Rankin Danielle A, Walters Maroya Spalding, Caicedo Luz, Gable Paige, Moulton-Meissner Heather A, Chan Allison, Burks Albert, Edwards Kendra, McAllister Gillian, Kent Alyssa, Laufer Halpin Alison, Moore Christina, McLemore Tracy, Thomas Linda, Dotson Nychie Q, Chu Alvina K
Florida Department of Health in Orange County, Orlando, Florida.
Bureau of Epidemiology, Florida Department of Health, Tallahassee, Florida.
Infect Control Hosp Epidemiol. 2024 Mar;45(3):292-301. doi: 10.1017/ice.2023.231. Epub 2024 Jan 10.
We investigated concurrent outbreaks of carrying (VIM-CRPA) and Enterobacterales carrying (KPC-CRE) at a long-term acute-care hospital (LTACH A).
We defined an incident case as the first detection of or from a patient's clinical cultures or colonization screening test. We reviewed medical records and performed infection control assessments, colonization screening, environmental sampling, and molecular characterization of carbapenemase-producing organisms from clinical and environmental sources by pulsed-field gel electrophoresis (PFGE) and whole-genome sequencing.
From July 2017 to December 2018, 76 incident cases were identified from 69 case patients: 51 had 11 had and 7 had and . Also, were identified from 7 Enterobacterales, and all were . We observed gaps in hand hygiene, and we recovered KPC-CRE and VIM-CRPA from drains and toilets. We identified 4 KPC alleles and 2 VIM alleles; 2 KPC alleles were located on plasmids that were identified across multiple Enterobacterales and in both clinical and environmental isolates.
Our response to a single patient colonized with VIM-CRPA and KPC-CRE identified concurrent CPO outbreaks at LTACH A. Epidemiologic and genomic investigations indicated that the observed diversity was due to a combination of multiple introductions of VIM-CRPA and KPC-CRE and to the transfer of carbapenemase genes across different bacteria species and strains. Improved infection control, including interventions that minimized potential spread from wastewater premise plumbing, stopped transmission.
我们调查了一家长期急性护理医院(LTACH A)中同时发生的携带VIM碳青霉烯酶的肺炎克雷伯菌(VIM-CRPA)和携带KPC碳青霉烯酶的肠杆菌科细菌(KPC-CRE)的暴发情况。
我们将首例病例定义为首次从患者的临床培养物或定植筛查试验中检测到VIM-CRPA或KPC-CRE。我们查阅了病历,并进行了感染控制评估、定植筛查、环境采样,以及通过脉冲场凝胶电泳(PFGE)和全基因组测序对临床和环境来源的产碳青霉烯酶生物体进行分子特征分析。
2017年7月至2018年12月,从69例病例患者中识别出76例首例病例:51例携带VIM-CRPA,11例携带KPC-CRE,7例同时携带VIM-CRPA和KPC-CRE。此外,从7株肠杆菌科细菌中鉴定出VIM-CRPA,且均为KPC-CRE。我们观察到手部卫生存在差距,并且从排水管道和厕所中分离出了KPC-CRE和VIM-CRPA。我们鉴定出4个KPC等位基因和2个VIM等位基因;2个KPC等位基因位于质粒上,这些质粒在多个肠杆菌科细菌中以及临床和环境分离株中均有发现。
我们对一名同时定植有VIM-CRPA和KPC-CRE的患者的应对措施,识别出了LTACH A同时发生的产碳青霉烯酶生物体暴发。流行病学和基因组学调查表明,观察到的多样性是由于VIM-CRPA和KPC-CRE的多次引入以及碳青霉烯酶基因在不同细菌物种和菌株之间的转移共同导致的。加强感染控制,包括采取措施尽量减少废水管道系统的潜在传播,阻止了传播。