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Methylphenidate for attention-deficit/hyperactivity disorder in children and adolescents: Cochrane systematic review with meta-analyses and trial sequential analyses of randomised clinical trials

Study question Is methylphenidate beneficial or harmful for the treatment of attention-deficit/hyperactivity disorder (ADHD) in children and adolescents? Methods Electronic databases were searched up to February 2015 for parallel and crossover randomised clinical trials comparing methylphenidate wit...

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Autores principales: Storebø, Ole Jakob, Krogh, Helle B, Ramstad, Erica, Moreira-Maia, Carlos R, Holmskov, Mathilde, Skoog, Maria, Nilausen, Trine Danvad, Magnusson, Frederik L, Zwi, Morris, Gillies, Donna, Rosendal, Susanne, Groth, Camilla, Rasmussen, Kirsten Buch, Gauci, Dorothy, Kirubakaran, Richard, Forsbøl, Bente, Simonsen, Erik, Gluud, Christian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group Ltd. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4659414/
https://www.ncbi.nlm.nih.gov/pubmed/26608309
http://dx.doi.org/10.1136/bmj.h5203
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author Storebø, Ole Jakob
Krogh, Helle B
Ramstad, Erica
Moreira-Maia, Carlos R
Holmskov, Mathilde
Skoog, Maria
Nilausen, Trine Danvad
Magnusson, Frederik L
Zwi, Morris
Gillies, Donna
Rosendal, Susanne
Groth, Camilla
Rasmussen, Kirsten Buch
Gauci, Dorothy
Kirubakaran, Richard
Forsbøl, Bente
Simonsen, Erik
Gluud, Christian
author_facet Storebø, Ole Jakob
Krogh, Helle B
Ramstad, Erica
Moreira-Maia, Carlos R
Holmskov, Mathilde
Skoog, Maria
Nilausen, Trine Danvad
Magnusson, Frederik L
Zwi, Morris
Gillies, Donna
Rosendal, Susanne
Groth, Camilla
Rasmussen, Kirsten Buch
Gauci, Dorothy
Kirubakaran, Richard
Forsbøl, Bente
Simonsen, Erik
Gluud, Christian
author_sort Storebø, Ole Jakob
collection PubMed
description Study question Is methylphenidate beneficial or harmful for the treatment of attention-deficit/hyperactivity disorder (ADHD) in children and adolescents? Methods Electronic databases were searched up to February 2015 for parallel and crossover randomised clinical trials comparing methylphenidate with placebo or no intervention in children and adolescents with ADHD. Meta-analyses and trial sequential analyses (TSA) were conducted. Quality was assessed using GRADE. Teachers, parents, and observers rated ADHD symptoms and general behaviour. Study answer and limitations The analyses included 38 parallel group trials (n=5111, median treatment duration 49 days) and 147 crossover trials (n=7134, 14 days). The average age across all studies was 9.7 years. The analysis suggested a beneficial effect of methylphenidate on teacher rated symptoms in 19 parallel group trials (standardised mean difference (SMD) −0.77, n=1698), corresponding to a mean difference of −9.6 points on the ADHD rating scale. There was no evidence that methylphenidate was associated with an increase in serious adverse events (risk ratio 0.98, nine trials, n=1532; TSA adjusted intervention effect RR 0.91). Methylphenidate was associated with an increased risk of non-serious adverse events (1.29, 21 trials, n=3132; TSA adjusted RR 1.29). Teacher rated general behaviour seemed to improve with methylphenidate (SMD −0.87, five trials, n=668) A change of 7 points on the child health questionnaire (CHQ) has been deemed a minimal clinically relevant difference. The change reported in a meta-analysis of three trials corresponds to a mean difference of 8.0 points on the CHQ (range 0-100 points), which suggests that methylphenidate may improve parent reported quality of life (SMD 0.61, three trials, n=514). 96.8% of trials were considered high risk of bias trials according to the Cochrane guidelines. All outcomes were assessed very low quality according to GRADE. What this study adds The results suggest that among children and adolescents with a diagnosis of ADHD, methylphenidate may improve teacher reported symptoms of ADHD and general behaviour and parent reported quality of life. However, given the risk of bias in the included studies, and the very low quality of outcomes, the magnitude of the effects is uncertain. Methylphenidate is associated with an increased risk of non-serious but not serious adverse events. Funding, competing interests, data sharing Region Zealand Research Foundation and Copenhagen Trial Unit. Competing interests are given in the full paper on bmj.com. Full data are available in the version of this review published in The Cochrane Library.
