The Ethics of Cancer Screening Based on Race and Ethnicity.

IF 19.6 1区 医学 Q1 MEDICINE, GENERAL & INTERNAL
Duco T Mülder, James F O'Mahony, Chyke A Doubeni, Iris Lansdorp-Vogelaar, Maartje H N Schermer
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Abstract

Racial and ethnic disparities in incidence and mortality are well documented for many types of cancer. As a result, there is understandable policy and clinical interest in race- and ethnicity-based clinical screening guidelines to address cancer health disparities. Despite the theoretical benefits, such proposals do not typically address associated ethical considerations. Using the examples of gastric cancer and esophageal adenocarcinoma, which have demonstrated disparities according to race and ethnicity, this article examines relevant ethical arguments in considering screening based on race and ethnicity.

Race- and ethnicity-based clinical preventive care services have the potential to improve the balance of harms and benefits of screening. As a result, programs focused on high-risk racial or ethnic groups could offer a practical alternative to screening the general population, in which the screening yield may be too low to demonstrate sufficient effectiveness. However, designing screening according to socially based categorizations such as race or ethnicity is controversial and has the potential for intersectional stigma related to social identity or other structurally mediated environmental factors. Other ethical considerations include miscategorization, unintended negative effects on health disparities, disregard for underlying risk factors, and the psychological costs of being assigned higher risk.

Given the ethical considerations, the practical application of race and ethnicity in cancer screening is most relevant in multicultural countries if and only if alternative proxies are not available. Even in those instances, policymakers and clinicians should carefully address the ethical considerations within the historical and cultural context of the intended population. Further research on alternative proxies, such as social determinants of health and culturally based characteristics, could provide more adequate factors for risk stratification.

基于种族和民族的癌症筛查伦理。
在许多类型的癌症中,种族和民族在发病率和死亡率方面的差异都有据可查。因此,人们对基于种族和民族的临床筛查指南的政策和临床兴趣是可以理解的,以解决癌症健康差异问题。尽管有理论上的好处,但这些建议通常并不涉及相关的伦理考虑。本文以胃癌和食管腺癌为例,探讨了在考虑基于种族和民族的筛查时的相关伦理论点。因此,以高风险种族或民族群体为重点的项目可以为普通人群筛查提供一个实用的替代方案,因为普通人群的筛查率可能太低,无法显示出足够的有效性。然而,根据种族或民族等社会分类来设计筛查是有争议的,有可能造成与社会身份或其他结构性环境因素相关的交叉污名。其他伦理方面的考虑还包括分类不当、对健康差异产生意想不到的负面影响、忽视潜在的风险因素以及被认为风险较高的心理代价。即使在这种情况下,政策制定者和临床医生也应在目标人群的历史和文化背景下仔细考虑伦理因素。对健康的社会决定因素和基于文化的特征等替代代用指标的进一步研究可为风险分层提供更充分的因素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Annals of Internal Medicine
Annals of Internal Medicine 医学-医学:内科
CiteScore
23.90
自引率
1.80%
发文量
1136
审稿时长
3-8 weeks
期刊介绍: Established in 1927 by the American College of Physicians (ACP), Annals of Internal Medicine is the premier internal medicine journal. Annals of Internal Medicine’s mission is to promote excellence in medicine, enable physicians and other health care professionals to be well informed members of the medical community and society, advance standards in the conduct and reporting of medical research, and contribute to improving the health of people worldwide. To achieve this mission, the journal publishes a wide variety of original research, review articles, practice guidelines, and commentary relevant to clinical practice, health care delivery, public health, health care policy, medical education, ethics, and research methodology. In addition, the journal publishes personal narratives that convey the feeling and the art of medicine.
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