High-dose versus low-dose valproate for the treatment of juvenile myoclonic epilepsy: Going from low to high.
High-dose versus low-dose valproate for the treatment of juvenile myoclonic epilepsy: Going from low to high.
复制标题
高剂量与低剂量丙戊酸,用于治疗青少年肌阵挛性癫痫:从低到高。
DOI:
10.1016/j.yebeh.2016.04.047
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发表时间:
2016-08
期刊:
影响因子:
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通讯作者:
Martínez-Juárez IE
中科院分区:
文献类型:
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作者:
Hernández-Vanegas LE;Jara-Prado A;Ochoa A;Rodríguez Y Rodríguez N;Durón RM;Crail-Meléndez D;Alonso ME;Delgado-Escueta AV;Martínez-Juárez IE
Juvenile myoclonic epilepsy (JME) is a genetic generalized epilepsy accounting for 3–12% of adult cases of epilepsy. Valproate has proven to be the first-choice drug in JME for controlling the most common seizure types: myoclonic, absence, and generalized tonic-clonic (GTC). In this retrospective study, we analyzed seizure outcome in patients with JME using valproate monotherapy for a minimum period of one year. Low valproate dose was considered to be 1000 mg/day or lower, while serum levels were considered to be low if they were at or below 50 mcg/dl. One hundred three patients met the inclusion criteria. Fifty-six patients (54.4%) were female. The current average age was 28.4 ± 7.4 years, while the age of epilepsy onset was 13.6 ± 2.9 years. Most patients corresponded to the subsyndrome of classic JME. Forty-six (44.7%) patients were free from all seizure types, and 76 (73.7%) patients were free from GTC seizures. No significant difference was found in seizure freedom among patients using a low dose of valproate versus a high dose (p=0.535), or among patients with low blood levels versus high blood levels (p=0.69). In patients with JME, it seems appropriate to use low doses of valproate (500 mg to 1,000 mg) for initial treatment and to evaluate to determine if freedom from seizures was attained.