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重症监护病房感染泛耐药和广泛耐药碳青霉烯酶-producing 革兰氏阴性菌的患者使用磷霉素治疗的结果。

Outcomes of critically ill intensive care unit patients treated with fosfomycin for infections due to pandrug-resistant and extensively drug-resistant carbapenemase-producing Gram-negative bacteria.

机构信息

First Department of Respiratory Medicine - Intensive Care Unit, University of Athens, Sotiria Chest Diseases and General Hospital, 152 Mesogeion Avenue, 115 27 Athens, Greece.

Sixth Department of Internal Medicine, Hygeia Hospital, 4 Erythrou Stavrou Street, 151 23 Marousi, Athens, Greece.

出版信息

Int J Antimicrob Agents. 2014 Jan;43(1):52-9. doi: 10.1016/j.ijantimicag.2013.09.010. Epub 2013 Oct 16.

Abstract

Fosfomycin is active in vitro against extensively drug-resistant (XDR) and pandrug-resistant (PDR) Pseudomonas aeruginosa and Klebsiella pneumoniae carbapenemase-producing strains; however, the in vivo effectiveness against such pathogens is almost unknown. A multicentre, observational, prospective case-series study was performed in 11 ICUs. All consecutive fosfomycin-treated patients suffering from XDR or PDR fosfomycin-susceptible, microbiologically documented infections were recorded. Clinical and microbiological outcomes were assessed. A safety analysis was performed. In total, 68 patients received fosfomycin during the study period, 48 of whom were considered suitable for effectiveness analysis based on predefined criteria. Bacteraemia and ventilator-associated pneumonia were the main infections. Carbapenemase-producing K. pneumoniae and P. aeruginosa were isolated in 41 and 17 cases, respectively. All isolates exhibited an XDR or PDR profile, being fosfomycin-susceptible by definition. Fosfomycin was administered intravenously at a median dose of 24g/day for a median of 14 days, mainly in combination with colistin or tigecycline. Clinical outcome at Day 14 was successful in 54.2% of patients, whilst failure, indeterminate outcome and superinfection were documented in 33.3%, 6.3% and 6.3%, respectively. All-cause mortality at Day 28 was 37.5%. Bacterial eradication was observed in 56.3% of cases. Fosfomycin resistance developed in three cases. The main adverse event was reversible hypokalaemia. In conclusion, fosfomycin could have a place in the armamentarium against XDR and PDR Gram-negative infections in the critically ill. Resistance development during therapy, which has been a matter of concern in previous studies, did not occur frequently. The necessity of combination with other antibiotics requires further investigation.

摘要

磷霉素在体外对广泛耐药(XDR)和泛耐药(PDR)铜绿假单胞菌和产碳青霉烯酶的肺炎克雷伯菌具有活性;然而,其对这些病原体的体内疗效几乎未知。一项多中心、观察性、前瞻性病例系列研究在 11 个 ICU 进行。记录了所有连续接受磷霉素治疗的 XDR 或 PDR 磷霉素敏感、微生物学确诊感染的患者。评估了临床和微生物学结局。进行了安全性分析。在研究期间,共有 68 名患者接受了磷霉素治疗,其中 48 名患者根据预设标准被认为适合进行有效性分析。菌血症和呼吸机相关性肺炎是主要感染。41 例和 17 例分别分离出产碳青霉烯酶的肺炎克雷伯菌和铜绿假单胞菌。所有分离株均表现出 XDR 或 PDR 表型,根据定义对磷霉素敏感。磷霉素静脉给药,中位数剂量为 24g/天,中位数疗程为 14 天,主要与多粘菌素或替加环素联合使用。第 14 天的临床结局在 54.2%的患者中成功,而失败、不确定结局和继发感染分别记录在 33.3%、6.3%和 6.3%的患者中。第 28 天的全因死亡率为 37.5%。在 56.3%的病例中观察到细菌清除。在 3 例中出现磷霉素耐药。主要不良事件是可逆性低钾血症。总之,磷霉素在治疗危重症患者的 XDR 和 PDR 革兰氏阴性感染方面可能具有一定地位。在以前的研究中,人们一直关注治疗过程中出现的耐药性,但在本研究中并未频繁发生。需要与其他抗生素联合使用,这需要进一步研究。

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