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首页> 外文期刊>Korean Circulation Journal >Effect of Pretreatment of Ezetimibe/Simvastatin on Arterial Healing and Endothelialization after Drug-Eluting Stent Implantation in a Porcine Coronary Restenosis Model
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Effect of Pretreatment of Ezetimibe/Simvastatin on Arterial Healing and Endothelialization after Drug-Eluting Stent Implantation in a Porcine Coronary Restenosis Model

机译:依泽替米贝/辛伐他汀的预处理对猪冠状动脉再狭窄模型中药物洗脱支架植入后动脉愈合和内皮化的影响

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Background and Objectives We sought to evaluate the effect of the early use of ezetimibe/simvastatin (Vytorin?) on arterial healing and endothelialization after the implantation of a drug-eluting stent (DES) in a porcine model of coronary restenosis. Materials and Methods A total of 20 pigs (40 coronary arteries) were randomly allocated to a pretreatment or no treatment group. The pretreatment group (n=20) received oral ezetimibe/simvastatin (10/20 mg) daily for 7 days before stenting and the no pretreatment group (n=20) did not. All pigs were treated with ezetimibe/simvastatin (10/20 mg) daily after stenting for 4 weeks. Stenting was performed using a bare-metal stent (BMS, n=10) and three types of DES: biolimus A9-eluting stent (BES, n=10), zotarolimus-eluting stent (ZES, n=10), and everolimus-eluting stents (EES, n=10). Four weeks later, pigs underwent a follow-up coronary angiography and were sacrificed for histopathologic analysis. Results There were no significant differences between the pretreatment and no pretreatment groups in the internal elastic lamina area, lumen area, neointima area, stenotic area, injury score, fibrin score, and inflammation score. In both groups, the fibrin score was higher in pigs with DES than in BMS, particularly in ZES and EES. The inflammatory score was not different between DES and BMS. Conclusion In a porcine model of coronary restenosis, pretreatment with ezetimibe/simvastatin before DES implantation failed to improve arterial healing and endothelialization compared to treatment after stenting.
机译:背景与目的我们试图评估在猪冠状动脉再狭窄模型中植入药物洗脱支架(DES)后早期使用依泽替米贝/辛伐他汀(Vytorin?)对动脉愈合和内皮化的影响。材料和方法将20头猪(40根冠状动脉)随机分配到一个预处理组或不进行治疗的组中。预处理组(n = 20)在支架置入前7天每天口服口服依泽替米贝/辛伐他汀(10/20 mg),无预处理组(n = 20)未接受。支架置入术后4周,每天用ezetimibe / simvastatin(10/20 mg)治疗所有猪。使用裸金属支架(BMS,n = 10)和三种类型的DES进行支架:Biolimus A9洗脱支架(BES,n = 10),佐他莫司洗脱支架(ZES,n = 10)和依维莫司-洗脱支架(EES,n = 10)。四周后,对猪进行了冠状动脉造影,并处死以进行组织病理学分析。结果预处理组与未预处理组之间的内部弹性椎板区域,管腔区域,新内膜区域,狭窄区域,损伤评分,纤维蛋白评分和炎症评分之间无显着差异。两组中,DES猪的血纤维蛋白评分均高于BMS,尤其是ZES和EES。 DES和BMS之间的炎症评分没有差异。结论在猪冠状动脉再狭窄模型中,与支架置入术相比,DES植入前用依泽替米贝/辛伐他汀进行的预处理未能改善动脉的愈合和内皮化。

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