Research Service, Michael E. DeBakey Veterans Affairs Medical Center, Houston, TX 77030, USA.
Parkinsons Dis. 2010 May 5;2010:569154. doi: 10.4061/2010/569154.
Objectives. To assess the feasibility of treating musculoskeletal pain in the lower back and/or lower extremities in persons with Parkinson's disease (PD) with cranial electrotherapy stimulation (CES). Design. Randomized, controlled, double-blind trial. Setting. Veterans Affairs Medical Center, Community. Participants. Nineteen persons with PD and pain in the lower back and/or lower extremities. Thirteen provided daily pain rating data. Intervention. Of the thirteen participants who provided daily pain data, 6 were randomly provided with active CES devices and 7 with sham devices to use at home 40 minutes per day for six weeks. They recorded their pain ratings on a 0-to-10 scale immediately before and after each session. Main Outcome Measure. Average daily change in pain intensity. Results. Persons receiving active CES had, on average, a 1.14-point decrease in pain compared with a 0.23-point decrease for those receiving sham CES (Wilcoxon Z = -2.20, P = .028). Conclusion. Use of CES at home by persons with PD is feasible and may be somewhat helpful in decreasing pain. A larger study is needed to determine the characteristics of persons who may experience meaningful pain reduction with CES. Guidelines for future studies are provided.
目的。评估经颅微电流刺激(CES)治疗帕金森病(PD)患者下背部和/或下肢骨骼肌肉疼痛的可行性。
设计。随机、对照、双盲试验。
地点。退伍军人事务医疗中心,社区。
参与者。19 名 PD 患者,下背部和/或下肢疼痛。13 名参与者提供每日疼痛评分数据。
干预措施。在提供每日疼痛数据的 13 名参与者中,随机为 6 名参与者提供了有效的 CES 设备,为 7 名参与者提供了假设备,供他们在家中每天使用 40 分钟,为期六周。他们在每次治疗前后立即用 0 到 10 的量表记录疼痛评分。
主要结果测量。疼痛强度的平均每日变化。
结果。与接受假 CES 的参与者相比,接受 CES 治疗的参与者的疼痛平均降低了 1.14 分,而接受假 CES 的参与者的疼痛平均降低了 0.23 分(Wilcoxon Z = -2.20,P =.028)。
结论。PD 患者在家中使用 CES 是可行的,并且可能在一定程度上有助于减轻疼痛。需要更大的研究来确定哪些人可能会从 CES 中获得有意义的疼痛缓解。为未来的研究提供了指南。