Division of Rheumatology, Department of Internal Medicine, Chonnam National University Medical School and Hospital, 42 Jebong-ro, Dong-gu, Gwangju, 61469, Republic of Korea.
Department of Neurosurgery, Chonnam National University Medical School and Hospital, Gwangju, Republic of Korea.
Sci Rep. 2020 Jul 21;10(1):12114. doi: 10.1038/s41598-020-69131-7.
Despite promising preliminary results of transcranial direct current stimulation (tDCS) treatment in patients with fibromyalgia (FM), several issues need to be addressed, including its limited efficacy, low response rate, and poor tolerability. We investigated the efficacy and safety of tDCS as an add-on treatment for chronic pain in Korean patients with FM. This study enrolled 46 patients who were refractory to pain medications from May 2016 to February 2017. A conventional tDCS device was used to supply 2 mA of current for 20 min on five consecutive days. The primary end-point was a change in visual analogue scale (VAS) pain score at the end of treatment; secondary end-points included changes in Fibromyalgia Impact Questionnaire (FIQ), Brief Pain Inventory (BPI), Brief Fatigue Inventory (BFI), Beck Depression Inventory (BDI), State-Trait Anxiety Inventory (STAI), and Medical Outcomes Study Sleep Scale (MOS-SS) scores. After tDCS, 46 patients showed clinical improvements in VAS pain scores on days 6, 13, and 36 compared with day 0 (p < 0.001). Improvement in FIQ was seen on day 13. The BDI decreased significantly on days 6 and 36, and BFI improved significantly on days 6 and 13. There were no significant improvements in STAI-I, STAI-II, and MOS-SS scores after tDCS. No serious adverse events were observed. Our results suggest that tDCS can result in significant pain relief in FM patients and may be an effective add-on treatment.
尽管经颅直流电刺激(tDCS)治疗纤维肌痛(FM)患者的初步结果令人鼓舞,但仍有几个问题需要解决,包括疗效有限、反应率低和耐受性差。我们研究了 tDCS 作为纤维肌痛韩国患者慢性疼痛附加治疗的疗效和安全性。这项研究纳入了 46 名 2016 年 5 月至 2017 年 2 月期间对疼痛药物无反应的患者。使用常规 tDCS 设备在连续 5 天内每天供应 2 mA 电流 20 分钟。主要终点是治疗结束时视觉模拟量表(VAS)疼痛评分的变化;次要终点包括纤维肌痛影响问卷(FIQ)、简明疼痛量表(BPI)、简明疲劳量表(BFI)、贝克抑郁量表(BDI)、状态-特质焦虑量表(STAI)和医疗结果研究睡眠量表(MOS-SS)评分的变化。在 tDCS 后,46 名患者在第 6、13 和 36 天的 VAS 疼痛评分与第 0 天相比有临床改善(p<0.001)。在第 13 天 FIQ 有所改善。BDI 在第 6 和第 36 天显著下降,BFI 在第 6 和第 13 天显著改善。在 tDCS 后,STAI-I、STAI-II 和 MOS-SS 评分没有显著改善。未观察到严重不良事件。我们的结果表明,tDCS 可使 FM 患者显著缓解疼痛,可能是一种有效的附加治疗方法。