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药物洗脱支架中远隔贴壁和分支支架内的延迟覆盖与贴壁良好的支架相比:光学相干断层成像的体内评估。

Delayed coverage in malapposed and side-branch struts with respect to well-apposed struts in drug-eluting stents: in vivo assessment with optical coherence tomography.

机构信息

Erasmus Medical Centre, Thoraxcenter, Rotterdam, Netherlands.

出版信息

Circulation. 2011 Aug 2;124(5):612-23. doi: 10.1161/CIRCULATIONAHA.110.014514. Epub 2011 Jul 18.

Abstract

BACKGROUND

Pathology studies on fatal cases of very late stent thrombosis have described incomplete neointimal coverage as common substrate, in some cases appearing at side-branch struts. Intravascular ultrasound studies have described the association between incomplete stent apposition (ISA) and stent thrombosis, but the mechanism explaining this association remains unclear. Whether the neointimal coverage of nonapposed side-branch and ISA struts is delayed with respect to well-apposed struts is unknown.

METHODS AND RESULTS

Optical coherence tomography studies from 178 stents implanted in 99 patients from 2 randomized trials were analyzed at 9 to 13 months of follow-up. The sample included 38 sirolimus-eluting, 33 biolimus-eluting, 57 everolimus-eluting, and 50 zotarolimus-eluting stents. Optical coherence tomography coverage of nonapposed side-branch and ISA struts was compared with well-apposed struts of the same stent by statistical pooled analysis with a random-effects model. A total of 34 120 struts were analyzed. The risk ratio of delayed coverage was 9.00 (95% confidence interval, 6.58 to 12.32) for nonapposed side-branch versus well-apposed struts, 9.10 (95% confidence interval, 7.34 to 11.28) for ISA versus well-apposed struts, and 1.73 (95% confidence interval, 1.34 to 2.23) for ISA versus nonapposed side-branch struts. Heterogeneity of the effect was observed in the comparison of ISA versus well-apposed struts (H=1.27; I(2)=38.40) but not in the other comparisons.

CONCLUSIONS

Coverage of ISA and nonapposed side-branch struts is delayed with respect to well-apposed struts in drug-eluting stents, as assessed by optical coherence tomography. Clinical Trial Registration- http://www.clinicaltrials.gov. Unique identifier: NCT00389220, NCT00617084.

摘要

背景

对极晚期支架血栓形成的致死病例进行的病理学研究表明,不完全的新生内膜覆盖是常见的病变基质,在某些情况下出现在分支支架的侧支。血管内超声研究描述了不完全支架贴壁(ISA)与支架血栓形成之间的关系,但解释这种关系的机制尚不清楚。非贴壁分支和 ISA 支架的新生内膜覆盖是否相对于贴壁良好的支架延迟尚不清楚。

方法和结果

对来自 2 项随机试验的 99 例患者的 178 个支架的光学相干断层扫描研究进行了分析,随访时间为 9 至 13 个月。样本包括 38 个西罗莫司洗脱支架、33 个比伐卢定洗脱支架、57 个依维莫司洗脱支架和 50 个佐他莫司洗脱支架。通过随机效应模型的统计合并分析比较了非贴壁分支和 ISA 支架与同一支架上贴壁良好的支架的光学相干断层扫描覆盖情况。共分析了 34120 个支架。非贴壁分支与贴壁良好的支架相比,延迟覆盖的风险比为 9.00(95%置信区间,6.58 至 12.32);ISA 与贴壁良好的支架相比,风险比为 9.10(95%置信区间,7.34 至 11.28);ISA 与非贴壁分支支架相比,风险比为 1.73(95%置信区间,1.34 至 2.23)。ISA 与贴壁良好的支架相比,存在效应异质性(H=1.27;I²=38.40),但其他比较无差异。

结论

药物洗脱支架的 ISA 和非贴壁分支支架的覆盖相对于贴壁良好的支架是延迟的,这可以通过光学相干断层扫描来评估。临床试验注册- http://www.clinicaltrials.gov。唯一标识符:NCT00389220,NCT00617084。

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