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Question clinique
Is 6 weeks of anticoagulant therapy for provoked venous thromboembolism noninferior to conventional 3-month therapy in patients younger than 21 years?
L’Essentiel
This study found that 6 weeks of treatment compared with 3 months of treatment for provoked venous thromboembolism in patients younger than 21 years clearly met noninferiority criteria. Specifically, 6 weeks of therapy resulted in (nonsignificantly) less recurrence of VTE and less incidence of clinically relevant bleeding. 1b
Référence
Plan de l'etude: Randomized controlled trial (single-blinded)
Financement: Government
Cadre: Inpatient (any location) with outpatient follow-up
Sommaire
Standard treatment for adults with provoked venous thromboembolism (provoked VTE; ie, temporally associated with a prothrombotic clinical risk factor) is 3 months of anticoagulant therapy. Whether this same duration is necessary for children is uncertain. These investigators identified patients younger than 21 years with an acute VTE diagnosed via standard imaging modalities and a provoking factor, including recent hospitalization, traumatic injury, or central venous catheterization. Exclusion criteria included history of VTE, active malignancy, systemic lupus erythematosus, isolated pulmonary embolism, and deficiencies of natural anticoagulants (ie, protein C, protein S, antithrombin). All participants initially received standard treatment with intravenous unfractionated heparin or subcutaneous low-molecular-weight (LMW) heparin followed by LMW heparin, fondaparinux, oral vitamin K antagonists, or direct oral anticoagulants. At 6 weeks, all patients underwent repeat imaging. Similarly, those patients initially noted at baseline to have antiphospholipid antibodies underwent follow-up testing. Those patients (n = 417) with venous flow occurring in the involved vessel segments and without persistent antiphospholipid antibodies randomly received (concealed allocation) assignment to either discontinue anticoagulant therapy or to continue anticoagulant therapy for a total of 3 months. Individuals assessing outcomes remained masked to treatment group assignment. Complete follow-up occurred for 89.9% of patients at 1 year. Using both intention-to-treat and per-protocol analyses, the primary outcome (recurrent VTE within 1 year) occurred less frequently in the 6-week group than in the 3-month group (0.97% vs 1.91% and 0.65% vs 1.40%, respectively). The primary safety outcome — clinically relevant bleeding events — also occurred less frequently in the 6-week group than in the 3-month group (0.65% vs 0.70% and 0.97% vs 2.38%, respectively). All outcomes met predetermined criteria for noninferiority. Similarly, other secondary outcomes, such as chronic venous insufficiency, occurred similarly in both treatment groups.
Reviewer
David C. Slawson, MD
Professor and Vice Chair of Family Medicine for Education and Scholarship
Atrium Health
Professor of Family Medicine, UNC Chapel Hill
Charlotte, NC