Long-term outcomes following drug-eluting stent implantation in unprotected left main bifurcation lesions

Chin Med J (Engl). 2007 Apr 5;120(7):545-51.

Abstract

Background: The safety and efficacy of drug-eluting stents (DES) implantation in unprotected left main (LM) bifurcation lesions has yet to be determined. The aim of the present report was to evaluate the long-term outcome following implantation of DES in unprotected LM bifurcation lesions.

Methods: We identified 70 consecutive patients treated with DES in unprotected LM bifurcation lesions from April 2003 to January 2005. Of them, 42 patients were treated with sirolimus-eluting stent (SES) and 28 patients were treated with paclitaxel-eluting stent (PES).

Results: Stents to the left anterior descending and to the circumflex were implanted in 62 patients. During 1-year follow-up, 3 (4.3%) patients died of cardiac causes. One of them had myocardial infarction and adjudicated as possibly due to stent thrombosis. Angiographic follow-up was available in 80% of patients. The per lesion restenosis rate was 13.4% in the entire cohort, of which 10.7% occurred in lesions treated with SES and 16.1% in those treated with PES (P = 0.58). All restenosis was focal and occurred in the lesions treated with a stent with stent size to post-procedural reference vessel diameter ratio < 1.0 (17.6% vs 0, P = 0.04). The per patient target lesion revascularization rate at 1 year was 17.1%. One year survival free from major adverse cardiac events was 77.1%.

Conclusions: Treatment of LM bifurcation lesions using DES is a safe and feasible way with a low one-year mortality. The need for revascularization in 17% of patients demands for improvement.

MeSH terms

  • Adult
  • Aged
  • Angioplasty, Balloon, Coronary / methods*
  • Coronary Angiography
  • Coronary Disease / mortality
  • Coronary Disease / therapy*
  • Coronary Restenosis / prevention & control
  • Drug Delivery Systems
  • Female
  • Humans
  • Male
  • Middle Aged
  • Myocardial Revascularization
  • Paclitaxel / administration & dosage*
  • Sirolimus / administration & dosage*
  • Stents*

Substances

  • Paclitaxel
  • Sirolimus