The purpose of this study is to describe the population pharmacokinetic characteristics of piperacillin/tazobactam after intravenous administration in pregnant women during pregnancy and delivery, and to evaluate pharmacodynamic effectiveness and safety of piperacillin/tazobactam in pregnant women whose baby are at high risk of developing early-onset sepsis after birth.
Study Type
OBSERVATIONAL
Enrollment
50
Piperacillin/Tazobactam, specification: 4g; 0.5g. Anti-infective therapy with piperacillin/tazobactam, specific regimen based on clinical practice, without intervention.
Shandong Provincial Hospital
Jinan, China
RECRUITINGClearance (L/h) of piperacillin/tazobactam
The mean population pharmacokintic parameter as well as its interindividual variability
Time frame: Through study completion, an average of 20 days.
Volume of Distribution (L) of piperacillin/tazobactam
The mean population pharmacokintic parameter as well as its interindividual variability
Time frame: Through study completion, an average of 20 days.
PD target attainment
PD target is defined as the time of free drug concentration beyond MIC during the dose interval
Time frame: Through study completion, an average of 20 days.
Adverse events
Drug-related adverse events and serious adverse events during the study.
Time frame: Through study completion, an average of 20 days.
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