4.2 Review

Ceftolozane/tazobactam for the treatment of complicated intra-abdominal infections

Journal

EXPERT OPINION ON PHARMACOTHERAPY
Volume 16, Issue 2, Pages 271-280

Publisher

INFORMA HEALTHCARE
DOI: 10.1517/14656566.2015.994504

Keywords

ceftolozane/tazobactam; complicated intra-abdominal infection; enterobacteriaceae; Gram-negative bacteria; multidrug resistance

Funding

  1. Pfizer
  2. AstraZeneca
  3. Bayer
  4. Cubist
  5. Merck
  6. Novartis
  7. Wyeth
  8. Rempex
  9. Tetraphase
  10. Cubist Pharmaceuticals

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Introduction: Decisions regarding empirical antimicrobial therapy for complicated intra-abdominal infections (cIAIs) are increasingly difficult because of the threat of antimicrobial resistance. Extended-spectrum beta-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.

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