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将新型口服抗凝药物纳入医院处方集。

Implementing the new oral anticoagulants into the hospital formulary.

机构信息

Thomas Jefferson University Hospitals, Jefferson Medical College, Philadelphia, Pennsylvania 19107, USA.

出版信息

Am J Hematol. 2012 May;87 Suppl 1:S127-32. doi: 10.1002/ajh.23208. Epub 2012 Apr 12.

Abstract

The new oral anticoagulants may prove to be one of most significant innovations in clinical practice in the past 60 years. Apixaban and rivaroxaban are direct inhibitors of Factor Xa, while dabigatran inhibits Factor IIa. The predictable pharmacological profile of these new agents allows physicians to prescribe these drugs without the need for routine coagulation monitoring, which is the mainstay of warfarin therapy. In addition, these new agents have not been shown to have any food interactions and minimal drug-drug interactions, interactions are limited to the p-glycoprotein (p-Gp) transporter or cytochrome P450 (CYP450) system, each drug is unique in its drug interaction profile, as will be discussed below. These unique pharmacokinetics profiles may usher in for clinicians a new era of managing thromboembolic disorders. In this article, the pharmacology of these new oral anticoagulants will be reviewed along with the major clinical trials evaluating the use of these agents for thromboembolic prophylaxis in patients undergoing total hip and knee arthroplastic surgery, the treatment of venous thromboembolic disorders and stroke prevention in atrial fibrillation. Am. J. Hematol., 2012. © 2012 Wiley Periodicals, Inc.

摘要

新的口服抗凝剂可能被证明是过去 60 年来临床实践中最重要的创新之一。阿哌沙班和利伐沙班是直接的 Xa 因子抑制剂,而达比加群则抑制 IIa 因子。这些新型药物可预测的药理学特性使医生能够在无需常规凝血监测的情况下开处方,而常规凝血监测是华法林治疗的主要手段。此外,这些新型药物没有显示出任何食物相互作用和最小的药物相互作用,相互作用仅限于 P-糖蛋白(p-Gp)转运体或细胞色素 P450(CYP450)系统,每种药物在药物相互作用谱方面都是独特的,如下文所述。这些独特的药代动力学特征可能为临床医生管理血栓栓塞性疾病带来新时代。本文将回顾这些新型口服抗凝剂的药理学,并讨论评估这些药物在全髋关节和膝关节成形术患者中用于血栓栓塞预防、静脉血栓栓塞性疾病治疗和心房颤动中风预防的主要临床试验。Am J Hematol,2012。©2012 年 Wiley Periodicals,Inc.

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