Currently submitted to: JMIR Preprints
Date Submitted: May 2, 2023
Open Peer Review Period: May 2, 2023 - Apr 16, 2024
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Pharmacotherapies for acute mania in adults: a systematic review and network meta-analysis of randomized controlled trials (AM-SRNMA 001)
ABSTRACT
Background:
Acute manía is a serious psychiatric disorder, and there is currently a lack of comparisons for drug treatment options, including monotherapies and adjuvant therapies, for adults with acute manía.
Objective:
The aim of this study was to provide evidence-based recommendations regarding the efficacy, safety, and tolerability of currently used pharmacological treatments for adults with acute bipolar mania.
Methods:
To achieve this, we conducted a systematic review and network meta-analysis (NMA) using R software and related packages. We searched primary clinical databases until February 2023 for reports of randomized controlled trials of drug treatments and adjunctive therapies for adults with acute bipolar mania, with outcomes including efficacy (mean change from baseline to endpoint in mania rating scores), safety (clinically significant adverse events from baseline to end of treatment), and tolerability (the proportion of patients who completed the whole trial to the planned endpoint).
Results:
A total of 113 studies were included in our analysis, in which 23,491 participants (50.38% males; mean age = 38.6 years; mean study duration = 3.39 weeks; mean manic baseline score = 29.37) were randomly allocated to one of 51 monotherapies, adjunctive treatments, or placebo. Our results showed that tamoxifen (mean difference, -22.31 [-25.97, -18.63]) and tamoxifen+ lithium or valproate (LIT/VAL) (-16.37 [-22.55, -10.25]) had the best and second-best clinical efficacy in adults with acute bipolar mania over the placebo. Furthermore, olanzapine, paliperidone, quetiapine, ziprasidone, risperidone, divalproex, and haloperidol were significantly better tolerated than placebo. Combination therapies of antipsychotics and LIT/VAL appeared to be more effective than their corresponding monotherapies. While pharmacotherapies were associated with specific common adverse events, we found no evidence of increased incidence of headache or depression events compared to the placebo.
Conclusions:
Overall, our NMAs provided important insights into the effectiveness, safety, and tolerability of pharmacological treatments for acute bipolar mania and can help guide treatment decisions for clinicians. Clinical Trial: CRD42023387438
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