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一项对113例接受丙戊酸缓释剂治疗的癫痫患者的回顾性研究。

A retrospective study of 113 epileptic patients treated with sustained-release valproate.

作者信息

Despland P A

机构信息

Neurology Department, University Hospital (CHUV), Lausanne, Switzerland.

出版信息

Epilepsia. 1994;35 Suppl 5:S99-100. doi: 10.1111/j.1528-1157.1994.tb05981.x.

Abstract

A retrospective study of 113 patients treated with a sustained-release form of valproate (SRF-VPA), known as the "chrono" formulation in most European countries, led to the following conclusions: Patients treated with the old VPA formulation could immediately receive the same daily dosage of SRF-VPA without loss of seizure control when administered as a single evening dose. The tolerability of SRF-VPA was good and twice or single daily dosing was preferred by all our patients. Whether or not SRF-VPA should be used as first or second-line treatment in partial seizures that do or do not secondarily generalize is unclear. Our study demonstrates that the efficacy of SRF-VPA is comparable with that of other major antiepileptic drugs such as carbamazepine (CBZ). In refractory seizures, the combination of SRF-VPA and CBZ seemed to be the most satisfactory treatment. Based on these results SRF-VPA is a promising drug for all types of seizures even in low daily dosage, but further clinical work is required to confirm our observations.

摘要

一项针对113例接受丙戊酸盐缓释制剂(SRF-VPA,在大多数欧洲国家称为“chrono”制剂)治疗的患者的回顾性研究得出了以下结论:接受旧的丙戊酸制剂治疗的患者,在作为单次晚间剂量给药时,可立即接受相同每日剂量的SRF-VPA,且不会失去对癫痫发作的控制。SRF-VPA的耐受性良好,我们所有患者均更倾向于每日给药两次或一次。SRF-VPA是否应用于继发或未继发全面性发作的部分性癫痫的一线或二线治疗尚不清楚。我们的研究表明,SRF-VPA的疗效与其他主要抗癫痫药物如卡马西平(CBZ)相当。在难治性癫痫发作中,SRF-VPA与CBZ联合使用似乎是最令人满意的治疗方法。基于这些结果,即使每日剂量较低,SRF-VPA对于所有类型的癫痫发作都是一种有前景的药物,但需要进一步的临床研究来证实我们的观察结果。

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