Cardiac and Noncardiac Fibrotic Reactions Caused by Ergot-and Nonergot-Derived Dopamine Agonists

被引:54
作者
Andersohn, Frank [1 ]
Garbe, Edeltraut [1 ,2 ]
机构
[1] Univ Bremen, Bremen Inst Prevent Res & Social Med, D-28359 Bremen, Germany
[2] Charite Univ Med Berlin, Inst Clin Pharmacol & Toxicol, Berlin, Germany
关键词
dopamine agonists; adverse effects; fibrosis; adverse drug reaction reporting systems; VALVULAR HEART-DISEASE; PLEUROPULMONARY CHANGES;
D O I
10.1002/mds.22385
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
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. (c) 2009 Movement Disorder Society
引用
收藏
页码:129 / 133
页数:5
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