Fiscella Kevin, Tobin Jonathan N, Carroll Jennifer K, He Hua, Ogedegbe Gbenga
Department of Family Medicine, University of Rochester Medical Center, Rochester, USA.
Family Medicine Research, 1381 South Ave, Rochester, NY, 14620, USA.
BMC Med Ethics. 2015 Sep 17;16(1):63. doi: 10.1186/s12910-015-0056-2.
Institutional review boards (IRBs) distinguish health care quality improvement (QI) and health care quality improvement research (QIR) based primarily on the rigor of the methods used and the purported generalizability of the knowledge gained. Neither of these criteria holds up upon scrutiny. Rather, this apparently false dichotomy may foster under-protection of participants in QI projects and over-protection of participants within QIR.
Minimal risk projects should entail minimal oversight including waivers for informed consent for both QI and QIR projects. Minimizing the burdens of conducting QIR, while ensuring minimal safeguards for QI projects, is needed to restore this imbalance in oversight. Potentially, such ethical oversight could be provided by the integration of Institutional Review Boards and Clinical Ethical Committees, using a more integrated and streamlined approach such as a two-step process involving a screening review, followed by a review by committee trained in QIR. Standards for such ethical review and training in these standards, coupled with rapid review cycles, could facilitate an appropriate level of oversight within the context of creating and sustaining learning health care systems. We argue that QI and QIR are not reliably distinguishable. We advocate for approaches that improve protections for QI participants while minimizing over-protection for participants in QIR through reasonable ethical oversight that aligns risk to participants in both QI and QIR with the needs of a learning health care system.
机构审查委员会(IRB)主要依据所使用方法的严谨性以及所获知识的所谓可推广性来区分医疗质量改进(QI)和医疗质量改进研究(QIR)。但经仔细审查,这两个标准都站不住脚。相反,这种看似错误的二分法可能会导致QI项目中参与者保护不足,而QIR中参与者保护过度。
低风险项目应进行最低限度的监督,包括免除QI和QIR项目的知情同意。需要在尽量减少QIR实施负担的同时,确保QI项目有最低限度的保障措施,以恢复这种监督方面的不平衡。潜在地,这种伦理监督可以通过整合机构审查委员会和临床伦理委员会来提供,采用一种更综合、简化的方法,比如两步流程,先进行筛选审查,然后由接受过QIR培训的委员会进行审查。这种伦理审查的标准以及这些标准的培训,再加上快速审查周期,可以在创建和维持学习型医疗系统的背景下促进适当水平的监督。我们认为QI和QIR并不能可靠地区分。我们主张采取一些方法,通过合理的伦理监督,在提高对QI参与者保护的同时,尽量减少对QIR参与者的过度保护,使QI和QIR中参与者面临的风险与学习型医疗系统的需求相匹配。