Abstract

ISSUE: Methicillin-resistant S. aureus (MRSA) has become a widespread nosocomial pathogen. The use of active surveillance cultures to detect nasal carriage of MRSA is recommended to identify carriers and initiate contact precautions. OBJECTIVE: To evaluate time to detection (TTD) of MRSA using chromogenic media compared to traditional culture methods from nasal surveillance cultures. METHODS: A total of 1133 nasal samples were plated to sheep blood agar (SBA) and BBL CHROMagar™ MRSA (C-MRSA, BBL, Sparks, Maryland). MRSA appear as mauve colonies on C-MRSA. All other organisms including methicillin-susceptible staphylococci are inhibited or produce a distinctly different colony color. If mauve colonies are detected at 24 hours, MRSA may be reported without further testing. At 48 hour detection, a slide coagulase needs to be completed. MRSA was identified from SBA by slide coagulase, exogenous DNase, and mannitol fermentation. Susceptibility testing was performed using agar dilution. RESULTS: Of the 1133 samples tested, 78 (7.4%) were positive for MRSA. Forty-one of 78 (53%) had a TTD of 24 hours from C-MRSA and 48 hours from SBA. Eleven of 78 (14%) had a TTD of 24 hours from C-MRSA and greater than 48 hours from SBA. At 24 hours, an additional 11 (14%) isolates were recovered on C-MRSA that were not detected on SBA. After 48 hours incubation, seven of 78 (9%) were detected on both media, while an additional five of 78 (6%) had TTD of 48 hours on C-MRSA and equal or greater than 72 hours on SBA. An additional two isolates were recovered on C-MRSA at 48 hours that were not detected on SBA and one isolate had a TTD of 72 hours from SBA and was not recovered on C-MRSA. CONCLUSION: Sixty-three of 78 (81%) of MRSA were reported at 24 hours using C-MRSA versus 48 hours or greater using traditional culture methods. Eleven of 63 (17%) were reported 3 or more days later than the C-MRSA result. Eleven of 63 (17%) were missed by traditional culture methods. A more rapid positive report from nares surveillance cultures may assist the infection control practitioner in identifying colonized patients, initiate contact precautions, and potentially decrease the spread of MRSA.

Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call