Tags

Type your tag names separated by a space and hit enter

The Effectiveness and Tolerability of Central Nervous System Stimulants in School-Age Children with Attention-Deficit/Hyperactivity Disorder and Disruptive Mood Dysregulation Disorder Across Home and School.

Abstract

OBJECTIVE

This study examines the effectiveness and tolerability of stimulants in children with attention-deficit/hyperactivity disorder (ADHD) and disruptive mood dysregulation disorder (DMDD).

METHODS

To be eligible, participants had to meet Diagnostic and Statistical Manual of Mental Disorders, 4th ed., Text Revision (DSM-IV) criteria for the combined subtype of ADHD and National Institute of Mental Health (NIMH) severe mood dysregulation criteria. The Diagnostic and Statistical Manual of Mental Disorders, 5th ed. (DSM-V) DMDD criteria were retrospectively assessed after the study was completed. An open-label medication trial lasting up to 6 weeks was completed to optimize the central nervous system (CNS) stimulant dose. Measures of affective symptoms, ADHD symptoms and other disruptive behaviors, impairment, and structured side effect ratings were collected before and after the medication trial.

RESULTS

Optimization of stimulant medication was associated with a significant decline in depressive symptoms on the Childhood Depression Rating Score-Revised Scale (p<0.05, Cohen's d=0.61) and Mood Severity Index score (p<0.05, Cohen's d=0.55), but not in manic-like symptoms on the Young Mania Rating Scale. There was a significant reduction in ADHD (p<0.05, Cohen's d=0.95), oppositional defiant disorder (ODD) (p<0.05, Cohen's d=0.5), and conduct disorder (CD) symptoms (p<0.05, Cohen's d=0.65) as rated by parents. There was also a significant reduction in teacher-rated ADHD (p<0.05, Cohen's d=0.33) but not in ODD symptoms. Medications were well tolerated and there was no increase in side effect ratings seen with dose optimization. Significant improvement in functioning was reported by clinicians and parents (all p's<0.05), but youth still manifested appreciable impairment at end-point.

CONCLUSIONS

CNS simulants were well tolerated by children with ADHD comorbid with a diagnosis of DMDD. CNS stimulants were associated with clinically significant reductions in externalizing symptoms, along with smaller improvements in mood. However, most participants still exhibited significant impairment, suggesting that additional treatments may be needed to optimize functioning.

Links

  • PMC Free PDF
  • PMC Free Full Text
  • Publisher Full Text
  • Authors+Show Affiliations

    ,

    1 Department of Psychiatry, Penn State University College of Medicine , Hershey, Pennsylvania.

    ,

    2 Center for Children and Families, Florida International University, Miami, Florida.

    ,

    3 Department of Psychiatry, Herbert Wertheim College of Medicine, Florida International University , Miami, Florida.

    ,

    2 Center for Children and Families, Florida International University, Miami, Florida.

    ,

    4 Department of School and Counseling Psychology, SUNY Buffalo , Buffalo, New York.

    ,

    1 Department of Psychiatry, Penn State University College of Medicine , Hershey, Pennsylvania.

    ,

    5 Department of Pediatrics, SUNY Buffalo School of Medicine , Buffalo, New York.

    ,

    6 Department of Psychiatry, SUNY Buffalo School of Medicine , Buffalo, New York.

    ,

    6 Department of Psychiatry, SUNY Buffalo School of Medicine , Buffalo, New York.

    ,

    2 Center for Children and Families, Florida International University, Miami, Florida.

    1 Department of Psychiatry, Penn State University College of Medicine , Hershey, Pennsylvania.

    Source

    MeSH

    Attention Deficit Disorder with Hyperactivity
    Attention Deficit and Disruptive Behavior Disorders
    Central Nervous System Stimulants
    Child
    Conduct Disorder
    Diagnostic and Statistical Manual of Mental Disorders
    Dose-Response Relationship, Drug
    Female
    Humans
    Male
    Mood Disorders
    Psychiatric Status Rating Scales
    Schools
    Treatment Outcome

    Pub Type(s)

