1 Hz rTMS of the right orbitofrontal cortex for major depression: Safety, tolerability and clinical outcomes

耐受性 眶额皮质 重性抑郁障碍 不利影响 磁刺激 萧条(经济学) 医学 精神科 背外侧前额叶皮质 心理学 听力学 前额叶皮质 内科学 刺激 认知 经济 宏观经济学
作者
Kfir Feffer,Peter Fettes,Peter Giacobbe,Zafiris J. Daskalakis,Daniel M. Blumberger,Jonathan Downar
出处
期刊:European Neuropsychopharmacology [Elsevier]
卷期号:28 (1): 109-117 被引量:75
标识
DOI:10.1016/j.euroneuro.2017.11.011
摘要

Conventional rTMS in major depressive disorder (MDD) targets the dorsolateral prefrontal cortex (DLPFC). However, many patients do not respond to DLPFC-rTMS. Recent evidence suggests that the right lateral orbitofrontal cortex (OFC) plays a key role in ‘non-reward’ functions and shows hyperconnectivity in MDD. OFC-rTMS has been used successfully in obsessive-compulsive disorder, and achieved remission in an MDD case nonresponsive to DLPFC- and DMPFC-rTMS. Here, we assess the safety and tolerability of right OFC-rTMS, and examine the effectiveness of inhibitory right OFC-rTMS in MDD, particularly among patients with previous nonresponse to DMPFC-rTMS. We performed a chart review to retrieve data on clinical characteristics, stimulation parameters, adverse events, and clinical symptom outcomes for a series of 42 patients with medication-resistant and/or DMPFC-rTMS-nonresponsive MDD, who underwent 20–30 sessions of 1 Hz right OFC-rTMS at a single Canadian clinic from 2015 to 2017. Over 882 sessions of treatment, there were no seizures, visual/ocular complications, or other serious or treatment-limiting adverse events. Pain ratings averaged 6–7/10 (10=maximum tolerable); no patient discontinued treatment prematurely due to pain. 15/42 patients (35.7%) achieved response (≥50% symptom reduction) and 10/42 (23.8%) achieved remission. Among the 30/42 patients who were previous nonresponders to DMPFC-rTMS, 9/30 (30.0%) achieved response and 7/30 (23.8%) achieved remission. Response distribution was sharply bimodal. 1 Hz right OFC-rTMS appears safe and tolerable, and may achieve remission in MDD patients even when conventional rTMS has failed. Sham-controlled follow-up studies may be warranted.
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