In vitro activity of imipenem/relebactam against Enterobacteriaceae and Pseudomonas aeruginosa isolated from intraabdominal and urinary tract infection samples: SMART Surveillance United States 2015-2017.

Gram-negative bacilli Imipenem/relebactam Intraabdominal infection Study for Monitoring Antimicrobial Resistance Trends (SMART) United States Urinary tract infection

Journal

Journal of global antimicrobial resistance
ISSN: 2213-7173
Titre abrégé: J Glob Antimicrob Resist
Pays: Netherlands
ID NLM: 101622459

Informations de publication

Date de publication:
06 2020
Historique:
received: 21 05 2019
revised: 17 10 2019
accepted: 27 10 2019
pubmed: 8 11 2019
medline: 24 6 2021
entrez: 8 11 2019
Statut: ppublish

Résumé

Antimicrobial resistance, including multidrug-resistance (MDR), is increasing, especially among Gram-negative bacilli. New agents are needed to treat infections caused by these pathogens. This report assessed the activity of imipenem/relebactam against Gram-negative bacilli from intraabdominal infections (IAIs) and urinary tract infections (UTIs) submitted to the SMART (Study for Monitoring Antimicrobial Resistance Trends) global surveillance programme in the United States from 2015 to 2017. Broth microdilution MICs for imipenem/relebactam and comparators were determined by a central laboratory against isolates of non-Proteeae Enterobacteriaceae (NPE) and Pseudomonas aeruginosa (P. aeruginosa). Imipenem/relebactam MICs were interpreted using United States Food and Drug Administration (FDA) breakpoints. 99.5% of NPE isolates collected from patients with IAIs (n=3633) and UTIs (n=3038) were susceptible to imipenem/relebactam, as were 77.9% of imipenem-nonsusceptible, 96.3% of Klebsiella pneumoniae carbapenemase (KPC)-positive, and 98.7% of MDR isolates from IAIs and UTIs combined. A total of 96.7% of IAI isolates (n=486) and 96.4% of UTI isolates (n=360) of P. aeruginosa were susceptible to imipenem/relebactam, as were 85.0% of imipenem-nonsusceptible and 87.3% of MDR isolates from IAIs and UTIs combined. Percent susceptibility to imipenem/relebactam for cefepime-, ceftazidime-, and piperacillin-tazobactam-nonsusceptible isolates was 98.3-98.8% for NPE and 87.3-90.0% for P. aeruginosa. Imipenem/relebactam demonstrated potent in vitro activity against NPE and P. aeruginosa isolates from IAIs and UTIs, including against resistant subsets, and will provide important coverage for IAIs and UTIs caused by β-lactam-resistant, MDR, and KPC-positive Gram-negative bacilli.

Identifiants

pubmed: 31698105
pii: S2213-7165(19)30290-5
doi: 10.1016/j.jgar.2019.10.028
pii:
doi:

Substances chimiques

Anti-Bacterial Agents 0
Azabicyclo Compounds 0
Imipenem 71OTZ9ZE0A
relebactam Y1MYA2UHFL

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

223-228

Informations de copyright

Copyright © 2019 International Society for Antimicrobial Chemotherapy. Published by Elsevier Ltd. All rights reserved.

Auteurs

James A Karlowsky (JA)

International Health Management Associates, Inc., Schaumburg, IL, USA; Department of Medical Microbiology and Infectious Diseases, Max Rady College of Medicine, University of Manitoba, Winnipeg, Canada.

Sibylle H Lob (SH)

International Health Management Associates, Inc., Schaumburg, IL, USA. Electronic address: shlob@ihma.com.

Krystyna M Kazmierczak (KM)

International Health Management Associates, Inc., Schaumburg, IL, USA.

Katherine Young (K)

Merck & Co., Inc., Kenilworth, NJ, USA.

Mary R Motyl (MR)

Merck & Co., Inc., Kenilworth, NJ, USA.

Daniel F Sahm (DF)

International Health Management Associates, Inc., Schaumburg, IL, USA.

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Classifications MeSH