The pharmacokinetics of piperacillin/tazobactam will be evaluated in twenty septic patients with renal failure undergoing continuous veno-venous hemodiafiltration.
The pharmacokinetics of piperacillin/tazobactam will be evaluated in twenty septic patients with renal failure undergoing continuous veno-venous hemodiafiltration. This is a prospective study. Continuous replacement therapy has a continuous effect on drug elimination which could compromise effective antibiotic treatment. Patients will receive a standard course of pip/tazo 4g intravenously 8 hourly administrated immediately when CVVHDF will be started. Blood samples will be collected at 30mn, 2h, 4h, 6h, 8h, 16h, 24h for the first and the second day. We will measure plasma piperacillin/tazobactam concentration and compare them to MICs for the whole dosing interval.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
10
piperacillin 4 g and tazobactam 500 mg during 30 min IV infusion every 8h during 2 consecutive days
Service de Néphrologie
Toulouse, France
Serum levels of both piperacillin and tazobactam (Cmin) during 2 daus
Time frame: 2 days
Body clearance
Time frame: 2 days
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