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药物洗脱支架中内皮与支架内血栓形成的范例

The paradigm of endothelium and stent thrombosis in DES.

作者信息

Onuma Yoshinobu, van Beusekom Heleen M M, Sorop Oana, van der Giessen Willem J

机构信息

Department of Cardiology, Erasmus MC, Rotterdam, The Netherlands.

出版信息

EuroIntervention. 2008 Aug;4 Suppl C:C17-21.

Abstract

Drug eluting stents (DES) have attracted considerable attention due to concerns of late stent thrombosis (LST) thought to be related to delayed endothelialisation. This hypothesis is based on clinical autopsy studies indicating an association between lack of endothelium and LST. However, meta-analysis of clinical trials does not support the notion that all DES induce more late stent thrombosis than BMS. In addition, preclinical data using animal models also do not necessarily support this hypothesis. Most animal models using single non-overlapping stents show no signs of delayed endothelialisation at all. Experiments with several DES in our laboratory using the porcine coronary artery model also suggest that DES show no differences in re-endothelialisation. They can however induce (late) differences in endothelial function, depending on the DES of choice. These phenomena are also described clinically in coronary segments distal from the DES. We hypothesise that DES do not necessarily delay endothelialisation but more likely induce late endothelial dysfunction that varies between DES.

摘要

药物洗脱支架(DES)由于被认为与延迟内皮化有关的晚期支架血栓形成(LST)问题而备受关注。这一假设基于临床尸检研究,该研究表明内皮缺失与LST之间存在关联。然而,临床试验的荟萃分析并不支持所有DES比裸金属支架(BMS)更易引发更多晚期支架血栓形成这一观点。此外,使用动物模型的临床前数据也不一定支持这一假设。大多数使用单个非重叠支架的动物模型根本没有延迟内皮化的迹象。我们实验室在猪冠状动脉模型中对几种DES进行的实验也表明,DES在再内皮化方面没有差异。然而,根据所选的DES,它们可能会诱导(晚期)内皮功能差异。这些现象在DES远端的冠状动脉节段中也有临床描述。我们推测,DES不一定会延迟内皮化,更有可能引发晚期内皮功能障碍,不同的DES之间存在差异。

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