Rationale: Deficiency in antithrombin (AT) can significantly increase the risk of venous thromboembolism (VTE). However, there is insufficient data on the efficacy and safety of anticoagulants in patients with AT deficiency, especially in children. In addition, Asian populations typically require a lower dose of rivaroxaban, and this may be even more pronounced in Asian children. This case aims to explore the potential efficacy and safety of a higher dose of rivaroxaban in an Asian child with AT deficiency and VTE.
Patient Concerns: A 15-year-old boy was referred to our center with severe deep vein thrombosis progression. The primary concern was the effective management of the thromboembolic events while minimizing the risk of bleeding, given the patient's young age and AT deficiency.
Diagnoses: The patient was diagnosed with pulmonary embolism and deep vein thrombosis with AT deficiency.
Interventions: The patient was treated with a higher dose of rivaroxaban, which was 15 mg twice a day for 3 weeks, followed by 20 mg per day for 6 months, which was a relatively high dose for an Asian child.
Outcomes: During the follow-up period, the patient did not experience any VTE events or bleeding events.
Lessons: This case provides additional data on the efficacy and safety of direct oral factor Xa inhibitors in patients with VTE and AT deficiency. It suggests that for Asian children with AT deficiency, considering a higher dose of rivaroxaban could be beneficial, especially when the children's height, weight, and age are close to adults.
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http://dx.doi.org/10.1097/MD.0000000000041629 | DOI Listing |
BMC Health Serv Res
March 2025
Faculty of Pharmacy, Shiraz University of Medical Sciences, Shiraz, Iran.
Background: Low-dose aspirin and rivaroxaban are the cornerstone treatment for cardiovascular prevention in patients with peripheral artery disease (PAD) and/or stable coronary artery disease (SCAD). The combination of rivaroxaban with aspirin imposes a synergistic effect on the inhibition of factor-induced platelet aggregation. The present work aimed at comparing the cost-utility and cost-effectiveness of rivaroxaban (2.
View Article and Find Full Text PDFReadily available and rapid turn-around, bedside assays to measure the effect of the direct oral anticoagulants (DOACs) are not available. This study evaluates a point-of-care (PoC) coagulometer to assess the anticoagulant effects of the DOACs and low molecular weight heparin. Studies were done in fresh spiked blood from healthy volunteers.
View Article and Find Full Text PDFLancet
March 2025
Univ Brest, INSERM U1304-GETBO, CIC INSERM 1412, Brest, France; Centre Hospitalier Universitaire Brest, Département de Médecine Interne et Pneumologie, Brest, France; FCRIN INNOVTE Network, Saint-Etienne, France.
Background: In patients with venous thromboembolism at high risk of recurrence for whom extended treatment with direct oral anticoagulants has been indicated, the optimal dose is unknown. We aimed to assess efficacy and safety of reduced-dose versus full-dose direct oral anticoagulants in patients in whom extended anticoagulation has been indicated.
Methods: RENOVE was a non-inferiority, investigator-initiated, multicentre, randomised, open-label, blinded endpoint trial done in 47 hospitals in France.
Medicine (Baltimore)
February 2025
Department of Pharmacy, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, China.
Rationale: Deficiency in antithrombin (AT) can significantly increase the risk of venous thromboembolism (VTE). However, there is insufficient data on the efficacy and safety of anticoagulants in patients with AT deficiency, especially in children. In addition, Asian populations typically require a lower dose of rivaroxaban, and this may be even more pronounced in Asian children.
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