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Optimum symptomatic control of Parkinson's disease with dopaminergic therapy.

Abstract
This paper presents a review of the literature on the therapeutic action and the side effects of the two main dopaminergic agents: L-DOPA/decarboxylase inhibitor (L-DOPA/DI) and bromocriptine (Parlodel used either as monotherapy or in combination in patients with Parkinson's disease. The combination of L-DOPA/DI and bromocriptine gives the best therapeutic efficacy (49% improvement) in the total score (bradykinesia, rigidity and tremor). However, treatment by monotherapy or combination gives the same pattern of activity: greatest improvement in tremor, followed by rigidity and bradykinesia. Improvement observed in the short term is not sustained over longer periods of time for monotherapy with either drug. The short-term side effects are similar for each treatment, whereas long-term complications (dyskinesia, end-of-dose deterioration and on-off phenomenon) appear only when levodopa is used, alone (high incidence) or in combination with bromocriptine (low incidence). The overall optimum treatment is obtained with a combination of L-DOPA/DI and bromocriptine.
AuthorsS Bouchard
JournalThe Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques (Can J Neurol Sci) Vol. 14 Issue 3 Suppl Pg. 460-5 (Aug 1987) ISSN: 0317-1671 [Print] England
PMID3676921 (Publication Type: Journal Article)
Chemical References
  • Drug Combinations
  • Bromocriptine
  • Levodopa
Topics
  • Aged
  • Bromocriptine (administration & dosage, adverse effects, therapeutic use)
  • Drug Combinations
  • Humans
  • Levodopa (administration & dosage, adverse effects, therapeutic use)
  • Middle Aged
  • Movement Disorders (etiology)
  • Parkinson Disease (complications, drug therapy)
  • Time Factors

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