Background: Infections due to carbapenem-resistant Gram-negative bacteria are emerging as an important challenge in health-care settings and a growing concern worldwide. Lateral flow immunoassay NG-Test CARBA 5 can detect the five most reported carbapenemases (KPC, OXA-48-like, VIM, IMP, and NDM). Direct testing of positive blood cultures could reduce time to detection. This study aims to validate and report on the diagnostic yield of a novel method for carbapenemase detection in positive blood culture vials using NG-Test CARBA 5.
Methods: We implemented an investigator-developed method for the direct testing of positive blood cultures using NG-Test CARBA 5. We compared results between genotypic, phenotypic, and direct NG-Test CARBA 5 in blood.
Results: A total of 32 isolates were tested (21 Enterobacterales and 11 ). Genotypic testing detected 23 carbapenemases. When comparing the results of NG-Test CARBA 5 in blood with genotypic testing, agreement was observed in 31/32 (97%) tests. The sensitivity, specificity, positive predictive value, and negative predictive value of the NG-Test CARBA 5 in blood were 93%, 100%, 100%, and 94%, respectively.
Conclusions: Our method using NG-Test CARBA 5 directly in blood culture samples presented an excellent diagnostic yield when compared to genotypic profiling and permits an accurate detection of carbapenemases.
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http://dx.doi.org/10.3390/antibiotics13111105 | DOI Listing |
Ann Clin Microbiol Antimicrob
December 2024
The Centre for Clinical Microbiology, University College London, London, UK.
Introduction: Colonisation and infection with Carbapenem-resistant Enterobacterales (CRE) in healthcare settings poses significant risks, especially for vulnerable patients. Genomic analysis can be used to trace transmission routes, supporting antimicrobial stewardship and informing infection control strategies. Here we used genomic analysis to track the movement and transmission of CREs within clinical and environmental samples.
View Article and Find Full Text PDFAntibiotics (Basel)
November 2024
Department of Infectious Diseases, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, 15 Vasco de Quiroga, Belisario Domínguez Secc 16, Tlalpan, Mexico City 14080, Mexico.
Background: Infections due to carbapenem-resistant Gram-negative bacteria are emerging as an important challenge in health-care settings and a growing concern worldwide. Lateral flow immunoassay NG-Test CARBA 5 can detect the five most reported carbapenemases (KPC, OXA-48-like, VIM, IMP, and NDM). Direct testing of positive blood cultures could reduce time to detection.
View Article and Find Full Text PDFPol J Microbiol
September 2024
The First Affiliated Hospital of Anhui Medical University, Hefei, China.
The global proliferation of carbapenemase-producing bacteria (CPB) has garnered significant attention worldwide. Early diagnosis of CPB and accurate identification of carbapenemases are crucial for preventing the spread of CPB and ensuring targeted antibiotic therapy. Therefore, efficient and accurate identification of carbapenemases is paramount in clinically treating diseases associated with CPB.
View Article and Find Full Text PDFAntibiotics (Basel)
August 2024
Department of Microbiology, AHEPA University Hospital, School of Medicine, Aristotle University of Thessaloniki, S. Kiriakidi Str. 1, 54636 Thessaloniki, Greece.
Carbapenemase-producing strains present a specific geographical distribution regarding the type of carbapenemase-encoding genes that they harbor. For more than twenty years, VIM-type enzymes were the only major carbapenemases that were detected among isolates in Greece until the emergence of NDM-1-encoding in early 2023. In the present study, we present the rapid reversal of the carbapenemase-producing epidemiology from - to -harbouring isolates that occurred in our hospital since then.
View Article and Find Full Text PDFJ Appl Microbiol
August 2024
Department of Laboratory Medicine, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430030, China.
Aims: Adequately and accurately identifying carbapenemase-producing Enterobacterales (CPE) is vital for selecting appropriate antimicrobial therapy and implementing effective infection control measures. This study aims to optimize the phenotypic detection method of carbapenemase for routine diagnostics in clinical microbiology laboratories.
Methods And Results: Carbapenemase genes in 2665 non-duplicate CRE clinical strains collected from various regions of China were confirmed through whole-genome sequencing (WGS).
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