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Real-life data for major adverse cardiac events in patients with ST-elevation myocardial infarction prasugrel versus
M H Satilmisoglu1, M Gul2, S Ozyilmaz3
1Department of Cardiology, Istanbul Mehmet Akif Ersoy Thoracic and Cardiovascular Surgery Training and Research Hospital, University of Health Sciences, Istanbul, Turkey. drmg23@gmail.com.
Insights
Prasugrel and ticagrelor show similar effectiveness for major adverse cardiac events in ST-elevation myocardial infarction (STEMI) patients after percutaneous coronary intervention (PCI). However, prasugrel was associated with fewer treatment discontinuations and better tolerability compared to ticagrelor.
Area of Science:
- Cardiology
- Pharmacology
- Clinical Medicine
Background:
- ST-segment-elevation myocardial infarction (STEMI) is a critical condition requiring prompt intervention.
- Oral antiplatelet therapy is essential post-percutaneous coronary intervention (PCI) to prevent thrombotic events.
- Prasugrel and ticagrelor are P2Y12 inhibitors used in STEMI patients, with differing clinical profiles.
Purpose of the Study:
- To compare the efficacy and safety of prasugrel versus ticagrelor in STEMI patients undergoing primary PCI.
- To evaluate major adverse cardiac events (MACE) and other clinical outcomes between the two antiplatelet agents.
- To assess treatment discontinuation rates and reasons, particularly dyspnea-related, between prasugrel and ticagrelor.
Main Methods:
- A prospective comparative study included 560 STEMI patients suitable for PCI.
- Patients received either prasugrel (n=232) or ticagrelor (n=328) as oral antiplatelet therapy.
- Follow-up averaged 10.9 months for prasugrel and 11.9 months for ticagrelor, monitoring MACE, mortality, bleeding, and stent thrombosis.
Main Results:
- Major adverse cardiac events occurred at similar rates: 7.3% for prasugrel vs. 7.9% for ticagrelor (p=0.793).
- Mortality rates were higher in the ticagrelor group (6.7%) but not statistically significant compared to prasugrel (3.4%, p=0.092).
- Treatment discontinuation was significantly higher with ticagrelor (14.3%) vs. prasugrel (8.6%, p=0.023), primarily due to dyspnea in the ticagrelor group (p=0.001).
Conclusions:
- Prasugrel and ticagrelor demonstrate comparable efficacy in preventing MACE in STEMI patients post-PCI.
- Prasugrel exhibits superior tolerability, leading to significantly lower treatment discontinuation rates compared to ticagrelor.
- The findings suggest prasugrel may be a preferred option when long-term adherence is a concern due to side effects like dyspnea.
Abstract:
We aimed to evaluate the major adverse cardiac events and other clinical outcomes in ST-segment-elevation myocardial infarction (STEMI) cases treated with prasugrel versus ticagrelor after percutaneous intervention (PCI). The study was a prospective comparative study into which 560 patients diagnosed with STEMI, being suitable for PCI, and prescribed with either prasugrel (n = 232) or ticagrelor (n = 328) as oral antiplatelet therapy were included. Patients were followed up for a mean of 10.9 ± 4.7 months and 11.9 ± 4.9 months for prasugrel and ticagrelor groups, respectively. The major adverse cardiac events developed in similar rates between prasugrel and ticagrelor groups (7.3% versus 7.9%, respectively, p = 0.793). Even if mortality rate was higher in ticagrelor group, the difference did not reach statistically significance (3.4% vs. 6.7%, p=0.092). Among all study population, stent thrombosis and minor bleeding was recorded only in 7 (1.2%) and 12 (2.1%) patients without significant difference between prasugrel and ticagrelor groups. Twenty patients (8.6%) in prasugrel group and 47 patients (14.3%) in ticagrelor group discontinued treatment (p = 0.023). In ticagrelor group, 12 patients discontinued treatment due to dyspnea, but none in prasugrel group (p = 0.001). Prasugrel and ticagrelor have similar effects on major adverse cardiac events in patients with STEMI undergoing primary PCI, but prasugrel seems more tolerated and less discontinued than ticagrelor.
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