Efficacy of sertraline in the treatment of children and adolescents with major depressive disorder - Two randomized controlled trials

被引:302
作者
Wagner, KD
Ambrosini, P
Rynn, M
Wohlberg, C
Yang, RY
Greenbaum, MS
Childress, A
Donnelly, C
Deas, D
机构
[1] Univ Texas, Med Branch, Dept Psychiat & Behav Sci, Div Child & Adolescent Psychiat, Galveston, TX 77555 USA
[2] Drexel Univ, Coll Med, Philadelphia, PA 19104 USA
[3] Univ Penn, Philadelphia, PA 19104 USA
[4] Pfizer Inc, New York, NY USA
[5] Ingenium Clin Res, Libertyville, IL USA
[6] Nevada Behav Hlth Inc, Las Vegas, NV USA
[7] Dartmouth Coll Sch Med, Lebanon, NH USA
[8] Med Univ S Carolina, Charleston, SC 29425 USA
来源
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION | 2003年 / 290卷 / 08期
关键词
D O I
10.1001/jama.290.8.1033
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Context The efficacy, safety, and tolerability of selective serotonin reuptake inhibitors (SSRIs) in the treatment of adults with major depressive disorder (MDD) are well established. Comparatively few data are available on the effects of SSRIs in depressed children and adolescents. Objective To evaluate the efficacy and safety of sertraline compared with placebo in treatment of pediatric patients with MDD. Design and Setting Two multicenter randomized, double-blind, placebo-controlled trials were conducted at 53 hospital, general practice, and academic centers in the United States, India, Canada, Costa Rica, and Mexico between December 1999 and May 2001 and were pooled a priori. Participants Three hundred seventy-six children and adolescents aged 6 to 17 years with Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition-defined MDD of at least moderate severity. Intervention Patients were randomly assigned to receive a flexible dosage (50-200 mg/d) of sertraline (n=189) or matching placebo tablets (n=187) for 10 weeks. Main Outcome Measures Change from baseline in the Children's Depression Rating Scale-Revised (CDRS-R) Best Description of Child total score and reported adverse events. Results Sertraline-treated patients experienced statistically significantly greater improvement than placebo patients on the CDRS-R total score (mean change at week 10, -30.24 vs -25.83, respectively; P=.001; overall mean change, -22.84 vs -20.19, respectively; P=.007). Based on a 40% decrease in the adjusted CDRS-R total score at study end point, 69% of sertraline-treated patients compared with 59% of placebo patients were considered responders (P=.05). Sertraline treatment was generally well tolerated. Seventeen sertraline-treated patients (9%) and 5 placebo patients (3%) prematurely discontinued the study because of adverse events. Adverse events that occurred in at least 5% of sertraline-treated patients and with an incidence of at least twice that in placebo patients included diarrhea, vomiting, anorexia, and agitation. Conclusion The results of this pooled analysis demonstrate that sertraline is an effective and well-tolerated short-term treatment for children and adolescents with MDD.
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页码:1033 / 1041
页数:9
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