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VUV luminescence due to 5d-4f transitions in $Gd^{3+}$ and $Lu^{3+}$ ions doped into fluoride crystals

机译:由于掺杂到氟化物晶体中的$ Gd ^ {3 +} $和$ Lu ^ {3 +} $离子中有5d-4f跃迁而引起的VUV发光

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摘要

This open-label extension evaluated the long-term efficacy and tolerability of rufinamide in patients with Lennox-Gastaut syndrome (LGS) who had previously completed a 12-week double-blind study.In total, 124 patients (aged 4-37 years), receiving 1-3 concomitant antiepileptic drugs, were treated with rufinamide approximately 25-60 mg/kg/day. Efficacy was assessed by seizure frequency; tolerability by adverse events (AEs) and laboratory tests.Overall, patients were treated with rufinamide for a median (range) of 432 (10-1149) days. Reductions in seizure frequency were observed throughout the study; during the last 12 months of treatment, 41.0% and 47.9% of patients had > or = 50% reduction in total and tonic-atonic seizure frequency, respectively. The most common AEs were vomiting (30.6%) and pyrexia (25.8%).In this open-label extension, rufinamide appeared to be an effective long-term adjunctive therapy for the treatment of LGS-associated seizures in children and young adults.
机译:这项公开标签的扩展评估了鲁芬酰胺对Lennox-Gastaut综合征(LGS)患者的长期疗效和耐受性,该患者先前已完成了为期12周的双盲研究,总共124例患者(4-37岁)接受1-3种抗癫痫药的同时接受约25-60 mg / kg /天的芦丁酰胺治疗。通过癫痫发作频率评估疗效;不良事件(AE)和实验室测试的耐受性总体而言,患者接受芦丁酰胺治疗的中位(范围)为432(10-1149)天。在整个研究中观察到癫痫发作频率降低;在治疗的最后12个月中,分别有41.0%和47.9%的患者的总发作次数和强直发作次数减少了50%。最常见的AE是呕吐(30.6%)和发热(25.8%)。在这种开放标签的扩展中,rufinamide似乎是一种有效的长期辅助疗法,可用于治疗儿童和年轻人的LGS相关性癫痫发作。

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