Literature DB >> 21904084

Exploring the impact of once-daily OROS® methylphenidate (MPH) on symptoms and quality of life in children and adolescents with ADHD transitioning from immediate-release MPH.

Andreas Kordon1, Kirsten Stollhoff, Käte Niederkirchner, Fritz Mattejat, Klaus Rettig, Barbara Schäuble.   

Abstract

OBJECTIVES: To explore the clinical and health-related quality of life (HRQoL) outcomes in children/adolescents with attention-deficit/hyperactivity disorder (ADHD) who required a therapy switch from immediate-release (IR) methylphenidate (MPH) and were initiated on Osmotic Release Oral System (OROS(®)) MPH.
METHODS: Prospective, noninterventional study including patients (aged 6-18 years) with a confirmed diagnosis of ADHD who transitioned from IR MPH to OROS(®) MPH based on medical needs. Patients were transitioned to OROS(®) MPH and were followed for 12 weeks. Attention-deficit/hyperactivity disorder symptoms, functional outcomes, HRQoL, and tolerability were assessed throughout the study.
RESULTS: 598 patients entered the intention-to-treat analysis. The mean OROS(®) MPH starting dose was 29.5 ± 12.0 mg/day, increasing slightly to 33.5 ± 13.2 mg/day at final visit. Compared with baseline, there were significant (all P < 0.0001) symptomatic, functional, and HRQoL improvements after transitioning from IR MPH to OROS(®) MPH as assessed by the Conners' Parent Rating Scale (from 29.0 ± 10.5 to 19.5 ± 11.1), Children's Global Assessment Scale (by 11.0 ± 13.3), and Inventory for Assessing Quality of Life (ILC) LQ0-28 scores (parents' rating from 17.2 ± 3.9 to 19.4 ± 4.0; patients' rating from 18.7 ± 4.0 to 20.5 ± 3.9). Overall, no significant changes in quality of sleep or appetite were observed. More than 70% of parents and physicians rated the effectiveness of OROS(®) MPH as at least "good" and were at least "satisfied" with OROS(®) MPH. The most common treatment-emergent adverse events were insomnia and anorexia. No clinically relevant changes in body weight or vital signs were observed.
CONCLUSIONS: In this naturalistic setting, transitioning from IR MPH to OROS(®) MPH, in patients who showed previously insufficient response and/or poor tolerability, was successful. Patients' and parents' HRQoL as well as burden of disease showed a clinically relevant improvement. OROS(®) MPH was generally safe and well tolerated.

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Year:  2011        PMID: 21904084     DOI: 10.3810/pgm.2011.09.2457

Source DB:  PubMed          Journal:  Postgrad Med        ISSN: 0032-5481            Impact factor:   3.840


  6 in total

Review 1.  A review of OROS methylphenidate (Concerta(®)) in the treatment of attention-deficit/hyperactivity disorder.

Authors:  Martin A Katzman; Tia Sternat
Journal:  CNS Drugs       Date:  2014-11       Impact factor: 5.749

2.  Improved functionality, health related quality of life and decreased burden of disease in patients with ADHD treated with OROS® MPH: is treatment response different between children and adolescents?

Authors:  Michael Berek; Andreas Kordon; Ludger Hargarter; Fritz Mattejat; Lara Slawik; Klaus Rettig; Barbara Schäuble
Journal:  Child Adolesc Psychiatry Ment Health       Date:  2011-07-26       Impact factor: 3.033

3.  Social adjustment and family function after drug switch from IR-methylphenidate to OROS-methylphenidate in patients with attention-deficit/hyperactivity disorder.

Authors:  Wen-Jiun Chou; Liang-Jen Wang; Chien-Ho Lin; Sun-Yuan Liang; Vincent Chin-Hung Chen; Yuh-Ming Hou; Rong-Rong Huang; Miao-Chun Chou; Chi-Yung Shang; Chi-Pui Ho; Meng-Chuan Lai
Journal:  Neuropsychiatr Dis Treat       Date:  2018-10-23       Impact factor: 2.570

Review 4.  Methylphenidate for attention deficit hyperactivity disorder (ADHD) in children and adolescents - assessment of adverse events in non-randomised studies.

Authors:  Ole Jakob Storebø; Nadia Pedersen; Erica Ramstad; Maja Lærke Kielsholm; Signe Sofie Nielsen; Helle B Krogh; Carlos R Moreira-Maia; Frederik L Magnusson; Mathilde Holmskov; Trine Gerner; Maria Skoog; Susanne Rosendal; Camilla Groth; Donna Gillies; Kirsten Buch Rasmussen; Dorothy Gauci; Morris Zwi; Richard Kirubakaran; Sasja J Håkonsen; Lise Aagaard; Erik Simonsen; Christian Gluud
Journal:  Cochrane Database Syst Rev       Date:  2018-05-09

5.  Brinp1(-/-) mice exhibit autism-like behaviour, altered memory, hyperactivity and increased parvalbumin-positive cortical interneuron density.

Authors:  James C Whisstock; Phillip I Bird; Susan R Berkowicz; Travis J Featherby; Zhengdong Qu; Aminah Giousoh; Natalie A Borg; Julian I Heng
Journal:  Mol Autism       Date:  2016-03-31       Impact factor: 7.509

6.  Hyperactive and impulsive behaviors of LMTK1 knockout mice.

Authors:  Miyuki Takahashi; Arika Sugiyama; Ran Wei; Shizuka Kobayashi; Kimiko Fukuda; Hironori Nishino; Roka Takahashi; Koji Tsutsumi; Ichiro Kita; Kanae Ando; Toshiya Manabe; Hiroyuki Kamiguchi; Mineko Tomomura; Shin-Ichi Hisanaga
Journal:  Sci Rep       Date:  2020-09-22       Impact factor: 4.379

  6 in total

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