Treatment of comorbid migraine and temporomandibular disorders: a factorial, double-blind, randomized, placebo-controlled study.

Daniela A G Goncalves, Cinara M Camparis, José G Speciali, Sabrina M Castanharo, Liliana T Ujikawa, Richard B Lipton, Marcelo E Bigal
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引用次数: 47

Abstract

Aims: To investigate the effectiveness of single and concomitant treatment of migraine and temporomandibular disorders (TMD) in women with the comorbidity.

Methods: Eligible female patients met International Classification of Headache Disorders, second edition (ICHD-2) criteria for migraine with or without aura and the Research Diagnostic Criteria for myofascial TMD (Grade ll or lll). After a run-in period (30 days), women with both migraine and TMD were enrolled into a four-arm, double-blind, placebo-controlled, factorial study testing the separate and joint effects of a migraine treatment (propranolol 90 mg) and a TMD treatment (stabilization splint [SS]) in four groups of patients. The four treatment groups were propranolol and SS (n = 22); propranolol placebo and SS (n = 23); propranolol and non-occlusal splint (NOS) (n = 23); and propranolol placebo and NOS (n = 21). The primary endpoint for migraine was change in headache days from baseline to the third month, and the secondary endpoint was change in days with at least moderate headache in the same period. The TMD endpoints included pain threshold and mandibular vertical range of motion. Data were analyzed using analysis of variance (ANOVA, Dunn's post-hoc test) or Kruskal-Wallis test.

Results: For the primary endpoint, in intention-to-treat (ITT) analyses (n = 94), propranolol and SS were associated with a nonsignificant reduction in the number of headache days, relative to all other groups. For per-protocol (PP) Completer analyses (n = 89), differences in the number of headache days reached significance (P < .05). The propranolol and SS group was significantly superior to the other groups on all other headache endpoints and in disability, in both ITT and PP analyses. No significant differences among groups were seen for the TMD parameters.

Conclusion: In women with TMD and migraine, migraine significantly improved only when both conditions were treated. The best treatment choice for TMD pain in women with migraine is yet to be defined.

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治疗合并偏头痛和颞下颌紊乱:一项因子、双盲、随机、安慰剂对照研究。
目的:探讨合并偏头痛和颞下颌紊乱(TMD)的女性患者单独和联合治疗的效果。方法:符合国际头痛疾病分类第2版(ICHD-2)偏头痛伴或不伴先兆标准和肌筋膜TMD研究诊断标准(ⅱ级或ⅱ级)的女性患者。经过一段磨合期(30天),同时患有偏头痛和TMD的女性被纳入一项四组、双盲、安慰剂对照、因子研究,对四组患者进行偏头痛治疗(普萘洛尔90mg)和TMD治疗(稳定夹板[SS])的单独和联合效果进行测试。4个治疗组分别为心得安和SS (n = 22);心得安安慰剂和SS (n = 23);心得安加无咬合夹板(NOS) (n = 23);心得安安慰剂和NOS (n = 21)。偏头痛的主要终点是从基线到第3个月头痛天数的变化,次要终点是在同一时间段内出现至少中度头痛的天数的变化。TMD终点包括疼痛阈值和下颌垂直运动范围。数据分析采用方差分析(ANOVA, Dunn’s事后检验)或Kruskal-Wallis检验。结果:对于主要终点,在意向治疗(ITT)分析(n = 94)中,相对于所有其他组,心得安和SS与头痛天数的无显著减少相关。对于每个方案(PP)完整分析(n = 89),头痛天数的差异达到显著性(P < 0.05)。在ITT和PP分析中,普萘洛尔和SS组在所有其他头痛终点和残疾方面均显著优于其他组。各组间TMD参数无显著差异。结论:在女性TMD和偏头痛患者中,只有当两种情况都得到治疗时,偏头痛才有明显改善。女性偏头痛患者TMD疼痛的最佳治疗选择尚未确定。
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来源期刊
Journal of orofacial pain
Journal of orofacial pain 医学-牙科与口腔外科
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