Marso S P, Lincoff A M, Ellis S G, Bhatt D L, Tanguay J F, Kleiman N S, Hammoud T, Booth J E, Sapp S K, Topol E J
Department of Cardiology, Cleveland Clinic Foundation, Cleveland, Ohio 44195, USA.
Circulation. 1999;100(25):2477-84. doi: 10.1161/01.cir.100.25.2477.
Stenting likely decreases the need for target-vessel revascularization procedures in diabetic patients compared with balloon angioplasty. However, the efficacy of stenting with platelet glycoprotein IIb/IIIa blockade has not yet been assessed in diabetics.
We analyzed the outcomes of 491 diabetic patients within the multicenter Evaluation of Platelet IIb/IIIa Inhibitor for Stenting Trial (EPISTENT). Diabetic patients were a prospectively defined subset: 173 were randomized to stent-placebo, 162 to stent-abciximab, and 156 to balloon angioplasty-abciximab. The main end point for this analysis was combined 6-month death, myocardial infarction (MI), or target-vessel revascularization (TVR). The composite end point occurred in 25.2% of stent-placebo, 23.4% of balloon-abciximab, and 13.0% of stent-abciximab patients (P=0.005). Abciximab therapy, irrespective of revascularization strategy (stent or balloon angioplasty), resulted in a significant reduction in the 6-month death or MI rate: 12.7% for stent-placebo, 7.8% for balloon angioplasty-abciximab, and 6.2% for the stent-abciximab group (P=0.029). The 6-month TVR rate was 16.6% for stent-placebo, 18.4% for balloon-abciximab, and 8.1% for stent-abciximab (P=0.021). Compared with stent-placebo, stent-abciximab therapy was associated with a significant increase in angiographic net gain (0.88 versus 0.55 mm; P=0.011) and a decrease in the late loss index (0.40 versus 0.60 mm; P=0.061). The 1-year mortality rate for diabetics was 4.1% for stent-placebo and 1. 2% for stent-abciximab patients (P=0.11).
The combination of stenting and abciximab therapy among diabetics resulted in a significant reduction in 6-month rates of death, MI, and TVR compared with stent-placebo or balloon-abciximab therapy.
与球囊血管成形术相比,支架置入术可能减少糖尿病患者进行靶血管血运重建术的需求。然而,血小板糖蛋白IIb/IIIa受体阻滞剂辅助支架置入术在糖尿病患者中的疗效尚未得到评估。
我们在多中心血小板IIb/IIIa受体抑制剂用于支架置入术试验(EPISTENT)中分析了491例糖尿病患者的治疗结果。糖尿病患者是一个前瞻性定义的亚组:173例被随机分配至支架-安慰剂组,162例至支架-阿昔单抗组,156例至球囊血管成形术-阿昔单抗组。该分析的主要终点是6个月时死亡、心肌梗死(MI)或靶血管血运重建(TVR)的复合终点。复合终点在支架-安慰剂组患者中的发生率为25.2%,球囊血管成形术-阿昔单抗组为23.4%,支架-阿昔单抗组为13.0%(P=0.005)。阿昔单抗治疗,无论血运重建策略(支架或球囊血管成形术)如何,均导致6个月时死亡或MI发生率显著降低:支架-安慰剂组为12.7%,球囊血管成形术-阿昔单抗组为7.8%,支架-阿昔单抗组为6.2%(P=0.029)。6个月时TVR发生率在支架-安慰剂组为1,6.6%,球囊血管成形术-阿昔单抗组为18.4%,支架-阿昔单抗组为8.1%(P=0.021)。与支架-安慰剂组相比,支架-阿昔单抗治疗使血管造影净增(0.88对0.55 mm;P=0.011)显著增加,晚期丢失指数降低(0.40对0.60 mm;P=0.061)。糖尿病患者1年死亡率在支架-安慰剂组为4.1%,支架-阿昔单抗组为1.2%(P=0.11)。
与支架-安慰剂或球囊血管成形术-阿昔单抗治疗相比,糖尿病患者采用支架置入术与阿昔单抗治疗相结合的方法可使6个月时死亡、MI和TVR发生率显著降低。