bThree chromogenic media, chromID MRSA SMART (SMART), chromID MRSA first generation (chromID), and Brilliance MRSA (OX2), were evaluated for methicillin-resistant Staphylococcus aureus (MRSA) screening using 1,220 samples. The sensitivity at 24 h was significantly better with the SMART agar (66.4%) than that with chromID agar (50.5%). Enrichment and incubation until 48 h are still needed for an optimal yield. M ethicillin-resistant Staphylococcus aureus (MRSA) is a major cause of nosocomial infections (1, 2). Asymptomatic carriers in the nose, throat, or on the skin represent the major reservoirs for MRSA transmission in hospitals (3, 4). Rapid identification of MRSA colonization is of utmost importance to identify carriers in order to implement infection control procedures and reduce patient-to-patient transmission (5-7). Several chromogenic agars have been specifically developed for MRSA screening. These media show superior sensitivity and specificity compared to those of conventional selective plates (8-10). The purpose of this study was to compare the performance of the new bioMérieux chromID MRSA SMART (SMART) agar with bioMérieux chromID MRSA first generation (chromID) and Oxoid Brilliance MRSA version 2 agar (OX2) with and without enrichment broth (EB).This prospective study was conducted between January and May 2014 at Hôpital Erasme, Brussels, Belgium, and Amphia Hospital, Breda, The Netherlands. Screening samples were collected from patients admitted to both hospitals using ESwab transport medium (Copan Diagnostics). The swabs were inoculated into EB supplemented with 6.5% NaCl (bioMérieux) and directly on the SMART, chromID, and OX2 agars, and a Colombia agar plate with 5% sheep blood (SBA) (growth control) at 35 to 37°C. EB was subcultured after 24 h onto secondary selective plates. Primary plates were examined at 24 h and 48 h, and secondary plates were examined after 24 h. The assessments included comparative amounts of growth of presumptive MRSA/sample and the amount of background flora able to grow on the three media. All suspected MRSA colonies were identified by matrix-assisted laser desorption ionization-time of flight mass spectrometry (MALDI-TOF MS), and methicillin susceptibility was determined by the cefoxitin disk method, as recommended by EUCAST (11).Each new MRSA isolate per patient and discrepant results between the three media were tested for the presence of the mecA gene by in-house PCR (Erasme) (12) or GeneXpert (Xpert SA nasal G3 kit version 4; Cepheid) (Amphia). Discrepant results (typical MRSA colonies and mecA negative) were further analyzed for the presence of the mecC gene, and the MICs to cefoxitin and oxacillin were determined (11, 13). The presence of MRSA recovered from at least one of the media (primary chromogenic agar or after enrichment) was considered the gold standard. True-positive results were defined as MRSA isolates showing characteristic colonies (color and morphology) confirmed by PCR, false-positive results as isolates with typical colonies not confirmed by PC...