Randomised clinical trial of moxifloxacin versus ertapenem in complicated
intra-abdominal infections: results of the PROMISE study.
Author(s): De Waele JJ(1), Tellado JM, Alder J, Reimnitz P, Jensen M, Hampel B, Arvis P.
Affiliation(s): Author information:
(1)Department of Critical Care Medicine, Ghent University Hospital, Ghent, Belgium.
Jan.DeWaele@UGent.be
Publication date & source: 2013, Int J Antimicrob Agents. , 41(1):57-64
Antibiotic therapy for complicated intra-abdominal infections (cIAIs) should
provide broad-spectrum coverage both Gram-positive and Gram-negative
microorganisms. The PROMISE study compared the clinical and bacteriological
efficacy and safety of moxifloxacin versus ertapenem for the treatment of cIAIs.
This randomised, prospective, double-dummy, double-blind, multicentre trial was
designed as a non-inferiority study. The safety and efficacy of 5-14 days of
daily intravenous moxifloxacin (400mg) or ertapenem (1g) were compared in
patients with cIAIs requiring surgery and parenteral antibiotic therapy. The
primary and secondary endpoints included clinical and bacteriological responses
at 21-28 days after the end of treatment (TOC), respectively. Of 830 enrolled
patients, 699 were efficacy valid. Moxifloxacin was non-inferior to ertapenem
regarding clinical success [89.5% (315/352) versus 93.4% (324/347); 95%
confidence interval (CI) -7.9%, 0.4%]. There were no significant differences
between groups for any of the primary causes or types of cIAI regarding clinical
response. Bacteriological success was achieved in 86.5% (257/297) of
moxifloxacin-treated patients and 90.2% (249/276) of ertapenem-treated patients
(95% CI -9.0%, 1.5%). There were no major differences between groups regarding
the frequency or types of organisms eradicated. The incidence of adverse events
(AEs) was higher with moxifloxacin than ertapenem (P=0.039), however a similar
number of drug-related AEs was seen in each group (P=1.000). Wound infections,
nausea and increased lipase were the most commonly reported AEs with both agents.
The results show that moxifloxacin is a valuable treatment option for a range of
community-acquired cIAIs with mild-to-moderate severity.
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