抗血栓治疗与体重的最新进展。ESC心血管药物治疗工作组和ESC血栓形成工作组临床共识声明。

IF 5.3 1区 医学 Q1 CARDIAC & CARDIOVASCULAR SYSTEMS
Bruna Gigante, Juan Tamargo, Stefan Agewall, Dan Atar, Jurrien Ten Berg, Gianluca Campo, Elisabetta Cerbai, Christina Christersson, Dobromir Dobrev, Péter Ferdinandy, Tobias Geisler, Diana A Gorog, Erik L Grove, Juan Carlos Kaski, Andrea Rubboli, Sven Wassmann, Håkan Wallen, Bianca Rocca
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引用次数: 0

摘要

肥胖和体重过轻是全球日益严重的健康问题,也是临床医生在抗血栓治疗方面面临的挑战,因为肥胖和体重过轻会带来血栓形成和/或出血的风险。本临床共识声明更新了 2018 年发布的上一份共识声明,根据世界卫生组织的体型分类,回顾了有关抗血栓药物的最新证据。该文件主要关注体重处于极端水平(即体重不足和中度至重度肥胖)的患者,根据现行指南,他们需要服用抗血栓药物来治疗或预防心血管疾病或静脉血栓栓塞。由于身体成分、新陈代谢和器官功能的深刻变化,药物药代动力学和药效学的改变,以及临床试验证据的薄弱或缺乏,管理这些人的抗血栓治疗或血栓预防具有挑战性。该文件还包括从硅学药代动力学/药效学模型中得出的人工智能模拟,它可以模拟药代动力学的变化,帮助确定体重严重不足或严重肥胖者的最佳抗血栓药物治疗方案。此外,世界各地经常对病态肥胖者实施减肥手术。根据手术类型的不同,减肥手术会导致代谢和胃肠道解剖结构发生特定和额外的变化,这也会影响抗血栓药物的药代动力学及其管理。本文件以现有文献为基础,就优化体重不足和各类肥胖患者的抗血栓药物管理提供了共识声明,同时强调了目前在这些复杂的临床环境中存在的知识空白,这就需要个性化医疗和精准药理学。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Update on antithrombotic therapy and body mass: a clinical consensus statement of the European Society of Cardiology Working Group on Cardiovascular Pharmacotherapy and the European Society of Cardiology Working Group on Thrombosis.

Obesity and underweight are a growing health problem worldwide and a challenge for clinicians concerning antithrombotic therapy, due to the associated risks of thrombosis and/or bleeding. This clinical consensus statement updates a previous one published in 2018, by reviewing the most recent evidence on antithrombotic drugs based on body size categories according to the World Health Organization classification. The document focuses mostly on individuals at the extremes of body weight, i.e. underweight and moderate-to-morbid obesity, who require antithrombotic drugs, according to current guidelines, for the treatment or prevention of cardiovascular diseases or venous thromboembolism. Managing antithrombotic therapy or thromboprophylaxis in these individuals is challenging, due to profound changes in body composition, metabolism and organ function, and altered drug pharmacokinetics and pharmacodynamics, as well as weak or no evidence from clinical trials. The document also includes artificial intelligence simulations derived from in silico pharmacokinetic/pharmacodynamic models, which can mimic the pharmacokinetic changes and help identify optimal regimens of antithrombotic drugs for severely underweight or severely obese individuals. Further, bariatric surgery in morbidly obese subjects is frequently performed worldwide. Bariatric surgery causes specific and additional changes in metabolism and gastrointestinal anatomy, depending on the type of the procedure, which can also impact the pharmacokinetics of antithrombotic drugs and their management. Based on existing literature, the document provides consensus statements on optimizing antithrombotic drug management for underweight and all classes of obese patients, while highlighting the current gaps in knowledge in these complex clinical settings, which require personalized medicine and precision pharmacology.

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来源期刊
European Heart Journal - Cardiovascular Pharmacotherapy
European Heart Journal - Cardiovascular Pharmacotherapy Medicine-Cardiology and Cardiovascular Medicine
CiteScore
10.10
自引率
14.10%
发文量
65
期刊介绍: The European Heart Journal - Cardiovascular Pharmacotherapy (EHJ-CVP) is an international, peer-reviewed journal published in English, specifically dedicated to clinical cardiovascular pharmacology. EHJ-CVP publishes original articles focusing on clinical research involving both new and established drugs and methods, along with meta-analyses and topical reviews. The journal's primary aim is to enhance the pharmacological treatment of patients with cardiovascular disease by interpreting and integrating new scientific developments in this field. While the emphasis is on clinical topics, EHJ-CVP also considers basic research articles from fields such as physiology and molecular biology that contribute to the understanding of cardiovascular drug therapy. These may include articles related to new drug development and evaluation, the physiological and pharmacological basis of drug action, metabolism, drug interactions, and side effects.
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