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吲哚洛尔辅助治疗难治性强迫症:一项双盲安慰剂对照试验。

Pindolol augmentation in treatment-resistant obsessive compulsive disorder: a double-blind placebo controlled trial.

作者信息

Dannon P N, Sasson Y, Hirschmann S, Iancu I, Grunhaus L J, Zohar J

机构信息

Psychiatry Department, Chaim Sheba Medical Center, Tel Hashomer, Israel.

出版信息

Eur Neuropsychopharmacol. 2000 May;10(3):165-9. doi: 10.1016/s0924-977x(00)00065-1.

DOI:10.1016/s0924-977x(00)00065-1
PMID:10793318
Abstract

OBJECTIVE

To evaluate the efficacy of pindolol augmentation in treatment-resistant obsessive compulsive disorder (OCD) patients who were unsuccessfully treated with serotonin reuptake inhibitors.

METHOD

Fourteen treatment-resistant OCD patients were treated with paroxetine for 17.4+/-2.1 weeks up to 60 mg/d after they failed at least two other serotonin reuptake inhibitor trials. The patients, who did not respond to open-label paroxetine treatment, were assigned to a double-blind, placebo-controlled pindolol (2.5 mgx3/d) augmentation. All the subjects were evaluated biweekly for a six-week period with the Yale-Brown Obsessive Compulsive Scale (Y-BOCS), Hamilton Anxiety Scale (HAM-Anx), and Montgomery Asberg Depression Rating Scale (MADRS). Data was analyzed by paired t-test, and ANOVA with repeated measures.

RESULTS

Pindolol augmentation to paroxetine (n=8) as compared to placebo augmentation (n=6), was associated with a significant (P<0.01) improvement in Y-BOCS as measured by paired t-test after the fourth week of the treatment and by ANOVA with repeated measures (df: 4.9, f: 3,3, P<0.006). Although no significant differences were found between placebo and pindolol groups on HAM-Anx and MADRS, a trend for improvement in the pindolol group was noted.

CONCLUSIONS

The results of our study demonstrated that pindolol may augment the therapeutic effect of paroxetine in treatment-resistant OCD patients.

摘要

目的

评估吲哚洛尔增效治疗对经5-羟色胺再摄取抑制剂治疗无效的难治性强迫症(OCD)患者的疗效。

方法

14名难治性OCD患者在至少两次其他5-羟色胺再摄取抑制剂试验失败后,接受帕罗西汀治疗17.4±2.1周,剂量高达60mg/d。对开放标签帕罗西汀治疗无反应的患者,被分配到双盲、安慰剂对照的吲哚洛尔(2.5mg×3/d)增效治疗组。所有受试者每两周接受一次评估,为期六周,使用耶鲁-布朗强迫症量表(Y-BOCS)、汉密尔顿焦虑量表(HAM-Anx)和蒙哥马利-阿斯伯格抑郁评定量表(MADRS)。数据采用配对t检验和重复测量方差分析进行分析。

结果

与安慰剂增效治疗组(n=6)相比,帕罗西汀联合吲哚洛尔增效治疗组(n=8)在治疗第四周后,通过配对t检验和重复测量方差分析(自由度:4.9,F:3.3,P<0.006)测量,Y-BOCS有显著改善(P<0.01)。虽然在HAM-Anx和MADRS上,安慰剂组和吲哚洛尔组之间未发现显著差异,但吲哚洛尔组有改善趋势。

结论

我们的研究结果表明,吲哚洛尔可能增强帕罗西汀对难治性OCD患者的治疗效果。

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