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帕罗西汀治疗惊恐障碍的双盲、固定剂量、安慰剂对照研究。

Double-blind, fixed-dose, placebo-controlled study of paroxetine in the treatment of panic disorder.

作者信息

Ballenger J C, Wheadon D E, Steiner M, Bushnell W, Gergel I P

机构信息

Paroxetine Panic Disorder Study Group, SmithKline Beecham Pharmaceuticals, Collegeville, Pa., USA.

出版信息

Am J Psychiatry. 1998 Jan;155(1):36-42. doi: 10.1176/ajp.155.1.36.

DOI:10.1176/ajp.155.1.36
PMID:9433336
Abstract

OBJECTIVE

This study was designed to determine the minimum paroxetine dose effective for treating panic disorder.

METHOD

Of 425 patients with DSM-III-R panic disorder with or without agoraphobia who underwent a 2-week drug-free screening period, 278 patients were randomly assigned to double-blind treatment with a 10-week course of placebo or paroxetine at a dose of 10, 20, or 40 mg/day.

RESULTS

At 40 mg/day, paroxetine was superior to placebo across the majority of outcome measures. Despite a mean of 9.5 to 11.6 full panic attacks during the screening period, 86.0% of the patients taking 40 mg of paroxetine, 65.2% of those taking 20 mg, 67.4% of those taking 10 mg, and 50.0% of the placebo-treated patients were free of full panic attacks during the 2 weeks ending at week 10. The 40-mg paroxetine group experienced significantly greater global improvement than the placebo group and significantly greater improvement in frequency of full and limited-symptom panic attacks, intensity of full panic attacks, phobic fear, anxiety, and depressive symptoms, usually evident by week 4. All doses of paroxetine were well tolerated, and adverse effects were consistent with those associated with selective serotonin reuptake inhibitors.

CONCLUSIONS

Paroxetine is an effective and well-tolerated short-term treatment of panic disorder. The minimum dose demonstrated to be significantly superior to placebo was 40 mg/day, although some patients did respond at lower doses.

摘要

目的

本研究旨在确定治疗惊恐障碍的帕罗西汀最小有效剂量。

方法

425例患有DSM-III-R惊恐障碍伴或不伴广场恐惧症的患者,经过2周的停药筛查期后,278例患者被随机分配接受为期10周的双盲治疗,分别服用安慰剂或剂量为10、20或40mg/天的帕罗西汀。

结果

在40mg/天的剂量下,帕罗西汀在大多数疗效指标上均优于安慰剂。尽管在筛查期平均有9.5至11.6次完全惊恐发作,但在第10周结束的2周内,服用40mg帕罗西汀的患者中有86.0%、服用20mg的患者中有65.2%、服用10mg的患者中有67.4%以及接受安慰剂治疗的患者中有50.0%无完全惊恐发作。40mg帕罗西汀组在总体改善方面显著优于安慰剂组,在完全和有限症状惊恐发作的频率、完全惊恐发作的强度、恐惧、焦虑和抑郁症状方面的改善也显著更大,通常在第4周时就很明显。所有剂量的帕罗西汀耐受性良好,不良反应与选择性5-羟色胺再摄取抑制剂相关的不良反应一致。

结论

帕罗西汀是治疗惊恐障碍的一种有效且耐受性良好的短期治疗药物。尽管有些患者在较低剂量下也有反应,但证明显著优于安慰剂的最小剂量为40mg/天。

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