Wagner Karen Dineen, Ambrosini Paul, Rynn Moira, Wohlberg Christopher, Yang Ruoyong, Greenbaum Michael S, Childress Ann, Donnelly Craig, Deas Deborah
University of Texas Medical Branch, Department of Psychiatry and Behavioral Sciences, Galveston 77555-0188, USA.
JAMA. 2003 Aug 27;290(8):1033-41. doi: 10.1001/jama.290.8.1033.
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.
To evaluate the efficacy and safety of sertraline compared with placebo in treatment of pediatric patients with MDD.
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.
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.
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.
Change from baseline in the Children's Depression Rating Scale-Revised (CDRS-R) Best Description of Child total score and reported adverse events.
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.
The results of this pooled analysis demonstrate that sertraline is an effective and well-tolerated short-term treatment for children and adolescents with MDD.
选择性5-羟色胺再摄取抑制剂(SSRIs)治疗成人重度抑郁症(MDD)的疗效、安全性及耐受性已得到充分证实。而关于SSRIs对抑郁儿童和青少年的影响的数据相对较少。
评估舍曲林治疗儿童MDD患者的疗效及安全性,并与安慰剂进行比较。
1999年12月至2001年5月期间,在美国、印度、加拿大、哥斯达黎加和墨西哥的53家医院、普通诊所及学术中心进行了两项多中心随机、双盲、安慰剂对照试验,并进行了预先汇总分析。
376名年龄在6至17岁之间、符合《精神疾病诊断与统计手册》第四版定义的至少中度严重程度的MDD儿童和青少年。
患者被随机分配接受灵活剂量(50 - 200毫克/天)的舍曲林(n = 189)或匹配的安慰剂片(n = 187),持续10周。
儿童抑郁评定量表修订版(CDRS - R)中儿童总体最佳描述得分相对于基线的变化以及报告的不良事件。
在CDRS - R总分上,舍曲林治疗组患者的改善在统计学上显著优于安慰剂组患者(第10周时的平均变化分别为 - 30.24和 - 25.83;P = 0.001;总体平均变化分别为 - 22.84和 - 20.19;P = 0.007)。根据研究终点时调整后的CDRS - R总分下降40%来计算,舍曲林治疗组69%的患者被视为有反应者,而安慰剂组为59%(P = 0.05)。舍曲林治疗一般耐受性良好。17名接受舍曲林治疗的患者(9%)和5名接受安慰剂治疗的患者(3%)因不良事件提前终止了研究。至少5%接受舍曲林治疗的患者出现且发生率至少为安慰剂组患者两倍的不良事件包括腹泻、呕吐、厌食和激越。
这项汇总分析的结果表明,舍曲林是治疗儿童和青少年MDD的一种有效且耐受性良好的短期治疗方法。