dc.contributorUniversidade Estadual Paulista (Unesp)
dc.contributorUniversidade de São Paulo (USP)
dc.contributorAlbert Einstein Coll Med
dc.contributorLabrys Biol Inc
dc.date.accessioned2014-12-03T13:07:06Z
dc.date.available2014-12-03T13:07:06Z
dc.date.created2014-12-03T13:07:06Z
dc.date.issued2013-09-01
dc.identifierJournal of Orofacial Pain. Hanover Park: Quintessence Publishing Co Inc, v. 27, n. 4, p. 325-335, 2013.
dc.identifier1064-6655
dc.identifierhttp://hdl.handle.net/11449/111246
dc.identifierWOS:000326428200005
dc.identifier8786391650842720
dc.description.abstractAims: 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 II or III). 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.
dc.languageeng
dc.publisherQuintessence Publishing Co Inc
dc.relationJournal of Orofacial Pain
dc.rightsAcesso restrito
dc.sourceWeb of Science
dc.subjectclinical trial
dc.subjectmigraine
dc.subjectocclusal splint
dc.subjectpropranolol
dc.subjecttemporomandibular disorders
dc.titleTreatment of Comorbid Migraine and Temporomandibular Disorders: A Factorial, Double-Blind, Randomized, Placebo-Controlled Study
dc.typeArtículos de revistas


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