Related Experiment Video
Updated: Mar 20, 2026

The Stroke Preclinical Assessment Network Multi-laboratory Model of Thromboembolic Stroke with Thrombolysis: TE-MCAo
Published on: December 19, 2025
Acute ischemic stroke after cardiac catheterization: the protamine low-dose recombinant tissue plasminogen activator
Carlos Guevara1, Alonso Quijada, Carolina Rosas
1aFacultad de Medicina, Universidad de Chile, Santiago bFacultad de Medicina, Universidad de Valparaiso, Valparaiso cUnidad de Hematologia dUnidad de Cardiologia, Universidad de Chile, Santiago, Chile.
Insights
Intravenous thrombolysis for acute ischemic stroke after cardiac catheterization is challenging. A novel approach using protamine followed by reduced-dose recombinant tissue plasminogen activator shows promise for safe and effective treatment.
Area of Science:
- Cardiology
- Neurology
- Pharmacology
Background:
- Intravenous thrombolysis is the gold standard for acute ischemic stroke.
- Its use after cardiac catheterization is not established due to bleeding risks associated with anticoagulation.
Observation:
- Three patients experienced acute ischemic stroke following cardiac catheterization.
- These patients had received unfractionated heparin, requiring reversal with protamine.
Findings:
- Off-label thrombolysis was successfully administered using reduced doses (0.6 mg/kg) of recombinant tissue plasminogen activator.
- This sequential protamine-recombinant tissue plasminogen activator strategy aimed to minimize bleeding risks.
Implications:
- This approach may offer a safer alternative for treating acute ischemic stroke post-cardiac catheterization.
- Further research is warranted to validate the efficacy and safety of this reduced-dose thrombolysis protocol.
Abstract:
: Intravenous thrombolysis is the preferred treatment for acute ischemic stroke; however, it remains unestablished in the area of cardiac catheterization. We report three patients with acute ischemic stroke after cardiac catheterization. After reversing the anticoagulant effect of unfractionated heparin with protamine, all of the patients were successfully off-label thrombolyzed with reduced doses of intravenous recombinant tissue plasminogen activator (0.6 mg/kg). This dose was preferred to reduce the risk of symptomatic cerebral or systemic bleeding. The sequential pathway of protamine recombinant tissue plasminogen activator at reduced doses may be safer for reducing intracranial or systemic bleeding events, whereas remaining efficacious for the treatment of acute ischemic stroke after cardiac catheterization.
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