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Efficacy and safety of intermittent theta burst stimulation versus high-frequency repetitive transcranial magnetic stimulation for patients with treatment-resistant depression: a systematic review.
Lan, Xian-Jun; Yang, Xin-Hu; Qin, Zhen-Juan; Cai, Dong-Bin; Liu, Qi-Man; Mai, Jian-Xin; Deng, Can-Jin; Huang, Xing-Bing; Zheng, Wei.
Afiliação
  • Lan XJ; The Brain Hospital of Guangxi Zhuang Autonomous Region, Liuzhou, China.
  • Yang XH; The Affiliated Brain Hospital of Guangzhou Medical University, Guangzhou, China.
  • Qin ZJ; The Brain Hospital of Guangxi Zhuang Autonomous Region, Liuzhou, China.
  • Cai DB; Shenzhen Traditional Chinese Medicine Hospital, Shenzhen, China.
  • Liu QM; The Affiliated Brain Hospital of Guangzhou Medical University, Guangzhou, China.
  • Mai JX; The Affiliated Brain Hospital of Guangzhou Medical University, Guangzhou, China.
  • Deng CJ; The Affiliated Brain Hospital of Guangzhou Medical University, Guangzhou, China.
  • Huang XB; The Affiliated Brain Hospital of Guangzhou Medical University, Guangzhou, China.
  • Zheng W; The Affiliated Brain Hospital of Guangzhou Medical University, Guangzhou, China.
Front Psychiatry ; 14: 1244289, 2023.
Article em En | MEDLINE | ID: mdl-37583841
ABSTRACT

Objective:

Intermittent theta-burst stimulation (iTBS), which is a form of repetitive transcranial magnetic stimulation (rTMS), can produce 600 pulses to the left dorsolateral prefrontal cortex (DLPFC) in a stimulation time of just over 3 min. The objective of this systematic review was to compare the safety and efficacy of iTBS and high-frequency (≥ 5 Hz) rTMS (HF-rTMS) for patients with treatment-resistant depression (TRD).

Methods:

Randomized controlled trials (RCTs) comparing the efficacy and safety of iTBS and HF-rTMS were identified by searching English and Chinese databases. The primary outcomes were study-defined response and remission.

Results:

Two RCTs (n = 474) investigating the efficacy and safety of adjunctive iTBS (n = 239) versus HF-rTMS (n = 235) for adult patients with TRD met the inclusion criteria. Among the two included studies (Jadad score = 5), all were classified as high quality. No group differences were found regarding the overall rates of response (iTBS group 48.0% versus HF-rTMS group 45.5%) and remission (iTBS group 30.0% versus HF-rTMS group 25.2%; all Ps > 0.05). The rates of discontinuation and adverse events such as headache were similar between the two groups (all Ps > 0.05).

Conclusion:

The antidepressant effects and safety of iTBS and HF-rTMS appeared to be similar for patients with TRD, although additional RCTs with rigorous methodology are needed.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Clinical_trials / Prognostic_studies / Systematic_reviews Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Clinical_trials / Prognostic_studies / Systematic_reviews Idioma: En Ano de publicação: 2023 Tipo de documento: Article