Chronic Arterial Responses to Polymer-Controlled Paclitaxel-Eluting Stents

Author:

Tanabe Kengo1,Serruys Patrick W.1,Degertekin Muzaffer1,Guagliumi Giulio1,Grube Eberhard1,Chan Charles1,Munzel Thomas1,Belardi Jorge1,Ruzyllo Witold1,Bilodeau Luc1,Kelbaek Henning1,Ormiston John1,Dawkins Keith1,Roy Louis1,Strauss Bradley H.1,Disco Clemens1,Koglin Jörg1,Russell Mary E.1,Colombo Antonio1

Affiliation:

1. From Thoraxcenter, Erasmus MC, Rotterdam, The Netherlands (K.T., P.W.S., M.D.); Ospedali Riuniti di Bergamo, Bergamo, Italy (G.G.); Heart Center Siegburg, Siegburg, Germany (E.G.); Singapore General Hospital, Singapore (C.C.); Universitaetsklinikum Eppendorf, Hamburg, Germany (T.M.); Instituto Cardiovascular de Buenos Aires, Buenos Aires, Argentina (J.B.); National Institute of Cardiology, Warsaw, Poland (W.R.); Montreal Heart Institute, Montreal, Canada (L.B.); Rigshospitalet, Heart Center,...

Abstract

Background— Polymer-controlled paclitaxel-eluting stents have shown a pronounced reduction in neointimal hyperplasia compared with bare metal stents (BMS). The aim of this substudy was to evaluate local arterial responses through the use of serial quantitative intravascular ultrasound (IVUS) analyses in the TAXUS II trial. Methods and Results— TAXUS II was a randomized, double-blind study with 536 patients in 2 consecutive cohorts comparing slow-release (SR; 131 patients) and moderate-release (MR; 135 patients) paclitaxel-eluting stents with BMS (270 patients). This IVUS substudy included patients treated with one study stent who underwent serial IVUS examination after the procedure and at 6-month follow-up (BMS, 152 patients; SR, 81; MR, 81). The analyzed stented segment (15 mm) was divided into 5 subsegments in which mean vessel area (VA), stent area (SA), lumen area (LA), intrastent neointimal hyperplasia area (NIHA), and peristent area (VA−SA) were measured. NIHA was significantly reduced in SR (0.7±0.9 mm 2 , P <0.001) and MR (0.6±0.8 mm 2 , P <0.001) compared with BMS (1.9±1.5 mm 2 ), with no differences between the two paclitaxel-eluting release formulations. Longitudinal distribution of neointimal hyperplasia throughout the paclitaxel-eluting stent was uniform. Neointimal growth was independent of peristent area at postprocedure examination in all groups. There were progressive increases in peristent area from BMS to SR to MR (0.5±1.7, 1.0±1.8, and 1.4±2.0 mm 2 , respectively; P <0.001). The increase in peristent area was directly correlated with increases in VA. Conclusions— Both SR and MR paclitaxel-eluting stents prevent neointimal formation to the same degree compared with BMS. However, the difference in peristent remodeling suggests a release-dependent effect between SR and MR.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Physiology (medical),Cardiology and Cardiovascular Medicine

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