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首页> 外文期刊>JACC. Cardiovascular interventions >Myocardial Blood Flow and Coronary Flow Reserve During 3 Years Following Bioresorbable Vascular Scaffold Versus Metallic Drug-Eluting Stent Implantation
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Myocardial Blood Flow and Coronary Flow Reserve During 3 Years Following Bioresorbable Vascular Scaffold Versus Metallic Drug-Eluting Stent Implantation

机译:血管血管支架与金属药物洗脱支架植入后3年内,心肌血流和冠状动脉流量储备

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OBJECTIVES The randomized clinical VANISH (Impact of Vascular Reparative Therapy on Vasomotor Function and Myocardial Perfusion: A Randomized [15O] H2O PET/ CT Study) trial was conducted to assess quantitative myocardial blood flow (MBF) during resting, hyperemia, and cold pressor testing (CPT) with positron emission tomographic perfusion imaging after the implantation of a bioresorbable everolimus-eluting scaffold compared with a drug-eluting stent. BACKGROUND Long-term resorption of the bioresorbable everolimus-eluting scaffold reinstates normal vessel geometry, allowing natural regeneration of the newly formed endothelium with revival of vasomotor function. METHODS Sixty patients (18 to 65 years of age) with single-vessel disease and type A or B1 lesions were randomized in a 1-to-1 fashion. Approximately 1 month, 1 year, and 3 years after device implantation, patients underwent [15O] H2O cardiac positron emission tomography. The primary endpoint was the interaction of device type and evolution over time of hyperemic MBF, coronary flow reserve, or CPT reserve. At 3-year follow-up, control invasive coronary angiography with optical coherence tomography was performed. RESULTS Fifty-nine (98%), 56 (93%), and 51 (85%) patients successfully completed 1-month, 1-year, and 3-year follow-up positron emission tomography, respectively, and no culprit vessel events were registered during follow-up time. The primary study endpoint (i. e., interaction between device type and time) was nonsignificant for hyperemic MBF, CPT reserve, and coronary flow reserve (p > 0.05 for all). In all patients, hyperemic MBF decreased from 1 to 3 years (p 1/4 0.02), while coronary flow reserve was lower at 3-year follow-up compared with 1-month and 1-year follow-up (p 1/4 0.03 for both). After 3 years, percentage area stenosis measured with optical coherence tomography was higher within the bioresorbable everolimus-eluting scaffold compared with the drug-eluting stent (p 1/4 0.03). CONCLUSIONS The hypothesized beneficial effects of scaffold resorption did not translate to improved MBF during maximal hyperemia or endothelium-dependent vasodilation by CPT. (J Am Coll Cardiol Intv 2019; 12: 967-79) (c) 2019 by the American College of Cardiology Foundation.
机译:目标随机临床消失(血管修复治疗对血管血管功能和心肌灌注的影响:进行随机化[150] H2O PET / CT研究)试验,以评估休息,充血和冷压力机测试期间的定量心肌血流(MBF) (CPT)具有正电子发射断层灌注灌注成像,其与药物洗脱支架相比,植入生物可吸收的everolimus洗脱的支架后。背景技术生物可吸收的血管血管洗脱支架的长期吸收恢复正常血管几何形状,允许新形成的内皮的自然再生具有血管运动功能的复苏。方法以单血管疾病和A型或B1病变为6​​0例患者(18至65岁)以1比1的方式随机化。在设备植入后约1个月,1年和3年,患者接受了[15o] H2O心脏正电子发射断层扫描。主要终点是设备类型和进化随时间的相互作用,随着时间的流逝MBF,冠状动脉储备或CPT储备。在3年的随访中,进行了控制侵入性冠状动脉造影,具有光学相干性断层扫描。结果59(98%),56(93%)和51名(85%)患者分别成功完成1个月,1年和3年后续正电子排放断层扫描,没有罪魁祸首事件在随访时间注册。主要研究终点(即,设备类型和时间之间的相互作用)对于多发MBF,CPT储备和冠状动物流量储备(P> 0.05)不显着。在所有患者中,血细胞MBF从1〜3年下降(p 1/4 0.02),而冠状动脉流量储备在3年后较低,与1个月和1年的随访相比(P 1/4两者0.03)。 3年后,与药物洗脱支架相比,使用光学相干断层扫描的光学相干断层扫描测量的百分比狭窄(P 1/4 0.03)较高。结论支架吸收的假设有益效果未转化为在最大高血量或内皮依赖性血管舒张期间改善MBF。 (J AM Coll Corniol Intv 2019; 12:967-79)(c)2019由美国心脏病学基础。

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  • 来源
    《JACC. Cardiovascular interventions》 |2019年第10期|共13页
  • 作者单位

    Vrije Univ Amsterdam Med Ctr Amsterdam UMC Dept Cardiol De Boelelaan 1117 NL-1081 HV Amsterdam;

    Vrije Univ Amsterdam Med Ctr Amsterdam UMC Dept Cardiol De Boelelaan 1117 NL-1081 HV Amsterdam;

    Vrije Univ Amsterdam Med Ctr Amsterdam UMC Dept Cardiol De Boelelaan 1117 NL-1081 HV Amsterdam;

    Vrije Univ Amsterdam Med Ctr Amsterdam UMC Dept Radiol &

    Nucl Med Amsterdam Netherlands;

    Vrije Univ Amsterdam Med Ctr Amsterdam UMC Dept Cardiol De Boelelaan 1117 NL-1081 HV Amsterdam;

    Vrije Univ Amsterdam Med Ctr Amsterdam UMC Dept Cardiol De Boelelaan 1117 NL-1081 HV Amsterdam;

    Vrije Univ Amsterdam Med Ctr Amsterdam UMC Dept Cardiol De Boelelaan 1117 NL-1081 HV Amsterdam;

    Vrije Univ Amsterdam Med Ctr Amsterdam UMC Dept Epidemiol &

    Biostat Amsterdam Netherlands;

    Vrije Univ Amsterdam Med Ctr Amsterdam UMC Dept Cardiol De Boelelaan 1117 NL-1081 HV Amsterdam;

    Vrije Univ Amsterdam Med Ctr Amsterdam UMC Dept Cardiol De Boelelaan 1117 NL-1081 HV Amsterdam;

    Radboud Univ Nijmegen Med Ctr Dept Cardiol Nijmegen Netherlands;

    Isala Heart Ctr Dept Cardiol Zwolle Netherlands;

    Vrije Univ Amsterdam Med Ctr Amsterdam UMC Dept Cardiol De Boelelaan 1117 NL-1081 HV Amsterdam;

    Vrije Univ Amsterdam Med Ctr Amsterdam UMC Dept Radiol &

    Nucl Med Amsterdam Netherlands;

    Vrije Univ Amsterdam Med Ctr Amsterdam UMC Dept Cardiol De Boelelaan 1117 NL-1081 HV Amsterdam;

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