Gabapentin as add-on therapy in refractory partial epilepsy: A double-blind, placebo-controlled, parallel-group study

被引:0
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作者
McLean, M
Ramsay, RE
Leppik, IE
Rowan, AJ
Shellenberger, MK
Wallace, J
机构
[1] Arizona Hlth Sci Ctr, Tucson, AZ USA
[2] Wake Forest Univ, Bowman Gray Sch Med, Winston Salem, NC USA
[3] Vet Adm Med Ctr, Bronx, NY 10468 USA
[4] DATAMAP, Freiburg, Germany
[5] Good Samaritan Hosp, Portland, OR 97209 USA
[6] Johns Hopkins Univ Hosp, Baltimore, MD 21287 USA
[7] Neurol Clin, Dallas, TX USA
[8] Parke Davis Pharmaceut Res, Ann Arbor, MI USA
[9] Univ Michigan, Med Ctr, Ann Arbor, MI USA
[10] Univ Minnesota, Minneapolis, MN 55455 USA
[11] MINCEP Epilepsy Care, Minneapolis, MN USA
[12] Univ Pittsburgh, Sch Med, Pittsburgh, PA 15260 USA
[13] Univ Virginia Hosp, Charlottesville, VA USA
[14] Univ Washington, Epilepsy Ctr, Seattle, WA 98195 USA
[15] Vanderbilt Univ Sch Med, Nashville, TN USA
[16] Univ Miami, Miami, FL 33152 USA
[17] Vet Adm Med Ctr, Miami, FL 33125 USA
[18] Vet Adm Med Ctr, West Haven, CT 06516 USA
[19] Vet Adm Med Ctr, Los Angeles, CA USA
[20] Univ Calif Los Angeles, Sch Med, Los Angeles, CA 90024 USA
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中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Gabapentin, administered as add-on therapy, was safe and effective in this 12-week, multicenter, placebo-controlled, parallel-group study in 306 patients with refractory partial epilepsy. For patients in each gabapentin treatment group (600, 1,200, or 1,800 mg/d), the mean response ratio, was significantly better than that of a placebo group. The percentage of patients achieving at least a 50% reduction in seizure frequency was 8% among placebo-treated patients and ranged from 18% to 26% for patients who received gabapentin. Adverse events were generally mild and transient and occurred at a slightly higher frequency among patients receiving gabapentin than among those receiving placebo. Gabapentin did not affect the serum concentrations of concurrent antiepileptic drugs and was not regularly associated with any deviations in clinical laboratory values. Gabapentin's low inherent toxicity and its lack of drug interactions make it an ideal candidate for use as add-on therapy in patients with refractory partial epilepsy.
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页码:S62 / S68
页数:7
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