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Protecting human subjects from harm in medical research: A proposal for improving risk judgments by institutional review boards

机译:保护人体免受医学研究的伤害:机构审查委员会提出的改善风险判断的建议

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摘要

Our concern for the way biomedical research is conducted has been evidenced in codes of ethics and in federal and international guidelines which emphasize the protection of the rights and welfare of research subjects. While there is agreement that research subjects ought to be protected from harm, Institutional Review Boards (IRBs) may be unable to assess meaningfully the risks of harm in relation to the hoped for benefits of research required in regulations and guidelines because they lack the technical and philosophical expertise to do so. In particular, IRBs are unable to make judgments about the risks of harm to subjects. Analysis of fundamental terms such as harm and risk led to the following conclusions. First, there can be several meanings of harm depending on whether a medical, philosophical or jurisprudential theory is adopted. Second, while risk is understood to express the probability and magnitude of a future harm, there are several objective and subjective considerations that affect the identification, estimation and evaluation of risk. Two considerations were found to be especially relevant: the availability of empirical data and the conduct of risk assessment by experts and non-experts. Emphasis should be placed on quantifying the risks of harm where possible and seeking methods for involving IRBs and subjects in risk judgments. Analysis of taxonomies by Jay Katz and Robert Levine showed them to be useful guides for identifying types of harm; however, they offered little insight as to how risk judgments might be improved. Decision analysis was found to be too restrictive for the protocol review environment although its quantitative, explicit and prescriptive features suggest that it is worthy of continued study. A four-cell matrix is developed that accounts for the contributions of IRBs and subjects in the presence and absence of data. Two cases are offered to illustrate the utility of the matrix for improving the risk judgments of IRBs.
机译:我们对生物医学研究方式的关注已在道德守则以及强调保护研究对象的权利和福利的联邦和国际准则中得到了证明。尽管已经同意应该保护研究对象免受伤害,但是机构审查委员会(IRB)可能无法根据法规和指南中要求的研究收益来有意义地评估伤害风险,因为他们缺乏技术和知识。这样做的哲学专业知识。特别是,IRB无法判断对受试者造成伤害的风险。对基本术语(例如危害和风险)的分析得出以下结论。首先,取决于是否采用医学,哲学或法学理论,伤害可能有多种含义。其次,虽然风险被理解为表示未来危害的可能性和严重程度,但还是有一些客观和主观的考虑因素会影响风险的识别,估计和评估。发现有两个考虑因素特别相关:经验数据的可用性以及专家和非专家进行的风险评估。应着重于在可能的情况下量化危害的风险,并寻求使IRB和主体参与风险判断的方法。 Jay Katz和Robert Levine对分类法的分析表明,它们是识别危害类型的有用指南。但是,他们对如何改进风险判断几乎没有见识。尽管决策分析的定量,明确和说明性特征表明它值得继续研究,但发现对于协议审查环境而言,决策分析过于严格。建立了一个四单元矩阵,该矩阵考虑了存在和不存在数据时IRB和受试者的贡献。提供了两种情况来说明矩阵在改善IRB风险判断方面的效用。

著录项

  • 作者

    Meslin, Eric Mark.;

  • 作者单位

    Georgetown University.;

  • 授予单位 Georgetown University.;
  • 学科 Philosophy.;Health sciences.
  • 学位 Ph.D.
  • 年度 1989
  • 页码 343 p.
  • 总页数 343
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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