Abstract

BackgroundRapid identification of positive blood cultures is important for initiation of optimal treatment in septic patients. Effects of automated, microarray-based rapid identification systems on antibiotic prescription against community-onset bacteremia (COB) remain unclear.MethodsWe prospectively enrolled 177 patients with 185 COB episodes (occurring within 72 h of admission) over 17 months. Bacteremia episodes due to gram-positive bacteria (GP) and gram-negative bacteria (GN) in the same patient were counted separately. For GP bacteremia, patients with ≥2 sets of positive blood cultures were included. The primary study objective was evaluating the rates of antibiotic prescription changes within 2 days of rapid identification using the Verigene system.ResultsBacteremia due to GN and GP included 144/185 (77.8%) and 41/185 (22.2%) episodes, respectively. Antibiotic prescription changes occurred in 51/185 cases (27.6% [95%CI:21.3–34.6%]) after Verigene analysis and 70/185 cases (37.8% [30.8–45.2%]) after conventional identification and susceptibility testing. Prescription changes after Verigene identification were more frequent in GP (17/41[41.5%]) than in GN (34/144[23.5%]). Among bacteremia due to single pathogen targeted by Verigene test, bacterial identification agreement between the two tests was high (GP: 38/39[97.4%], GN: 116/116[100%]). The Verigene test correctly predicted targeted antimicrobial resistance. The durations between the initiation of incubation and reporting of the results for the Verigene system and conventional test was 28.3 h (IQR: 25.8–43.4 h) and 90.6 h (68.3–118.4 h), respectively. In only four of the seven episodes of COB in which two isolates were identified by conventional tests, the Verigene test correctly identified both organisms.ConclusionWe observed a high rate of antibiotic prescription changes after the Verigene test in a population with COB especially in GP. The Verigene test would be a useful tool in antimicrobial stewardship programs among patients with COB.

Highlights

  • Rapid identification of positive blood cultures is important for the rapid initiation of optimal treatment in patients with bacteremia, increasing the opportunity for antimicrobial stewardship programs (ASPs) [1]

  • Among bacteremia due to single pathogen targeted by Verigene test, bacterial identification agreement between the two tests was high (GP: 38/39[97.4%], gram-negative bacteria (GN): 116/116[100%])

  • We observed a high rate of antibiotic prescription changes after the Verigene test in a population with community-onset bacteremia (COB) especially in gram-positive bacteria (GP)

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Summary

Introduction

Rapid identification of positive blood cultures is important for the rapid initiation of optimal treatment in patients with bacteremia, increasing the opportunity for antimicrobial stewardship programs (ASPs) [1]. Among the variety of available rapid identification systems, the Verigene gram-positive and gram-negative blood culture nucleic acid test (BC-GP, BC-GN; Nanosphere Inc., Northbrook, IL, USA), an automated microarray-based rapid identification system, is able to identify multiple bacterial species and their resistance genes, and the microbiological and clinical utility and impact of automated systems have been reported [2,3,4,5]. Considering its ability to identify common resistance genes and some typical healthcare-associated bacteria (e.g., methicillin-resistant Staphylococcus aureus [MRSA], Pseudomonas aeruginosa, Acinetobacter spp., and Serratia marcescens), the use of the Verigene system is expected to have clinical impact, including effects on antimicrobial prescriptions against hospital-acquired bacteremia. Microarray-based rapid identification systems on antibiotic prescription against community-onset bacteremia (COB) remain unclear

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