OBJECTIVE: To study vancomycin-resistant enterococci (VRE) gastrointestinal
colonization prevalence in high-risk hospitalized patients and to assess t
he cost and utility of this laboratory-based surveillance.
SETTING: Large university teaching hospital.
DESIGN: Quarterly prevalence culture survey of 50 stool specimens submitted
for Clostridium difficile toxin A assay from October 1996 through June 199
9 (n = 526). Screening culture survey of all C difficile-positive stool spe
cimens from July 1998 through June 1999 (n = 140).
PATIENTS: Specimens for analysis were collected from patients who were admi
tted to the hospital and who had C difficile toxin A testing ordered. Patie
nt samples were excluded from analysis if they were obtained from patients
not hospitalized at UCLA Medical Center, if the C difficile toxin assay res
ult was indeterminate, or if the patient was known to have previous VRE col
onization or infection.
RESULTS: During quarterly surveillance, VRE was detected in 19.8%, C diffic
ile toxin A in 9.5%, and both VRE and C difficile toxin A in 3.2% of stool
specimens submitted for C difficile toxin assay. Patients whose stool speci
mens were positive for C difficile toxin A were significantly more likely t
han those whose specimens were negative to have VRE detected (odds ratio, 2
.3; 95% confidence interval, 1.2-4.5). Based on these findings, in July 199
8, we began routine screening of all C difficile-positive stool specimens f
or VRE. From July 1998 through June 1999, 58 (41.4%) of 140 patients with C
difficile-positive specimens had VRE newly detected in the stool. The comb
ined cost of the two laboratory-based surveillance strategies was approxima
tely $62 per VRE-positive patient identified and $5,800 per year.
CONCLUSION: Quarterly surveillance of stool submitted for C difficile assay
combined with screening all C difficile-positive stools is a cost-effectiv
e and efficient strategy for detecting VRE stool colonization among high-ri
sk hospitalized patients. Such a laboratory-based surveillance should be in
cluded as part of a comprehensive program to limit nosocomial VRE transmiss
ion.