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Risk factors for fecal carriage of carbapenemase producing Enterobacteriaceae among intensive care unit patients from a tertiary care center in India

机译:印度三级护理中心重症监护病房患者粪便携带产生碳青霉烯酶的肠杆菌科细菌的风险因素

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Background Resistance amongst the commensal flora is a serious threat because a very highly populated ecosystem like the gut, may at a later stage, be a source of extra intestinal infections, resistant strains may spread to other host or transfer genetic resistance element to other members of micro-biota including pathogens. This study was carried out to assess fecal colonization by carbapenemase producing Enterobacteriaceae (CPE) and associated risk factors among 100 patients admitted to intensive care unit (ICU). The phenotypic and molecular characterizations of CPE were also included. Results Colonization with CPE was observed in 6.6?% (8/122) controls. Among ICU patients, fecal carriage of CPE was significantly higher on day 4 (D4) (22?%) as compared to day 1 (D1) (11?%) ( p value 0.002). The carbapenemase genes detected included OXA- 48, 181, KPC and NDM-1 with NDM-1 being the predominant carbapenemase in both ICU D1 and D4. Among the 50 CPE isolates, 8 (16?%) were susceptible to meropenem and imipenem (Minimum inhibitory concentration; MIC?≤?1?mg/L) and all were susceptible to colistin (MIC range 0.125 - 1?mg/L) and tigecycline (MIC range 0.06- 1.5?mg/L). The risk factors associated with CPE carriage were duration of ICU stay, use of ventilator and aminoglycosides. Conclusions Prior colonization with CPE could result in their influx and spread in ICU, challenging infection control measures. Exposure to ICU further increases risk of colonization with diverse carbapenemase-producing Enterobacteriaceae. Gut colonization with these strains may be a source of endogenous infection and horizontal transfer of these genes in future.
机译:背景共生菌群之间的抗药性是一个严重的威胁,因为像肠道这样人口稠密的生态系统可能会在以后阶段成为肠道外感染的来源,抗药性菌株可能会传播到其他宿主或将遗传抗性成分​​转移到其他宿主微生物群,包括病原体。这项研究旨在评估100例重症监护病房(ICU)患者中产生碳青霉烯酶的肠杆菌科(CPE)的粪便定植及相关危险因素。还包括CPE的表型和分子表征。结果在6.6%(8/122)的对照组中观察到了CPE的定植。在ICU患者中,与第一天(D1)(11%)相比,第四天(D4)(22%)的粪便CPE显着更高(p值0.002)。检测到的碳青霉烯酶基因包括OXA-48、181,KPC和NDM-1,其中IDM D1和D4中NDM-1是主要的碳青霉烯酶。在50种CPE分离株中,有8种(16%)对美罗培南和亚胺培南敏感(最低抑菌浓度;MIC≥1?mg / L),都对粘菌素敏感(MIC在0.125-1?mg / L范围内)和替加环素(MIC范围为0.06- 1.5?mg / L)。与CPE携带相关的危险因素是ICU停留时间,使用呼吸机和氨基糖苷类药物。结论预先用CPE定植可能导致它们流入ICU并在ICU中传播,这对感染控制措施提出了挑战。暴露于ICU会进一步增加产生各种碳青霉烯酶的肠杆菌科细菌定植的风险。这些菌株的肠道定植可能是将来这些基因内源性感染和水平转移的来源。

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