The Challenge of Treating Infections Caused by Metallo-β-Lactamase-Producing Gram-Negative Bacteria: A Narrative Review.

IF 13 1区 医学 Q1 PHARMACOLOGY & PHARMACY Drugs Pub Date : 2024-10-28 DOI:10.1007/s40265-024-02102-8
Carmen Hidalgo-Tenorio, German Bou, Antonio Oliver, Montserrat Rodríguez-Aguirregabiria, Miguel Salavert, Luis Martínez-Martínez
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Abstract

Gram-negative multidrug-resistant (MDR) bacteria, including Enterobacterales, Acinetobacter baumannii, and Pseudomonas aeruginosa, pose a significant challenge in clinical practice. Infections caused by metallo-β-lactamase (MBL)-producing Gram-negative organisms, in particular, require careful consideration due to their complexity and varied prevalence, given that the microbiological diagnosis of these pathogens is intricate and compounded by challenges in assessing the efficacy of anti-MBL antimicrobials. We discuss both established and new approaches in the treatment of MBL-producing Gram-negative infections, focusing on 3 strategies: colistin; the recently approved combination of aztreonam with avibactam (or with ceftazidime/avibactam); and cefiderocol. Despite its significant activity against various Gram-negative pathogens, the efficacy of colistin is limited by resistance mechanisms, while nephrotoxicity and acute renal injury call for careful dosing and monitoring in clinical practice. Aztreonam combined with avibactam (or with avibactam/ceftazidime if aztreonam plus avibactam is not available) exhibits potent activity against MBL-producing Gram-negative pathogens. Cefiderocol in monotherapy is effective against a wide range of multidrug-resistant organisms, including MBL producers, and favorable clinical outcomes have been observed in various clinical trials and case series. After examining scientific evidence in the management of infections caused by MBL-producing Gram-negative bacteria, we have developed a comprehensive clinical algorithm to guide therapeutic decision making. We recommend reserving colistin as a last-resort option for MDR Gram-negative infections. Cefiderocol and aztreonam/avibactam represent favorable options against MBL-producing pathogens. In the case of P. aeruginosa with MBL-producing enzymes and with difficult-to-treat resistance, cefiderocol is the preferred option. Further research is needed to optimize treatment strategies and minimize resistance.

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治疗产生金属-β-乳酰胺酶的革兰氏阴性细菌引起的感染所面临的挑战:综述。
革兰氏阴性耐多药(MDR)细菌,包括肠杆菌、鲍曼不动杆菌和铜绿假单胞菌,给临床实践带来了巨大挑战。产金属-β-内酰胺酶(MBL)的革兰氏阴性菌引起的感染因其复杂性和不同的流行率而尤其需要慎重考虑,因为这些病原体的微生物学诊断错综复杂,而且在评估抗MBL抗菌药的疗效方面也面临挑战。我们讨论了治疗产生 MBL 的革兰氏阴性菌感染的既有方法和新方法,重点讨论了三种策略:可乐定;最近批准的阿曲南加阿维巴坦(或头孢唑肟/阿维巴坦)组合;以及头孢啶醇。尽管大肠杆菌素对各种革兰氏阴性病原体具有显著的活性,但其疗效受到耐药机制的限制,同时肾毒性和急性肾损伤要求在临床实践中谨慎用药和监测。氨曲南与阿维菌素联用(如果没有氨曲南和阿维菌素,则与阿维菌素/头孢唑肟联用)对产生 MBL 的革兰氏阴性病原体具有强效作用。头孢妥昔洛单药治疗对多种耐多药病菌(包括产生 MBL 的病菌)有效,各种临床试验和病例系列观察到了良好的临床效果。在研究了治疗由产 MBL 革兰阴性菌引起的感染的科学证据后,我们制定了一套全面的临床算法来指导治疗决策。我们建议将可乐定作为 MDR 革兰氏阴性菌感染的最后选择。头孢克肟和阿曲南类/阿维菌素是对付产生 MBL 的病原体的有利选择。如果铜绿假单胞菌能产生 MBL 酶,且具有难以治疗的耐药性,则首选头孢代醇。要优化治疗策略并尽量减少耐药性,还需要进一步的研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Drugs
Drugs 医学-毒理学
CiteScore
22.70
自引率
0.90%
发文量
134
审稿时长
3-8 weeks
期刊介绍: Drugs is a journal that aims to enhance pharmacotherapy by publishing review and original research articles on key aspects of clinical pharmacology and therapeutics. The journal includes: Leading/current opinion articles providing an overview of contentious or emerging issues. Definitive reviews of drugs and drug classes, and their place in disease management. Therapy in Practice articles including recommendations for specific clinical situations. High-quality, well designed, original clinical research. Adis Drug Evaluations reviewing the properties and place in therapy of both newer and established drugs. AdisInsight Reports summarising development at first global approval. Moreover, the journal offers additional digital features such as animated abstracts, video abstracts, instructional videos, and podcasts to increase visibility and educational value. Plain language summaries accompany articles to assist readers with some knowledge of the field in understanding important medical advances.
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