“认识到偏见就是消除偏见”:关于偏见数据集如何导致有色人种(POC)和女性患者长期误诊的文献综述

Shreerachita Satish, Zoya Pal
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引用次数: 0

摘要

健康差距不成比例地影响少数群体患者。各种因素造成健康不平等,包括社会经济地位、偏见和歧视。从历史上看,医疗文献中偏向白人男性的样本偏见导致某些群体在科学文献中的代表性不足,特别是有色人种(POC)和女性群体。许多医疗保健研究中的革命性研究使用了有偏差的样本,这挑战了它们对POC和女性人群的普遍性。这篇综述探讨了在精神病学和生物医学环境中,这些文献空白导致POC和女性患者误诊的机制。方法:通过全面的文献回顾,调查:(1)文献中对少数民族的错误描述;(2)女性和POC人群的疾病和疾病的症状学和病因学差异;(3)在公认的诊断措施和标准中的偏差。研究人员使用PubMed、PsychINFO和Google Scholar等电子数据库来搜索关键词,包括“健康不平等”、“跨文化有效性”、“种族差异”、“性别差异”、“诊断延迟”、“误诊”、“临床异质性”。结果:87项研究被检查,38项研究被纳入综述。研究结果表明,对群体成员的错误分类、对少数群体身份的概念化不佳、对症状变化的理解不足、排除社会背景、缺乏文化敏感的方法、有偏见的诊断工具以及历史数据集中缺乏不同的样本,这些都导致了医学文献中少数群体代表性的有害缺陷。讨论:医疗文献的偏见导致了医学研究中少数民族人口的系统性代表性不足,并导致了这些群体的误诊和随后的卫生不平等。目前的研究结果强调有必要以合理的怀疑态度看待过去的健康研究,并呼吁优先考虑包容性和多样化的研究。结论:这篇综述揭示了如何通过强调少数民族人群在医疗保健领域的差异影响以及确定使这些差异持续存在的因素来弥补有偏见的研究造成的文献不足。必须对所检查的因素进行进一步研究,以制定方法,减少POC和女性患者的误诊率和随后的卫生不平等现象。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
“A Bias Recognized is A Bias Sterilized”: A Literature Review on How Biased Datasets Have Led to the Long-standing Misdiagnosing of People of Color (POC) and Female Patients
Introduction: Health disparities disproportionately impact minority group patients. Various factors perpetuate health inequity, including socioeconomic status, prejudice and discrimination. Historically, sample biases favoring White males in healthcare literature have led to the underrepresentation of certain groups in scientific literature, particularly people of color (POC) and female populations. Many revolutionary studies in healthcare research have used biased samples, which challenges their generalizability to POC and female populations. This review explores the mechanisms by which these gaps in the literature have led to the misdiagnoses of POC and female patients in psychiatric and biomedical settings. Methods: A comprehensive literature review was conducted to investigate: (1) misrepresentation of minority groups in literature, (2) variation in the symptomatology and etiology of disorders and diseases in female and POC populations; and (3) biases within accepted diagnostic measures and criteria. Electronic databases such as PubMed, PsychINFO and Google Scholar were used to search key terms including ‘health inequity’, ‘cross-cultural validity’, ‘racial disparities’, ‘sex disparities’, ‘diagnostic delays’, ‘misdiagnosis’, ‘clinical heterogeneity’. Results: Eighty-seven studies were examined, and 38 studies were included in the review. Findings suggest that misclassification of group membership, poor conceptualizations of minority identities, inadequate understanding of symptomatology variation, exclusion of social context, lack of culturally sensitive approaches, biased diagnostic tools and an absence of diverse samples in historical datasets have resulted in a harmful deficit in minority representation within medical literature. Discussion: Bias in healthcare literature has led to the systematic underrepresentation of minority populations in medical research and contributes to the misdiagnosis and subsequent health inequities within these groups. Present findings emphasize the necessity to regard past health research with reasonable skepticism and a call for prioritization of inclusive and diverse research. Conclusion: This review sheds light on how to bridge the literature deficit caused by biased research through highlighting how minority populations are differentially impacted within the healthcare field and identifying factors that perpetuate these disparities. Further research on the examined factors must be conducted to develop approaches to mitigate misdiagnosis rates and subsequent health inequities among POC and female patients.
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