Literature DB >> 16225407

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

Summer Johnson1, Nancy E Kass, Marvin Natowicz.   

Abstract

Protecting the confidentiality of medical information has been an issue of great interest in the fields of bioethics, public policy, and law. Few empirical studies have addressed patient experiences and attitudes toward disclosure of private medical information in multiple contexts such as health insurance, employment, and the family. Furthermore, it is unclear whether differences exist in experiences and attitudes about privacy between those living with a serious medical condition versus those who have a child with a medical condition. The study sought to determine whether attitudes and experiences related to medical privacy and confidentiality differ between affected adults and parents of affected children. Interviews were conducted with 296 adults and parents of children with sickle cell disease (SCD), cystic fibrosis (CF), or diabetes mellitus (DM). This cross-sectional study collected data regarding their experiences, attitudes, and beliefs concerning medical privacy and confidentiality. Multinomial logistic regression analysis was conducted on quantitative data. Qualitative analysis was conducted on data from open-ended response items. Parents disclose their child's diagnosis to others more often than affected adults disclose their own disease status. Parents are less likely than affected adults to regret their disclosure, to hope others do not find out, to have been pressured to share information, and to be asked about their disease by employers. Affected adults express greater concern about disclosure, a greater prevalence and greater fear of discrimination, and experience greater pressure from family members to disclose. Clinicians and researchers working with these populations should consider these differences in privacy and disclosure. Further study is necessary to examine the implications of these differences in attitudes and experiences concerning insurance, employment, and social interactions among persons with these conditions.

Entities:  

Keywords:  Empirical Approach; Professional Patient Relationship

Mesh:

Year:  2005        PMID: 16225407     DOI: 10.1089/gte.2005.9.269

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


  4 in total

1.  Managing the need to tell: Triggers and strategic disclosure of thalassemia major in Singapore.

Authors:  Neha Kumar; Erin Turbitt; Barbara B Biesecker; Ilana M Miller; Breana Cham; Katherine C Smith; Rajiv N Rimal
Journal:  Am J Med Genet A       Date:  2019-03-01       Impact factor: 2.802

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

Authors:  Nancy E Kass; Amy M Medley; Marvin R Natowicz; Sara Chandros Hull; Ruth R Faden; Laura Plantinga; Lawrence O Gostin
Journal:  Am J Med Genet A       Date:  2007-04-01       Impact factor: 2.802

3.  Research participants' attitudes towards the confidentiality of genomic sequence information.

Authors:  Leila Jamal; Julie C Sapp; Katie Lewis; Tatiane Yanes; Flavia M Facio; Leslie G Biesecker; Barbara B Biesecker
Journal:  Eur J Hum Genet       Date:  2013-11-27       Impact factor: 4.246

Review 4.  Disclosure of genetic information within families.

Authors:  Agatha M Gallo; Denise B Angst; Kathleen A Knafl
Journal:  Am J Nurs       Date:  2009-04       Impact factor: 2.220

  4 in total

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