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Imipenem/cilastatin/relebactam

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dc.contributor.author Mansour, Hanine
dc.contributor.author Oweini, Ahmad E. L
dc.contributor.author Chahine, Elias B.
dc.contributor.author Karaoui, Lamis R.
dc.date.accessioned 2022-04-06T12:41:57Z
dc.date.available 2022-04-06T12:41:57Z
dc.date.copyright 2021 en_US
dc.date.issued 2022-04-06
dc.identifier.issn 1079-2082 en_US
dc.identifier.uri http://hdl.handle.net/10725/13461
dc.description.abstract Purpose The pharmacology, pharmacokinetics, pharmacodynamics, antimicrobial activity, efficacy, safety, and current regulatory status of imipenem/cilastatin/relebactam are reviewed. Summary Imipenem/cilastatin/relebactam is a newly approved anti-infective combination of a well-established β-lactam and a new β-lactamase inhibitor for the treatment of complicated urinary tract infections (cUTIs), including pyelonephritis, and complicated intra-abdominal infections (cIAIs) caused by susceptible gram-negative bacteria in patients 18 years of age or older with limited or no alternative treatment options. The antibiotic is also indicated for the treatment of hospital-acquired bacterial pneumonia (HABP) and ventilator-associated bacterial pneumonia (VABP). The antibiotic is active in vitro against a wide range of pathogens, including multidrug-resistant (MDR) Pseudomonas aeruginosa and carbapenem-resistant Enterobacterales (CRE) such as Klebsiella pneumoniae carbapenemase. The addition of relebactam does not restore the activity of imipenem against metallo-β-lactamase (MBL)–producing Enterobacterales and carbapenem-resistant Acinetobacter baumannii. Two phase 3 clinical trials of imipenem/cilastatin/relebactam were conducted. In the RESTORE-IMI 1 trial, the efficacy and safety of imipenem/cilastatin/relebactam was found to be comparable to that of imipenem/cilastatin plus colistin for the treatment of infections caused by imipenem-nonsusceptible gram-negative bacteria in patients with HABP/VABP, cUTIs, and cIAIs, with a significantly lower incidence of nephrotoxicity reported with the new antibiotic. The RESTORE-IMI 2 trial demonstrated the noninferiority of imipenem/cilastatin/relebactam to piperacillin/tazobactam for the treatment of HABP/VABP. Commonly reported adverse events in clinical trials included anemia, elevated liver enzymes, electrolyte imbalances, nausea, vomiting, diarrhea, headache, fever, phlebitis and/or infusion-site reactions, and hypertension. Conclusion Imipenem/cilastatin/relebactam is a new β-lactam/β-lactamase inhibitor combination with activity against MDR gram-negative bacteria, including many CRE but excluding MBL-producing Enterobacterales and carbapenem-resistant Acinetobacter baumannii. It is approved for the treatment of cUTIs, cIAIs, and HABP/VABP. en_US
dc.language.iso en en_US
dc.title Imipenem/cilastatin/relebactam en_US
dc.type Article en_US
dc.description.version Published en_US
dc.title.subtitle A new carbapenem β-lactamase inhibitor combination en_US
dc.author.school SOP en_US
dc.author.idnumber 201205628 en_US
dc.author.idnumber 200101817 en_US
dc.author.department Pharmacy Practice en_US
dc.relation.journal American Journal of Health-System Pharmacy en_US
dc.journal.volume 78 en_US
dc.journal.issue 8 en_US
dc.article.pages 678-683 en_US
dc.keywords β-lactam/β-lactamase inhibitor en_US
dc.keywords Imipenem/cilastatin en_US
dc.keywords Intraabdominal infection en_US
dc.keywords Pneumonia en_US
dc.keywords Relebactam en_US
dc.keywords Urinary tract infection en_US
dc.identifier.doi https://doi.org/10.1093/ajhp/zxab012 en_US
dc.identifier.ctation Mansour, H., Ouweini, A. E., Chahine, E. B., & Karaoui, L. R. (2021). Imipenem/cilastatin/relebactam: A new carbapenem β-lactamase inhibitor combination. American Journal of Health-System Pharmacy, 78(8), 674-683. en_US
dc.author.email hanine.mansour@lau.edu.lb en_US
dc.author.email lamis.karaoui@lau.edu.lb en_US
dc.identifier.tou http://libraries.lau.edu.lb/research/laur/terms-of-use/articles.php en_US
dc.identifier.url https://academic.oup.com/ajhp/article/78/8/674/6134520?login=true en_US
dc.orcid.id https://orcid.org/0000-0001-6383-0288 en_US
dc.orcid.id https://orcid.org/ 0000-0002-7857-7374 en_US
dc.author.affiliation Lebanese American University en_US


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