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Safinamide in the treatment pathway of Parkinson’s Disease: a European Delphi Consensus
被引:0
|作者:
Fabrizio Stocchi
Angelo Antonini
Daniela Berg
Bruno Bergmans
Wolfgang Jost
Regina Katzenschlager
Jaime Kulisevsky
Per Odin
Francesc Valldeoriola
K. Ray Chaudhuri
机构:
[1] University and IRCCS San Raffaele Pisana,Department of Neurology
[2] Center for Rare Neurological Diseases (ERN-RND),Parkinson and Movement Disorders Unit
[3] Department of Neuroscience University of Padua,Department of Neurology, UKSH, Campus Kiel
[4] Christian-Albrechts-University Kiel,Department of Neurodegeneration
[5] Hertie-Institute of Clinical Brain Research Tübingen,Department of Neurology, AZ St
[6] Campus Brugge,Jan Brugge
[7] Ghent University Hospital,Oostende AV
[8] Parkinson-Klinik Ortenau,Department of Neurology
[9] Department of Neurology and Karl Landsteiner Institute for Neuroimmunological and Neurodegenerative Disorders Klinik Donaustadt,Movement Disorders Unit, Neurology Department
[10] Hospital de la Santa Creu i Sant Pau,Department of Medicine
[11] Autonomous University of Barcelona,Division of Neurology, Dept of Clinical Sciences Lund
[12] Centro de Investigación en Red sobre Enfermedades Neurodegenerativas (CIBERNED),Hospital Clinic de Barcelona, 16493, Movement Disorders Unit
[13] Lund University,Parkinson Foundation Centre of Excellence
[14] Universitat de Barcelona Institute of Neurosciences,undefined
[15] Institut d’Investigacions Biomèdiques August Pi i Sunyer,undefined
[16] Centro de Investigación Biomédica en Red sobre Enfermedades Neurodegenerativas,undefined
[17] Neurology Service,undefined
[18] King’s College Hospital and Kings College,undefined
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摘要:
Safinamide is a highly selective, reversible MAO B-inhibitor recently marketed in European and North American countries. To better define clinical indications regarding motor and non-motor symptoms, targeted population and safety of this compound, ten movement disorders specialists, experts in their field, convened and developed a panel of statements on: the role of glutamate in Parkinson’s disease, introduction to fluctuations, efficacy of safinamide on motor symptoms, motor complications and non-motor symptoms, quality of life, safety of safinamide and target population for use. Strong consensus was reached for all the statements on the efficacy of safinamide on motor symptoms, motor fluctuations, quality of life and safety. Among non-motor symptoms, a positive consensus was reached for the symptoms sleep/fatigue, mood, and pain while there was a lack of consensus for the statements regarding the efficacy of safinamide in improving cognition, urinary and sexual functions. The statement on orthostatic hypotension obtained a negative consensus. The consistent and large agreement reached in this Delphi panel perfectly reflects the perception of efficacy, safety and tolerability of safinamide as evident from pivotal trials and clinical practice and shows how these findings may guide movement disorders specialists in their clinical therapeutic approach. The impact of non-motor symptoms in PD is considerable, and management remains an unmet need. In this context, the ability of safinamide to impact some non-motor symptoms may represent the most promising and distinctive feature of this compound and deserves further investigations.
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