Spectra VRE (Remel, Lenexa, KS) is a chromogenic medium designed to recover and differentiate vancomycin-resistant Enterococcus faecium and Enterococcus faecalis (VRE). This medium was compared to bile esculin azide agar (BEAV) and was 98.2% sensitive and 99.3% specific compared to BEAV, which was 87.6% sensitive and 87.1% specific at 24 h.Two Enterococcus species, E. faecalis and E. faecium, cause the majority of human enterococcal infections (1). The rapid strain identification for patients colonized in the gastrointestinal tract with vancomycin-resistant strains of these species (VRE) is critical, as infection with these organisms can result in endocarditis, urinary tract, bloodstream, and wound infections with reduced therapeutic options (3). Screening for VRE is essential for the proper implementation of isolation precautions, as asymptomatic carriers serve as reservoirs for VRE infection or transmission (4, 7, 9). Successful identification of patients colonized with VRE requires rapid and accurate screening tests that are easily interpretable. The purpose of this multicenter study was to compare the performance of a new chromogenic medium, Spectra VRE, to bile esculin azide agar supplemented with 6 g vancomycin/ml (BEAV; Remel) as a means of screening stool specimens for VRE colonization.Stool specimens were collected from inpatients in sterile containers for Clostridium difficile testing and stored at 4°C for up to 3 days. Specimens were plated with a sterile Dacron swab to BEAV and Spectra VRE and streaked for isolation by the quadrant technique. Inoculated plates were incubated at 35°C in ambient air and examined for growth at 18, 24, and 48 h. Pink, purple, or dark blue colonies on Spectra VRE were presumptively identified as vancomycinresistant E. faecium. Light blue colonies on Spectra VRE were presumptively identified as vancomycin-resistant E. faecalis. Presumed VRE colonies on BEAV appeared dark brown or black.Presumptive VRE from Spectra VRE and BEAV were subcultured to tryptic soy agar plates (TSA; Remel) and incubated at 35°C for 24 h. Catalase-negative, Gram-positive cocci positive for L-pyrrolidonyl--naphthylamide (PYR; Remel) were further identified using methyl-␣-Dglucopyranoside (MDG; Remel), motility test medium (Remel), PB arabinose (Remel), and colony morphology on blood agar. VRE isolates were identified based on the following performance characteristics: E. faecalis, MDG-neg-* Corresponding author. Mailing address: