Risk Stratification after an Acute Coronary Syndrome: Significance of Antithrombotic Therapy
Victoria A Brazhnik1,2, Larisa O Minushkina1, Olga I Boeva1
1Central State Medical Academy of Department of Presidential Affairs, 121359 Moscow, Russia.
Insights
De-escalating antiplatelet therapy (APT) after acute coronary syndromes (ACS) and percutaneous coronary intervention (PCI) is safe and reduces mortality. This strategy, switching from potent to less potent drugs, shows a lower death rate without increasing bleeding or recurrent events.
Area of Science:
- Cardiology
- Clinical Practice
- Pharmacotherapy
Background:
- Assessing antiplatelet therapy (APT) de-escalation impact on life expectancy post-acute coronary syndromes (ACS) and percutaneous coronary intervention (PCI) is crucial in real-world settings.
- The ORACLE II trial (NCT04068909) enrolled 1803 patients with ACS and PCI indications.
Purpose of the Study:
- To evaluate the effect of APT de-escalation on mortality and clinical outcomes in patients after ACS and PCI.
- To identify predictors of death in this patient population.
Main Methods:
- A multicenter observational study (ORACLE II) involving 1803 patients.
- Classification tree method used for death predictor analysis.
- Pseudorandomization employed to adjust for clinical parameters between therapy groups.
Main Results:
- Age, antithrombotic therapy choice, chronic heart failure history, and uric acid level were key death predictors.
- A death prediction model demonstrated 82.1% sensitivity in training and 79.2% in testing cohorts.
- Patients undergoing APT de-escalation (357 patients) exhibited a lower all-cause death rate compared to those on continuous potent therapy, with no significant difference in bleeding or recurrent coronary events.
Conclusions:
- APT de-escalation from potent to moderate regimens after ACS and PCI is associated with improved survival.
- Individualizing antiplatelet therapy strategies in patients post-ACS warrants further investigation.
Abstract:
The impact of the de-escalation strategy of antiplatelet therapy (APT) on the life expectancy after acute coronary syndromes (ACS) and percutaneous coronary intervention (PCI) requires an assessment in real clinical practice. Into the Russian multicentral observational trial (ORACLE II ClinicalTrials.gov number, NCT04068909), 1803 patients with ACS and PCI indications were enrolled. During 12 months of follow-up, 228 all-cause deaths have occurred. The analysis of death predictors was carried out by the classification tree method. Age, an option of antithrombotic therapy, a history of chronic heart failure, and uric acid level had the greatest prognostic value. The death prediction model's sensitivity was 82.1% in the training cohort and 79.2% in the test cohort. During the observation period, ticagrelor was replaced with clopidogrel (APT de-escalation) in 357 patients. The groups of patients with different antiplatelet therapy options were adjusted for clinical parameters by the pseudorandomization method. The de-escalation group had the lowerest all-cause death rate. The incidence of bleeding and recurrent nonfatal coronary events in the study groups did not differ significantly. Thus, the APT regimen's advantage of changing from the maximum in the first weeks after ACS to moderate at follow-up has been confirmed. There is an obvious need to study the possibilities of individualizing antiplatelet therapy in patients after acute coronary syndromes.
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