Cardiocentro Ticino Institute, Ente Ospedaliero Cantonale, Lugano, Switzerland.
Department of Biomedical Sciences, University of Italian Switzerland, Lugano, Switzerland.
JAMA Cardiol. 2024 Jan 1;9(1):35-44. doi: 10.1001/jamacardio.2023.4316.
Abbreviated dual antiplatelet therapy (DAPT) reduces bleeding with no increase in ischemic events in patients at high bleeding risk (HBR) undergoing percutaneous coronary intervention (PCI).
To evaluate the association of sex with the comparative effectiveness of abbreviated vs standard DAPT in patients with HBR.
DESIGN, SETTING, AND PATIENTS: This prespecified subgroup comparative effectiveness analysis followed the Management of High Bleeding Risk Patients Post Bioresorbable Polymer Coated Stent Implantation With an Abbreviated vs Standard DAPT Regimen (MASTER DAPT) trial, a multicenter, randomized, open-label clinical trial conducted at 140 sites in 30 countries and performed from February 28, 2017, to December 5, 2019. A total of 4579 patients with HBR were randomized at 1 month after PCI to abbreviated or standard DAPT. Data were analyzed from July 1 to October 31, 2022.
Abbreviated (immediate DAPT discontinuation, followed by single APT for ≥6 months) or standard (DAPT for ≥2 additional months, followed by single APT for 11 months) treatment groups.
One-year net adverse clinical events (NACEs) (a composite of death due to any cause, myocardial infarction, stroke, or major bleeding), major adverse cardiac or cerebral events (MACCEs) (a composite of death due to any cause, myocardial infarction, or stroke), and major or clinically relevant nonmajor bleeding (MCB).
Of the 4579 patients included in the analysis, 1408 (30.7%) were women and 3171 (69.3%) were men (mean [SD] age, 76.0 [8.7] years). Ischemic and bleeding events were similar between sexes. Abbreviated DAPT was associated with comparable NACE rates in men (hazard ratio [HR], 0.97 [95% CI, 0.75-1.24]) and women (HR, 0.87 [95% CI, 0.60-1.26]; P = .65 for interaction). There was evidence of heterogeneity of treatment effect by sex for MACCEs, with a trend toward benefit in women (HR, 0.68 [95% CI, 0.44-1.05]) but not in men (HR, 1.17 [95% CI, 0.88-1.55]; P = .04 for interaction). There was no significant interaction for MCB across sex, although the benefit with abbreviated DAPT was relatively greater in men (HR, 0.65 [95% CI, 0.50-0.84]) than in women (HR, 0.77 [95% CI, 0.53-1.12]; P = .46 for interaction). Results remained consistent in patients with acute coronary syndrome and/or complex PCI.
These findings suggest that women with HBR did not experience higher rates of ischemic or bleeding events compared with men and may derive particular benefit from abbreviated compared with standard DAPT owing to these numerically lower rates of events.
ClinicalTrials.gov Identifier: NCT03023020.
在高出血风险(HBR)接受经皮冠状动脉介入治疗(PCI)的患者中,缩短双联抗血小板治疗(DAPT)可减少出血,而不会增加缺血事件。
评估性别与高出血风险患者中缩短与标准 DAPT 比较的有效性的相关性。
设计、地点和患者:这是一项预先指定的亚组比较有效性分析,遵循了《生物可吸收聚合物涂层支架植入后高出血风险患者管理中缩短与标准 DAPT 方案的比较》(MASTER DAPT)试验,这是一项多中心、随机、开放标签临床试验,在 30 个国家的 140 个地点进行,于 2017 年 2 月 28 日至 2019 年 12 月 5 日进行。共有 4579 名 HBR 患者在 PCI 后 1 个月随机分为缩短或标准 DAPT 组。数据分析于 2022 年 7 月 1 日至 10 月 31 日进行。
缩短(立即停止 DAPT,随后至少 6 个月单抗血小板治疗)或标准(DAPT 至少 2 个月,随后 11 个月单抗血小板治疗)治疗组。
一年净不良临床事件(NACEs)(任何原因导致的死亡、心肌梗死、卒中和主要出血的复合事件)、主要不良心脑事件(MACCEs)(任何原因导致的死亡、心肌梗死或卒中的复合事件)和主要或临床相关非主要出血(MCB)。
在分析中包括的 4579 名患者中,1408 名(30.7%)为女性,3171 名(69.3%)为男性(平均[标准差]年龄,76.0[8.7]岁)。男性和女性的缺血和出血事件相似。在男性(风险比[HR],0.97[95%置信区间,0.75-1.24])和女性(HR,0.87[95%置信区间,0.60-1.26])中,缩短 DAPT 与相似的 NACE 发生率相关(P=0.65 用于交互作用)。在 MACCEs 方面,存在治疗效果的性别异质性证据,女性有获益趋势(HR,0.68[95%置信区间,0.44-1.05]),但男性没有(HR,1.17[95%置信区间,0.88-1.55];P=0.04 用于交互作用)。在 MCB 方面,性别之间没有显著的交互作用,尽管缩短 DAPT 在男性(HR,0.65[95%置信区间,0.50-0.84])中的获益相对大于女性(HR,0.77[95%置信区间,0.53-1.12];P=0.46 用于交互作用)。在急性冠状动脉综合征和/或复杂 PCI 的患者中,结果仍然一致。
这些发现表明,与男性相比,HBR 女性没有经历更高的缺血或出血事件发生率,并且由于这些事件发生率较低,与标准 DAPT 相比,她们可能特别受益于缩短 DAPT。
ClinicalTrials.gov 标识符:NCT03023020。