Literature DB >> 21927977

Family physicians' awareness and knowledge of the Genetic Information Non-Discrimination Act (GINA).

Amanda L Laedtke1, Suzanne M O'Neill, Wendy S Rubinstein, Kristen J Vogel.   

Abstract

Historically, physicians have expressed concern about their patients' risk of genetic discrimination, which has acted as a barrier to uptake of genetic services. The Genetic Information Nondiscrimination Act of 2008 (GINA) is intended to protect patients against employer and health insurance discrimination. Physicians' awareness and knowledge of GINA has yet to be evaluated. In 2009, we mailed surveys to 1500 randomly selected members of the American Academy of Family Physicians. Questions measured physicians' current knowledge of GINA and their level of concern for genetic discrimination. In total, 401 physicians completed the survey (response rate 26.9%). Approximately half (54.5%) of physicians had no awareness of GINA. Of physicians who reported basic knowledge of GINA, the majority were aware of the protections offered for group health insurance (92.7%), private health insurance (82.9%), and employment (70.7%). Fewer physicians were aware of GINA's limitations regarding life insurance (53.7%) and long-term care insurance (58.8%). Physicians demonstrated highest levels of concern for health insurance, life insurance, and long-term care insurance discrimination, with less concern for employer and family/social discrimination. Level of concern for the risk of genetic discrimination did not correlate significantly with awareness of GINA. Approximately 17 months after GINA was signed into federal law, physicians' knowledge remained limited regarding the existence of this legislation and relevant details. Physicians who are aware of GINA continue to have significant concerns regarding the risk of genetic discrimination. This study reveals the need to further educate physicians about the existence of GINA and the protections offered.

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Year:  2011        PMID: 21927977     DOI: 10.1007/s10897-011-9405-6

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


  23 in total

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3.  Genetic discrimination: the clinician perspective.

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6.  Concerns in a primary care population about genetic discrimination by insurers.

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8.  An investigation of genetic counselors' discussion of genetic discrimination with cancer risk patients.

Authors:  Nicole L Pfeffer; Patricia McCarthy Veach; Bonnie S LeRoy
Journal:  J Genet Couns       Date:  2003-10       Impact factor: 2.537

9.  Patients' fear of genetic discrimination by health insurers: the impact of legal protections.

Authors:  M A Hall; S S Rich
Journal:  Genet Med       Date:  2000 Jul-Aug       Impact factor: 8.822

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Authors:  S J Hayflick; M P Eiff; L Carpenter; J Steinberger
Journal:  Genet Med       Date:  1998 Nov-Dec       Impact factor: 8.822

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  27 in total

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5.  The Undergraduate Training in Genomics (UTRIG) Initiative: early & active training for physicians in the genomic medicine era.

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Journal:  Per Med       Date:  2018-05-30       Impact factor: 2.512

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8.  Genetic information, non-discrimination, and privacy protections in genetic counseling practice.

Authors:  Anya E R Prince; Myra I Roche
Journal:  J Genet Couns       Date:  2014-07-27       Impact factor: 2.537

9.  Evolution of Hereditary Breast Cancer Genetic Services: Are Changes Reflected in the Knowledge and Clinical Practices of Florida Providers?

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10.  "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
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