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J Am Coll Cardiol, 2003; 42:971-977, doi:10.1016/S0735-1097(03)00911-2
© 2003 by the American College of Cardiology Foundation
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Outcomes of optimal or "stent-like"balloon angioplasty in acutemyocardial infarction: the CADILLAC trial

David A. Cox, MD, FACC*,*, Gregg W. Stone, MD, FACC{dagger}, Cindy L. Grines, MD FACC{ddagger}, Thomas Stuckey, MD, FACC§, David J. Cohen, MD||, James E. Tcheng, MD, FACC, Eulogio Garcia, MD#, Giulio Guagliumi, MD**, Robert S. Iwaoka, MD, FACC*, Martin Fahy, MSc{dagger}, Mark Turco, MD, FACC{dagger}{dagger}, Alexandra J. Lansky, MD, FACC{dagger}, John J. Griffin, MD, FACC{ddagger}{ddagger}, Roxana Mehran, MD, FACC{dagger} CADILLAC Investigators

* Mid Carolina Cardiology, Charlotte, North Carolina, USA
{dagger} The Cardiovascular Research Foundation and Lenox Hill Heart and Vascular Institute, New York, New York, USA
{ddagger} William Beaumont Hospital, Royal Oak, Michigan, USA
§ Moses Cone Memorial Hospital, Greensboro, North Carolina, USA
|| Beth Israel Deaconess Medical Center, Boston, Massachusetts, USA
Duke Clinical Research Institute, Durham, North Carolina, USA
# Hospital Gregorio Maranon, Madrid, Spain
** Ospedali Riuniti di Bergamo, Bergamo, Italy
{dagger}{dagger} Doylestown Hospital, Doylestown, Pennsylvania, USA
{ddagger}{ddagger} Virginia Beach General Hospital, Virginia Beach, Virginia, USA



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Figure 1 Individual and composite adverse event rates at 30 days (upper graph) and 1 year (lower graph) in patients achieving optimal percutaneous transluminal coronary angioplasty (PTCA) results randomized to pre-procedural abciximab administration (white bars) versus no pre-procedural abciximab. The p values for all two-way comparisons in both graphs are non-significant. TVR = target vessel revascularization.

 


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Figure 2 Subgroup analysis for the one-year composite end point of death, disabling stroke, reinfarction, or ischemic target vessel revascularization, comparing patients achieving an optimal percutaneous transluminal coronary angioplasty (PTCA) result (n = 415) with all patients randomized to stent implantation (n = 1,036), displayed as hazard ratios (black boxes) with 95% confidence intervals (CI) (horizontal limit lines). OR = odds ratio.

 




 
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