Abstract | BACKGROUND AND PURPOSE: METHODS: We performed a systematic online search for clinical trials for pramipexole ER treatment up to 1 August 2016. We assessed differences in Unified Parkinson's Disease Rating Scale (UPDRS) scores, percentage of 'on' time or 'off' time, withdrawals, adverse events (AEs) and life quality between pramipexole ER and pramipexole IR or placebo. Data analyses were performed by the Cochrane Collaboration's Review Manager 5.3 software. RESULTS: Six randomized controlled trials were included. Compared with placebo, pramipexole ER achieved a significant improvement in the UPDRS Part II + III score [weighted mean difference, -4.81; 95% confidence interval (CI), -6.40 to -3.23], whereas no significant difference was found in the UPDRS Part III + III score between pramipexole ER and pramipexole IR groups (weighted mean difference, -0.26; 95% CI, -1.15 to 0.64). No differences were found in total AEs (relative risk, 0.97; 95% CI, 0.92 to 1.03), drug-related AEs (relative risk, 0.97; 95% CI, 0.92 to 1.03) or the commonly reported AEs between pramipexole ER and pramipexole IR. CONCLUSIONS:
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Authors | T Shen, R Ye, B Zhang |
Journal | European journal of neurology
(Eur J Neurol)
Vol. 24
Issue 6
Pg. 835-843
(06 2017)
ISSN: 1468-1331 [Electronic] England |
PMID | 28480621
(Publication Type: Journal Article, Review)
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Copyright | © 2017 EAN. |
Chemical References |
- Antiparkinson Agents
- Benzothiazoles
- Delayed-Action Preparations
- Pramipexole
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Topics |
- Antiparkinson Agents
(administration & dosage, adverse effects, therapeutic use)
- Benzothiazoles
(administration & dosage, adverse effects, therapeutic use)
- Delayed-Action Preparations
(administration & dosage, adverse effects, therapeutic use)
- Double-Blind Method
- Drug Administration Schedule
- Humans
- Mental Status and Dementia Tests
- Parkinson Disease
(diagnosis, drug therapy)
- Pramipexole
- Quality of Life
- Randomized Controlled Trials as Topic
- Severity of Illness Index
- Treatment Outcome
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