A prospective study on the use of rivastigmine transdermal patch in Alzheimer's dementia in a routine clinical setting

Abstract

There is not much published literature on the use of rivastigmine patch in a “routine” clinical setting.ObjectivesIn this naturalistic longitudinal observational study we sought to evaluate the safety, tolerability and efficacy of the rivastigmine patch in patients with early and late onset moderate Alzheimer’s disease in a routine clinical setting.MethodsOut of all routine clinical referrals, the first 30 patients with diagnosis of moderate Alzheimer’s dementia who were started on rivastigmine patch were included in the study. Rivastigmine patch dose was titrated from 4.6 to 9.5mg/24 hours as appropriate. The primary outcome measure was safety and tolerability, measured by the incidence of adverse events and discontinuation due to any reason. The secondary outcome measure was to examine improvement on global, functional and behavioral domains as demonstrated by the MMSE (Mini Mental State Examination) score, BADLS (Bristol Activities of Daily Living Skills) score, patient and carer feedback and clinical judgment.ResultsAdverse events were reported in 20% of patients and 10% of total patients needed discontinuation of treatment. Improvement on global, functional and behavioral domains was observed in two thirds of patients whereas one third showed a relative decline. The most common side effect was skin irritation or erythema.ConclusionsThe rivastigmine transdermal patch may provide a treatment option for those patients who require a change in their current oral cholinesterase inhibitor therapy due to safety or tolerability concerns.

Cognitive, functional and behavioral assessment: Alzheimer's disease

“… 41 However, only one study analyzing its application in AD patients was identified. 42 The BADL was used in studies of dementia patients 43 , 44 but no studies on its adaptation or validation for use in the Brazilian population were available.…”