Literature DB >> 17290434

Access to health insurance: experiences and attitudes of those with genetic versus non-genetic medical conditions.

Nancy E Kass1, Amy M Medley, Marvin R Natowicz, Sara Chandros Hull, Ruth R Faden, Laura Plantinga, Lawrence O Gostin.   

Abstract

While studies reveal that individuals with both genetic and other chronic medical conditions have difficulty obtaining health insurance, no large-scale studies have compared the health insurance experiences of these groups. The goal of this study was to document and compare the health insurance experiences, attitudes, and beliefs of persons with genetic conditions to those of persons with or at risk for other serious medical conditions. We interviewed approximately 100 adults or parents of children with one of each of the following medical conditions: sickle cell disease (SCD), cystic fibrosis (CF), diabetes, and HIV, and 200 adults with or at risk for breast (BC) or colon cancer (CC). The interview included items related to respondents' experiences and attitudes regarding health insurance. Twenty-seven percent of 597 total respondents self-reported having been denied health insurance or offered insurance at a prohibitive rate. Respondents with single-gene disorders (CF and SCD) were twice as likely to report this as those with non-genetic conditions. Legislation that exists to limit genetic discrimination in insurance addresses genetic risks or traits only, however, rather than protecting those with actual disease. Thus, current legislation may not address the challenges faced by individuals like those in this study, who try to maintain access to health insurance when they or their children are symptomatic with a genetic or other serious health condition. More than one-third of all respondents thought there was a high chance they would be denied health insurance in the future or their insurance would become unaffordable. That individuals with all six health conditions expressed concern regarding their ability to obtain future health insurance suggests policy proposals should be broad-based, addressing the needs and concerns of individuals with diverse health conditions.

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Year:  2007        PMID: 17290434      PMCID: PMC4815905          DOI: 10.1002/ajmg.a.31576

Source DB:  PubMed          Journal:  Am J Med Genet A        ISSN: 1552-4825            Impact factor:   2.802


  16 in total

1.  Individual, family, and societal dimensions of genetic discrimination: a case study analysis.

Authors:  Lisa N Geller; Joseph S Alper; Paul R Billings; Carol I Barash; Jonathan Beckwith; Marvin R Natowicz
Journal:  Sci Eng Ethics       Date:  1996-01       Impact factor: 3.525

2.  "Genetic exceptionalism" in medicine: clarifying the differences between genetic and nongenetic tests.

Authors:  Michael J Green; Jeffrey R Botkin
Journal:  Ann Intern Med       Date:  2003-04-01       Impact factor: 25.391

3.  A scarlet letter or a red herring?

Authors:  William J Nowlan
Journal:  Nature       Date:  2003-01-23       Impact factor: 49.962

Review 4.  Genetic information and life insurance: a 'real' risk?

Authors:  Yann Joly; Bartha M Knoppers; Béatrice Godard
Journal:  Eur J Hum Genet       Date:  2003-08       Impact factor: 4.246

5.  Disclosure of genetic tests for health insurance: is it ethical not to?

Authors:  Nick Raithatha; Richard D Smith
Journal:  Lancet       Date:  2004-01-31       Impact factor: 79.321

6.  Drafting the Genetic Privacy Act: science, policy, and practical considerations.

Authors:  G J Annas; L H Glantz; P A Roche
Journal:  J Law Med Ethics       Date:  1995       Impact factor: 1.718

7.  National health information privacy: regulations under the Health Insurance Portability and Accountability Act.

Authors:  L O Gostin
Journal:  JAMA       Date:  2001-06-20       Impact factor: 56.272

8.  Disclosure, confidentiality, and families: experiences and attitudes of those with genetic versus nongenetic medical conditions.

Authors:  Laura Plantinga; Marvin R Natowicz; Nancy E Kass; Sara Chandros Hull; Lawrence O Gostin; Ruth R Faden
Journal:  Am J Med Genet C Semin Med Genet       Date:  2003-05-15       Impact factor: 3.908

9.  Disclosure of personal medical information: differences among parents and affected adults for genetic and nongenetic conditions.

Authors:  Summer Johnson; Nancy E Kass; Marvin Natowicz
Journal:  Genet Test       Date:  2005

10.  Genetic discrimination: perspectives of consumers.

Authors:  E V Lapham; C Kozma; J O Weiss
Journal:  Science       Date:  1996-10-25       Impact factor: 47.728

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  12 in total

Review 1.  Genetic testing in psychiatry: a review of attitudes and beliefs.

Authors:  Ryan E Lawrence; Paul S Appelbaum
Journal:  Psychiatry       Date:  2011       Impact factor: 2.458

Review 2.  Global trends on fears and concerns of genetic discrimination: a systematic literature review.

Authors:  Annet Wauters; Ine Van Hoyweghen
Journal:  J Hum Genet       Date:  2016-01-07       Impact factor: 3.172

3.  Civilian and military genetics: nondiscrimination policy in a post-GINA world.

Authors:  Susannah Baruch; Kathy Hudson
Journal:  Am J Hum Genet       Date:  2008-10       Impact factor: 11.025

4.  Attitudes and beliefs of African-Americans toward genetics, genetic testing, and sickle cell disease education and awareness.

Authors:  Katie A Long; Stephen B Thomas; Robin E Grubs; Elizabeth A Gettig; Lakshmanan Krishnamurti
Journal:  J Genet Couns       Date:  2011-07-12       Impact factor: 2.537

5.  You never call, you never write: why return of 'omic' results to research participants is both a good idea and a moral imperative.

Authors:  Misha Angrist
Journal:  Per Med       Date:  2011-11       Impact factor: 2.512

6.  Perception, experience, and response to genetic discrimination in Huntington disease: the international RESPOND-HD study.

Authors:  Cheryl Erwin; Janet K Williams; Andrew R Juhl; Michelle Mengeling; James A Mills; Yvonne Bombard; Michael R Hayden; Kimberly Quaid; Ira Shoulson; Sandra Taylor; Jane S Paulsen
Journal:  Am J Med Genet B Neuropsychiatr Genet       Date:  2010-07       Impact factor: 3.568

7.  Private Insurance Coverage for Diabetes Before and After Enactment of the Preexisting Condition Mandate of the Affordable Care Act, 2005-2016.

Authors:  Mary A M Rogers; Catherine Kim; Joyce M Lee; Tanima Basu; Renuka Tipirneni
Journal:  Am J Public Health       Date:  2019-02-21       Impact factor: 9.308

8.  Evolving perspectives on genetic discrimination in health insurance among health care providers.

Authors:  Carin R Huizenga; Katrina Lowstuter; Kimberly C Banks; Veronica I Lagos; Virginia O Vandergon; Jeffrey N Weitzel
Journal:  Fam Cancer       Date:  2010-06       Impact factor: 2.375

9.  Study protocol: the Australian genetics and life insurance moratorium-monitoring the effectiveness and response (A-GLIMMER) project.

Authors:  Louise Keogh; Paul Lacaze; Jane Tiller; Aideen McInerney-Leo; Andrea Belcher; Tiffany Boughtwood; Penny Gleeson; Martin Delatycki; Kristine Barlow-Stewart; Ingrid Winship; Margaret Otlowski
Journal:  BMC Med Ethics       Date:  2021-05-21       Impact factor: 2.652

10.  Legal update: living with the Genetic Information Nondiscrimination Act.

Authors:  Cheryl Erwin
Journal:  Genet Med       Date:  2008-12       Impact factor: 8.822

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