4.4 Article

Comparison of Outcomes and Prognosis of Patients With Versus Without Newly Diagnosed Diabetes Mellitus After Primary Percutaneous Coronary Intervention for ST-Elevation Myocardial Infarction (the HORIZONS-AMI Study)

Journal

AMERICAN JOURNAL OF CARDIOLOGY
Volume 119, Issue 12, Pages 1917-1923

Publisher

EXCERPTA MEDICA INC-ELSEVIER SCIENCE INC
DOI: 10.1016/j.amjcard.2017.03.016

Keywords

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Funding

  1. Eli Lilly
  2. Indianapolis
  3. Indiana/Daiichi-Sankyo, Inc., Tokyo, Japan
  4. Bristol-Myers Squibb, New York, New York
  5. AstraZeneca, Cambridge, England
  6. Medicines Company, Parsippany, New Jersey
  7. OrbusNeich, Fort Lauderdale, Florida
  8. Bayer, Leverkusen, Germany
  9. CSL Behring, King of Prussia, Pennsylvania
  10. Abbott Laboratories, St. Paul, Minnesota
  11. Watermark Research Partners, Indianapolis, Indiana
  12. Novartis Pharmaceuticals, Basel, Switzerland
  13. Medtronic, Santa Rosa, California
  14. AUM Cardiovascular, Inc., Northfield, Minnesota
  15. Beth Israel Deaconess Medical Center, Boston, Massachusetts

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A history of diabetes mellitus (DM) is an independent predictor for adverse events in patients with acute ST-segment elevation myocardial infarction (STEMI) undergoing primary percutaneous coronary intervention. Outcomes of patients with STEMI and newly diagnosed DM (NDM) are less well described. We used the Harmonizing Outcomes with Revascularization and Stents in Acute Myocardial Infarction (HORIZONS-AMI) trial database to identify the outcomes at 30 days and 3 years according to no, known, and NDM in patients with STEMI. In HORIZONS-AMI, 3,602 patients with STEMI were randomized to bivalirudin versus heparin and a glycoprotein IIb/IIIa inhibitor, and eligible patients were randomized again to a paclitaxel-eluting stent or a bare-metal stent. DM was defined as a history of hyperglycemia managed by insulin, oral hypoglycemic agents, or diet. NDM was defined as the absence of previous diagnosis or treatment for DM at baseline and its addition at discharge. DM was present in 593/3,599 patients (16.5%), and. NDM was diagnosed in 130 cases (3.6%). Compared with nondiabetics, those with DM and NDM had higher 3-year rates of death (11.4% and 12.0% vs 5.6%, respectively, p<0.0001) and major adverse cardiac events (29.6% and 30.2% vs 19.9%, respectively, p<0.0001). There were no significant differences in adverse events between new and known diabetic patients. DM and NDM were independent predictors of 3-year mortality and 3-year major adverse cardiac events. In conclusion, patients with NDM have a similarly poor prognosis after primary percutaneous coronary intervention in STEMI as those with previously established DM. (C) 2017 Elsevier Inc. All rights reserved.

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