Dementia & Neuropsychologia (Sep 2022)

Evidence from Cochrane systematic reviews on pharmacological treatment compared to placebo for panic disorder

  • Manuelle Mastrorocco Brand Rosa,
  • Yara Dadalti Fragoso,
  • Ana Carolina Lemes Scaciota,
  • Giuliana Raduan Crizol,
  • Mileny Esbravatti Stephano Colovati,
  • Eduardo Calmon de Moura,
  • Ana Luiza Cabrera Martimbianco

DOI
https://doi.org/10.1590/1980-5764-dn-2022-0022
Journal volume & issue
Vol. 16, no. 4
pp. 411 – 417

Abstract

Read online

ABSTRACT. Panic disorder is an anxiety condition characterized by recurrent and unexpected panic attacks. The comparison between active treatment and placebo is essential to analyze an intervention’s efficacy and safety. It is important to identify and summarize the studies with higher evidence to assist health professionals and public policy managers in clinical decision-making. Objective: The aim of this study was to identify and summarize all Cochrane systematic reviews (SRs) that compared the efficacy and safety of any drug treatment compared to placebo for panic disorder patients. Methods: SRs published in the Cochrane Library were included without date restriction. All outcomes presented were analyzed. The methodological quality of the SRs was evaluated using the AMSTAR-2 tool. Results: We included three Cochrane SRs of high methodological quality on the effects of antidepressants, benzodiazepines, and azapirones for panic disorder. All medications showed benefits in response to treatment, symptom improvement, and reduced panic attacks. Dropouts were lower with tricyclic antidepressants and benzodiazepines and higher with azapirones. The occurrence of adverse events was higher for drug groups. Conclusions: Very low to moderate certainty evidence (GRADE) showed that antidepressants and benzodiazepines seem to improve clinical symptoms in individuals with short-term panic disorder compared to placebo. In addition, the use of azapirones seems to have greater adherence by patients than placebo. However, there is insufficient evidence to support its clinical efficacy.

Keywords