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May 1, 2018EuroIntervention33 citations

The efficacy of early versus delayed P2Y12 inhibition in percutaneous coronary intervention for ST-elevation myocardial infarction: a systematic review and meta-analysis

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ABAnne Bellemain-AppaixCBCéline BéguéDBDeepak L. Bhatt

Key Result

Early P2Y12 inhibition significantly reduced major adverse cardiac events compared to delayed inhibition in STEMI patients undergoing PCI (OR 0.73; 95% CI 0.61-0.88; p=0.0008).

Study Design

Type

Meta-Analysis (n=9,648)

Structured PICO

Does early P2Y12 inhibition reduce MACE in patients undergoing PCI for STEMI compared to delayed P2Y12 inhibition?

P
Population
9,648 STEMI patients scheduled for PCI included across 7 randomized controlled trials.
I
Intervention
Early P2Y12 inhibition
C
Comparator
Delayed P2Y12 inhibition
O
Outcome
Major adverse cardiac events (MACE) at the shortest follow-up availablecomposite

Early P2Y12 inhibition in STEMI patients undergoing PCI significantly reduces MACE and myocardial infarction without increasing major bleeding compared to delayed administration.

Main Result

Odds Ratio: 0.73 (95% CI 0.61–0.88)

p-value: p=0.0008

Abstract

AIMS: The aim of this meta-analysis was to compare the benefit of "early" vs. "delayed" P2Y12 inhibition in patients undergoing percutaneous coronary intervention (PCI) for ST-elevation myocardial infarction (STEMI). METHODS AND RESULTS: We conducted a meta-analysis including seven randomised controlled trials (RCTs) which compared early vs. delayed P2Y12inhibition in STEMI patients scheduled for PCI, providing data on major adverse cardiac events (MACE), all-cause death, and major bleeding. The primary endpoint was MACE. Secondary endpoints included stent thrombosis and the use of GP IIb/IIIa inhibitors (GPI). All endpoints were analysed at the shortest follow-up available. A total of 9,648 patients were included ("early"=4,792, "delayed"=4,856). "Early" P2Y12 inhibition was associated with a significant reduction in MACE rate (OR 0.73, 95% CI: 0.61-0.88, p=0.0008), myocardial infarction (OR 0.71, 95% CI: 0.57-0.90, p=0.004), bail-out GPI use (OR 0.87, 95% CI: 0.75-1.00, p=0.04) and improved coronary reperfusion before PCI (OR for Thrombolysis In Myocardial Infarction TIMI flow grade 2-3=1.12, 95% CI: 1.00-1.26, p=0.04). Major bleeding was not increased (OR 0.87, 95% CI: 0.62-1.21, p=0.41). CONCLUSIONS: A strategy of early effective P2Y12 inhibition in PCI of STEMI appears to improve coronary reperfusion before PCI, and reduce MACE, MI and bail-out GPI use without increase of major bleeding.

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Cite This Study

Bellemain-Appaix et al. (2018) conducted a meta-analysis in ST-elevation myocardial infarction (STEMI) (n=9,648). Early P2Y12 inhibition vs. Delayed P2Y12 inhibition was evaluated on Major adverse cardiac events (MACE) (OR 0.73, 95% CI 0.61-0.88, p=0.0008). Early P2Y12 inhibition significantly reduced major adverse cardiac events compared to delayed inhibition in STEMI patients undergoing PCI (OR 0.73; 95% CI 0.61-0.88; p=0.0008).

synapsesocial.com/papers/6a209bee4b6e681fc6911352https://doi.org/10.4244/eij-d-17-00852
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