2007
DOI: 10.1345/aph.1h113
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Rotigotine: Transdermal Dopamine Agonist Treatment of Parkinson's Disease and Restless Legs Syndrome

Abstract: Longer trials are required to determine whether transdermal rotigotine will reduce development of dyskinesias and motor fluctuations in Parkinson's disease and augmentation and rebound in RLS by preventing pulsatile dopamine stimulation associated with levodopa and other dopamine agonists.

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Cited by 62 publications
(12 citation statements)
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“…Donepezil, pramipexole and L -dopa have also been reported to be effective, though experience is limited to case reports [65, 66]. Restless legs syndrome is readily responsive to DAs [67, 68]. Use of hypnotics should be limited to cases that do not respond to behavioral modifications and other measures, as there are no efficacy data for specific hypnotic agents in PD.…”
Section: Treatment Of Non-motor Symptomsmentioning
confidence: 99%
“…Donepezil, pramipexole and L -dopa have also been reported to be effective, though experience is limited to case reports [65, 66]. Restless legs syndrome is readily responsive to DAs [67, 68]. Use of hypnotics should be limited to cases that do not respond to behavioral modifications and other measures, as there are no efficacy data for specific hypnotic agents in PD.…”
Section: Treatment Of Non-motor Symptomsmentioning
confidence: 99%
“…Levodopa's short elimination half-life causes fluctuating plasma concentrations that are closely correlated with motor performance [27]. Rotigotine (Neupro; Schwarz Pharma, Monheim, Germany), a nonergolinic dopamine agonist, is newly approved for treating early-stage idiopathic Parkinson's disease [28]. Neupro is a transdermal delivery system that provides rotigotine continuously over a 24-hour period [29].…”
Section: New Drugs In Psychiatry and Neurologymentioning
confidence: 99%
“…However, the transdermal delivery system bypasses the gastrointestinal system and provides constant systemic levels. Rotigotine is dispersed in a silicone adhesive and spread evenly over the silicone backing of the patch [25]. In a study in which eight healthy volunteers were exposed to rotigotine transdermal patch (2.0 mg/24 h), the median peak plasma concentration was 0.215 ng/ml [26].…”
Section: Pharmacology and Pharmacokineticsmentioning
confidence: 99%
“…In the liver, rotigotine undergoes extensive metabolism by means of conjugation (sulfation, glucuronidation) or catalysis by the P450 cytochrome system [25]. Inactive metabolites are excreted primarily in urine (∼ 71%) and to a lesser degree in feces [30][31][32].…”
Section: Pharmacology and Pharmacokineticsmentioning
confidence: 99%
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