). Both groups recalled a lower proportion of information about hereditary cancer than about genetics (P=0.005). Relatives who learnt the information from the patient alone recalled significantly less accurate information than those informed directly by genetics health professionals (P=0.001). Following genetic counselling about a BRCA1/2 mutation, accuracy of recall was low among patients and relatives, particularly about hereditary cancer. Multiple sources of information, including direct contact with genetics health professionals, may improve the accuracy of information among relatives.

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Year:  2014        PMID: 24848747      PMCID: PMC4297912          DOI: 10.1038/ejhg.2014.84

Source DB:  PubMed          Journal:  Eur J Hum Genet        ISSN: 1018-4813            Impact factor:   4.246


  26 in total

1.  The impact of proband mediated information dissemination in families with a BRCA1/2 gene mutation.

Authors:  E Sermijn; G Goelen; E Teugels; L Kaufman; M Bonduelle; B Neyns; B Poppe; A De Paepe; J De Grève
Journal:  J Med Genet       Date:  2004-03       Impact factor: 6.318

2.  The development of a methodology for examining the process of family communication of genetic test results.

Authors:  Jonathan A Smith; Caroline Dancyger; Melissa Wallace; Chris Jacobs; Susan Michie
Journal:  J Genet Couns       Date:  2010-09-11       Impact factor: 2.537

3.  Satisfaction with genetic counseling: dimensions and measurement.

Authors:  S Shiloh; O Avdor; R M Goodman
Journal:  Am J Med Genet       Date:  1990-12

Review 4.  Process and outcome in communication of genetic information within families: a systematic review.

Authors:  Clara L Gaff; Angus J Clarke; Paul Atkinson; Stephanie Sivell; Glyn Elwyn; Rachel Iredale; Hazel Thornton; Joanna Dundon; Chris Shaw; Adrian Edwards
Journal:  Eur J Hum Genet       Date:  2007-07-04       Impact factor: 4.246

Review 5.  Communicating genetic information in families--a review of guidelines and position papers.

Authors:  Laura E Forrest; Martin B Delatycki; Loane Skene; MaryAnne Aitken
Journal:  Eur J Hum Genet       Date:  2007-03-28       Impact factor: 4.246

6.  How families communicate about HNPCC genetic testing: findings from a qualitative study.

Authors:  Susan K Peterson; Beatty G Watts; Laura M Koehly; Sally W Vernon; Walter F Baile; Wendy K Kohlmann; Ellen R Gritz
Journal:  Am J Med Genet C Semin Med Genet       Date:  2003-05-15       Impact factor: 3.908

7.  To tell or not to tell: barriers and facilitators in family communication about genetic risk.

Authors:  K Forrest; S A Simpson; B J Wilson; E R van Teijlingen; L McKee; N Haites; E Matthews
Journal:  Clin Genet       Date:  2003-10       Impact factor: 4.438

8.  Understanding why negative genetic test results sometimes fail to reassure.

Authors:  Susan Michie; Jonathan A Smith; Victoria Senior; Theresa M Marteau
Journal:  Am J Med Genet A       Date:  2003-06-15       Impact factor: 2.802

9.  A theory of medical decision making and health: fuzzy trace theory.

Authors:  Valerie F Reyna
Journal:  Med Decis Making       Date:  2008-11-17       Impact factor: 2.583

10.  A whisper-game perspective on the family communication of DNA-test results: a retrospective study on the communication process of BRCA1/2-test results between proband and relatives.

Authors:  Joël Vos; Fred Menko; Anna M Jansen; Christi J van Asperen; Anne M Stiggelbout; Aad Tibben
Journal:  Fam Cancer       Date:  2011-03       Impact factor: 2.375

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  7 in total

Review 1.  Family Communication, Risk Perception and Cancer Knowledge of Young Adults from BRCA1/2 Families: a Systematic Review.

Authors:  Alison L Young; Phyllis N Butow; Janine Vetsch; Veronica F Quinn; Andrea F Patenaude; Katherine M Tucker; Claire E Wakefield
Journal:  J Genet Couns       Date:  2017-06-30       Impact factor: 2.537

2.  A Qualitative Study to Explore the Views and Attitudes towards Prenatal Testing in Adults Who Have Muenke Syndrome and their Partners.

Authors:  Julie Phipps; Heather Skirton
Journal:  J Genet Couns       Date:  2017-03-22       Impact factor: 2.537

3.  The Long and Short of Genetic Counseling Summary Letters: A Case-control Study.

Authors:  J Roggenbuck; R Temme; D Pond; J Baker; K Jarvis; M Liu; S Dugan; N J Mendelsohn
Journal:  J Genet Couns       Date:  2014-12-14       Impact factor: 2.537

Review 4.  Communication about genetic testing with breast and ovarian cancer patients: a scoping review.

Authors:  Chris Jacobs; Christine Patch; Susan Michie
Journal:  Eur J Hum Genet       Date:  2018-12-20       Impact factor: 4.246

5.  Public support for healthcare-mediated disclosure of hereditary cancer risk information: Results from a population-based survey in Sweden.

Authors:  Andreas Andersson; Carolina Hawranek; Anna Öfverholm; Hans Ehrencrona; Kalle Grill; Senada Hajdarevic; Beatrice Melin; Emma Tham; Barbro Numan Hellquist; Anna Rosén
Journal:  Hered Cancer Clin Pract       Date:  2020-09-15       Impact factor: 2.857

6.  Healthcare professionals' responsibility for informing relatives at risk of hereditary disease.

Authors:  Kalle Grill; Anna Rosén
Journal:  J Med Ethics       Date:  2020-11-27       Impact factor: 2.903

7.  Characteristics and experiences of patients from a community-based and consumer-directed hereditary cancer population screening initiative.

Authors:  Veronica Greve; Katherine Odom; Susanna Pudner; Neil E Lamb; Sara J Cooper; Kelly East
Journal:  HGG Adv       Date:  2021-08-24
  7 in total

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