Registry data evaluating the effectiveness of drug-eluting stents for the treatment of symptomatic in-stent restenosis

Heart Lung Circ. 2006 Oct;15(5):300-5. doi: 10.1016/j.hlc.2006.06.002. Epub 2006 Jul 28.

Abstract

Background: In this new-era of drug-eluting stents (DES) the impact of symptomatic in-stent restenosis (ISR) is diminishing. However, world wide bare-metal stents remain widely used and therefore, it is imperative to establish a simple and effective form of treatment. The objective of this registry database was to evaluate the 'real-world' effectiveness of DES for the treatment of symptomatic bare-metal stent ISR.

Methods: All patients presenting with symptomatic ISR were evaluated between February 2003 and February 2005. Patients had 9-month angiographic follow-up with primary endpoint evaluation of binary restenosis (>50%). Secondary endpoints included in-segment late loss, target lesion revascularization (TLR) and the difference in late loss between sirolimus (n=23) and paciltaxel (n=36) eluting stents.

Results: Fifty eight patients with fifty nine ISR lesions were evaluated, 36% of patients had diabetes mellitus. All procedures were performed safely with no adverse peri-procedural events documented. At 9-month follow-up the median in-segment late loss was 0.24 mm (IQR 0.1, 0.53), with a binary restenosis rate of 17%. At long-term follow-up greater than 1 year, the incidence of TLR was 10%. No difference in the angiographic parameter of in-segment late loss was seen between the sirolimus and paclitaxel-eluting stents.

Conclusions: In this cohort of patients with long-term angiographic and clinical follow-up, DES is an effective and safe treatment for symptomatic bare-metal stent ISR.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antineoplastic Agents, Phytogenic / pharmacology
  • Blood Vessel Prosthesis Implantation / instrumentation*
  • Coated Materials, Biocompatible*
  • Coronary Angiography
  • Coronary Restenosis / diagnostic imaging
  • Coronary Restenosis / surgery*
  • Female
  • Follow-Up Studies
  • Humans
  • Immunosuppressive Agents / pharmacology
  • Male
  • Middle Aged
  • Paclitaxel / pharmacology*
  • Prosthesis Failure
  • Reoperation
  • Retrospective Studies
  • Sirolimus / pharmacology*
  • Stents*
  • Time Factors
  • Treatment Outcome

Substances

  • Antineoplastic Agents, Phytogenic
  • Coated Materials, Biocompatible
  • Immunosuppressive Agents
  • Paclitaxel
  • Sirolimus