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维拉帕米添加治疗难治性癫痫的临床研究
引用本文:汪银洲,林才经,许文华,程琼,林守华,庄文景,江秀龙,雷惠新. 维拉帕米添加治疗难治性癫痫的临床研究[J]. 中国急救医学, 2006, 26(8): 561-563
作者姓名:汪银洲  林才经  许文华  程琼  林守华  庄文景  江秀龙  雷惠新
作者单位:1. 福建医科大学附属医院神经内科,福建,福州,350001
2. 福建医科大学附属省立医院急救中心,福建,福州,350001
3. 安徽医科大学附属省立医院神经内科,安徽,合肥,230001
基金项目:福建省青年科技人才创新基金
摘    要:目的 研究维拉帕米作为添加剂,采用剂量递增法治疗难治性癫痫部分性发作的疗效和安全性。方法 对48例难治性部分性发作患者(男28例,女20例,年龄14~56岁)进行维拉帕米添加治疗的开放性自身对照研究,原服用的抗癫痫药种类和剂量不变。维拉帕米剂量递增给药方法为:第1周120mg/d,第2周240mg/d,第3周360mg/d,第4周420mg/d,分2次口服,连续观察半年。结果 43例完成维拉帕米剂量递增添加治疗。总有效率为65%,其中单纯部分性发作(SPS)有效率为78%,复杂部分性发作(CPS)为65%,继发性全身性发作(SGS)为54%。同添加治疗前比较,总的发作频率减少为68%,其中SPS为72%,CPS为65%,SGS为59%。脑电图呈中度或重度异常的患者比例由74%下降到45%。治疗前后血压、心率、心电图及肝、肾、血、尿等化验检查均无明显变化。抗癫痫药血药浓度除卡马西平升高外(P〈0.05),其余未见明显变化。7例患者出现轻度副反应,但未影响治疗。结论 维拉帕米作为添加剂,用剂量递增法治疗难治性癫痫部分性发作,疗效确切,安全性较高。

关 键 词:维拉帕米  癫痫  部分性  耐药
文章编号:1002-1949(2006)08-0561-03
收稿时间:2006-06-20
修稿时间:2006-06-20

Verapamil used as an add-on therapy in an increasing dosage for the treatment of drug-resistance partial epilepsy
WANG Yin - zhou, LIN Cai -ring, XU Wen - hua ,et al.. Verapamil used as an add-on therapy in an increasing dosage for the treatment of drug-resistance partial epilepsy[J]. Chinese Journal of Critical Care Medicine, 2006, 26(8): 561-563
Authors:WANG Yin - zhou   LIN Cai -ring   XU Wen - hua   et al.
Affiliation:Department of Neurology., Fujian Provincial Hospital, Fuzhou 350001, China
Abstract:Objective To study the efficacy and safety of verapamil used as an add-on therapy with increasing dosage for the treatment of drug-resistance partial seizures(DRPS).Methods 48 patients with DRPS received verapamil add-on therapy more than 6 months from Jan 2001 to Jan 2005 in addition to the medication of existing antiepileptic drug.The administration of verapamil in increasing dosage was executed as follows:the initial dosage was 120 mg/d in the first week,240 mg/d for the second week,360 mg/d for the third week and 420 mg/d for the forth week.The patients were studied continuously for 6 months.Results 2 patients dropped out for personal reasons,three cases discontinued verapamil add-on therapy because of untolerable adverse effects of increase dosage.43 cases accomplished the whole course of 6-months treatment.Total effective ratio was 65%,in which there was 78% for simple partial seizurew(SPS),65% for complex partial seizures(CPS) and 54% for the secondary general seizures(SGS).There was a seizure reduction of 68% as compared with pre-verapamil treatment period(P<0.01),showing 72% for SPS,65% for CPS and 59% for SGS respectively.The patients with severe and mediate abnormal EEG reduced a ratio from 76% to 47%.The changes of blood pressure,heart rate,EKG,and clinical tests of liver,kidney,blood and urine in the pre-verapamil add-on period were insignificant as compared with post-verapamil add-on period.The blood level of antiepiletic drugs were also insignificant as compared with post-verapamil add-on period,except for cabamazpine(P<0.05).7 cases had manifestations of mildly adverse effects,but no influence on the treatment.Conclusion Verapamil as an add-on therapy with increasing dosage has a definite efficacy and a higher safety for the treatment of DRPS.
Keywords:Verapamil   Epilepsy   Partial   Drug - resistance
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