4.6 Article

Comparative Effectiveness and Safety of New-Generation Versus Early-Generation Drug-Eluting Stents According to Complexity of Coronary Artery Disease A Patient-Level Pooled Analysis of 6,081 Patients

Journal

JACC-CARDIOVASCULAR INTERVENTIONS
Volume 8, Issue 13, Pages 1657-1666

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.jcin.2015.08.013

Keywords

coronary artery disease complexity; drug-eluting stent(s); percutaneous coronary intervention; SYNTAX score

Funding

  1. Italian Society of Cardiology
  2. Veronesi Foundation
  3. Medtronic
  4. Biotronik
  5. Veronesi Foundation-Cardiovascular research
  6. AstraZeneca
  7. Biosensors International
  8. Eli Lilly
  9. Medicines Company
  10. Abbott Vascular
  11. Biosensors
  12. St. Jude Medical
  13. Abbott
  14. Boston Scientific
  15. Edwards Lifesciences, Inc.
  16. St. Jude

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OBJECTIVES The purpose of this study was to compare the 2-year safety and effectiveness of new-versus early-generation drug-eluting stents (DES) according to the severity of coronary artery disease (CAD) as assessed by the SYNTAX (Synergy between Percutaneous Coronary Intervention with Taxus and Cardiac Surgery) score. BACKGROUND New-generation DES are considered the standard-of-care in patients with CAD undergoing percutaneous coronary intervention. However, there are few data investigating the effects of new-over early-generation DES according to the anatomic complexity of CAD. METHODS Patient-level data from 4 contemporary, all-comers trials were pooled. The primary device-oriented clinical endpoint was the composite of cardiac death, myocardial infarction, or ischemia-driven target-lesion revascularization (TLR). The principal effectiveness and safety endpoints were TLR and definite stent thrombosis (ST), respectively. Adjusted hazard ratios (HRs) with 95% confidence intervals (CIs) were calculated at 2 years for overall comparisons, as well as stratified for patients with lower (SYNTAX score <= 11) and higher complexity (SYNTAX score >11). RESULTS A total of 6,081 patients were included in the study. New-generation DES (n = 4,554) compared with earlygeneration DES (n = 1,527) reduced the primary endpoint (HR: 0.75 [95% CI: 0.63 to 0.89]; p = 0.001) without interaction (p = 0.219) between patients with lower (HR: 0.86 [95% CI: 0.64 to 1.16]; p = 0.322) versus higher CAD complexity (HR: 0.68 [95% CI: 0.54 to 0.85]; p = 0.001). In patients with SYNTAX score >11, new-generation DES significantly reduced TLR (HR: 0.36 [95% CI: 0.26 to 0.51]; p < 0.001) and definite ST (HR: 0.28 [95% CI: 0.15 to 0.55]; p < 0.001) to a greater extent than in the low-complexity group (TLR p(int) = 0.059; ST p(int) = 0.013). New-generation DES decreased the risk of cardiac mortality in patients with SYNTAX score >11 (HR: 0.45 [95% CI: 0.27 to 0.76]; p = 0.003) but not in patients with SYNTAX score <= 11 (p(int) = 0.042). CONCLUSIONS New-generation DES improve clinical outcomes compared with early-generation DES, with a greater safety and effectiveness in patients with SYNTAX score >11. (C) 2015 by the American College of Cardiology Foundation.

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