Is ertapenem (Invanz) more effective than piperacillin/tazobactam (Zosyn) for treating intra-abdominal abscesses?

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Last updated: April 1, 2025View editorial policy

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From the Guidelines

Neither ertapenem nor Zosyn (piperacillin-tazobactam) can be definitively considered "stronger" for intra-abdominal abscesses as both are effective options, but their selection depends on specific clinical factors.

Key Considerations

  • Zosyn may be preferred for more complex intra-abdominal infections due to its broader coverage against Pseudomonas aeruginosa and certain resistant gram-negative organisms.
  • Ertapenem (typically dosed at 1g IV daily) provides excellent coverage against many common intra-abdominal pathogens including Enterobacteriaceae and anaerobes, but lacks Pseudomonas coverage.
  • Zosyn (typically dosed at 3.375g IV every 6 hours or 4.5g every 6 hours) is often chosen for healthcare-associated infections or when Pseudomonas is suspected.

Clinical Decision Making

The choice between these agents should consider local resistance patterns, patient factors such as renal function, prior antibiotic exposure, and whether the infection is community-acquired or healthcare-associated, as recommended by guidelines from the Surgical Infection Society and the Infectious Diseases Society of America 1.

Treatment Approach

Both antibiotics should be part of a comprehensive treatment approach that may include drainage of the abscess when possible.

Duration of Therapy

Regardless of which antibiotic is chosen, duration of therapy typically ranges from 5-14 days depending on the adequacy of source control and clinical response.

Resistance and Safety

It's also important to consider the potential for resistance and the safety profile of each antibiotic, with ertapenem being a carbapenem and thus carrying a risk of promoting carbapenem-resistant Enterobacteriaceae, as noted in guidelines 1.

Final Recommendation

The selection of ertapenem or Zosyn should be based on individual patient factors, local epidemiology, and the specific characteristics of the infection, with the goal of optimizing outcomes in terms of morbidity, mortality, and quality of life.

From the FDA Drug Label

14 CLINICAL STUDIES 14.1 Adults Complicated Intra-Abdominal Infections Ertapenem was evaluated in adults for the treatment of complicated intra-abdominal infections in a randomized, double-blind, non-inferiority clinical trial. This trial compared ertapenem (1 g intravenously once a day) with piperacillin/tazobactam (3. 375 g intravenously every 6 hours) for 5 to 14 days and enrolled 665 patients with localized complicated appendicitis, and any other complicated intra-abdominal infection including colonic, small intestinal, and biliary infections and generalized peritonitis The combined clinical and microbiologic success rates in the microbiologically evaluable population at 4 to 6 weeks posttherapy (test-of-cure) were 83.6% (163/195) for ertapenem and 80. 4% (152/189) for piperacillin/tazobactam.

The clinical success rates of ertapenem and piperacillin/tazobactam (Zosyn) for complicated intra-abdominal infections were 83.6% and 80.4%, respectively.

  • Ertapenem had a slightly higher success rate than Zosyn.
  • However, the study was designed as a non-inferiority trial, which means that ertapenem was compared to Zosyn to determine if it was not significantly worse, rather than directly comparing which one is stronger. Based on the provided data, it can be said that ertapenem is not significantly weaker than Zosyn for the treatment of complicated intra-abdominal infections, but it is not possible to conclude that it is stronger 2.

From the Research

Comparison of Ertapenem and Zosyn for Intraabdominal Abscess

  • Ertapenem has been shown to have potent bactericidal activity against a range of pathogens responsible for intra-abdominal infections, including Gram-negative and Gram-positive bacteria, as well as anaerobic bacteria 3.
  • In a study comparing ertapenem to piperacillin/tazobactam, ertapenem was found to be equivalent in efficacy for the treatment of complicated intra-abdominal infections, with clinical success rates of 79.3% and 76.2%, respectively 4.
  • A meta-analysis of randomized-controlled trials found no difference in clinical success rates between ertapenem and comparators, including piperacillin/tazobactam, for the treatment of complicated intra-abdominal infections 5.
  • Another study found that ertapenem was not inferior to piperacillin-tazobactam for the treatment of community-acquired intra-abdominal infections requiring surgical intervention, with favorable clinical response rates of 90% and 94%, respectively 6.
  • Ertapenem has a broad spectrum of in vitro activity against Gram-negative pathogens, including extended-spectrum beta-lactamase (ESBL)- and AmpC-producing Enterobacteriaceae, Gram-positive pathogens, and anaerobic pathogens, making it an effective option for the empirical treatment of complicated community-acquired bacterial infections 7.

Key Findings

  • Ertapenem has potent bactericidal activity against a range of pathogens responsible for intra-abdominal infections.
  • Ertapenem is equivalent in efficacy to piperacillin/tazobactam for the treatment of complicated intra-abdominal infections.
  • Ertapenem is not inferior to piperacillin-tazobactam for the treatment of community-acquired intra-abdominal infections requiring surgical intervention.
  • Ertapenem has a broad spectrum of in vitro activity against Gram-negative and Gram-positive pathogens, as well as anaerobic pathogens.

Pathogen Coverage

  • Ertapenem covers a range of pathogens, including:
  • Gram-negative bacteria: Escherichia coli, Klebsiella pneumoniae, Klebsiella oxytoca, Klebsiella ozaenae, Enterobacter cloacae, and Proteus mirabilis.
  • Gram-positive bacteria: Methicillin-susceptible Staphylococcus aureus (MSSA) and Enterococcus faecalis.
  • Anaerobic bacteria: Bacteroides fragilis.

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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