Abstract

BackgroundThe rise of methicillin-resistant Staphylococcus aureus (MRSA) is a global health concern. Paucity of data on MRSA carriage prevalence and diagnostic methods in resource-limited settings hampers efforts to define the problem and plan an appropriate response. Additionally, high variability in cost and logistical characteristics of MRSA screening methods may impede infection control efforts. We compared the performance of locally-available chromogenic agar BD CHROMagar MRSA II and two PCR-based assays (Hain GenoQuick MRSA and Cepheid Xpert SA Complete) for the detection of asymptomatic MRSA carriage in nasal swabs.ResultsDuring 2015, we enrolled 500 patients from five hospital wards at a Ugandan regional referral hospital. We found 30% prevalence of methicillin-sensitive Staphylococcus aureus (MSSA) nasal carriage, and 5.4% MRSA nasal carriage prevalence. Compared to a composite reference standard defined as a positive test result on any one of the three assays, Hain GenoQuick MRSA demonstrated the highest sensitivity (96%) followed by direct plating on CHROMagar at (70%), with the lowest sensitivity observed with Xpert SA Complete (52%). Cepheid Xpert provided the most rapid results (< 1 h) but was the most expensive (US $45–50/test). Substantially more labor was required for the Hain GenoQuick MRSA compared to Xpert SA Complete or CHROMagar tests.ConclusionMRSA nasal carriage prevalence rates were low, and high diagnostic sensitivity was achieved using Hain GenoQuick MRSA. Chromogenic media had significantly lower sensitivity, but may represent a viable local option given its lower cost compared to PCR-based assays.

Highlights

  • The rise of methicillin-resistant Staphylococcus aureus (MRSA) is a global health concern

  • MRSA infections remain a significant cause of hospital-acquired infections [4, 5]; accounting for up to 75% of all S. aureus isolates from patients with skin and soft-tissue infections among patients seen in emergency departments in the United States [3]

  • Of 500 samples tested for MRSA using the Cepheid Xpert SA Complete assay, one yielded an invalid result, leaving 499 samples for analysis

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Summary

Introduction

The rise of methicillin-resistant Staphylococcus aureus (MRSA) is a global health concern. MRSA infections remain a significant cause of hospital-acquired infections [4, 5]; accounting for up to 75% of all S. aureus isolates from patients with skin and soft-tissue infections among patients seen in emergency departments in the United States [3]. In many high-resource settings, patients are tested for MRSA carriage on hospital admission and may undergo isolation or decontamination to reduce MRSA transmission [7, 8]. Towards this end, several detection methods have been used to evaluate MRSA carriage, including polymerase chain reaction (PCR)-based assays

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