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ADHD, comorbid disorders and psychosocial functioning: How representative is a child cohort study? Findings from a national patient registry

BACKGROUND: Cohort studies often report findings on children with Attention Deficit Hyperactivity Disorder (ADHD) but may be biased by self-selection. The representativeness of cohort studies needs to be investigated to determine whether their findings can be generalised to the general child populat...

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Autores principales: Oerbeck, Beate, Overgaard, Kristin Romvig, Aspenes, Stian Thoresen, Pripp, Are Hugo, Mordre, Marianne, Aase, Heidi, Reichborn-Kjennerud, Ted, Zeiner, Pal
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5240379/
https://www.ncbi.nlm.nih.gov/pubmed/28095819
http://dx.doi.org/10.1186/s12888-017-1204-7
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author Oerbeck, Beate
Overgaard, Kristin Romvig
Aspenes, Stian Thoresen
Pripp, Are Hugo
Mordre, Marianne
Aase, Heidi
Reichborn-Kjennerud, Ted
Zeiner, Pal
author_facet Oerbeck, Beate
Overgaard, Kristin Romvig
Aspenes, Stian Thoresen
Pripp, Are Hugo
Mordre, Marianne
Aase, Heidi
Reichborn-Kjennerud, Ted
Zeiner, Pal
author_sort Oerbeck, Beate
collection PubMed
description BACKGROUND: Cohort studies often report findings on children with Attention Deficit Hyperactivity Disorder (ADHD) but may be biased by self-selection. The representativeness of cohort studies needs to be investigated to determine whether their findings can be generalised to the general child population. The aim of the present study was to examine the representativeness of child ADHD in the Norwegian Mother and Child Cohort Study (MoBa). METHODS: The study population was children born between January 1, 2000 and December 31, 2008 registered with hyperkinetic disorders (hereafter ADHD) in the Norwegian Patient Registry during the years 2008–2013, and two groups of children with ADHD were identified in: 1. MoBa and 2. The general child population. We used the multiaxial International Classification of Diseases (ICD-10) and compared the proportions of comorbid disorders (axes I–III), abnormal psychosocial situations (axis V) and child global functioning (axis VI) between these two groups. We also compared the relative differences in the multiaxial classifications for boys and girls and for children with/without axis I comorbidity, respectively in these two groups of children with ADHD. RESULTS: A total of 11 119 children were registered with ADHD, with significantly fewer in MoBa (1.45%) than the general child population (2.11%), p < 0.0001. The proportions of comorbid axis I, II, and III disorders were low, with no significant group differences. Compared with the general child population with ADHD, children with ADHD in MoBa were registered with fewer abnormal psychosocial situations (axis V: t = 7.63, p < .0001; d = -.18) and better child global functioning (axis VI: t = 7.93, p < 0.0001; d = .17). When analysing relative differences in the two groups, essentially the same patterns were found for boys and girls and for children with/without axis I comorbidity. CONCLUSIONS: Self-selection was found to affect the proportions of ADHD, psychosocial adversity and child global functioning in the cohort. However, the differences from the general population were small. This indicates that studies on ADHD and multiaxial classifications in MoBa, as well as other cohort studies with similar self-selection biases, may have reasonable generalisability to the general child population.
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spelling pubmed-52403792017-01-19 ADHD, comorbid disorders and psychosocial functioning: How representative is a child cohort study? Findings from a national patient registry Oerbeck, Beate Overgaard, Kristin Romvig Aspenes, Stian Thoresen Pripp, Are Hugo Mordre, Marianne Aase, Heidi Reichborn-Kjennerud, Ted Zeiner, Pal BMC Psychiatry Research Article BACKGROUND: Cohort studies often report findings on children with Attention Deficit Hyperactivity Disorder (ADHD) but may be biased by self-selection. The representativeness of cohort studies needs to be investigated to determine whether their findings can be generalised to the general child population. The aim of the present study was to examine the representativeness of child ADHD in the Norwegian Mother and Child Cohort Study (MoBa). METHODS: The study population was children born between January 1, 2000 and December 31, 2008 registered with hyperkinetic disorders (hereafter ADHD) in the Norwegian Patient Registry during the years 2008–2013, and two groups of children with ADHD were identified in: 1. MoBa and 2. The general child population. We used the multiaxial International Classification of Diseases (ICD-10) and compared the proportions of comorbid disorders (axes I–III), abnormal psychosocial situations (axis V) and child global functioning (axis VI) between these two groups. We also compared the relative differences in the multiaxial classifications for boys and girls and for children with/without axis I comorbidity, respectively in these two groups of children with ADHD. RESULTS: A total of 11 119 children were registered with ADHD, with significantly fewer in MoBa (1.45%) than the general child population (2.11%), p < 0.0001. The proportions of comorbid axis I, II, and III disorders were low, with no significant group differences. Compared with the general child population with ADHD, children with ADHD in MoBa were registered with fewer abnormal psychosocial situations (axis V: t = 7.63, p < .0001; d = -.18) and better child global functioning (axis VI: t = 7.93, p < 0.0001; d = .17). When analysing relative differences in the two groups, essentially the same patterns were found for boys and girls and for children with/without axis I comorbidity. CONCLUSIONS: Self-selection was found to affect the proportions of ADHD, psychosocial adversity and child global functioning in the cohort. However, the differences from the general population were small. This indicates that studies on ADHD and multiaxial classifications in MoBa, as well as other cohort studies with similar self-selection biases, may have reasonable generalisability to the general child population. BioMed Central 2017-01-17 /pmc/articles/PMC5240379/ /pubmed/28095819 http://dx.doi.org/10.1186/s12888-017-1204-7 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Oerbeck, Beate
Overgaard, Kristin Romvig
Aspenes, Stian Thoresen
Pripp, Are Hugo
Mordre, Marianne
Aase, Heidi
Reichborn-Kjennerud, Ted
Zeiner, Pal
ADHD, comorbid disorders and psychosocial functioning: How representative is a child cohort study? Findings from a national patient registry
title ADHD, comorbid disorders and psychosocial functioning: How representative is a child cohort study? Findings from a national patient registry
title_full ADHD, comorbid disorders and psychosocial functioning: How representative is a child cohort study? Findings from a national patient registry
title_fullStr ADHD, comorbid disorders and psychosocial functioning: How representative is a child cohort study? Findings from a national patient registry
title_full_unstemmed ADHD, comorbid disorders and psychosocial functioning: How representative is a child cohort study? Findings from a national patient registry
title_short ADHD, comorbid disorders and psychosocial functioning: How representative is a child cohort study? Findings from a national patient registry
title_sort adhd, comorbid disorders and psychosocial functioning: how representative is a child cohort study? findings from a national patient registry
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5240379/
https://www.ncbi.nlm.nih.gov/pubmed/28095819
http://dx.doi.org/10.1186/s12888-017-1204-7
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