The Journal of Clinical Pharmacology · 2011 · 40 citations · 14 references
PharmacyPharmacokineticsPharmacologyDrug ClearanceHemodialysisRenal PharmacokineticsPharmacokinetics In Renal ImpairmentRenal Dose AdjustmentRenal Function TestsRenal PharmacologyConcentration-time Data AnalysisConcentration-time RelationshipPharmacokinetic ParametersPharmacokinetics In Kidney DiseaseRenal Function EvaluationRenal Function LossRenal Impairment ClearanceTandem Mass Spectrometry
The pharmacokinetic parameters of tigecycline were assessed in subjects with severe renal impairment (creatinine clearance <30 mL/min, n = 6), subjects receiving hemodialysis (4 received tigecycline before and 4 received tigecycline after hemodialysis), and subjects with age-adjusted, normal renal function (n = 6) after administration of single 100-mg doses. Serial serum and urine samples were collected and assayed using validated liquid chromatography with tandem mass spectrometer (LC/MS/MS) methods. Concentration-time data were then analyzed using noncompartmental pharmacokinetic methods. Tigecycline renal clearance in subjects with normal renal function represented approximately 20% of total systemic clearance. Tigecycline clearance was reduced by approximately 20%, and area under the tigecycline concentration-time curve increased by approximately 30% in subjects with severe renal impairment. Tigecycline was not efficiently removed by dialysis; thus, it can be administered without regard to timing of hemodialysis. Based on these pharmacokinetic data, tigecycline requires no dosage adjustment in patients with renal impairment.
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Evelyn J. Ellis‐Grosse, Timothy Babinchak, Nathalie Dartois et al. · Clinical Infectious Diseases · 2005 · 415 citations · Full text
Timothy Babinchak, Evelyn J. Ellis‐Grosse, Nathalie Dartois et al. · Clinical Infectious Diseases · 2005 · 384 citations · Full text