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首页> 外文期刊>Journal of affective disorders >Efficacy, predictors of therapy response, and safety of sertraline in routine clinical practice: prospective, open-label, non-interventional postmarketing surveillance study in 1878 patients.
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Efficacy, predictors of therapy response, and safety of sertraline in routine clinical practice: prospective, open-label, non-interventional postmarketing surveillance study in 1878 patients.

机译:常规临床实践中的功效,治疗反应的预测指标和舍曲林的安全性:1878例患者的前瞻性,开放标签,非干预售后监测研究。

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摘要

BACKGROUND: It is well established that subjects participating in controlled clinical trials may not be representative of patients seen in actual practice. Given that efficacy and safety of sertraline have been investigated almost exclusively in controlled clinical trials, the aim of this study was to investigate efficacy, safety, and predictors of treatment response to sertraline in routine clinical practice. METHODS: A total of 1878 depressed outpatients (69.5% female; mean age, 50.3 years) participated in this prospective, open-label, non-interventional, postmarketing surveillance study of sertraline. The primary study outcome was change in depression severity as assessed independently with the Patient Health Questionnaire (PHQ-9) depression scale and Clinical Global Impression (CGI) scales after 12 weeks of treatment. Stepwise logistic regression analyses were used to identify independent predictors of treatment response. RESULTS: Using standard criteria to define clinical improvement, responder rates were 87.7% (PHQ-9) and 87.2% (CGI), respectively. Remission, i.e. a PHQ-9 score of 5 or below, occurred in 56.9% of patients. Independent baseline predictors of CGI treatment response were: non-chronic course of depression (OR=2.8, p < 0.001), non-psychiatric treatment setting (OR=2.5, p < 0.001), absence of comorbid physical disease (OR=1.9, p < 0.001), depression-related work disability (OR=1.9, p < 0.001), and no previous antidepressant medication (OR=1.5, p=0.03). Adverse events were reported by 4.8% of patients. LIMITATIONS: Lack of a control group limits the conclusions that can be drawn from this study. CONCLUSIONS: For treatment of depressive disorders in routine outpatient settings, sertraline is safe and efficacious. Patients without prior episodes of depression, without medical comorbidity, and those with higher levels of depression-related functional limitations are most likely to respond to sertraline treatment.
机译:背景:众所周知,参加对照临床试验的受试者可能无法代表实际实践中出现的患者。鉴于舍曲林的功效和安全性几乎仅在对照临床试验中进行了研究,因此本研究的目的是研究常规临床实践中对舍曲林的治疗功效,安全性和预测指标。方法:共有1878名抑郁症门诊患者(女性为69.5%;平均年龄为50.3岁)参加了这项舍曲林前瞻性,开放标签,非干预,上市后监测研究。主要研究结果是治疗12周后根据患者健康问卷(PHQ-9)抑郁量表和临床总体印象(CGI)量表独立评估的抑郁严重程度变化。逐步逻辑回归分析用于确定治疗反应的独立预测因子。结果:使用标准标准定义临床改善,缓解率分别为87.7%(PHQ-9)和87.2%(CGI)。 56.9%的患者出现缓解,即PHQ-9得分为5或更低。 CGI治疗反应的独立基线预测因素包括:非慢性抑郁症病程(OR = 2.8,p <0.001),非精神病学治疗设置(OR = 2.5,p <0.001),没有合并症的身体疾病(OR = 1.9 p <0.001),与抑郁相关的工作障碍(OR = 1.9,p <0.001),并且以前没有抗抑郁药物(OR = 1.5,p = 0.03)。 4.8%的患者报告了不良事件。局限性:缺乏对照组限制了可以从这项研究中得出的结论。结论:舍曲林对于常规门诊患者的抑郁性疾病是安全有效的。既往没有抑郁发作,无医学合并症的患者,以及与抑郁相关的功能受限水平较高的患者,最有可能对舍曲林治疗产生反应。

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