对于无血栓的隐静脉移植物病变,移植内阿昔单抗和维拉帕米联合直接支架植入术是一种安全有效的预防慢流无回流现象的策略。

Sanjiv Sharma, Joel A Lardizabal, Sarabjeet Singh, Rasham Sandhu, Brijesh K Bhambi
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引用次数: 7

摘要

未标记:隐静脉移植物(SVG)支架植入术中的慢流无回流现象(SF-NR)与远端斑块栓塞、血小板活化和微血管痉挛的发生有关。我们的文章讨论了一些与SVG经皮冠状动脉介入治疗(SVG PCI)中预防慢流/无回流现象的策略相关的专利。方法:回顾163例连续10年无明显大血栓且未使用远端栓塞保护装置的SVG病变行PCI治疗的患者资料。新策略组患者在直接支架植入后预防性给予阿昔单抗和维拉帕米(n=91)。对照组(n=72)由在常规远端栓塞保护装置可用之前接受常规PCI技术的患者组成,目标病变进行球囊预扩张,然后放置支架,可选择使用维拉帕米或静脉注射阿昔单抗。在移植静脉中可见较大血栓的患者被排除在研究之外,因为这些患者使用远端栓塞保护(过滤器)进行了PCI。结果:与新策略组相比,对照组SF-NR (TIMI 0-1流)发生的频率更高(18% vs. 1%, P=0.0001)。对照组1例患者在pci术后出现持续性SF-NR和急性心肌梗死后死亡。新策略组无死亡报告。在对照组中,13%的患者在PCI后出现心脏酶升高,是正常的3倍,而新策略组为1% (P < 0.05)。结论:近年来,一些远端栓塞保护装置已获得专利,以最大限度地减少慢流/无回流现象的机会。在精心挑选的无明显大血栓的SVG病变亚组中,预防性地在移植物内给予阿昔单抗和维拉帕米,并在没有预扩张的情况下直接支架置入移植物病变,可以安全地完成,没有明显的慢流/无回流现象风险。我们为无血栓的SVG病变经皮冠状动脉介入治疗的三步策略申请专利。
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Intra-graft abciximab and verapamil combined with direct stenting is a safe and effective strategy to prevent slow-flow and no-reflow phenomenon in saphenous vein graft lesions not associated with thrombus.

Unlabelled: Slow flow and no-reflow phenomenon (SF-NR) in saphenous vein grafts (SVG) stenting is related to the occurrence of distal plaque embolization, platelet activation and microvascular vasospasm. Our article discusses few of the patents related to strategies for preventing slow-flow/no-reflow phenomenon in SVG percutaneous coronary intervention (SVG PCI).

Methods: Data from 163 consecutive patients who underwent PCI of SVG lesions without visible macro-thrombus without use of distal embolic protection device over a 10-year period were reviewed. Patients in the novel strategy group received prophylactic intra-graft administration of abciximab and verapamil followed by direct stenting (n=91). The control group (n=72) comprised of patients who had undergone conventional PCI technique before the routine availability of distal embolic protection devices, with balloon pre-dilatation of the target lesion followed by stent deployment and optional use of intragraft verapamil or intravenous abciximab. Patients with visible macro-thrombus in the vein graft were excluded from the study, since these patients underwent PCI with use of the distal embolic protection (filter).

Results: SF-NR (TIMI 0-1 flow) occurred more frequently in the control group compared to the novel strategy group (18% vs. 1%, P=0.0001). One patient in the control group died after developing persistent SF-NR and acute MI post-PCI. No death was reported in the novel strategy group. In the control group, 13% patients developed cardiac enzyme elevation 3 times more than normal after the PCI as compared to 1% in the novel strategy group (P < 0.05).

Conclusions: In recent years several distal embolic protection devices have been granted patents for minimizing the chance of slow-flow/no-reflow phenomenon. In carefully selected subgroup of SVG lesions without visible macrothrombus, a strategy of prophylactic intra-graft administration of abciximab and verapamil, combined with direct stenting of the graft lesion without pre-dilatation, can be safely accomplished without any significant risk of slow-flow/no-reflow phenomenon. We propose a patent to this 3-step strategy of percutaneous coronary intervention of SVG lesions not associated with thrombus.

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Patents and Heart Valve Surgery - III: Percutaneous Heart Valves. Patents and Heart Valve Surgery - III: Percutaneous Heart Valves. New frontiers in the management of acute coronary syndromes: cangrelor and elinogrel. Blockade of renin angiotensin system in heart failure post-myocardial infarction: what is the best therapy? Ticagrelor: a novel drug for an old problem.
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