Department of Cardiology, St. Antonius Hospital, Nieuwegein, the Netherlands.
EuroIntervention. 2017 Aug 4;13(5):e522-e530. doi: 10.4244/EIJ-D-17-00261.
The PRISON IV trial investigated the next-generation sirolimus-eluting stent (SES) with ultra-thin struts and biodegradable polymer against the second-generation everolimus-eluting stent (EES) with thin struts and durable polymer in patients with successfully recanalised chronic total occlusions (CTO). In this study, we examined the secondary optical coherence tomography endpoints.
The main PRISON IV trial randomised 330 patients to either SES or EES. At nine months, 281 (85%) patients underwent repeat angiography. Of these, 60 consecutive patients received optical coherence tomography divided over both stent groups. The mean number of struts analysed was 750±337 and 633±358 in SES and EES patients, respectively (p=0.07). The minimal lumen area, minimal stent area, maximal neointima area and neointimal thickness were comparable between the groups (4.8±2.1 and 4.4±1.5 mm2; 5.3±1.8 and 5.3±1.4 mm2; 2.5±2.0 and 2.2±1.5 mm2; 0.7±1.7 and 0.4±0.2 mm). The percentage of uncovered struts was higher with EES (6.2±7.5% and 11.9±13.4%, p=0.04), whereas the percentage of malapposed struts and mean number of coronary evaginations were significantly higher with SES (2.9±4.0% and 1.2±2.4%, p=0.02; 18.5±17.7 and 5.3±3.1, p=0.004).
The optical coherence tomography findings of this substudy demonstrated improved strut coverage with ultra-thin strut SES with bioresorbable polymer compared to thin-strut EES with durable polymer in CTO. On the other hand, SES showed a higher rate of stent strut malappositon and coronary evaginations. The clinical relevance of these findings remains to be demonstrated.
PRISON IV 试验旨在比较新一代载有超亲水性聚合物的雷帕霉素洗脱支架(SES)与载有亲水性聚合物的第二代依维莫司洗脱支架(EES)在成功开通的慢性完全闭塞病变(CTO)患者中的疗效。本研究旨在分析次要光学相干断层成像(OCT)终点。
PRISON IV 试验共纳入 330 例患者,随机分至 SES 组或 EES 组。9 个月时,281 例(85%)患者接受了再次冠状动脉造影。其中,SES 组和 EES 组分别有 60 例患者接受了光学相干断层成像检查。SES 组和 EES 组分析的支架梁数分别为 750±337 个和 633±358 个(p=0.07)。两组间最小管腔面积、最小支架面积、最大新生内膜面积和内膜厚度无显著差异(分别为 4.8±2.1 和 4.4±1.5mm2;5.3±1.8 和 5.3±1.4mm2;2.5±2.0 和 2.2±1.5mm2;0.7±1.7 和 0.4±0.2mm)。EES 组的未覆盖支架梁比例更高(6.2±7.5%和 11.9±13.4%,p=0.04),而 SES 组的支架梁贴壁不良比例和冠状动脉瘤样扩张比例更高(2.9±4.0%和 1.2±2.4%,p=0.02;18.5±17.7 和 5.3±3.1,p=0.004)。
本亚组研究的光学相干断层成像结果显示,在 CTO 患者中,与载有亲水性聚合物的第二代依维莫司洗脱支架相比,载有超亲水性聚合物的新一代雷帕霉素洗脱支架具有更好的支架梁覆盖率。然而,SES 组的支架梁贴壁不良和冠状动脉瘤样扩张比例更高。这些发现的临床意义仍有待进一步证实。