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Mizuo, Y., Yamamoto, M., Kuno, S., Hasegawa, K., Hattori, N., Kagimura, T., Sarashina, A., Rascol, O., Schapira, A.H.V., Barone, P., Hauser, R., Poewe, W., The Pramipexole ER Study Group (2012) Efficacy and Safety of Extended- versus Immediate- Release Pramipexole in Japanese Patients with Advanced and L-dopa-Undertreated Parkinson Disease: A Double-Blind, Randomized Trial. Clinical Neuropharmacology, 35, 174-181.
http://dx.doi.org/10.1097/WNF.0b013e31825f77b9
has been cited by the following article:
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TITLE:
Self-Reported Adherence after Overnight Switching from Immediate- to Extended-Release Pramipexole in Parkinson’s Disease
AUTHORS:
Mutsumi Iijima, Mikio Osawa, Kenji Maruyama, Shinichiro Uchiyama, Kazuo Kitagawa
KEYWORDS:
Parkinson’s Disease, Timing Adherence, Pramipexole, Extended-Release, Immediate-Release, Motor Function
JOURNAL NAME:
Advances in Parkinson's Disease,
Vol.4 No.1,
February
5,
2015
ABSTRACT: Background: Drug adherence decreased in patients with Parkinson’ s disease (PD) because of taking many different types of drugs. We evaluated drug adherence after switching from immediate-release (IR) to once-daily extended-release (ER) pramipexole (PPX) in PD. Methods: This study included 35 PD patients (20 men, 15 women); 10 were taking oral PPX alone, and 25 were also using another anti-PD drug. PPX-IR was switched overnight to PPX-ER without gradual tapering. One month after switching, improvement in timing adherence and reduction in medication burden were evaluated by a questionnaire using a visual analog scale (VAS) (0: No change; 10: Better). Motor function was assessed using part III of the Unified Parkinson’s Disease Rating Scale (UPDRS). Results: The VAS score for improvement in timing adherence was 8.1 ± 0.5 (mean ± standard error), and that for reduction in medication burden was 7.3 ± 0.6. There was a significant negative correlation (ρ = -0.43, p = 0.01) between the VAS score and number of types of medications. The UPDRS part III score improved significantly after switching (p