Hidalgo-Tenorio Carmen, Bou German, Oliver Antonio, Rodríguez-Aguirregabiria Montserrat, Salavert Miguel, Martínez-Martínez Luis
Hospital Universitario Virgen de las Nieves de Granada, Instituto de Investigación Biosanitario de Granada (IBS-Granada), Granada, Spain.
Departamento de Medicina, Universidad de Granada, Granada, Spain.
Drugs. 2024 Dec;84(12):1519-1539. doi: 10.1007/s40265-024-02102-8. Epub 2024 Oct 28.
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.
革兰氏阴性多重耐药(MDR)细菌,包括肠杆菌科、鲍曼不动杆菌和铜绿假单胞菌,在临床实践中构成了重大挑战。由产金属β-内酰胺酶(MBL)的革兰氏阴性菌引起的感染尤其需要谨慎考虑,因为其复杂性和不同的流行率,鉴于这些病原体的微生物学诊断复杂,且评估抗MBL抗菌药物疗效时面临诸多挑战。我们讨论了治疗产MBL革兰氏阴性菌感染的既定方法和新方法,重点关注三种策略:黏菌素;最近批准的氨曲南与阿维巴坦(或与头孢他啶/阿维巴坦)的联合用药;以及头孢地尔。尽管黏菌素对各种革兰氏阴性病原体具有显著活性,但其疗效受到耐药机制的限制,而肾毒性和急性肾损伤要求在临床实践中谨慎给药和监测。氨曲南与阿维巴坦联合使用(如果没有氨曲南加阿维巴坦,则与阿维巴坦/头孢他啶联合使用)对产MBL革兰氏阴性病原体具有强大活性。头孢地尔单药治疗对包括产MBL菌在内的多种多重耐药菌有效,并且在各种临床试验和病例系列中观察到了良好的临床结果。在研究了产MBL革兰氏阴性菌感染管理中的科学证据后,我们制定了一个全面的临床算法来指导治疗决策。我们建议将黏菌素保留为MDR革兰氏阴性菌感染的最后手段。头孢地尔和氨曲南/阿维巴坦是针对产MBL病原体的有利选择。对于产MBL酶且耐药难以治疗的铜绿假单胞菌,头孢地尔是首选。需要进一步研究以优化治疗策略并尽量减少耐药性。