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Randomized Trial of Stents versus Bypass Surgery for Left Main Coronary Artery Disease:

Randomized Trial of Stents versus Bypass Surgery for Left Main Coronary Artery Disease:. Five-Year Outcomes of the PRECOMBAT Study. Jung-Min Ahn, MD. On behalf of the PRECOMBAT Investigators Professor of Medicine, University of Ulsan College of Medicine,

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Randomized Trial of Stents versus Bypass Surgery for Left Main Coronary Artery Disease:

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  1. Randomized Trial of Stents versus Bypass Surgery for Left Main Coronary Artery Disease: Five-Year Outcomes of the PRECOMBAT Study Jung-Min Ahn, MD. On behalf of the PRECOMBAT Investigators Professor of Medicine, University of Ulsan College of Medicine, Heart Institute, Asan Medical Center, Seoul, Korea

  2. Introduction Recent guidelines considered PCI to be a potential alternative to CABG for ULMCA stenosis, based on several large registries and randomized trials. However, the durable effect of PCI remains in debate and limited data exist regarding the long-term comparison studies between PCI and CABG.

  3. PRECOMBAT Trial Design • DESIGN: a prospective, open-label, randomized trial • OBJECTIVE: To compare PCI with sirolimus-eluting stents and CABG surgery for optimal revascularization of patients with ULMCA stenosis. • PRINCIPAL INVESTIGATOR • Seung-Jung Park, MD, PhD, Asan Medical Center, Seoul, Korea

  4. 600 patients were randomized 300 patients assigned to PCI 300 patients assigned to CABG 24 treated with CABG 276 treated with PCI 0medically treated 248 treated with CABG 51 treated with PCI 1 medically treated 3 lost to FU 2lost to FU 297 remained at 2 years 298 remained at 2 years 18 lost to FU 23 lost to FU 275 remained at 5 years 279 remained at 5 years

  5. Major Inclusion Criteria  18 years of age. Significant de novo ULMCA stenosis (>50%) Left main lesion and lesions outside ULMCA (if present) potentially comparably treatable with PCI and CABG, determined by physician and operators Objective evidence of ischemia or ischemic symptom with angina or NSTEMI

  6. Major Exclusion Criteria Any contraindication to dual antiplatelet therapy Any previous PCI within 1 year Previous CABG Chronic total occlusion > 1 AMI within 1 week Shock or LV EF < 30% Planed surgery Disabled stroke Other comorbidity, such as CRF, liver disease, etc

  7. Study Procedures Sirolimus-eluting Cypher stent for all lesions Strong recommendation of IVUS-guidance Other adjunctive devices at the operator’s discretion Use of LIMA to LAD anastomosis Off- or on-pump surgery at the operator’s discretion Dual antiplatelet therapy at least for 6 months after PCI Standard medical treatment after PCI and CABG

  8. Follow-up Clinical follow-up at 30 days and 6, 9, 12 months, and annually thereafter, via clinic visit or telephone interview. Routine angiographic follow-up at 8-10 months after PCI. Ischemia-guided angiographic follow-up after CABG. Retrospective SYNTAX score measurement in the Core Lab, CVRF, Seoul, Korea

  9. Primary End Point Cumulative rate of major adverse cardiac or cerebrovascular events (MACCE) at 5-year after randomization Death from any cause Myocardial infarction (MI) Stroke Ischemia-driven target vessel revascularization (TVR)

  10. Definition MI Within 48 hours: new Q waves AND CK-MB  5 times After 48 hours: new Q waves OR CK-MB > 1 time plus ischemic symptoms or signs Stroke: confirmed by imaging studies and neurologist TVR Ischemia-driven: ischemic symptom, sign OR angiographic stenosis > 70% Clinical-driven: ischemia symptom or sign

  11. Power Calculation Assumed 1-year rate of primary end point in the CABG group : 13%. A noninferiority margin : 7% A one-sided type I error rate : 0.05 Power : 80% Calculated sample size : a total of 572 patients (286 per group) Final sample size : 600 patients (300 per group) assuming 5% of loss

  12. Statistical Analysis Kaplan-Meier method to estimate cumulative event rates, and log-rank test to compare them Cox proportional hazards model to calculate hazard ratios and 95% confidence intervals Subgroups analysis performed using the Cox regression model with tests for interaction. Primary analysis based on an intention-to-treat principle.

  13. Baseline Clinical Characteristics

  14. Baseline Clinical Characteristics

  15. Baseline Angiographic Characteristics

  16. Procedural Characteristics PCI (N=300) CABG (N=300)

  17. Primary End Point of MACCE

  18. Death, MI or Stroke

  19. Death

  20. Cardiac Death

  21. Myocardial Infarction

  22. Stroke

  23. Ischemia-Driven TVR

  24. Clinical-driven TVR

  25. Conclusion At 5 years, no difference in MACCE was found between patients assigned to PCI with sirolimus-eluting stents and those who underwent CABG, supporting current guidelines stating that left main stenting is a feasible revascularization strategy for patients with suitable coronary anatomy.

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