Pharmacokinetics of topiramate in patients with renal impairment, end-stage renal disease undergoing hemodialysis, or hepatic impairment

被引:12
|
作者
Manitpisitkul, Prasarn [1 ]
Curtin, Christopher R. [1 ]
Shalayda, Kevin [1 ]
Wang, Shean-Sheng [1 ]
Ford, Lisa [1 ]
Heald, Donald L. [1 ]
机构
[1] Janssen Res & Dev LLC, Raritan, NJ 08869 USA
关键词
End-stage renal disease; Epilepsy; Hepatic impairment; Renal impairment; Topiramate; CHRONIC KIDNEY-DISEASE; ANTIEPILEPTIC DRUG; ESLICARBAZEPINE ACETATE; DOSE PHARMACOKINETICS; PHARMACODYNAMICS; CARBAMAZEPINE; GABAPENTIN; MODERATE; THERAPY; PLASMA;
D O I
10.1016/j.eplepsyres.2014.03.011
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Purpose: Topiramate is primarily renally excreted. Chronic renal and hepatic impairment can affect the clearance of topiramate. Therefore, the objective was to establish dosage guidelines for topiramate in chronic renal impairment, end-stage renal disease (ESRD) undergoing hemodialysis, or chronic hepatic impairment patients. Methods: In 3 separate open-label, parallel group studies (n = 5-7/group), in patients with mild moderate and severe renal impairment (based on creatinine clearance), ESRD requiring hemodialysis, or moderate-severe hepatic impairment (based on Child-Pugh classification) and matching healthy participants, pharmacokinetics of a single oral 100 mg topiramate was determined. Results: Compared with healthy controls, overall exposure (AUC(0-infinity)) for topiramate was higher in mild moderate (85%) and severe renal impairment (117%), consistent with significantly (p < 0.05) lower apparent total body clearance (CL/F) and renal clearance (CLR), leading to longer elimination half-life. Both CLR and CL/F of topirannate correlated well with renal function. CL/F was comparable in ESRD and severe renal impairment. Half of usual starting and maintenance dose is recommended in moderate-severe renal impairment patients, and those with ESRD. Hemodialysis effectively removed plasma topiramate with mean dialysis clearance approximately 12-fold greater than CL/F (123.5 mL/min versus 10.8 mL/min). Compared with healthy matched, patients with moderate severe hepatic impairment exhibited small increase (29%) in topiramate peak plasma concentrations and AUC(0-infinity) values, consistent with lower CL/F (26%). Topiramate was generally well tolerated. Conclusion: Half of usual dose is recommended for moderate severe renal impairment and ESRD. Supplemental dose may be required during hemodialysis. Dose adjustments might not be required in moderate severe hepatic impairments; however, the small sample size limits generalization. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:891 / 901
页数:11
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