Cargando…

Treatment with Methylphenidate for Attention Deficit Hyperactivity Disorder (ADHD) and the Risk of All-Cause Poisoning in Children and Adolescents: A Self-Controlled Case Series Study

BACKGROUND: Children and adolescents with attention deficit hyperactivity disorder (ADHD) are at higher risk of all-cause poisoning by drugs and chemicals (intentional or accidental). Currently, there is limited data on whether medication treatment for ADHD can reduce the risk of all-cause poisoning...

Descripción completa

Detalles Bibliográficos
Autores principales: Gao, Le, Man, Kenneth K. C., Chan, Esther W., Chui, Celine S. L., Li, Xue, Coghill, David, Hon, Kam Lun, Tse, Man Li, Lum, Terry Y. S., Wong, Kirstie H. T. W., Ip, Patrick, Wong, Ian C. K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8310501/
https://www.ncbi.nlm.nih.gov/pubmed/34283391
http://dx.doi.org/10.1007/s40263-021-00824-x
_version_ 1783728776561033216
author Gao, Le
Man, Kenneth K. C.
Chan, Esther W.
Chui, Celine S. L.
Li, Xue
Coghill, David
Hon, Kam Lun
Tse, Man Li
Lum, Terry Y. S.
Wong, Kirstie H. T. W.
Ip, Patrick
Wong, Ian C. K.
author_facet Gao, Le
Man, Kenneth K. C.
Chan, Esther W.
Chui, Celine S. L.
Li, Xue
Coghill, David
Hon, Kam Lun
Tse, Man Li
Lum, Terry Y. S.
Wong, Kirstie H. T. W.
Ip, Patrick
Wong, Ian C. K.
author_sort Gao, Le
collection PubMed
description BACKGROUND: Children and adolescents with attention deficit hyperactivity disorder (ADHD) are at higher risk of all-cause poisoning by drugs and chemicals (intentional or accidental). Currently, there is limited data on whether medication treatment for ADHD can reduce the risk of all-cause poisoning. METHODS: Patients aged 5–18 years with a methylphenidate (MPH) prescription and an incident poisoning diagnosis between January 2001 and June 2020 were identified from the Hong Kong Clinical Data Analysis and Reporting System. A self-controlled case series study design was used to compare the incidence rate ratios (IRRs) of all-cause poisoning during different risk windows (30 days before the first MPH prescription, exposure periods within 30 days of the first prescription, and periods of subsequent exposure) compared with the reference window (other non-exposure periods). RESULTS: 42,203 patients were prescribed ADHD medication in Hong Kong during the study period. Of these, 417 patients who had both an MPH prescription and poisoning incident recorded were included in the main analysis. Compared with other non-exposed periods, a higher risk of poisoning was found in the 30 days before the first prescription (IRR 2.64, 95% confidence interval [CI] 1.33–5.22) and exposure periods within 30 days of the first prescription (IRR 2.18, 95% CI 1.06–4.48), but not during prolonged exposure. However, compared with 30 days before the first prescription as well as exposure periods within 30 days of the first prescription, there was a lower risk during the subsequent exposure (IRRs 0.49 and 0.60, respectively). Similar results to the main analysis were also found in the subgroup analysis of intentional poisoning and females, but not in that of accidental poisoning and males. CONCLUSIONS: The risk of all-cause poisoning was higher shortly before and after the first MPH prescription and became lower during the subsequent prescription period. Our results do not support an association between the use of MPH and an increased risk of all-cause poisoning in children and adolescents and, in fact, suggest that longer-term use of MPH may be associated with a lower risk of all-cause poisoning, although this latter finding requires further study. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s40263-021-00824-x.
format Online
Article
Text
id pubmed-8310501
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Springer International Publishing
record_format MEDLINE/PubMed
spelling pubmed-83105012021-07-27 Treatment with Methylphenidate for Attention Deficit Hyperactivity Disorder (ADHD) and the Risk of All-Cause Poisoning in Children and Adolescents: A Self-Controlled Case Series Study Gao, Le Man, Kenneth K. C. Chan, Esther W. Chui, Celine S. L. Li, Xue Coghill, David Hon, Kam Lun Tse, Man Li Lum, Terry Y. S. Wong, Kirstie H. T. W. Ip, Patrick Wong, Ian C. K. CNS Drugs Original Research Article BACKGROUND: Children and adolescents with attention deficit hyperactivity disorder (ADHD) are at higher risk of all-cause poisoning by drugs and chemicals (intentional or accidental). Currently, there is limited data on whether medication treatment for ADHD can reduce the risk of all-cause poisoning. METHODS: Patients aged 5–18 years with a methylphenidate (MPH) prescription and an incident poisoning diagnosis between January 2001 and June 2020 were identified from the Hong Kong Clinical Data Analysis and Reporting System. A self-controlled case series study design was used to compare the incidence rate ratios (IRRs) of all-cause poisoning during different risk windows (30 days before the first MPH prescription, exposure periods within 30 days of the first prescription, and periods of subsequent exposure) compared with the reference window (other non-exposure periods). RESULTS: 42,203 patients were prescribed ADHD medication in Hong Kong during the study period. Of these, 417 patients who had both an MPH prescription and poisoning incident recorded were included in the main analysis. Compared with other