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首页> 外文期刊>International journal of infectious diseases : >Extended-spectrum beta-lactamase-producing Enterobacteriaceae (ESBL-PE) infections: are carbapenem alternatives achievable in daily practice?
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Extended-spectrum beta-lactamase-producing Enterobacteriaceae (ESBL-PE) infections: are carbapenem alternatives achievable in daily practice?

机译:产生广谱β-内酰胺酶的肠杆菌科细菌(ESBL-PE)感染:在日常实践中是否可以使用碳青霉烯替代品?

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Objectives: To avoid the use of carbapenems, alternatives such as cephamycin, piperacillin-tazobactam, and others are suggested for the treatment of extended-spectrum beta-lactamase-producing Enterobacteriaceae (ESBL-PE) infections. The aim of this study was to evaluate the frequency and the feasibility of antimicrobial de-escalation for ESBL-PE-related infections. Methods: A prospective observational, bi centric cohort study was conducted. All patients with ESBL-PE infections were included. De-escalation was systematically suggested if patients were clinically stable and the isolate was susceptible to possible alternatives. Results: Seventy-nine patients were included: 36 (45.6%) were children, 27 (34.1%) were hospitalized in intensive care units, and 37 (47%) were immunocompromised. Urinary tract infections, pneumonia, and catheter-related bloodstream infections accounted for 45.6%, 19%, and 10%, respectively, of the cohort. Escherichia coli, Klebsiella pneumoniae, and Enterobacter cloacae were the three most frequent causative organisms isolated. On day 5, 47 (59.2%) of the patients were still receiving carbapenems. Antimicrobial resistance (44.7%), infection relapse (26.9%), and clinical instability (19.2%) were the most important reasons for not prescribing alternatives. E. coli-related infections appeared to be a protective factor against maintaining the carbapenem prescription (odds ratio 0.11, 95% confidence interval 0.041-0.324; p=0.0013). Conclusions: In clinical practice, less than 50% of patients with ESBL-PE-related infections were de-escalated after empirical treatment with carbapenems.
机译:目的:为避免使用碳青霉烯类药物,建议使用其他替代品,例如头孢菌素,哌拉西林-他唑巴坦等,用于治疗产生广谱β-内酰胺酶的肠杆菌科(ESBL-PE)感染。这项研究的目的是评估针对ESBL-PE相关感染的抗菌药物降级的频率和可行性。方法:进行了一项前瞻性观察性,双中心队列研究。包括所有ESBL-PE感染的患者。如果患者临床稳定并且分离株易于选择,则系统地建议降级。结果:共纳入79例患者:儿童36(45.6%),重症监护病房住院的27(34.1%),以及免​​疫功能低下的37(47%)。尿路感染,肺炎和导管相关的血流感染分别占队列的45.6%,19%和10%。大肠埃希菌,肺炎克雷伯菌和阴沟肠杆菌是三种最常见的致病菌。在第5天,仍有47名(59.2%)患者接受碳青霉烯类药物治疗。抗菌药物耐药性(44.7%),感染复发(26.9%)和临床不稳定(19.2%)是不开处方的最重要原因。大肠杆菌相关感染似乎是维持碳青霉烯处方的保护因素(赔率比为0.11,95%置信区间为0.041-0.324; p = 0.0013)。结论:在临床实践中,用碳青霉烯类药物进行经验性治疗后,不到50%的ESBL-PE相关感染患者逐渐消退。

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