PK/PD of Extended-infusion Meropenem, Piperacillin-tazobactam and Cefepime in the Early Phase of Septic Shock (PAACS)
Septic Shock
About this trial
This is an interventional treatment trial for Septic Shock focused on measuring Septic shock, Beta Lactams, Extended infusion, PK/PD
Eligibility Criteria
Inclusion Criteria:
- Septic shock
- Meropenem, piperacillin-tazobactam or cefepime started after enrollment
Exclusion Criteria:
- Pregnancy
- Central nervous system infection
- Burns
Sites / Locations
- Chu BesanconRecruiting
Arms of the Study
Arm 1
Arm 2
Arm 3
Active Comparator
Active Comparator
Active Comparator
MEROPENEM
PIPERACILLIN-TAZOBACTAM
CEFEPIME
After enrollment, patients of MEROPENEM arm will receive an initial 2g bolus of MEROPENEM and 2g infusion over 3 hours every eight hours, during 48 hours, without modification of rhythm and dose according to renal function.
After enrollment, patients of PIPERACILLIN - TAZOBACTAM arm will receive an initial 4g bolus of PIPERACILLIN - TAZOBACTAM and a 16g continuous infusion per day, during 48 hours, without modification of rhythm and dose according to renal function.
After enrollment, patients of CEFEPIME arm will receive an initial 2g bolus of CEFEPIME and a 6g continuous infusion per day, during 48 hours, without modification of rhythm and dose according to renal function.