Complicated intra-abdominal infections usually mandate prompt surgical intervention supplemented by appropriate antimicrobial
therapy. The aim of this study was to demonstrate that ertapenem was not inferior to piperacillin-tazobactam for the treatment
of community-acquired intra-abdominal infections. A randomized open-label active-comparator clinical trial was conducted at
48 medical centers on four continents from December 2001 to February 2003. Adult patients with intra-abdominal infections
requiring surgery were randomized to receive either ertapenem 1 g daily or piperacillin/tazobactam 13.5 g daily in 3–4 divided
doses. The primary analysis of efficacy was the clinical response rate in clinically and microbiologically evaluable patients
at the test-of-cure assessment 2 weeks after completion of therapy. All treated patients were included in the safety analysis.
Patient demographics, disease characteristics, and treatment duration in both treatment groups were generally similar. The
most commonly isolated pathogens at baseline were
E coli (greater than 50% of cases in each group) and
B fragilis (~9%). Favorable clinical response rates were 107/119 (90%) for ertapenem recipients and 107/114 (94%) for piperacillin/tazobactam
recipients. The frequencies of drug-related adverse events, most commonly diarrhea and elevated serum alanine aminotransferase
levels, were similar in both treatment groups. Six of 180 ertapenem recipients (3%) and two of 190 piperacillin/tazobactam
recipients (1%) had serious drug-related adverse experiences. In this study, ertapenem and piperacillin/tazobactam were comparably
safe and effective treatments for adult patients with complicated intra-abdominal infections.
Key words Intra-abdominal infection - ertapenem - piperacillin-tazobactam
Supported and sponsored by Merck & Co., Inc.