Piribedil and bromocriptine in Parkinson's disease: a single-blind crossover study

Acta Neurol Scand. 2003 Mar;107(3):202-6. doi: 10.1034/j.1600-0404.2003.02104.x.

Abstract

Introduction: Clinicians switch from one dopamine agonist to another for various reasons. However, each change may inadvertently result in certain potential risks such as decreased medication efficacy or new side-effects.

Objective: We evaluated the tolerability of a switch of bromocriptine to piribedil using two conversion ratios as a primary outcome measure, with motor function as a secondary outcome measure, in patients with mild to moderate Parkinson's disease (PD).

Methods: Twenty consecutive patients with mild to moderate PD (Hoehn and Yahr, stage II-III) on treatment with stable doses of bromocriptine and levodopa were randomized to two groups of 10 patients each, to receive piribedil based on 1:5 or 1:10 conversion ratios. Blinded evaluations were performed: 1) United Parkinson's Diseased Rating Scale (UPDRS) scores both in 'on' and 'off', 2) Open-ended interviews for adverse events, 3) Epworth Sleepiness Scale, 4) Purdue Pegboard assessment during 'on' and 'off', 5) Hand-arm movement test during 'on' and 'off', and 6) Walking test during 'on' and 'off'.

Results: Major adverse events included 'sleep attacks' in one patient and minor side-effects included giddiness, nausea, hallucinations, sleepiness and lethargy. However, these were mild and 19 (95%) of the 20 patients completed the study. There was a significant improvement in both the UPDRS 'off' total and motor scores at 1 month compared with baseline for the group on 1:10 ratio. The walking times during the 'off' state at 1 and 2 months were significantly better compared with baseline in the 1:5 group. There were otherwise no significant differences in the rating tests during both 'off' and 'on' states before and after the bromocriptine switch.

Conclusions: We demonstrated that patients with mild to moderate PD who were on relatively low doses of bromocriptine can be safely switched to piribedil based on a conversion ratio of either 1:5 or 1:10. However, the higher conversion ratio has to be carried out with caution in patients with daytime somnolence.

Publication types

  • Clinical Trial
  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Administration, Oral
  • Aged
  • Antiparkinson Agents / administration & dosage
  • Antiparkinson Agents / adverse effects
  • Antiparkinson Agents / pharmacology*
  • Bromocriptine / administration & dosage
  • Bromocriptine / adverse effects
  • Bromocriptine / pharmacology*
  • Cross-Over Studies
  • Female
  • Hallucinations / chemically induced
  • Humans
  • Male
  • Middle Aged
  • Nausea / chemically induced
  • Parkinson Disease / drug therapy*
  • Parkinson Disease / pathology
  • Piribedil / administration & dosage
  • Piribedil / adverse effects
  • Piribedil / pharmacology*
  • Psychomotor Agitation / etiology
  • Severity of Illness Index
  • Single-Blind Method
  • Sleep Wake Disorders / chemically induced
  • Treatment Outcome

Substances

  • Antiparkinson Agents
  • Bromocriptine
  • Piribedil