电休克疗法
磁刺激
难治性抑郁症
医学
萧条(经济学)
随机对照试验
重性抑郁障碍
心理学
麻醉
认知
刺激
精神科
内科学
宏观经济学
经济
作者
Maud Rothärmel,Pierre Quesada,Thomas Husson,Ghina Harika‐Germaneau,Clément Nathou,Julien Guehl,Marine Dalmont,Gaëlle Opolczynski,Iris Miréa-Grivel,Bruno Millet,Emmanuel Gérardin,Vincent Compère,Sonia Dollfus,Némat Jaafari,Jacques Bénichou,Caroline Thill,Olivier Guillin,Virginie Moulier
标识
DOI:10.1017/s0033291721003810
摘要
Abstract Background Electroconvulsive therapy (ECT) is one of the most effective treatments for treatment-resistant depression (TRD). However, due to response delay and cognitive impairment, ECT remains an imperfect treatment. Compared to ECT, repetitive transcranial magnetic stimulation (rTMS) is less effective at treating severe depression, but has the advantage of being quick, easy to use, and producing almost no side effects. In this study, our objective was to assess the priming effect of rTMS sessions before ECT on clinical response in patients with TRD. Methods In this multicenter, randomized, double-blind, sham-controlled trial, 56 patients with TRD were assigned to active or sham rTMS before ECT treatment. Five sessions of active/sham neuronavigated rTMS were administered over the left dorsolateral prefrontal cortex (20 Hz, 90% resting motor threshold, 20 2 s trains with 60-s intervals, 800 pulses/session) before ECT (which was active for all patients) started. Any relative improvements were then compared between both groups after five ECT sessions, in order to assess the early response to treatment. Results After ECT, the active rTMS group exhibited a significantly greater relative improvement than the sham group [43.4% (28.6%) v. 25.4% (17.2%)]. The responder rate in the active group was at least three times higher. Cognitive complaints, which were assessed using the Cognitive Failures Questionnaire, were higher in the sham rTMS group compared to the active rTMS group, but this difference was not corroborated by cognitive tests. Conclusions rTMS could be used to enhance the efficacy of ECT in patients with TRD. ClinicalTrials.gov: NCT02830399.
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