Bonanni Enrica, Galli Renato, Maestri Michelangelo, Pizzanelli Chiara, Fabbrini Monica, Manca Maria Laura, Iudice Alfonso, Murri Luigi
Department of Neurosciences, Section of Neurology, University of Pisa, Italy.
Epilepsia. 2004 Apr;45(4):333-7. doi: 10.1111/j.0013-9580.2004.47803.x.
Limited research has focused to date on objective neurophysiological evaluation of daytime sleepiness in patients treated with newer antiepileptic drugs (AEDs), especially when used as monotherapy. This study was aimed at assessing occurrence of daytime sleepiness in newly diagnosed, drug-naïve patients with partial epilepsy receiving initial topiramate (TPM) monotherapy.
Daytime vigilance was assessed in 14 consecutive, newly diagnosed and never medicated adult patients with focal epilepsy, receiving monotherapy with TPM. At baseline and 2 months after slowly titrated therapy with TPM, 200 mg/day, patients underwent the Multiple Sleep Latency Test (MSLT), visual simple and choice reaction times (VRT), and self-rated their own degree of sleepiness with the Epworth Sleepiness Scale. A group of 14 age- and gender-matched healthy volunteers served as controls.
At baseline, mean daytime sleep latencies on the MSLT were comparable in patients and in controls. Two months after TPM monotherapy, MSLT scores did not significantly change in patients as compared with pretreatment values. Accordingly, subjective daytime sleepiness and VRTs, which were comparable in controls and in untreated patients at baseline, did not change in patients after TPM monotherapy.
Study results suggest that an initial short-course monotherapy with TPM, 200 mg/day, does not impair daytime vigilance in newly diagnosed adult patients with partial seizures.
迄今为止,针对使用新型抗癫痫药物(AEDs)治疗的患者,尤其是单药治疗时白天嗜睡的客观神经生理学评估的研究有限。本研究旨在评估新诊断的、未接受过药物治疗的部分性癫痫患者接受初始托吡酯(TPM)单药治疗时白天嗜睡的发生率。
对14例连续的、新诊断的且从未接受过药物治疗的局灶性癫痫成年患者进行TPM单药治疗,并评估其白天的警觉性。在基线期以及以200mg/天的TPM缓慢滴定治疗2个月后,患者接受多次睡眠潜伏期试验(MSLT)、视觉简单反应时间和选择反应时间(VRT),并使用爱泼华嗜睡量表对自己的嗜睡程度进行自评。14名年龄和性别匹配的健康志愿者作为对照组。
在基线期,患者和对照组的MSLT平均白天睡眠潜伏期相当。TPM单药治疗2个月后,患者的MSLT评分与治疗前相比无显著变化。因此,在基线期对照组和未治疗患者中相当的主观白天嗜睡和VRT,在TPM单药治疗后的患者中没有变化。
研究结果表明,初始短期使用200mg/天的TPM单药治疗不会损害新诊断的部分性发作成年患者的白天警觉性。