Department of Cardiology, Thoraxcenter, Erasmus MC Rotterdam, the Netherlands and Department of Cardiology, Kocaeli University, Kocaeli, Turkey.
Neth Heart J. 2009 Apr;17(4):177-80. doi: 10.1007/BF03086242.
Drug-eluting stents (DES) significantly reduce the risk of restenosis after percutaneous coronary revascularisation, but an increased risk of late stent thrombosis (LST) has been put forward as a major safety concern. Meta-analysis of clinical trials, however, does not support this caveat. Even so, many interventional cardiologists think that LST is associated with DES and related to delayed endothelialisation. This hypothesis is based on autopsy studies and clinical intracoronary angioscopy. In autopsy studies, differences between endothelialisation of DES and baremetal stents (BMS) have been reported. Most preclinical studies, however, have failed to show any significant differences in endothelialisation between DES and BMS. Our own studies, using the porcine coronary artery model, also suggest that DES show no differences in re-endothelialisation. However, DES do delay vascular healing and induce endothelial dysfunction. This paper will review clinical and animal studies which consider re-endothelialisation and LST. (Neth Heart J 2009;17:177-81.).
药物洗脱支架 (DES) 可显著降低经皮冠状动脉血运重建后的再狭窄风险,但有研究提出迟发性支架内血栓形成 (LST) 的风险增加是一个主要的安全隐患。然而,临床试验的荟萃分析并不支持这一说法。即便如此,许多介入心脏病学家认为 LST 与 DES 有关,且与血管内皮延迟愈合有关。这一假说基于尸检研究和临床冠状动脉血管内镜检查。在尸检研究中,已经报道了 DES 和裸金属支架 (BMS) 的内皮化之间的差异。然而,大多数临床前研究未能显示 DES 和 BMS 之间在内皮化方面有任何显著差异。我们自己使用猪冠状动脉模型的研究也表明,DES 在再内皮化方面没有差异。然而,DES 确实会延迟血管愈合并引起内皮功能障碍。本文将回顾考虑再内皮化和 LST 的临床和动物研究。(Neth Heart J 2009;17:177-81.)。