Literature DB >> 18373400

Cancer genetics evaluation: barriers to and improvements for referral.

Rachael Brandt1, Zonera Ali, Allison Sabel, Terri McHugh, Paul Gilman.   

Abstract

Despite the availability of cancer susceptibility testing, little information exists regarding physicians' selection and referral of eligible patients. This study provides insight into whom, why, and when physicians refer for cancer genetics evaluation, as well as their comfort level within this role. Eighty-two physicians (51 primary care, 15 gynecology, 11 surgery and 5 oncology) completed a survey (response rate: 34%) regarding cancer genetics referral practices. Of these, 59% reported an awareness of the hospital's cancer genetics program. Program awareness was greater among oncologists, surgeons, and gynecologists than among primary care physicians (p < 0.0001). Patients were referred for enhanced risk assessment (88%), improved medical management (85%), and concern for family members (83%). Patient eligibility was based on family cancer history (96%), patient cancer history (83%), and patient request (73%). Patients were not referred mainly due to patient disinterest (54%) or physician concern about either insurance coverage (44%) or insurance discrimination (31%). Primary care physicians were less comfortable with identifying patients for referral (p < 0.001) and with discussing genetics (p < 0.002) than specialists. The largest barriers to referral were lack of program awareness and limited knowledge regarding patient eligibility, improved insurance coverage, and antidiscrimination legislation. Physician-targeted marketing and education may improve the referral process.

Entities:  

Mesh:

Year:  2008        PMID: 18373400     DOI: 10.1089/gte.2007.0036

Source DB:  PubMed          Journal:  Genet Test        ISSN: 1090-6576


  17 in total

1.  Access to genetic testing and genetic counseling in vulnerable populations: the d/Deaf and hard of hearing population.

Authors:  Sandra Cooke-Hubley; Victor Maddalena
Journal:  J Community Genet       Date:  2011-05-01

2.  Barriers to and motivations for physician referral of patients to cancer genetics clinics.

Authors:  Carrie F Prochniak; Lisa J Martin; Erin M Miller; Sara C Knapke
Journal:  J Genet Couns       Date:  2011-08-13       Impact factor: 2.537

3.  Randomized Noninferiority Trial of Telephone Delivery of BRCA1/2 Genetic Counseling Compared With In-Person Counseling: 1-Year Follow-Up.

Authors:  Anita Y Kinney; Laurie E Steffen; Barbara H Brumbach; Wendy Kohlmann; Ruofei Du; Ji-Hyun Lee; Amanda Gammon; Karin Butler; Saundra S Buys; Antoinette M Stroup; Rebecca A Campo; Kristina G Flores; Jeanne S Mandelblatt; Marc D Schwartz
Journal:  J Clin Oncol       Date:  2016-06-20       Impact factor: 44.544

4.  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

Review 5.  Genetics, genomics, and cancer risk assessment: State of the Art and Future Directions in the Era of Personalized Medicine.

Authors:  Jeffrey N Weitzel; Kathleen R Blazer; Deborah J MacDonald; Julie O Culver; Kenneth Offit
Journal:  CA Cancer J Clin       Date:  2011-08-19       Impact factor: 508.702

6.  Expanding access to BRCA1/2 genetic counseling with telephone delivery: a cluster randomized trial.

Authors:  Anita Y Kinney; Karin M Butler; Marc D Schwartz; Jeanne S Mandelblatt; Kenneth M Boucher; Lisa M Pappas; Amanda Gammon; Wendy Kohlmann; Sandra L Edwards; Antoinette M Stroup; Saundra S Buys; Kristina G Flores; Rebecca A Campo
Journal:  J Natl Cancer Inst       Date:  2014-11-05       Impact factor: 13.506

7.  Cancer genetic risk assessment and referral patterns in primary care.

Authors:  Hetal S Vig; Joanne Armstrong; Brian L Egleston; Carla Mazar; Michele Toscano; Angela R Bradbury; Mary B Daly; Neal J Meropol
Journal:  Genet Test Mol Biomarkers       Date:  2009-12

8.  Personalized medicine and genomics: challenges and opportunities in assessing effectiveness, cost-effectiveness, and future research priorities.

Authors:  Rena Conti; David L Veenstra; Katrina Armstrong; Lawrence J Lesko; Scott D Grosse
Journal:  Med Decis Making       Date:  2010-01-04       Impact factor: 2.583

9.  "Would you test your children without their consent?" and other sticky dilemmas in the field of cancer genetic testing.

Authors:  Karina L Brierley; Danielle C Bonadies; Anne Moyer; Ellen T Matloff
Journal:  Fam Cancer       Date:  2014-09       Impact factor: 2.375

10.  Patient-reported hereditary breast and ovarian cancer in a primary care practice.

Authors:  John M Quillin; Alexander H Krist; Maria Gyure; Rosalie Corona; Vivian Rodriguez; Joseph Borzelleca; Joann N Bodurtha
Journal:  J Community Genet       Date:  2013-07-20
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