Rapid identification from rectal swabs of the clinically most relevant carbapenemase genes from gram-negative bacteria using the BD MAX Check-Points CPO Assay.


Journal

Diagnostic microbiology and infectious disease
ISSN: 1879-0070
Titre abrégé: Diagn Microbiol Infect Dis
Pays: United States
ID NLM: 8305899

Informations de publication

Date de publication:
Jan 2022
Historique:
received: 19 04 2021
revised: 01 09 2021
accepted: 17 09 2021
pubmed: 23 10 2021
medline: 21 1 2022
entrez: 22 10 2021
Statut: ppublish

Résumé

We conducted an international multicentre evaluation to assess the clinical performance characteristics of the new multiplex PCR-based BD MAX Check-Points CPO assay to detect the 5 major carbapenemase families: KPC, VIM/IMP (tested simultaneously), NDM and OXA-48 compared to a reference method consisting of 2 culture methods (to improve recovery of CPO isolates from the rectal swabs), followed by carbapenem susceptibility testing and sequencing of target carbapenemase genes. Tests were performed from rectal swab specimens in ESwab collection and transport devices. Positive percent agreement (PPA) for BD MAX Check-Points CPO for KPC and OXA-48 were 88.2% (95% CI:72.6-96.7) and 96.2% (95% CI:80.4-99.9), respectively. Negative percent agreement was ≥99% for each gene. Insufficient samples (≤10) were positive for VIM/IMP or NDM tests to calculate meaningful PPA values. The BD MAX Check-Points CPO assay represents an accurate tool for rapid recognition of patients with rectal colonization by the most commonly encountered CPOs.

Identifiants

pubmed: 34678712
pii: S0732-8893(21)00246-7
doi: 10.1016/j.diagmicrobio.2021.115554
pii:
doi:

Substances chimiques

Anti-Bacterial Agents 0
Bacterial Proteins 0
Carbapenems 0
beta-Lactamases EC 3.5.2.6
carbapenemase EC 3.5.2.6

Types de publication

Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

115554

Informations de copyright

Copyright © 2021 Elsevier Inc. All rights reserved.

Auteurs

Sergio García-Fernández (S)

Servicio de Microbiología, Hospital Universitario Ramón y Cajal and Instituto Ramón y Cajal de Investigación Sanitaria (IRYCIS), Madrid, Spain; Red Española de Investigación en Patología Infecciosa (REIPI), Madrid, Spain; Servicio de Microbiología, Hospital Universitario Marqués de Valdecilla-IDIVAL, Santander, Spain (Present address).

Patricia J Simner (PJ)

Division of Medical Microbiology, Department of Pathology, Johns Hopkins School of Medicine, Baltimore, Maryland, USA.

Gina Thomson (G)

Department of Pathology and Laboratory Medicine, School of Medicine, University of Louisville, Louisville, Kentucky, USA.

Matthew Faron (M)

Department of Pathology, Medical College of Wisconsin, Milwaukee, Wisconsin, USA.

Ron Bosboom (R)

Rijnstate Hospital, Arnhem, the Netherlands.

Arjanne van Griethuijsen (A)

Ziekenhuis Gelderse Vallei, Ede, the Netherlands.

María García-Castillo (M)

Servicio de Microbiología, Hospital Universitario Ramón y Cajal and Instituto Ramón y Cajal de Investigación Sanitaria (IRYCIS), Madrid, Spain; Red Española de Investigación en Patología Infecciosa (REIPI), Madrid, Spain.

Renee Harris (R)

Servicio de Microbiología, Hospital Universitario Marqués de Valdecilla-IDIVAL, Santander, Spain (Present address).

Nathan A Ledeboer (NA)

Department of Pathology, Medical College of Wisconsin, Milwaukee, Wisconsin, USA.

Rafael Cantón (R)

Servicio de Microbiología, Hospital Universitario Ramón y Cajal and Instituto Ramón y Cajal de Investigación Sanitaria (IRYCIS), Madrid, Spain; Red Española de Investigación en Patología Infecciosa (REIPI), Madrid, Spain. Electronic address: rafael.canton@salud.madrid.org.

Kenneth S Thomson (KS)

Department of Pathology and Laboratory Medicine, School of Medicine, University of Louisville, Louisville, Kentucky, USA.

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Classifications MeSH