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心房颤动合并慢性肾脏病患者的口服抗凝治疗

Oral Anticoagulant Treatment in Patients with Atrial Fibrillation and Chronic Kidney Disease.

作者信息

Stoica Mihai Ciprian, Gáll Zsolt, Gliga Mirela Liana, Căldăraru Carmen Denise, Székely Orsolya

机构信息

Department of Nephrology/Internal Medicine, Mures County Clinical Hospital, 540103 Târgu Mureș, Romania.

Department of Pharmacology and Clinical Pharmacy, George Emil Palade University of Medicine, Pharmacy, Science and Technology of Târgu Mureș, 540142 Târgu Mureș, Romania.

出版信息

Medicina (Kaunas). 2021 Apr 27;57(5):422. doi: 10.3390/medicina57050422.

Abstract

Over the past few decades, a series of innovative medicines have been developed in order to optimize anticoagulation therapy for atrial fibrillation (AF). As a result, a number of nonvitamin K antagonist oral anticoagulants (NOAC) that directly target the enzymatic activity of factor II and factor Xa have been successfully licensed providing a more predictable effect and better safety profile compared to conventional anticoagulants (heparins and vitamin K antagonists (VKAs)). However, comparative efficacy and safety data is limited in patients with advanced chronic kidney disease (i.e., CKD stage 4/5 and end stage renal disease) because patients with estimated glomerular filtration rate (eGFR) < 30 mL/min/1.73 m were actively excluded from landmark trials, thus representing a major clinical limitation for the currently available agents. However, the renal function of AF patients can be altered over time. On the other hand, patients with CKD have an increased risk of developing AF. This review article will provide an overview of current concepts and recent evidence guiding the clinical use of NOACs in patients with CKD requiring chronic anticoagulation, and the associated risks and benefits of treatment in this specific patient population.

摘要

在过去几十年里,为了优化心房颤动(AF)的抗凝治疗,已经研发出一系列创新药物。因此,一些直接靶向凝血因子II和因子Xa酶活性的非维生素K拮抗剂口服抗凝剂(NOAC)已成功获批,与传统抗凝剂(肝素和维生素K拮抗剂(VKA))相比,其效果更可预测,安全性更高。然而,对于晚期慢性肾脏病(即CKD 4/5期和终末期肾病)患者,比较疗效和安全性的数据有限,因为估算肾小球滤过率(eGFR)<30 mL/min/1.73 m²的患者被主动排除在标志性试验之外,这是目前可用药物的一个主要临床局限性。然而,AF患者的肾功能会随时间发生改变。另一方面,CKD患者发生AF的风险增加。本文综述将概述当前的概念和最新证据,指导NOACs在需要长期抗凝的CKD患者中的临床应用,以及在这一特定患者群体中治疗的相关风险和益处。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e52/8147111/3dc430fb451b/medicina-57-00422-g001.jpg

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