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硫酸右苯丙胺(Attentin)在儿童和青少年注意力缺陷多动障碍常规治疗中的有效性和安全性:一项为期12个月的非干预性研究结果

Effectiveness and safety of dexamphetamine sulfate (Attentin) in the routine treatment of children and adolescents with ADHD: results from a 12-month non-interventional study.

作者信息

Uebel-von Sandersleben Henrik, Dangel Oliver, Fischer Roland, Ruhmann Michaela, Huss Michael

机构信息

University Medical Center Göttingen, Department of Child and Adolescent Psychiatry and Psychotherapy, Göttingen, Germany.

MEDICE Arzneimittel Pütter GmbH & Co KG; Iserlohn, Germany.

出版信息

Scand J Child Adolesc Psychiatr Psychol. 2021 Apr 23;9:73-86. doi: 10.21307/sjcapp-2021-009. eCollection 2021.

Abstract

BACKGROUND

Randomized controlled trials have shown that dexamphetamine sulfate (DEX) is efficacious in the treatment of attention-deficit/hyperactivity disorder (ADHD) in children and adolescents; however, data on the effectiveness and safety of DEX in routine practice are scarce.

OBJECTIVE

This study investigated the long-term effectiveness and safety of Attentin (immediate-release DEX) in children and adolescents with ADHD in routine practice.

METHODS

ATTENTION was a multicenter, prospective, observational, non-interventional study that enrolled pediatric patients with ADHD (aged 6-17 years) with a clinically inadequate response to previous methylphenidate (MPH) treatment. Patients were assessed at baseline and two follow-up visits after approx. 6 and 12 months of DEX treatment. The primary endpoint was the investigator-rated ADHD rating scale IV (ADHD-RS-IV) total score change from baseline to the first follow-up visit.

RESULTS

The study enrolled 140 patients (mean age: 11.2 years). Significant reductions in ADHD-RS-IV total scores were observed in the titration phase and were maintained up to the second follow-up visit. The mean ADHD-RS-IV total score change from baseline to the first follow-up visit was -11.9 (27.1 vs. 13.4, < .001). Beneficial effects of DEX were observed on both ADHD-RS-IV subscales ('hyperactivity/impulsivity' and 'inattention') and in both children and adolescents. Clinical response, defined as a reduction in the ADHD-RS-IV total score of at least 30% at the first follow-up visit, was observed in 78.1% of patients. Patients reported an average onset of action of 36.2 minutes and an average duration of action of 6.5 hours after intake of the first dose of DEX in the morning. DEX was well tolerated. Small significant increases in mean systolic and diastolic blood pressure compared to baseline were observed.

CONCLUSIONS

Attentin is an effective and well-tolerated long-term treatment for pediatric ADHD patients with a clinically inadequate response to previous MPH treatment.

摘要

背景

随机对照试验表明,硫酸右苯丙胺(DEX)在治疗儿童和青少年注意力缺陷多动障碍(ADHD)方面有效;然而,关于DEX在常规临床实践中的有效性和安全性的数据却很稀少。

目的

本研究调查了Attentin(速释DEX)在常规临床实践中治疗患有ADHD的儿童和青少年的长期有效性和安全性。

方法

ATTENTION是一项多中心、前瞻性、观察性、非干预性研究,纳入了对先前哌甲酯(MPH)治疗临床反应不足的ADHD儿科患者(6至17岁)。在基线以及DEX治疗约6个月和12个月后的两次随访中对患者进行评估。主要终点是研究者评定的ADHD评定量表IV(ADHD-RS-IV)从基线到首次随访的总分变化。

结果

该研究纳入了140名患者(平均年龄:11.2岁)。在滴定阶段观察到ADHD-RS-IV总分显著降低,并持续到第二次随访。从基线到首次随访,ADHD-RS-IV总分的平均变化为-11.9(27.1对13.4,P<0.001)。在ADHD-RS-IV的两个分量表(“多动/冲动”和“注意力不集中”)以及儿童和青少年中均观察到了DEX的有益效果。在首次随访时,78.1%的患者出现了临床反应,定义为ADHD-RS-IV总分降低至少30%。患者报告,早晨服用第一剂DEX后,平均起效时间为36.2分钟,平均作用持续时间为6.5小时。DEX耐受性良好。与基线相比,平均收缩压和舒张压有小幅显著升高。

结论

对于先前MPH治疗临床反应不足的儿科ADHD患者,Attentin是一种有效且耐受性良好的长期治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2b73/8077785/91eea3abc0b9/sjcapp-09-009-g001.jpg

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