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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

机译:与药物洗脱支架中支撑良好的支杆相比,不良支杆和侧支杆支杆的延迟覆盖:光学相干断层扫描的体内评估

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摘要

textabstractBackground-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; I2=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.
机译:关于晚期支架内血栓形成的致命病例的背景病理研究表明,不完整的新内膜覆盖是常见的基质,某些情况下出现在侧支杆上。血管内超声研究已经描述了不完全的支架并置(ISA)与支架血栓形成之间的关联,但尚不清楚解释这种关联的机制。尚不清楚相对于布置良好的支撑杆,新的内膜未覆盖侧支和ISA支撑杆是否延迟。方法和结果在2项随机试验中,对99例患者的178个支架进行了光学相干断层扫描研究,并随访了9至13个月。样品包括38个西罗莫司洗脱支架,33个生物lim莫司洗脱支架,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汇总分析,比较了未并置的侧支和ISA支杆的光学相干层析成像覆盖率与同一支架的并置好的支杆。总共分析了34120个支杆。对于无支腿的支具与支配良好的支杆,延迟承保的风险比为9.00(95%置信区间,6.58至12.32);对于有支配结构的支支,ISA分别为9.10(95%置信区间,7.34至11.28),以及1.73 ISA与无支腿侧支杆相比(95%置信区间,1.34至2.23)。在ISA与布置良好的支撑杆(H = 1.27; I2 = 38.40)的比较中观察到了效果的异质性,但在其他比较中没有观察到。结论通过光学相干断层扫描技术评估,相对于药物洗脱支架中布置良好的支撑杆,ISA和未布置的侧支撑杆的覆盖范围有所延迟。临床试验注册-http:// www。临床试验网唯一标识符:NCT00389220,NCT00617084。

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