Newcorn Jeffrey H, Michelson David, Kratochvil Christopher J, Allen Albert J, Ruff Dustin D, Moore Rodney J
Mount Sinai Medical Center, Department of Psychiatry, One Gustave L Levy Place, Box 1230, New York, NY 10029, USA.
Pediatrics. 2006 Dec;118(6):e1701-6. doi: 10.1542/peds.2005-2999. Epub 2006 Nov 13.
Data from acute studies of atomoxetine in patients with attention-deficit/hyperactivity disorder suggest that a dose of approximately 1.2 mg/kg per day is required to attain a maximal symptom response. However, lower doses could be effective during maintenance treatment, which would reduce drug exposure and potential problems related to tolerability during chronic treatment.
Patients 6 to 16 years of age who had a robust response to an initial acute trial of atomoxetine were assigned randomly under double-blind conditions to continue treatment for up to 8 months with either the dose to which they had responded acutely (1.2-1.8 mg/kg per day, N = 116, continued same dose) or a lower dose (0.5 mg/kg per day, N = 113, low dose). The primary outcome measure was relapse, defined as an Attention-Deficit/Hyperactivity Disorder Rating Scale-IV-Parent Version: Investigator-Administered and Scored total score returned to > or = 90% of the original baseline value (before acute treatment) for 2 consecutive visits. Mean change in Attention-Deficit/Hyperactivity Disorder Rating Scale total score was assessed as a secondary outcome.
At randomization, symptom severity was low and similar in both groups. At end point, relapse rates did not differ between the groups. Mean change in Attention-Deficit/Hyperactivity Disorder Rating Scale total score from the conclusion of acute treatment to end point also was not different between groups. Reports of affective lability were higher in the patients in the low-dose group. Also, increases in heart rate (compared with when atomoxetine was started) were higher in the patients in the continued same-dose group than in the low-dose group. Finally, increases in weight over the course of the trial were greater for the low-dose group than the continued same-dose group.
For patients who experience a robust response to atomoxetine, it may be possible to retain the response during maintenance treatment with a reduced dose of atomoxetine.
来自对注意缺陷/多动障碍患者进行的托莫西汀急性研究的数据表明,每天约1.2毫克/千克的剂量才能获得最大症状缓解。然而,较低剂量在维持治疗期间可能有效,这将减少药物暴露以及慢性治疗期间与耐受性相关的潜在问题。
对托莫西汀初始急性试验有强烈反应的6至16岁患者,在双盲条件下随机分配,用他们急性反应时的剂量(每天1.2 - 1.8毫克/千克,N = 116,继续相同剂量)或较低剂量(每天0.5毫克/千克,N = 113,低剂量)持续治疗长达8个月。主要结局指标为复发,定义为注意缺陷/多动障碍评定量表-IV-家长版:研究者施测并计分的总分连续2次访视恢复至≥急性治疗前原始基线值的90%。注意缺陷/多动障碍评定量表总分的平均变化作为次要结局进行评估。
随机分组时,两组症状严重程度均较低且相似。在终点时,两组复发率无差异。从急性治疗结束到终点,两组注意缺陷/多动障碍评定量表总分的平均变化也无差异。低剂量组患者情感不稳定的报告较多。此外,继续相同剂量组患者心率增加幅度(与开始使用托莫西汀时相比)高于低剂量组。最后,试验过程中低剂量组体重增加幅度大于继续相同剂量组。
对于对托莫西汀有强烈反应的患者,在维持治疗期间降低托莫西汀剂量可能仍能保持疗效。