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Updated: Aug 27, 2026

Nanomechanics of Drug-target Interactions and Antibacterial Resistance Detection
Published on: October 25, 2013
Clostridium difficile and vancomycin-resistant enterococcus: the new nosocomial alliance
R D Poduval1, R P Kamath, M Corpuz
1Department of Medicine, Our Lady of Mercy Medical Center, Bronx, New York 10466, USA.
Objectives:
The aims of this study were to determine the frequency of the association between Clostridium difficile (C. difficile) and vancomycin-resistant Enterococcus (VRE) and delineate the role of C. difficile coinfection as a predictor of VRE infection versus colonization and adverse outcome.
Methods:
Patients with both C. difficile colitis and VRE (CD/VRE) were compared to patients with VRE alone with regard to demographics, comorbidity, prior antibiotic therapy, and coinfection with methicillin-resistant Staphylococcus aureus and funguria. C. difficile as a predictor of VRE infection (VRE-I) versus colonization (VRE-C) and adverse outcome was also studied.
Results:
Eighty-nine patients with VRE infection or colonization were studied. This included 31 cases of VRE-I and 58 VRE-C. C. difficile was isolated in 17 (19.1%) of patients; of these C. difficile was isolated before VRE in 9 patients and after VRE in 8. The two groups did not differ in age, residence, or comorbidity. C. difficile coinfection was not predictive of VRE-I versus VRE-C, nor was it associated with increased length of stay or mortality. However, the mortality rates in both groups was high, around 30%. A significant association was noted between the use of vancomycin and metronidazole (before the isolation of VRE) and C. difficile coinfection (p = 0.03 and p = 0.001, respectively). A high incidence of nosocomial coinfection with methicillin-resistant Staphylococcus aureus, funguria, and gram-negative sepsis was noted in both groups; the association with funguria was statistically significant (p = 0.029).
Conclusions:
In conclusion, C. difficile coinfection is common in patients with VRE infection or colonization and is significantly associated with other nosocomial dilemmas like funguria. This may result in the emergence of highly virulent pathogens including vancomycin-resistant C. difficile, posing new challenges in the management of nosocomial diarrheas.
Insights
Clostridium difficile (C. difficile) coinfection is common in patients with vancomycin-resistant Enterococcus (VRE). This coinfection is linked to other hospital-acquired infections like funguria but does not predict VRE infection severity or patient outcomes.
Area of Science:
- Infectious Diseases
- Microbiology
- Hospital Epidemiology
Background:
- Vancomycin-resistant Enterococcus (VRE) and Clostridium difficile (C. difficile) are significant healthcare-associated pathogens.
- Coinfection with these organisms presents complex clinical challenges.
- Understanding the interplay between C. difficile and VRE is crucial for effective patient management.
Purpose of the Study:
- To determine the frequency of C. difficile and VRE coinfection.
- To assess C. difficile coinfection as a predictor of VRE infection versus colonization.
- To evaluate the impact of C. difficile coinfection on adverse outcomes in VRE patients.
Main Methods:
- Retrospective comparison of patients with C. difficile colitis and VRE (CD/VRE) versus VRE alone.
- Analysis of demographics, comorbidities, prior antibiotic use, and coinfections.
- Statistical evaluation of C. difficile as a predictor for VRE infection/colonization and adverse outcomes.
Main Results:
- C. difficile was isolated in 19.1% of VRE patients.
- C. difficile coinfection did not predict VRE infection/colonization or adverse outcomes like mortality.
- Significant associations were found between vancomycin/metronidazole use and C. difficile coinfection, and between coinfection and funguria.
Conclusions:
- C. difficile coinfection is frequent in VRE patients and associated with other nosocomial infections, such as funguria.
- The emergence of highly virulent pathogens, including vancomycin-resistant C. difficile, poses management challenges.
- Further research is needed to understand the clinical implications of these coinfections.
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