Pilgrim T, Windecker S
Department of Cardiology, Bern University Hospital, Bern, Switzerland.
Minerva Cardioangiol. 2009 Oct;57(5):611-20.
Drug-eluting stents (DES) have reduced the risk of repeat revascularization procedures by 50-70% compared with bare metal stents across a wide range of lesion and patients subsets. Stent thrombosis is a rare but devastating adverse event, which results in abrupt closure of the treated artery with the incumbent risk of sudden death or myocardial infarction. Although stent thrombosis has been recognized as a shortcoming of coronary artery stents since there inception, very late stent thrombosis occurring more than one year after stent implantation emerged as a new entity complicating the use of DES. The mechanisms leading to very late ST are complex and only incompletely understood. Delayed healing and incomplete re-endothelialization emerged as prevailing mechanism of thrombosis in autopsy studies. Various components of DES may give rise to very late stent thrombosis, notably the polymers used for controlled drug-release. Newer generation DES attempt to address these concerns by aiming at improved vascular healing while maintaining potent neointimal suppression.
与裸金属支架相比,药物洗脱支架(DES)在广泛的病变和患者亚组中已将重复血管重建手术的风险降低了50%至70%。支架血栓形成是一种罕见但具有毁灭性的不良事件,它会导致治疗的动脉突然闭塞,存在猝死或心肌梗死的风险。尽管自冠状动脉支架问世以来,支架血栓形成就被认为是其一个缺点,但支架植入一年多后发生的极晚期支架血栓形成已成为一个使DES使用复杂化的新问题。导致极晚期支架血栓形成的机制很复杂,目前仅不完全清楚。尸检研究表明,延迟愈合和不完全再内皮化是血栓形成的主要机制。DES的各种成分可能导致极晚期支架血栓形成,特别是用于控制药物释放的聚合物。新一代DES试图通过在保持有效抑制新生内膜的同时改善血管愈合来解决这些问题。