کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
6232093 1608147 2015 11 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Comparative efficacy and acceptability of atomoxetine, lisdexamfetamine, bupropion and methylphenidate in treatment of attention deficit hyperactivity disorder in children and adolescents: A meta-analysis with focus on bupropion
ترجمه فارسی عنوان
کارآزمایی بالینی و پذیرش آتوموکسستین، لیسکسمافاتامین، بوپروپیون و متیل فنیدات در درمان اختلال بیش فعالی کم توجهی در کودکان و نوجوانان: یک متاآنالیز با تمرکز بر بوپروپیون
موضوعات مرتبط
علوم پزشکی و سلامت پزشکی و دندانپزشکی روانپزشکی و بهداشت روانی
چکیده انگلیسی

ObjectivesThere is a lack of comparative effectiveness research among attention deficit hyperactivity disorder (ADHD) drugs in terms of efficacy and acceptability, where bupropion is compared with atomoxetine, lisdexamfetamine and methylphenidate. The main aim of this work was to compare the efficacy and acceptability of these drugs in children and adolescents using a metaanalysis.MethodsA literature search was conducted to identify double-blind, placebo-controlled, noncrossover studies of ADHD. PubMed/Medline and Clinicaltrials.gov were searched. Comparative drug efficacy to placebo was calculated based on the standardized mean difference (SMD), while the comparative drug acceptability (all cause discontinuation) to placebo was estimated on the odds ratio (OR).ResultsIn total 28 trials were included in the meta-analysis. Efficacy in reducing ADHD symptoms compared to placebo was small for bupropion (SMD=−0.32, 95% CI; −0.69, 0.05), while modest efficacy was shown for atomoxetine (SMD=−0.68, 95% CI; −0.76, −0.59) and methylphenidate (SMD=−0.75, 95% CI; −0.98, −0.52) and high efficacy was observed for lisdexamfetamine (SMD=−1.28, 95% CI; −1.84, −0.71). Compared to placebo treatment discontinuation was statistically significantly lower for methylphenidate (OR=0.35, 95% CI; 0.24, 0.52), while it was not significantly different for atomoxetine (OR=0.91, 95% CI; 0.66, 1.24), lisdexamfetamine (OR=0.60, 95% CI, 0.22, 1.65), and bupropion (OR=1.64, 95% CI; 0.5, 5.43).LimitationsThe heterogeneity was high, except in atomoxetine trials. The crossover studies were excluded. The effect sizes at specific time points were not computed. Studies with comorbid conditions, except those reporting on oppositional defiant disorder, were also excluded. All studies involving MPH were combined.ConclusionsThe results suggest that lisdexamfetamine has the best benefit risk balance and has promising potential for treating children and adolescents with ADHD. More research is needed for a better clinical evaluation of bupropion.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Journal of Affective Disorders - Volume 178, 1 June 2015, Pages 149-159
نویسندگان
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