Efficacy and tolerability of paroxetine for the long-term treatment of generalized anxiety disorder

被引:80
作者
Stocchi, F
Nordera, G
Jokinen, RH
Lepola, UM
Hewett, K
Bryson, H
Iyengar, MK
机构
[1] Ist Ric Carattere Sci Neuromed, Neurol Inst, I-86077 Pozzelli, Isernia, Italy
[2] Casa Cura Villa Margherita, Vicenza, Italy
[3] Psychiat Res Clin Turku, Turku, Finland
[4] Oulu Univ, Psychiat Res Clin, Dept Psychiat, Kuopio, Finland
[5] GlaxoSmithKleine Pharmaceut, Harlow, Essex, England
[6] GlaxoSmithKleine Pharmaceut, Upper Providence, PA USA
关键词
D O I
10.4088/JCP.v64n0305
中图分类号
B849 [应用心理学];
学科分类号
040203 ;
摘要
Background: Paroxetine has demonstrated efficacy in depression and anxiety disorders, including generalized anxiety disorder (GAD). This 32-week study evaluated the maintained efficacy and safety of paroxetine in GAD by assessing the potential for relapse after discontinuation of medication. Method: Adults (N = 652) with DSM-IV GAD and a Clinical Global Impressions-Severity of Illness (CGI-S) score greater than or equal to 4 received paroxetine (20-50 mg/day) for 8 weeks. Patients whose CGI-S score had decreased by at least 2 points to greater than or equal to 3 at week 8 were randomly assigned to double-blind treatment with paroxetine (N = 278) or placebo (N = 288) for a further 24 weeks. The primary efficacy parameter was the proportion of patients relapsing (an increase in CGI-S score of at least 2 points to a score greater than or equal to 4 or withdrawal resulting from lack of efficacy) during double-blind treatment. Results: Significantly fewer paroxetine than placebo patients relapsed during the 24-week double-blind phase (10.9% vs. 39.9%; p < .001). Placebo patients were almost 5 times more likely to relapse than paroxetine patients (estimated hazard ratio = 0.213 [95% CI = 0.1 to 0.3]; p < .001). Statistical significance in favor of paroxetine was demonstrated for all secondary efficacy parameters, including functional status. Twice as many paroxetine patients as placebo patients (73%) achieved remission. Paroxetine was well tolerated, with no unexpected adverse events reported. Conclusion: Paroxetine was found to be effective and well tolerated for both the short- and long-term treatment of DSM-IV GAD. Continued treatment with paroxetine significantly reduced the potential for relapse of GAD symptoms.
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收藏
页码:250 / 258
页数:9
相关论文
共 37 条
  • [1] Venlafaxine extended release (ER) in the treatment of generalised anxiety disorder - Twenty-four-week placebo-controlled dose-ranging study
    Allgulander, C
    Hackett, D
    Salinas, E
    [J]. BRITISH JOURNAL OF PSYCHIATRY, 2001, 179 : 15 - 22
  • [2] Ballenger JC, 1999, J CLIN PSYCHIAT, V60, P29
  • [3] BELLEW KM, 2000, 153 ANN M AM PSYCH A, P124
  • [4] CLAGHORN JL, 1993, J CLIN PSYCHOPHARM, V13, pS23
  • [5] Efficacy, safety, and tolerability of venlafaxine extended release and buspirone in outpatients with generalized anxiety disorder
    Davidson, JRT
    DuPont, RL
    Hedges, D
    Haskins, JT
    [J]. JOURNAL OF CLINICAL PSYCHIATRY, 1999, 60 (08) : 528 - 535
  • [6] DUNBAR G, 1995, EUR NEUROPSYCHOPHARM, P372
  • [7] Efficacy of venlafaxine extended-release capsules in nondepressed outpatients with generalized anxiety disorder - A 6-month randomized controlled trial
    Gelenberg, AJ
    Lydiard, RB
    Rudolph, RL
    Aguiar, L
    Haskins, JT
    Salinas, E
    [J]. JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2000, 283 (23): : 3082 - 3088
  • [8] Guy W., 1976, ECDEU ASSESSMENT MAN, P217, DOI DOI 10.1016/J.BIOPHA.2016.11.034
  • [9] HAIR T, 2000, INT J NEUROPSYCHOPH, V3, pS227
  • [10] Hamilton M, 1976, ECDEU ASSESSMENT MAN, P193