S. Daenen et al., CONTINUOUS-INFUSION OF CEFTAZIDIME IN FEBRILE NEUTROPENIC PATIENTS WITH ACUTE MYELOID-LEUKEMIA, European journal of clinical microbiology & infectious diseases, 14(3), 1995, pp. 188-192
Twelve febrile patients with severe neutropenia, who had undergone agg
ressive chemotherapy for acute myeloid leukemia, were treated empirica
lly with a continuous infusion of ceftazidime 100 mg/kg/day after a 50
0 mg loading dose, in order to study the pharmacokinetics of ceftazidi
me after continuous infusion and to examine the clinical applicability
of continuous infusion in this patient population. Three patients had
a slight decrease in renal function. All patients attained a steady-s
tate ceftazidime serum level of > 20 mu g/ml within 180 to 240 min, wh
ich was considered effective against most pathogens in neutropenic pat
ients. The median volume of distribution for the patient group was 29.
1 I, the elimination half-life was 2.5 h and the clearance of ceftazid
ime was 7.7 I/h. A subnormal kidney function influenced half-lives and
clearance (but not volume of distribution), as expected. When precaut
ions were taken to avoid known interactions between ceftazidime and ot
her compounds to be infused simultaneously, continuous infusion of cef
tazidime was applicable for treatment of neutropenic patients without
major side effects.