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Decolonization with Mupirocin and Subsequent Risk of Methicillin-Resistant Staphylococcus aureus Carriage in Veterans
Richard E Nelson1, Makoto Jones, Michael A Rubin
1George E. Whalen Department of Veterans Affairs Medical Center, 500 Foothill Drive, GRECC-182, Salt Lake City, UT, 84148, USA, Richard.Nelson@utah.edu.
Introduction:
Hospital-acquired methicillin-resistant Staphylococcus aureus (MRSA) infections remain one of the leading causes of preventable patient mortality in the US. Eradication of MRSA through decolonization could prevent both MRSA infections and transmission; however, there is currently no consensus within the infectious disease community on the proper role of decolonization in the prevention of infections. The purpose of this study was to assess the impact of decolonization with mupirocin on subsequent MRSA carriage.
Methods:
Patients included in this study were those with an inpatient admission to a Department of Veterans Affairs (VA) hospital between January 1, 2008 and December 31, 2009 who had a positive MRSA screen on admission and a subsequent re-admission during the same time period. Exposure to mupirocin on the initial hospital admission was measured using Barcode Medication Administration data and MRSA carriage was measured using microbiology text reports and lab data containing results from surveillance swabs collected from the nares. Chi-square tests were used to test for differences in re-admission MRSA carriage rates between mupirocin-receiving and non-mupirocin-receiving patients.
Results:
Of the 25,282 MRSA-positive patients with a subsequent re-admission included in the present study cohort, 1,183 (4.7%) received mupirocin during their initial hospitalization. Among the patients in the present study cohort who were re-admitted within 30 days, those who received mupirocin were less likely to test positive for MRSA carriage than those who did not receive mupirocin (27.2% vs. 55.1%, P < 0.001). The proportion of those who tested positive for MRSA during re-admissions that occurred 30-60 days, 60-120 days, and >120 days were 33.9, 37.3, and 41.0%, respectively, among mupirocin patients and 52.7%, 53.0%, and 51.9%, respectively, for patients who did not receive mupirocin (P < 0.001 at each time point).
Conclusion:
Patients decolonized with mupirocin in VA hospitals were less likely to be colonized with MRSA on re-admission as long as 4 months after decolonization.
Insights
Hospital-acquired methicillin-resistant Staphylococcus aureus (MRSA) decolonization with mupirocin significantly reduced MRSA carriage in patients upon re-admission. This finding supports mupirocin
Area of Science:
- Infectious Diseases
- Hospital Epidemiology
- Antimicrobial Stewardship
Background:
- Hospital-acquired methicillin-resistant Staphylococcus aureus (MRSA) infections are a major cause of preventable patient mortality in the US.
- Decolonization strategies, including mupirocin use, are explored to prevent MRSA infections and transmission.
- There is ongoing debate regarding the optimal role of decolonization in infection prevention protocols.
Purpose of the Study:
- To evaluate the effectiveness of mupirocin decolonization in reducing subsequent methicillin-resistant Staphylococcus aureus (MRSA) carriage.
- To assess the impact of mupirocin treatment on MRSA colonization rates in patients readmitted to VA hospitals.
Main Methods:
- Retrospective cohort study of 25,282 patients admitted to VA hospitals between 2008-2009 with positive MRSA screening.
- Mupirocin exposure was identified through Barcode Medication Administration data.
- MRSA carriage on readmission was determined via microbiology reports and surveillance swab results; chi-square tests compared carriage rates.
Main Results:
- Of 25,282 MRSA-positive patients, 4.7% received mupirocin during initial hospitalization.
- Patients receiving mupirocin showed significantly lower MRSA carriage rates upon 30-day readmission (27.2% vs. 55.1%, P < 0.001).
- Reduced MRSA carriage in mupirocin recipients persisted for up to 4 months post-decolonization across different readmission time points (P < 0.001).
Conclusions:
- Mupirocin decolonization in VA hospital settings is associated with a sustained reduction in MRSA colonization.
- The findings suggest mupirocin decolonization is an effective strategy for decreasing MRSA carriage in patients upon hospital readmission.
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