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spelling pubmed-46594142015-12-01 Methylphenidate for attention-deficit/hyperactivity disorder in children and adolescents: Cochrane systematic review with meta-analyses and trial sequential analyses of randomised clinical trials Storebø, Ole Jakob Krogh, Helle B Ramstad, Erica Moreira-Maia, Carlos R Holmskov, Mathilde Skoog, Maria Nilausen, Trine Danvad Magnusson, Frederik L Zwi, Morris Gillies, Donna Rosendal, Susanne Groth, Camilla Rasmussen, Kirsten Buch Gauci, Dorothy Kirubakaran, Richard Forsbøl, Bente Simonsen, Erik Gluud, Christian BMJ Research Study question Is methylphenidate beneficial or harmful for the treatment of attention-deficit/hyperactivity disorder (ADHD) in children and adolescents? Methods Electronic databases were searched up to February 2015 for parallel and crossover randomised clinical trials comparing methylphenidate with placebo or no intervention in children and adolescents with ADHD. Meta-analyses and trial sequential analyses (TSA) were conducted. Quality was assessed using GRADE. Teachers, parents, and observers rated ADHD symptoms and general behaviour. Study answer and limitations The analyses included 38 parallel group trials (n=5111, median treatment duration 49 days) and 147 crossover trials (n=7134, 14 days). The average age across all studies was 9.7 years. The analysis suggested a beneficial effect of methylphenidate on teacher rated symptoms in 19 parallel group trials (standardised mean difference (SMD) −0.77, n=1698), corresponding to a mean difference of −9.6 points on the ADHD rating scale. There was no evidence that methylphenidate was associated with an increase in serious adverse events (risk ratio 0.98, nine trials, n=1532; TSA adjusted intervention effect RR 0.91). Methylphenidate was associated with an increased risk of non-serious adverse events (1.29, 21 trials, n=3132; TSA adjusted RR 1.29). Teacher rated general behaviour seemed to improve with methylphenidate (SMD −0.87, five trials, n=668) A change of 7 points on the child health questionnaire (CHQ) has been deemed a minimal clinically relevant difference. The change reported in a meta-analysis of three trials corresponds to a mean difference of 8.0 points on the CHQ (range 0-100 points), which suggests that methylphenidate may improve parent reported quality of life (SMD 0.61, three trials, n=514). 96.8% of trials were considered high risk of bias trials according to the Cochrane guidelines. All outcomes were assessed very low quality according to GRADE. What this study adds The results suggest that among children and adolescents with a diagnosis of ADHD, methylphenidate may improve teacher reported symptoms of ADHD and general behaviour and parent reported quality of life. However, given the risk of bias in the included studies, and the very low quality of outcomes, the magnitude of the effects is uncertain. Methylphenidate is associated with an increased risk of non-serious but not serious adverse events. Funding, competing interests, data sharing Region Zealand Research Foundation and Copenhagen Trial Unit. Competing interests are given in the full paper on bmj.com. Full data are available in the version of this review published in The Cochrane Library. BMJ Publishing Group Ltd. 2015-11-25 /pmc/articles/PMC4659414/ /pubmed/26608309 http://dx.doi.org/10.1136/bmj.h5203 Text en © Storebø et al 2015 http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/.
spellingShingle Research
Storebø, Ole Jakob
Krogh, Helle B
Ramstad, Erica
Moreira-Maia, Carlos R
Holmskov, Mathilde
Skoog, Maria
Nilausen, Trine Danvad
Magnusson, Frederik L
Zwi, Morris
Gillies, Donna
Rosendal, Susanne
Groth, Camilla
Rasmussen, Kirsten Buch
Gauci, Dorothy
Kirubakaran, Richard
Forsbøl, Bente
Simonsen, Erik
Gluud, Christian
Methylphenidate for attention-deficit/hyperactivity disorder in children and adolescents: Cochrane systematic review with meta-analyses and trial sequential analyses of randomised clinical trials
title Methylphenidate for attention-deficit/hyperactivity disorder in children and adolescents: Cochrane systematic review with meta-analyses and trial sequential analyses of randomised clinical trials
title_full Methylphenidate for attention-deficit/hyperactivity disorder in children and adolescents: Cochrane systematic review with meta-analyses and trial sequential analyses of randomised clinical trials
title_fullStr Methylphenidate for attention-deficit/hyperactivity disorder in children and adolescents: Cochrane systematic review with meta-analyses and trial sequential analyses of randomised clinical trials
title_full_unstemmed Methylphenidate for attention-deficit/hyperactivity disorder in children and adolescents: Cochrane systematic review with meta-analyses and trial sequential analyses of randomised clinical trials
title_short Methylphenidate for attention-deficit/hyperactivity disorder in children and adolescents: Cochrane systematic review with meta-analyses and trial sequential analyses of randomised clinical trials
title_sort methylphenidate for attention-deficit/hyperactivity disorder in children and adolescents: cochrane systematic review with meta-analyses and trial sequential analyses of randomised clinical trials
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4659414/
https://www.ncbi.nlm.nih.gov/pubmed/26608309
http://dx.doi.org/10.1136/bmj.h5203
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