Psychopharmacotherapy of panic disorder: 8-week randomized trial with clonazepam and paroxetine
The objective of the present randomized, open-label, naturalistic 8-week study was to compare the efficacy and safety of treatment with clonazepam (N = 63) and paroxetine (N = 57) in patients with panic disorder with or without agoraphobia. Efficacy assessment included number of panic attacks and cl...
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doaj-d41503778dab4295b4457c91d37f8d912020-11-24T23:51:12ZengAssociação Brasileira de Divulgação CientíficaBrazilian Journal of Medical and Biological Research1414-431X2011-04-01444366373S0100-879X2011000400015Psychopharmacotherapy of panic disorder: 8-week randomized trial with clonazepam and paroxetineA.E. Nardi0A.M. Valença1R.C. Freire2M.D. Mochcovitch3R. Amrein4A. Sardinha5M.N. Levitan6I. Nascimento7V.L. de-Melo-Neto8A.L. King9A.C. de O. e Silva10A.B. Veras11G.P. Dias12G.L. Soares-Filho13R.T. da Costa14M.A. Mezzasalma15M.R. de Carvalho16A.C. de Cerqueira17J.E. Hallak18J.A. Crippa19M. Versiani20Universidade Federal do Rio de JaneiroUniversidade Federal do Rio de JaneiroUniversidade Federal do Rio de JaneiroUniversidade Federal do Rio de JaneiroUniversidade Federal do Rio de JaneiroUniversidade Federal do Rio de JaneiroUniversidade Federal do Rio de JaneiroUniversidade Federal do Rio de JaneiroUniversidade Federal do Rio de JaneiroUniversidade Federal do Rio de JaneiroUniversidade Federal do Rio de JaneiroUniversidade Federal do Rio de JaneiroUniversidade Federal do Rio de JaneiroUniversidade Federal do Rio de JaneiroUniversidade Federal do Rio de JaneiroUniversidade Federal do Rio de JaneiroUniversidade Federal do Rio de JaneiroUniversidade Federal do Rio de JaneiroUniversidade de São PauloUniversidade de São PauloUniversidade Federal do Rio de JaneiroThe objective of the present randomized, open-label, naturalistic 8-week study was to compare the efficacy and safety of treatment with clonazepam (N = 63) and paroxetine (N = 57) in patients with panic disorder with or without agoraphobia. Efficacy assessment included number of panic attacks and clinician ratings of the global severity of panic disorders with the clinical global impression (CGI) improvement (CGI-I) and CGI severity (CGI-S) scales. Most patients were females (69.8 and 68.4% in the clonazepam and paroxetine groups, respectively) and age (mean ± SD) was 35.9 ± 9.6 years for the clonazepam group and 33.7 ± 8.8 years for the paroxetine group. Treatment with clonazepam versus paroxetine resulted in fewer weekly panic attacks at week 4 (0.1 vs 0.5, respectively; P < 0.01), and greater clinical improvements at week 8 (CGI-I: 1.6 vs 2.9; P = 0.04). Anxiety severity was significantly reduced with clonazepam versus paroxetine at weeks 1 and 2, with no difference in panic disorder severity. Patients treated with clonazepam had fewer adverse events than patients treated with paroxetine (73 vs 95%; P = 0.001). The most common adverse events were drowsiness/fatigue (57%), memory/concentration difficulties (24%), and sexual dysfunction (11%) in the clonazepam group and drowsiness/fatigue (81%), sexual dysfunction (70%), and nausea/vomiting (61%) in the paroxetine group. This naturalistic study confirms the efficacy and tolerability of clonazepam and paroxetine in the acute treatment of patients with panic disorder.http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X2011000400015&lng=en&tlng=enParoxetineClonazepamPanic disorderEfficacySafety |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
