预防支架内再狭窄。

C R Narins, S G Ellis
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引用次数: 0

摘要

尽管支架植入对特定病变类型的再狭窄率有有利影响,但支架内再狭窄仍然是一个常见且难以处理的实体。组织学上,支架内再狭窄似乎几乎完全源于新生内膜增生,在支架植入后比球囊血管成形术后更常见。支架内再狭窄最有力的预测因素包括糖尿病的存在、较大的病变长度、较小的血管直径和支架扩张不足。已经提出了几种策略作为减少支架内再狭窄发生率的手段。也许其中最重要的是临时支架的使用策略,即只有在球囊血管成形术后达到次优结果时才进行支架植入。最近来自EPILOG和EPILOG支架试验的数据表明,使用IIb/IIIa受体拮抗剂可能会增强临时支架置入的策略。当使用支架时,适当的部署是必不可少的。辅助IVUS成像在支架植入过程中指导正确球囊大小从而降低再狭窄风险的能力目前是随机试验的主题。根据初步的研究结果,血管内放疗作为一种抑制内膜增生从而减少支架内再狭窄发生的手段似乎具有很大的潜力,大规模的安全性和有效性试验正在进行中。其他以药理学和器械为导向的策略也同样在进行评估。总之,虽然冠状动脉支架的可用性毫无疑问提高了冠状动脉血管成形术的安全性和有效性,但我们仍然需要以客观的方式确定如何以及何时最好地使用这些设备。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Prevention of in-stent restenosis.

Despite the favourable impact of stent implantation on restenosis rates for selected lesion types, in-stent restenosis remains a commonly encountered and difficult to manage entity. Histologically, in-stent restenosis appears to derive almost exclusively from neointimal hyperplasia, which appears to be more abundant following stent implantation than balloon angioplasty. The most powerful predictors of in-stent restenosis include the presence of diabetes, greater lesion length, small vessel caliber, and inadequate stent expansion. Several strategies have been proposed as a means to reduce the incidence of in-stent restenosis. Perhaps the most important among these relates to a strategy of provisional stent use, whereby stenting is undertaken only if suboptimal results are achieved following balloon angioplasty. Recent data from the EPILOG and EPILOG-stent trials suggest that the use of IIb/IIIa receptor antagonists may enhance the strategy of provisional stenting. When stents are used, adequate deployment is essential. The ability of adjunct IVUS imaging to guide proper balloon sizing during stent implantation and consequently reduce the risk of restenosis is currently the subject of randomized trials. Based on preliminary study results, intravascular radiation appears to hold great potential as a means to inhibit neointimal hyperplasia and consequently reduce the occurrence of in-stent restenosis, and large scale safety and efficacy trials are in progress. Other pharmacologic- and device-oriented strategies are likewise undergoing evaluation. In conclusion, while the availability of coronary stents has without question improved the safety and efficacy of coronary angioplasty, it remains critical that we continue to determine in an objective manner how and when best to use these devices.

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