THE THERAPEUTIC USE OF TRANSCRANIAL MAGNETIC STIMULATION IN MAJOR DEPRESSION

被引:0
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作者
Nemeth, Viola Luca [1 ]
Csifcsak, Gabor [2 ]
Kincses, Zsigmond Tamas [3 ]
Janka, Zoltan [3 ]
Must, Anita [1 ]
机构
[1] Szegedi Tud Egyet, Altalanos Orvostud Kar, Neurol Klin, Tisza Lajos Krt 107-109, H-6725 Szeged, Hungary
[2] Szegedi Tud Egyet, Bolcseszettud Kar, Pszichol Int, H-6725 Szeged, Hungary
[3] Szegedi Tud Egyet, Altalanos Orvostud Kar, Pszichiatriai Klin, H-6725 Szeged, Hungary
来源
关键词
major depression; repetitive transcranial magnetic stimulation; treatment outcome; DORSOLATERAL PREFRONTAL CORTEX; INTRINSIC FUNCTIONAL CONNECTIVITY; TREATMENT-RESISTANT DEPRESSION; CEREBRAL-BLOOD-FLOW; HUMAN MOTOR CORTEX; HIGH-FREQUENCY; DOUBLE-BLIND; ELECTROCONVULSIVE-THERAPY; ANTIDEPRESSANT EFFICACY; BRAIN-STIMULATION;
D O I
暂无
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
The antidepressive effect of repetitive transcranial magnetic stimulation (rTMS) has been investigated for almost 20 years now. Several studies have been published aiming to identify the exact and reliable parameters leading to the desired therapeutic effect. However, the related literature shows great variability. The current overview aims to provide a comprehensive overview of factors associated with the therapeutic effect of rTMS in major depression. High frequency stimulation of the left dorsolateral prefrontal cortex (DLPFC) for 3-6 weeks leads to mood improvement comparable to the effect of antidepressive medications in 35-40% of patients. Pharmacotherapy resistant patients treated with rTMS reach remission for 3 months on average. Low frequency stimulation of the right DLPFC appears to be similarly effective, though much less investigated so far. In addition to the exact delineation of the stimulation area, treatment outcome is also related to stimulation intensity as well as the number of sessions and impulses. Considering the safety and tolerability aspects of rTMS, it might be a significant therapeutic support for therapy resistant patients. Above this, patients diagnosed with major depression might benefit from the additional positive influence of rTMS improving the effect of antidepressive medication. Based on converging research evidence, the Food and Drug Administration (FDA) agency approved the use of rTMS as a treatment option for therapy resistant major depression in 2008. So far, in Hungary rTMS is primarily considered as a promising tool in research settings only. Hopefully, patients suffering from major depression will increasingly benefit from the positive therapeutic effect of this intervention.
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页码:89 / 97
页数:9
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