Genetic discrimination by insurance companies in Aotearoa New Zealand: experiences and views of health professionals

被引:0
|
作者
Fraser, Harry [1 ]
Gamet, Kimberley [1 ]
Jackson, Sally [2 ]
Shelling, Andrew Neil [3 ]
Lacaze, Paul [4 ]
Tiller, Jane [4 ,5 ]
机构
[1] Auckland City Hosp, Genet Hlth Serv New Zealand Northern Hub, Auckland, New Zealand
[2] Wellington Reg Hosp, Genet Hlth Serv New Zealand Cent Hub, Wellington, New Zealand
[3] Univ Auckland, Fac Med & Hlth Sci, Auckland, New Zealand
[4] Monash Univ, Sch Publ Hlth & Prevent Med, Publ Hlth Genom, Melbourne, Australia
[5] Australian Genom, Melbourne, Australia
关键词
KNOWLEDGE;
D O I
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中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
AIMS: Genetic discrimination in insurance is a significant clinical, research and consumer issue. Recently, the Australian life insurance industry introduced a partial moratorium on the use of genetic test results. However, in Aotearoa New Zealand, both life and health insurers can still use genetic results legally to discriminate against applicants. We aimed to document experiences and concerns of New Zealand-based health professionals (HPs) around the potential misuse of genetic test results for insurance purposes.METHODS: We administered an online survey to New Zealand HPs who discuss genetic testing with patients, their experiences regarding the use of genetic test results in insurance and views on regulation.RESULTS: Twenty-three New Zealand HPs responded, 15 of whom worked in genetics clinics, representing >60% of the total New Zealand clinical genetics workforce. Eleven respondents reported having patients who experienced adverse outcomes related to insurance based on genetic results. Respondents reported patients sometimes/often delayed (n=11) or refused (n=4) genetic testing due to insurance concerns. Over 80% of those who answered (n=17/21) believe insurers' use of genetic results should be legally regulated.CONCLUSION: New Zealand HPs have concerns about insurance companies using genetic test results in underwriting, including the effect on patients, and strongly believe government legislation is required.
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页码:32 / 52
页数:21
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