non-exposed periods, a higher risk of poisoning was found in the 30 days before the first prescription (IRR 2.64, 95% confidence interval [CI] 1.33–5.22) and exposure periods within 30 days of the first prescription (IRR 2.18, 95% CI 1.06–4.48), but not during prolonged exposure. However, compared with 30 days before the first prescription as well as exposure periods within 30 days of the first prescription, there was a lower risk during the subsequent exposure (IRRs 0.49 and 0.60, respectively). Similar results to the main analysis were also found in the subgroup analysis of intentional poisoning and females, but not in that of accidental poisoning and males. CONCLUSIONS: The risk of all-cause poisoning was higher shortly before and after the first MPH prescription and became lower during the subsequent prescription period. Our results do not support an association between the use of MPH and an increased risk of all-cause poisoning in children and adolescents and, in fact, suggest that longer-term use of MPH may be associated with a lower risk of all-cause poisoning, although this latter finding requires further study. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s40263-021-00824-x. Springer International Publishing 2021-07-20 2021 /pmc/articles/PMC8310501/ /pubmed/34283391 http://dx.doi.org/10.1007/s40263-021-00824-x Text en © The Author(s) 2021 https://creativecommons.org/licenses/by-nc/4.0/Open AccessThis article is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License, which permits any non-commercial use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) .
spellingShingle Original Research Article
Gao, Le
Man, Kenneth K. C.
Chan, Esther W.
Chui, Celine S. L.
Li, Xue
Coghill, David
Hon, Kam Lun
Tse, Man Li
Lum, Terry Y. S.
Wong, Kirstie H. T. W.
Ip, Patrick
Wong, Ian C. K.
Treatment with Methylphenidate for Attention Deficit Hyperactivity Disorder (ADHD) and the Risk of All-Cause Poisoning in Children and Adolescents: A Self-Controlled Case Series Study
title Treatment with Methylphenidate for Attention Deficit Hyperactivity Disorder (ADHD) and the Risk of All-Cause Poisoning in Children and Adolescents: A Self-Controlled Case Series Study
title_full Treatment with Methylphenidate for Attention Deficit Hyperactivity Disorder (ADHD) and the Risk of All-Cause Poisoning in Children and Adolescents: A Self-Controlled Case Series Study
title_fullStr Treatment with Methylphenidate for Attention Deficit Hyperactivity Disorder (ADHD) and the Risk of All-Cause Poisoning in Children and Adolescents: A Self-Controlled Case Series Study
title_full_unstemmed Treatment with Methylphenidate for Attention Deficit Hyperactivity Disorder (ADHD) and the Risk of All-Cause Poisoning in Children and Adolescents: A Self-Controlled Case Series Study
title_short Treatment with Methylphenidate for Attention Deficit Hyperactivity Disorder (ADHD) and the Risk of All-Cause Poisoning in Children and Adolescents: A Self-Controlled Case Series Study
title_sort treatment with methylphenidate for attention deficit hyperactivity disorder (adhd) and the risk of all-cause poisoning in children and adolescents: a self-controlled case series study
topic Original Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8310501/
https://www.ncbi.nlm.nih.gov/pubmed/34283391
http://dx.doi.org/10.1007/s40263-021-00824-x
work_keys_str_mv AT gaole treatmentwithmethylphenidateforattentiondeficithyperactivitydisorderadhdandtheriskofallcausepoisoninginchildrenandadolescentsaselfcontrolledcaseseriesstudy
AT mankennethkc treatmentwithmethylphenidateforattentiondeficithyperactivitydisorderadhdandtheriskofallcausepoisoninginchildrenandadolescentsaselfcontrolledcaseseriesstudy
AT chanestherw treatmentwithmethylphenidateforattentiondeficithyperactivitydisorderadhdandtheriskofallcausepoisoninginchildrenandadolescentsaselfcontrolledcaseseriesstudy
AT chuicelinesl treatmentwithmethylphenidateforattentiondeficithyperactivitydisorderadhdandtheriskofallcausepoisoninginchildrenandadolescentsaselfcontrolledcaseseriesstudy
AT lixue treatmentwithmethylphenidateforattentiondeficithyperactivitydisorderadhdandtheriskofallcausepoisoninginchildrenandadolescentsaselfcontrolledcaseseriesstudy
AT coghilldavid treatmentwithmethylphenidateforattentiondeficithyperactivitydisorderadhdandtheriskofallcausepoisoninginchildrenandadolescentsaselfcontrolledcaseseriesstudy
AT honkamlun treatmentwithmethylphenidateforattentiondeficithyperactivitydisorderadhdandtheriskofallcausepoisoninginchildrenandadolescentsaselfcontrolledcaseseriesstudy
AT tsemanli treatmentwithmethylphenidateforattentiondeficithyperactivitydisorderadhdandtheriskofallcausepoisoninginchildrenandadolescentsaselfcontrolledcaseseriesstudy
AT lumterryys treatmentwithmethylphenidateforattentiondeficithyperactivitydisorderadhdandtheriskofallcausepoisoninginchildrenandadolescentsaselfcontrolledcaseseriesstudy
AT wongkirstiehtw treatmentwithmethylphenidateforattentiondeficithyperactivitydisorderadhdandtheriskofallcausepoisoninginchildrenandadolescentsaselfcontrolledcaseseriesstudy
AT ippatrick treatmentwithmethylphenidateforattentiondeficithyperactivitydisorderadhdandtheriskofallcausepoisoninginchildrenandadolescentsaselfcontrolledcaseseriesstudy
AT wongianck treatmentwithmethylphenidateforattentiondeficithyperactivitydisorderadhdandtheriskofallcausepoisoninginchildrenandadolescentsaselfcontrolledcaseseriesstudy