Chlorhexidine and Mupirocin for Clearance of Methicillin-Resistant Staphylococcus aureus Colonization After Hospital Discharge: A Secondary Analysis of the Changing Lives by Eradicating Antibiotic Resistance Trial

Author:

Miller Loren G1,Singh Raveena2,Eells Samantha J1,Gillen Daniel2,McKinnell James A1,Park Steven2,Tjoa Tom2,Chang Justin2,Rashid Syma2,Macias-Gil Raul1,Heim Lauren2,Gombosev Adrijana2,Kim Diane2,Cui Eric2,Lequieu Jennifer2,Cao Chenghua2,Hong Suzie S2,Peterson Ellena M2,Evans Kaye D2,Launer Bryn1,Tam Steven2,Bolaris Michael1,Huang Susan S2

Affiliation:

1. Infectious Disease Clinical Outcomes Research Unit, Division of Infectious Disease, Los Angeles Biomedical Research Institute, Harbor–UCLA Medical Center , Torrance, California , USA

2. Division of Infectious Diseases and Health Policy Research Institute, University of California, Irvine School of Medicine , Irvine, California , USA

Abstract

Abstract Background The CLEAR Trial demonstrated that a multisite body decolonization regimen reduced post-discharge infection and hospitalization in methicillin-resistant Staphylococcus aureus (MRSA) carriers. Here, we describe decolonization efficacy. Methods We performed a large, multicenter, randomized clinical trial of MRSA decolonization among adult patients after hospital discharge with MRSA infection or colonization. Participants were randomized 1:1 to either MRSA prevention education or education plus decolonization with topical chlorhexidine, oral chlorhexidine, and nasal mupirocin. Participants were swabbed in the nares, throat, axilla/groin, and wound (if applicable) at baseline and 1, 3, 6, and 9 months after randomization. The primary outcomes of this study are follow-up colonization differences between groups. Results Among 2121 participants, 1058 were randomized to decolonization. By 1 month, MRSA colonization was lower in the decolonization group compared with the education-only group (odds ration [OR] = 0.44; 95% confidence interval [CI], .36–.54; P ≤ .001). A similar magnitude of reduction was seen in the nares (OR = 0.34; 95% CI, .27–.42; P < .001), throat (OR = 0.55; 95% CI, .42–.73; P < .001), and axilla/groin (OR = 0.57; 95% CI, .43–.75; P < .001). These differences persisted through month 9 except at the wound site, which had a relatively small sample size. Higher regimen adherence was associated with lower MRSA colonization (P ≤ .01). Conclusions In a randomized, clinical trial, a repeated post-discharge decolonization regimen for MRSA carriers reduced MRSA colonization overall and at multiple body sites. Higher treatment adherence was associated with greater reductions in MRSA colonization.

Funder

Agency for Healthcare Research and Quality

National Institutes of Health

National Center for Research Resources

National Center for Advancing Translational Sciences

University of California

Los Angeles Clinical and Translational Science Institute

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Microbiology (medical)

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