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Long-Term Treatment of Bipolar Disorder with Valproate: Updated Systematic Review and Meta-analyses.
Yee, Caitlin S; Vázquez, Gustavo H; Hawken, Emily R; Biorac, Aleksandar; Tondo, Leonardo; Baldessarini, Ross J.
Afiliação
  • Yee CS; From the Department of Psychiatry (Drs. Yee, Vázquez, and Hawken) and Centre for Neuroscience Studies (Drs. Vázquez and Biorac), Queen's University School of Medicine, Kingston, Ontario; International Consortium for Mood & Psychotic Disorder Research, McLean Hospital, Belmont, MA (Drs. Vázquez, Tondo, and Baldessarini); Harvard Medical School (Drs. Tondo and Baldessarini); Lucio Bini Mood Disorder Centers, Cagliari and Rome (Dr. Tondo).
Harv Rev Psychiatry ; 29(3): 188-195, 2021.
Article em En | MEDLINE | ID: mdl-33795581
ABSTRACT
LEARNING

OBJECTIVE:

After participating in this activity, learners should be better able to• Evaluate the evidence regarding the effectiveness of long-term treatment of bipolar disorder with valproate.

BACKGROUND:

Prophylactic treatment is critical for bipolar disorder (BD) patients. Valproate is commonly used for this purpose but lacks regulatory approval and carries appreciable risks.

METHODS:

Systematic literature searching through June 2020 sought prospective trials lasting ≥12 months with adults diagnosed with BD to support comparisons of risk of new illness episodes with valproate versus placebo or other agents.

RESULTS:

Included were 13 reports involving 9240 subjects treated for an average of 29.1 months (range, 12-124) in 21 trials 9 were blinded, randomized trials (RCTs) of valproate versus placebo (n = 3), lithium (5), or olanzapine (1); 2 were unblinded RCTs versus lithium (1) or quetiapine (1); and 10 were open-label trials versus lithium (5), quetiapine (2), carbamazepine (1), lamotrigine (1), or olanzapine (1). Random-effects meta-analysis found valproate superior to placebo in 3 trials (odds ratio [OR] = 0.42 [95% confidence level (CI), 0.30-0.60]; p < .0001). In 11 trials, protective effects with valproate and lithium were similar (OR = 1.20 [CI, 0.81-1.79]; p = .36), as well in 5 comparisons versus antipsychotics quetiapine and olanzapine (OR = 0.96 [CI, 0.66-1.40]; p = .84), and 2 versus other mood-stabilizing anticonvulsants (carbamazepine and lamotrigine) (OR = 1.30 [CI, 0.75-2.26]; p = .34). Valproate was nonsignificantly more effective versus new mania than depression (χ2 = 3.03; p = .08).

CONCLUSIONS:

Valproate was more effective than placebo in preventing new BD episodes of mania or depression, and not significantly different from lithium, second-generation antipsychotics, or other anticonvulsants. Overall benefits were nonsignificantly greater versus mania than bipolar depression.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Antipsicóticos / Transtorno Bipolar Tipo de estudo: Clinical_trials / Systematic_reviews Limite: Adult / Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Antipsicóticos / Transtorno Bipolar Tipo de estudo: Clinical_trials / Systematic_reviews Limite: Adult / Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article