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比伐卢定在 COVID-19 体外膜肺氧合期间用于维持静脉-静脉体外膜氧合抗凝。

Bivalirudin for Maintenance Anticoagulation During Venovenous Extracorporeal Membrane Oxygenation for COVID-19.

机构信息

Department of Anesthesiology and Perioperative Medicine, Mayo Clinic, Rochester, MN.

Department of Cardiovascular Surgery, Mayo Clinic, Rochester, MN.

出版信息

J Cardiothorac Vasc Anesth. 2021 Apr;35(4):1149-1153. doi: 10.1053/j.jvca.2020.06.059. Epub 2020 Jun 25.

DOI:10.1053/j.jvca.2020.06.059
PMID:32660924
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7315936/
Abstract

In its severe manifestation, coronavirus disease 2019 (COVID-19) compromises oxygenation in a manner that is refractory to maximal conventional support and requires escalation to extracorporeal membrane oxygenation (ECMO). Maintaining ECMO support for extended durations requires a delicately balanced anticoagulation strategy to maintain circuit viability by preventing thrombus deposition while avoiding excessive anticoagulation yielding hemorrhage-a task that is complicated in COVID-19 secondary to an inherent hypercoagulable state. Bivalirudin, a member of the direct thrombin inhibitor drug class, offers potential advantages during ECMO, including to its ability to exert its effect by directly attaching to and inhibiting freely circulating and fibrin-bound thrombin. Herein, the successful use of an anticoagulation strategy using the off-label use of a continuous infusion of bivalirudin in a case of severe hypoxemic and hypercarbic respiratory failure caused by COVID-19 requiring venovenous ECMO is reported. Importantly, therapeutic anticoagulation intensity was achieved rapidly with stable pharmacokinetics, and there was no need for any circuit interventions throughout the patient's 27-day ECMO course. In COVID-19, bivalirudin offers a potential option for maintaining systemic anticoagulation during ECMO in a manner that may mitigate the prothrombotic nature of the underlying pathophysiologic state.

摘要

在严重的表现中,2019 年冠状病毒病(COVID-19)以对抗最大常规支持的方式损害氧合作用,需要升级为体外膜氧合(ECMO)。为了延长 ECMO 支持时间,需要一种精心平衡的抗凝策略,通过防止血栓沉积来维持回路的存活,同时避免过度抗凝导致出血——在 COVID-19 中,由于固有的高凝状态,这一任务变得复杂。比伐卢定是直接凝血酶抑制剂药物类别的成员,在 ECMO 期间提供了潜在的优势,包括其通过直接附着并抑制游离循环和纤维蛋白结合的凝血酶来发挥作用的能力。在此,报告了一例 COVID-19 导致严重低氧和高碳酸呼吸衰竭需要静脉-静脉 ECMO 的病例,成功使用了一种连续输注比伐卢定的抗凝策略。重要的是,在整个患者 27 天的 ECMO 过程中,迅速达到了治疗性抗凝强度,并且不需要进行任何回路干预。在 COVID-19 中,比伐卢定为 ECMO 期间维持全身抗凝提供了一种潜在选择,可能减轻潜在病理生理状态的血栓形成性质。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8a8b/7315936/ff9b30d9a75b/gr1_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8a8b/7315936/ff9b30d9a75b/gr1_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8a8b/7315936/ff9b30d9a75b/gr1_lrg.jpg

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