4.6 Article

Long-Term Impact of Chronic Kidney Disease in Patients With ST-Segment Elevation Myocardial Infarction Treated With Primary Percutaneous Coronary Intervention The HORIZONS-AMI (Harmonizing Outcomes With Revascularization and Stents in Acute Myocardial Infarction) Trial

Journal

JACC-CARDIOVASCULAR INTERVENTIONS
Volume 4, Issue 9, Pages 1011-1019

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.jcin.2011.06.012

Keywords

bivalirudin; chronic kidney disease; ST-segment elevation myocardial infarction

Funding

  1. Medicines Company
  2. Boston Scientific
  3. Medtronic Vascular
  4. LightLab Imaging
  5. Labcoat
  6. Abbott
  7. Adamed
  8. AstraZeneca
  9. Biotronik
  10. Balton
  11. Bayer
  12. BBraun
  13. BioMatrix
  14. Boehringer Ingelheim
  15. Bristol-Myers Squibb
  16. Cordis
  17. Cook
  18. Eli Lilly
  19. EuroCor
  20. Glaxo
  21. Invatec
  22. Medtronic
  23. MSD
  24. Nycomed
  25. Orbus-Neich
  26. Pfizer
  27. Possis
  28. Promed
  29. Sanofi-Aventis
  30. Siemens
  31. Solvay
  32. Terumo
  33. Tyco
  34. BMS/Sanofi-Aventis

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Objectives This study sought to investigate the impact of chronic kidney disease (CKD) in patients undergoing percutaneous coronary intervention (PCI) for ST-segment elevation myocardial infarction (STEMI) with different antithrombotic strategies. Background CKD is associated with increased risk of adverse ischemic and hemorrhagic events after primary PCI for STEMI. Methods HORIZONS-AMI (Harmonizing Outcomes With Revascularization and Stents in Acute Myocardial Infarction) trial was a multicenter, international, randomized trial comparing bivalirudin monotherapy or heparin plus a glycoprotein Ilb/Illa inhibitor (GPI) during primary PCI in STEMI. CKD, defined as creatinine clearance <60 ml/min, was present at baseline in 554 of 3,397 patients (16.3%). Patients were followed for 3 years. Net adverse cardiac event (NACE) was defined as the composite of death, reinfarction, ischemia-driven target vessel revascularization (TVR), stroke or noncoronary artery bypass grafting (CABG)-related major bleeding. Results Patients with CKD compared with patients without had higher rates of NACE (41.4% vs. 23.8%, p < 0.0001), death (18.7% vs. 4.4%, p < 0.0001), and major bleeding (19.3% vs. 6.7%, p < 0.0001). Multivariable analysis identified baseline creatinine as an independent predictor of death at 3 years (hazard ratio: 1.51, 95% confidence interval: 1.21 to 1.87, p < 0.001). Patients with CKD randomized to bivalirudin monotherapy versus heparin plus GPI had no significant difference in major bleeding (19.0% vs. 19.6%, p = 0.72) or death (19.0% vs. 18.4%, p = 0.88) at 3 years. In patients with CKD, there was no difference in the rates of TVR in bare-metal stents (BMS) versus drug-eluting stents (DES) at 3 years (14.1% vs. 15.1%, p = 0.8). Conclusions STEMI patients with CKD have significantly higher rates of death and major bleeding compared with those without CKD. In patients with CKD, there appears to be no benefit of bivalirudin compared with heparin + GPI, or DES versus BMS during primary PCI in improving clinical outcomes. (J Am Coll Cardiol Intv 2011;4:1011-9) (C) 2011 by the American College of Cardiology Foundation

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