布里瓦拉作为发育性脑病变的儿童的附加疗法:一项对42名患者的研究
Roberto H Caraballo1, Gabriela Reyes1, Santiago Chacón2
1Department of Neurology, Juan P Garrahan Hospital, Buenos Aires, Argentina.
布里瓦拉 (BRV) 有效地减少了发育性脑病变 (DEE) 的儿童的发作,超过70%的儿童出现了显著的改善. 这种附加疗法在儿科患者中证明了安全性和耐受性.
科学领域:
- 儿科神经学 儿科神经学
- 发病学 (Epileptology) 是一个专业的学科.
- 药理学 药理学是指药理学的学科.
背景情况:
- 发育性脑病变 (DEE) 是儿童发作的严重综合征.
- 耐治疗的DEE在儿科神经病学中带来了重大挑战.
- 布里瓦拉 (BRV) 是一种抗药,具有独特的药理学特征.
研究的目的:
- 评估布里瓦拉 (BRV) 作为DEE儿科患者的附加治疗的疗效和安全性.
- 评估BRV在治疗耐药病例中的有效性.
- 探索BRV在患有特定伴随性疾病 (如行为障碍) 的患者中的实用性.
主要方法:
- 在阿根廷的四个中心对42名患有DEE的儿科患者的医疗记录进行了回顾性分析.
- 患者在2021年1月至2023年7月期间接受了BRV作为附加疗法.
- 收集的数据包括发作频率,EEG异常和不良事件.
主要成果:
- 在62.1%的患者 (>50%的减少) 观察到发作频率显著减少,23.8%的患者经历了25-50%的减少.
- 三名患者 (9.5%) 实现了无性发作,而响应者中的间脉脑电图异常得到改善.
- 副作用 (昏昏欲睡,易怒,食欲下降) 是轻微的,在大多数情况下不会导致停止治疗.
结论:
- 布里瓦拉是一种有效且耐受性良好的补充治疗,用于患有DEE的儿科患者.
- 对于有行为障碍的患者,即使没有先前的 levetiracetam (LEV) 治疗,也可以考虑 BRV.
- 这项研究支持BRV作为一种有价值的治疗选择,用于治疗儿童难以治疗的.
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