Division of Infectious Diseases, American University of Beirut Medical Center, Beirut, Lebanon.
Department of Health Science, University of Genoa, Genoa, Italy; Infectious Diseases Clinic, Ospedale Policlinico San Martino Hospital - IRCCS, Genoa, Italy.
Int J Antimicrob Agents. 2022 Sep;60(3):106633. doi: 10.1016/j.ijantimicag.2022.106633. Epub 2022 Jul 1.
Multidrug-resistant (MDR) Gram-negative bacteria (GNB) pose a critical threat to global healthcare, worsening outcomes and increasing mortality among infected patients. Carbapenemase- and extended-spectrum β-lactamase-producing Enterobacterales, as well as carbapenemase-producing Pseudomonas and Acinetobacter spp., are common MDR pathogens. New antibiotics and combinations have been developed to address this threat. Clinical trial findings support several combinations, notably ceftazidime-avibactam (CZA, a cephalosporin-β-lactamase inhibitor combination), which is effective in treating complicated urinary tract infections (cUTI), complicated intra-abdominal infections and hospital-acquired and ventilator-associated pneumonia caused by GNBs. Other clinically effective combinations include meropenem-vaborbactam (MVB), ceftolozane-tazobactam (C/T) and imipenem-relebactam (I-R). Cefiderocol is a recent siderophore β-lactam antibiotic that is useful against cUTIs caused by carbapenem-resistant Enterobacterales (CRE) and is stable against many β-lactamases. Carbapenem-resistant Enterobacterales are a genetically heterogeneous group that vary in different world regions and are a substantial cause of infections, among which Klebsiella pneumoniae are the most common. Susceptible CRE infections can be treated with fluoroquinolones, aminoglycosides or fosfomycin, but alternatives include CZA, MVB, I-R, cefiderocol, tigecycline and eravacycline. Multidrug-resistant Acinetobacter baumannii and Pseudomonas aeruginosa are increasingly common pathogens producing a range of different carbapenemases, and infections are challenging to treat, often requiring novel antibiotics or combinations. Currently, no single agent can treat all MDR-GNB infections, but new β-lactam-β-lactamase inhibitor combinations are often effective for different infection sites and, when used appropriately, have the potential to improve outcomes. This article reviews clinical studies investigating novel β-lactam approaches for treatment of MDR-GNB infections.
耐多药(MDR)革兰氏阴性菌(GNB)对全球医疗保健构成严重威胁,使感染患者的预后恶化并增加死亡率。产碳青霉烯酶和超广谱β-内酰胺酶的肠杆菌科,以及产碳青霉烯酶的假单胞菌和不动杆菌属,是常见的 MDR 病原体。已经开发了新的抗生素和组合来应对这一威胁。临床试验结果支持几种组合,特别是头孢他啶-阿维巴坦(CZA,一种头孢菌素-β-内酰胺酶抑制剂组合),它在治疗复杂尿路感染(cUTI)、复杂腹腔内感染以及由 GNB 引起的医院获得性和呼吸机相关性肺炎方面非常有效。其他具有临床疗效的组合包括美罗培南-法硼巴坦(MVB)、头孢洛扎-他唑巴坦(C/T)和亚胺培南-雷利巴坦(I-R)。头孢地尔是一种最近的铁载体β-内酰胺抗生素,对耐碳青霉烯肠杆菌科(CRE)引起的 cUTI 有效,并且对许多β-内酰胺酶稳定。耐碳青霉烯肠杆菌科是一组遗传异质性的细菌,在不同的世界区域有所不同,是感染的主要原因之一,其中肺炎克雷伯菌最为常见。对敏感的 CRE 感染可使用氟喹诺酮类、氨基糖苷类或磷霉素治疗,但替代方案包括 CZA、MVB、I-R、头孢地尔、替加环素和依拉环素。多药耐药的鲍曼不动杆菌和铜绿假单胞菌是越来越常见的产生多种不同碳青霉烯酶的病原体,感染难以治疗,通常需要新型抗生素或组合。目前,没有单一药物可以治疗所有 MDR-GNB 感染,但新的β-内酰胺-β-内酰胺酶抑制剂组合通常对不同的感染部位有效,并且在适当使用时,有可能改善结果。本文综述了用于治疗 MDR-GNB 感染的新型β-内酰胺方法的临床研究。