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长期应用舒马曲坦/萘普生钠治疗偏头痛对血压的评价。

Evaluation of the migraine treatment sumatriptan/naproxen sodium on blood pressure following long-term administration.

机构信息

Calhoun Cardiology Center, University of Connecticut School of Medicine, Farmington, CT 06030-3940, USA.

出版信息

J Clin Hypertens (Greenwich). 2011 Dec;13(12):910-6. doi: 10.1111/j.1751-7176.2011.00554.x. Epub 2011 Nov 11.

Abstract

Anti-inflammatory and pain therapies have been associated with blood pressure (BP) destabilization. Hence, the effects on BP of sumatriptan/naproxen sodium in fixed-dose combination, sumatriptan 85 mg, and naproxen sodium 500 mg administered intermittently for the acute treatment of migraine attacks were assessed. Patients with migraine with or without aura and no history of hypertension were randomized to sumatriptan/naproxen sodium (n=135), sumatriptan (n=136), or naproxen sodium (n=136) to treat migraine attacks for 6 months in a double-blind, parallel-group trial. Following a treated migraine attack, patients performed 2 consecutive days of self-measured BPs beginning ≥24 hours after the last dose of study medication and transmitted them by a transtelephonic modem. The primary end point was the change from baseline in self-measured BP at 6 months. Changes in self-measured BP from baseline to 6 months for sumatriptan/naproxen sodium were -2.1/-1.5 mm Hg (95% confidence intervals, -3.4 to -0.8 for systolic and -2.6 to -0.3 for diastolic). Mean changes from baseline in self-measured BP did not differ among the 3 treatment groups. Additional categorical analyses did not show increases from baseline with sumatriptan/naproxen sodium relative to either of the monotherapy groups. Intermittent acute migraine treatment with sumatriptan/naproxen sodium for up to 6 months was associated with clinically insignificant decreases in self-measured BP that were similar to those with sumatriptan or naproxen alone in normotensive patients with migraine.

摘要

抗炎和止痛疗法与血压(BP)不稳定有关。因此,评估了固定剂量组合舒马曲坦/萘普生钠(舒马曲坦 85mg 和萘普生钠 500mg)、舒马曲坦(n=136)和萘普生钠(n=136)间歇性给药治疗偏头痛发作时对 BP 的影响。有或无先兆偏头痛且无高血压病史的患者被随机分为舒马曲坦/萘普生钠(n=135)、舒马曲坦(n=136)或萘普生钠(n=136),以在双盲、平行组试验中接受偏头痛发作的 6 个月治疗。在治疗后的偏头痛发作后,患者在最后一次研究药物剂量后至少 24 小时开始连续 2 天进行自我测量 BP,并通过远程调制解调器传输。主要终点是 6 个月时自我测量 BP 相对于基线的变化。舒马曲坦/萘普生钠从基线到 6 个月的自我测量 BP 变化为-2.1/-1.5mmHg(95%置信区间,收缩压为-3.4 至-0.8,舒张压为-2.6 至-0.3)。3 个治疗组之间从基线到 6 个月的自我测量 BP 变化无差异。额外的分类分析未显示与舒马曲坦/萘普生钠相比,从基线开始与任何单药治疗组相比均无增加。在无高血压的偏头痛患者中,间歇性急性偏头痛治疗使用舒马曲坦/萘普生钠长达 6 个月,与单独使用舒马曲坦或萘普生钠相比,自我测量 BP 仅出现临床意义上的降低。

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