Literature DB >> 21845493

Reading between the lines: a comparison of responders and non-responders to a family history questionnaire and implications for cancer genetic counselling.

Julia H Appleby-Tagoe1, William D Foulkes, Laura Palma.   

Abstract

Family history questionnaires (FHQ) are useful tools for cancer genetic counseling, providing an informational basis for pedigree construction and individualized cancer risk assessment. Reported return rates of mailed FHQs amongst familial cancer clinics that utilize them are lower than desired however, and it is unknown whether patients perceive required completion of a FHQ as a barrier to access of cancer genetics services. This study critically evaluated the use of a mailed FHQ for all routine new patient referrals to a single hereditary cancer clinic in Quebec, Canada. Reasons for response/non-response to a FHQ and the effect of administration of a questionnaire on patients' self-reported level of motivation to pursue genetic counseling, were examined. Of 112 eligible individuals referred during the study period, 86 completed a semi-structured telephone survey; of these, 45% had returned the mailed FHQ prior to the telephone survey (Responders) and 55% had not (Non-responders). Overall, the majority of participants indicated a FHQ is an acceptable and understandable method of collecting family history information. Most prevalent reasons for not returning the FHQ were (bad) timing (56%), and difficulty accessing family history information (46%). Non-response was significantly associated with difficulty in asking relatives for the requested information (p = 0.011), and Non-responders cited fewer overall perceived benefits of cancer genetic counseling as compared with Responders (p < 0.0001). One quarter of Non-responders returned the mailed FHQ following administration of the telephone survey, suggesting implementation of a follow-up prompt is a cost-effective way to increase response.

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Year:  2011        PMID: 21845493     DOI: 10.1007/s10897-011-9399-0

Source DB:  PubMed          Journal:  J Genet Couns        ISSN: 1059-7700            Impact factor:   2.537


  14 in total

1.  Proband family uptake of familial-genetic counselling.

Authors:  L Hagoel; S Dishon; R Almog; Z Silman; S Bisland-Becktell; G Rennert
Journal:  Psychooncology       Date:  2000 Nov-Dec       Impact factor: 3.894

2.  The psychological impact of a cancer family history questionnaire completed in general practice.

Authors:  V Leggatt; J Mackay; T M Marteau; J R Yates
Journal:  J Med Genet       Date:  2000-06       Impact factor: 6.318

3.  Ethnicity, but not cancer family history, is related to response to a population-based mailed questionnaire.

Authors:  Cristina Mancuso; Gord Glendon; Lynn Anson-Cartwright; Ellen Juqing Shi; Irene Andrulis; Julia Knight
Journal:  Ann Epidemiol       Date:  2004-01       Impact factor: 3.797

4.  Psychological and social determinants of women's decisions to undergo genetic counseling and testing for breast cancer.

Authors:  M Cappelli; L Surh; L Humphreys; S Verma; D Logan; A Hunter; J Allanson
Journal:  Clin Genet       Date:  1999-06       Impact factor: 4.438

5.  The use of family history questionnaires: an examination of genetic risk estimates and genetic testing eligibility in the non-responder population.

Authors:  Susan Randall Armel; Kara Hitchman; Kathryn Millar; Laura Zahavich; Rochelle Demsky; Joan Murphy; Barry Rosen
Journal:  J Genet Couns       Date:  2011-03-30       Impact factor: 2.537

6.  Factors influencing patients' decisions to decline cancer genetic counseling services.

Authors:  K P Geer; M E Ropka; W F Cohn; S M Jones; S Miesfeldt
Journal:  J Genet Couns       Date:  2001-02       Impact factor: 2.537

7.  The effectiveness of family history questionnaires in cancer genetic counseling.

Authors:  Susan Randall Armel; Jeanna McCuaig; Amy Finch; Rochelle Demsky; Tony Panzarella; Joan Murphy; Barry Rosen
Journal:  J Genet Couns       Date:  2009-05-21       Impact factor: 2.537

8.  Barriers to participating in genetic counseling and BRCA testing during primary treatment for breast cancer.

Authors:  Kathryn J Schlich-Bakker; Herman F J ten Kroode; Carla C Wárlám-Rodenhuis; Jan van den Bout; Margreet G E M Ausems
Journal:  Genet Med       Date:  2007-11       Impact factor: 8.822

9.  Psychosocial predictors of BRCA counseling and testing decisions among urban African-American women.

Authors:  Hayley S Thompson; Heiddis B Valdimarsdottir; Chantal Duteau-Buck; Josephine Guevarra; Dana H Bovbjerg; Cassandra Richmond-Avellaneda; David Amarel; Diana Godfrey; Karen Brown; Kenneth Offit
Journal:  Cancer Epidemiol Biomarkers Prev       Date:  2002-12       Impact factor: 4.254

10.  Acceptance of and attitude toward genetic testing for hereditary nonpolyposis colorectal cancer: a comparison of participants and nonparticipants in genetic counseling.

Authors:  Monika Keller; Ralf Jost; Martina Kadmon; Hans-Peter Wüllenweber; Carrie Mastromarino Haunstetter; Frank Willeke; Christine Jung; Johannes Gebert; Christian Sutter; Christian Herfarth; Markus W Büchler
Journal:  Dis Colon Rectum       Date:  2004-02       Impact factor: 4.585

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  4 in total

1.  Who is being referred to cancer genetic counseling? Characteristics of counselees and their referral.

Authors:  E van Riel; S van Dulmen; M G E M Ausems
Journal:  J Community Genet       Date:  2012-03-17

2.  All in the Family: Barriers and Motivators to the Use of Cancer Family History Questionnaires and the Impact on Attendance Rates.

Authors:  Susan Randall Armel; Jeanna McCuaig; Nicole Gojska; Rochelle Demsky; Manjula Maganti; Joan Murphy; Barry Rosen
Journal:  J Genet Couns       Date:  2015-01-07       Impact factor: 2.537

3.  An internal performance assessment of CancerGene Connect: an electronic tool to streamline, measure and improve the genetic counseling process.

Authors:  Mary Pritzlaff; Arielle Yorczyk; Linda S Robinson; Sara Pirzadeh-Miller; Tirun Lin; David Euhus; Theodora S Ross
Journal:  J Genet Couns       Date:  2014-06-12       Impact factor: 2.537

Review 4.  A systematic review of factors that act as barriers to patient referral to genetic services.

Authors:  Türem Delikurt; Graham R Williamson; Violetta Anastasiadou; Heather Skirton
Journal:  Eur J Hum Genet       Date:  2014-09-10       Impact factor: 4.246

  4 in total

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