Department of Radiation Medicine, Oregon Health & Science University, Portland, Oregon, USA.
Department of Radiation Oncology, The Ohio State University, Columbus, Ohio, USA.
J Appl Clin Med Phys. 2024 Apr;25(4):e14261. doi: 10.1002/acm2.14261. Epub 2024 Jan 9.
To identify high-priority risks in a clinical trial investigating the use of radiation to alleviate COVID-19 pneumonia using a multi-phase failure modes and effects analysis (FMEA).
A comprehensive FMEA survey of 133 possible causes of failure was developed for the clinical trial workflow (Phase I). The occurrence, severity, and detection risk of each possible cause of failure was scored by three medical physicists. High-risk potential failure modes were identified using the risk priority number (RPN) and severity scores, which were re-scored by 13 participants in radiation oncology (Phase II). Phase II survey scores were evaluated to identify steps requiring possible intervention and examine risk perception patterns. The Phase II participants provided consensus scores as a group.
Thirty high-priority failure modes were selected for the Phase II survey. Strong internal consistency was shown in both surveys using Cronbach's alpha (α ≥ 0.85). The 10 failures with the largest median RPN values concerned SARS-CoV-2 transmission (N = 6), wrong treatment (N = 3), and patient injury (N = 1). The median RPN was larger for COVID-related failures than other failure types, primarily due to the perceived difficulty of failure detection. Group re-scoring retained 8/10 of the highest-priority risk steps that were identified in the Phase II process, and discussion revealed interpretation differences of process steps and risk evaluation. Participants who were directly involved with the trial working group had stronger agreement on severity scores than those who were not.
The high ranking of failures concerning SARS-CoV-2 transmission suggest that these steps may require additional quality management intervention when treating critically ill COVID-19+ patients. The results also suggest that a multi-phase FMEA survey led by a facilitator may be a useful tool for assessing risks in radiation oncology procedures, supporting future efforts to adapt FMEA to clinical procedures.
通过多阶段失效模式与影响分析(FMEA),确定使用辐射缓解 COVID-19 肺炎的临床试验中的高优先级风险。
针对临床试验工作流程(第一阶段),开发了一项综合的 FMEA 调查,涵盖了 133 种可能导致失败的原因。三位医学物理学家对每种可能导致失败的原因的发生、严重程度和检测风险进行了评分。使用风险优先数(RPN)和严重程度评分确定高风险潜在失效模式,然后由 13 名放射肿瘤学参与者(第二阶段)重新评分。评估第二阶段调查评分,以确定需要干预的步骤,并检查风险感知模式。第二阶段参与者作为一个小组提供了共识评分。
选择了 30 个高优先级失效模式进行第二阶段调查。两个阶段的调查都表现出了很强的内部一致性,克朗巴赫的α值(α≥0.85)。第二阶段调查中,RPN 值中位数最大的 10 个失效模式涉及 SARS-CoV-2 传播(N=6)、错误治疗(N=3)和患者损伤(N=1)。与其他失效类型相比,与 COVID 相关的失效的 RPN 值中位数更大,主要是因为检测失效的难度较大。重新评分保留了第二阶段过程中确定的 8/10 个最高优先级风险步骤,讨论揭示了对过程步骤和风险评估的不同解释。直接参与试验工作组的参与者对严重程度评分的一致性强于未参与的参与者。
SARS-CoV-2 传播相关失效的高排名表明,在治疗重症 COVID-19+患者时,这些步骤可能需要额外的质量管理干预。结果还表明,由主持人领导的多阶段 FMEA 调查可能是评估放射肿瘤学程序风险的有用工具,为未来将 FMEA 应用于临床程序的努力提供支持。