Department of Infection Control of Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo, São Paulo, Brazil.
Department of Infectious Diseases and LIM-54, Universidade de São Paulo, São Paulo, Brazil.
J Antimicrob Chemother. 2019 Jan 1;74(1):177-181. doi: 10.1093/jac/dky406.
In vitro and clinical studies using parenteral fosfomycin have suggested the possibility of using this drug against infections caused by MDR microorganisms. The aim of this study was to describe a case series of patients treated with fosfomycin who had severe infections caused by pan-drug-resistant Gram-negative bacteria.
We describe a prospective series of cases of hospitalized patients with infections caused by Gram-negative bacteria resistant to β-lactams and colistin, treated with 16 g of fosfomycin daily for 10-14 days. Isolates were tested for antimicrobial susceptibility and synergism of fosfomycin with meropenem. We tested for resistance genes and performed typing using PCR and WGS.
Thirteen patients received fosfomycin (seven immunosuppressed); they had bloodstream infections (n = 11; 85%), ventilator-associated pneumonia (n = 1; 8%) and surgical site infection (n = 1; 8%), caused by Klebsiella pneumoniae (n = 9), Serratia marcescens (n = 3) and Pseudomonas aeruginosa (n = 1). Overall, eight (62%) patients were cured. Using time-kill assays, synergism between fosfomycin and meropenem occurred in 9 (82%) of 11 isolates. Typing demonstrated that K. pneumoniae were polyclonal. Eight patients (62%) had possible adverse events, but therapy was not discontinued.
Fosfomycin may be safe and effective against infections caused by pan-drug-resistant Gram-negative microorganisms with different antimicrobial resistance mechanisms and there seems to be synergism with meropenem.
体外和临床研究表明,注射用磷霉素有可能用于治疗由耐多药微生物引起的感染。本研究旨在描述一组使用磷霉素治疗的严重感染泛耐药革兰氏阴性细菌的患者病例系列。
我们描述了一组接受磷霉素治疗的住院患者的前瞻性病例系列,这些患者患有对β-内酰胺类和粘菌素耐药的革兰氏阴性菌感染,每天接受 16 克磷霉素治疗 10-14 天。对分离物进行了药敏试验和磷霉素与美罗培南协同作用的检测。我们检测了耐药基因,并使用 PCR 和 WGS 进行了分型。
13 名患者接受了磷霉素治疗(7 名免疫抑制患者);他们患有血流感染(n=11;85%)、呼吸机相关性肺炎(n=1;8%)和手术部位感染(n=1;8%),由肺炎克雷伯菌(n=9)、粘质沙雷氏菌(n=3)和铜绿假单胞菌(n=1)引起。总体而言,8 名(62%)患者治愈。使用时间杀伤试验,11 株分离物中有 9 株(82%)显示出磷霉素和美罗培南之间的协同作用。分型表明肺炎克雷伯菌是多克隆的。8 名(62%)患者可能发生不良反应,但未停止治疗。
磷霉素对具有不同抗菌耐药机制的泛耐药革兰氏阴性微生物引起的感染可能是安全有效的,并且与美罗培南似乎存在协同作用。