Journal of Antimicrobial Chemotherapy (1999) 43, 309-311
© 1999 The British Society for Antimicrobial Chemotherapy
Brief reports |
Continuous infusion ceftazidime in intensive care: a randomized controlled trial
a Royal Brisbane Hospital, Division of Anaesthesiology and Intensive Care, University of Queensland, Brisbane, Australia b Prince of Wales Hospital, Department of Anaesthesia and Intensive Care, Chinese University of Hong Kong, Hong Kong c Department of Anaesthesia, Christchurch Hospital, Christchurch, New Zealand
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.
* Correspondence address: Intensive Care Facility, Royal Brisbane Hospital and University of Queensland, Herston Road, Herston, Brisbane, 4029 Queensland, Australia. Tel:+61-7-3253-8897; Fax:+61-7-3253-3542; E-mail:jlipman{at}gasbone.herston.uq.edu.au
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