TY - JOUR
T1 - Short- and long-term clinical and quantitative angiographic results with the new, less shortening wallstent for vessel reconstruction in chronic total occlusion
T2 - A quantitative angiographic study
AU - Ozaki, Yukio
AU - Violaris, Andonis G.
AU - Hamburger, Jaap
AU - Melkert, Rein
AU - Foley, David
AU - Keane, David
AU - De Feyter, Pim
AU - Serruys, Patrick W.
N1 - Funding Information:
From the Catheterization Laboratory, Thoraxcenter, Erasmus UniversiW, Rotterdam, The Netherlands. Dr. Ozaki is the recipient of a grant from the Takeda Medical Research (Yaisha Ijo) Foundation, Osaka, Japan. Dr. Violaris is the recipient of an International Travel fellowship from the Wellcome Trust, London, England, United Kingdom. Dr. Keane is the recipient of a travel grant from the Peel Medical Research Trust, London. Manuscript received November 3, 1995; revised manuscript received February 9, 1996, accepted March 27, 1996. Address for correspondence: Professor Patrick W. Serruys, Catheterization Laboratory, Thoraxcenter, Erasmus University Rotterdam, Postbus 1738, 3000 DR Rotterdam, The Netherlands.
PY - 1996/8
Y1 - 1996/8
N2 - Objectives. This study was designed to examine whether oversized implantation of the new, less shortening Wallstent provides a more favorable long-term clinical and angiographic outcome in chronic total occlusions than does conventional coronary balloon angioplasty. Background. Restenosis and reocclusion remain major limitations of balloon angioplasty for chronic total occlusions. Enforced mechanical remodeling by implantation of the oversized Wallstent may prevent elastic recoil and improve accommodation of intimal hyperplasia. Methods. Lumen dimension was measured by a computer- based quantitative coronary angiography system (CAAS II). These measurements (before and after intervention and at 6-month follow-up) were compared between the groups with Wallstent implantation (20 lesions, 20 patients) and conventional balloon angioplasty (266 lesions, 249 patients) for treatment of chronic total occlusion. Acute gain (minimal lumen diameter after intervention minus that before intervention), late loss (minimal lumen diameter after intervention minus that at follow-up) and net gain (acute gain minus late loss) were examined. Results. Wallstent deployment was successful in all patients. High pressure intra-Wallstent balloon inflation (mean ± SD 14 ± 3 atm) was performed in all lesions. Although vessel size did not differ between the Wallstent and balloon angioplasty groups, acute gain was significantly greater in the Wallstent group (2.96 ± 0.55 vs. 1.61 ± 0.34 mm, p < 0.0001). Although late loss was also significantly larger in the Wallstent group (0.81 ± 0.95 vs. 0.43 ± 0.68 mm, p < 0.05), net gain was still significantly greater in this group (2.27 ± 1.00 vs. 1.18 ± 0.69 mm, p < 0.0001). Angiographic restenosis (≤50% diameter stenosis) occurred at 6 months in 29% of lesions in the Wallstent group and in 45% of those in the balloon angioplasty group (p = 0.5150). Conclusions. Implantation of the oversized Wallstent, with full coverage of the lesion length, ensures resetting of the vessel size to its original caliber before disease and allows greater accommodation of intimal hyperplasia and chronic vessel recoil. Wallstent implantation provides a more favorable short- and long- term clinical and angiographic outcome than does conventional balloon angioplasty for chronic total occlusions.
AB - Objectives. This study was designed to examine whether oversized implantation of the new, less shortening Wallstent provides a more favorable long-term clinical and angiographic outcome in chronic total occlusions than does conventional coronary balloon angioplasty. Background. Restenosis and reocclusion remain major limitations of balloon angioplasty for chronic total occlusions. Enforced mechanical remodeling by implantation of the oversized Wallstent may prevent elastic recoil and improve accommodation of intimal hyperplasia. Methods. Lumen dimension was measured by a computer- based quantitative coronary angiography system (CAAS II). These measurements (before and after intervention and at 6-month follow-up) were compared between the groups with Wallstent implantation (20 lesions, 20 patients) and conventional balloon angioplasty (266 lesions, 249 patients) for treatment of chronic total occlusion. Acute gain (minimal lumen diameter after intervention minus that before intervention), late loss (minimal lumen diameter after intervention minus that at follow-up) and net gain (acute gain minus late loss) were examined. Results. Wallstent deployment was successful in all patients. High pressure intra-Wallstent balloon inflation (mean ± SD 14 ± 3 atm) was performed in all lesions. Although vessel size did not differ between the Wallstent and balloon angioplasty groups, acute gain was significantly greater in the Wallstent group (2.96 ± 0.55 vs. 1.61 ± 0.34 mm, p < 0.0001). Although late loss was also significantly larger in the Wallstent group (0.81 ± 0.95 vs. 0.43 ± 0.68 mm, p < 0.05), net gain was still significantly greater in this group (2.27 ± 1.00 vs. 1.18 ± 0.69 mm, p < 0.0001). Angiographic restenosis (≤50% diameter stenosis) occurred at 6 months in 29% of lesions in the Wallstent group and in 45% of those in the balloon angioplasty group (p = 0.5150). Conclusions. Implantation of the oversized Wallstent, with full coverage of the lesion length, ensures resetting of the vessel size to its original caliber before disease and allows greater accommodation of intimal hyperplasia and chronic vessel recoil. Wallstent implantation provides a more favorable short- and long- term clinical and angiographic outcome than does conventional balloon angioplasty for chronic total occlusions.
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U2 - 10.1016/S0735-1097(96)00155-6
DO - 10.1016/S0735-1097(96)00155-6
M3 - Article
C2 - 8800109
AN - SCOPUS:0030220711
SN - 0735-1097
VL - 28
SP - 354
EP - 360
JO - Journal of the American College of Cardiology
JF - Journal of the American College of Cardiology
IS - 2
ER -