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Fergus, Icilma

Mayo Clinic

Mount Sinai Hospital

Citations 2

Everolimus‐eluting stents and zotarolimus‐eluting stents for percutaneous coronary interventions
Ye, Zhong, Wu, Chuntao , Walford, Gary, Holmes, David R. , Jacobs, Alice K. , Stamato, Nicholas J., Venditti, Ferdinand J. , Sharma, Samin, Fergus, Icilma, King, Spencer B., Hannan, Edward L. , Sharma, Samin

Catheterization and Cardiovascular Interventions | June 18, 2012 | Volume: 81 | Issue: 7 | Pages: 1097-1105

10.1002/ccd.24512 Get It

ObjectivesTo compare 2‐year outcomes (mortality, mortality/myocardial infarction (MI), target vessel PCI (TVPCI), and target lesion PCI (TLPCI)) for patients receiving EES and ZES.BackgroundThe utilization of drug‐eluting coronary stents (DES) among patients undergoing percutaneous coronary interventions (PCI) has increased dramatically in the last decade. Everolimus‐eluting stents (EES) and ENDEAVOR zotarolimus eluting stents (ZES) constitute the latest generation of approved DES in the United States, but little is known about their relative effectiveness.MethodsNew York patients undergoing EES and ZES revascularization without any other type of stent between 7/08 and 12/08 were propensity matched at the hospital level using multiple patient, operator, and hospital characteristics, and matched patients were followed through the end of 2010 to obtain comparative 2‐year outcomes.ResultsA total of 3286 patients were propensity‐matched. Patients receiving EES had a significantly lower TVPCI rate (9.0% vs. 11.9%, AHR = 1.31, 95% CI (1.04, 1.65)) and a significantly lower TLPCI rate (6.0% vs. 8.3%, AHR = 1.35, 95% CI (1.02, 1.79)). There was no significant difference between EES and ZES for mortality or MI/mortality.ConclusionsThere were no significant differences in the hard endpoints of death or MI between patients who received EES versus those who received ZES (ENDEAVOR). Patients with EES experienced lower repeat revascularization rates than patients with ZES at 24 months. © 2012 Wiley Periodicals, Inc.
Impact of Incomplete Revascularization on Long-Term Mortality After Coronary Stenting
Wu, Chuntao , Dyer, Anne-Marie, King, Spencer B., Walford, Gary, Holmes, David R. , Stamato, Nicholas J., Venditti, Ferdinand J. , Sharma, Samin K., Fergus, Icilma, Jacobs, Alice K. , Sharma, Samin K., Hannan, Edward L.

Circulation: Cardiovascular Interventions | October 5, 2011 | Volume: 4 | Issue: 5 | Pages: 413-421

10.1161/circinterventions.111.963058 Get It

Background— The impact of incomplete revascularization (IR) on adverse outcomes after percutaneous coronary intervention remains inconclusive, and few studies have examined mortality during follow-ups longer than 5 years. The objective of this study is to test the hypothesis that IR is associated with higher risk of long-term (8-year) mortality after stenting for multivessel coronary disease. Methods and Results— A total of 13 016 patients with multivessel disease who had undergone stenting procedures with bare metal stents in 1999 to 2000 were identified in the New York State's Percutaneous Coronary Intervention Reporting System. A logistic regression model was fit to predict the probability of achieving complete revascularization (CR) in these patients using baseline risk factors; then, the CR patients were matched to the IR patients with similar likelihoods of achieving CR. Each patient's vital status was followed through 2007 using the National Death Index, and the difference in long-term mortality between IR and CR was compared. It was found that CR was achieved in 29.2% (3803) of the patients. For the 3803 pair-matched patients, the respective 8-year survival rates were 80.8% and 78.5% for CR and IR ( P =0.04), respectively. The risk of death was marginally significantly higher for IR (hazard ratio=1.12; 95% confidence interval, 1.01–1.26, P =0.04). The 95% bootstrap confidence interval for the hazard ratio was 0.98 to 1.32. Conclusions— IR may be associated with higher risk of long-term mortality after stenting with BMS in patients with multivessel disease. More prospective studies are needed to further test this association.