Rapid detection of imipenem/relebactam susceptibility/resistance in Enterobacterales
Détails
ID Serval
serval:BIB_F24D1BAD2273
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Institution
Titre
Rapid detection of imipenem/relebactam susceptibility/resistance in Enterobacterales
Périodique
Clinical Microbiology and Infection
ISSN
1198-743X
ISSN-L
1198-743X
Statut éditorial
Publié
Date de publication
11/2023
Peer-reviewed
Oui
Volume
29
Numéro
11
Pages
1453.e1-1453.e5
Langue
anglais
Résumé
The treatment options for infections caused by carbapenem-resistant Enterobacterales are scarce and the development of new antibiotics is an urgent necessity. Imipenem/relebactam (IPR) has been recently introduced for treating severe infections related to multidrug-resistant bacteria. However, IPR resistance has already been reported in Enterobacterales, thus its rapid detection may be interesting for clinical decision-making. The aim of the study was to develop a rapid and accurate test, namely the Rapid IPR Nordmann Poirel (NP) test, for the identification of IPR resistance among multidrug-resistant Enterobacterales.
The Rapid IPR NP test is based on the detection of glucose metabolization because of bacterial growth in the presence of IPR. Bacterial growth is visually detectable by a colour change of the red phenol pH indicator, turning from red to yellow subsequent to the acidification of the medium upon bacterial growth. Cultures of a total of 94 Enterobacterales isolates were selected for evaluating the performance of the Rapid IPR NP test.
The sensitivity and specificity of the test were found to be 95.2% (95.2%, CI 84.2-98.7%) and 100% (100%, CI 93.1-100%), respectively. All the results were obtained within 3 hours incubation time at 35°C ± 2°C, which is a gain of time of at least 15 hours when compared with currently used antimicrobial susceptibility. The test showed two very major errors corresponding to OXA-48-producing Klebsiella pneumoniae isolates with MICs of IPR at 8 mg/L.
The Rapid IPR NP test is simple to perform and interpret, and shows excellent performances. Thus, it may suitable for implementation in clinical microbiology routine laboratories.
The Rapid IPR NP test is based on the detection of glucose metabolization because of bacterial growth in the presence of IPR. Bacterial growth is visually detectable by a colour change of the red phenol pH indicator, turning from red to yellow subsequent to the acidification of the medium upon bacterial growth. Cultures of a total of 94 Enterobacterales isolates were selected for evaluating the performance of the Rapid IPR NP test.
The sensitivity and specificity of the test were found to be 95.2% (95.2%, CI 84.2-98.7%) and 100% (100%, CI 93.1-100%), respectively. All the results were obtained within 3 hours incubation time at 35°C ± 2°C, which is a gain of time of at least 15 hours when compared with currently used antimicrobial susceptibility. The test showed two very major errors corresponding to OXA-48-producing Klebsiella pneumoniae isolates with MICs of IPR at 8 mg/L.
The Rapid IPR NP test is simple to perform and interpret, and shows excellent performances. Thus, it may suitable for implementation in clinical microbiology routine laboratories.
Mots-clé
Infectious Diseases, Microbiology (medical), General Medicine
Pubmed
Web of science
Création de la notice
03/08/2023 15:00
Dernière modification de la notice
16/04/2024 6:11