Differential antibiotic-induced endotoxin release in severe melioidosis

J Infect Dis. 2000 Mar;181(3):1014-9. doi: 10.1086/315306.

Abstract

Severe melioidosis is a life-threatening, systemic bacterial infection caused by Burkholderia pseudomallei. A prospective, randomized treatment trial was conducted in northeast Thailand to compare ceftazidime (a penicillin-binding protein [PBP]-3-specific agent that causes release of large amounts of endotoxin in vitro) and imipenem (a PBP-2-specific agent that kills B. pseudomallei more rapidly but releases low amounts of endotoxin) in severe melioidosis over a 6-h time course after the first dose of antibiotic. Despite similar clinical, microbiological, endotoxin, and cytokine measures at study entry, ceftazidime-treated patients (n=34) had significantly greater systemic endotoxin (P<.001) than patients treated with imipenem (n=34) after the first dose of antibiotic. No overall difference in mortality was observed (35% in both groups [95% confidence interval, 20%-50%]). Differential antibiotic-induced endotoxin release is demonstrable in severe melioidosis. These differences in endotoxin release did not appear to have a significant impact on survival in this group of patients.

Publication types

  • Clinical Trial
  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Anti-Bacterial Agents / therapeutic use*
  • Ceftazidime / therapeutic use*
  • Cytokines / blood
  • Endotoxins / metabolism*
  • Female
  • Humans
  • Imipenem / therapeutic use*
  • Male
  • Melioidosis / drug therapy*
  • Melioidosis / immunology
  • Melioidosis / mortality
  • Middle Aged
  • Prospective Studies

Substances

  • Anti-Bacterial Agents
  • Cytokines
  • Endotoxins
  • Imipenem
  • Ceftazidime