Targeted intranasal mupirocin to prevent colonization and infection by community-associated methicillin-resistant Staphylococcus aureus strains in soldiers:: A cluster randomized controlled trial

被引:107
作者
Ellis, Michael W.
Griffith, Matthew E.
Dooley, David P.
McLean, Joseph C.
Jorgensen, James H.
Patterson, Jan E.
Davis, Kepler A.
Hawley, Joshua S.
Regules, Jason A.
Rivard, Robert G.
Gray, Paula J.
Ceremuga, Julia M.
DeJoseph, Mary A.
Hospenthal, Duane R.
机构
[1] Audie L Murphy Mem Vet Adm Med Ctr, San Antonio, TX USA
[2] DD Eisenhower Army Med Ctr, Dept Med Infect Dis, Ft Gordon, GA USA
[3] Brooke Army Med Ctr, Dept Med Infect Dis, Ft Sam Houston, TX 78234 USA
[4] Brooke Army Med Ctr, Dept Prevent Med, Ft Sam Houston, TX 78234 USA
[5] Brooke Army Med Ctr, Pathol & Area Lab Serv, Ft Sam Houston, TX 78234 USA
[6] Univ Texas, Hlth Sci Ctr, Dept Pathol, San Antonio, TX USA
[7] Univ Texas, Hlth Sci Ctr, Dept Med Infect Dis, San Antonio, TX USA
关键词
D O I
10.1128/AAC.01086-06
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Community-associated methicillin-resistant Staphylococcus aureus (CA-MRSA) is an emerging pathogen that primarily manifests as uncomplicated skin and soft tissue infections. We conducted a cluster randomized, double-blind, placebo-controlled trial to determine whether targeted intranasal mupirocin therapy in CAMRSA-colonized soldiers could prevent infection in the treated individual and prevent new colonization and infection within their study groups. We screened 3,447 soldiers comprising 14 training classes for CA-MRSA colonization from January to December 2005. Each training class was randomized to either the mupirocin or placebo study group, and the participants identified as CA-MRSA colonized were treated with either mupirocin or placebo. All participants underwent repeat screening after 8 to 10 weeks and were monitored for 16 weeks for development of infection. Of 3,447 participants screened, 134 (3.9%) were initially colonized with CAMRSA. Five of 65 (7.7%; 95% confidence interval [95% CI], 4.0% to 11.4%) placebo-treated participants and 7 of 66 (10.6%; 95% CI, 7.9% to 13.3%) mupirocin-treated participants developed infections; the difference in the infection rate of the placebo- and mupirocin -treated groups was -2.9% (95% CI, -7.5% to 1.7%). Of those not initially colonized with CA-MRSA, 63 of 1,459 (4.3%; 95% CI, 2.7% to 5.9%) of the placebo group and 56 of 1,607 (3.5%; 95% CI, 2.6% to 5.2%) of the mupirocin group developed infections; the difference in the infection rate of the placebo and mupirocin groups was 0.8% (95% CI, -1.0% to 2.7%). Of 3,447 participants, 3,066 (89%) were available for the second sampling and completed follow-up. New CA-MRSA colonization occurred in 24 of 1,459 (1.6%; 95% CI, 0.05% to 2.8%) of the placebo group participants and 23 of 1,607 (1.4%; 95% CI, 0.05% to 2.3%) of the mupirocin group participants; the difference in the infection rate of the placebo and mupirocin groups was 0.2% (95% CI, -1.3% to 1.7%). Despite CA-MRSA eradication in colonized participants, this study showed no decrease in infections in either the mupirocin -treated individuals or within their study group. Furthermore, CA-MRSA eradication did not prevent new colonization within the study group.
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页码:3591 / 3598
页数:8
相关论文
共 53 条
[1]  
[Anonymous], 1999, MMWR-MORBID MORTAL W, V48, P707
[2]   Community-onset methicillin-resistant Staphylococcus aureus associated with antibiotic use and the cytotoxin Panton-Valentine leukocidin during a furunculosis outbreak in rural Alaska [J].
Baggett, HC ;
Hennessy, TW ;
Rudolph, K ;
Bruden, D ;
Reasonover, A ;
Parkinson, A ;
Sparks, R ;
Donlan, RM ;
Martinez, P ;
Mongkolrattanothai, K ;
Butler, JC .
JOURNAL OF INFECTIOUS DISEASES, 2004, 189 (09) :1565-1573
[3]   PULSED-FIELD GEL-ELECTROPHORESIS AS A REPLACEMENT FOR BACTERIOPHAGE-TYPING OF STAPHYLOCOCCUS-AUREUS [J].
BANNERMAN, TL ;
HANCOCK, GA ;
TENOVER, FC ;
MILLER, JM .
JOURNAL OF CLINICAL MICROBIOLOGY, 1995, 33 (03) :551-555
[4]  
Bending M, 1996, J AM SOC NEPHROL, V7, P2403
[5]   Emergence of community-associated methicillin-resistant Staphylococcus aureus at a Memphis, Tennessee children's hospital [J].
Buckingham, SC ;
McDougal, LK ;
Cathey, LD ;
Comeaux, K ;
Craig, AS ;
Fridkin, SK ;
Tenover, FC .
PEDIATRIC INFECTIOUS DISEASE JOURNAL, 2004, 23 (07) :619-624
[6]  
*CDCP, 2003, MMWR-MORBID MORTAL W, V52, P793
[7]  
Centers for Disease Control and Prevention (CDC), 2003, MMWR Morb Mortal Wkly Rep, V52, P88
[8]   Mupirocin prophylaxis misses by a nose [J].
Chambers, HF ;
Winston, LG .
ANNALS OF INTERNAL MEDICINE, 2004, 140 (06) :484-485
[9]   The emergence of mupirocin resistance: a challenge to infection control and antibiotic prescribing practice [J].
Cookson, BD .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 1998, 41 (01) :11-18
[10]   Community-associated methicillin-resistant Staphylococcus aureus:: The way to the wound is through the nose [J].
Creech, CB ;
Talbot, TR ;
Schaffner, W .
JOURNAL OF INFECTIOUS DISEASES, 2006, 193 (02) :169-171