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J Am Coll Cardiol Intv, 2009; 2:542-549, doi:10.1016/j.jcin.2009.03.014
© 2009 by the American College of Cardiology Foundation
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Clinical Research

Characterization of Post-Operative Risk Associated With Prior Drug-Eluting Stent Use

Saif Anwaruddin, MD*, Arman T. Askari, MD*, Hammad Saudye, MD§, Lilian Batizy, MS{ddagger}, Penny L. Houghtaling, MS{ddagger}, Mohammad Alamoudi, MD||, Michael Militello, PharmD{dagger}, Kamran Muhammad, MD*, Samir Kapadia, MD*, Stephen G. Ellis, MD*,*

* Department of Cardiovascular Medicine, Cleveland Clinic, Cleveland, Ohio
{dagger} Department of Pharmacy, Cleveland Clinic, Cleveland, Ohio
{ddagger} Department of Quantitative Health Sciences, Cleveland Clinic, Cleveland, Ohio
§ Department of Internal Medicine, Cleveland Clinic, Cleveland, Ohio
|| Department of Internal Medicine, University of Missouri-Kansas City, Kansas City, Missouri

* Reprint requests and correspondence: Dr. Stephen G. Ellis, Director, Sones Cardiac Catheterization Laboratory, Cleveland Clinic, 9500 Euclid Avenue, Cleveland, Ohio 44195 (Email: elliss{at}ccf.org).

Objectives: The aim of this study was to assess risk of inpatient surgery at any time after percutaneous coronary intervention (PCI) with drug-eluting stents (DES).

Background: Risk of adverse events, including stent thrombosis (ST), in patients undergoing surgical procedures with prior DES remains poorly defined.

Methods: Outcomes of consecutive patients having inpatient surgical procedures after PCI with DES, placed from April 28, 2003 until December 31, 2006 at a tertiary-care medical center, were studied. Primary and secondary end points were 30-day post-operative risk of the Academic Research Consortium (ARC) definite and modified probable definitions of ST and combined 30-day post-operative risk of death, nonfatal myocardial infarction (MI), or ST, respectively. Multivariable logistic regression analyses were used to determine independent risk factors.

Results: Six hundred six inpatient surgeries on 481 patients with a mean time from PCI to surgery of 1.07 ± 0.89 years were evaluated. The primary and secondary end points occurred after 11 (2.0%) and 56 (9%) surgeries, respectively. Risk of the combined end point and ST decreased significantly in the first 1 to 6 months after PCI (p < 0.0001 and p < 0.014, respectively); however, risk persisted when time between PCI and surgery was >12 months. Independent correlates of the combined end point include emergency surgery, antecedent MI, the pre-operative use of intravenous heparin, and atherosclerotic lesion length treated with DES. Oral antiplatelet status at time of surgery was not a correlate of events.

Conclusions: Risk of 30-day post-operative adverse events, including ST, remains significantly higher when surgery is performed soon after PCI, while intermediate-term risk extending at least 2 to 3 years remains important.

Key Words: drug-eluting stents • perioperative risk • stent thrombosis

Abbreviations and Acronyms
  ARC = Academic Research Consortium
  BMS = bare-metal stent(s)
  DES = drug-eluting stent(s)
  MI = myocardial infarction
  PCI = percutaneous coronary intervention
  ST = stent thrombosis




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P. B. Berger, N. S. Kleiman, M. J. Pencina, W.-H. Hsieh, S. R. Steinhubl, A. Jeremias, A. Sonel, K. Browne, G. Barseness, D. J. Cohen, et al.
Frequency of Major Noncardiac Surgery and Subsequent Adverse Events in the Year After Drug-Eluting Stent Placement: Results From the EVENT (Evaluation of Drug-Eluting Stents and Ischemic Events) Registry
J. Am. Coll. Cardiol. Intv., September 1, 2010; 3(9): 920 - 927.
[Abstract] [Full Text] [PDF]



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