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共病和多种药物治疗对舍曲林在老年抑郁症患者中临床效用的影响:一项开放性多中心研究。

Effects of comorbidity and polypharmacy on the clinical usefulness of sertraline in elderly depressed patients: an open multicentre study.

作者信息

Arranz F J, Ros S

机构信息

Department of Psychiatry, Hospital del Mar, Autonomous University of Barcelona, Spain.

出版信息

J Affect Disord. 1997 Dec;46(3):285-91. doi: 10.1016/s0165-0327(97)00092-x.

Abstract

Antidepressant therapy in the elderly age group is frequently complicated by medical comorbidity, polypharmacy and increased sensitivity to drug effects. A nonblind, noncomparative, observational, multicentre study over 8 weeks was conducted to assess the effectiveness and tolerability of sertraline (50-200 mg/day) in 1437 elderly depressed outpatients with a mean (S.D.) age of 68 (6.3) years (range 60-92) in routine clinical practise. Depressive symptoms were monitored using the Montgomery Asberg Depression Rating Scale (MADRS) at baseline and at weeks 2, 4, 6 and 8. The mean dose of sertraline at the final visit was 85.2 mg/day (48% of patients were given the initial dose throughout the study). At the end of the study, mean percentage change of MADRS score from baseline was 61% (P < 0.001). A > or = 50% decrease in MADRS score was obtained in 70% of patients. Sertraline was well tolerated. Side effects occurred in 23% of patients, although only 5.1% withdrew because of adverse events. There were no significant differences in the antidepressant effectiveness or occurrence of side effects when patients with and without concomitant pathologic conditions or with and without concurrent medications were compared. These findings indicate the absence of clinically important drug interaction and confirm the effectiveness and safety of sertraline in routine clinical practise for treating elderly depressed outpatients.

摘要

老年人群的抗抑郁治疗常常因合并内科疾病、多种药物联合使用以及对药物效应的敏感性增加而变得复杂。在常规临床实践中,对1437名年龄平均(标准差)为68(6.3)岁(范围60 - 92岁)的老年抑郁症门诊患者进行了一项为期8周的非盲、非对照、观察性多中心研究,以评估舍曲林(50 - 200毫克/天)的有效性和耐受性。在基线以及第2、4、6和8周时,使用蒙哥马利 - 阿斯伯格抑郁评定量表(MADRS)监测抑郁症状。末次访视时舍曲林的平均剂量为85.2毫克/天(48%的患者在整个研究过程中给予初始剂量)。研究结束时,MADRS评分相对于基线的平均变化百分比为61%(P < 0.001)。70%的患者MADRS评分下降≥50%。舍曲林耐受性良好。23%的患者出现副作用,不过只有5.1%的患者因不良事件而退出。比较有或无合并病理状况以及有或无同时使用药物的患者时,抗抑郁效果或副作用的发生情况没有显著差异。这些发现表明不存在具有临床重要意义的药物相互作用,并证实了舍曲林在常规临床实践中治疗老年抑郁症门诊患者的有效性和安全性。

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