OBJECTIVE: Our purpose was to study the pharmacokinetics of ceftazidim
e at different stages of pregnancy and in the nonpregnant state to det
ermine whether glomerular filtration rate is altered and whether tubul
ar secretions occurs. STUDY DESIGN: Twelve pregnant women with asympto
matic bacteruria were given a bolus dose of 400 mg of ceftazidime foll
owed by a constant infusion for 4 hours. Inulin was infused simultaneo
usly to determine glomerular filtration rate. Blood samples were drawn
every 30 minutes. Urine was collected immediately after the bolus dos
e and then every hour. The same study procedure was then repeated twic
e: 2 weeks before the expected delivery and after termination of breas
t-feeding. RESULTS: At term clearance values were raised by 50% to 100
% compared with the values found in the postpartum period. At all obse
rvation points a close correlation between inulin and ceftazidime clea
rance values were found. CONCLUSION: The results strongly indicate tha
t ceftazidime is excreted exclusively by glomerular filtration with no
tubular reabsorbtion. During pregnancy the excretion pattern is unalt
ered, but renal elimination is increased.