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Effect of preventive (β blocker) treatment behavioural migraine management or their combination on outcomes of optimised acute treatment in frequent migraine: randomised controlled trial

机译:预防性(β受体阻滞剂)治疗行为性偏头痛治疗或其组合对频繁偏头痛的最佳急性治疗效果的影响:随机对照试验

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摘要

>Objective To determine if the addition of preventive drug treatment (β blocker), brief behavioural migraine management, or their combination improves the outcome of optimised acute treatment in the management of frequent migraine.>Design Randomised placebo controlled trial over 16 months from July 2001 to November 2005.>Setting Two outpatient sites in Ohio, USA.>Participants 232 adults (mean age 38 years; 79% female) with diagnosis of migraine with or without aura according to International Headache Society classification of headache disorders criteria, who recorded at least three migraines with disability per 30 days (mean 5.5 migraines/30 days), during an optimised run-in of acute treatment.>Interventions Addition of one of four preventive treatments to optimised acute treatment: β blocker (n=53), matched placebo (n=55), behavioural migraine management plus placebo (n=55), or behavioural migraine management plus β blocker (n=69).>Main outcome measure The primary outcome was change in migraines/30 days; secondary outcomes included change in migraine days/30 days and change in migraine specific quality of life scores.>Results Mixed model analysis showed statistically significant (P≤0.05) differences in outcomes among the four added treatments for both the primary outcome (migraines/30 days) and the two secondary outcomes (change in migraine days/30 days and change in migraine specific quality of life scores). The addition of combined β blocker and behavioural migraine management (−3.3 migraines/30 days, 95% confidence interval −3.2 to −3.5), but not the addition of β blocker alone (−2.1 migraines/30 days, −1.9 to −2.2) or behavioural migraine management alone (−2.2 migraines migraines/30 days, −2.0 to −2.4), improved outcomes compared with optimised acute treatment alone (−2.1 migraines/30 days, −1.9 to −2.2). For a clinically significant (≥50% reduction) in migraines/30 days, the number needed to treat for optimised acute treatment plus combined β blocker and behavioural migraine management was 3.1 compared with optimised acute treatment alone, 2.6 compared with optimised acute treatment plus β blocker, and 3.1 compared with optimised acute treatment plus behavioural migraine management. Results were consistent for the two secondary outcomes, and at both month 10 (the primary endpoint) and month 16.>Conclusion The addition of combined β blocker plus behavioural migraine management, but not the addition of β blocker alone or behavioural migraine management alone, improved outcomes of optimised acute treatment. Combined β blocker treatment and behavioural migraine management may improve outcomes in the treatment of frequent migraine.>Trial registration Clinical trials .
机译:>目的,以确定在预防频繁偏头痛的过程中添加预防性药物治疗(β受体阻滞剂),短暂的行为性偏头痛治疗或其组合是否可以改善优化的急性治疗的效果。>设计从2001年7月至2005年11月的16个月中进行的随机安慰剂对照试验。>设置位于美国俄亥俄州的两个门诊站点。>参与者 232名成人(平均年龄38岁; 79%女性)根据国际头痛协会对头痛疾病标准的分类诊断为有偏头痛或无先兆偏头痛,在优化的急性治疗磨合期间,每30天至少记录3例偏头痛(平均5.5偏头痛/ 30天) 。>干预在优化的急性治疗中添加四种预防性治疗方法之一:β受体阻滞剂(n = 53),匹配的安慰剂(n = 55),行为偏头痛治疗加安慰剂(n = 55)或行为偏头痛管理ENT加β受体阻滞剂(n = 69)。>主要结局指标:主要结局为偏头痛/ 30天的变化;次要结局包括偏头痛天数/ 30天的改变和偏头痛特定生活质量得分的改变。>结果混合模型分析显示,两种治疗方法在四种添加治疗之间的结局具有统计学意义(P≤0.05)主要结局(偏头痛/ 30天)和两个次要结局(偏头痛天/ 30天的变化以及偏头痛特定生活质量得分的变化)。联合使用β受体阻滞剂和行为偏头痛治疗(-3.3偏头痛/ 30天,95%置信区间-3.2至-3.5),但不单独添加β受体阻滞剂(-2.1偏头痛/ 30天,-1.9至-2.2 )或仅行为偏头痛治疗(-2.2偏头痛/ 30天,-2.0至-2.4),与单独优化的急性治疗(-2.1偏头痛/ 30天,-1.9至-2.2)相比,改善了预后。对于临床上显着(≥50%的偏头痛)/ 30天偏头痛,与单独的最佳急性治疗相比,最佳的急性治疗加β受体阻滞剂和行为偏头痛联合治疗所需的治疗数量为3.1,与最佳的急性治疗加β相比为2.6阻滞剂和3.1与优化的急性治疗加行为偏头痛治疗相比。结果与两个次要结果一致,在第10个月(主要终点)和第16个月都一致。>结论联合使用β受体阻滞剂和行为偏头痛治疗,但不单独应用β受体阻滞剂或单独进行行为偏头痛管理,可改善优化急性治疗的效果。 β受体阻滞剂联合行为偏头痛治疗可以改善频发偏头痛的治疗效果。>试验注册临床试验。

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