Abstract
Surveillance for methicillin-resistant Staphylococcus aureus (MRSA) colonization can be an important element for infection control programs when managing a multidrug-resistant pathogen such as MRSA. The sensitivity and speed of laboratory testing affects the proportion of appropriate isolation days captured, which determines the success or failure of a MRSA control program. Chromogenic culture, CHROMagar MRSA (BBL, Becton Dickinson, Sparks, MD) and MRSA Select (Bio-Rad, Hercules, CA), with and without broth enrichment and real-time polymerase chain reaction (PCR; BD GeneOhm MRSA, BD Diagnostics, San Diego, CA), were compared andfound to have a wide range of sensitivities (78.5%-98.2%), specificities (91.6%-100.0%), and turnaround times (2-72 hours). Real-time PCR provided the most rapid results and demonstrated the highest sensitivity followed by broth-enriched culture and then direct plating for MRSA detection in nasal swabs. There was no substantial difference in the labor required for any of the 3 approaches. © American Society for Clinical Pathology.
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CITATION STYLE
Paule, S. M., Mehta, M., Hacek, D. M., Gonzalzles, T.-M., Robicsek, A., & Peterson, L. R. (2009). Chromogenic Media vs Real-Time PCR for Nasal Surveillance of Methicillin-Resistant Staphylococcus aureus. American Journal of Clinical Pathology, 131(4), 532–539. https://doi.org/10.1309/ajcp18onzutdugaq
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