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Prevention with low-dose aspirin plus dipyridamole in patients with disabling stroke
Diederik W J Dippel1, Lisette Maasland, Patricia Halkes
1Department of Neurology, Erasmus MC University Medical Center, Rotterdam, The Netherlands. d.dippel@erasmusmc.nl
Insights
The combination of aspirin and dipyridamole effectively reduces vascular events in patients post-stroke, regardless of stroke severity. This combination therapy offers consistent benefits across all modified Rankin Scale scores.
Area of Science:
- Neurology
- Cardiology
- Clinical Pharmacology
Background:
- Low-dose aspirin plus dipyridamole is established for secondary stroke prevention.
- Its efficacy in patients with disabling strokes (higher mRS scores) remains less understood.
Purpose of the Study:
- To evaluate the effectiveness of aspirin plus dipyridamole versus aspirin alone in patients with varying stroke severities.
- Specifically assess outcomes based on modified Rankin Scale (mRS) scores at baseline.
Main Methods:
- Reanalysis of data from 5700 patients in ESPRIT and ESPS-2 trials.
- Stratified analysis based on baseline mRS scores (0-5).
- Proportional hazards regression used to estimate treatment effects and test for interactions.
Main Results:
- The combination therapy showed a relative risk of 0.79 (95% CI, 0.69-0.91) for vascular events compared to aspirin alone across all mRS scores.
- Benefits were observed across mRS subcategories 0-4 for vascular events and stroke.
- A trend towards benefit was suggested for patients with mRS score 5, though data were limited.
Conclusions:
- The combination of low-dose aspirin and dipyridamole provides consistent benefits in preventing vascular events.
- This efficacy extends across all stroke severity levels, as indicated by the modified Rankin Scale scores.
Background And Purpose:
The combination of low-dose aspirin and dipyridamole is more effective than aspirin alone in reducing the risk of recurrent stroke and other major cardiovascular events in patients with a recent transient ischemic attack or minor stroke. It is unknown whether this also applies to patients with a disabling stroke.
Methods:
We reanalyzed the data of 5700 patients from ESPRIT and ESPS-2 to study the effect of aspirin and dipyridamole according to modified Rankin scale (mRS) score at baseline. Primary outcome was vascular events (stroke, myocardial infarction, or vascular death). We used proportional hazards regression to estimate the treatment effect across mRS strata at baseline, and we tested for interactions with treatment.
Results:
In total, 426 patients (7.5%) had mRS score of 4 or 5 at baseline. The risk of an outcome event increased with mRS score. The relative risk associated with the combination of aspirin and dipyridamole compared to aspirin alone in patients with mRS score 0 to 5 was 0.79 (95% confidence interval, 0.69-0.91). The relative risk according to mRS subcategory score 0 to 4 at baseline varied between 0.73 and 0.96 for vascular events and between 0.62 and 0.96 for stroke. The number of patients with mRS score 5 was too small for reliable estimates, but the data suggest a beneficial effect. There was no evidence of interaction between treatment effect and mRS score at baseline.
Conclusions:
The beneficial effect of the combination of low-dose aspirin and dipyridamole was present in all subcategories of the mRS score.
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