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失效模式与效应分析如何改进 ART 中心的工作流程?

How can the failure mode and effect analysis improve the working processes in the ART center?

机构信息

BetaPlus Center for Reproductive Medicine, Ulica Charlesa Darwina 6H, 10 000 Zagreb, Croatia.

出版信息

Eur J Obstet Gynecol Reprod Biol. 2024 Nov;302:43-55. doi: 10.1016/j.ejogrb.2024.08.041. Epub 2024 Aug 28.

DOI:10.1016/j.ejogrb.2024.08.041
PMID:39217759
Abstract

OBJECTIVE(S): Assisted reproductive technology (ART) Centers and laboratories perform complex tasks with patients and their gametes/embryos daily. The degree of problems/non-conformances in such surroundings must be minimized at zero point. This study aimed to establish the proper risk management system with well-defined process steps to prevent and eliminate problems/non-conformances.

STUDY DESIGN

Failure mode and effect analysis (FMEA) was introduced in the ART Center and the IVF laboratory. ART Center working processes were grouped into the categories of Clinical procedures, Forms, Identification, Personnel, Patients, and Facility. Working processes in the IVF laboratory were grouped into the categories of Consumables, Media, Equipment, Personnel, Working space, and Procedures. The traceability and safety of the working processes were evaluated before and after corrective measures regarding risk priority number (RPN). The severity (S), occurrence (O), and detection (D) index of problems/non-conformance were scaled from 1 to 5. The RPN was calculated by multiplying the SOD index, and the cut-off value for RPN was ≥12.

RESULTS

The increased RPN was found in the following working processes of the ART Center: Embryo transfer and pregnancy (RPN = 18) in the category of Clinical procedures; Informed consents and agreements (RPN = 16) in the category Forms; Continuous education of the knowledge and skills (RPN = 12) in Personnel category; Space conditions (RPN = 24) and Equipment (RPN = 12) in the category Facility. In the IVF laboratory, increased RPN was found in the following working processes: Production of the plasticware (RPN = 12), Transport (RPN = 12) and Storage (RPN = 12) in the category Consumables; Media production (RPN = 16) in category Media; Alarm notification system for the critical equipment (RPN = 12) in category Equipment; Personnel number and qualifications (RPN = 12), Standard operative procedures (SOP) (RPN = 12) and Continuous education of the knowledge and skills (RPN = 12) in category Personnel; Working conditions (RPN = 18) and Security (RPN = 20) in Working space; Patient identification (RPN = 20), Biological samples identification (RPN = 20), Records (RPN = 12), ART procedure (RPN = 30), Embryo transfer (RPN = 30) and Cryopreservation and thawing of biological samples (RPN = 30) in category Procedures. According to the RPN score, corrective measures were implemented. Most RPN scores were reduced after the implementation of the electronic witnessing system in patient/sample tracing steps. Phases Patient identification and Biological sample identification showed a double reduction of RPN scores, from 20 to 10. Also, for critical steps in ART procedures, Embryo transfer, Cryopreservation, and thawing of biological samples, the RPN score was reduced from 30 to 10. Proper education of personnel was another corrective measure that significantly contributed to a reduction of RPN scores in most of the categories.

CONCLUSION(S): The FMEA analysis is useful in recognizing the critical steps of an ART Center. The RPN scores for patient traceability were successfully reduced using the electronic witnessing system. Nonetheless, the study has certain limitations, as FMEA is highly dependent on the specific healthcare organization, adherence to national guidelines, and the subjective nature of SOD and RPN evaluations.

摘要

目的

辅助生殖技术(ART)中心和实验室每天都要处理患者及其配子/胚胎的复杂任务。必须将此类环境中的问题/不符合项的程度降到最低。本研究旨在建立适当的风险管理系统,制定明确的流程步骤,以预防和消除问题/不符合项。

研究设计

失败模式与效应分析(FMEA)被引入到 ART 中心和体外受精(IVF)实验室。ART 中心的工作流程被分为临床程序、表格、识别、人员、患者和设施六类。IVF 实验室的工作流程分为耗材、培养基、设备、人员、工作空间和程序六类。在采取纠正措施前后,根据风险优先数(RPN)评估工作流程的可追溯性和安全性。问题/不符合项的严重度(S)、发生度(O)和检出度(D)指数从 1 到 5 进行划分。RPN 通过 SOD 指数相乘计算得出,RPN 的截断值为≥12。

结果

ART 中心的胚胎移植和妊娠(临床程序类,RPN=18)、知情同意书和协议(表格类,RPN=16)、人员的知识和技能的持续教育(人员类,RPN=12)、空间条件(设施类,RPN=24)和设备(设施类,RPN=12)的工作流程 RPN 增加。在 IVF 实验室,增加的 RPN 见于以下工作流程:塑料器皿的生产(耗材类,RPN=12)、运输(耗材类,RPN=12)和储存(耗材类,RPN=12)、培养基的生产(培养基类,RPN=16)、关键设备的报警通知系统(设备类,RPN=12)、人员数量和资质(人员类,RPN=12)、标准操作程序(SOP)(人员类,RPN=12)和知识和技能的持续教育(人员类,RPN=12)、工作条件(工作空间类,RPN=18)和安全(工作空间类,RPN=20)、患者识别(程序类,RPN=20)、生物样本识别(程序类,RPN=20)、记录(程序类,RPN=12)、ART 程序(程序类,RPN=30)、胚胎移植(程序类,RPN=30)和生物样本的冷冻保存和解冻(程序类,RPN=30)。根据 RPN 评分实施了纠正措施。在实施患者/样本追踪步骤的电子见证系统后,大多数 RPN 评分都有所降低。在患者识别和生物样本识别两个环节,RPN 评分从 20 降至 10,实现了双重降低。ART 程序中的关键步骤,如胚胎移植、冷冻保存和生物样本解冻,RPN 评分从 30 降至 10。对人员进行适当的教育也是一项纠正措施,这对降低大多数类别中的 RPN 评分起到了重要作用。

结论

失败模式与效应分析有助于识别 ART 中心的关键步骤。使用电子见证系统成功降低了患者追踪的 RPN 评分。然而,FMEA 高度依赖于特定的医疗保健组织、对国家指南的遵守情况,以及 SOD 和 RPN 评估的主观性,因此本研究存在一定的局限性。

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