Posterior-superior insular deep transcranial magnetic stimulation alleviates peripheral neuropathic pain — A pilot double-blind, randomized cross-over study

医学 神经病理性疼痛 磁刺激 麻醉 随机对照试验 止痛药 刺激 不利影响 脑深部刺激 致盲 内科学 帕金森病 疾病
作者
Liu Dongyang,Ana Mércia Fernandes,Pedro Henrique Martins da Cunha,Raissa Tibes,João Ricardo Sato,Clarice Listik,Camila Squarzoni Dale,Gabriel Taricani Kubota,Ricardo Galhardoni,Manoel Jacobsen Teixeira,Valquíria Aparecida da Silva,Jefferson Rosí,Daniel Ciampi de Andrade
出处
期刊:Neurophysiologie Clinique-clinical Neurophysiology [Elsevier]
卷期号:51 (4): 291-302 被引量:37
标识
DOI:10.1016/j.neucli.2021.06.003
摘要

Peripheral neuropathic pain (pNeP) is prevalent, and current treatments, including drugs and motor cortex repetitive transcranial magnetic stimulation (rTMS) leave a substantial proportion of patients with suboptimal pain relief.We explored the intensity and short-term duration of the analgesic effects produced in pNeP patients by 5 days of neuronavigated deep rTMS targeting the posterior superior insula (PSI) with a double-cone coil in a sham-controlled randomized cross-over trial.Thirty-one pNeP patients received induction series of five active or sham consecutive sessions of daily deep-rTMS to the PSI in a randomized sequence, with a washout period of at least 21 days between series. The primary outcome [number of responders (>50% pain intensity reduction from baseline in a numerical rating scale ranging from 0 to 10)] was significantly higher after real (58.1%) compared to sham (19.4%) stimulation (p = 0.002). The number needed to treat was 2.6, and the effect size was 0.97 [95% CI (0.6; 1.3)]. One week after the 5th stimulation day, pain scores were no longer different between groups, and no difference in neuropathic pain characteristics and interference with daily living were present. No major side effects occurred, and milder adverse events (i.e., short-lived headaches after stimulation) were reported in both groups. Blinding was effective, and analgesic effects were not affected by sequence of the stimulation series (active-first or sham-first), age, sex or pain duration of participants.PSI deep-rTMS was safe in refractory pNeP and was able to provide significant pain intensity reduction after a five-day induction series of treatments. Post-hoc assessment of neuronavigation targeting confirmed deep-rTMS was delivered within the boundaries of the PSI in all participants.PSI deep-rTMS provided significant pain relief during 5-day induction sessions compared to sham stimulation.
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