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Antiplatelet therapy following ischaemic stroke - Continue or change pre-existing therapy?
Wardati Mazlan-Kepli1, Rachael L MacIsaac1, Matthew Walters1
1Institute of Cardiovascular and Medical Sciences, University of Glasgow, Queen Elizabeth University Hospital, Glasgow, UK.
Insights
Changing antiplatelet therapy after an ischaemic stroke did not affect the risk of recurrent stroke or bleeding. This study suggests current antiplatelet regimens can be continued post-stroke in most patients.
Area of Science:
- Neurology
- Cardiology
- Clinical Trials
Background:
- Antiplatelet therapy is standard post-ischaemic stroke.
- Many patients are already on antiplatelets before stroke.
- Optimal antiplatelet strategy post-stroke remains unclear.
Purpose of the Study:
- To investigate if changing antiplatelet regimen after ischaemic stroke impacts outcomes.
- To compare risks of recurrent stroke and bleeding between patients who change or continue antiplatelet therapy.
Main Methods:
- Retrospective analysis of 1129 ischaemic stroke patients from the Virtual International Stroke Trials Archive.
- Comparison of patients who changed antiplatelet regimen versus those who continued.
- Primary outcome: recurrent ischaemic stroke within 90 days.
- Secondary outcomes: intracranial haemorrhage (ICH) and extracranial haemorrhage (ECH).
Main Results:
- No significant difference in recurrent ischaemic stroke rates between groups (4.1% vs. 4.3%).
- Similar rates of ICH between groups (2.4% vs. 2.6%).
- Slightly higher, but not statistically significant, ECH rates in the group that changed regimen (4.7% vs. 2.9%).
Conclusions:
- Changing antiplatelet regimen post-ischaemic stroke is not associated with altered early risk of recurrent stroke or bleeding.
- Findings based on non-randomized registry data with low event rates.
- Further research may be needed to confirm these findings in diverse patient populations.
Introduction:
Antiplatelet therapy is routinely prescribed early after ischaemic stroke. Many patients will already be taking antiplatelet therapy and it is unknown whether these patients should continue the same antiplatelet treatment or switch to a different regimen.
Methods:
We selected patients with ischaemic stroke from the Virtual International Stroke Trials Archive database who were prescribed antiplatelets both before and after their stroke and who had detailed records of adverse events after stroke. We compared patients who changed to a new antiplatelet regimen after their stroke to those who continued the same regimen. The primary outcome was recurrent ischaemic stroke within 90 days after their index stroke and the secondary outcome was intracranial haemorrhage (ICH) or extracranial haemorrhage (ECH). We used logistic regression analysis and adjusted for age and baseline NIHSS.
Results:
A total of 1129 participants were included. Of these, 538 subjects changed antiplatelet regimen post stroke and 591 continued the same regimen. A recurrent ischaemic event occurred in 4.1% of subjects who changed regimen and 4.3% who continued unchanged (adjusted OR = 0.93; 95% CI 0.54-1.75, p = 0.929). The incidence of ICH and ECH within the first 90 days was similar in both groups (2.4% vs. 2.6% (adjusted OR = 1.02; 95% CI 0.48-2.18, p = 0.955) and 4.7% vs. 2.9% (adjusted OR = 1.82; 95% CI 0.96-3.43, p = 0.065), respectively).
Discussion:
The analysis was performed using a non-randomised registry data.
Conclusion:
In patients who suffer ischaemic stroke whilst taking antiplatelets, a change in antiplatelet regimen was not associated with an altered risk of early recurrent ischaemic stroke rate or bleeding. However, the results must be interpreted in view of the low event rates.
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