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优化产超广谱β-内酰胺酶肠杆菌科导致的血流感染的治疗。

Optimizing therapy of bloodstream infection due to extended-spectrum β-lactamase-producing Enterobacteriaceae.

机构信息

Infectious Diseases Department, Bellvitge University Hospital, IDIBELL, University of Barcelona, Barcelona.

REIPI (Spanish Network for Research in Infectious Disease), Instituto de Salud Carlos III, Madrid, Spain.

出版信息

Curr Opin Crit Care. 2019 Oct;25(5):438-448. doi: 10.1097/MCC.0000000000000646.

Abstract

PURPOSE OF REVIEW

Infections due to extended-spectrum β-lactamase-producing Enterobacteriaceae (ESBL-E) are increasing worldwide. Carbapenems are usually regarded as the antibiotics of choice for the treatment of serious ESBL infections. However, because of the alarming emergence or carbapenem resistance, interest in effective alternatives has emerged. The present review summarizes the findings published on the antibiotics currently available for treatment of patients with an ESBL-E bloodstream infection (BSI).

RECENT FINDINGS

Meropenem and imipenem are the drugs recommended for treatment of ESBL BSIs in critically ill patients, and in infections with high bacterial loads or elevated β-lactam minimum inhibitory concentrations. Ertapenem should be reserved for patients with less severe presentations, and should be used at high doses. In milder presentations or BSIs from low-risk sources, other carbapenem-sparing alternatives could be considered: cephamycins, fluoroquinolones, and particularly a β-lactam/β-lactam inhibitor combination (particularly piperacillin/tazobactam). Optimized dosing of piperacillin/tazobactam is recommended (high doses and extended infusion). There are few data on the use of the promising newly available drugs (e.g. ceftolozane/tazobactam, ceftazidime/avibactam, cefiderocol, and plazomicin), and it seems reasonable to reserve them as last-resort drugs.

SUMMARY

Carbapenems should be used in patients with serious infections; alternatives could be used individually, particularly for definitive treatment of patients with milder presentations.

摘要

目的综述

产超广谱β-内酰胺酶肠杆菌科(ESBL-E)引起的感染在全球范围内不断增加。碳青霉烯类抗生素通常被认为是治疗严重 ESBL 感染的首选抗生素。然而,由于碳青霉烯类耐药性的惊人出现,人们对有效替代品的兴趣日益浓厚。本综述总结了目前已发表的关于治疗产 ESBL-E 血流感染(BSI)患者的抗生素的研究结果。

最近的发现

美罗培南和亚胺培南是推荐用于治疗危重症患者 ESBL BSI 以及细菌负荷量高或β-内酰胺最低抑菌浓度升高的感染的药物。厄他培南应保留给病情较轻的患者,并应使用高剂量。在病情较轻或来自低危源的 BSI 中,可以考虑其他碳青霉烯类药物节约替代品:头孢菌素类、氟喹诺酮类,特别是β-内酰胺/β-内酰胺抑制剂联合用药(特别是哌拉西林/他唑巴坦)。推荐优化哌拉西林/他唑巴坦的给药剂量(高剂量和延长输注)。关于新出现的有前途的药物(例如头孢他啶/阿维巴坦、头孢唑肟/avibactam、头孢地尔和硫酸帕拉米韦)的使用数据很少,将其保留作为最后手段的药物似乎是合理的。

总结

在严重感染的患者中应使用碳青霉烯类抗生素;对于病情较轻的患者,可以单独使用替代药物,特别是用于明确治疗。

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