Key result
Selective triple antithrombotic therapy was not associated with a significant difference in net adverse clinical events compared to ticagrelor-based dual antiplatelet therapy in patients with anterior STEMI and apical dysfunction (OR 1.87, p=0.169).
Why the study?
Does systematic ticagrelor-based DAPT reduce net adverse clinical events compared to selective triple antithrombotic therapy in patients with anterior STEMI and apical dysfunction?
Cohort (n=177)
Yes
Does systematic ticagrelor-based DAPT reduce net adverse clinical events compared to selective triple antithrombotic therapy in patients with anterior STEMI and apical dysfunction?
Odds Ratio: 1.87 (95% CI 0.77–4.54)
Absolute Event Rate: 27% vs 19%
p-value: p=0.169
In patients with anterior STEMI and apical dysfunction, systematic ticagrelor-based DAPT was associated with similar ischemic outcomes but significantly less major bleeding compared to selective triple antithrombotic therapy.
No practice change warranted in STEMI with apical dysfunction; hypothesis-generating for randomized confirmation of ticagrelor-DAPT.
Antithrombotic management of STEMI patients with apical dysfunction, but without demonstrable thrombus, is controversial. Triple antithrombotic therapy (TATT, defined as the addition of oral anticoagulation to dual antiplatelet therapy, or DAPT) may be associated with increased bleeding, while DAPT alone may not adequately protect against cardio-embolic events. We undertook a dual-center study of anterior STEMI patients treated with primary PCI (pPCI) from 2013 to 2015 and presenting presumed new apical dysfunction. The Centre hospitalier de l'Université de Montréal (CHUM) uses a strategy of selective TATT, whereas the Centre hospitalier universitaire de Sherbrooke (CHUS) has favored ticagrelor-based DAPT for all patients since 2013. The primary composite outcome consisted of death, MI, stroke, revascularization, and BARC 3 to 5 bleeding up to 4-months follow-up. We identified 177 cases (69 CHUM; 108 CHUS). Baseline characteristics were similar and procedural success was high (97%). There was no difference in post-procedure LVEF (39 ± 9% vs 37 ± 9%) or the extent of apical dysfunction. The primary composite outcome occurred in 27% with the selective TATT strategy compared to 19% with ticagrelor-DAPT (p = 0.342). Thus, this retrospective dual-center analysis does not support a strategy of conventional TATT over ticagrelor-based DAPT for patients with apical dysfunction following anterior STEMI treated with pPCI. A pragmatic randomized trial is needed to provide a definitive answer to this clinical conundrum.
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Bastiany et al. (2018) conducted a cohort in Anterior STEMI with apical dysfunction (n=177). Selective triple antithrombotic therapy (TATT) vs. Ticagrelor-based dual antiplatelet therapy (DAPT) was evaluated on Net adverse clinical event (NACE) composite outcome (OR 1.87, 95% CI 0.77-4.54, p=0.169). Selective triple antithrombotic therapy was not associated with a significant difference in net adverse clinical events compared to ticagrelor-based dual antiplatelet therapy in patients with anterior STEMI and apical dysfunction (OR 1.87, p=0.169).
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