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1.
Eur J Hum Genet ; 28(1): 108-113, 2020 01.
Artigo em Inglês | MEDLINE | ID: mdl-31281182

RESUMO

We report previously undocumented evidence of genetic discrimination by Australian insurance companies, obtained through direct consumer reports. We surveyed 174 consumers with cancer-predisposing variants, recruited by cancer organisations Lynch Syndrome Australia and Pink Hope. Questions related to experiences accessing risk-rated insurance after genetic testing. Results indicate that both legal (permitted under current regulation) and illegal discrimination is occurring. Although some respondents had not applied for risk-rated insurance, or had insurance in place before genetic testing (n = 100), those seeking new policies (n = 74) commonly experienced difficulties obtaining insurance (86%, 64/74). Of those experiencing difficulties, 50% (32/64) had no prior history or symptoms of cancer, and had undertaken risk reduction through surveillance and/or preventative surgery. Seventy-seven percent (49/64) reported difficulties related to life insurance. Follow-up telephone interviews with four respondents further described cases of apparent illegal breaches. All reports of discrimination identified were, to our knowledge, previously unreported in the literature. The number of cases suggests a systemic problem with the Australian life insurance industry. We support calls for government oversight of the inherently conflicted model of industry self-regulation in Australia, and an immediate ban on the use of genetic test results in insurance underwriting.


Assuntos
Neoplasias Colorretais Hereditárias sem Polipose/psicologia , Predisposição Genética para Doença , Seleção Tendenciosa de Seguro , Seguro Saúde/estatística & dados numéricos , Austrália , Neoplasias Colorretais Hereditárias sem Polipose/economia , Neoplasias Colorretais Hereditárias sem Polipose/epidemiologia , Testes Genéticos/estatística & dados numéricos , Humanos , Pacientes/psicologia , Discriminação Social , Inquéritos e Questionários
2.
Eur J Hum Genet ; 28(1): 137, 2020 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-31358952

RESUMO

An amendment to this paper has been published and can be accessed via a link at the top of the paper.

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