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Time Course of Death After Acute Coronary Syndrome Treated With Dual Antiplatelet Therapy for 1 Year
Victor L Serebruany1, Jean-Francois Tanguay2, Milana L Gurvich3
1Department of Neurology, Johns Hopkins University, Baltimore, Md.
Insights
Dual antiplatelet therapy (DAPT) after acute coronary syndrome shows most deaths occur within the first week. This finding supports shorter DAPT durations for improved survival and reduced bleeding risks.
Area of Science:
- Cardiology
- Clinical Trials
- Pharmacology
Background:
- Excess mortality is a primary concern following acute coronary syndrome (ACS) despite dual antiplatelet therapy (DAPT).
- Shorter DAPT durations may reduce bleeding risks while maintaining vascular protection and improving survival.
- Understanding the precise timing of post-ACS deaths is crucial for optimizing DAPT duration.
Purpose of the Study:
- To analyze the timing of death events in patients treated with DAPT after ACS.
- To inform optimal DAPT treatment duration based on mortality patterns.
Main Methods:
- Post hoc analysis of the Platelet Inhibition and Outcomes (PLATO) trial data.
- Examination of all-cause individual death events plotted over 365 days post-ACS.
- Analysis included 913 fatalities from patients on aspirin/ticagrelor or aspirin/clopidogrel.
Main Results:
- The majority of deaths (22.1%) occurred within the first week after ACS.
- Peak mortality was observed on Days 1, 2, and 3 post-event.
- Mortality rates gradually declined after Day 10 and Day 60, reaching background levels by Day 220.
Conclusions:
- The timing of mortality suggests that a DAPT duration shorter than 12 months may be sufficient.
- This supports focusing on mortality reduction strategies with potentially shorter DAPT regimens.
Background:
Excess mortality remains the cornerstone concern despite dual antiplatelet therapy (DAPT) after acute coronary syndrome. Some data suggest that shorter periods than 12 months of DAPT diminish bleeding risks yet still provide adequate vascular protection and improving survival. However, the precise timing of deaths after acute coronary syndrome has not been mapped in many studies. This knowledge may be critical for defining optimal treatment duration.
Methods:
Access was gained to the data set for the Platelet Inhibition and Outcomes (PLATO) trial, which was issued by the Food and Drug Administration, in which post hoc analyses of timing of death events during DAPT (with either aspirin/ticagrelor or aspirin/clopidogrel) were performed. All-cause individual deaths were counted and plotted over time from day 1 to day 365 after the index event.
Results:
Among 18,624 enrollees, 938 total deaths were reported to the Food and Drug Administration in PLATO. After exclusion of deceased patients with missing dates, randomization errors, and deaths beyond 1 year of follow-up, 913 fatalities (509 after clopidogrel and 404 after ticagrelor) were analyzed. The PLATO records did not indicate where exactly deaths occurred making impossible to triage in the hospital versus outpatient fatalities. Most frequent deaths occurred within the Day 1 (n = 41); Day 2 (n = 48); and Day 3 (n = 33) and overall during the first week (n = 202; 22.1%) after the index acute coronary syndrome, with a gradual decline after Day 10 and Day 60, reaching background counts after Day 220.
Conclusion:
Focusing on mortality reduction, this large data set may support a shorter than 12 months' duration of DAPT.
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