The Journal of Clinical Pharmacology · 2001 · 23 citations · 4 references
PharmacyClinical PharmacokineticsPharmacologyDialysisDrug ClearanceHemodialysisContinuous Renal Replacement TherapyPharmacokinetics In Critical IllnessRenal ClearanceRenal Drug ClearanceRenal PharmacologyContinuous HemodialysisContinuous Veno-venous HemodialysisDrug Clearance By HemodialysisDrug Clearance During HemodialysisDrug Elimination Half-lifeMedication Clearance By HemodialysisMidazolam InfusionSieving Coefficient
The aim of the study was to investigate the pharmacokinetics and removal of midazolam and unconjugated and glucuronidated 1-hydroxy-midazolam in 4 intensive care patients on continuous venovenous hemodialysis. Plasma midazolam and its metabolites were assessed by HPLC from blood samples collected during continuous infusion and after the end of infusion. Additional samples from the arterial and venous bloodlines and ultrafiltrate were drawn to calculate sieving coefficient and clearance of ultrafiltration. The elimination half-life of midazolam ranged from 7.6 to 22.8 hours. The clearance of ultrafiltration was between 0.13 and 4.7 ml/min and reached approximately 11% of the total clearance. The range of sieving coefficient was from 0.006 to 0.26, with an average fraction removal of 0.2%. 1-Hydroxy-midazolam glucuronide was removed by continuous hemodialysis (sieving 0.36 to 0.63), with a clearance of ultrafiltration ranging from 7.8 to 12.0 ml/min. These preliminary results showed that midazolam is not removed efficiently, and approximately half of the 1-hydroxy-midazolam glucuronide was removed by dialysis.
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Prolonged sedation due to accumulation of conjugated metabolites of midazolam
Tilman Bauer, R Ritz, C. Haberthür et al. · The Lancet · 1995 · 336 citations