Julius Center for Health Sciences and Primary Care, University Medical Center Utrecht, Utrecht University, Utrecht, The Netherlands.
Department of Medical Microbiology and Infectious Diseases, Erasmus MC University Medical Center, P.O. Box 2040, 3000 CA, Rotterdam, The Netherlands.
Antimicrob Resist Infect Control. 2022 Apr 4;11(1):55. doi: 10.1186/s13756-022-01095-x.
Hospital outbreaks of multidrug resistant Pseudomonas aeruginosa are often caused by Pseudomonas aeruginosa clones which produce metallo-β-lactamases, such as Verona Integron-encoded Metallo-β-lactamase (VIM). Although different sources have been identified, the exact transmission routes often remain unknown. However, quantifying the role of different transmission routes of VIM-PA is important for tailoring infection prevention and control measures. The aim of this study is to quantify the relative importance of different transmission routes by applying a mathematical transmission model using admission and discharge dates as well as surveillance culture data of patients.
We analyzed VIM-PA surveillance data collected between 2010 and 2018 of two intensive-care unit (ICU) wards for adult patients of the Erasmus University Medical Center Rotterdam using a mathematical transmission model. We distinguished two transmission routes: direct cross-transmission and a persistent environmental route. Based on admission, discharge dates, and surveillance cultures, we estimated the proportion of transmissions assigned to each of the routes.
Our study shows that only 13.7% (95% CI 1.4%, 29%) of the transmissions that occurred in these two ICU wards were likely caused by cross-transmission, leaving the vast majority of transmissions (86.3%, 95% CI 71%, 98.6%) due to persistent environmental contamination.
Our results emphasize that persistent contamination of the environment may be an important driver of nosocomial transmissions of VIM-PA in ICUs. To minimize the transmission risk from the environment, potential reservoirs should be regularly and thoroughly cleaned and disinfected, or redesigned.
医院多重耐药铜绿假单胞菌的爆发通常是由产生金属β-内酰胺酶的铜绿假单胞菌克隆引起的,例如 Verona 整合子编码的金属β-内酰胺酶(VIM)。尽管已经确定了不同的来源,但确切的传播途径通常仍不清楚。然而,量化 VIM-PA 不同传播途径的作用对于制定感染预防和控制措施非常重要。本研究的目的是通过应用数学传播模型,利用患者的入院和出院日期以及监测培养数据来量化不同传播途径的相对重要性。
我们分析了 2010 年至 2018 年间鹿特丹伊拉斯姆斯大学医学中心两个成人重症监护病房(ICU)的 VIM-PA 监测数据,使用数学传播模型进行分析。我们区分了两种传播途径:直接交叉传播和持续的环境传播。根据入院、出院日期和监测培养,我们估计了每种途径分配的传播比例。
我们的研究表明,这两个 ICU 病房发生的传播中,只有 13.7%(95%CI 1.4%,29%)可能是由交叉传播引起的,而绝大多数传播(86.3%,95%CI 71%,98.6%)是由于环境持续污染所致。
我们的研究结果强调,环境的持续污染可能是 ICU 中 VIM-PA 医院传播的重要驱动因素。为了最大限度地降低环境传播的风险,应定期彻底清洁和消毒或重新设计潜在的污染源。