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氨己烯酸作为婴儿痉挛症的初始治疗:一项欧洲回顾性调查。喜保宁国际研究人员及同行评审小组。

Vigabatrin as initial therapy for infantile spasms: a European retrospective survey. Sabril IS Investigator and Peer Review Groups.

作者信息

Aicardi J, Mumford J P, Dumas C, Wood S

机构信息

Institute of Child Health, University of London, England.

出版信息

Epilepsia. 1996 Jul;37(7):638-42. doi: 10.1111/j.1528-1157.1996.tb00627.x.

Abstract

PURPOSE

The efficacy and tolerability of vigabatrin (VGB) as an add-on therapy in the treatment of infantile spasm (IS) prompted physicians to explore its use as the first drug in this seizure type.

METHODS

Our retrospective study included 250 infants diagnosed with IS; the data obtained were subjected to peer-group review. Of this infant population, 192 infants were considered to have classic IS and had received VGB as their first treatment for the spasms. There was a slight preponderance of boys (57%) in this population. Mean age of IS onset was 5.8 months; 60% had typical hypsarrhythmia.

RESULTS

Initial suppression of spasms was obtained in 68% of infants with a median time to response of 4 days at an average VGB dose of 99 mg/kg/day. The best response was seen in those infants with tuberous sclerosis (96% response) and in those younger than 3 months at onset of spasms (90% response). Of these infants, 43 (22%) of 192 subsequently had other types of seizures, and a recurrence of infantile spasms occurred in 28 (21%) of 131 responders. At the end of this study, 96 of 192 infants who could be evaluated were seizure free with VGB monotherapy. Treatment appeared to be well tolerated, with only 33 (13%) infants with adverse events, of which the most common were somnolence (15 patients) and hyperkinesia (eight patients). In only two cases did adverse events require VGB withdrawal.

CONCLUSION

This study supports the opinion that VGB may be considered an initial treatment for IS regardless of cause.

摘要

目的

氨己烯酸(VGB)作为婴儿痉挛症(IS)附加治疗的疗效和耐受性促使医生探索将其作为这种癫痫类型的首选药物。

方法

我们的回顾性研究纳入了250例诊断为IS的婴儿;所获得的数据经过同行评审。在这一婴儿群体中,192例婴儿被认为患有典型IS,并接受了VGB作为痉挛的首次治疗。该群体中男孩略占多数(57%)。IS发病的平均年龄为5.8个月;60%有典型的高峰失律。

结果

68%的婴儿痉挛得到初步抑制,平均VGB剂量为99mg/kg/天时,中位反应时间为4天。在患有结节性硬化症的婴儿(96%有反应)和痉挛发作时年龄小于3个月的婴儿(90%有反应)中观察到最佳反应。在这些婴儿中,192例中有43例(22%)随后出现了其他类型的癫痫发作,131例有反应的婴儿中有28例(21%)婴儿痉挛复发。在本研究结束时,192例可评估的婴儿中有96例通过VGB单药治疗无癫痫发作。治疗耐受性良好,只有33例(13%)婴儿出现不良事件,其中最常见的是嗜睡(15例患者)和运动亢进(8例患者)。只有2例不良事件需要停用VGB。

结论

本研究支持以下观点,即无论病因如何,VGB均可被视为IS的初始治疗药物。

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