Literature DB >> 12704638

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

Laura Plantinga1, Marvin R Natowicz, Nancy E Kass, Sara Chandros Hull, Lawrence O Gostin, Ruth R Faden.   

Abstract

Despite policy attention to medical privacy and patient confidentiality, little empirical work exists documenting and comparing experiences of persons with genetic versus nongenetic medical conditions concerning persons' disclosure to others as well as their views about appropriate confidentiality to and within families. The goal of this cross-sectional interview study with nearly 600 participants was to document and compare the experiences, attitudes, and beliefs of persons with strictly genetic conditions to those of persons with or at risk for other serious medical conditions in terms of the degree to which they have disclosed to others that they have the condition and their views about how others ought to maintain the confidentiality of that information. While almost all participants reported that family members knew about their condition, results suggest participants want to control that disclosure themselves and do not want doctors to disclose information to family members without their knowledge. Similarly, participants do not think family members should be able to get information about them without their knowledge but feel overwhelmingly that it is a person's responsibility to disclose information about hereditary conditions to other family members. Ambivalence about confidentiality was evident: while most participants did not mind doctors sharing information with other doctors when it was for their benefit, the majority also felt that doctors should be punished for releasing information without their permission. The views and experiences reported here generally did not differ by whether participants had genetic versus nongenetic conditions, suggesting that the extensive policy focus on genetic information may be unwarranted. Copyright 2002 Wiley-Liss, Inc.

Entities:  

Keywords:  Empirical Approach; Genetics and Reproduction

Mesh:

Year:  2003        PMID: 12704638      PMCID: PMC4809525          DOI: 10.1002/ajmg.c.10006

Source DB:  PubMed          Journal:  Am J Med Genet C Semin Med Genet        ISSN: 1552-4868            Impact factor:   3.908


  9 in total

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Journal:  J Law Med Ethics       Date:  1998       Impact factor: 1.718

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Journal:  N Engl J Med       Date:  2001-08-02       Impact factor: 91.245

4.  Distinguishing genetic from nongenetic medical tests: some implications for antidiscrimination legislation.

Authors:  Joseph S Alper; Jon Beckwith
Journal:  Sci Eng Ethics       Date:  1998-04       Impact factor: 3.525

5.  Genetic privacy and the law: an end to genetics exceptionalism.

Authors:  L O Gostin; J G Hodge
Journal:  Jurimetrics       Date:  1999

6.  ASHG statement. Professional disclosure of familial genetic information. The American Society of Human Genetics Social Issues Subcommittee on Familial Disclosure.

Authors: 
Journal:  Am J Hum Genet       Date:  1998-02       Impact factor: 11.025

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 of familial genetic information: perceptions of the duty to inform.

Authors:  L S Lehmann; J C Weeks; N Klar; L Biener; J E Garber
Journal:  Am J Med       Date:  2000-12-15       Impact factor: 4.965

9.  Genetic discrimination: perspectives of consumers.

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

  9 in total
  15 in total

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Review 3.  Can you keep a (genetic) secret? The genetic privacy movement.

Authors:  Margaret Everett
Journal:  J Genet Couns       Date:  2004-08       Impact factor: 2.537

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5.  Disclosing Genetic Information to Family Members About Inherited Cardiac Arrhythmias: An Obligation or a Choice?

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6.  Information-seeking and sharing behavior following genomic testing for diabetes risk.

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7.  Patient experiences with pharmacogenetic testing in a primary care setting.

Authors:  Susanne B Haga; Rachel Mills; Jivan Moaddeb; Nancy Allen Lapointe; Alex Cho; Geoffrey S Ginsburg
Journal:  Pharmacogenomics       Date:  2016-09-20       Impact factor: 2.533

8.  A place for genetic uncertainty: parents valuing an unknown in the meaning of disease.

Authors:  Ian Whitmarsh; Arlene M Davis; Debra Skinner; Donald B Bailey
Journal:  Soc Sci Med       Date:  2007-06-11       Impact factor: 4.634

9.  A clinical perspective on ethical arguments around prenatal diagnosis and preimplantation genetic diagnosis for later onset inherited cancer predispositions.

Authors:  Tara Clancy
Journal:  Fam Cancer       Date:  2009-07-31       Impact factor: 2.375

10.  Should healthcare providers have a duty to warn family members of individuals with an HNPCC-causing mutation? A survey of patients from the Ontario Familial Colon Cancer Registry.

Authors:  Kelly Kohut; Michael Manno; Steven Gallinger; Mary Jane Esplen
Journal:  J Med Genet       Date:  2007-06       Impact factor: 6.318

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