Geriatric Research, Education, and Clinical Center, Cleveland VA Medical Center, Cleveland, Ohio, USA.
Antimicrob Resist Infect Control. 2014 Jan 21;3(1):4. doi: 10.1186/2047-2994-3-4.
Failures to follow recommendations for reprocessing of surgical instruments may place patients at risk for exposure to pathogenic microorganisms. When such failures occur, medical facilities often face considerable uncertainty and challenges in assessing the actual risks of disease transmission.
In 2011, staff at an Ohio hospital determined that surgical instruments inside a Steriset Container had inadvertently been autoclaved on a gravity cycle rather than on the recommended pre-vacuum cycle, potentially exposing 72 patients who underwent surgery with the instruments to risk of infection. To provide an assessment of the level of risk, we tested the effectiveness of the machine washer/disinfector step and of the sterilization process inside the Steriset Container on the gravity cycle for killing of Geobacillus stearothermophilus spores, Clostridium difficile spores, and methicillin-resistant Staphylococcus aureus (MRSA). Based on the test results, the risk of transmission of MRSA by the instruments was calculated and the risk of transmission of hepatitis B virus was estimated.
The machine washer/disinfector consistently reduced MRSA recovery by a factor of 1:100,000. The sterilization process inside the Steriset Container consistently reduced MRSA concentrations by a factor of >1:10,000,000 and killed 105C. difficile spores and 105G. stearothermophilus spores. The risk of MRSA transmission due to the incident was calculated to be 1 in 100 trillion.
The risk for transmission of infection due to the failure to follow recommended sterilization processes was negligible based upon complete killing of G. stearothermophilus biological indicator spores, C. difficile spores, and MRSA under conditions that replicated the incident where proper procedures were not followed. Such real-time assessments of the risks associated with specific incidents may provide evidence-based information that can be used to inform decisions regarding disclosure of the incident to patients.
未能遵循手术器械再处理的建议可能使患者面临暴露于病原体的风险。当这种失败发生时,医疗机构在评估疾病传播的实际风险时往往面临相当大的不确定性和挑战。
2011 年,俄亥俄州一家医院的工作人员发现,Steriset 容器内的手术器械意外地在重力循环中而不是在推荐的预真空循环中进行了高压灭菌,可能使接受这些器械进行手术的 72 名患者面临感染风险。为了评估风险水平,我们测试了机器清洗器/消毒器步骤以及重力循环中 Steriset 容器内的灭菌过程对嗜热脂肪芽孢杆菌孢子、艰难梭菌孢子和耐甲氧西林金黄色葡萄球菌(MRSA)的杀菌效果。根据测试结果,计算了器械传播 MRSA 的风险,并估计了乙型肝炎病毒传播的风险。
机器清洗器/消毒器始终将 MRSA 的回收减少了 1:100000 的因素。Steriset 容器内的灭菌过程始终将 MRSA 浓度降低了 >1:10000000 的因素,并杀死了 105C. 艰难梭菌孢子和 105G. 嗜热脂肪芽孢杆菌孢子。由于该事件,MRSA 传播的风险估计为 1 万亿分之一。
根据未遵循推荐的灭菌过程导致感染传播的风险可以忽略不计,因为在未遵循适当程序的情况下,G. stearothermophilus 生物指示剂孢子、C. difficile 孢子和 MRSA 被完全杀死。这种对与特定事件相关的风险进行实时评估可能提供基于证据的信息,可用于告知向患者披露事件的决策。