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. 2020 Mar 13;11:116. doi: 10.3389/fneur.2020.00116

Table 2.

Medication of the study population.

PD patients
(n = 1,385)
Patients with WO (n = 763) Patients without WO (n = 622) p
Levodopa-benserazide, n(%)a,$ 1206 (87.1%) 680 (89.2%) 526 (84.6%) 0.010*
Levodopa-cabidopa, n(%)a,$ 402 (29.0%) 275 (36.0%) 127 (20.4%) <0.001*
Pramipexole, n(%)a,$ 587 (42.4%) 344 (45.1%) 243 (39.1%) 0.024*
Piribedil, n(%)a,$ 261 (18.8%) 147 (19.3%) 114 (18.3%) 0.657
Bromocriptine, n(%)a,$ 5 (0.4%) 3 (0.4%) 2 (0.3%) 0.825
Rasagiline, n(%)a,$ 22 (1.6%) 13 (1.7%) 9 (1.4%) 0.704
Selegiline, n(%)a,$ 227 (16.4%) 136 (17.8%) 91 (14.6%) 0.110
Trihexyphenidyl 86 (6.2%) 50 (6.6%) 36 (5.8%) 0.557
Amantadine, n(%)a,$ 128 (9.2%) 89 (11.7%) 39 (6.3%) 0.001*
Entacapone, n(%)a,$ 15 (1.1%) 10 (1.3%) 5 (0.8%) 0.440
Numbers of medications 2 (1, 3) 2 (2, 3) 2 (1, 2) <0.001*
Medical treatment strategies, n(%)a,$ <0.001*
Levodopa monotherapy 390 (28.2%) 185 (24.2%) 205 (33.0%)
Levodopa plus other drugs 902 (65.1%) 541 (70.9%) 361 (58.0%)
DA monotherapy 77 (5.6%) 28 (3.7%) 49 (7.9%)
Non-dopaminergic treatment 16 (1.2%) 9 (1.2%) 7 (1.1%)

WO, Wearing-off; DA, dopamine agonist.

a

Presented as number(percentage).

$

Data were analyzed by χ2 test.

*

p < 0.05 of the comparison between two groups.