Transdermal rivastigmine: management of cutaneous adverse events and review of the literature.
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| Title: | Transdermal rivastigmine: management of cutaneous adverse events and review of the literature. |
|---|---|
| Authors: | Greenspoon J (AUTHOR), Herrmann N (AUTHOR), Adam DN (AUTHOR), Greenspoon, Jill (AUTHOR), Herrmann, Nathan (AUTHOR), Adam, David N (AUTHOR) |
| Source: | CNS Drugs. 2011, Vol. 25 Issue 7, p575-583. 9p. |
| Abstract: | Alzheimer's disease is a chronic neurodegenerative disorder resulting in part from the degeneration of cholinergic neurons in the brain. Rivastigmine, a cholinesterase inhibitor, is commonly used as a treatment for dementia due to its ability to moderate cholinergic neurotransmission; however, treatment with oral rivastigmine can lead to gastrointestinal adverse effects such as nausea and vomiting. Transdermal administration of rivastigmine can minimize these adverse effects by providing continuous delivery of the medication, while maintaining the effectiveness of the oral treatment. While the transdermal form of rivastigmine has been found to have fewer systemic adverse effects compared with the oral form, cutaneous reactions, such as contact dermatitis, can lead to discontinuation of the drug in its transdermal form. Lack of patient compliance with regard to applying the patch to the designated site, applying the patch for the correct length of time or rotating patch application sites increases the risk of cutaneous adverse reactions. This article outlines the diagnosis and management of irritant contact dermatitis and allergic contact dermatitis secondary to transdermal rivastigmine. The large majority of reactions to transdermal patches are of an irritant type, which can be diagnosed clinically by the presence of a pruritic, erythematous, eczematous plaque strictly confined to the borders of the patch. In contrast, an allergic reaction can be differentiated by the presence of vesicles and/or oedema, erythema beyond the boundaries of the transdermal patch and lack of improvement of the lesion 48 hours after removal of the offending treatment. By encouraging the patient to follow a regular rotation schedule for the patch, and using lipid-based emollients for irritant dermatitis and pre- and post-treatment topical corticosteroids for allergic dermatitis, cutaneous reactions can often be alleviated and patients can continue with their medication regimen. Other simple changes to a patient's treatment routine, including minimizing the use of harsh soaps, avoiding recently shaven or damaged areas of skin and carefully removing the patch after use, can help to further decrease the risk of dermatitis development. [ABSTRACT FROM AUTHOR] |
| Copyright of CNS Drugs is the property of Springer Nature and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.) | |
| Database: | Psychology and Behavioral Sciences Collection |
| FullText | Text: Availability: 0 |
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| Header | DbId: pbh DbLabel: Psychology and Behavioral Sciences Collection An: 104650518 AccessLevel: 6 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.2165/11592230-000000000-00000 Languages: – Code: eng Text: English PhysicalDescription: Pagination: PageCount: 9 StartPage: 575 Titles: – TitleFull: Transdermal rivastigmine: management of cutaneous adverse events and review of the literature. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Greenspoon J – PersonEntity: Name: NameFull: Herrmann N – PersonEntity: Name: NameFull: Adam DN – PersonEntity: Name: NameFull: Greenspoon, Jill – PersonEntity: Name: NameFull: Herrmann, Nathan – PersonEntity: Name: NameFull: Adam, David N IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 07 Text: 2011 Type: published Y: 2011 Identifiers: – Type: issn-print Value: 11727047 Numbering: – Type: volume Value: 25 – Type: issue Value: 7 Titles: – TitleFull: CNS Drugs Type: main |
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