Key result
Dual antiplatelet therapy for more than 13 months following percutaneous coronary intervention for acute coronary syndrome was associated with a higher non-adjusted incidence of Major Adverse Cardiovascular Events (17.3% vs. 11.6%) compared to 13 months or less.
Why the study?
Studies have provided inconclusive evidence on the effects of prolonged dual antiplatelet therapy following percutaneous revascularization for acute coronary syndrome.
Does prolonged dual antiplatelet therapy (>13 months) improve clinical outcomes in acute coronary syndrome patients treated with percutaneous coronary intervention who are event-free at 1 year?
Observational (n=750)
Yes
Does prolonged dual antiplatelet therapy (>13 months) improve clinical outcomes in acute coronary syndrome patients treated with percutaneous coronary intervention who are event-free at 1 year?
Answers are grounded in this paper and cite their sources.
Multicenter registry study observes higher rates of adverse cardiovascular events with prolonged dual antiplatelet therapy in acute coronary syndrome, highlighting the need for tailored strategies.
Background The optimal duration of dual antiplatelet therapy (DAPT) ought to be determined taking into account individual ischaemic or bleeding events risks. To date, studies have provided inconclusive evidence on the effects of prolonged DAPT. We sought to evaluate the long-term outcomes of this strategy following percutaneous revascularization in the context of acute coronary syndrome (ACS). Methods Retrospectively from four centers in Madrid, we identified 750 consecutive ACS patients, divided in two groups of DAPT duration: <13 months and >13 months, with a mean follow-up of 48 months. Results Patients with DAPT > 13 months had a higher non-adjusted incidence of Major Adverse Cardiovascular Events (11.6% vs. 17.3%) and new revascularization (3.7% vs. 8.7%). Differences in all-cause death, cardiac death, myocardial infarction, stent thrombosis and stroke were non-significant. There was no difference in the incidence of major bleeding (7.4% vs. 6.3%). Multivariable Cox regression analysis showed that the independent risk predictors of MACE were age (HR: 1.04, 95% CI: 1.02–1.06, p < 0.001) and multivessel disease (HR: 2.29, 95% CI: 1.32–3.95, p = 0.003), whereas the independent protective predictor was normal hemoglobin (HR: 0.88, 95% CI: 0.78–0.98, p = 0.022). Conclusions In this real-world registry cohort of ACS patients treated with PCI and 1 year of DAPT in Spain, we report a trend of increased rate of MACE and new revascularization not associated with TVR in patients with longer DAPT. Our findings support the need for future randomized controlled trials to confirm or refute these results.
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Vergara-Uzcategui et al. (2023) conducted an observational in Acute coronary syndrome (ACS) (n=750). Dual antiplatelet therapy (DAPT) >13 months vs. Dual antiplatelet therapy (DAPT) ≤13 months was evaluated on Major Adverse Cardiovascular Events (MACE) (p=0.040). Dual antiplatelet therapy for more than 13 months following percutaneous coronary intervention for acute coronary syndrome was associated with a higher non-adjusted incidence of Major Adverse Cardiovascular Events (17.3% vs. 11.6%) compared to 13 months or less.
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