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1000 Titel
  • Methylphenidate treatment of adult ADHD patients improves the degree of ADHD severity under routine conditions
1000 Autor/in
  1. Retz, Wolfgang |
  2. Rösler, Michael |
  3. Fischer, Roland |
  4. Ose, Claudia |
  5. Ammer, Richard |
1000 Erscheinungsjahr 2020
1000 Publikationstyp
  1. Artikel |
1000 Online veröffentlicht
  • 2020-09-03
1000 Erschienen in
1000 Quellenangabe
  • 127(10):1427-1434
1000 Copyrightjahr
  • 2020
1000 Lizenz
1000 Verlagsversion
  • https://doi.org/10.1007/s00702-020-02226-7 |
  • https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7497302/ |
1000 Publikationsstatus
1000 Sprache der Publikation
1000 Abstract/Summary
  • Attention-deficit hyperactivity disorder (ADHD) is associated with substantial personal and social impairments. Besides psychosocial interventions, current guidelines recommend a therapy with methylphenidate (MPH). This prospective, non-interventional study aims to investigate the efficacy and tolerability of MPH treatment of adult ADHD patients in a real-world setting. 468 adult patients with newly diagnosed ADHD were observed for 12-14 weeks. Primary efficacy endpoint was the clinical global impression (CGI) by the physician. Secondary endpoints comprise patient evaluation (Wender-Reimherr self-report, WR-SR), safety, tolerability, and dosage of MPH. With a mean daily dose of 35.8 (±17.0) mg MPH, the population of patients being severely/most extremely ill or markedly ill decreased by 64% and 61%, respectively. According to physicians' assessment (CGI), 74.5% of patients were identified as treatment responders. The total score of patient-based assessment (WR-SR) improved by 23.5% (50.1 ± 40.3 points) with the most profound improvement in attention deficit (-30.0%), disorganization (-26.6%), and hyperactivity / unrest (-23.3%). Self-evaluation revealed a responder rate of 35.4%. In summary, MPH treatment improves the degree of ADHD severity under routine conditions. In addition, activities of daily living were facilitated when taking MPH. The rather poor responder rates determined by patient assessment as well as the comparatively low applied mean daily dose of 35.8 mg (median 40 mg) indicate sub-optimal dosing under routine conditions, not exploiting the full beneficial therapeutic potential of MPH.
1000 Sacherschließung
lokal Double-Blind Method [MeSH]
lokal Adult [MeSH]
lokal Humans [MeSH]
lokal Prospective Studies [MeSH]
lokal Methylphenidate/therapeutic use [MeSH]
lokal Treatment Outcome [MeSH]
lokal Delayed-Action Preparations/therapeutic use [MeSH]
lokal Methylphenidate
lokal Symptoms relief
lokal Efficacy
lokal Attention Deficit Disorder with Hyperactivity/drug therapy [MeSH]
lokal Activities of Daily Living [MeSH]
lokal Psychiatry and Preclinical Psychiatric Studies - Original Article
lokal Dosage
lokal ADHD therapy
lokal Tolerability
lokal Central Nervous System Stimulants/therapeutic use [MeSH]
1000 Liste der Beteiligten
  1. https://frl.publisso.de/adhoc/uri/UmV0eiwgV29sZmdhbmc=|https://frl.publisso.de/adhoc/uri/UsO2c2xlciwgTWljaGFlbA==|https://frl.publisso.de/adhoc/uri/RmlzY2hlciwgUm9sYW5k|https://frl.publisso.de/adhoc/uri/T3NlLCBDbGF1ZGlh|https://orcid.org/0000-0003-0167-4894
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1000 Erstellt am 2023-11-18T05:58:22.271+0100
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