TY - JOUR
T1 - Bupropion versus methylphenidate in the treatment of children with attention-deficit/hyperactivity disorder
T2 - Randomized double-blind study
AU - Jafarinia, Morteza
AU - Mohammadi, Mohammad Reza
AU - Modabbernia, Amirhossein
AU - Ashrafi, Mandana
AU - Khajavi, Danial
AU - Tabrizi, Mina
AU - Yadegari, Noorollah
AU - Akhondzadeh, Shahin
PY - 2012/7
Y1 - 2012/7
N2 - Objective To compare the safety and efficacy of bupropion with methylphenidate in children and adolescents with attention-deficit/hyperactivity disorder (ADHD). Methods In a 6-week randomized double-blind study, 44 patients with a DSM-IV-TR diagnosis of ADHD were randomly assigned to receive bupropion 100-150 mg/day (100 mg/day for <30 kg and 150 mg/day for >30 kg) or methylphenidate 20-30 mg/day. Symptoms were assessed using Teacher and Parent Attention-Deficit/Hyperactivity Disorder Rating Scale-IV (ADHD-RS-IV) at baseline and weeks 3 and 6. Results Forty patients had at least one post-baseline measurement, and 38 patients completed the trial. No significant difference was found between the two groups on the Parent and Teacher ADHD-RS-IV scores ([F(1, 38) = 0.266, p = 0.609] and [F(1, 38) = 0.001, p = 0.972], respectively). By week 6, 18 patients (90%) in each group achieved response on the Parent scale (Fisher's exact test p-value = 1.0). With the Teacher ADHD-RS-IV used, eight (40%) patients in the bupropion group and 12 (60%) patients in the methylphenidate group achieved response by week 6 (χ2(1) = 1.600, p = 0.206). Headache was observed more frequently in the methylphenidate group. Frequency of other side effects was not significantly different between the two groups. Conclusions Bupropion has a comparable safety and efficacy profile with methylphenidate in children and adolescents with ADHD.
AB - Objective To compare the safety and efficacy of bupropion with methylphenidate in children and adolescents with attention-deficit/hyperactivity disorder (ADHD). Methods In a 6-week randomized double-blind study, 44 patients with a DSM-IV-TR diagnosis of ADHD were randomly assigned to receive bupropion 100-150 mg/day (100 mg/day for <30 kg and 150 mg/day for >30 kg) or methylphenidate 20-30 mg/day. Symptoms were assessed using Teacher and Parent Attention-Deficit/Hyperactivity Disorder Rating Scale-IV (ADHD-RS-IV) at baseline and weeks 3 and 6. Results Forty patients had at least one post-baseline measurement, and 38 patients completed the trial. No significant difference was found between the two groups on the Parent and Teacher ADHD-RS-IV scores ([F(1, 38) = 0.266, p = 0.609] and [F(1, 38) = 0.001, p = 0.972], respectively). By week 6, 18 patients (90%) in each group achieved response on the Parent scale (Fisher's exact test p-value = 1.0). With the Teacher ADHD-RS-IV used, eight (40%) patients in the bupropion group and 12 (60%) patients in the methylphenidate group achieved response by week 6 (χ2(1) = 1.600, p = 0.206). Headache was observed more frequently in the methylphenidate group. Frequency of other side effects was not significantly different between the two groups. Conclusions Bupropion has a comparable safety and efficacy profile with methylphenidate in children and adolescents with ADHD.
KW - adolescent
KW - attention-deficit/hyperactivity disorder
KW - bupropion
KW - children
KW - methylphenidate
UR - http://www.scopus.com/inward/record.url?scp=84864128978&partnerID=8YFLogxK
U2 - 10.1002/hup.2242
DO - 10.1002/hup.2242
M3 - Article
C2 - 22806822
AN - SCOPUS:84864128978
SN - 0885-6222
VL - 27
SP - 411
EP - 418
JO - Human Psychopharmacology
JF - Human Psychopharmacology
IS - 4
ER -