Imipenem-Cilastatin-Relebactam: A Novel β-Lactam-β-Lactamase Inhibitor Combination for the Treatment of Multidrug-Resistant Gram-Negative Infections

被引:63
作者
Smith, Jordan R. [1 ,2 ]
Rybak, Jeffrey M. [3 ]
Claeys, Kimberly C. [4 ]
机构
[1] High Point Univ, Fred Wilson Sch Pharm, Dept Clin Sci, 1 Univ Pkwy, High Point, NC 27268 USA
[2] Cone Hlth, Greensboro, NC USA
[3] Univ Tennessee, Coll Pharm, Dept Clin Pharm & Translat Sci, Memphis, TN USA
[4] Univ Maryland, Sch Pharm, Baltimore, MD 21201 USA
来源
PHARMACOTHERAPY | 2020年 / 40卷 / 04期
关键词
beta-lactams; infectious disease; imipenem; relebactam; PENICILLIN-BINDING PROTEINS; N-FORMIMIDOYL THIENAMYCIN; ANTIMICROBIAL SUSCEPTIBILITY; PSEUDOMONAS-AERUGINOSA; CEFTAZIDIME-AVIBACTAM; ESCHERICHIA-COLI; UNITED-STATES; IN-VITRO; PHARMACOKINETICS; ANTIBIOTICS;
D O I
10.1002/phar.2378
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Imipenem-cilastatin-relebactam (IMI-REL) is a novel beta-lactam-beta-lactamase inhibitor combination recently approved for the treatment of complicated urinary tract infections (cUTIs) and complicated intraabdominal infections (cIAIs). Relebactam is a beta-lactamase inhibitor with the ability to inhibit a broad spectrum of beta-lactamases such as class A and class C beta-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.
引用
收藏
页码:343 / 356
页数:14
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