Artigo Acesso aberto Produção Nacional Revisado por pares

Treatment of Bipolar Depression with Deep TMS: Results from a Double-Blind, Randomized, Parallel Group, Sham-Controlled Clinical Trial

2017; Springer Nature; Volume: 42; Issue: 13 Linguagem: Inglês

10.1038/npp.2017.26

ISSN

1740-634X

Autores

Diego Freitas Tavares, Martin Luiz Myczkowski, Rodrigo Lancelote Alberto, Leandro Valiengo, Rosa M. Rı́os, Pedro Caldana Gordon, Bernardo Sampaio-Júnior, Izio Klein, Carlos Gustavo Mansur, Marco Antônio Marcolin, Beny Lafer, Ricardo Alberto Moreno, Wagner F. Gattaz, Zafiris J. Daskalakis, André R. Brunoni,

Tópico(s)

Electroconvulsive Therapy Studies

Resumo

Bipolar depression (BD) is a highly prevalent condition with limited therapeutic options. Deep (H1-coil) transcranial magnetic stimulation (dTMS) is a novel TMS modality with established efficacy for unipolar depression. We conducted a randomized sham-controlled trial to evaluate the efficacy and safety of dTMS in treatment-resistant BD patients. Patients received 20 sessions of active or sham dTMS over the left dorsolateral prefrontal cortex (H1-coil, 55 18 Hz 2 s 120% MT trains). The primary outcome was changes in the 17-item Hamilton Depression Rating Scale (HDRS-17) from baseline to endpoint (week 4). Secondary outcomes were changes from baseline to the end of the follow-up phase (week 8), and response and remission rates. Safety was assessed using a dTMS adverse effects questionnaire and the Young Mania Rating Scale to assess treatment-emergent mania switch (TEMS). Out of 50 patients, 43 finished the trial. There were 2 and 5 dropouts in the sham and active groups, respectively. Active dTMS was superior to sham at end point (difference favoring dTMS=4.88; 95% CI 0.43 to 9.32, p=0.03) but not at follow-up. There was also a trend for greater response rates in the active (48%) vs sham (24%) groups (OR=2.92; 95% CI=0.87 to 9.78, p=0.08). Remission rates were not statistically different. No TEMS episodes were observed. Deep TMS is a potentially effective and well-tolerated add-on therapy in resistant bipolar depressed patients receiving adequate pharmacotherapy.

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