Abstract

Previous reports demonstrated a bleeding avoidance potential of angiotensin converting enzyme inhibitor (ACEI)/angiotensin receptor blocker (ARB) and β-blocker. It remains unclear whether early guideline-directed medical therapy [GDMT, i.e., the combined use of β-blocker, angiotensin converting enzyme inhibitor (ACEI)/angiotensin receptor blocker (ARB) and statin] confers protection against bleeding in the setting of high-intensity antithrombotic therapy. We assessed associations between the use of early (within the first 24h) GDMT and in-hospital major bleeds, ischemic events and mortality among ST-elevation myocardial infarction (STEMI) patients treated with percutaneous coronary intervention (PCI) in the Improving Care for Cardiovascular Disease in China-Acute Coronary Syndrome project. Among 34,538 STEMI patients without contra-indications to GDMT and eligible for analysis, 35.5% received early GDMT. In a 1-to-2 propensity-score matched cohort, compared with non-early GDMT, early GDMT was associated with a 25% reduction in major bleeds [odds ratio (OR) 0.75, 95% confidence interval (CI) 0.60-0.94], with parallel reductions in ischemic events (OR 0.60, 95%CI 0.45-0.78) and in-hospital mortality (OR 0.43, 95%CI 0.31-0.61). Early GDMT-associated reduction in major bleeds was generally consistently observed across different major bleeding definitions and in sensitivity analyses. Additionally, no significant interaction was observed in subgroup analyses. In a large nationwide registry, early initiation of GDMT was associated with reduced risk for in-hospital major bleeds in STEMI patients treated with PCI. To improve the outcome of STEMI, further effort should be made to reinforce the early use of GDMT in this patient population.

Highlights

  • Attribute to continued improvement of technical and procedural advances, the outcomes of ST-elevation myocardial infarction (STEMI) patients after percutaneous coronary intervention (PCI) has been dramatically improved.[1, 2] Notably, there has been a concomitant increase in bleeding events associated with the use of more potent, longer-duration perioperative antithrombotic therapy in this patient population.[3]

  • In a large nationwide registry, early initiation of guideline-directed medical therapy (GDMT) was associated with reduced risk for in-hospital major bleeds in STEMI patients treated with PCI

  • Paralleled with reductions in ischemic events and in-hospital mortality, early initiation of GDMT was associated with a 28% reduction in major bleeding risk among STEMI patients treated with PCI

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Summary

Introduction

Attribute to continued improvement of technical and procedural advances, the outcomes of ST-elevation myocardial infarction (STEMI) patients after percutaneous coronary intervention (PCI) has been dramatically improved.[1, 2] Notably, there has been a concomitant increase in bleeding events associated with the use of more potent, longer-duration perioperative antithrombotic therapy in this patient population.[3]. Initiation of guideline-directed medical therapy (GDMT), which includes a combined use of statin, βblocker and angiotensin-converting enzyme inhibitor (ACEI)/angiotensin receptor blocker (ARB), has been recommended in current guidelines for the secondary prevention of atherosclerotic cardiovascular disease (ASCVD) after STEMI.[6,7,8] it's worth noting that recent studies have suggested that individual component of GDMT, such as ACEI/ARB and β-blocker, had potential in reducing bleeding risk.[9, 10] To our knowledge, the impact of GDMT on the risk of bleeding in eligible patients treated with PCI for STEMI remains unclear. Previous reports demonstrated a bleeding avoidance potential of angiotensin converting enzyme inhibitor (ACEI)/angiotensin receptor blocker (ARB) and β-blocker. It remains unclear whether guideline-directed medical therapy [GDMT, i.e., the combined use of β-blocker, angiotensin converting enzyme inhibitor (ACEI)/angiotensin receptor blocker (ARB) and statin] confers protection against bleeding in the setting of high-intensity antithrombotic therapy

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