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Social and ethical implications of genomics, race, ethnicity, and health inequities.

机译:基因组学,种族,种族和健康不平等对社会和伦理的影响。

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摘要

OBJECTIVES: To review ethical, ethnic/ancestral, and societal issues of genetic and genomic information and technologies in the context of racial and ethnic health disparities. DATA SOURCES: Research and journal articles, government reports, web sites. CONCLUSION: As knowledge of human genetic variation and its link to diseases continues to grow, some see race and ethnicity well poised to serve as genetic surrogates in predicting disease etiology and treatment response. However, stereotyping and bias in clinical interactions can be barriers to effective treatment for racial and ethnic minority patients. IMPLICATIONS FOR NURSING PRACTICE: The nursing profession has a key role in assuring that genomic health care does not enhance racial and ethnic health inequities. This will require utilization of new genomic knowledge and caring for each patient as an individual in a culturally and clinically appropriate manner.
机译:目标:在种族和族裔健康差异的背景下,审查遗传和基因组信息和技术的伦理,族裔/祖传和社会问题。数据来源:研究和期刊文章,政府报告,网站。结论:随着对人类遗传变异及其与疾病联系的认识的不断增长,一些人认为种族和种族已准备好作为遗传替代物来预测疾病的病因和治疗反应。但是,临床互动中的陈规定型观念和偏见可能成为有效治疗种族和少数族裔患者的障碍。护理实践的意义:护理行业在确保基因组医疗保健不会加剧种族和族裔健康不平等方面起着关键作用。这将需要利用新的基因组学知识并以文化和临床上适当的方式照顾每一位患者。

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