Continuous infusion ceftazidime in intensive care: a randomized controlled trial

J Antimicrob Chemother. 1999 Feb;43(2):309-11. doi: 10.1093/jac/43.2.309.

Abstract

We randomized 18 critically ill patients to receive ceftazidime 6 g/day by continuous infusion or bolus dosing (2 g 8 hourly), each with a loading dose of 12 mg/kg ceftazidime. During the first 8 h, plasma ceftazidime concentration fell below 40 mg/L in only one patient (trough 38 mg/L) from the infusion group, compared with eight from the bolus group (2-33 mg/L) for periods ranging from 73 to 369 min. Thereafter all infusion patients remained above 40 mg/L for 40 h of study versus 20-30% of bolus patients. The pharmacokinetic and pharmacodynamic characteristics of ceftazidime suggest that continuous infusions should be clinically investigated in outcome studies.

Publication types

  • Clinical Trial
  • Randomized Controlled Trial

MeSH terms

  • Adult
  • Ceftazidime / administration & dosage*
  • Ceftazidime / blood
  • Cephalosporins / administration & dosage*
  • Cephalosporins / blood
  • Critical Care*
  • Humans
  • Infusions, Intravenous
  • Middle Aged

Substances

  • Cephalosporins
  • Ceftazidime