Prospective evaluation of a screening algorithm for carbapenemase-producing Enterobacteriaceae.


Journal

Journal of clinical laboratory analysis
ISSN: 1098-2825
Titre abrégé: J Clin Lab Anal
Pays: United States
ID NLM: 8801384

Informations de publication

Date de publication:
Mar 2019
Historique:
received: 13 08 2018
revised: 05 10 2018
accepted: 07 10 2018
pubmed: 6 11 2018
medline: 30 4 2019
entrez: 4 11 2018
Statut: ppublish

Résumé

Carbapenemase-producing Enterobacteriaceae (CPE) have become a major public health issue. The objective of the present study was to prospectively assess the analytical performance of a CPE detection algorithm based on phenotypic tests (the screening test) and MALDI-ToF hydrolysis (the confirmatory test). Over a 6-month period and based on a disk diffusion method, 74 carbapenem-resistant strains were included in this study. Of the collected isolates, 54 turned out to be negative after phenotypic tests. Hence, 20 strains (including all of the CPEs) were checked with the confirmation test. Seven strains were positive. After molecular biology assessments in a reference center, three of the seven were found to be false positives. The algorithm had a negative predictive value and a sensitivity of 100%, a specificity of 77%, and a positive predictive value of 20%. The algorithm has a 24-hour turnaround time and helps to avoid using expensive molecular biology tests; we consider that it can be used on a routine basis for screening clinical strains.

Sections du résumé

BACKGROUND BACKGROUND
Carbapenemase-producing Enterobacteriaceae (CPE) have become a major public health issue. The objective of the present study was to prospectively assess the analytical performance of a CPE detection algorithm based on phenotypic tests (the screening test) and MALDI-ToF hydrolysis (the confirmatory test).
METHODS METHODS
Over a 6-month period and based on a disk diffusion method, 74 carbapenem-resistant strains were included in this study.
RESULTS RESULTS
Of the collected isolates, 54 turned out to be negative after phenotypic tests. Hence, 20 strains (including all of the CPEs) were checked with the confirmation test. Seven strains were positive. After molecular biology assessments in a reference center, three of the seven were found to be false positives. The algorithm had a negative predictive value and a sensitivity of 100%, a specificity of 77%, and a positive predictive value of 20%.
CONCLUSION CONCLUSIONS
The algorithm has a 24-hour turnaround time and helps to avoid using expensive molecular biology tests; we consider that it can be used on a routine basis for screening clinical strains.

Identifiants

pubmed: 30390351
doi: 10.1002/jcla.22706
pmc: PMC6818548
doi:

Substances chimiques

Anti-Bacterial Agents 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e22706

Informations de copyright

© 2018 Wiley Periodicals, Inc.

Références

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pubmed: 28980084
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pubmed: 25355766
J Clin Microbiol. 2011 Aug;49(8):2798-803
pubmed: 21632895
Antimicrob Agents Chemother. 1995 Jun;39(6):1211-33
pubmed: 7574506
BMC Infect Dis. 2017 Jan 17;17(1):78
pubmed: 28095794
Emerg Infect Dis. 2011 Oct;17(10):1791-8
pubmed: 22000347
Clin Microbiol Infect. 2010 Feb;16(2):112-22
pubmed: 20085605
J Antimicrob Chemother. 2014 Oct;69(10):2706-12
pubmed: 24942333
J Antimicrob Chemother. 2016 Jan;71(1):135-40
pubmed: 26462984
J Clin Lab Anal. 2019 Mar;33(3):e22706
pubmed: 30390351
Trends Mol Med. 2012 May;18(5):263-72
pubmed: 22480775

Auteurs

Morgane Choquet (M)

Department of Bacteriology, Amiens University Hospital, Amiens, France.
Microbiology Research Unit, AGIR EA4294, Jules Verne University of Picardie, Amiens, France.

Raphaël Guiheneuf (R)

Department of Bacteriology, Amiens University Hospital, Amiens, France.
Microbiology Research Unit, AGIR EA4294, Jules Verne University of Picardie, Amiens, France.

Sandrine Castelain (S)

Department of Bacteriology, Amiens University Hospital, Amiens, France.
Microbiology Research Unit, AGIR EA4294, Jules Verne University of Picardie, Amiens, France.

Emilie Pluquet (E)

Department of Bacteriology, Amiens University Hospital, Amiens, France.
Microbiology Research Unit, AGIR EA4294, Jules Verne University of Picardie, Amiens, France.

Véronique Decroix (V)

Department of Bacteriology, Amiens University Hospital, Amiens, France.
Microbiology Research Unit, AGIR EA4294, Jules Verne University of Picardie, Amiens, France.

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Classifications MeSH