Literature DB >> 19408048

Recall of and reactions to a surgeon referral letter for BRCA genetic counseling among high-risk breast cancer patients.

Susan T Vadaparampil1, Gwendolyn P Quinn, Cheryl A Miree, Jennifer Brzosowicz, Bradford Carter, Christine Laronga.   

Abstract

BACKGROUND: The oncology care setting represents an important opportunity to identify and refer women at increased risk for hereditary breast and ovarian cancer. However, little is known about the effectiveness of provider approaches to inform patients of hereditary cancer risk or patient uptake of genetic counseling (GC). This qualitative study examined the impact of a surgeon referral letter on recently diagnosed breast cancer patients' uptake of BRCA GC.
METHODS: Qualitative open-ended, in-depth interviews were conducted with 26 high-risk breast cancer patients sent a referral letter for BRCA GC by their surgeon. Data were analyzed by a grounded theory approach.
RESULTS: Most women (approximately 80%) recalled receiving the letter, and 62% of all (n = 16) women pursued GC. Recall of the letter did not seem to be associated with uptake of GC (P = .49, Fisher's exact test). The results highlight key areas for improvement that may help increase the impact of the letter. Half of the women in this sample believed that the letter was sent to all breast cancer patients, rather than those with specific risk factors. Few women mentioned any implications for the information obtained during GC or testing regarding their current breast cancer diagnosis or treatment. Of the women who did not attend, many perceived that dealing with the GC and testing process in the midst of a cancer diagnosis and treatment was overwhelming. Among the women who had chosen not to attend GC, most stated they would reconsider after completing their treatment.
CONCLUSIONS: Patient recall of a surgeon referral letter does not seem to increase the number of high-risk women who attend GC after a breast cancer diagnosis. The letter approach in its current format does not seem to be a wholly effective means of communicating with some patients who may be overwhelmed by their cancer diagnosis or unaware that GC and testing may have implications for their current treatment decisions, possibly resulting in a missed opportunity to engage in informed decision making.

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Year:  2009        PMID: 19408048     DOI: 10.1245/s10434-009-0479-4

Source DB:  PubMed          Journal:  Ann Surg Oncol        ISSN: 1068-9265            Impact factor:   5.344


  16 in total

1.  A model for patient-direct screening and referral for familial cancer risk.

Authors:  Kristin B Niendorf; Melissa A Geller; Rachel Isaksson Vogel; Timothy R Church; Anna Leininger; Angela Bakke; Robert D Madoff
Journal:  Fam Cancer       Date:  2016-10       Impact factor: 2.375

2.  Incorporating information regarding preimplantation genetic diagnosis into discussions concerning testing and risk management for BRCA1/2 mutations: a qualitative study of patient preferences.

Authors:  Karen Hurley; Lisa R Rubin; Allison Werner-Lin; Michal Sagi; Yelena Kemel; Rikki Stern; Aliza Phillips; Ina Cholst; Noah Kauff; Kenneth Offit
Journal:  Cancer       Date:  2012-06-26       Impact factor: 6.860

3.  Why Is Cancer Genetic Counseling Underutilized by Women Identified as at Risk for Hereditary Breast Cancer? Patient Perceptions of Barriers Following a Referral Letter.

Authors:  Alyssa Kne; Heather Zierhut; Shari Baldinger; Karen K Swenson; Pamela Mink; Patricia McCarthy Veach; Michaela L Tsai
Journal:  J Genet Couns       Date:  2016-11-08       Impact factor: 2.537

4.  Utilization of clinical genetic counseling among childhood and young adult cancer survivors in a registry trial.

Authors:  Nassim Anderson; Arash Delavar; Danielle Novetsky Friedman; Vijai Joseph; Nidha Mubdi; Kevin C Oeffinger; Charles A Sklar; Kenneth Offit; Matthew Matasar; Nirupa Raghunathan; Zoltan Antal; David Straus; Michael Walsh; Alicia Latham; Emily S Tonorezos
Journal:  J Community Genet       Date:  2020-07-16

5.  Satisfaction with physician recommendation for and information about genetic counseling among breast cancer patients.

Authors:  Susan T Vadaparampil; Gwendolyn P Quinn; Ji-Hyun Lee; Teri Malo; Xiuhua Zhao; Cheryl Miree; Jennifer Brzosowicz
Journal:  Breast J       Date:  2010-12-06       Impact factor: 2.431

6.  Cognitive and psychological impact of BRCA genetic counseling in before and after definitive surgery breast cancer patients.

Authors:  Juliette Christie; Gwendolyn P Quinn; Teri Malo; Ji-Hyun Lee; Xiuhua Zhao; Jessica McIntyre; Jennifer Brzosowicz; Paul B Jacobsen; Susan T Vadaparampil
Journal:  Ann Surg Oncol       Date:  2012-07-06       Impact factor: 5.344

Review 7.  Genetic risk assessments in individuals at high risk for inherited breast cancer in the breast oncology care setting.

Authors:  Tuya Pal; Susan T Vadaparampil
Journal:  Cancer Control       Date:  2012-10       Impact factor: 3.302

8.  Health beliefs associated with readiness for genetic counseling among high risk breast cancer survivors.

Authors:  Maija Reblin; Monica L Kasting; Kelli Nam; Courtney L Scherr; Jongphil Kim; Ram Thapa; Cathy D Meade; M Catherine Lee; Tuya Pal; Gwendolyn P Quinn; Susan T Vadaparampil
Journal:  Breast J       Date:  2018-11-28       Impact factor: 2.431

9.  A pilot study of hereditary breast and ovarian knowledge among a multiethnic group of Hispanic women with a personal or family history of cancer.

Authors:  Susan T Vadaparampil; Gwendolyn P Quinn; Brent J Small; Jessica McIntyre; Claudia Aguado Loi; Zuheily Closser; Clement K Gwede
Journal:  Genet Test Mol Biomarkers       Date:  2010-02

10.  Development and Pilot Testing of a Decision Aid for Genomic Research Participants Notified of Clinically Actionable Research Findings for Cancer Risk.

Authors:  Amanda M Willis; Sian K Smith; Bettina Meiser; Mandy L Ballinger; David M Thomas; Martin Tattersall; Mary-Anne Young
Journal:  J Genet Couns       Date:  2018-02-17       Impact factor: 2.537

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