Cardiovascular Research Foundation, 111 East 59th Street, New York, NY 10022, USA.
Am Heart J. 2010 Feb;159(2):271-7. doi: 10.1016/j.ahj.2009.11.008.
Animal models show impairment of arterial healing after drug-eluting stents (DES) compared with bare-metal stents (BMS). Virtual histology intravascular ultrasound (VH-IVUS) offers an opportunity to assess lesion morphology in vivo.
We used VH-IVUS in 80 patients to assess long-term (median = 10 months) native artery vascular responses after 76 implantations of DES compared with 32 BMS. The presence of "necrotic core abutting the lumen" was evaluated at baseline and follow-up.
At baseline, necrotic core abutting the lumen through the stent struts was observed in 76% of DES and 75% of BMS. Although the percentage of necrotic core within the plaque behind the stents did not change during follow-up in DES (23% [18%, 28%] to 22% [17%, 27%], P = .57) or BMS (22% [19%, 27%] to 20% [12%, 26%], P = .29), necrotic core abutting the lumen through the stent struts decreased more in BMS (75% to 19%, P < .001) than DES (76% to 61%, P = .036) because of the lack of an overlying, protective neointima in DES-treated lesions. Furthermore, within the adjacent reference segments, the incidence of necrotic core abutting the lumen decreased in BMS-treated lesions (proximal 23% to 0%, P = .023; distal 21% to 0%, P = .023), but not in DES (proximal 22% to 17%, P = .48; distal 23% to 21%, P = .82).
Serial VH-IVUS analysis of DES-treated lesions showed a greater frequency of unstable lesion morphometry at follow-up compared with BMS. The apparent mechanism was a suppression of the protective neointimal hyperplasia layer coupled with a lack of vulnerable plaque resolution at reference segments in DES compared with BMS.
动物模型显示药物洗脱支架(DES)与裸金属支架(BMS)相比,动脉愈合受损。虚拟组织学血管内超声(VH-IVUS)提供了一种活体评估病变形态的机会。
我们使用 VH-IVUS 评估了 80 例患者的 76 例 DES 植入物与 32 例 BMS 植入物后 10 个月的原生动脉血管反应。在基线和随访时评估“紧贴管腔的坏死核心”的存在情况。
在基线时,DES 组 76%和 BMS 组 75%的支架内可见紧贴支架的管腔的坏死核心。尽管 DES 组(23%[18%,28%]至 22%[17%,27%],P=.57)或 BMS 组(22%[19%,27%]至 20%[12%,26%],P=.29)支架后斑块内的坏死核心百分比在随访期间没有变化,但 BMS 组支架内紧贴管腔的坏死核心减少更多(75%降至 19%,P<.001),而 DES 组减少较少(76%降至 61%,P=.036),因为 DES 治疗的病变缺乏覆盖的保护新生内膜。此外,在相邻的参考节段中,BMS 治疗的病变中紧贴管腔的坏死核心的发生率降低(近端 23%降至 0%,P=.023;远端 21%降至 0%,P=.023),但 DES 治疗的病变中无此变化(近端 22%降至 17%,P=.48;远端 23%降至 21%,P=.82)。
DES 治疗的病变的连续 VH-IVUS 分析显示,与 BMS 相比,在随访时不稳定的病变形态更为常见。明显的机制是在 DES 中抑制了保护性的新生内膜增生层,同时与 BMS 相比,参考节段中易损斑块的消退受到抑制。