2010
DOI: 10.1111/j.1755-5949.2010.00141.x
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Drug Profile: Transdermal Rivastigmine Patch in the Treatment of Alzheimer Disease

Abstract: Cholinesterase inhibitors constitute one of the mainstays of treatment of Alzheimer disease (AD). Gastrointestinal side effects, difficulty accessing therapeutic doses and poor patient compliance have been identified as barriers to effective treatment with these substances. The rivastigmine transdermal patch provides continuous delivery of drug through the skin into the bloodstream, avoiding the fluctuations in plasma concentration associated with oral administration. This pharmacokinetic profile is associated… Show more

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Cited by 28 publications
(23 citation statements)
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“…Authors have alleged that, in general, patches would be advantageous for informal caregivers providing care at home [13,15,19,20,37,38,39]. However, in this study, almost every institutionalized patient received rivastigmine by transdermal route.…”
Section: Discussionmentioning
confidence: 83%
“…Authors have alleged that, in general, patches would be advantageous for informal caregivers providing care at home [13,15,19,20,37,38,39]. However, in this study, almost every institutionalized patient received rivastigmine by transdermal route.…”
Section: Discussionmentioning
confidence: 83%
“…Recently, for rivastigmine, a transdermal formulation (‘patch’) has been introduced [10]. Potential advantages were shown, such as improved drug delivery due to different pharmacokinetic features, and better tolerability [11,12,13]. The claim of ease of administration is particularly interesting regarding the caregiver burden.…”
Section: Introductionmentioning
confidence: 99%
“…This formulation provides smooth and continuous drug delivery through the skin and into the bloodstream, avoiding first‐pass effects in the gut and the liver 12 . The indication for rivastigmine transdermal patch is the symptomatic treatment of mild to moderate Alzheimer's dementia 13 . With this formulation, trough levels at steady state are approximately 50% of peak levels, in contrast to oral administration, with which concentrations fall off to virtually zero between doses.…”
Section: Introductionmentioning
confidence: 99%