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The Legacy of the U. S. Public Health Services Study of Untreated Syphilis in African American Men at Tuskegee on the Affordable Care Act and Health Care Reform Fifteen Years After President Clinton’s Apology

机译:在克林顿总统道歉之后在Tuskegee对非洲裔美国男子在非洲裔美国男子的非洲裔美国男子未经处理的梅毒研究的遗产

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摘要

This special issue addresses the legacy of the United States Public Health Service Syphilis Study on health reform, particularly the Affordable Care Act (ACA). The 12 manuscripts cover the history and current practices of ethical abuses affecting American Indians, Latinos, Asian Americans and African Americans in the United States and in one case, internationally. Commentaries and essays include the voice of a daughter of one of the study participants in which we learn of the stigma and maltreatment some of the families experienced and how the study has impacted generations within the families. Consideration is given in one essay to utilizing narrative storytelling with the families to help promote healing.This article provides the reader a roadmap to the themes that emerged from the collection of articles. These themes include population versus individual consent issues, need for better government oversight in research and health care, the need for overhauling our bioethics training to develop a population level, culturally driven approach to research bioethics. The articles challenge and inform us that some of our assumptions about how the consent process best works to protect racial/ethnic minorities may be merely assumptions and not proven facts. Articles challenge the belief that low participation rates seen in biomedical studies have resulted from the legacy of the USPHS Syphilis Study rather than a confluence of factors rooted in racism, bias and negative treatment. Articles in this special issue challenge the “cultural paranoia” of mistrust and provide insights into how the distrust may serve to lengthen rather than shorten the lives of racial/ethnic minorities who have been used as guinea pigs on more than one occasion. We hope that the guidance offered on the importance of developing a new framework to bioethics can be integrated into the foundation of health care reform.
机译:本特刊探讨了美国公共卫生服务梅毒研究机构关于医疗改革的遗留问题,特别是《平价医疗法案》(ACA)。这12篇手稿涵盖了在美国乃至国际上影响美国印第安人,拉美裔,亚裔美国人和非裔美国人的道德虐待的历史和当前做法。评论和文章包括一位研究参与者的女儿的声音,我们从中了解到一些经历过的家庭受到的污名和虐待,以及这项研究如何影响了家庭中的后代。在一篇文章中考虑了与家人一起利用叙事叙事来促进康复。本文为读者提供了从文章集中出现的主题的路线图。这些主题包括人口与个人同意问题,需要对政府在研究和医疗保健方面进行更好的监督,需要对我们的生物伦理学培训进行全面改革以开发人口层次,文化驱动的研究生物伦理学的方法。这些文章挑战并告知我们,关于同意过程如何最好地保护种族/族裔少数群体的一些假设可能仅仅是假设,而不是事实。文章挑战了这样一种信念,即生物医学研究中的低参与率是由于USPHS梅毒研究的遗留下来的,而不是源于种族主义,偏见和负面对待的因素的融合。这一期特刊的文章挑战了不信任的“文化偏执”,并提供了有关不信任如何延长而不是缩短曾多次被用作豚鼠的种族/族裔人的寿命的见解。我们希望,就开发新的生物伦理学框架的重要性提供的指导意见可以纳入卫生保健改革的基础。

著录项

  • 期刊名称 other
  • 作者

    Vickie M. Mays;

  • 作者单位
  • 年(卷),期 -1(22),6
  • 年度 -1
  • 页码 411–418
  • 总页数 8
  • 原文格式 PDF
  • 正文语种
  • 中图分类
  • 关键词

    Tuskegee research bioethics survivors;

    机译:塔斯基吉;研究生物伦理学;幸存者;
  • 入库时间 2022-08-21 11:23:13

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