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Add-on rTMS for the acute treatment of depressive symptoms is probably more effective in adolescents than in adults: Evidence from real-world clinical practice

耐受性 哈姆德 焦虑 磁刺激 汉密尔顿焦虑量表 萧条(经济学) 评定量表 心情 心理学 随机对照试验 临床试验 医学 精神科 临床心理学 内科学 不利影响 刺激 经济 宏观经济学 发展心理学
作者
Tianhong Zhang,Jun‐Juan Zhu,Lihua Xu,XiaoChen Tang,HuiRu Cui,YanYan Wei,Yan Wang,Qiang Hu,Zhenying Qian,Xiaohua Liu,Yingying Tang,Chunbo Li,Jijun Wang
出处
期刊:Brain Stimulation [Elsevier]
卷期号:12 (1): 103-109 被引量:44
标识
DOI:10.1016/j.brs.2018.09.007
摘要

Background Repetitive transcranial magnetic stimulation (rTMS) is considered as an effective treatment for adults with major depressive disorder. However, it remains unknown whether rTMS has comparable or better efficacy in adolescents. Objective The current naturalistic study aimed to investigate the efficacy and clinical outcome of add-on rTMS in a large sample of adolescent patients compared to adult patients. Methods This study included 117 patients (42 adolescents vs. 75 adults) with mood or anxiety disorders who were treated with at least 10 sessions of rTMS. rTMS was applied over the left dorsolateral prefrontal cortex (10 Hz). Symptoms of depression and anxiety were measured using the Hamilton Rating Scale for Depression (HAMD) and the Hamilton Rating Scale for Anxiety (HAMA) respectively, at baseline and after 2 and 4 weeks of follow-up. Comparisons of clinical improvement and rates of response/remission were made across age groups. Major findings and conclusions All the age groups showed significant improvements in clinical symptoms. No safety or tolerability concerns were identified. Symptomatic improvements and response/remission rates were more significant in adolescent patients than in adults. Decrease in HAMD and HAMA scores after 2 weeks and 4 weeks of rTMS treatment were positively correlated in adolescents, but not in adults. General linear model repeated measures demonstrated significant effect of time × age group interaction on the HAMD score, in response to 10 sessions of rTMS. Add-on rTMS is feasible, tolerable, effective and more applicable to adolescents with mood or anxiety disorders. However, double-blinded and sham-controlled trials are needed for validating this conclusion.
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