Methicillin-resistant Staphylococcus aureus (MRSA) is a major cause of health care-associated infections. Multiple factors, including transmission from unrecognized reservoirs of MRSA, are responsible for failure to control the spread of MRSA. We conducted prospective surveillance to determine the frequency of gastrointestinal colonization with MRSA among patients and its possible impact on nosocomial transmission of MRSA. Stool specimens submitted for Clostridium difficile toxin A/B assays were routinely inoculated on colistinnaladixic acid agar plates, and S. aureus was identified by using standard methods. Methicillin resistance was confirmed by growth on oxacillin-salt screening agar. For patients whose stool yielded MRSA, information regarding any previous cultures positive for MRSA or other organisms that would require contact precautions was obtained from the laboratory's computer system. During a 1-year period, 151 (9.8%) of 1,543 patients who had one or more stool specimens screened had MRSA in their stool. Ninety-three ( Screening of patients at high risk of colonization by methicillin-resistant Staphylococcus aureus (MRSA) has been recommended as a measure for controlling transmission of the organism in health care settings (24). Culture of specimens from the anterior nares and other body sites, such as wounds from high-risk individuals, often identifies patients with unrecognized MRSA colonization (9,12,19,38). Although gastrointestinal tract colonization by MRSA has been reported previously (4, 10, 29), culturing the stool specimens of patients who have been hospitalized for more than 3 days for potential pathogens is generally not recommended (33, 39). We conducted prospective surveillance of stool specimens in a hospital where MRSA is highly endemic to determine the frequency of MRSA gastrointestinal colonization among high-risk patients. A secondary aim of the study was to determine if recognition of gastrointestinal colonization by MRSA would affect the implementation of barrier precautions designed to reduce the spread of MRSA.
MATERIALS AND METHODSAs part of ongoing surveillance for MRSA in a 450-bed university-affiliated teaching hospital, all stool specimens submitted to the clinical microbiology laboratory for Clostridium difficile toxin A/B testing were inoculated onto colistinnaladixic acid (CNA) agar plates that were incubated under aerobic conditions at 36°C overnight. This approach was taken because it seemed likely that patients at risk of antibiotic-associated diarrhea due to C. difficile would also be at increased risk of carrying other resistant pathogens such as MRSA. Colonies growing on CNA agar with morphology characteristic of S. aureus were identified by using coagulase tests. Those identified as S. aureus were inoculated onto commercially available oxacillin-salt screening agar (BBL, Cockeysville, MD), and those capable of growing on oxacillin-salt screening agar were classified as MRSA. The number of colonies of MRSA growing on CNA plates was recorded as 1ϩ to 4ϩ, with 4ϩ re...