Abstract
The objective of this study was to determine if the current dosage regimen for chloramphenicol (CAP)
administered to children with severe malaria (SM) for presumptive treatment of concomitant bacterial
meningitis achieves steady state plasma CAP concentrations within the reported therapeutic range
of 10–25 mg/l. Fifteen children (11 male, 4 female) with a median age of 45 months (range:
10–108 months) and having SM, were administered multiple intravenous doses (25 mg/kg, 6 hourly for
72 h) of chloramphenicol sodium succinate (CAPS) for presumptive treatment of concomitant bacterial
meningitis. Blood samples were collected over 72 h, and plasma CAPS, CAP and CSF CAP concentrations
determined by high performance liquid chromatography. Average steady state CAP
concentrations were approximately 17 mg/l, while mean fraction unbound (0.49) and CSF/plasma
concentration ratio (0.65) were comparable to previously reported values in Caucasian children.
Clearance was variable (mean=4.3 l/h), and trough plasma concentrations during the first dosing
interval were approximately 6 mg/l. Simulations indicated that an initial of loading dose of 40 mg/kg
CAPS, followed by a maintenance dose of 25 mg/kg every 6 h would result in trough CAP
concentrations of approximately 10 mg/l and peak concentrations <25 mg/l throughout the treatment
period. The current dosage regimen for CAP needs to include a loading dose of 40 mg/kg CAPS to
rapidly achieve plasma CAP concentrations within the reported therapeutic range.
