Related Experiment Video
Updated: Jun 7, 2026

Microfluidics in Assessing Platelet Function
Published on: November 8, 2024
Antiplatelet therapy following cardiac valve replacement-a comparative study of aspirin and ticlopidine
1Department of Cardiovascular Surgery, Hachioji Medical Center. Tokyo Medical College, Tatemachi 1163, Hachioji City.
Insights
Aspirin and ticlopidine are effective antiplatelet agents for preventing thromboembolism after cardiac valve replacement. Both drugs demonstrated low thromboembolism rates with comparable safety profiles in this study.
Area of Science:
- Cardiovascular Medicine
- Pharmacology
- Hematology
Background:
- Antiplatelet agents like aspirin and ticlopidine are crucial for preventing thromboembolism in patients with cardiac valve replacements.
- Warfarin is concurrently administered to maintain specific therapeutic ranges (Thrombotest 10-25%, PT-INR 1.6-3.0).
Purpose of the Study:
- To compare the clinical efficacy and safety of daily low-dose aspirin versus ticlopidine in patients following cardiac valve replacement.
- To evaluate the incidence of thromboembolic events and hemorrhagic complications in both treatment groups.
Main Methods:
- A prospective study involving 100 patients undergoing aortic or mitral valve replacement.
- Patients were randomized to receive either daily aspirin (81 mg) or ticlopidine (300 mg) for a mean follow-up of approximately 52 months.
- Thromboembolism and hemorrhagic complication rates were recorded. Laboratory parameters including liver function tests and lipid profiles were monitored.
Main Results:
- Both aspirin and ticlopidine groups exhibited low incidences of thromboembolism (1.0/100 patient-years for ticlopidine, 1.9/100 patient-years for aspirin).
- Hemorrhagic complication rates were similar between groups (2.9 for ticlopidine, 2.3 for aspirin).
- Ticlopidine significantly reduced ADP-induced platelet aggregation, while no significant differences in other clinical outcomes or adverse reactions were noted between the two agents.
Conclusions:
- Both aspirin and ticlopidine are safe and effective antiplatelet therapies for patients with cardiac valve replacements.
- While ticlopidine demonstrates superior inhibition of platelet aggregation, clinical outcomes regarding thromboembolism and bleeding are comparable to aspirin in this patient cohort.
Abstract:
The antiplatelet agents, aspirin and ticlopidine, are widely used to prevent thromboembolism following cardiac valve replacement. To compare the clinical effects of each platelet inhibitor, a daily dose of ticlopidine 300 mg was given to 50 patients who underwent aortic valve or mitral valve replacement with an average age of 56.9 years over a mean 52.6 months after surgery. 50 more patients with an average age of 50.2 years were given a daily dose of aspirin 81 mg over a mean 51.3 months after surgery. Warfarin was given to maintain thrombotest values at 10 to 25% (PT-INR at 1.6-3.0). The incidence of thromboembolism was low in both groups; 1.0/100 patient years in the ticlopidine group and 1.9 in the aspirin group. Hemorrhagic complications, hematuria and ecchymosis, showed an incidence of 2.9 in the ticlopidine group and 2.3 in the aspirin group. Slight increases in GOT and GTP were observed in 4 and 18% of cases and elevated total cholesterol and neutral fat in 2 and 18% of cases. No adverse reactions were reported. With the exception of a significant decrease in ADP-induced platelet aggregation in patients who took ticlopidine, there were no significant differences observed between the two groups.
Related Concept Videos
Antiplatelet Drugs: Prostaglandin Synthesis, P2Y12 and Glycoprotein IIb/IIIa Inhibitors
Prostaglandin synthesis inhibitors, exemplified by the widely known aspirin, wield their power by irreversibly acetylating...
Venous Thrombosis III: Interprofessional Care
Coronary Artery Disease V: Interprofessional Care
Peripheral Artery Disease III: Interprofessional Care
Anticoagulant Drugs: Vitamin K Antagonists and Direct Oral Anticoagulants
Warfarin, a prominent vitamin K antagonist family member, exerts its effect by inhibiting the enzyme VKORC1 (vitamin K epoxide reductase complex 1). By hindering this enzyme, warfarin...
Anticoagulant Drugs: Low-Molecular-Weight Heparins
