International Centre for Circulatory Health, Imperial College London, London, United Kingdom.
EuroIntervention. 2013 Mar;8(11):1315-25. doi: 10.4244/EIJV8I11A200.
Left main stenting is increasingly performed and often involves deployment of a single stent across vessels with marked disparity in diameters. Knowing stent expansion capacity is critical to ensure adequate strut apposition after post-dilatation of the stent has been performed. Coronary stents are usually manufactured in only two or three different model designs with each design having a different maximal expansion capacity. Information about the different workhorse designs and their maximal achievable diameter is not commonly provided by manufacturers but, in the absence of this critically important information, stents implanted in segments with major changes in vessel diameter have the potential to become grossly overstretched and to remain incompletely apposed.
We examined the differences in workhorse designs of six commercially available drug-eluting stents (DES): the PROMUS Element, Taxus Liberté, XIENCE Prime, Resolute Integrity, BioMatrix Flex and Cypher Select stents. Using micro-computed tomography, we tested oversizing capabilities above nominal pressures for the different workhorse designs of the six DES using 4.0, 5.0 and 6.0 mm post-dilatation balloons inflated to 14 atmospheres. MLD could be increased significantly in all stents, only restricted by workhorse design limitations. Minimal inner lumen diameter (MLD) achieved after two successive 6.0 mm post-dilatations of the largest design (4.0 mm stent) was 5.7 mm for the Element, 5.6 mm for the XIENCE Prime, 6.0 mm for the Taxus, 5.4 mm for the Resolute Integrity, 5.9 mm for the BioMatrix and 5.8 mm for the Cypher stent. Significant deformations were observed during stent oversizing with large changes in terms of cell opening and crowns expansion. These are affected by design structure and reveal important differences among all stents tested. Such extensive deformations may alter the functional ability of an individual stent to scaffold a lesion and prevent restenosis.
Stent selection based on stent model design may be critical, particularly for treatment of large artery and left main bifurcations where overexpansion is normally required to optimise results and ensure full expansion of the stent.
左主干支架置入术的应用日益增多,通常涉及在直径明显差异的血管中植入单个支架。了解支架的扩张能力对于确保支架扩张后支架支柱充分贴壁至关重要。冠状动脉支架通常仅采用两种或三种不同的模型设计制造,每种设计的最大扩张能力都不同。不同的主力设计及其最大可实现直径的信息通常不会由制造商提供,但在缺乏这些极其重要的信息的情况下,在血管直径发生重大变化的节段中植入的支架有可能被严重过度拉伸并保持不完全贴壁。
我们检查了六种市售药物洗脱支架(DES)的主力设计差异:PROMUS Element、Taxus Liberté、XIENCE Prime、Resolute Integrity、BioMatrix Flex 和 Cypher Select 支架。使用微计算机断层扫描,我们使用直径为 4.0、5.0 和 6.0 毫米的后扩张球囊在 14 个大气压下对六种 DES 的不同主力设计进行了名义压力以上的过扩张能力测试。在所有支架中,支架的最大扩张能力都可以显著增加,仅受主力设计限制。最大设计(4.0 毫米支架)连续两次 6.0 毫米后扩张后的最小内腔直径(MLD)分别为 Element 支架 5.7 毫米、XIENCE Prime 支架 5.6 毫米、Taxus 支架 6.0 毫米、Resolute Integrity 支架 5.4 毫米、BioMatrix 支架 5.9 毫米和 Cypher 支架 5.8 毫米。在支架过度扩张过程中观察到明显的变形,支架支柱开口和冠部扩张发生了很大的变化。这些变化受到设计结构的影响,并揭示了所有测试支架之间的重要差异。这种广泛的变形可能会改变单个支架支撑病变和预防再狭窄的功能能力。
基于支架模型设计的支架选择可能至关重要,特别是在治疗大动脉和左主干分叉等部位,通常需要过度扩张以优化结果并确保支架完全扩张。