首页> 外文期刊>Cardiovascular revascularization medicine: including molecular interventions >A prospective multicenter registry of laser therapy for degenerated saphenous vein graft stenosis: The COronary graft Results following Atherectomy with Laser (CORAL) trial
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A prospective multicenter registry of laser therapy for degenerated saphenous vein graft stenosis: The COronary graft Results following Atherectomy with Laser (CORAL) trial

机译:退行性大隐静脉移植物狭窄的激光治疗的前瞻性多中心研究:冠脉搭桥术(CORAL)试验后的冠状动脉移植结果

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Purpose: The primary aim of this study was to prospectively evaluate the safety and efficacy of Excimer laser atherectomy as a primary treatment strategy in consecutively eligible patients presenting for percutaneous coronary intervention (PCI) of degenerated saphenous vein graft (SVG) lesions using a multicenter registry. Prior single-center experience suggested that laser atherectomy may decrease acute procedural complications during treatment of degenerated SVGs, including lesions not amenable to distal protection devices (DPDs). Methods and materials: The COronary graft Results following Atherectomy with Laser investigators enrolled 98 patients at 18 centers between June 23, 2003, and October 4, 2004, with greater than 50% stenosis of an SVG who presented for PCI due to angina pectoris or objective evidence of myocardial ischemia in a concordant myocardial distribution. Laser atherectomy was planned. Patients were excluded if the operator planned to utilize a DPD. Inclusion and exclusion criteria were aligned to those in the Saphenous vein graft Angioplasty Free of Emboli Randomized (SAFER) trial. Results: The primary end point [30-day major adverse cardiac events (MACE)] occurred in 18/98 (18.4%) patients driven primarily by non-q-wave myocardial infarction. Major procedural complications included no reflow (. n=5) and major dissection (. n=1). No perforations occurred. Univariate predictors of 30-day MACE included lesion length, vessel angulation, plaque burden, SVG degeneracy score, number of laser pulses used, and larger-sized laser catheters. Conclusions: This study demonstrated that Excimer laser atherectomy of diseased SVGs is feasible with results comparable to the 30-day MACE in the control population from the SAFER trial. Whether the addition of laser to embolic protection devices is of any clinical utility remains to be tested in future studies.
机译:目的:本研究的主要目的是前瞻性评估准分子激光旋磨术作为连续治疗合格的使用多中心注册表对变性大隐静脉移植(SVG)病变进行经皮冠状动脉介入治疗(PCI)的合格患者的主要治疗策略的安全性和有效性。先前的单中心经验表明,激光斑块切除术可以降低退化性SVG的治疗过程中的急性手术并发症,包括远端保护装置(DPD)不适合的病变。方法和材料:2003年6月23日至2004年10月4日,在18个中心进行的激光研究者进行冠脉搭桥术后的冠状动脉移植结果纳入了SVG狭窄程度超过50%的人,这些人由于心绞痛或客观原因而接受PCI心肌分布一致的心肌缺血证据。计划进行激光斑块切除术。如果操作员计划使用DPD,则将患者排除在外。纳入和排除标准与无栓塞大隐静脉移植血管成形术(SAFER)试验中的标准一致。结果:主要终点[30天主要不良心脏事件(MACE)]发生在18/98(18.4%)主要由非q波心肌梗死驱动的患者中。主要的手术并发症包括无回流(.n = 5)和主要解剖(.n = 1)。没有发生穿孔。 30天MACE的单变量预测因素包括病变长度,血管成角,斑块负担,SVG退化评分,使用的激光脉冲数和较大尺寸的激光导管。结论:这项研究表明,对患病的SVG进行准分子激光旋切术是可行的,其结果与SAFER试验中对照组的30天MACE相当。在栓塞保护装置中增加激光是否具有任何临床实用性,仍有待进一步研究。

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