Views Of Primary Care Providers On Testing Patients For Genetic Risks For Common Chronic Diseases

被引:65
作者
Hauser, Diane [1 ]
Obeng, Aniwaa Owusu [2 ,3 ,4 ,5 ]
Fei, Kezhen [3 ,6 ]
Ramos, Michelle A. [3 ,6 ]
Horowitz, Carol R. [3 ,6 ]
机构
[1] Icahn Sch Med Mt Sinai, Inst Family Hlth, Ctr Hlth Equ & Community Engaged Res, New York, NY 10029 USA
[2] Icahn Sch Med Mt Sinai, Charles Bronfman Inst Personalized Med, New York, NY 10029 USA
[3] Icahn Sch Med Mt Sinai, Ctr Hlth Equ & Community Engaged Res, New York, NY 10029 USA
[4] Mt Sinai Hosp, Clin Pharmacogen, New York, NY 10029 USA
[5] Mt Sinai Hosp, Pharm Dept, New York, NY 10029 USA
[6] Icahn Sch Med Mt Sinai, Dept Populat Hlth Sci & Policy, New York, NY 10029 USA
关键词
GENOMIC MEDICINE; AFRICAN-AMERICAN; RACE; HEALTH; PHARMACOGENOMICS; ATTITUDES; ANCESTRY; SERVICES; ASSOCIATION; INFORMATION;
D O I
10.1377/hlthaff.2017.1548
中图分类号
R19 [保健组织与事业(卫生事业管理)];
学科分类号
摘要
We surveyed 488 primary care providers in community and academic practices in New York City in the period 2014-16 about their views on genetic testing for chronic diseases. The majority of the providers, most of whom were current or recent physicians in training, had had formal genetics education and had positive views of the utility of genetic testing. However, they felt unprepared to work with patients at high risk for genetic conditions and were not confident about interpreting test results. Many were concerned that genetic testing might lead to insurance discrimination and lacked trust in companies that offer genetic tests. These findings point to some of the attitudes and knowledge gaps among the providers that should be considered in the clinical implementation of genomic medicine for chronic conditions. Enhanced training, guidelines, clinical tools, and awareness of patient protections might support the effective adoption of genomic medicine by primary care providers.
引用
收藏
页码:793 / 800
页数:8
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