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Use of Serotonin Norepinephrine Reuptake Inhibitors in the Treatment of Attention-Deficit Hyperactivity Disorder in Pediatrics

机译:5-羟色胺去甲肾上腺素再摄取抑制剂在儿科注意缺陷多动障碍的治疗中的应用

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Objective: To review the current literature on the efficacy and safety of serotonin norepinephrine reuptake inhibitors in the treatment of attention-deficit hyperactivity disorder (ADHD) in the pediatric population. Data Sources: A literature search from 1996 to August 2013 was conducted using MEDLINE, CINAHL, and EMBASE databases. Search terms included attention-deficit hyperactivity disorder, serotonin norepinephrine reuptake inhibitor, pediatric attention-deficit hyperactivity disorder, venlafaxine, duloxetine, desvenlafaxine, milnacipran, and nefazodone. Study Selection and Data Extraction: Relevant articles on duloxetine and venlafaxine for the treatment of pediatric ADHD were reviewed; 5 studies on venlafaxine and 1 study on duloxetine were evaluated. Studies included open-label and randomized, double-blind trials. Case studies in pediatric populations and all studies in adult populations were excluded. Data Synthesis: Patients 6 to 17 years old were evaluated in the venlafaxine and duloxetine studies. Trials on venlafaxine, ranging from 2 to 6 weeks, showed patient improvement as measured by the Conners Rating Scale and ADHD Rating Scale. Venlafaxine was initiated at 12.5 to 25 mg/d and titrated up to 1.4 to 3.8 mg/kg/d to a maximum of 150 mg/d. Duloxetine showed minimal efficacy in treating ADHD symptoms at doses of 60 mg/d at 6 weeks. The most common side effects for venlafaxine and duloxetine included drowsiness and decreased appetite, respectively. Conclusions: Data for venlafaxine and duloxetine are limited. However, venlafaxine may be considered as an alternative agent when patients cannot tolerate or fail stimulants, tricyclic antidepressants, or bupropion. Duloxetine has been studied in children; however, with only 1 study available, it is difficult to recommend.
机译:目的:综述有关5-羟色胺去甲肾上腺素再摄取抑制剂治疗小儿注意缺陷多动障碍(ADHD)的有效性和安全性的文献。数据来源:使用MEDLINE,CINAHL和EMBASE数据库进行了1996年至2013年8月的文献检索。搜索词包括注意缺陷多动障碍,5-羟色胺去甲肾上腺素再摄取抑制剂,儿科注意缺陷多动障碍,文拉法辛,度洛西汀,去甲文拉法辛,米那普仑和奈法唑酮。研究选择和数据提取:综述了有关度洛西汀和文拉法辛治疗小儿ADHD的相关文章;评估了5项关于文拉法辛的研究和1项关于度洛西汀的研究。研究包括开放标签和随机,双盲试验。排除了儿科人群的案例研究和成人人群的所有研究。数据综合:在文拉法辛和度洛西汀研究中评估了6至17岁的患者。根据Conners评分量表和ADHD评分量表,对文拉法辛进行2到6周的试验显示患者的病情好转。文拉法辛起始剂量为12.5至25 mg / d,滴定至1.4至3.8 mg / kg / d至最高150 mg / d。度洛西汀在6周时以60 mg / d的剂量治疗ADHD症状的疗效最低。文拉法辛和度洛西汀最常见的副作用分别是嗜睡和食欲下降。结论:文拉法辛和度洛西汀的数据有限。但是,当患者不能耐受或无法使用兴奋剂,三环类抗抑郁药或安非他酮时,文拉法辛可被视为替代药物。已经对儿童进行了度洛西汀的研究。但是,只有一项研究可用,因此很难推荐。

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