Abbott Lura, Grady Christine
Department of Bioethics, National Institutes of Health, Clinical Center, Building 10/1C118, Bethesda, MD 20892, USA.
J Empir Res Hum Res Ethics. 2011 Mar;6(1):3-19. doi: 10.1525/jer.2011.6.1.3.
Institutional review boards (IRBs) are integral to the U.S. system of protection of human research participants. Evaluation of IRBs, although difficult, is essential. To date, no systematic review of IRB studies has been published. We conducted a systematic review of empirical studies of U.S. IRBs to determine what is known about the function of IRBs and to identify gaps in knowledge. A structured search in PubMed identified forty-three empirical studies evaluating U.S. IRBs. Studies were included if they reported an empirical investigation of the structure, process, outcomes, effectiveness, or variation of U.S. IRBs. The authors reviewed each study to extract information about study objectives, sample and methods, study results, and conclusions. Empirical evidence collected in forty-three published studies shows that for review of a wide range of types of research, U.S. IRBs differ in their application of the federal regulations, in the time they take to review studies, and in the decisions made. Existing studies show evidence of variation in multicenter review, inconsistent or ambiguous interpretation of the federal regulations, and inefficiencies in review. Despite recognition of a need to evaluate effectiveness of IRB review, no identified published study included an evaluation of IRB effectiveness. Multiple studies evaluating the structure, process, and outcome of IRB review in the United States have documented inconsistencies and inefficiencies. Efforts should be made to address these concerns. Additional research is needed to understand how IRBs accomplish their objectives, what issues they find important, what quality IRB review is, and how effective IRBs are at protecting human research participants.
机构审查委员会(IRB)是美国保护人类研究受试者体系不可或缺的一部分。对IRB进行评估虽有难度,但至关重要。迄今为止,尚未发表对IRB研究的系统综述。我们对美国IRB的实证研究进行了系统综述,以确定关于IRB功能的已知情况,并找出知识空白。在PubMed中进行的结构化检索确定了43项评估美国IRB的实证研究。如果研究报告了对美国IRB的结构、流程、结果、有效性或差异的实证调查,则将其纳入。作者对每项研究进行了审查,以提取有关研究目标、样本和方法、研究结果及结论的信息。在43项已发表研究中收集的实证证据表明,对于广泛类型的研究审查,美国IRB在联邦法规的应用、审查研究所需的时间以及做出的决定方面存在差异。现有研究显示了多中心审查存在差异、对联邦法规的解释不一致或含混不清以及审查效率低下的证据。尽管认识到需要评估IRB审查的有效性,但未发现已发表的研究包括对IRB有效性的评估。多项评估美国IRB审查的结构、流程和结果的研究记录了不一致和效率低下的情况。应努力解决这些问题。需要进行更多研究,以了解IRB如何实现其目标、它们认为哪些问题重要、IRB审查的质量如何以及IRB在保护人类研究受试者方面的有效性如何。