Bacterial infection Renal Insufficiency
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: • Admission to the ICU of the Zaandam Medical Center during the study period • Expected to be undergoing CVVHD for >24 h • Treatment with ciprofloxacin for any infection or suspected infection, as judged by the attending physician. • Age >= 18 years
Exclusion criteria
Exclusion criteria: • Cessation of renal replacement therapy before obtainment of a through sample • No CRRT delivered during >25 % of the interval between obtainment of peak and through plasma samples.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary endpoint in our study is the theoretical pharmacodynamic breakpoint for efficacy, calculated by means of the following formula: TP BPeff = AUC24-ss / 125 (where AUC24-ss is the estimated AUC at steady state during a 12 h dosing interval multiplied by 2) | — |
Secondary
| Measure | Time frame |
|---|---|
| The secondary endpoint in our study is the theoretical pharmacodynamic breakpoint for the emergence of resistance, calculated by means of the following formula: TP BPres = Cmax-ss / 10 (where Cmax-ss is the estimated plasma concentration 30 minutes after ending a ciprofloxacin infusion at steady state) | — |
Countries
Netherlands