Physical Medicine and Rehabilitation, Fatih Sultan Mehmet Training and Research Hospital, Istanbul, Turkey.
Istsanbul Haydarpasa Numune Training and Research Hospital, Istanbul, Turkey.
Somatosens Mot Res. 2021 Dec;38(4):327-332. doi: 10.1080/08990220.2021.1977265. Epub 2021 Sep 20.
Myofascial pain syndrome (MPS) is a common problem in the general population. MPS should not be a local/peripheral painful syndrome and considered to be a syndrome of central sensitivity. We aimed to investigate the effect of pregabalin in patients with MPS in this study.
We randomized 40 patients into two groups, and 17 patients per group completed the study. Female patients in group I received pregabalin and exercise therapy, whereas those in group II received exercise therapy alone. All patients were evaluated as follows: for pain by visual analog scale (VAS); trigger-point pressure pain threshold-(PPT) by algometry; neuropathic pain using the Douleur Neuropathique en 4 Questions (DN4) and quality of life with the Short Form-36 (SF36). Evaluations were performed pre-treatment and at the end of the first and third months of treatment. Clinical trial ID: NCT04600037, retrospectively registered 20/10/2020.
In group I, significant improvements were observed in VAS, trigger-point-PPT, physical component summary-SF-36, at the first and third months. In group II, statistically significant improvements were observed in VAS, trigger-point-PPT after the first and third months. Group I showed statistically better improvements in VAS, trigger points-PPT, physical component summary-SF36 compared with group II by the third month.
Pregabalin treatment is effective for controlling trigger points. Pregabalin treatment is also more effective than exercise treatment at improving quality of life in patients with MPS.
肌筋膜疼痛综合征(MPS)是一种常见的人群疾病。MPS 不应是局部/外周性疼痛综合征,而应被认为是一种中枢敏化综合征。在本研究中,我们旨在研究普瑞巴林对 MPS 患者的疗效。
我们将 40 名患者随机分为两组,每组 17 名患者完成了研究。组 I 的女性患者接受普瑞巴林和运动疗法,而组 II 的患者仅接受运动疗法。所有患者均接受以下评估:疼痛采用视觉模拟评分(VAS);触痛点压痛阈值(PPT)采用压力测定法;神经病理性疼痛采用 4 个问题的神经病理性疼痛问卷(DN4),生活质量采用 36 项简短健康调查问卷(SF36)。评估在治疗前、治疗第 1 个月和第 3 个月进行。临床试验 ID:NCT04600037,2020 年 10 月 20 日回溯注册。
在组 I 中,VAS、触痛点 PPT、SF-36 生理成分总分在第 1 个月和第 3 个月均有显著改善。在组 II 中,VAS 和触痛点 PPT 在第 1 个月和第 3 个月均有统计学显著改善。在第 3 个月,组 I 在 VAS、触痛点 PPT、SF36 生理成分总分方面的改善明显优于组 II。
普瑞巴林治疗对控制触发点有效。普瑞巴林治疗在改善 MPS 患者的生活质量方面比运动治疗更有效。