Literature DB >> 32961619

Overnight switch from rasagiline to safinamide in Parkinson's disease patients with motor fluctuations: a tolerability and safety study.

F Stocchi1,2, L Vacca1, P Grassini1, C Tomino2, G Caminiti3, M Casali1, V D'Antoni3, M Volterrani3, M Torti1.   

Abstract

BACKGROUND AND
PURPOSE: When switching between monoamine oxidase type B (MAO-B) inhibitors, a 15-day suspension period is a precautionary measure to avoid a serotonin syndrome and hypertensive crisis. However, this indication results in a major inconvenience for parkinsonian patients because of the worsening of their clinical condition. In routine clinical practice, neurologists often perform a substitution of these two drugs without solution of continuity (i.e. overnight), to avoid worsening of fluctuations and prolonged OFF periods. Therefore, a safety open label study was performed to investigate the possible risks of switching overnight from rasagiline to safinamide.
METHODS: The study population included 20 advanced patients with Parkinson's disease on stable treatment with rasagiline and levodopa (alone or in combination with other anti-parkinsonian medication). The possible occurrence of serotonin syndrome and hypertension was monitored through a strict clinical observation and a 24-h Holter recording (ABPM) performed twice, whilst subjects were on rasagiline and immediately after switching to safinamide.
RESULTS: No cases of serotonin syndrome or hypertensive crisis occurred during the study. Changes that were not significant occurred in the primary end-point: 24-h mean blood pressure (BP) had a mild +4.4% increase in the ABPM2 versus ABPM1 (P = 0.17), 24-h systolic and diastolic BP values were slightly higher at ABPM2 compared to ABPM1 (respectively +3.3%, P = 0.13; and 5.4%, P = 0.08) and 24-h systolic BP variability was unchanged between the two ABPM evaluations (from 8.6 ± 2.9 to 8.9 ± 1.8; P = 0.27).
CONCLUSION: The results of the present study confirm that the overnight switch from rasagiline to safinamide is safe and well tolerated by patients.
© 2020 European Academy of Neurology.

Entities:  

Keywords:  MAO-B inhibitors; Parkinson's disease; blood pressure; overnight switch; serotonin syndrome

Year:  2020        PMID: 32961619     DOI: 10.1111/ene.14552

Source DB:  PubMed          Journal:  Eur J Neurol        ISSN: 1351-5101            Impact factor:   6.089


  4 in total

1.  Safinamide in the treatment pathway of Parkinson's Disease: a European Delphi Consensus.

Authors:  Fabrizio Stocchi; Angelo Antonini; Daniela Berg; Bruno Bergmans; Wolfgang Jost; Regina Katzenschlager; Jaime Kulisevsky; Per Odin; Francesc Valldeoriola; K Ray Chaudhuri
Journal:  NPJ Parkinsons Dis       Date:  2022-02-21

2.  Prescription Pattern of Monoamine Oxidase B Inhibitors Combined with Levodopa: A Retrospective Observational Analysis of Italian Healthcare Administrative Databases.

Authors:  Giulia Ronconi; Silvia Calabria; Carlo Piccinni; Letizia Dondi; Antonella Pedrini; Immacolata Esposito; Alice Addesi; Luisa Sambati; Nello Martini
Journal:  Drugs Real World Outcomes       Date:  2022-06-13

3.  Collective Expert Perspectives on the Use of Safinamide as Adjunctive Therapy for Parkinson's Disease: Online-Based Delphi Survey.

Authors:  Atsushi Takeda; Yoshio Tsuboi; Masahiro Nomoto; Hideki Mochizuki; Nobutaka Hattori
Journal:  Parkinsons Dis       Date:  2022-07-15

Review 4.  The Current Evidence for the Use of Safinamide for the Treatment of Parkinson's Disease.

Authors:  Giovanni Abbruzzese; Paolo Barone; Leonardo Lopiano; Fabrizio Stocchi
Journal:  Drug Des Devel Ther       Date:  2021-06-10       Impact factor: 4.162

  4 in total

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