Department of Cardiology, Shonan Kamakura General Hospital, 1370‐1 Okamoto, Kamakura, Kanagawa 247‐0072, Japan.
J Interv Cardiol. 2013 Apr;26(2):114-22. doi: 10.1111/j.1540-8183.2013.12019.x. Epub 2013 Feb 5.
To evaluate the risk of long-term dual antiplatelet therapy (DAT) following drug-eluting stent (DES) implantation in octogenarians.
DES implantation requires DAT; however, DAT-associated risk in octogenarians remains unclear.
Two-hundred and six consecutive octogenarians (130 men, 83.3 ± 3.4 years) underwent stent implantation (104 bare metal stents [BMSs] and 102 DESs) and 38.0 ± 13.2 months of follow-up.
Significantly more DES patients received DAT. The incidence of bleeding events was similar in the DES and BMS groups for 1 year (total: 10.8% vs 5.8%, P = 0.19; major: 4.9% vs 2.9%, P = 0.70). However, after 2 years, significantly more bleeding events occurred in the DES group than the BMS group (total: 2 years, 21.6% vs 9.6%, P = 0.02; 3 years, 29.4% vs 11.5%, P = 0.001; 4 years, 31.4% vs 15.4%, P = 0.007; major: 2 years, 12.7% vs 3.8%, P = 0.04; 3 years, 18.6% vs 5.8%, P = 0.005; 4 years, 19.6% vs 6.7%, P = 0.006). Overall, significantly more total bleeding events (31.4% vs 15.4%, P = 0.007) and major bleeding events (19.2% vs 6.7%, P = 0.006) were observed in the DES group than in the BMS group. The adjusted hazard ratios and 95% confidence intervals (CI) were as follows: total bleeding events, 2.203 (95% CI: 1.065-4.556; P = 0.033); major bleeding events, 4.324 (1.506-12.414; P = 0.007).
DAT was associated with an increased risk of bleeding events in octogenarians after 2 years. DAT discontinuation should be considered for octogenarians 1-year post-DES implantation.
评估老年患者接受药物洗脱支架(DES)植入后长期双联抗血小板治疗(DAT)的风险。
DES 植入需要 DAT;然而,80 岁以上患者 DAT 的相关风险尚不清楚。
206 例连续的 80 岁以上患者(130 名男性,83.3±3.4 岁)接受了支架植入(104 个裸金属支架 [BMS] 和 102 个 DES)和 38.0±13.2 个月的随访。
DES 患者接受 DAT 的比例明显更高。DES 组和 BMS 组在 1 年时出血事件的发生率相似(总出血:10.8%比 5.8%,P=0.19;大出血:4.9%比 2.9%,P=0.70)。然而,2 年后,DES 组出血事件的发生率明显高于 BMS 组(总出血:2 年,21.6%比 9.6%,P=0.02;3 年,29.4%比 11.5%,P=0.001;4 年,31.4%比 15.4%,P=0.007;大出血:2 年,12.7%比 3.8%,P=0.04;3 年,18.6%比 5.8%,P=0.005;4 年,19.6%比 6.7%,P=0.006)。总体而言,DES 组的总出血事件(31.4%比 15.4%,P=0.007)和大出血事件(19.2%比 6.7%,P=0.006)明显多于 BMS 组。调整后的危险比和 95%置信区间(CI)如下:总出血事件,2.203(95%CI:1.065-4.556;P=0.033);大出血事件,4.324(1.506-12.414;P=0.007)。
DAT 与 2 年后 80 岁以上患者出血事件风险增加相关。DES 植入后 1 年应考虑停止 DAT。