NEW TREATMENTS FOR PANIC

Authors
Citation
Jc. Ballenger, NEW TREATMENTS FOR PANIC, European psychiatry, 13, 1998, pp. 75-81
Citations number
12
Categorie Soggetti
Psychiatry
Journal title
ISSN journal
09249338
Volume
13
Year of publication
1998
Supplement
2
Pages
75 - 81
Database
ISI
SICI code
0924-9338(1998)13:<75:>2.0.ZU;2-U
Abstract
Panic disorder is a chronic condition for many patients and can be soc ially, emotionally and occupationally disabling. Until recently, clomi pramine and alprazolam were the only drugs approved for its treatment. While widely used in the US and Europe, both belong to drug classes ( tricyclics and benzodiazepines) with well-recognised side effects that can be problematic and thus limit their use. Recently, paroxetine bec ame the first selective serotonin reuptake inhibitor to receive approv al and licensing for panic disorder. The short- and long-term efficacy and tolerability of paroxetine in panic disorder has been established in clinical trials of almost 1,000 patients meeting Diagnostic and St atistical Manual (DSM)-IIIR criteria for panic disorder, with or witho ut agoraphobia. In a 12-week double-blind study of 120 panic patients receiving standardised cognitive therapy, paroxetine was significantly more effective than placebo in reducing panic attack frequency. In a 1 a-week placebo-controlled comparison in 367 panic patients, paroxeti ne was at least as effective as clomipramine and better tolerated. The re was also some evidence that paroxetine had an earlier onset of acti on than clomipramine. A 9-month extension of the placebo-controlled co mparison with clomipramine showed that the efficacy of paroxetine and clomipramine is maintained when treatment is continued into the longer term. In a relapse prevention study, 105 responders to 3 months' trea tment with paroxetine or placebo were re-randomised, either to continu e existing treatment or to receive placebo for 3 months. Only 5% of pa tients who continued to take paroxetine experienced a relapse compared with 30% of those who switched to placebo (P = 0.002). Paroxetine was generally well tolerated. In the short-term trials, the frequency of withdrawals due to adverse events (7.3%) was lower than that for place bo (11.4%) or clomipramine (14.9%). In the longer term, the dropout ra te due to adverse events increased in the clomipramine group (19.0%) b ut was unchanged in the paroxetine group (7.4%). Since most patients w ith panic disorder will require prolonged treatment, the long-term tol erability of paroxetine and its lack of potential for dependence are i mportant advantages that will encourage good compliance with treatment and improve the quality of life of patients. (C) 1998, Elsevier, Pari s.