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Low-Dose Ticagrelor in Patients With High Ischemic Risk and Previous Myocardial Infarction: A Multicenter Prospective
Arturo Cesaro1,2, Vittorio Taglialatela3, Felice Gragnano1,2
1Department of Translational Medical Sciences, University of Campania "Luigi Vanvitelli," Naples, Italy.
Insights
Prolonged dual antiplatelet therapy with low-dose ticagrelor after myocardial infarction (MI) is effective and safe in real-world practice. This study found low rates of ischemic events and no major bleeding in patients treated beyond 12 months post-MI.
Area of Science:
- Cardiology
- Pharmacology
- Clinical Research
Background:
- Prolonged dual antiplatelet therapy (DAPT) after myocardial infarction (MI) aims to reduce long-term ischemic events.
- The PEGASUS-TIMI 54 trial demonstrated efficacy of low-dose ticagrelor (60 mg twice daily) plus aspirin post-MI.
- Real-world data on the use and outcomes of prolonged low-dose ticagrelor therapy are limited.
Purpose of the Study:
- To evaluate the real-world prescription criteria, clinical characteristics, and 1-year outcomes of patients receiving low-dose ticagrelor for prolonged DAPT after MI.
- To assess the safety and effectiveness of ticagrelor 60 mg in a real-world cohort based on Italian national regulations.
Main Methods:
- A prospective, real-world study enrolling 181 consecutive patients eligible for ticagrelor 60 mg in three Italian centers.
- Data collection included patient demographics, prescription criteria, major adverse cardiovascular events (MACE), and bleeding events over a median follow-up of 18 months.
- Analysis focused on 1-year outcomes, including rates of MI, stroke/transient ischemic attack, and major bleeding.
Main Results:
- Multivessel coronary disease (72.4%) was the most common prescription criterion; chronic kidney disease (15.5%) was the least common.
- At 1-year follow-up, the rate of MACE was 4.97%, comprising 3.86% for MI and 1.1% for stroke/transient ischemic attack.
- No major bleeding events were reported during the follow-up period.
Conclusions:
- Real-world use of low-dose ticagrelor for prolonged DAPT in patients with previous MI is effective in reducing ischemic events.
- The treatment demonstrated a favorable safety profile, with no major bleeding observed in this cohort.
- Findings support the use of ticagrelor 60 mg for extended DAPT in selected post-MI patients in routine clinical practice.
Abstract:
Prolonged dual antiplatelet therapy after 12 months in patients with previous myocardial infarction (MI) is attractive to reduce long-term ischemic complications. In the PEGASUS-TIMI 54, the use of low-dose ticagrelor (60 mg b.i.d.) plus aspirin after 12 months from MI reduced the risk of ischemic events, at the price of limited increase on bleeding complications. However, data on the use of low-dose ticagrelor in real-world practice lack. We aim at providing data on prescription/eligibility criteria and outcomes in patients receiving low-dose ticagrelor in the real-world setting. We enrolled consecutive patients eligible for ticagrelor 60 mg according to Italian national regulation in 3 high-volume centers and collected 1-year outcomes. The primary objective of the study is to generate real-world data about clinical characteristics, eligibility criteria, major adverse cardiovascular events, bleeding, and adverse event in patients receiving low-dose ticagrelor from our cohort. One hundred eighty-one patients were consecutively enrolled with a median follow-up of 18 months. The most used and the least used prescription criteria were multivessel coronary disease (72.4%) and chronic kidney disease (15.5%), respectively. At 1-year follow-up, the rate of major adverse cardiovascular events was 4.97%; of these, 3.86% of patients had a MI, and 1.1% had a stroke/transient ischemic attack, whereas no major bleeding occurred. In conclusion, in a real-world study, including patients with previous MI, low-dose ticagrelor for prolonged dual antiplatelet therapy showed to be effective and safe, with no major bleeding occurring at follow-up.
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