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The ergoline dopamine agonists should only be used in exceptional circumstances and after the non-ergoline agonist have been tried.
Fibrotic reactions: Ergot-derived dopamine-receptor agonists, bromocriptine, cabergoline, and pergolide, have been associated with pulmonary, retroperitoneal, and pericardial fibrotic reactions.
Exclude cardiac valvulopathy with echocardiography before starting treatment with these ergot derivatives for Parkinson's disease or chronic endocrine disorders (excludes suppression of lactation); it may also be appropriate to measure the erythrocyte sedimentation rate and serum creatinine and to obtain a chest X-ray. Patients should be monitored for dyspnoea, persistent cough, chest pain, cardiac failure, and abdominal pain or tenderness. If long-term treatment is expected, then lung-function tests may also be helpful. Patients taking cabergoline or pergolide should be regularly monitored for cardiac fibrosis by echocardiography (within 3–6 months of initiating treatment and subsequently at 6–12 month intervals).
Ergot derivatives (bromocriptine, cabergoline and pergolide) act by direct stimulation of surviving dopamine receptors. Although effective, they have no advantages over levodopa. They should be reserved for patients in whom levodopa alone is no longer adequate or who, despite careful titration, cannot tolerate levodopa. They are sometimes useful in reducing "off" periods in ameliorating fluctuations in the later stage of Parkinson's disease.
Excessive daytime sleepiness and sudden onset of sleep can occur with dopaminergic drugs. Patients starting treatment with these drugs should be warned of the possibility of these effects and of the need to exercise caution when driving or operating machinery.
Indications
Dose
Notes
Indications
Dose
Notes