Radic Julia A E, Beauprie Ian, Chiasson Paula, Kiss Zelma H T, Brownstone Robert M
1Department of Surgery (Neurosurgery),Dalhousie University,Halifax,Nova Scotia.
2Department of Anaesthesia,Dalhousie University,Halifax,Nova Scotia.
Can J Neurol Sci. 2015 Nov;42(6):401-9. doi: 10.1017/cjn.2015.292. Epub 2015 Sep 1.
Chronic motor cortex stimulation (MCS) has been used to treat medically refractory neuropathic pain over the past 20 years. We investigated this procedure using a prospective multicentre randomized blinded crossover trial.
Twelve subjects with three different neuropathic pain syndromes had placement of MCS systems after which they were randomized to receive low ("subtherapeutic") or high ("therapeutic") stimulation for 12 weeks, followed by a crossover to the other treatment group for 12 weeks. The primary outcome measure was the pain visual analogue scale (VAS). Secondary outcome measures included McGill Pain Questionnaire (MPQ), Beck Depression Inventory-II, medication log, work status, global impression of change, and SF-36 quality of life scale.
The trial was halted early due to lack of efficacy. One subject withdrew early due to protocol violation and five subjects withdrew early due to transient adverse events. Six subjects with upper extremity pain completed the study. There was no significant change in VAS with low or high stimulation and no significant improvement in any of the outcome measures from low to high stimulation. SF-36 role physical and mental health scores were worse with high compared to low stimulation (p=0.024, p=0.005).
We failed to show that MCS is an effective treatment for refractory upper extremity neuropathic pain and suggest that previous studies may have been skewed by placebo effects, or ours by nocebo. We suggest that a healthy degree of skepticism is warranted when considering this invasive therapy for upper extremity pain syndromes.
在过去20年中,慢性运动皮层刺激(MCS)已被用于治疗药物难治性神经性疼痛。我们通过一项前瞻性多中心随机双盲交叉试验对该治疗方法进行了研究。
12名患有三种不同神经性疼痛综合征的受试者植入了MCS系统,之后他们被随机分为接受低强度(“亚治疗性”)或高强度(“治疗性”)刺激12周,然后交叉至另一治疗组再接受12周刺激。主要结局指标为疼痛视觉模拟量表(VAS)。次要结局指标包括麦吉尔疼痛问卷(MPQ)、贝克抑郁量表第二版、用药记录、工作状态、总体变化印象以及SF-36生活质量量表。
由于缺乏疗效,该试验提前终止。1名受试者因违反方案提前退出,5名受试者因短暂不良事件提前退出。6名上肢疼痛受试者完成了研究。低强度或高强度刺激时VAS均无显著变化,从低强度刺激到高强度刺激,任何结局指标均无显著改善。与低强度刺激相比,高强度刺激时SF-36生理职能和精神健康评分更差(p=0.024,p=0.005)。
我们未能证明MCS是治疗难治性上肢神经性疼痛的有效方法,并表明既往研究可能受到安慰剂效应的影响,而我们的研究可能受到反安慰剂效应的影响。我们建议,在考虑将这种侵入性治疗用于上肢疼痛综合征时,应保持适度的怀疑态度。