New and extended-action treatments in the management of ADHD: a critical appraisal of lisdexamfetamine in adults and children
Diana Domnitei, Vishal MadaanDepartment of Psychiatry, Creighton University Medical Center, Omaha, NE, USAAbstract: Treatment guidelines from the American Academy of Child and Adolescent Psychiatry and the American Academy of Pediatrics state that stimulant medications have the most evidence for saf...
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Dove Medical Press
2010
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oai:doaj.org-article:76a7b95d9d09471b84ee133aa3c5f4112021-12-02T02:34:00ZNew and extended-action treatments in the management of ADHD: a critical appraisal of lisdexamfetamine in adults and children1176-63281178-2021https://doaj.org/article/76a7b95d9d09471b84ee133aa3c5f4112010-05-01T00:00:00Zhttp://www.dovepress.com/new-and-extended-action-treatments-in-the-management-of-adhd-a-critica-a4457https://doaj.org/toc/1176-6328https://doaj.org/toc/1178-2021Diana Domnitei, Vishal MadaanDepartment of Psychiatry, Creighton University Medical Center, Omaha, NE, USAAbstract: Treatment guidelines from the American Academy of Child and Adolescent Psychiatry and the American Academy of Pediatrics state that stimulant medications have the most evidence for safety and efficacy in the treatment of childhood attention deficit hyperactivity disorder (ADHD). Longer-acting stimulants are thus considered as first-line for management of ADHD symptoms. Over the years, concerns about the abuse potential of stimulants have led to the development of alternative formulations of these agents. One such recent development, lisdexamfetamine (LDX) was FDA approved for treating ADHD in children in early 2007 and in adults in early 2008. LDX is a prodrug, which when orally ingested, is converted to l-lysine and active d-amphetamine, which is responsible for its therapeutic activity. This unique formulation may lead to a possible reduction of the abuse potential, by bypassing the first-pass metabolism. In fact, a statistically significant difference for the ‘liking’ effects on the Drug Questionnaire Response has been reported with intravenous LDX compared to d-amphetamine. LDX appears to have an efficacy and tolerability profile comparable to other extended-release stimulant formulations used to treat ADHD, but reduced potential for abuse-related liking effects when compared to equivalent amounts of immediate-release d-amphetamine. The most common adverse events include decreased appetite, insomnia, upper abdominal pain, headache, irritability, weight loss, and nausea.Keywords: lisdexamfetamine, attention deficit hyperactivity disorder, adults, children Diana DomniteiVishal MadaanDove Medical PressarticleNeurosciences. Biological psychiatry. NeuropsychiatryRC321-571Neurology. Diseases of the nervous systemRC346-429ENNeuropsychiatric Disease and Treatment, Vol 2010, Iss Issue 1, Pp 273-279 (2010) |
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Neurosciences. Biological psychiatry. Neuropsychiatry RC321-571 Neurology. Diseases of the nervous system RC346-429 |
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Neurosciences. Biological psychiatry. Neuropsychiatry RC321-571 Neurology. Diseases of the nervous system RC346-429 Diana Domnitei Vishal Madaan New and extended-action treatments in the management of ADHD: a critical appraisal of lisdexamfetamine in adults and children |
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Diana Domnitei, Vishal MadaanDepartment of Psychiatry, Creighton University Medical Center, Omaha, NE, USAAbstract: Treatment guidelines from the American Academy of Child and Adolescent Psychiatry and the American Academy of Pediatrics state that stimulant medications have the most evidence for safety and efficacy in the treatment of childhood attention deficit hyperactivity disorder (ADHD). Longer-acting stimulants are thus considered as first-line for management of ADHD symptoms. Over the years, concerns about the abuse potential of stimulants have led to the development of alternative formulations of these agents. One such recent development, lisdexamfetamine (LDX) was FDA approved for treating ADHD in children in early 2007 and in adults in early 2008. LDX is a prodrug, which when orally ingested, is converted to l-lysine and active d-amphetamine, which is responsible for its therapeutic activity. This unique formulation may lead to a possible reduction of the abuse potential, by bypassing the first-pass metabolism. In fact, a statistically significant difference for the ‘liking’ effects on the Drug Questionnaire Response has been reported with intravenous LDX compared to d-amphetamine. LDX appears to have an efficacy and tolerability profile comparable to other extended-release stimulant formulations used to treat ADHD, but reduced potential for abuse-related liking effects when compared to equivalent amounts of immediate-release d-amphetamine. The most common adverse events include decreased appetite, insomnia, upper abdominal pain, headache, irritability, weight loss, and nausea.Keywords: lisdexamfetamine, attention deficit hyperactivity disorder, adults, children |
format |
article |
author |
Diana Domnitei Vishal Madaan |
author_facet |
Diana Domnitei Vishal Madaan |
author_sort |
Diana Domnitei |
title |
New and extended-action treatments in the management of ADHD: a critical appraisal of lisdexamfetamine in adults and children |
title_short |
New and extended-action treatments in the management of ADHD: a critical appraisal of lisdexamfetamine in adults and children |
title_full |
New and extended-action treatments in the management of ADHD: a critical appraisal of lisdexamfetamine in adults and children |
title_fullStr |
New and extended-action treatments in the management of ADHD: a critical appraisal of lisdexamfetamine in adults and children |
title_full_unstemmed |
New and extended-action treatments in the management of ADHD: a critical appraisal of lisdexamfetamine in adults and children |
title_sort |
new and extended-action treatments in the management of adhd: a critical appraisal of lisdexamfetamine in adults and children |
publisher |
Dove Medical Press |
publishDate |
2010 |
url |
https://doaj.org/article/76a7b95d9d09471b84ee133aa3c5f411 |
work_keys_str_mv |
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