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Ceftolozane/tazobactam for the treatment of complicated intra-abdominal infections
Christian Eckmann1, Joseph Solomkin
1Klinikum Peine, Academic Hospital of Medical University Hannover, Department of General, Visceral and Thoracic Surgery , Virchowstrasse 8h, D-31221, Peine , Germany +49 0 5171 931530 ; +49 0 5171 931549 ; christian.eckmann@klinikum-peine.de.
Introduction:
Decisions regarding empirical antimicrobial therapy for complicated intra-abdominal infections (cIAIs) are increasingly difficult because of the threat of antimicrobial resistance. Extended-spectrum β-lactamase (ESBL)-producing Enterobacteriaceae are a particular challenge, as is multidrug-resistant (MDR) Pseudomonas aeruginosa, both of which are encountered in cIAI. Ceftolozane/tazobactam is a new antimicrobial that provides an effective solution for treating cIAI.
Areas Covered:
Evidence concerning the mechanism of action of ceftolozane/tazobactam, its in vitro activity against common cIAI pathogens, and pharmacokinetic and pharmacodynamic properties are reviewed. The clinical efficacy and safety of ceftolozane/tazobactam plus metronidazole, as determined by the Phase II and III clinical trials in hospitalized adults with cIAI, are discussed.
Expert Opinion:
Ceftolozane/tazobactam has demonstrated efficacy and safety in patients with cIAI, including those who are infected with ESBL-producing Enterobacteriaceae and P. aeruginosa. High rates of clinical cure by ceftolozane/tazobactam in Phase II and III trials suggest that this antimicrobial will be valuable for treating infections caused by MDR Gram-negative bacteria. In recent years, clinicians have become dependent on carbapenems for treating MDR infections. There is concern that this could lead to emergence of carbapenem-resistant strains, emphasizing the importance of antimicrobial stewardship. Ceftolozane/tazobactam appears to be an effective carbapenem-sparing alternative for treating cIAI.
Insights
Ceftolozane/tazobactam offers an effective treatment for complicated intra-abdominal infections (cIAIs), including those caused by resistant bacteria like extended-spectrum β-lactamase (ESBL)-producing Enterobacteriaceae and multidrug-resistant Pseudomonas aeruginosa.
Area of Science:
- Infectious Diseases
- Pharmacology
- Antimicrobial Resistance
Background:
- Complicated intra-abdominal infections (cIAIs) present treatment challenges due to rising antimicrobial resistance.
- Extended-spectrum β-lactamase (ESBL)-producing Enterobacteriaceae and multidrug-resistant (MDR) Pseudomonas aeruginosa are significant pathogens in cIAIs.
- Ceftolozane/tazobactam is a novel antimicrobial agent developed to address these challenges.
Purpose of the Study:
- To review the mechanism of action, in vitro activity, and pharmacokinetic/pharmacodynamic properties of ceftolozane/tazobactam.
- To discuss the clinical efficacy and safety of ceftolozane/tazobactam plus metronidazole in treating cIAIs.
- To evaluate ceftolozane/tazobactam as a carbapenem-sparing option for MDR Gram-negative bacterial infections.
Main Methods:
- Review of scientific literature on ceftolozane/tazobactam.
- Analysis of in vitro data against common cIAI pathogens.
- Examination of Phase II and III clinical trial data for efficacy and safety in hospitalized adults with cIAI.
Main Results:
- Ceftolozane/tazobactam demonstrates potent in vitro activity against key cIAI pathogens.
- Phase II and III trials show high clinical cure rates for ceftolozane/tazobactam plus metronidazole in cIAI patients.
- The agent is effective in patients with infections caused by ESBL-producing Enterobacteriaceae and P. aeruginosa.
Conclusions:
- Ceftolozane/tazobactam is an effective and safe treatment option for cIAIs.
- It provides a valuable therapeutic choice for infections involving ESBL-producing Enterobacteriaceae and MDR P. aeruginosa.
- Ceftolozane/tazobactam represents an important carbapenem-sparing alternative, aiding antimicrobial stewardship efforts against MDR Gram-negative bacteria.
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