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我们是否应该以及如何优化碳青霉烯类耐药鲍曼不动杆菌引起的严重医院获得性肺炎时的头孢地尔的给药方案?一种观点。

Should we, and how to, optimize cefiderocol administration during severe nosocomial pneumonia due to carbapenem-resistant Acinetobacter baumanii? A viewpoint.

机构信息

Infectious disease department, Raymond-Poincaré University Hospital, Garches, France.

Infectious disease department, Raymond-Poincaré University Hospital, Garches, France.

出版信息

J Glob Antimicrob Resist. 2024 Sep;38:140-145. doi: 10.1016/j.jgar.2024.05.014. Epub 2024 Jun 5.

Abstract

OBJECTIVES

Acinetobacter baumannii is classified by the centre for Disease Control and Prevention (CDC) as an "urgent threat" due to its ability to acquire and develop resistance to multiple classes of antibiotics. As a result, it is one of the most concerning pathogens in healthcare settings, with increasing incidence of infections due to carbapenem-resistant Acinetobacter baumannii (CRAB) associated with high morbidity and mortality rates. Therefore, there are ongoing efforts to find novel treatment options, one of which is cefiderocol. We aim to review available evidence on cefiderocol use for severe nosocomial pneumonia due to carbapenem-resistant Acinetobacter baumannii.

METHODS

A comprehensive review was conducted from 2017 to 2023, covering articles from databases such as Pubmed, Scopus, and Embase, along with conference proceedings from ECCMID 2023. The primary focus was on severe nosocomial pneumonia due A. baumannii and cefiderocol.

DISCUSSION

Cefiderocol, targeting periplasmic space Penicillin-Binding Proteins (PBPs) via siderophore transport pathways, exhibits promise against multi-drug resistant Gram-negative bacilli. Its effectiveness in treating CRAB pneumonia remains debated. The CREDIBLE trial reported higher mortality with cefiderocol compared to the best available treatment, while other cohort studies showed contrasting outcomes. Patient variations and pharmacokinetic factors may underlie these discrepancies. The recommended cefiderocol dosage regimen may fall short of desired pharmacokinetic targets, especially in critically ill patients and lung infections. Pulmonary factors hindering cefiderocol's entry into bacteria through iron transporters are overlooked in clinical breakpoints. Optimized dosing or combination regimens may enhance infection site exposure and outcomes.

CONCLUSIONS

Further research is needed to determine the optimal cefiderocol dosage and administration (mono vs. dual therapy, continuous vs. intermittent infusion), in severe Acinetobacter baumannii nosocomial pneumonia.

摘要

目的

由于鲍曼不动杆菌能够获得并发展对多种类抗生素的耐药性,因此被疾病控制与预防中心(CDC)归类为“紧急威胁”。因此,它是医疗机构中最令人关注的病原体之一,由于耐碳青霉烯鲍曼不动杆菌(CRAB)相关的感染发病率不断增加,导致发病率和死亡率很高。因此,人们正在努力寻找新的治疗选择,其中之一是头孢他啶-阿维巴坦。我们旨在回顾关于头孢他啶-阿维巴坦治疗耐碳青霉烯鲍曼不动杆菌引起的严重医院获得性肺炎的现有证据。

方法

从 2017 年到 2023 年进行了全面审查,涵盖了来自 Pubmed、Scopus 和 Embase 等数据库的文章以及 2023 年 ECCMID 会议的会议记录。主要重点是耐碳青霉烯鲍曼不动杆菌引起的严重医院获得性肺炎和头孢他啶-阿维巴坦。

讨论

头孢他啶-阿维巴坦通过铁载体转运途径靶向周质空间青霉素结合蛋白(PBP),对多种耐药革兰氏阴性杆菌具有潜力。它在治疗 CRAB 肺炎方面的疗效仍存在争议。CREDIBLE 试验报告称,与最佳可用治疗相比,头孢他啶-阿维巴坦的死亡率更高,而其他队列研究则显示出相反的结果。患者差异和药代动力学因素可能是这些差异的基础。建议的头孢他啶-阿维巴坦剂量方案可能达不到预期的药代动力学目标,尤其是在重症患者和肺部感染患者中。临床折点忽略了阻碍头孢他啶-阿维巴坦通过铁载体进入细菌的肺部因素。优化剂量或联合方案可能会增强感染部位的暴露和结果。

结论

需要进一步研究确定头孢他啶-阿维巴坦在严重鲍曼不动杆菌医院获得性肺炎中的最佳剂量和给药方式(单药与双药治疗、连续与间歇性输注)。

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