Abstract |
We performed a retrospective analysis of the Efficacy And Safety Evaluation in Parkinson's Disease (EASE-PD) Adjunct Study, assessing the minimum time to symptom improvement after initiation of ropinirole prolonged release (2-24 mg/day) versus placebo in patients with moderate-to-advanced PD not optimally controlled with levodopa. Ropinirole prolonged release was superior to placebo at Week 2 for change from baseline in "off" time (adjusted mean treatment difference [AMTD] - 0.7 hours; 95% confidence interval [CI], -1.1, -0.2; P = 0.0029), and "on" time without troublesome dyskinesia (0.4 hours; 95%CI, 0.01, 0.88; P = 0.0444). At Week 4, improvements were seen in change from baseline in Unified Parkinson's Disease Rating Scale total motor score (AMTD, -3.1; 95%CI, -4.4, -1.8; P < 0.0001), activities of daily living score (AMTD, -1.1; 95%CI, -1.7, -0.5; P = 0.0004), and the cardinal symptoms of PD compared with placebo. These analyses indicate that once-daily, adjunctive ropinirole prolonged release can offer PD symptom control 2 weeks after treatment initiation.
|
Authors | Bonnie P Hersh, Nancy L Earl, Robert A Hauser, Mark Stacy |
Journal | Movement disorders : official journal of the Movement Disorder Society
(Mov Disord)
Vol. 25
Issue 7
Pg. 927-31
(May 15 2010)
ISSN: 1531-8257 [Electronic] United States |
PMID | 20461810
(Publication Type: Journal Article, Multicenter Study, Randomized Controlled Trial, Research Support, Non-U.S. Gov't)
|
Copyright | (c) 2010 Movement Disorder Society. |
Chemical References |
- Delayed-Action Preparations
- Dopamine Agonists
- Indoles
- ropinirole
|
Topics |
- Aged
- Delayed-Action Preparations
- Dopamine Agonists
(therapeutic use)
- Double-Blind Method
- Female
- Humans
- Indoles
(therapeutic use)
- Male
- Movement Disorders
(diagnosis, epidemiology)
- Parkinson Disease
(drug therapy, epidemiology)
- Severity of Illness Index
- Treatment Outcome
|