Clinical gains from including both dextroamphetamine and methylphenidate in stimulant trials.

Objective: The purpose of this study was to investigate clinical gains from including both dextroamphetamine and methylphenidate in stimulant trials.Method: Thirty-six medication-naïve children ages 9-14 years diagnosed with attention-deficit/hyperactivity disorder (ADHD) were enrolled for 6 weeks i...

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Publicado en:Journal of Child & Adolescent Psychopharmacology Vol. 23; no. 9; pp. 597 - 605
Autores principales: Ramtvedt, Bjørn E, Røinås, Elisabeth, Aabech, Henning S, Sundet, Kjetil S
Formato: research randomized controlled trial Journal Article
Publicado: Mary Ann Liebert, Inc. Nov2013
Acceso en línea:Ver este registro en EBSCOhost
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      dt: Nov2013
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      pub: Mary Ann Liebert, Inc.
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        10.1089/cap.2012.0085
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        atl: Clinical gains from including both dextroamphetamine and methylphenidate in stimulant trials.
      aug:
        au:
          Ramtvedt, Bjørn E
          Røinås, Elisabeth
          Aabech, Henning S
          Sundet, Kjetil S
        affil: 1 østfold Hospital Trust , Neuropsychiatric Unit, Fredrikstad, Norway .
      sug:
        subj:
          Attention Deficit Hyperactivity Disorder Drug Therapy
          Central Nervous System Stimulants Therapeutic Use
          Dextroamphetamine Therapeutic Use
          Methylphenidate Therapeutic Use
          Adolescence
          Attention Deficit Hyperactivity Disorder Physiopathology
          Central Nervous System Stimulants Administration and Dosage
          Child
          Clinical Assessment Tools
          Crossover Design
          Dextroamphetamine Administration and Dosage
          Diagnosis, Computer Assisted
          Double-Blind Studies
          Female
          Human
          Male
          Methylphenidate Administration and Dosage
          Parents
          Questionnaires
          Time Factors
          Treatment Outcomes
          Adolescent: 13-18 years
          Child: 6-12 years
          Female
          Male
      ab: Objective: The purpose of this study was to investigate clinical gains from including both dextroamphetamine and methylphenidate in stimulant trials.Method: Thirty-six medication-naïve children ages 9-14 years diagnosed with attention-deficit/hyperactivity disorder (ADHD) were enrolled for 6 weeks in a crossover trial, with 2 weeks of methylphenidate, dextroamphetamine, and placebo, in a randomly assigned, counterbalanced sequence. Outcome measures constituted a computer-based continuous performance test combined with a motion tracking system (Qb Test) and an ADHD questionnaire rated by parents and teachers.Results: Group analyses found significant treatment effects of similar size for the two stimulants on both outcome measures. Single-subject analyses revealed that each stimulant produced a favourable response in 26 children; however, an individual child frequently responded qualitatively or quantitatively differently to the two stimulants. By including both stimulants in the trial, the number of favorable responders increased from 26 (72%) to 33 (92%). In children with favorable responses of unequal strength to the two stimulants, a shift from inferior drug to best drug was associated with a 64% mean increase in the overall response strength score, as measured by the ADHD questionnaire.Conclusions: The likelihood of a favorable response and optimal response strength is increased by including both stimulants in the stimulant trial. The study was first registered in clinical trials 28 September 2010. Clinical Trials.gov Identifier: NCT01220440.
      pubtype: Academic Journal
      doctype:
        research
        randomized controlled trial
        Journal Article
      ougenre: Article
    language: English
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