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Τρίτη 31 Οκτωβρίου 2017

Performance of an ESBL-PCR assay for rapid and direct detection of ESBL carriage from rectal swabs and enrichment broth.

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Performance of an ESBL-PCR assay for rapid and direct detection of ESBL carriage from rectal swabs and enrichment broth.

J Hosp Infect. 2017 Oct 25;:

Authors: van den Bijllaardt W, Janssens MM, Buiting AG, Muller AE, Mouton JW, Verweij JJ

Abstract
BACKGROUND: ESBL screening and contact precautions on patients at high risk for ESBL carriage are considered important infection control measures. Since contact precautions are costly and may negatively impact patient care, rapid exclusion of ESBL carriage and therefore earlier discontinuation of contact precautions are desired.
AIM: In the present study, the performance of an ESBL PCR targeting blaCTX-M genes was evaluated as a screening assay for ESBL carriage.
METHODS: Two methods were assessed: PCR performed directly on rectal swabs and PCR on enrichment broth after incubation overnight. The reference standard was culture of ESBL producing Enterobacteriaceae on selective agar after overnight enrichment and confirmation by the combination disk diffusion method. Microarray (Checkpoints. NL) was used for discrepancy analysis. A secondary analysis was performed to evaluate the added value of including a blaSHV target in the PCR.
FINDINGS: A total of 551 rectal swabs from 385 patients were included of which 28 (5%) were ESBL positive in culture. The sensitivity, specificity, PPV and NPV were 86%, 98%, 67% and 99%, respectively, for PCR directly on swabs, and 96%, 98%, 75% and 100%, respectively, for PCR on enrichment broth. Adding a blaSHV target to the assay resulted in a lower PPV without increasing the sensitivity and NPV.
CONCLUSION: Screening for ESBL by PCR directly on rectal swabs has a high negative predictive value, is up to 48 hours faster than traditional culture and therefore facilitates earlier discontinuation of contact precautions, thereby improving patient care and saving valuable resources in the hospital.

PMID: 29080706 [PubMed - as supplied by publisher]



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