Ochała Andrzej, Smolka Grzegorz, Wojakowski Wojciech, Gabrylewicz Bogna, Garbocz Piotr, Tendera Michał
Third Department of Cardiology, Medical University of Silesia, ul. Ziołowa 45-47, 40-635 Katowice, Poland.
Kardiol Pol. 2007 Jun;65(6):672-80; discussion 681-3.
Myocardial reperfusion following primary percutaneous coronary intervention (pPCI) is limited due to, among other things, microembolic events. Abciximab and a mechanical system of distal protection both reduce their incidence during PCI.
Prospective, randomised study to compare effectiveness of abciximab and protection devices in reduction of microembolic complications during pPCI.
One hundred and twenty consecutive patients with ST elevation acute myocardial infarction referred for pPCI after coronary angiography were randomly assigned to the following groups: Group A (n=63), treated with abciximab; and Group B (n=57), treated using the distal protection system. Primary endpoint was blood flow through the infarct-related artery (IRA) using TIMI grading after pPCI; secondary endpoints included myocardial perfusion assessment using myocardial blush grade (MBG), ST resolution and improvement of echocardiographic left ventricular ejection fraction (LVEF) after pPCI.
TIMI grade 3 flow after pPCI was obtained in 89% of patients in both groups, TIMI grade 2 flow in 5% (NS). Myocardial perfusion after pPCI assessed with MBG scored 3 in 66% of patients in group A and 62% of patients in group B (NS). ST resolution was present in 62% (26-84) in group A and 68% (41 - 86) in group B (NS). Logistic regression analysis showed no significant influence of selected variables on the primary endpoint. Analysis performed in the distal protection group revealed significant effects on the following factors on the final TIMI flow in IRA: presence of thrombus prior to pPCI (p=0.026), presence of residual thrombus after aspiration (p <0.001), and IRA diameter of > or =3.5 mm (p=0.01). Median LVEF in group A at sixth month of follow-up was 46% (44-50%), similar to group B - 46% (45-49%) (NS).
Use of the PercuSurge distal protection device during pPCI allows angiographic and electrocardiographic measures of reperfusion to be improved. It has a similar effect on left ventricular systolic function as administration of abciximab. The device seems to be useful in patients with culprit artery diameter of > or =3.0 mm, and optimally > or =3.5 mm and thrombus visible on angiography. Successful initial thrombectomy prior to deployment of stent seems particularly important when using the PercuSurge system.
除其他因素外,微栓塞事件限制了直接经皮冠状动脉介入治疗(pPCI)后的心肌再灌注。阿昔单抗和远端保护机械系统均可降低PCI期间微栓塞事件的发生率。
进行前瞻性随机研究,比较阿昔单抗和保护装置在减少pPCI期间微栓塞并发症方面的有效性。
120例在冠状动脉造影后接受pPCI的ST段抬高型急性心肌梗死连续患者被随机分为以下组:A组(n = 63),接受阿昔单抗治疗;B组(n = 57),使用远端保护系统治疗。主要终点是pPCI后使用TIMI分级评估梗死相关动脉(IRA)的血流;次要终点包括使用心肌 blush分级(MBG)评估心肌灌注、ST段回落以及pPCI后超声心动图左心室射血分数(LVEF)的改善情况。
两组中89%的患者在pPCI后获得TIMI 3级血流,5%的患者获得TIMI 2级血流(无显著性差异)。用MBG评估pPCI后的心肌灌注情况,A组66%的患者评分为3,B组62%的患者评分为3(无显著性差异)。A组62%(26 - 84)的患者ST段回落,B组68%(41 - 86)的患者ST段回落(无显著性差异)。逻辑回归分析显示所选变量对主要终点无显著影响。在远端保护组进行的分析表明,以下因素对IRA最终的TIMI血流有显著影响:pPCI前存在血栓(p = 0.026)、抽吸后存在残余血栓(p <0.001)以及IRA直径≥3.5 mm(p = 0.01)。随访6个月时,A组的LVEF中位数为46%(44 - 50%),与B组相似,为46%(45 - 49%)(无显著性差异)。
在pPCI期间使用PercuSurge远端保护装置可改善再灌注的血管造影和心电图指标。其对左心室收缩功能的影响与给予阿昔单抗相似。该装置似乎对罪犯血管直径≥3.0 mm且最好≥3.5 mm以及血管造影可见血栓的患者有用。在使用PercuSurge系统时,在支架置入前成功进行初始血栓切除术似乎尤为重要。