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A Placebo-Controlled Trial of Antibiotics for Smaller Skin Abscesses.

Authors :
Daum, Robert S
Daum, Robert S
Miller, Loren G
Immergluck, Lilly
Fritz, Stephanie
Creech, C Buddy
Young, David
Kumar, Neha
Downing, Michele
Pettibone, Stephanie
Hoagland, Rebecca
Eells, Samantha J
Boyle, Mary G
Parker, Trisha Chan
Chambers, Henry F
DMID 07-0051 Team
Daum, Robert S
Daum, Robert S
Miller, Loren G
Immergluck, Lilly
Fritz, Stephanie
Creech, C Buddy
Young, David
Kumar, Neha
Downing, Michele
Pettibone, Stephanie
Hoagland, Rebecca
Eells, Samantha J
Boyle, Mary G
Parker, Trisha Chan
Chambers, Henry F
DMID 07-0051 Team
Source :
The New England journal of medicine; vol 376, iss 26, 2545-2555; 0028-4793
Publication Year :
2017

Abstract

BackgroundUncomplicated skin abscesses are common, yet the appropriate management of the condition in the era of community-associated methicillin-resistant Staphylococcus aureus (MRSA) is unclear.MethodsWe conducted a multicenter, prospective, double-blind trial involving outpatient adults and children. Patients were stratified according to the presence of a surgically drainable abscess, abscess size, the number of sites of skin infection, and the presence of nonpurulent cellulitis. Participants with a skin abscess 5 cm or smaller in diameter were enrolled. After abscess incision and drainage, participants were randomly assigned to receive clindamycin, trimethoprim-sulfamethoxazole (TMP-SMX), or placebo for 10 days. The primary outcome was clinical cure 7 to 10 days after the end of treatment.ResultsWe enrolled 786 participants: 505 (64.2%) were adults and 281 (35.8%) were children. A total of 448 (57.0%) of the participants were male. S. aureus was isolated from 527 participants (67.0%), and MRSA was isolated from 388 (49.4%). Ten days after therapy in the intention-to-treat population, the cure rate among participants in the clindamycin group was similar to that in the TMP-SMX group (221 of 266 participants [83.1%] and 215 of 263 participants [81.7%], respectively; P=0.73), and the cure rate in each active-treatment group was higher than that in the placebo group (177 of 257 participants [68.9%], P<0.001 for both comparisons). The results in the population of patients who could be evaluated were similar. This beneficial effect was restricted to participants with S. aureus infection. Among the participants who were initially cured, new infections at 1 month of follow-up were less common in the clindamycin group (15 of 221, 6.8%) than in the TMP-SMX group (29 of 215 [13.5%], P=0.03) or the placebo group (22 of 177 [12.4%], P=0.06). Adverse events were more frequent with clindamycin (58 of 265 [21.9%]) than with TMP-SMX (29 of 261 [11.1%]) or placebo (32 of 255 [1

Details

Database :
OAIster
Journal :
The New England journal of medicine; vol 376, iss 26, 2545-2555; 0028-4793
Notes :
application/pdf, The New England journal of medicine vol 376, iss 26, 2545-2555 0028-4793
Publication Type :
Electronic Resource
Accession number :
edsoai.on1391613498
Document Type :
Electronic Resource