Target lesion revascularisation in patients treated with a sirolimus-eluting or paclitaxel-eluting stent

Heart. 2007 Jun;93(6):694-7. doi: 10.1136/hrt.2006.100594. Epub 2006 Dec 28.

Abstract

Objective: To identify risk factors for clinical-driven target lesion revascularisation (TLR) in patients treated with sirolimus-eluting (Cypher) or paclitaxel-eluting (Taxus) stents in a real-world scenario.

Design: From 1 January 2003 to 18 May 2005, all patients treated with a Cypher or Taxus stent were consecutively registered and followed for 9 months. Re-intervention was driven by clinical symptoms.

Setting: Western Denmark Heart Registry.

Patients: 4432 patients with 6102 lesions treated with a Cypher (n = 3791 lesions) or Taxus (n = 2311 lesions) stent.

Interventions: Percutaneous coronary intervention.

Main outcome measures: TLR, defined as either new percutaneous coronary intervention or coronary artery bypass graft operation of the target lesion, within 9 months from the index procedure.

Results: TLR within 9 months was performed in 2.5% of lesions treated with the Cypher stent and in 3.3% of lesions treated with the Taxus stent (OR 1.36, 95% CI 1.00 to 1.84). After adjustment by multivariate logistic regression, Taxus stent implantation was an independent predictor of TLR (OR 1.43, 95% CI 1.05 to 1.95). Implantation of >1 stent per lesion (OR 1.62, 95% CI 1.13 to 2.33) and reference diameter <2.8 mm (OR 1.42, 95% CI 1.00 to 2.02) were also identified as independent predictors of TLR.

Conclusions: These data from the registry reflect a real-world clinical scenario with operator-driven use of drug-eluting stents and symptom-driven re-intervention. In this setting, use of the Taxus stent, implantation of multiple stents per lesion and stent implantation in small vessels were independent predictors of TLR.

Publication types

  • Comparative Study

MeSH terms

  • Analysis of Variance
  • Angioplasty, Balloon, Coronary
  • Coronary Restenosis / epidemiology
  • Coronary Restenosis / therapy*
  • Coronary Stenosis / therapy*
  • Denmark
  • Drug Delivery Systems
  • Equipment Design
  • Humans
  • Logistic Models
  • Paclitaxel / administration & dosage*
  • Registries
  • Risk Factors
  • Sirolimus / administration & dosage*
  • Stents*
  • Treatment Outcome

Substances

  • Paclitaxel
  • Sirolimus