Clinic Hospital no. 7, Medical University of Silesia, Silesian Medical Center, Katowice, Poland.
Kardiol Pol. 2010 Jan;68(1):11-20.
Even up-to-date reperfusion therapy using primary percutaneous intervention (PCI) in acute myocardial infarction does not result in improvement of the left ventricular (LV) function in all patients. Cellular myoblasty, a novel method using mononuclear bone marrow cells (BMC), can be applied in the infarcted myocardium area to stimulate regeneration and to limit the organ damage. However, the impact of intracoronary BMC administration on the effect of PCI is not clear.
To assess angiographic outcomes in patients with anterior myocardial infarction and LV dysfunction, undergoing intracoronary BMC administration after a successful primary PCI.
The study group consisted of 40 patients (mean age 56.2 years) with LV ejection fraction below 40%, in whom 20 ml of BMC were administered to the infarct-related artery (IRA) distally to the occlusion. The control group comprised 25 age- and sex-matched patients with similar values of LV ejection fraction undergoing bare metal stenting of IRA without BMC administration. Quantitative coronary angiography was performed 6 months later to assess IRA patency.
The reference diameter of the stented artery decreased in the study group from 3.22 +/- 0.28 mm to 3.16 +/- 0.18 mm (p < 0.05) and in the control group from 3.22 +/- 0.31 mm to 3.15 +/- 0.28 mm (p < 0.082); also in the area of the implanted stent the diameter decreased from 3.57 +/- 0.21 mm to 2.96 +/- 0.79 mm in the study group vs. 3.48 +/- 0.22 mm to 3.01 +/- 0.35 mm in the control group. For lumen diameter measured 10 mm distally to the stent, the diameter loss was similar in both groups. In 6 patients from the BMC treated group and in 3 patients from the control group there was asymptomatic lumen reduction > 70% (NS).
The results of our study show that BMC administration into IRA is safe. The degree of lumen loss in the stent area was larger in the BMC group than in the control group. There was no significant difference in the lumen change distally to the stent; the artery diameter loss in both groups was similar, and the improvement in LV ejection fraction was greater in the BMC-treated group.
即使在急性心肌梗死中采用经皮直接冠状动脉介入治疗(PCI)进行最新的再灌注治疗,也不能改善所有患者的左心室(LV)功能。使用单核骨髓细胞(BMC)的新型细胞肌源性疗法可应用于梗塞心肌区域,刺激再生并限制器官损伤。然而,经冠状动脉内 BMC 给药对 PCI 效果的影响尚不清楚。
评估在前壁心肌梗死和 LV 功能障碍患者中,经皮直接冠状动脉介入治疗(PCI)成功后行冠状动脉内 BMC 给药的血管造影结果。
研究组包括 40 名(平均年龄 56.2 岁)LV 射血分数低于 40%的患者,其中 20ml 的 BMC 被给予梗塞相关动脉(IRA)闭塞段远端。对照组由 25 名年龄和性别匹配的 LV 射血分数相似的患者组成,他们接受 IRA 的裸金属支架置入术,而不给予 BMC 治疗。6 个月后进行定量冠状动脉造影,以评估 IRA 通畅性。
研究组的支架血管参考直径从 3.22±0.28mm 减少至 3.16±0.18mm(p<0.05),对照组从 3.22±0.31mm 减少至 3.15±0.28mm(p<0.082);在植入支架的区域,直径也从 3.57±0.21mm 减少至研究组的 2.96±0.79mm,对照组为 3.48±0.22mm 减少至 3.01±0.35mm。在支架远端 10mm 处测量管腔直径时,两组的管腔丢失相似。在 BMC 治疗组的 6 名患者和对照组的 3 名患者中,无症状的管腔减少>70%(无统计学差异)。
我们的研究结果表明,IRA 内 BMC 给药是安全的。在 BMC 组,支架区域的管腔丢失程度大于对照组。支架远端的管腔变化无显著差异;两组的动脉直径丢失相似,BMC 治疗组的 LV 射血分数改善更大。