护身符后单抗血小板、双抗血小板或口服抗凝的结果:来自EMERGE LAA批准后研究的见解

IF 1.9 Q3 CARDIAC & CARDIOVASCULAR SYSTEMS
Atman P Shah, James V Freeman, Mohamad Alkhouli, Himanshu Agarwal, Megan Coylewright, Akash Makkar, Jordan Anderson, Ryan Gage, Xavier Freixa, Jens Erik Nielsen-Kudsk, Dhanunjaya Lakkireddy
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引用次数: 0

摘要

背景:护身符左心耳闭塞(LAAO)后不同抗血栓策略的相关结果尚未得到很好的描述。目的:本分析比较了在EMERGE LAA批准后研究中接受双重抗血小板治疗(DAPT)与单一抗血小板治疗(SAPT)或口服抗凝(OAC)的出院患者在Amulet植入后的结果。方法:纳入2021年8月14日至2023年12月15日期间成功植入护符出院并进入国家心血管数据登记处(NCDR) LAAO登记处的患者。全因死亡、卒中、大出血或全身性栓塞的安全性终点和缺血性卒中、全身性栓塞或心血管性死亡的有效性终点通过6个月以及主要不良事件进行评估。结果:共纳入11445例患者,其中DAPT出院9355例(81.7%),SAPT出院606例(5.3%),OAC出院1484例(13.0%)。SAPT组患者有更多的合并症,并且在护身符植入前出血风险最大。在45天,95%的患者实现了临床相关的闭合(≤3mm的装置周围泄漏)。6个月时,DAPT、SAPT和OAC组的安全终点率分别为8.8%、7.0%和7.0% (p = 0.045), DAPT、SAPT和OAC组的有效终点率分别为2.1%、1.6%和1.7% (p = 0.511)。尽管基线出血风险较高,但SAPT组在6个月内的出血率在数值上低于DAPT组(DAPT为4.8%,SAPT为3.9%;HR 1.23[0.78, 1.95]),与器械相关的血栓发生率无差异(DAPT 0.8% vs. SAPT 0.8%;Hr 0.91[0.33, 2.50])。然而,在调整基线特征差异后,在45天或6个月时,三个用药组之间的任何临床事件均无显著差异(p > 0.05)。结论:在目前接受Amulet LAAO治疗的患者队列中,LAA完全闭合率很高,SAPT成为当前DAPT方案的可行替代方案,可能降低高风险患者出血并发症的风险,同时不影响疗效。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Outcomes for single antiplatelet, dual antiplatelet, or oral anticoagulation after Amulet: Insights from EMERGE LAA post-approval study.

Background: Outcomes associated with different antithrombotic strategies after Amulet left atrial appendage occlusion (LAAO) are not well described.

Objective: This analysis compared outcomes from patients discharged on dual antiplatelet therapy (DAPT) versus single antiplatelet therapy (SAPT) or oral anticoagulation (OAC) following Amulet implant in the EMERGE LAA post-approval study.

Methods: Patients with a successful Amulet implant and discharged from the hospital between August 14, 2021 and December 15, 2023 and entered into the National Cardiovascular Data Registry (NCDR) LAAO Registry were included. A safety endpoint of all-cause death, stroke, major bleeding, or systemic embolism and effectiveness endpoint of ischemic stroke, systemic embolism, or cardiovascular death were assessed through 6 months as well as major adverse events.

Results: A total of 11,445 patients were included in this analysis with 9355 discharged on DAPT (81.7 %), 606 on SAPT (5.3 %), and 1484 on OAC (13.0 %). Patients in the SAPT group had more comorbid conditions and were at the greatest bleeding risk pre-Amulet implant. At 45-days, clinically relevant closure (≤3 mm peri-device leak) was achieved in >95 % of all patients. At 6 months, the safety endpoint rates were 8.8 %, 7.0 %, and 7.0 % in the DAPT, SAPT, and OAC groups, respectively (p = 0.045) and effectiveness endpoint rates were 2.1 %, 1.6 %, and 1.7 % in the DAPT, SAPT, and OAC groups, respectively (p = 0.511). Despite higher baseline bleeding risk, the SAPT group had numerically lower bleeding rates than the DAPT group through 6 months (DAPT 4.8 % vs. SAPT 3.9 %; HR 1.23 [0.78, 1.95]) with no difference in device-related thrombus rates (DAPT 0.8 % vs. 0.8 % SAPT; HR 0.91 [0.33, 2.50]). However, after adjusting for differences in baseline characteristics, no significant differences (p > 0.05) were noted for any clinical events between the three medication groups at 45 days or 6 months.

Conclusion: In the present cohort of patients treated with Amulet LAAO there were high rates of LAA complete closure, and SAPT emerged as a viable alternative to the current DAPT regimen potentially reducing the risk of bleeding complications in patients at high risk without compromising effectiveness.

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来源期刊
Cardiovascular Revascularization Medicine
Cardiovascular Revascularization Medicine CARDIAC & CARDIOVASCULAR SYSTEMS-
CiteScore
3.30
自引率
5.90%
发文量
687
审稿时长
36 days
期刊介绍: Cardiovascular Revascularization Medicine (CRM) is an international and multidisciplinary journal that publishes original laboratory and clinical investigations related to revascularization therapies in cardiovascular medicine. Cardiovascular Revascularization Medicine publishes articles related to preclinical work and molecular interventions, including angiogenesis, cell therapy, pharmacological interventions, restenosis management, and prevention, including experiments conducted in human subjects, in laboratory animals, and in vitro. Specific areas of interest include percutaneous angioplasty in coronary and peripheral arteries, intervention in structural heart disease, cardiovascular surgery, etc.
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