Volume 4 Supplement 1

Antimicrobial Resistance and Infection Control: Abstracts from the 3rd International Conference on Prevention and Infection Control (ICPIC 2015)

Open Access

Recurrence and mortality following treatment for Clostridum difficile infection with metronidazole or vancomycin

  • V Stevens1,
  • R Nelson1,
  • K Khader1,
  • M Jones1,
  • K Brown1,
  • M Samore1 and
  • M Rubin1
Antimicrobial Resistance and Infection Control20154(Suppl 1):O38

https://doi.org/10.1186/2047-2994-4-S1-O38

Published: 16 June 2015

Introduction

Metronidazole is considered first-line therapy for patients with mild to moderate Clostridium difficile infection (CDI), but was recently shown to be inferior to vancomycin for clinical cure. The effect of treatment choice on downstream outcomes such as recurrence and risk of death is not well understood.

Objectives

To evaluate the impact of vancomycin or metronidazole on CDI recurrence and 30-day mortality.

Methods

A retrospective cohort study of patients with CDI who were treated with vancomycin or metronidazole in the US Department of Veterans Affairs healthcare system between 1 January 2005 and 31 December 2012. A diagnosis of CDI was based on a positive enzyme immunoassay or cytotoxin test. CDI treatment was defined as administration or dispensing of vancomycin (oral or compounded) or metronidazole (oral or intravenous) within two days before or after the positive CDI result. Each patient treated with vancomycin was matched with up to four patients treated with metronidazole on propensity score, which included comorbidity, utilization, and diagnosis of CDI in the ICU as a proxy for disease severity. Patients were followed for recurrence within 8 weeks and for mortality at 30 days after infection.

Results

There were 2,104 CDI patients treated with vancomycin matched with 8,014 CDI patients treated with metronidazole. Overall, 1,674 (16.5%) patients experienced a recurrence and 1,177 (11.6%) of patients died within 30 days. There was no difference in the risk of recurrence by treatment group (15.8% vs. 16.7% for vancomycin and metronidazole, p=0.32), but fewer patients who received vancomycin died (8.6% vs. 12.4%, RR 0.69, 95% CI 0.59 – 0.80).

Conclusion

Recurrence rates were similar between treatment groups, but the risk of 30-day mortality was significantly reduced among patients who received vancomycin. The choice of treatment for CDI has become increasingly complex with the number of options available, and evidence regarding clinical cure, recurrence, mortality, and cost must all be taken into consideration. If validated, our observation that vancomycin results in a lower mortality rate may justify the additional costs of treatment relative to metronidazole.

Disclosure of interest

None declared.

Authors’ Affiliations

(1)
IDEAS 2.0 Center, Veterans Affairs Salt Lake City Health Care System (VASLCHCS)

Copyright

© Stevens et al; licensee BioMed Central Ltd. 2015

This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

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