Efficacy and tolerability of tolcapone compared with bromocriptine in levodopa-treated parkinsonian patients
The catechol‐O‐methyltransferase inhibitor tolcapone was compared with the dopamine agonist bromocriptine in an open‐label, randomized trial involving 146 levodopa‐treated parkinsonian patients with end‐of‐dose deterioration of efficacy. Tolcapone was given at a dosage of 200 mg three times daily; b...
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Published in: | Movement disorders Vol. 14; no. 1; pp. 38 - 44 |
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Format: | Journal Article |
Language: | English |
Published: |
New York
John Wiley & Sons, Inc
01-01-1999
Wiley |
Subjects: | |
Online Access: | Get full text |
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Summary: | The catechol‐O‐methyltransferase inhibitor tolcapone was compared with the dopamine agonist bromocriptine in an open‐label, randomized trial involving 146 levodopa‐treated parkinsonian patients with end‐of‐dose deterioration of efficacy. Tolcapone was given at a dosage of 200 mg three times daily; bromocriptine was titrated from 1.25 mg once daily at baseline to, at most, 10 mg three times daily by day 24 (mean final dose 22.4 mg/day). After 8 weeks, the tolcapone group had a significant reduction in daily levodopa dose compared with the bromocriptine group (p < 0.05). No significant differences in the “on/off” time and motor disability were seen between the tolcapone and bromocriptine treatment groups. Bromocriptine induced more hallucinations, orthostatic hypotension, and nausea, whereas tolcapone therapy was associated with more muscle cramps and dystonia. These results suggest that when added to levodopa therapy, the two drugs have a different side effect profile, with the advantages for tolcapone being absence of titration and quicker efficacy. |
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Bibliography: | F. Hoffmann-La Roche Ltd, Basel, Switzerland ark:/67375/WNG-L1L0030Z-Q ArticleID:MDS1008 istex:796F1D2ADEC1CDC906C2A7DB15116C142B327396 ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0885-3185 1531-8257 |
DOI: | 10.1002/1531-8257(199901)14:1<38::AID-MDS1008>3.0.CO;2-I |