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Published on: May 28, 2019
Dipyridamole may be used safely in patients with ischaemic heart disease
D M Humphreys1, J Street, H Schumacher
1Boehringer Ingelheim GmbH, Germany.
Insights
Dipyridamole combined with aspirin is safe for preventing secondary strokes in patients with cerebrovascular disease and mild to moderate ischemic heart disease. Clinical trials show no increased cardiac risk at recommended doses.
Area of Science:
- Cardiology
- Neurology
- Pharmacology
Background:
- Up to 50% of patients with cerebrovascular disease also have ischemic heart disease.
- Dipyridamole plus aspirin enhances secondary stroke risk reduction compared to aspirin alone.
- The cardiac safety of dipyridamole in patients with concurrent ischemic heart disease requires clarification.
Purpose of the Study:
- To evaluate the risk of cardiac adverse events associated with dipyridamole treatment in patients with co-existing ischemic heart disease.
Main Methods:
- Systematic review of published literature, safety reports, and randomized controlled trials.
- Analysis focused on trials involving antiplatelet agents for stroke prevention and dipyridamole for cardiovascular indications.
Main Results:
- Early reports of cardiac adverse effects were linked to high-dose dipyridamole used in cardiac imaging stress tests.
- Randomized controlled trials found no evidence of increased mortality.
- Only isolated cases of significant cardiac morbidity were observed at recommended oral doses for ischemic heart disease patients.
Conclusions:
- Dipyridamole is safe for secondary stroke prevention in patients with cerebrovascular disease and mild to moderate ischemic heart disease.
- Recommended oral doses do not appear to increase cardiac risk in this patient population.
Abstract:
It is thought that up to 50% of patients with cerebrovascular disease will have concurrent ischaemic heart disease. Dipyridamole co-formulated with aspirin has been shown to increase the relative reduction in risk of second stroke in patients with prior stroke/transient ischaemic attack beyond that obtaining with aspirin alone. We have sought to resolve the question of whether dipyridamole treatment increases the risk of cardiac adverse events in patients with co-existing ischaemic heart disease. The published literature, periodic safety update reports, the randomised controlled trials of antiplatelet agents in stroke prevention and those including dipyridamole in cardiovascular indications, have been reviewed and analysed. The early reports of serious adverse cardiac effect attributable to dipyridamole occurred in patients with severe coronary artery disease using dipyridamole as a stress test adjunct to cardiac imaging. The randomised controlled trials databases show no evidence of mortality and only isolated cases of significant cardiac morbidity attributable to dipyridamole at recommended oral doses in patients with ischaemic heart disease. We conclude that patients with cerebrovascular and mild to moderate concomitant ischaemic heart disease may be treated safely with dipyridamole for the secondary prevention of stroke.
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