Shimizu Kazuhiro, Sasaki Takeshi, Todani Shunsuke, Ito Takuro, Iwakawa Masahiro, Sugizaki Yuta, Sato Shuji, Nakagami Takahiro, Mikamo Hiroshi, Kinoshita Toshio
Department of Internal Medicine, Toho University Sakura Medical Center Sakura Japan.
Clinical Physiological Function Laboratory, Toho University Sakura Medical Center Sakura Japan.
Circ Rep. 2024 May 22;6(6):217-222. doi: 10.1253/circrep.CR-24-0042. eCollection 2024 Jun 10.
Factor Xa inhibitors, such as rivaroxaban, are increasing the convenience of treatment for deep vein thrombosis (DVT). Limited evidence exists regarding clot evaluation at 3 months after treatment for DVT. We retrospectively analyzed the clinical course of symptomatic proximal DVT in patients who received 3 months of anticoagulation treatment at our hospital. Patients treated with the rivaroxaban single-drug approach were classified as group A (n=42). Patients treated with unfractionated heparin (UFH) or subcutaneous fondaparinux followed by vitamin K antagonist comprised group B (n=60) as an historical cohort. The quantitative ultrasound thrombosis (QUT) score was used to quantify clot burden before and after treatment. No significant differences were observed in patient characteristics between the groups. Serum D-dimer levels in both groups significantly improved after treatment. Clot volume assessed using QUT also reduced significantly in both groups. The QUT score in groups A and B improved from 7.5 [4.8, 12.0] to 3.0 [1.8, 5.0; P=0.000] and 7.0 [4.0, 9.8] to 3.0 [2.0, 5.0; P=0.000], respectively. The change in QUT (∆QUT) was significantly greater in group A compared with group B (-4.5 [-8.25, -2.0] vs. -2.0 [-6.0, 0.0]; P=0.005). We were able to demonstrate the effectiveness of DVT treatment using rivaroxaban over a period of 3 months from onset, in terms of clot regression evaluated using the QUT score.