TY - JOUR
T1 - Safinamide in clinical practice :
T2 - A Spanish multicenter cohort study
AU - Martí-Andrés, Gloria
AU - Jiménez-Bolaños, Rayco
AU - Arbelo, José Matías
AU - Pagonabarraga Mora, Javier
AU - Duran-Herrera, Carmen
AU - Valenti-Azcarate, Rafael
AU - Luquin, Maria-Rosario
PY - 2019
Y1 - 2019
N2 - Safinamide is an approved drug for the treatment of motor fluctuations of Parkinson's Disease (PD) patients with a potential benefit on non-motor symptoms (NMS). A retrospective multicenter cohort study was conducted, in which the clinical effect of safinamide on both motor and NMS was assessed by the Clinical Global Impression of Change scale. Furthermore, we assessed the appearance of adverse events (AEs) and its effect on dyskinesia, that were also recorded in non-fluctuating PD patients and in those previously treated with rasagiline. We included 213 PD patients who received safinamide in addition to their regular levodopa therapy. Thirty-five withdrew prematurely from safinamide, mainly because of AEs. Out of 178, clinical improvement on motor and NMS was found in 76.4% and 26.2%, respectively. A total of 44 reported AEs of mild intensity. We did not find a difference concerning the clinical benefit or AEs when comparing either patients who had or had not been taking Monoamine Oxidase B Inhibitor (MAOB-I) previously or between patients with and without motor complications. Safinamide is an effective and safe add-on to levodopa drug for PD patients. Moreover, safinamide could elicit an additional clinical improvement in PD patients previously treated with other MAOB-I and in non-fluctuating patients with suboptimal motor control.
AB - Safinamide is an approved drug for the treatment of motor fluctuations of Parkinson's Disease (PD) patients with a potential benefit on non-motor symptoms (NMS). A retrospective multicenter cohort study was conducted, in which the clinical effect of safinamide on both motor and NMS was assessed by the Clinical Global Impression of Change scale. Furthermore, we assessed the appearance of adverse events (AEs) and its effect on dyskinesia, that were also recorded in non-fluctuating PD patients and in those previously treated with rasagiline. We included 213 PD patients who received safinamide in addition to their regular levodopa therapy. Thirty-five withdrew prematurely from safinamide, mainly because of AEs. Out of 178, clinical improvement on motor and NMS was found in 76.4% and 26.2%, respectively. A total of 44 reported AEs of mild intensity. We did not find a difference concerning the clinical benefit or AEs when comparing either patients who had or had not been taking Monoamine Oxidase B Inhibitor (MAOB-I) previously or between patients with and without motor complications. Safinamide is an effective and safe add-on to levodopa drug for PD patients. Moreover, safinamide could elicit an additional clinical improvement in PD patients previously treated with other MAOB-I and in non-fluctuating patients with suboptimal motor control.
KW - Adverse drug event
KW - Drug-Induced
KW - Dyskinesia
KW - Motor complications
KW - Parkinson's Disease
KW - Safinamide
U2 - 10.3390/brainsci9100272
DO - 10.3390/brainsci9100272
M3 - Article
C2 - 31614574
SN - 2076-3425
VL - 9
JO - Brain Sciences
JF - Brain Sciences
IS - 10
ER -