    Clinical Trial
    Journal Article
    Research Support, N.I.H., Extramural

    Language

    eng

    PubMed ID

    26771437

    Citation

    Baweja, Raman, et al. "The Effectiveness and Tolerability of Central Nervous System Stimulants in School-Age Children With Attention-Deficit/Hyperactivity Disorder and Disruptive Mood Dysregulation Disorder Across Home and School." Journal of Child and Adolescent Psychopharmacology, vol. 26, no. 2, 2016, pp. 154-63.
    Baweja R, Belin PJ, Humphrey HH, et al. The Effectiveness and Tolerability of Central Nervous System Stimulants in School-Age Children with Attention-Deficit/Hyperactivity Disorder and Disruptive Mood Dysregulation Disorder Across Home and School. J Child Adolesc Psychopharmacol. 2016;26(2):154-63.
    Baweja, R., Belin, P. J., Humphrey, H. H., Babocsai, L., Pariseau, M. E., Waschbusch, D. A., ... Waxmonsky, J. G. (2016). The Effectiveness and Tolerability of Central Nervous System Stimulants in School-Age Children with Attention-Deficit/Hyperactivity Disorder and Disruptive Mood Dysregulation Disorder Across Home and School. Journal of Child and Adolescent Psychopharmacology, 26(2), pp. 154-63. doi:10.1089/cap.2015.0053.
    Baweja R, et al. The Effectiveness and Tolerability of Central Nervous System Stimulants in School-Age Children With Attention-Deficit/Hyperactivity Disorder and Disruptive Mood Dysregulation Disorder Across Home and School. J Child Adolesc Psychopharmacol. 2016;26(2):154-63. PubMed PMID: 26771437.
    * Article titles in AMA citation format should be in sentence-case
    TY - JOUR T1 - The Effectiveness and Tolerability of Central Nervous System Stimulants in School-Age Children with Attention-Deficit/Hyperactivity Disorder and Disruptive Mood Dysregulation Disorder Across Home and School. AU - Baweja,Raman, AU - Belin,Peter J, AU - Humphrey,Hugh H, AU - Babocsai,Lysett, AU - Pariseau,Meaghan E, AU - Waschbusch,Daniel A, AU - Hoffman,Martin T, AU - Akinnusi,Opeolowa O, AU - Haak,Jenifer L, AU - Pelham,William E, AU - Waxmonsky,James G, Y1 - 2016/01/15/ PY - 2017/03/01/pmc-release PY - 2016/1/16/entrez PY - 2016/1/16/pubmed PY - 2017/1/4/medline SP - 154 EP - 63 JF - Journal of child and adolescent psychopharmacology JO - J Child Adolesc Psychopharmacol VL - 26 IS - 2 N2 - OBJECTIVE: This study examines the effectiveness and tolerability of stimulants in children with attention-deficit/hyperactivity disorder (ADHD) and disruptive mood dysregulation disorder (DMDD). METHODS: To be eligible, participants had to meet Diagnostic and Statistical Manual of Mental Disorders, 4th ed., Text Revision (DSM-IV) criteria for the combined subtype of ADHD and National Institute of Mental Health (NIMH) severe mood dysregulation criteria. The Diagnostic and Statistical Manual of Mental Disorders, 5th ed. (DSM-V) DMDD criteria were retrospectively assessed after the study was completed. An open-label medication trial lasting up to 6 weeks was completed to optimize the central nervous system (CNS) stimulant dose. Measures of affective symptoms, ADHD symptoms and other disruptive behaviors, impairment, and structured side effect ratings were collected before and after the medication trial. RESULTS: Optimization of stimulant medication was associated with a significant decline in depressive symptoms on the Childhood Depression Rating Score-Revised Scale (p<0.05, Cohen's d=0.61) and Mood Severity Index score (p<0.05, Cohen's d=0.55), but not in manic-like symptoms on the Young Mania Rating Scale. There was a significant reduction in ADHD (p<0.05, Cohen's d=0.95), oppositional defiant disorder (ODD) (p<0.05, Cohen's d=0.5), and conduct disorder (CD) symptoms (p<0.05, Cohen's d=0.65) as rated by parents. There was also a significant reduction in teacher-rated ADHD (p<0.05, Cohen's d=0.33) but not in ODD symptoms. Medications were well tolerated and there was no increase in side effect ratings seen with dose optimization. Significant improvement in functioning was reported by clinicians and parents (all p's<0.05), but youth still manifested appreciable impairment at end-point. CONCLUSIONS: CNS simulants were well tolerated by children with ADHD comorbid with a diagnosis of DMDD. CNS stimulants were associated with clinically significant reductions in externalizing symptoms, along with smaller improvements in mood. However, most participants still exhibited significant impairment, suggesting that additional treatments may be needed to optimize functioning. SN - 1557-8992 UR - https://www.unboundmedicine.com/medline/citation/26771437/The_Effectiveness_and_Tolerability_of_Central_Nervous_System_Stimulants_in_School_Age_Children_with_Attention_Deficit/Hyperactivity_Disorder_and_Disruptive_Mood_Dysregulation_Disorder_Across_Home_and_School_ L2 - https://www.liebertpub.com/doi/full/10.1089/cap.2015.0053?url_ver=Z39.88-2003&amp;rfr_id=ori:rid:crossref.org&amp;rfr_dat=cr_pub=pubmed DB - PRIME DP - Unbound Medicine ER -