Comparative analysis of neointimal coverage with paclitaxel and zotarolimus drug-eluting stents, using optical coherence tomography 6 months after implantation

Arch Cardiovasc Dis. 2009 Aug-Sep;102(8-9):617-24. doi: 10.1016/j.acvd.2009.05.010. Epub 2009 Sep 16.

Abstract

Background: Intrastent thrombosis, while rare, has a poor prognosis. Strut non-coverage is one causal factor, especially in cases of resistance to or premature discontinuation of dual antiplatelet therapy.

Aim: To compare neointimal coverage with paclitaxel and zotarolimus drug-eluting stents, using optical coherence tomography (OCT).

Methods: Twenty-two drug-eluting stents (11 paclitaxel-eluting stents and 11 zotarolimus-eluting stents) were examined by OCT, 6 months after implantation. Mean neointimal strut-coverage thickness and percentage neointimal hyperplasia were measured every millimetre. On each OCT image, struts were classified into one of four categories: well-apposed to vessel wall with apparent neointimal coverage; well-apposed to vessel wall without neointimal coverage; malapposed to the vessel wall; or located on a major side branch.

Results: OCT analysis showed a lower percentage of neointimal hyperplasia with paclitaxel-eluting stents than with zotarolimus-eluting stents (17% vs 38% and mean thickness 154 microm vs 333 microm, respectively; p<0.0001). The rate of strut-coverage was greater with zotarolimus-eluting stents than with paclitaxel-eluting stents (99.1% vs 87.1%, respectively; p<0.0001). A non-covered/covered strut ratio greater than 0.3 was observed in 0.5% of zotarolimus-eluting stent OCT images compared with 18% of paclitaxel-eluting stent OCT images (p<0.0001).

Conclusion: Six months after implantation, neointimal hyperplasia was greater with zotarolimus-eluting stents compared with paclitaxel-eluting stents. Conversely, neointimal strut-coverage was better with zotarolimus-eluting stents.

Publication types

  • Comparative Study

MeSH terms

  • Adult
  • Aged
  • Angioplasty / adverse effects
  • Angioplasty / instrumentation*
  • Cardiovascular Agents / administration & dosage*
  • Cell Proliferation / drug effects
  • Coronary Angiography
  • Coronary Artery Disease / therapy*
  • Coronary Restenosis / etiology
  • Coronary Restenosis / pathology
  • Coronary Restenosis / prevention & control*
  • Coronary Thrombosis / etiology
  • Coronary Thrombosis / pathology
  • Coronary Thrombosis / prevention & control*
  • Drug-Eluting Stents*
  • Female
  • Humans
  • Hyperplasia
  • Male
  • Middle Aged
  • Paclitaxel / administration & dosage*
  • Platelet Aggregation Inhibitors / therapeutic use
  • Predictive Value of Tests
  • Sirolimus / administration & dosage
  • Sirolimus / analogs & derivatives*
  • Time Factors
  • Tomography, Optical Coherence*
  • Treatment Outcome
  • Tunica Intima / drug effects*
  • Tunica Intima / pathology

Substances

  • Cardiovascular Agents
  • Platelet Aggregation Inhibitors
  • zotarolimus
  • Paclitaxel
  • Sirolimus