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Xarelto治疗静脉血栓效果怎样?

Author: Medicalhalo
Release time: 2025-10-19 11:44:20

Rivaroxaban (Xarelto) is produced by Bayer Healthcare Co., Ltd. Its main clinical indications are: 1. Used in adult patients undergoing elective hip or knee replacement surgery to prevent venous thrombosis (VTE). 2. Used to treat venous thrombosis (DVT) in adults and reduce the risk of DVT recurrence and pulmonary embolism (PE) after acute DVT. 3. For use in adult patients with nonvalvular atrial fibrillation who have one or more risk factors (e.g., congestive heart failure, hypertension, age ≥75 years, diabetes, history of stroke or transient ischemic attack) to reduce the risk of stroke and systemic embolism.

An international scientific research team published a paper in the journal "The Lancet" stating that through analysis of data from a multi-center, randomized, double-blind clinical trial called "BECORD4", among a total of more than 3,000 patients, researchers confirmed that compared with standard therapy using enoxaparin, patients treated with rivaroxaban (Xarelto, Xarelto) reduced the risk of venous thromboembolism after orthopedic surgery by about one-third. "This is the first oral anticoagulant drug with better efficacy than the current standard therapy. Therefore, it may become a new clinical treatment option for preventing severe blood clots after major orthopedic surgery," said Professor A. Turpai from McMaster University in Canada. "At the same time, this new drug also has better economics."

Rivaroxaban (Xarelto) is a highly selective oral drug that directly inhibits factor Xa. By inhibiting factor Xa, it can interrupt the intrinsic and extrinsic pathways of the coagulation cascade and inhibit thrombin generation and thrombosis. Rivaroxaban (Xarelto) does not inhibit thrombin (activated factor II) and has not been shown to have an effect on platelets. A dose-dependent inhibitory effect of rivaroxaban (Xarelto) on factor Xa activity has been observed in humans. The effect of rivaroxaban (Xarelto, Xarelto) on prothrombin time (PT) has a dose-effect relationship. If NeopLastin is used for content measurement, it is closely related to the plasma concentration (correlation coefficient is 0.98). Different results may occur with other reagents.

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