4.4 Article

Comparison of Clinical Trial Outcome Patterns in Patients Following Acute Coronary Syndromes and in Patients With Chronic Stable Atherosclerosis

期刊

CLINICAL CARDIOLOGY
卷 37, 期 6, 页码 337-342

出版社

WILEY-BLACKWELL
DOI: 10.1002/clc.22255

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资金

  1. Merck Co.
  2. Aastrom Biosciences
  3. Anthera Pharmaceuticals
  4. AstraZeneca Pharmaceuticals
  5. Bristol-Myers Squibb
  6. Cardiovascular Systems
  7. Centocor Research Development
  8. Edwards Lifesciences
  9. Eli Lilly
  10. Ethicon
  11. Johnson & Johnson Pharmaceutical Research Development
  12. Juventas Therapeutics
  13. KAI Pharmaceuticals
  14. Karo Bio
  15. Medtronic
  16. Novartis Pharmaceuticals
  17. Orexigen Therapeutics
  18. Pfizer
  19. Regado Biosciences
  20. Resverlogix
  21. Roche
  22. Sanofi
  23. Schering-Plough
  24. Scios
  25. Takeda Pharmaceuticals North America
  26. VIVUS
  27. Amarin
  28. AstraZeneca
  29. Eisai
  30. sanofi-aventis
  31. Athera Biotechnologies
  32. Boehringer-Ingelheim
  33. GlaxoSmithKline
  34. Abbott
  35. Merck/ScheringPlough
  36. Bristol-Myers Squibb/Pfizer

向作者/读者索取更多资源

Background: The transition of patients with atherosclerotic vascular disease from the acute phase of the disease to the chronic stable atherosclerosis (CSA) phase has not been well characterized. We sought to compare ischemic and bleeding outcomes in hospitalized patients enrolled in clinical trials of non-ST-elevation acute coronary syndrome (ACS) with patients enrolled in outpatient trials of CSA. Hypothesis: The risk for recurrent events will differ between the 2 populations. Methods: Patient-level outcome data were evaluated from 3 consecutive trials of patients with ACS with long-term follow-up and 2 trials of patients with CSA. Kaplan-Meier curves were generated for ischemic and bleeding outcomes. Results: In total, 37 370 patients were included in these analyses. Of these, 28 489 (76.2%) were from ACS trials and 8881 (23.8%) from chronic trials. During the first year of follow-up, 1353 deaths, 1081 cardiovascular (CV) deaths, 2113 myocardial infarctions (MIs), and 397 strokes occurred across the trials. Six-month Kaplan-Meier event rates for CV death, MI, or stroke were higher in the ACS trials compared with the CSA trials (8.6% vs 2.7%), as were the 1-year CV death rate (3.6% vs 1.7%) and 1-year rates for GUSTO moderate or severe bleeding (6.0% vs 1.3%). Qualitatively, the Kaplan-Meier curves appear to show an early increased risk as well as a continued increased risk over time. Conclusions: Patients with ACS enrolled while in the hospital appear to have different risk profiles for ischemic and bleeding outcomes compared with outpatients enrolled with CSA, including those patients with ACS after the acute phase.

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