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首页> 外文期刊>Headache >Long-term tolerability of sumatriptan nasal spray in adolescent patients with migraine.
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Long-term tolerability of sumatriptan nasal spray in adolescent patients with migraine.

机译:舒马曲坦鼻喷雾剂对青少年偏头痛患者的长期耐受性。

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摘要

OBJECTIVE: This 1-year, open-label, multicenter study was designed to assess the long-term tolerability and efficacy of sumatriptan nasal spray 20 mg in adolescent patients with migraine. METHODS: A prospective, multicenter, open-label study was conducted in patients aged 12 to 17 years who were allowed to treat an unlimited number of migraines at severe, moderate, or mild pain intensity with sumatriptan nasal spray for up to 1 year. All patients started the study at the 20-mg dose of sumatriptan nasal spray. Dose could be adjusted downward to 5 mg at the discretion of the investigator to optimize therapy. RESULTS: A total of 484 adolescent migraineurs treated 4676 migraines with sumatriptan nasal spray 20 mg (3593 during the first 6 months and 1083 during the second 6 months). A total of 3940 migraines and 699 migraines were treated with one and two 20-mg doses of sumatriptan nasal spray, respectively. Only 10 patients (treating 42 migraines) took the 5-mg dose of sumatriptan nasal spray. The overall percentage of migraines treated with either one 20-mg dose or one, two, or three 20-mg doses with at least 1 drug-related adverse event was 19%. The most common specific drug-related adverse event was unpleasant taste, reported in 17% of migraines. No other single drug-related adverse event was reported in more than 1% of migraines over the 1-year treatment period. When unpleasant taste was excluded from the adverse-event tabulations, the percentages of migraines with at least 1 drug-related adverse event after one or one, two, or three 20-mg doses declined to 4% and 3%, respectively. No patient experienced any drug-related changes in 12-lead ECGs, vital signs, or nasal assessments; and no clinically meaningful changes in clinical laboratory values were observed. Across all migraines with evaluable efficacy data (n=4334), headache relief was reported in 43% of migraines at 1 hour and in 59% at 2 hours after dosing with sumatriptan nasal spray 20 mg. Of the 2561 migraines with headache relief 2 hours postdose,headache recurrence was reported within 24 hours of initial dosing in 7% of migraines. None of the efficacy or tolerability results varied as a function of time in the study (ie, first 6 months vs. second 6 months). CONCLUSION: Sumatriptan nasal spray 20 mg is generally well tolerated and may be beneficial during long-term use by adolescent migraineurs ages 12 to 17 years.
机译:目的:这项为期一年的开放标签,多中心研究旨在评估舒马普坦鼻腔喷雾剂20 mg对青少年偏头痛患者的长期耐受性和疗效。方法:一项前瞻性,多中心,开放标签的研究在12至17岁的患者中进行,这些患者被允许使用舒马曲坦鼻喷剂治疗重度,中度或轻度疼痛程度不限的偏头痛,长达1年。所有患者均以20 mg舒马曲坦鼻喷雾剂开始研究。研究者可酌情将剂量下调至5 mg,以优化治疗。结果:总共484名青少年偏头痛患者使用20 mg舒马曲坦鼻喷剂治疗了4676例偏头痛(头6个月为3593头,后6个月为1083头)。分别用一剂和两剂20 mg舒马曲坦鼻喷剂治疗总共3940例偏头痛和699例偏头痛。仅10例患者(治疗42例偏头痛)服用了5 mg剂量的舒马曲坦鼻喷雾剂。用一剂20 mg或一剂,二剂或三剂20 mg剂量治疗且至少有一种与药物相关的不良事件治疗的偏头痛的总百分比为19%。最常见的与药物相关的特定不良事件是令人不快的味道,据报道有17%的偏头痛。在1年的治疗期内,没有超过1%的偏头痛报告有其他与单一药物相关的不良事件。当从不良事件列表中排除令人不快的味道时,在一次或一次,两次或三次20 mg剂量后出现至少1种与药物相关的不良事件的偏头痛的百分比分别下降至4%和3%。没有患者在12导联心电图,生命体征或鼻腔评估中出现任何与药物相关的变化;并且未观察到临床实验室值的临床意义变化。在所有具有可评估疗效数据的偏头痛中(n = 4334),舒马普坦鼻喷剂20 mg给药后1小时出现头痛缓解的比例为1%,2小时出现头痛缓解的比例为59%。用药2小时后缓解头痛的2561例偏头痛中,有7%的偏头痛在初次给药后24小时内复发。在研究中,疗效或耐受性结果均未随时间变化(即前6个月对后6个月)。结论:舒马曲坦鼻喷雾剂20 mg通常耐受性良好,在12至17岁的青少年偏头痛患者长期使用期间可能有益。

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