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Antimicrobial Agents and Chemotherapy, June 1999, p. 1412-1416, Vol. 43, No. 6
0066-4804/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
Randomized, Placebo-Controlled, Double-Blind Trial To Evaluate
the Efficacy of Mupirocin for Eradicating Carriage of
Methicillin-Resistant Staphylococcus aureus
Stephan
Harbarth,1,
Sasi
Dharan,1
Nadia
Liassine,2
Pascale
Herrault,1
Raymond
Auckenthaler,2 and
Didier
Pittet1,*
Infection Control
Program1 and Clinical Microbiology
Laboratory,2 University Hospitals of Geneva,
CH-1211 Geneva 14, Switzerland
Received 21 December 1998/Returned for modification 8 March
1999/Accepted 7 April 1999
Mupirocin has been widely used for the clearance of nasal
methicillin-resistant Staphylococcus aureus (MRSA) carriage
during outbreaks, but no placebo-controlled trial has evaluated its
value for eradicating MRSA carriage at multiple body sites in settings where MRSA is not epidemic. In a 1,500-bed teaching hospital with endemic MRSA, 102 patients colonized with MRSA were randomized into a
double-blind, placebo-controlled trial and treated with either
mupirocin (group M) or placebo (group P) applied to the anterior nares
for 5 days; both groups used chlorhexidine soap for body washing.
Follow-up screening, susceptibility testing, and genotyping were
performed to evaluate treatment success, mupirocin or chlorhexidine
resistance, and exogenous recolonization. At baseline, MRSA carriage
was 60% in the nares, 38% in the groin, and 62% in other sites (skin
lesions, urine). The MRSA eradication rate (all body sites) was 25% in
group M (12 of 48 patients), compared to 18% in group P (9 of 50 patients; relative risk [RR], 0.72; 95% confidence interval
[CI95], 0.33 to 1.55). At the end of follow-up, 44% of
patients (19 of 43) were free of nasal MRSA in group M, compared to
23% (11 of 44) in group P (RR, 0.57; CI95, 0.31 to 1.04).
Ten patients developed MRSA infections (three in group M and seven in
group P). One mupirocin treatment failure was due to exogenous MRSA
recolonization. No MRSA isolate showed chlorhexidine resistance or
high-level mupirocin resistance; however, we observed an association
(P = 0.003) between low-level mupirocin resistance at
study entry (prevalence, 23%) and subsequent treatment failure in both
study arms. These results suggest that nasal mupirocin is only
marginally effective in the eradication of multisite MRSA carriage in a
setting where MRSA is endemic.
*
Corresponding author. Mailing address: Infection
Control Program, University Hospitals of Geneva, CH-1211 Geneva 14, Switzerland. Phone: 41-22-372 98 28. Fax: 41-22-372 39 87. E-mail:
didier.pittet{at}hcuge.ch.

Present address: Department of Epidemiology, Harvard School of
Public Health, Boston, MA
02215.
Antimicrobial Agents and Chemotherapy, June 1999, p. 1412-1416, Vol. 43, No. 6
0066-4804/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
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