A controlled, prospective, 1-year trial of citalopram in the treatment of panic disorder

被引:82
作者
Lepola, UM
Wade, AG
Leinonen, EV
Koponen, HJ
Frazer, J
Sjodin, I
Penttinen, JT
Pedersen, T
Lehto, HJ
机构
[1] Psychiat Res Clin Kuopio, FIN-70110 Kuopio, Finland
[2] Univ Helsinki, Helsinki, Finland
[3] Oulu Univ, Oulu, Finland
[4] Clydebank Hlth Ctr, Clydebank, Scotland
[5] Tampere Univ Hosp, Tampere, Finland
[6] Moisio Hosp, Mikkeli, Finland
[7] Frazer Med Res Ltd, Bradford, W Yorkshire, England
[8] Linkoping Univ Hosp, Psychiat Clin, S-58185 Linkoping, Sweden
[9] Psychiat Res Clin Turku, Turku, Finland
[10] H Lundbeck & Co AS, Copenhagen, Denmark
[11] Oy H Lundbeck Ab, Turku, Finland
关键词
D O I
10.4088/JCP.v59n1006
中图分类号
B849 [应用心理学];
学科分类号
040203 ;
摘要
Background: The objective of this study was to evaluate the efficacy and tolerability of citalopram in the long-term treatment of adult outpatients with panic disorder with or without agoraphobia. Method: Patients in this double-blind, parallel-group trial were assigned to 1 of 3 fixed dosage ranges of citalopram (10 or 15 mg/day, 20 or 30 mg/day, or 40 or 60 mg/day), 1 dosage range of clomipramine (60 or 90 mg/day), or placebo. After the completed 8-week acute treatment period, the eligible patients could continue the treatment for up to 1 year. Of the 475 patients who were randomly assigned for the short-term trial, 279 agreed to continue double-blind treatment at their assigned doses. The primary efficacy measure used was the Clinical Anxiety Scale panic attack item, and the response was defined as no panic attacks (score of 0 or 1). The other key measures used were the Physician's Global Improvement Scale, the Patient's Global Improvement Scale, and the Hamilton Rating Scale for Anxiety (HAM-A). Results: In all drug-treated groups, except the group receiving the lowest citalopram dose, the treatment outcome was generally better than with placebo. As determined by a life table analysis of response, the probability of response during the 12 months was significantly greater with all treatment regimens than with placebo (p <.05), with citalopram 20 or 30 mg/day demonstrating the best response. Panic attacks tended to disappear in all patients remaining in the study until the end of follow-up. Analysis of the difference in the number of patients in different treatment groups remaining in the study (perhaps the best measure of long-term efficacy) also demonstrated that the patients treated with citalopram in dosage ranges of 20 or 30 mg/day and 40 or 60 mg/day had better response than placebo-treated patients (p <.0002 and p <.004, respectively). HAM-A and Global Improvement Scale scores also showed that patients treated with active drug showed greater improvement than placebo-treated patients. All treatment groups showed no new or exceptional adverse event clusters. Conclusion: Citalopram in the dosage range of 20 to 60 mg/day is effective, well tolerated, and safe in the long-term treatment of patients who have panic disorder.
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页码:528 / 534
页数:9
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