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生酮饮食治疗肌阵挛-失张力癫痫患者

Ketogenic diet in patients with myoclonic-astatic epilepsy.

作者信息

Caraballo Roberto Horacio, Cersósimo Ricardo Oscar, Sakr Diego, Cresta Araceli, Escobal Nidia, Fejerman Natalio

机构信息

Servicio de Neurología, Hospital de Pediatría "Prof Dr Juan P Garrahan", Buenos Aires, Argentina.

出版信息

Epileptic Disord. 2006 Jun;8(2):151-5.

Abstract

For more than 80 years, the ketogenic diet has been used as an alternative to antiepileptic drugs for patients with refractory epilepsy. Myoclonic-astatic epilepsy in early childhood is one of the malignant epilepsy syndromes that often proves refractory to antiepileptic drugs treatment. Objective. In this prospective study we assess the efficacy and tolerability of the ketogenic diet in patients with myoclonic-astatic epilepsy. Material and methods. Between March 1, 1990 and August 31, 2004, 30 patients who met diagnostic criteria of myoclonic-astatic epilepsy were seen at our department. Eleven of them were placed on the ketogenic diet using the Hopkins protocol and were followed for a minimum of 18 months. Results. The children had previously received a mean of 5.2 different antiepileptic drugs and were on a mean of 2.2 antiepileptic drugs when the diet was started. Eighteen months after initiating the diet, six of the patients (54.5%) remained on the diet. Two patients (18%) were seizure-free, two (18%) had a 75-99% decrease in seizures, and the remaining two children (18%) had a 50% to 74% decrease in seizures. The first two patients were tapered off the diet after remaining seizure-free, without antiepileptic drugs for several years. In the two patients who had sporadic seizures, antiepileptic drugs were reduced to one, and in the last two the seizure frequency was significantly reduced. No differences in seizure control were found when compared for age, sex, or seizure type. Five of our patients discontinued the ketogenic diet in less than 3 months (four because of lack of effectiveness and one because of persistent vomiting). Conclusion. The ketogenic diet is a promising therapy for patients with myoclonic-astatic epilepsy, with over half the children showing a > 50% reduction in seizures, and seizure-freedom in 18%. In drug resistant cases of myoclonic-astatic epilepsy, the diet should be considered early in the course of this syndrome and not as a last resort.

摘要

八十多年来,生酮饮食一直被用作难治性癫痫患者抗癫痫药物的替代疗法。儿童早期肌阵挛-无动性癫痫是一种恶性癫痫综合征,通常对抗癫痫药物治疗无效。目的。在这项前瞻性研究中,我们评估生酮饮食对肌阵挛-无动性癫痫患者的疗效和耐受性。材料与方法。1990年3月1日至2004年8月31日期间,30例符合肌阵挛-无动性癫痫诊断标准的患者在我科就诊。其中11例采用霍普金斯方案进行生酮饮食,并至少随访18个月。结果。这些儿童此前平均接受过5.2种不同的抗癫痫药物治疗,开始饮食时平均正在服用2.2种抗癫痫药物。开始饮食18个月后,6例患者(54.5%)仍在坚持饮食。2例患者(18%)无癫痫发作,2例(18%)癫痫发作减少75% - 99%,其余2例儿童(18%)癫痫发作减少50%至74%。前2例患者在多年无癫痫发作且未服用抗癫痫药物后逐渐停用饮食。在2例偶发癫痫发作的患者中,抗癫痫药物减至1种,最后2例患者癫痫发作频率显著降低。在年龄、性别或癫痫发作类型方面比较时,未发现癫痫控制方面的差异。我们的5例患者在不到3个月内停止了生酮饮食(4例因无效,1例因持续呕吐)。结论。生酮饮食是治疗肌阵挛-无动性癫痫患者的一种有前景的疗法,超过半数的儿童癫痫发作减少>50%,18%的儿童无癫痫发作。在肌阵挛-无动性癫痫的耐药病例中,应在该综合征病程早期考虑采用饮食疗法,而不应作为最后的手段。

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