Palo Renda J, Dulaney Bumpers Qran, Mohsenian Yasamin
Sterile Processing and Supply Chain, Seattle Children's Hospital, Seattle, Wash.
Pediatr Qual Saf. 2020 Dec 28;6(1):e371. doi: 10.1097/pq9.0000000000000371. eCollection 2021 Jan-Feb.
At Seattle Children's Hospital, in November 2016, the operating room (OR) physicians reported experiencing a high number of issues occurring during cases and believed a significant amount was related to sterile processing department (SPD) errors. These errors, hereafter called "defects," were not defined or routinely reported. There was no method of capturing these defects. There was no root cause analysis or trending of defect data. This project aimed to improve the quality of surgical instruments received in the OR.
The SPD and OR leaders collaborated to develop an OR Case Sign-Out form to capture defects during the case. The data were triaged and assigned to specific departments for root cause analysis. The SPD related data were depicted with a Pareto chart to highlight the most significant opportunities for improvement. We developed a driver diagram and identified the following interventions: orientation and competency, technician OR rotation, capacity/full-time employee analysis, surgical instruments inventory, instrument pouch work trigger, work environment, preventative maintenance, and instrument wrap reduction.
A 56% improvement in "Non-Sterile" defects was achieved. While a centerline shift in "Sterile" defects was not observed, the most significant "Sterile" defect, "breach of soft instrument wrap," dropped from 8 occurrences (at baseline) to 1. The number of OR case sign-out forms collected plateaued at 47%, which could indicate missing defect data.
SPD improved quality in the OR by reducing instrument defects. The physicians gained a mechanism for reporting barriers and tracking improvements. Ultimately, the utilization of lean tools and a quality improvement approach helped drive process changes, creating a more efficient, collaborative, and safe procedural environment for patients and staff.
2016年11月,在西雅图儿童医院,手术室(OR)医生报告称,手术过程中出现了大量问题,并且认为其中很大一部分与无菌处理部门(SPD)的错误有关。这些错误,以下称为“缺陷”,此前未进行定义或常规报告。没有收集这些缺陷的方法。没有对缺陷数据进行根本原因分析或趋势分析。该项目旨在提高手术室收到的手术器械的质量。
SPD和手术室负责人合作开发了一份手术室病例交接表,以在手术过程中捕捉缺陷。对数据进行分类,并分配给特定部门进行根本原因分析。用帕累托图描绘与SPD相关的数据,以突出最显著的改进机会。我们绘制了驱动图,并确定了以下干预措施:入职培训和能力培训、技术人员手术室轮岗、工作量/全职员工分析、手术器械库存、器械包工作触发机制、工作环境、预防性维护以及减少器械包装。
“非无菌”缺陷减少了56%。虽然未观察到“无菌”缺陷的中心线偏移,但最显著的“无菌”缺陷“软器械包装破损”从(基线时的)8次降至1次。收集的手术室病例交接表数量稳定在47%,这可能表明存在缺陷数据缺失的情况。
SPD通过减少器械缺陷提高了手术室的质量。医生们获得了一种报告障碍和跟踪改进情况的机制。最终,精益工具和质量改进方法的运用有助于推动流程变革,为患者和工作人员创造了一个更高效、协作性更强且安全的手术环境。