| Literature DB >> 27575912 |
Elif Aktaş1, Gülşah Malkoçoğlu2, Barış Otlu3, Ayşegül Çopur Çiçek4, Canan Külah5, Füsun Cömert5, Cemal Sandallı6, Nafia Canan Gürsoy3, Duygu Erdemir1, Mehmet Emin Bulut1.
Abstract
Timely detection of carbapenemases by both phenotypic and genotypic methods is essential for developing strategies to control the spread of infections by carbapenem-resistant isolates and related morbidity and mortality. The aim of this study was to compare the performance of a commercial kit, the RAPIDEC® CARBA NP, and an in-house technique, the carbapenem inactivation method (CIM), against a panel of 136 carbapenemase- and noncarbapenemase-producing Enterobacteriaceae, Acinetobacter baumannii, and Pseudomonas aeruginosa isolates. RAPIDEC CARBA NP displayed 99% sensitivity and 100% specificity, whereas the sensitivity and specificity were 78% and 100% for the CIM test, respectively. A slight modification of the CIM test, a prolonged incubation time of 4 hours instead of two, increased the sensitivity of the test to 90% by diminishing false negativity particularly for A. baumannii. In conclusion, both tests possess a high performance and are practical for the detection of carbapenemases. Although RAPIDEC CARBA NP is a more rapid and reliable method, the CIM test may represent a useful tool for microbiology laboratories due to its simplicity and availability at any laboratory with low cost.Entities:
Keywords: CARBA NP; CIM; carbapenemase
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Year: 2016 PMID: 27575912 DOI: 10.1089/mdr.2016.0092
Source DB: PubMed Journal: Microb Drug Resist ISSN: 1076-6294 Impact factor: 3.431