Key result
P2Y12 inhibitor pretreatment in STEMI linked to ~39% reduction in definite stent thrombosis and lower mortality.
Why the study?
While dual antiplatelet therapy with aspirin and P2Y12 inhibitors improves outcomes in STEMI, the optimal timing of its initiation remains uncertain.
Does pretreatment with P2Y12 inhibitors improve clinical outcomes in patients with STEMI undergoing primary PCI?
Meta-Analysis (n=79,300)
Does pretreatment with P2Y12 inhibitors improve clinical outcomes in patients with STEMI undergoing primary PCI?
Odds Ratio: 0.61 (95% CI 0.38–0.98)
Pretreatment with P2Y12 inhibitors in STEMI patients undergoing primary PCI is associated with reduced definite stent thrombosis, all-cause death, and cardiogenic shock without increasing major bleeding.
Supports P2Y12 pretreatment in STEMI primary PCI; confirms lower stent thrombosis and mortality without excess bleeding.
Dual antiplatelet therapy with aspirin and P2Y12 inhibitors in patients with ST-segment elevation myocardial infarction (STEMI) has been shown to be associated with better outcomes. Yet, there is uncertainty regarding the optimal timing for its initiation. We performed a systematic review and meta-analysis of evidence on pretreatment with P2Y12 inhibitors in combination with aspirin in patients with STEMI undergoing primary percutaneous coronary intervention (PCI). We performed a systematic search of electronic databases PubMed, CENTRAL, and Scopus until April 2022. Studies were eligible if they compared P2Y12 inhibitor upstream administration with downstream use in patients with STEMI submitted to PCI. Studies with patients receiving fibrinolysis or medical therapy only were excluded. Outcomes were assessed at the shortest follow-up available. Of 2491 articles, 3 RCT and 16 non-RCT studies were included, with a total of 79,300 patients (66.1% pretreated, 66.0% treated with clopidogrel). Pretreatment was associated with reduction in definite stent thrombosis (odds ratio [OR] 0.61 [0.38-0.98]), all-cause death (OR 0.77 [0.60-0.97]), and cardiogenic shock (OR 0.60 [0.48-0.75]). It was also associated with a lower incidence of thrombolysis in myocardial infarction flow <3 pre-PCI (OR 0.78 [0.67-0.92]). However, incidence of recurrent MI was not significantly reduced (OR 0.93 [0.57-1.52]). Regarding safety, pretreatment was not associated with a higher risk of major bleeding events (OR 0.83 [0.75-0.92]). Pretreatment with dual antiplatelet therapy, including a P2Y12 inhibitor, was associated with better pre-PCI coronary perfusion, lower incidence of definite stent thrombosis, cardiogenic shock, and, possibly, all-cause mortality with no sign of potential harm encountered.
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Presume et al. (2023) conducted a meta-analysis in ST-segment elevation myocardial infarction (STEMI) (n=79,300). P2Y12 inhibitor pretreatment (upstream administration) vs. Downstream use was evaluated on Definite stent thrombosis (OR 0.61, 95% CI 0.38-0.98). Pretreatment with P2Y12 inhibitors in STEMI patients undergoing primary PCI was associated with reduced definite stent thrombosis (OR 0.61; 95% CI 0.38-0.98) and all-cause death (OR 0.77).
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