Department of Prosthetic Dentistry, Faculty of Medicine, Institute of Dentistry, University of Turku, Turku, Finland.
J Oral Rehabil. 2012 Apr;39(4):252-60. doi: 10.1111/j.1365-2842.2011.02261.x. Epub 2011 Oct 11.
The long-term effectiveness of a prefabricated oral appliance (R) was compared with a stabilisation appliance (S) in patients with myofascial pain. Sixty-five patients diagnosed with myofascial pain at two centres for Stomatognathic Physiology in Sweden and Finland were included in a randomised controlled trial using Research Diagnostic Criteria for Temporomandibular Disorders, with history questionnaires and clinical examinations performed by blinded examiners at baseline and at 6- and 12-month follow-ups. Patients were randomly assigned either to the R or the S group. Treatment outcome was measured according to IMMPACT for four chronic pain outcome domains: pain intensity, overall improvement, physical functioning and emotional functioning. Physical functioning was classified for Graded Chronic Pain severities and assessed by the Jaw Functional Limitation scale. Emotional functioning composed of scores of non-specific physical symptoms and depression. There were no differences between groups at baseline. At both follow-ups, all outcome domains showed significant within-group improvement, without significant differences between groups. At 12 months, 72% of all patients reported a 30% reduction in worst pain and 63% of the patients a 50% reduction in worst pain. Overall improvement 'better' to 'symptom-free' was observed in 81% in the R and 64% in the S group at the 12-month follow-up. Graded Chronic Pain, Functional Limitation of the Jaw, non-specific physical symptoms and depression showed statistically significant reduction at 12-month follow-up. Results support the hypothesis that the effectiveness of the prefabricated appliance is similar to that of the stabilisation appliance in the long-term when treating patients with myofascial pain.
预制口腔矫治器(R)与稳定器(S)治疗肌筋膜疼痛患者的长期疗效比较。在瑞典和芬兰的两个口腔生理学中心,根据颞下颌关节紊乱研究诊断标准,对 65 名肌筋膜疼痛患者进行了一项随机对照试验,纳入了病史问卷和临床检查,由盲法检查者在基线和 6 个月及 12 个月随访时进行。患者被随机分配到 R 组或 S 组。根据 IMPACT 对四个慢性疼痛结局领域进行治疗结局测量:疼痛强度、整体改善、身体功能和情绪功能。身体功能按 Graded Chronic Pain 严重程度分类,并通过 Jaw Functional Limitation 量表进行评估。情绪功能由非特异性躯体症状和抑郁的评分组成。基线时两组间无差异。在两次随访中,所有结局领域均显示出显著的组内改善,两组间无显著差异。在 12 个月时,所有患者中有 72%报告最差疼痛减轻 30%,63%报告最差疼痛减轻 50%。在 12 个月的随访中,R 组 81%和 S 组 64%的患者总体改善为“更好”至“无症状”。Graded Chronic Pain、Jaw 功能受限、非特异性躯体症状和抑郁在 12 个月随访时均显示出统计学显著减轻。结果支持以下假设,即治疗肌筋膜疼痛患者时,预制矫治器的疗效与稳定器相似,具有长期疗效。