Sertraline for Preventing Mood Disorders Following Traumatic Brain Injury A Randomized Clinical Trial

被引:51
作者
Jorge, Ricardo E. [1 ]
Acion, Laura [1 ,2 ,3 ]
Burin, Debora I. [4 ]
Robinson, Robert G. [5 ]
机构
[1] Baylor Coll Med, Menninger Dept Psychiat & Behav Sci, One Baylor Plaza, Houston, TX 77030 USA
[2] Univ Iowa, Iowa Consortium Subst Abuse Res & Evaluat, Iowa City, IA USA
[3] Univ Buenos Aires, CONICET, Fac Ciencias Exactas & Nat, Inst Calculo, Buenos Aires, DF, Argentina
[4] Univ Buenos Aires, CONICET, Fac Psicol, Buenos Aires, DF, Argentina
[5] Univ Iowa, Dept Psychiat, Iowa City, IA 52242 USA
基金
美国国家卫生研究院;
关键词
MAJOR DEPRESSIVE DISORDER; BLUNT HEAD-INJURY; PSYCHIATRIC-DISORDERS; AXIS-I; ASSOCIATION; ILLNESS; RISK; ESCITALOPRAM; RELATIVES; ONSET;
D O I
10.1001/jamapsychiatry.2016.2189
中图分类号
R749 [精神病学];
学科分类号
100204 [神经病学];
摘要
IMPORTANCE Prevention is more effective than treatment to decrease the burden of significant medical conditions such as depressive disorders, a major cause of disability worldwide. Traumatic brain injury (TBI) is a candidate for selective strategies to prevent depression given the incidence, prevalence, and functional effect of depression that occurs after TBI. OBJECTIVE To assess the efficacy of sertraline treatment in preventing depressive disorders following TBI. DESIGN, SETTING, AND PARTICIPANTS A double-blind, placebo-controlled, parallel-group randomized clinical trial was conducted at a university hospital from July 3, 2008, to September 17, 2012, with 24 weeks of follow-up. A consecutive sample of 534 patients aged 18 to 85 years, hospitalized for mild, moderate, or severe TBI, was eligible for the study. Ninety-four patients consented to participate and were randomized (46 to placebo and 48 to sertraline), of whom 79 (84%) completed the study. Intention-to-treat data analysis was conducted from July 1, 2014, to December 31, 2015. INTERVENTIONS Placebo or sertraline, 100 mg/d, for 24 weeks or until development of a mood disorder. MAIN OUTCOMES AND MEASURES Time to onset of depressive disorders, as defined by the DSM-IV, associated with TBI. RESULTS Of the 94 patients in the study (38 female and 56 male; 92 white), the number needed to treat to prevent depression after TBI at 24 weeks was 5.9 (95% CI, 3.1-71.1; chi(2) = 4.6; P = .03) for sertraline treatment vs placebo. The influence of sertraline in the course of neuropsychological variables was not detected. The intervention was well tolerated, and adverse effects were mild in both the sertraline and placebo groups. CONCLUSIONS AND RELEVANCE Sertraline appears to be efficacious to prevent the onset of depressive disorders following TBI. Future studies should replicate these findings in a large sample of patients with TBI and depict their long-term physical, cognitive, behavioral, and functional outcomes.
引用
收藏
页码:1041 / 1047
页数:7
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