Antibiotic treatment for 6 days versus 12 days in patients with severe cellulitis: a multicentre randomized, double-blind, placebo-controlled, non-inferiority trial.


Journal

Clinical microbiology and infection : the official publication of the European Society of Clinical Microbiology and Infectious Diseases
ISSN: 1469-0691
Titre abrégé: Clin Microbiol Infect
Pays: England
ID NLM: 9516420

Informations de publication

Date de publication:
May 2020
Historique:
received: 28 05 2019
revised: 16 09 2019
accepted: 17 09 2019
pubmed: 17 10 2019
medline: 5 1 2021
entrez: 17 10 2019
Statut: ppublish

Résumé

To investigate whether antibiotic treatment of 6 days' duration is non-inferior to treatment for 12 days in patients hospitalized for cellulitis. This multicentre, randomized, double-blind, placebo-controlled, non-inferiority trial enrolled adult patients hospitalized for severe cellulitis who were treated with intravenous flucloxacillin. At day 6 participants with symptom improvement who were afebrile were randomized between an additional 6 days of oral flucloxacillin or placebo in a 1:1 ratio, stratified for diabetes and hospital. The primary outcome was cure by day 14, without relapse by day 28. Secondary outcomes included a modified cure assessment and relapse rate by day 90. Between August 2014 and June 2017, 151 of 248 included participants were randomized. The intention-to-treat population consisted of 76 and 73 participants allocated to 12 and 6 days of antibiotic therapy, respectively (mean age 62 years, 67% males, 24% diabetics); 38/76 (50.0%) and 36/73 (49.3%) were cured in the 12- and 6-day groups respectively (ARR 0.7 percentage points, 95%CI: -15.0 to 16.3). Cure rates were 56/76 (73.7%) and 49/73 (67.1%) with the modified cure assessment (ARR 6.6, 95%CI: -8.0 to 20.8). After initial cure without relapse, day 90 relapse rates were higher in the 6-day group (6% versus 24%, p < 0.05). Given the wide confidence intervals, we can neither confirm nor refute our hypothesis that 6 days of therapy is non-inferior to 12 days of therapy. However, a 6-day course resulted in significantly more frequent relapses by day 90. These findings require confirmation in future studies.

Identifiants

pubmed: 31618678
pii: S1198-743X(19)30504-X
doi: 10.1016/j.cmi.2019.09.019
pii:
doi:

Substances chimiques

Anti-Bacterial Agents 0
Floxacillin 43B2M34G2V

Types de publication

Equivalence Trial Journal Article Multicenter Study Randomized Controlled Trial

Langues

eng

Sous-ensembles de citation

IM

Pagination

606-612

Commentaires et corrections

Type : CommentIn

Informations de copyright

Copyright © 2019. Published by Elsevier Ltd.

Auteurs

D R Cranendonk (DR)

Amsterdam UMC, University of Amsterdam, Department of Medicine, Division of Infectious Diseases, Amsterdam, the Netherlands; Amsterdam UMC, University of Amsterdam, Centre for Experimental and Molecular Medicine, Amsterdam Infection & Immunity Institute, Amsterdam, the Netherlands. Electronic address: d.r.cranendonk@amc.uva.nl.

B C Opmeer (BC)

Amsterdam UMC, University of Amsterdam, Clinical Research Unit, Amsterdam, the Netherlands.

M A van Agtmael (MA)

Amsterdam UMC, Vrije Universiteit Amsterdam, Department of Internal Medicine, Amsterdam, the Netherlands.

J Branger (J)

Department of Internal Medicine, Flevoziekenhuis, Almere, the Netherlands.

K Brinkman (K)

Department of Internal Medicine, OLVG-Oost, Amsterdam, the Netherlands.

A I M Hoepelman (AIM)

Department of Internal Medicine, University Medical Centre, University of Utrecht, Utrecht, the Netherlands.

F N Lauw (FN)

Department of Internal Medicine, MC Slotervaart, Amsterdam, the Netherlands.

J J Oosterheert (JJ)

Department of Internal Medicine, University Medical Centre, University of Utrecht, Utrecht, the Netherlands.

A H Pijlman (AH)

Department of Internal Medicine, St Antonius Ziekenhuis, Utrecht, the Netherlands.

S U C Sankatsing (SUC)

Department of Internal Medicine, Diakonessenhuis, Utrecht, the Netherlands.

R Soetekouw (R)

Department of Internal Medicine, Spaarne Gasthuis, Haarlem, the Netherlands.

J Veenstra (J)

Department of Internal Medicine, OLVG-West, Amsterdam, the Netherlands.

P J de Vries (PJ)

Department of Internal Medicine, Tergooiziekenhuizen, Hilversum, the Netherlands.

J M Prins (JM)

Amsterdam UMC, University of Amsterdam, Department of Medicine, Division of Infectious Diseases, Amsterdam, the Netherlands.

W J Wiersinga (WJ)

Amsterdam UMC, University of Amsterdam, Department of Medicine, Division of Infectious Diseases, Amsterdam, the Netherlands; Amsterdam UMC, University of Amsterdam, Centre for Experimental and Molecular Medicine, Amsterdam Infection & Immunity Institute, Amsterdam, the Netherlands.

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Classifications MeSH