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Effect of Extended Dual Antiplatelet Therapy on the Prognosis of Patients With ST Segment Elevation Myocardial
Ya-Chao Li1, Jing-Yao Wang1, Meng-Jie Lei1
1Department of Cardiology, Langfang People's Hospital, Hebei Medical University Langfang Core Laboratory of Precision Treatment of Coronary Artery Disease Langfang Hebei China.
Insights
Extending dual antiplatelet therapy (DAPT) to 18-24 months for ST-segment elevation myocardial infarction (STEMI) patients after percutaneous coronary intervention (PCI) did not reduce major adverse cardiovascular events. However, extended DAPT significantly increased bleeding events.
Area of Science:
- Cardiology
- Interventional Cardiology
- Pharmacology
Background:
- Dual antiplatelet therapy (DAPT) is standard after percutaneous coronary intervention (PCI) for ST-segment elevation myocardial infarction (STEMI).
- Optimal DAPT duration remains a key clinical question, balancing ischemic event prevention against bleeding risk.
Purpose of the Study:
- To evaluate the impact of extending DAPT duration to 18-24 months versus standard 12-month therapy on prognosis in STEMI patients undergoing PCI.
Main Methods:
- A retrospective study of 757 STEMI patients undergoing PCI.
- Patients were divided into standard (12 months DAPT) and extended (18-24 months DAPT) groups.
- Primary endpoint: Major adverse cardiovascular and cerebrovascular events (MACCEs); Secondary endpoint: Bleeding events.
Main Results:
- No statistically significant difference in MACCEs between the standard and extended DAPT groups (4.6% vs. 3.9%, p=0.66).
- The incidence of bleeding events was significantly higher in the extended DAPT group (10.7%) compared to the standard group (5.2%, p=0.007).
Conclusions:
- Continuing DAPT for 18-24 months in STEMI patients undergoing PCI does not reduce ischemic events.
- Extended DAPT duration is associated with an increased risk of bleeding events, particularly minor bleeding.
Background And Aims:
To inquire the effect of extending the duration of dual antiplatelet therapy (DAPT) to 18-24 months on the prognosis of patients with ST segment elevation myocardial infarction (STEMI) undergoing percutaneous coronary intervention (PCI).
Methods:
A retrospective investigation were conducted on 757 patients with STEMI from a single center from September 2016 to August 2020. Based on the duration of postoperative DAPT, patients were divided into a standard group (n = 326) and an extended group (n = 431). Those in the standard group received aspirin 100 mg + ticagrelor 90 mg or clopidogrel 75 mg for 12 months, after which the drug regimen was changed to aspirin 100 mg, once per day. Those in the extended group received aspirin 100 mg + ticagrelor 90 mg or clopidogrel 75 mg that was continued for 18-24 months. The duration of DAPT in all patients was ≥ 12 months, and the follow-up time was 12 months, 18 months, and 24 months after PCI. The primary end point was major adverse cardiovascular and cerebrovascular events (MACCEs) during the follow-up period, including composite end points of cardiac death, myocardial infarction, ischemia-driven revascularization, and stroke. The major safety endpoint was bleeding events.
Results:
The results showed that during follow-up, the difference in the incidence of MACCEs between the two groups (4.6% vs. 3.9%, χ² = 0.198, p = 0.66) was not statistically significant, but the incidence of bleeding events in the standard group was significantly lower than that in the extended group (5.2% vs. 10.7%, χ² = 7.242, p = 0.007).
Conclusion:
For patients with STEMI undergoing PCI, continuing DAPT to 18-24 months did not reduce ischemic events but increased the incidence of bleeding events, especially minor bleeding events.
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