Center of Reproductive Medicine, Department of Obstetrics and Gynecology, Azienda Unità Sanitaria Locale-IRCCS di Reggio Emilia, Viale Risorgimento 80, 42123 Reggio Emilia, Italy.
Unit of Medical Genetics, Azienda Ospedaliero-Universitaria di Ferrara, Via Fossato di Mortara, 74, 44121 Ferrara, Italy.
Biomed Res Int. 2021 Oct 21;2021:1126270. doi: 10.1155/2021/1126270. eCollection 2021.
In IVF centers, risk assessment applies to complex processes potentially accounting for adverse events and reactions that undergo well-established legislative oversight, and nonconformances (NCs), that lack of established tracking systems. NCs account for an integral part of the quality management system, so that their documentation is important. The study evaluated the performance of a customized tool for incident reporting (IR) to track and characterize NCs in a public IVF center. IVF operators used the IVF-customized IR tool to record NCs at the moment of detection or subsequently, and in a time-saving manner during daily practice. From February 2015 to February 2020, 635 NCs were reported leading to the implementation of 10 operative instructions and 3 procedures with corrective strategies. NCs referred to the IVF laboratory were the most numerically meaningful (454/635, 71.5%). The majority (352/454, 77.5%) accounted for NCs related to procedures of sample management; considering the analytical phase as all the procedures involving sample treatment, the intra-analytical phase (176/352, 50%) has always been more subject to NCs compared to pre- (102/352, 29%) and postanalytical (74/352, 21%) phases. Our experience showed that the IVF-customized IR tool is suitable for application in IVF with regard to NC reports and documentation, as it identifies the most vulnerable steps of treatments. It manages NCs over the time, but it requires a contextual understanding of its application in order to avoid NC underestimates that could negatively influence the safety and quality aspects of IVF treatments.
在体外受精中心,风险评估适用于可能导致不良事件和反应的复杂过程,这些过程需要经过完善的立法监督和缺乏既定跟踪系统的不符合项 (NC)。NC 是质量管理体系的一个组成部分,因此其文件记录非常重要。本研究评估了一个定制的不良事件报告 (IR) 工具在一个公共体外受精中心跟踪和描述 NC 的性能。体外受精操作人员使用 IVF 定制的 IR 工具在检测到或随后的时间,以及在日常实践中节省时间的方式记录 NC。从 2015 年 2 月到 2020 年 2 月,报告了 635 例 NC,导致实施了 10 项操作指令和 3 项带有纠正策略的程序。NC 涉及体外受精实验室的数量最多(454/635,71.5%)。大多数(352/454,77.5%)与样本管理程序的 NC 有关;考虑到分析阶段是所有涉及样本处理的程序,与预分析阶段(102/352,29%)和后分析阶段(74/352,21%)相比,分析阶段(176/352,50%)总是更容易出现 NC。我们的经验表明,IVF 定制的 IR 工具适用于体外受精中的 NC 报告和文件记录,因为它可以识别出治疗中最脆弱的步骤。它可以随着时间的推移管理 NC,但需要对其应用有深入的了解,以避免 NC 低估,从而对体外受精治疗的安全性和质量产生负面影响。