A.E. Nardi A.M. Valença R.C. Freire M.D. Mochcovitch R. Amrein A. Sardinha M.N. Levitan I. Nascimento V.L. de-Melo-Neto A.L. King A.C. de O. e Silva A.B. Veras G.P. Dias G.L. Soares-Filho R.T. da Costa M.A. Mezzasalma M.R. de Carvalho A.C. de Cerqueira J.E. Hallak J.A. Crippa M. Versiani |
spellingShingle |
A.E. Nardi A.M. Valença R.C. Freire M.D. Mochcovitch R. Amrein A. Sardinha M.N. Levitan I. Nascimento V.L. de-Melo-Neto A.L. King A.C. de O. e Silva A.B. Veras G.P. Dias G.L. Soares-Filho R.T. da Costa M.A. Mezzasalma M.R. de Carvalho A.C. de Cerqueira J.E. Hallak J.A. Crippa M. Versiani Psychopharmacotherapy of panic disorder: 8-week randomized trial with clonazepam and paroxetine Brazilian Journal of Medical and Biological Research Paroxetine Clonazepam Panic disorder Efficacy Safety |
author_facet |
A.E. Nardi A.M. Valença R.C. Freire M.D. Mochcovitch R. Amrein A. Sardinha M.N. Levitan I. Nascimento V.L. de-Melo-Neto A.L. King A.C. de O. e Silva A.B. Veras G.P. Dias G.L. Soares-Filho R.T. da Costa M.A. Mezzasalma M.R. de Carvalho A.C. de Cerqueira J.E. Hallak J.A. Crippa M. Versiani |
author_sort |
A.E. Nardi |
title |
Psychopharmacotherapy of panic disorder: 8-week randomized trial with clonazepam and paroxetine |
title_short |
Psychopharmacotherapy of panic disorder: 8-week randomized trial with clonazepam and paroxetine |
title_full |
Psychopharmacotherapy of panic disorder: 8-week randomized trial with clonazepam and paroxetine |
title_fullStr |
Psychopharmacotherapy of panic disorder: 8-week randomized trial with clonazepam and paroxetine |
title_full_unstemmed |
Psychopharmacotherapy of panic disorder: 8-week randomized trial with clonazepam and paroxetine |
title_sort |
psychopharmacotherapy of panic disorder: 8-week randomized trial with clonazepam and paroxetine |
publisher |
Associação Brasileira de Divulgação Científica |
series |
Brazilian Journal of Medical and Biological Research |
issn |
1414-431X |
publishDate |
2011-04-01 |
description |
The objective of the present randomized, open-label, naturalistic 8-week study was to compare the efficacy and safety of treatment with clonazepam (N = 63) and paroxetine (N = 57) in patients with panic disorder with or without agoraphobia. Efficacy assessment included number of panic attacks and clinician ratings of the global severity of panic disorders with the clinical global impression (CGI) improvement (CGI-I) and CGI severity (CGI-S) scales. Most patients were females (69.8 and 68.4% in the clonazepam and paroxetine groups, respectively) and age (mean ± SD) was 35.9 ± 9.6 years for the clonazepam group and 33.7 ± 8.8 years for the paroxetine group. Treatment with clonazepam versus paroxetine resulted in fewer weekly panic attacks at week 4 (0.1 vs 0.5, respectively; P < 0.01), and greater clinical improvements at week 8 (CGI-I: 1.6 vs 2.9; P = 0.04). Anxiety severity was significantly reduced with clonazepam versus paroxetine at weeks 1 and 2, with no difference in panic disorder severity. Patients treated with clonazepam had fewer adverse events than patients treated with paroxetine (73 vs 95%; P = 0.001). The most common adverse events were drowsiness/fatigue (57%), memory/concentration difficulties (24%), and sexual dysfunction (11%) in the clonazepam group and drowsiness/fatigue (81%), sexual dysfunction (70%), and nausea/vomiting (61%) in the paroxetine group. This naturalistic study confirms the efficacy and tolerability of clonazepam and paroxetine in the acute treatment of patients with panic disorder. |
topic |
Paroxetine Clonazepam Panic disorder Efficacy Safety |
url |
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X2011000400015&lng=en&tlng=en |
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