Key result
Ergot-derived dopamine agonists were associated with increased reporting odds ratios for fibrotic reactions, whereas nonergot-derived drugs showed no such safety signals.
Why the study?
Do ergot-derived and nonergot-derived dopamine agonists increase the risk of cardiac and noncardiac fibrotic reactions?
Observational
Do ergot-derived and nonergot-derived dopamine agonists increase the risk of cardiac and noncardiac fibrotic reactions?
Ergot-derived dopamine agonists are associated with an increased risk of cardiac and noncardiac fibrotic reactions, whereas nonergot-derived dopamine agonists do not show this safety signal.
May favor nonergot-derived agents to reduce fibrosis risk; leaves open prospective confirmation before practice change.
There is growing evidence that the ergot-derived dopamine agonists cabergoline and pergolide can cause fibrotic cardiac valvulopathy. Data on other fibrotic reactions and nonergot-derived dopamine agonists are sparse. Aim of this study was to investigate whether there are signals that dopamine agonists are related to cardiac and other fibrotic reactions. We identified all reports of fibrotic reactions at the heart, lung, and retroperitoneal space associated with dopamine agonists within the US Adverse Event Reporting System database. Disproportionality analyses were used to calculate adjusted reporting odds ratios (RORs). For ergot-derived dopamine agonists (bromocriptine, cabergoline, pergolide), the RORs of all reactions under study were increased, whereas no such increases were observed for nonergot-derived drugs (apomorphine, pramipexole, ropinirole, rotigotine). Fibrotic reactions due to ergot-derived dopamine agonists may not be limited to heart valves. For nonergot-derived dopamine agonists, no drug safety signals were evident.
No takes yet. Share an insight, caveat, or question.
Andersohn et al. (2008) conducted an observational in Fibrotic reactions. Ergot-derived and nonergot-derived dopamine agonists was evaluated on Reporting odds ratios (RORs) of fibrotic reactions at the heart, lung, and retroperitoneal space. Ergot-derived dopamine agonists were associated with increased reporting odds ratios for fibrotic reactions, whereas nonergot-derived drugs showed no such safety signals.
Synapse has enriched 2 closely related papers on similar clinical questions. Consider them for comparative context: