Smith Jordan R, Rybak Jeffrey M, Claeys Kimberly C
Department of Clinical Sciences, Fred Wilson School of Pharmacy, High Point University, High Point, North Carolina.
Cone Health, Greensboro, North Carolina.
Pharmacotherapy. 2020 Apr;40(4):343-356. doi: 10.1002/phar.2378. Epub 2020 Mar 9.
Imipenem-cilastatin-relebactam (IMI-REL) is a novel β-lactam-β-lactamase inhibitor combination recently approved for the treatment of complicated urinary tract infections (cUTIs) and complicated intraabdominal infections (cIAIs). Relebactam is a β-lactamase inhibitor with the ability to inhibit a broad spectrum of β-lactamases such as class A and class C β-lactamases, including carbapenemases. The addition of relebactam to imipenem restores imipenem activity against several imipenem-resistant bacteria, including Enterobacteriaceae and Pseudomonas aeruginosa. Clinical data demonstrate that IMI-REL is well tolerated and effective in the treatment of cUTIs and cIAIs due to imipenem-resistant bacteria. In a phase III trial comparing IMI-REL with imipenem plus colistin, favorable clinical response was achieved in 71% and 70% of patients, respectively. Available clinical and pharmacokinetic data support the approved dosage of a 30-minute infusion of imipenem 500 mg-cilastatin 500 mg-relebactam 250 mg every 6 hours, along with dosage adjustments based on renal function. In this review, we describe the chemistry, mechanism of action, spectrum of activity, pharmacokinetics and pharmacodynamics, and clinical efficacy, and safety and tolerability of this new agent. The approval of IMI-REL represents another important step in the ongoing fight against multidrug-resistant gram-negative pathogens.
亚胺培南-西司他丁-雷利巴坦(IMI-REL)是一种新型的β-内酰胺类-β-内酰胺酶抑制剂组合,最近被批准用于治疗复杂性尿路感染(cUTIs)和复杂性腹腔内感染(cIAIs)。雷利巴坦是一种β-内酰胺酶抑制剂,能够抑制多种β-内酰胺酶,如A类和C类β-内酰胺酶,包括碳青霉烯酶。在亚胺培南中加入雷利巴坦可恢复亚胺培南对多种耐亚胺培南细菌的活性,包括肠杆菌科细菌和铜绿假单胞菌。临床数据表明,IMI-REL对耐亚胺培南细菌引起的cUTIs和cIAIs治疗耐受性良好且有效。在一项将IMI-REL与亚胺培南加黏菌素进行比较的III期试验中,分别有71%和70%的患者获得了良好的临床反应。现有的临床和药代动力学数据支持每6小时静脉输注30分钟的500mg亚胺培南-500mg西司他丁-250mg雷利巴坦的批准剂量,并根据肾功能进行剂量调整。在本综述中,我们描述了这种新药的化学结构、作用机制、活性谱、药代动力学和药效学以及临床疗效、安全性和耐受性。IMI-REL的批准是在对抗多重耐药革兰氏阴性病原体的持续斗争中的又一重要步骤。