Department of Pharmacy Practice and Science, PGY2 Infectious Diseases Pharmacy Resident University of Maryland School of Pharmacy ,St. Baltimore, MD, USA.
Department of Pharmacy Practice and Science, Assistant Professor, University of Maryland School of Pharmacy 20 N Pine St. Baltimore , MD,USA.
Expert Opin Pharmacother. 2021 Feb;22(3):265-271. doi: 10.1080/14656566.2020.1840552. Epub 2020 Nov 2.
: Nosocomial pneumonias are the second most common healthcare-associated infections (HCAIs), often associated with the presence of , , , species, and species. Increasing use of carbapenems has led to an increase in the prevalence of carbapenem-resistant gram-negative organisms, such as carbapenem-resistant Enterobacterales (CRE), (CRPA), and (CRAB), limiting treatment options for patients at high-risk of multi-drug resistant (MDR) gram-negative pathogens. : The purpose of this review is to discuss the role of meropenem/vaborbactam, a beta-lactam combined with a novel non-beta-lactam cyclic boronic acid beta-lactamase inhibitor (BLI), for the treatment of nosocomial pneumonia based on its chemistry, pharmacokinetics/dynamics, microbiological spectrum of activity, mechanisms of resistance, safety, and clinical efficacy. : Currently, any utilization of meropenem/vaborbactam beyond its FDA-approved indication for complicated urinary tract infections is considered off-label use; however, based on the pulmonary penetration of meropenem/vaborbactam, it is highly likely to be a safe and effective alternative to more toxic agents, like aminoglycosides and polymixins, for targeted therapy in pulmonary infections due to CRE. Unfortunately, the multifactorial resistance pattern of CRPA and other non-lactose-fermenting gram-negative bacteria restricts activity against these organisms which are common pathogens implicated in nosocomial pneumonia.
医院获得性肺炎是第二大常见的医院获得性感染(HAIs),常与 、 、 、 种和 种的存在有关。碳青霉烯类药物的使用增加导致了碳青霉烯类耐药革兰氏阴性菌(如耐碳青霉烯肠杆菌科(CRE)、耐碳青霉烯肺炎克雷伯菌(CRPA)和耐碳青霉烯鲍曼不动杆菌(CRAB))的流行率增加,限制了高风险多重耐药(MDR)革兰氏阴性病原体患者的治疗选择。本文旨在讨论美罗培南/沃博巴坦的作用,这是一种β-内酰胺类药物与新型非β-内酰胺类环状硼酸β-内酰胺酶抑制剂(BLI)的组合,用于治疗医院获得性肺炎,其依据为其化学、药代动力学/药效学、微生物活性谱、耐药机制、安全性和临床疗效。目前,任何超出美罗培南/沃博巴坦 FDA 批准的复杂尿路感染适应证的使用都被认为是超适应证使用;然而,基于美罗培南/沃博巴坦的肺部渗透特性,它极有可能成为针对 CRE 引起的肺部感染的更具毒性药物(如氨基糖苷类和多黏菌素)的安全有效替代物。不幸的是,CRPA 和其他非乳糖发酵革兰氏阴性菌的多因素耐药模式限制了对这些常见医院获得性肺炎病原体的活性。