Recent advances and knowledge gaps in anticoagulation strategy with durable left ventricular assist devices.

IF 7.4 3区 医学 Q1 CARDIAC & CARDIOVASCULAR SYSTEMS
Katrina F Etts, Ashwin A Pillai, John Marchuk-Welsby, Abhishek Jaiswal
{"title":"Recent advances and knowledge gaps in anticoagulation strategy with durable left ventricular assist devices.","authors":"Katrina F Etts, Ashwin A Pillai, John Marchuk-Welsby, Abhishek Jaiswal","doi":"10.33963/v.phj.113979","DOIUrl":null,"url":null,"abstract":"<p><p>Driven by technological advancements, donor shortages, and an aging population, utilization of left ventricular assist devices (LVAD), both as a bridge to transplant and as destination therapy, has risen in recent years for symptomatic patients with end-stage heart failure. With wide blood flow pathways, friction-free movement, and intrinsic pulsatility that reduce shear stress and promote more favorable intrapump blood flow, the incidence of adverse events such as device failure and thromboembolism has been significantly reduced in patients receiving the latest LVAD, the HeartMate 3 (HM3; Abbott Laboratories, Abbott Park, IL, US). However, hemocompatibility related complications, especially bleeding, remain common and a major cause of morbidity and hospitalization. This has prompted interest in less aggressive antithrombotic strategies for LVAD patients. Recent evidence has demonstrated that aspirin can be safely omitted in most HM3 recipients, substantially reducing bleeding without increasing thromboembolic events. Moreover, the direct oral anticoagulant apixaban has emerged as a promising alternative to warfarin in selected LVAD patients, with the potential to reduce bleeding risk without compromising protection against thrombotic complications. However, randomized phase III evidence remains limited, and important knowledge gaps persist in this population. This review summarizes contemporary antithrombotic strategies in HM3 recipients, evaluates emerging evidence supporting apixaban and aspirin withdrawal, and highlights remaining knowledge gaps. We also outline future directions, including ongoing randomized clinical trials, novel anticoagulants targeting factors XI and XII, and artificial intelligence-based approaches to individualized anticoagulation. As the field continues to evolve, personalized antithrombotic strategies have the potential to optimize hemocompatibility while improving clinical outcomes and quality of life in patients receiving durable LVAD.</p>","PeriodicalId":17784,"journal":{"name":"Kardiologia polska","volume":" ","pages":""},"PeriodicalIF":7.4000,"publicationDate":"2026-08-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Kardiologia polska","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.33963/v.phj.113979","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CARDIAC & CARDIOVASCULAR SYSTEMS","Score":null,"Total":0}
引用次数: 0

Abstract

Driven by technological advancements, donor shortages, and an aging population, utilization of left ventricular assist devices (LVAD), both as a bridge to transplant and as destination therapy, has risen in recent years for symptomatic patients with end-stage heart failure. With wide blood flow pathways, friction-free movement, and intrinsic pulsatility that reduce shear stress and promote more favorable intrapump blood flow, the incidence of adverse events such as device failure and thromboembolism has been significantly reduced in patients receiving the latest LVAD, the HeartMate 3 (HM3; Abbott Laboratories, Abbott Park, IL, US). However, hemocompatibility related complications, especially bleeding, remain common and a major cause of morbidity and hospitalization. This has prompted interest in less aggressive antithrombotic strategies for LVAD patients. Recent evidence has demonstrated that aspirin can be safely omitted in most HM3 recipients, substantially reducing bleeding without increasing thromboembolic events. Moreover, the direct oral anticoagulant apixaban has emerged as a promising alternative to warfarin in selected LVAD patients, with the potential to reduce bleeding risk without compromising protection against thrombotic complications. However, randomized phase III evidence remains limited, and important knowledge gaps persist in this population. This review summarizes contemporary antithrombotic strategies in HM3 recipients, evaluates emerging evidence supporting apixaban and aspirin withdrawal, and highlights remaining knowledge gaps. We also outline future directions, including ongoing randomized clinical trials, novel anticoagulants targeting factors XI and XII, and artificial intelligence-based approaches to individualized anticoagulation. As the field continues to evolve, personalized antithrombotic strategies have the potential to optimize hemocompatibility while improving clinical outcomes and quality of life in patients receiving durable LVAD.

耐用左心室辅助装置抗凝策略的最新进展和知识差距。
近年来,在技术进步、供体短缺和人口老龄化的推动下,对于有症状的终末期心力衰竭患者,左心室辅助装置(LVAD)作为移植的桥梁和终点治疗的使用率有所上升。使用最新LVAD HeartMate 3 (HM3;雅培实验室,雅培Park, IL, US)的患者,由于宽阔的血流通道、无摩擦运动和内在的脉动性减少了剪切应力,促进了更有利的泵内血流,因此设备故障和血栓栓塞等不良事件的发生率显著降低。然而,与血液相容性相关的并发症,特别是出血,仍然很常见,是发病和住院的主要原因。这引起了对LVAD患者的低侵略性抗血栓策略的兴趣。最近的证据表明,在大多数HM3受体中可以安全地省略阿司匹林,在不增加血栓栓塞事件的情况下大大减少出血。此外,直接口服抗凝药物阿哌沙班已成为选择性LVAD患者华法林的一种有希望的替代方案,具有降低出血风险而不影响对血栓并发症的保护的潜力。然而,随机III期证据仍然有限,在这一人群中仍然存在重要的知识差距。本综述总结了HM3受体的当代抗血栓策略,评估了支持阿哌沙班和阿司匹林停药的新证据,并强调了仍然存在的知识空白。我们还概述了未来的发展方向,包括正在进行的随机临床试验,新型抗凝剂靶向因子XI和XII,以及基于人工智能的个体化抗凝方法。随着该领域的不断发展,个性化的抗血栓策略有可能优化血液相容性,同时改善持久LVAD患者的临床结果和生活质量。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Kardiologia polska
Kardiologia polska 医学-心血管系统
CiteScore
3.00
自引率
24.20%
发文量
431
审稿时长
3-6 weeks
期刊介绍: Kardiologia Polska (Kardiol Pol, Polish Heart Journal) is the official peer-reviewed journal of the Polish Cardiac Society (PTK, Polskie Towarzystwo Kardiologiczne) published monthly since 1957. It aims to provide a platform for sharing knowledge in cardiology, from basic science to translational and clinical research on cardiovascular diseases.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信
小红书