4.4 Article

Effect of Smoking on Infarct Size and Major Adverse Cardiac Events in Patients With Large Anterior ST-Elevation Myocardial Infarction (from the INFUSE-AMI Trial)

Journal

AMERICAN JOURNAL OF CARDIOLOGY
Volume 118, Issue 8, Pages 1097-1104

Publisher

EXCERPTA MEDICA INC-ELSEVIER SCIENCE INC
DOI: 10.1016/j.amjcard.2016.07.019

Keywords

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Funding

  1. Boston Scientific
  2. Medtronic
  3. Abbott Vascular
  4. Abiomed
  5. St. Jude Medical
  6. Vascular Dynamics
  7. Eli Lilly
  8. Edwards Lifescience
  9. Cardiovascular Systems Inc.
  10. PiCardia
  11. AstraZeneca
  12. Atrium Medical Corporation
  13. Bayer
  14. Boehringer Ingelheim
  15. Biosensors International
  16. Biotronik
  17. BMS/Sanofi-Aventis
  18. Edwards Lifesciences
  19. Daiichi Sankyo
  20. Magnet
  21. Menarini
  22. St. Jude
  23. Medicines Company
  24. DSI
  25. OrbusNeich
  26. CSL Behring
  27. Janssen Pharmaceuticals Inc.
  28. Merck Co.
  29. Osprey Medical Inc.
  30. Watermark Research Partners
  31. Angel Medical Corporation
  32. Atrium Medical Systems
  33. Bristol Meyers
  34. Squibb Company
  35. Ikaria, Inc.
  36. Janssen Pharmaceuticals
  37. Johnson & Johnson Corporation
  38. Lantheus Medical Imaging
  39. Medtronic Vascular, Inc.
  40. Portola Pharmaceuticals
  41. Stealth Peptides, Inc.
  42. Volcano Corp
  43. Walk Vascular

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We sought to investigate the effect of smoking on infarct size (IS) and major adverse cardiac events (MACE) in patients with large anterior ST-elevation myocardial infarction undergoing primary percutaneous coronary intervention. Participants from the Intracoronary Abciximab and Aspiration Thrombectomy in Patients with Large Anterior Myocardial Infarction study were categorized according to smoking status (current or previous smoking vs no history of smoking). The primary imaging outcome was cardiac magnetic resonance imaging assessed IS of left ventricular mass (%) at 30 days. The primary clinical outcome was the rate of MACE at 30 days and 1 year, defined as the composite of death, reinfarction, new-onset heart failure, or rehospitalization. Of 447 patients enrolled in Intracoronary Abciximab and Aspiration Thrombectomy in Patients with Large Anterior Myocardial Infarction, 271 (60.6%) were current or past smokers. Compared with nonsmokers, smokers were almost 10 years younger and had a lower prevalence of clinical co-morbidities. Smokers had better procedural success and angiographic reperfusion compared with nonsmokers. At 30 days, there were no differences between smokers and nonsmokers in median IS (16.8% vs 17.4%, p = 0.67) or metrics of left ventricular function. By multivariable linear regression analysis, smoking was not significantly associated with IS at 30 days (beta coefficient: 0.83, p = 0.42). At 1 year, smokers had lower crude rates of MACE (7.6% vs 15%, p = 0.01). After multi variable adjustment, there were no significant differences in 1-year MACE between smokers and nonsmokers (adjusted hazard ratio 0.73, 95% CI 0.40 to 1.33, p = 0.30). In conclusion, smoking history had no significant effect on IS at 30 days. Although current or previous smokers had lower rates of 1-year MACE than those with no history of smoking, adjustment for baseline characteristics rendered this association nonsignificant. These findings support the hypothesis that the smoker's paradox is largely attributable to differences in demographic and clinical baseline risk, rather than differences in IS after primary percutaneous coronary intervention. (C) 2016 Elsevier Inc. All rights reserved.

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