Division of Cardiac Surgery, Department of Clinical Research, Boca Raton Regional Hospital, Florida Atlantic University, Boca Raton, Florida, USA.
Division of Cardiovascular and Thoracic Surgery, Missouri Baptist Medical Center, St. Louis, Missouri, USA.
J Card Surg. 2022 Jul;37(7):1969-1977. doi: 10.1111/jocs.16492. Epub 2022 Apr 9.
Compared to conventional aspirin therapy, ticagrelor did not improve vein graft patency 1 year after coronary bypass surgery (CABG) in the ticagrelor antiplatelet therapy to reduce graft events and thrombosis (TARGET) trial. However, it is unknown whether ticagrelor may impact graft patency long-term following surgery.
In the TARGET multicenter trial, 250 CABG patients were randomized to aspirin 81 mg or ticagrelor 90 mg twice daily. In this observational analysis, 2 years after surgery, vein graft occlusion and clinical events were compared among subjects who agreed to a second year of double-blind study drug administration (N = 156).
Two-year graft assessment was performed for 142 patients (80 aspirin patients, 62 ticagrelor patients, 425 total grafts), with an overall 2-year graft occlusion rate of 10.6%. Vein graft occlusion at 2 years, the primary outcome of this study, did not significantly differ between the two groups (15.7% vs. 13.2%, aspirin vs. ticagrelor, p = .71). The incidence of vein grafts with any disease (stenosis or occlusion) did not significantly differ between the groups (19.4% vs. 19.8%, aspirin vs. ticagrelor, p = 1.00), and the number of patients with vein graft disease did not significantly differ between the groups (30.0% vs. 29.0%, aspirin vs. ticagrelor, p = 1.00). Vein grafts developing new disease did not significantly differ between the two groups (1.5% vs. 3.8%, aspirin vs. ticagrelor, p = .41). Freedom from major adverse cardiovascular events at 2 years was similar between the groups (p = .75).
Compared to conventional aspirin therapy, ticagrelor did not significantly reduce vein graft disease 2 years after CABG.
与传统的阿司匹林治疗相比,替格瑞洛并没有改善冠状动脉旁路移植术(CABG)后 1 年的静脉移植物通畅率,这在替格瑞洛抗血小板治疗减少移植物事件和血栓形成(TARGET)试验中有所体现。然而,尚不清楚替格瑞洛是否会对手术后的移植物通畅率产生长期影响。
在 TARGET 多中心试验中,250 例 CABG 患者被随机分为阿司匹林 81mg 或替格瑞洛 90mg,每日两次。在这项观察性分析中,手术后 2 年,根据同意进行第二年双盲研究药物治疗的受试者,比较静脉移植物闭塞和临床事件(N=156)。
对 142 例患者(阿司匹林 80 例,替格瑞洛 62 例,共 425 例静脉移植物)进行了 2 年的移植物评估,总体 2 年的移植物闭塞率为 10.6%。本研究的主要终点为 2 年时的静脉移植物闭塞,两组之间没有显著差异(15.7%比 13.2%,阿司匹林组比替格瑞洛组,p=0.71)。两组之间静脉移植物任何疾病(狭窄或闭塞)的发生率没有显著差异(19.4%比 19.8%,阿司匹林组比替格瑞洛组,p=1.00),两组静脉移植物疾病患者的数量也没有显著差异(30.0%比 29.0%,阿司匹林组比替格瑞洛组,p=1.00)。两组之间新发生的静脉移植物疾病没有显著差异(1.5%比 3.8%,阿司匹林组比替格瑞洛组,p=0.41)。两组在 2 年内的主要不良心血管事件发生率无显著差异(p=0.75)。
与传统的阿司匹林治疗相比,替格瑞洛在 CABG 后 2 年并没有显著降低静脉移植物疾病。