Key result
Discontinuing ergot-derived dopamine agonists regressed valve abnormalities in ~1/3 of multivalvular and ~1/2 of monovalvular cases, whereas continuation led to 7 new cases of severe regurgitation.
Why the study?
Does discontinuation of ergot-derived dopamine agonists improve echocardiographic cardiac valvulopathy in patients with Parkinson's disease?
Cohort (n=101)
Does discontinuation of ergot-derived dopamine agonists improve echocardiographic cardiac valvulopathy in patients with Parkinson's disease?
Discontinuation of ergot-derived dopamine agonists leads to regression of valvulopathy in some patients, while continuation is associated with progressive valve damage.
May support discontinuation for regression in affected patients; leaves open need for randomized confirmation before practice change.
AIMS: In a previous echocardiographic prevalence study we reported a significant increase in the frequency of heart valve regurgitation in patients with Parkinson's disease taking the ergot-derived dopamine agonists pergolide and cabergoline versus controls. We followed-up our original cohort of patients to ascertain whether valvulopathy regressed after discontinuation of treatment and/or its incidence increased over time. METHODS: Prospective follow-up of 101 patients treated with ergot-derived dopamine agonists included in the prevalence study: 53 given pergolide and 48 cabergoline (64% male; 66.4 ± 8.7 years of age, 11.5 ± 5.9 years of disease, 21.8 ± 5.9 months of follow-up); 55 stopped treatment while 46 continued. The main outcomes measures, were: echocardiographic quantification of regurgitant valve disease, abnormal leaflet, or cusp thickening and measurement of mitral valve tenting area. RESULTS: Valve abnormalities regressed in about one third of patients with significant multivalvular and in about half of the patients with monovalvular regurgitation who withdrew; no progression was observed in remaining patients. Patients continuing ergot-derived dopamine agonists showed progression of cardiac valvulopathy: seven new cases with three to four regurgitation grade of any valve occurred during follow-up; this regarded also patients who had been on pergolide for many years. CONCLUSION: Owing to the persistence of risk of heart valve damage over time and the lack of its mid-term reversibility in many patients, we believe that pergolide and cabergoline should be prescribed only when therapeutic alternatives with a better risk/benefit ratio are unavailable and the patient has access to echocardiography.
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Zanettini et al. (2010) conducted a cohort in Parkinson's disease with ergot-derived dopamine agonist treatment (n=101). Discontinuation of ergot-derived dopamine agonists vs. Continuation of ergot-derived dopamine agonists was evaluated on Echocardiographic quantification of regurgitant valve disease, abnormal leaflet, or cusp thickening and measurement of mitral valve tenting area. Discontinuing ergot-derived dopamine agonists regressed valve abnormalities in ~1/3 of multivalvular and ~1/2 of monovalvular cases, whereas continuation led to 7 new cases of severe regurgitation.
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