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药物洗脱支架再狭窄中厚帽新生动脉粥样硬化和围手术期心肌梗死增加:药物洗脱支架和裸金属支架的多模式血管内影像学。

Increased thin-cap neoatheroma and periprocedural myocardial infarction in drug-eluting stent restenosis: multimodality intravascular imaging of drug-eluting and bare-metal stents.

机构信息

Division of Cardiology, Mount Sinai School of Medicine, New York, NY.

出版信息

Circ Cardiovasc Interv. 2013 Oct 1;6(5):507-17. doi: 10.1161/CIRCINTERVENTIONS.112.000248. Epub 2013 Sep 24.

Abstract

BACKGROUND

Re-endothelialization is delayed after drug-eluting stent (DES) implantation. In this setting, neointima is more prone to become lipid laden and develop neoatherosclerosis (NA), potentially increasing plaque vulnerability.

METHODS AND RESULTS

Optical coherence tomography and near-infrared spectroscopy with intravascular ultrasound were used to characterize NA in 65 (51 DES and 14 bare-metal stents) consecutive symptomatic patients with in-stent restenosis. Median duration poststent implantation was 33 months. Optical coherence tomography-verified NA was observed in 40 stents with in-stent restenosis (62%), was more prevalent in DES than bare-metal stents (68% versus 36%; P=0.02), and demonstrated significantly higher prevalence of thin-cap neoatheroma (47% versus 7%; P=0.01) in DES. Near-infrared spectroscopy assessment demonstrated that the total lipid core burden index (34 [interquartile range, 12-92] versus 9 [interquartile range, 0-32]; P<0.001) and the density of lipid core burden index (lipid core burden index/4 mm, 144 [interquartile range, 60-285] versus 26 [interquartile range, 0-86]; P<0.001) were higher in DES compared with bare-metal stents. Topographically, NA was classified as I (thin-cap NA), II (thick-cap NA), and III (peri-strut NA). Type I thin-cap neoatheroma was more common in DES (20% versus 3%; P=0.01) and in areas of the stented segment without significant in-stent restenosis (71%). Periprocedural myocardial infarction occurred only in DES (11 versus 0; P=0.05), of which 6 (55%) could be attributed to segments with >70% in-stent restenosis. By logistic regression, prior DES was the only independent predictor of both NA (odds ratio, 7.0; 95% confidence interval, 1.7-27; P=0.006) and periprocedural myocardial infarction (odds ratio, 1.8; 95% confidence interval, 1.1-2.4; P=0.05).

CONCLUSIONS

In-stent thin-cap neoatheroma is more prevalent, is distributed more diffusely across the stented segment, and is associated with increased periprocedural myocardial infarction in DES compared with bare-metal stents. These findings support NA as a mechanism for late DES failure.

摘要

背景

药物洗脱支架(DES)植入后再内皮化延迟。在这种情况下,新生内膜更容易富含脂质并发展为新生动脉粥样硬化(NA),从而潜在地增加斑块的脆弱性。

方法和结果

使用光学相干断层扫描和血管内超声对 65 例(51 例 DES 和 14 例裸金属支架)连续症状性支架内再狭窄患者的 NA 进行特征描述。支架植入后中位时间为 33 个月。在 40 个支架内再狭窄(62%)中观察到光学相干断层扫描证实的 NA,DES 中 NA 的发生率高于裸金属支架(68%对 36%;P=0.02),DES 中薄帽新生动脉粥样硬化的发生率明显更高(47%对 7%;P=0.01)。近红外光谱评估显示,总脂质核心负荷指数(34 [四分位间距,12-92] 对 9 [四分位间距,0-32];P<0.001)和脂质核心负荷指数密度(脂质核心负荷指数/4mm,144 [四分位间距,60-285] 对 26 [四分位间距,0-86];P<0.001)在 DES 中均高于裸金属支架。从拓扑学角度来看,NA 分为 I 型(薄帽新生动脉粥样硬化)、II 型(厚帽新生动脉粥样硬化)和 III 型(支架内新生动脉粥样硬化)。DES 中更常见 I 型(薄帽新生动脉粥样硬化)(20%对 3%;P=0.01)和支架段无明显支架内再狭窄的区域(71%)。仅 DES 术中发生心肌梗死(11 例对 0 例;P=0.05),其中 6 例(55%)可归因于>70%的支架内再狭窄节段。通过逻辑回归,DES 是 NA(优势比,7.0;95%置信区间,1.7-27;P=0.006)和围手术期心肌梗死(优势比,1.8;95%置信区间,1.1-2.4;P=0.05)唯一的独立预测因素。

结论

DES 中支架内薄帽新生动脉粥样硬化更为普遍,在支架段内分布更为弥散,与裸金属支架相比,围手术期心肌梗死的发生率更高。这些发现支持 NA 是 DES 晚期失败的机制。

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