Lisdexamfetamine Dimesylate: A Review in Paediatric ADHD
Drugs, ISSN: 1179-1950, Vol: 78, Issue: 10, Page: 1025-1036
2018
- 17Citations
- 85Captures
- 1Mentions
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
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Metrics Details
- Citations17
- Citation Indexes16
- 16
- CrossRef1
- Policy Citations1
- Policy Citation1
- Captures85
- Readers85
- 85
- Mentions1
- References1
- Wikipedia1
Article Description
Lisdexamfetamine dimesylate (lisdexamfetamine; Elvanse; Tyvense), an orally-active dexamfetamine prodrug, is indicated in the EU for the treatment of attention-deficit hyperactivity disorder (ADHD) in children aged ≥ 6 years (including adolescents) when the response to previous methylphenidate (MPH) treatment is clinically inadequate. The original approval of the drug was based on the results of phase III trials in children and adolescents with ADHD who had an inadequate response to previous pharmacotherapy (e.g. MPH) or were treatment naïve. In these studies, short-term treatment with flexibly-dosed lisdexamfetamine demonstrated greater efficacy than atomoxetine, based on a prospective comparison, and osmotic-release oral system (OROS)-MPH, based on a post hoc comparison. Improvements in ADHD symptoms were accompanied by improvements in health-related quality of life and functioning that were maintained as long as treatment with lisdexamfetamine was continued in a long-term extension of one of these trials. In subsequent phase IV head-to-head studies in adolescents with ADHD and an inadequate response to previous pharmacotherapy, lisdexamfetamine demonstrated greater efficacy than OROS-MPH when both medications were force-titrated, but not when they were flexibly-titrated. Lisdexamfetamine was generally well tolerated, with an adverse event profile (e.g. decreased appetite, headache, weight reduction, insomnia and irritability) typical of that reported for other stimulants. Thus, lisdexamfetamine provides an alternative option for the treatment of children and/or adolescents with ADHD who have not responded adequately to previous ADHD pharmacotherapies.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85048827240&origin=inward; http://dx.doi.org/10.1007/s40265-018-0936-0; http://www.ncbi.nlm.nih.gov/pubmed/29923015; http://link.springer.com/10.1007/s40265-018-0936-0; https://dx.doi.org/10.1007/s40265-018-0936-0; https://link.springer.com/article/10.1007/s40265-018-0936-0
Springer Science and Business Media LLC
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