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Efficacy of early vs. late use of frovatriptan combined with dexketoprofen vs. frovatriptan alone in the acute treatment of migraine attacks with or without aura

机译:早期和晚期使用氟哌曲坦联合右旋酮洛芬与氟哌曲坦单独或联合使用在急性先兆偏头痛发作或不先兆发作中的疗效

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Early triptan use after headache onset may help improve the efficacy of acute migraine treatment. This may be particularly the case when triptan therapy is combined with a nonsteroidal anti-inflammatory drug (NSAID). The objective of this is to assess whether the combination of frovatriptan 2.5 mg + dexketoprofen 25 or 37.5 mg (FroDex25 and FroDex37.5) is superior to frovatriptan 2.5 mg alone (Frova) in the acute treatment of migraine attacks in patients who took the drug within 30 min from the onset of pain (early use) or after (late use). A total of 314 subjects with a history of migraine with or without aura were randomized into a double-blind, multicenter, parallel group, pilot study to Frova, FroDex25 or FroDex37.5 and were required to treat at least one migraine attack. In the present post hoc analysis, traditional migraine endpoints were compared across study drugs for subgroups of the 279 patients of the full analysis set according to early (n = 172) or late (n = 107) drug use. The proportion of patients pain free at 2 h in the early drug use subgroup was 33 % with Frova, 50 % with FroDex25 and 51 % with FroDex37.5 mg (p = NS combinations vs. monotherapy), while in the late drug use subgroup was 22, 51 and 50 % (p < 0.05 FroDex25 and FroDex37.5 vs. Frova), respectively. Pain-free episodes at 4 h were 54 % for early and 34 % for late use of Frova, 71 and 57 % with FroDex25 and 74 and 68 % with FroDex37.5 (p < 0.05 for early and p < 0.01 for late use vs. Frova). The proportion of sustained pain free at 24 h was 26 % under Frova, 43 % under FroDex25 mg and 40 % under FroDex37.5 mg (p = NS FroDex25 or 37.5 vs. Frova) in the early drug intake subgroup, while it was 19 % under Frova, 43 % under FroDex25 mg and 45 % under FroDex37.5 mg (p < 0.05 FroDex25 and FroDex37.5 vs. Frova) in the late drug intake subgroup. Risk of relapse at 48 h was similar (p = NS) among study drug groups (Frova: 25 %, FroDex25: 21 %, and FroDex37.5: 37 %) for the early as well as for the late drug use subgroup (14, 42 and 32 %). FroDex was found to be more effective than Frova taken either early or late. The intrinsic pharmacokinetic properties of the two single drug components made FroDex combination particularly effective within the 2-48-h window from the onset of the acute migraine attack. The efficacy does not seem to be influenced by the time of drug use relative to the onset of headache.
机译:头痛发作后及早使用曲普坦可能有助于提高急性偏头痛治疗的疗效。当曲普坦疗法与非甾体类抗炎药(NSAID)联合使用时,尤其如此。这样做的目的是评估在服用药物的偏头痛发作的急性治疗中,frovatriptan 2.5 mg +右酮洛芬25或37.5 mg(FroDex25和FroDex37.5)的组合是否优于单独使用frovatriptan 2.5 mg(Frova)的组合在疼痛发作(早期使用)或疼痛发作(晚期使用)后30分钟内。总共314名有或没有先兆偏头痛病史的受试者被随机分为双盲,多中心,平行组,对Frova,FroDex25或FroDex37.5进行了初步研究,并被要求治疗至少一次偏头痛发作。在目前的事后分析中,根据药物使用的早期(n = 172)或晚期(n = 107),对整个分析集中279例患者的亚组之间的传统偏头痛终点进行了比较。在早期用药亚组中,使用Frova的患者在2小时无疼痛的比例为33%,使用FroDex25的患者为50%,使用FroDex37.5 mg的患者为51%(p = NS组合vs.单一疗法),而在晚期药物使用亚组分别为22%,51%和50%(相对于Frova,p <0.05 FroDex25和FroDex37.5)。早期使用Frova的无痛发作为54%,晚期使用为34%,FroDex25分别为71和57%,FroDex37.5为74和68%(早期使用p <0.05,晚期使用p <0.01 Frova)。在早期药物摄入亚组中,在Frova下24小时持续无痛的比例为26%,在FroDex25 mg下为43%,在FroDex37.5 mg下为40%(p = NS FroDex25或37.5 vs. Frova),为19岁。在晚期药物摄入亚组中,在Frova下为100%,在FroDex25 mg下为43%,在FroDex37.5 mg下为45%(与Frova相比p <0.05 FroDex25和FroDex37.5)。在早期和晚期用药亚组中,研究药物组(Frova:25%,FroDex25:21%,FroDex37.5:37%)在48 h复发的风险相似(p = NS)(14) ,42%和32%)。发现FroDex比早期或晚期服用Frova更有效。从急性偏头痛发作开始的2-48小时内,两种单一药物成分的内在药代动力学特性使FroDex组合特别有效。相对于头痛的发作,疗效似乎不受药物使用时间的影响。

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