Kapoor Nikhil, Yalamanchili Venkata, Siddiqui Tariq, Raza Syed, Leesar Massoud A
Division of Cardiology, University of Louisville, Louisville, Kentucky.
Catheter Cardiovasc Interv. 2014 Jun 1;83(7):1045-54. doi: 10.1002/ccd.25248. Epub 2014 Jan 31.
Despite the use of embolic protection devices, no-reflow can still occur during saphenous vein grafts (SVGs) intervention. High-dose intracoronary adenosine infusion preconditions the myocardium, improves coronary flow, and prevents no-reflow. The role of high-dose intragraft adenosine infusion on protection of microvascular function and prevention of no-reflow has not been investigated
We investigated the cardioprotective effect of high-dose intragraft adenosine infusion, compared with placebo, on microvascular function and prevention of no-reflow during SVGs intervention.
We randomized 22 patients with SVGs stenoses to receive either a 10-min intragraft adenosine infusion (200 μg/min; total dose = 2,000 μg) or normal saline prior to stenting. Average peak velocity (APV), coronary flow velocity reserve (CVR), thrombolysis in myocardial infarction (TIMI) frame count (TFC), TIMI myocardial perfusion grade (TMPG), and the rate of no-reflow were compared between the two groups before adenosine or saline infusions and after stenting
After stenting, hyperemic APV, CVR, and TMPG were significantly higher in the adenosine-treated group than in the control group (60 ± 18 vs. 35 ± 10 cm/sec; 2.6 ± 0.54 vs. 1.8 ± 0.47; and 2.8 ± 0.90 vs. 2.1 ± 0.80, respectively; P < 0.05. TFC was significantly lower in the adenosine-treated group than in the control group (14 ± 3.0 vs. 26 ± 13; P < 0.05). In the control group, four patients (36%) developed no-reflow compared to none in the adenosine-treated patient; P < 0.05 CONCLUSIONS: This study provides the first evidence that high-dose intragraft adenosine infusion compared with placebo protects microvascular function and prevents no-reflow during SVGs intervention.
尽管使用了栓塞保护装置,但在隐静脉移植血管(SVG)介入过程中仍可能发生无复流现象。大剂量冠状动脉内输注腺苷可使心肌预处理,改善冠状动脉血流,并预防无复流。大剂量移植血管内输注腺苷对微血管功能保护及预防无复流的作用尚未得到研究。
我们研究了与安慰剂相比,大剂量移植血管内输注腺苷对SVG介入过程中微血管功能及预防无复流的心脏保护作用。
我们将22例SVG狭窄患者随机分为两组,一组在支架置入前接受10分钟的移植血管内腺苷输注(200μg/分钟;总剂量=2000μg),另一组接受生理盐水输注。比较两组在腺苷或生理盐水输注前及支架置入后的平均峰值流速(APV)、冠状动脉血流储备(CVR)、心肌梗死溶栓(TIMI)帧数(TFC)、TIMI心肌灌注分级(TMPG)以及无复流发生率。
支架置入后,腺苷治疗组的充血性APV、CVR和TMPG显著高于对照组(分别为60±18 vs. 35±10cm/秒;2.6±0.54 vs. 1.8±0.47;2.8±0.90 vs. 2.1±0.80;P<0.05)。腺苷治疗组的TFC显著低于对照组(14±3.0 vs. 26±13;P<0.05)。对照组有4例患者(36%)发生无复流,而腺苷治疗组无患者发生无复流;P<0.05。
本研究首次证明,与安慰剂相比,大剂量移植血管内输注腺苷可在SVG介入过程中保护微血管功能并预防无复流。