Oliva Angelo, Angiolillo Dominick J, Valgimigli Marco, Cao Davide, Sartori Samantha, Bangalore Sripal, Bhatt Deepak L, Campo Gianluca, Chehab Bassem M, Choi James W, de la Torre Hernandez Jose M, Feng Yihan, Ge Junbo, Gitto Mauro, Hermiller James, Krucoff Mitchell W, Kunadian Vijay, Makkar Raj R, Maksoud Aziz, Neumann Franz-Josef, Picon Hector, Saito Shigeru, Sardella Gennaro, Thiele Holger, Toelg Ralph, Varenne Olivier, Vogel Birgit, Vranckx Pascal, Windecker Stephan, Mehran Roxana
Mount Sinai Fuster Heart Hospital, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Department of Biomedical Sciences, Humanitas University, Pieve Emanuele, Italy.
EuroIntervention. 2025 Jun 16;21(12):e668-e680. doi: 10.4244/EIJ-D-24-00897.
In patients with diabetes mellitus (DM) and high bleeding risk (HBR) undergoing percutaneous coronary intervention (PCI), the optimal duration of dual antiplatelet therapy (DAPT) remains uncertain.
We sought to compare early DAPT discontinuation in DM and non-DM patients enrolled in the prospective XIENCE Short DAPT programme.
The effects of 1- versus 3-month DAPT on ischaemic and bleeding outcomes were compared using propensity score stratification. The primary endpoint was a composite of all-cause death or myocardial infarction (MI) at 1 year. The incidence of Bleeding Academic Research Consortium (BARC) Type 2 to 5 bleeding was the key secondary endpoint.
Out of 3,352 included patients, 1,299 (38.8%) had DM; diabetic patients had a higher 1-year incidence of death or MI (DM vs non-DM: 10.1% vs 6.6%) and similar BARC 2-5 bleeding (DM vs non-DM: 9.5% vs 9.2%). With 1- versus 3-month DAPT, the incidence of death or MI did not statistically differ in DM patients (adjusted hazard ratio [adjHR] 0.70, 95% confidence interval [CI]: 0.47-1.05) and non-DM patients (adjHR 1.26, 95% CI: 0.87-1.81), although heterogeneity by DM status was evident (p for interaction=0.015). BARC 2-5 bleeding was numerically lower with 1-month DAPT in both groups (DM: adjHR 0.67, 95% CI: 0.45-1.01; non-DM: adjHR 0.78, 95% CI: 0.56-1.07; p for interaction=0.973).
Among HBR patients with DM undergoing PCI, 1-month DAPT, as compared to 3-month DAPT, was not associated with an excess of fatal or non-fatal MI and even reduced the occurrence of bleeding. These findings should be interpreted in the context of a predominantly stable patient population with low procedural complexity and may not be generalisable to higher-risk cases.
在接受经皮冠状动脉介入治疗(PCI)的糖尿病(DM)和高出血风险(HBR)患者中,双联抗血小板治疗(DAPT)的最佳持续时间仍不确定。
我们试图比较参加前瞻性XIENCE短期DAPT项目的DM患者和非DM患者早期停用DAPT的情况。
使用倾向评分分层比较1个月与3个月DAPT对缺血和出血结局的影响。主要终点是1年时全因死亡或心肌梗死(MI)的复合终点。出血学术研究联盟(BARC)2至5型出血的发生率是关键次要终点。
在3352例纳入患者中,1299例(38.8%)患有DM;糖尿病患者1年时死亡或MI的发生率较高(DM组与非DM组:10.1%对6.6%),BARC 2 - 5型出血发生率相似(DM组与非DM组:9.5%对9.2%)。对于1个月与3个月DAPT,DM患者(调整后风险比[adjHR] 0.70,95%置信区间[CI]:0.47 - 1.05)和非DM患者(adjHR 1.26,95% CI:0.87 - 1.81)死亡或MI的发生率在统计学上无差异,尽管按DM状态存在异质性(交互作用p = 0.015)。两组中1个月DAPT时BARC 2 - 5型出血在数值上均较低(DM组:adjHR 0.67,95% CI:0.45 - 1.01;非DM组:adjHR 0.78,95% CI:0.56 - 1.07;交互作用p = 0.973)。
在接受PCI的HBR DM患者中,与3个月DAPT相比,1个月DAPT与致命或非致命MI的增加无关,甚至减少了出血的发生。这些发现应在主要为病情稳定、手术复杂性低的患者群体背景下进行解读,可能不适用于更高风险的病例。