Abstract
Background and Objectives: Although current guidelines recommend early initiation of statin in patients with acute myocardial infarction (AMI), there is no consensus for optimal timing of statin initiation. Methods: A total of 3,921 statin-naïve patients undergoing percutaneous coronary intervention were analyzed, and divided into 3 groups according to statin initiation time: group 1 (statin initiation 24 hours after admission), group 2 (24–48 hours) and group 3 (≥48 hours). We also made 3 stratified models to reduce bias: model 1 (24 hours vs. ≥24 hours), model 2 (48 hours vs. ≥48 hours) and model 3 (24 hours vs. 24–48 hours). The endpoint was major adverse cardiac events (MACE; composite of cardiac death, myocardial infarction and target-vessel revascularization) during median 3.8 years. Results: During follow-up, incidence of MACE was lower in early statin group in both model 1 (14.3% vs. 18.4%, hazard ratio [HR], 0.77; 95% confidence interval [CI], 0.66–0.91; p=0.002) and model 2 (14.6% vs. 19.7%, HR, 0.81; 95% CI, 0.67–0.97; p=0.022). After propensity-score matching, results remained unaltered. Statin initiation 24 hours reduced MACE compared to statin initiation ≥24 hours in model 1. Statin initiation 48 hours also reduced MACE compared to statin initiation later in model 2. However, there was no difference in incidence of MACE between statin initiation 24 hours and 24–48 hours) in model 3. Conclusions: Early statin therapy within 48 hours after admission in statin-naïve patients with AMI reduced long-term clinical outcomes compared with statin initiation later.
Original language | English |
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Pages (from-to) | 419-433 |
Number of pages | 15 |
Journal | Korean Circulation Journal |
Volume | 49 |
Issue number | 5 |
DOIs | |
State | Published - May 2019 |
Bibliographical note
Publisher Copyright:© 2019. The Korean Society of Cardiology This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (https://creativecommons.org/licenses/by-nc/4.0) which permits unrestricted noncommercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
Keywords
- Hydroxymethylglutaryl-CoA reductase inhibitors
- Myocardial infarction
- Percutaneous coronary intervention