Why the study?
The clinical profile, evolution, and complications of rivaroxaban treatment in real-life patients presenting with venous thromboembolism needed analysis.
Does rivaroxaban provide effective and safe treatment for venous thromboembolism in a real-world setting?
Does rivaroxaban provide effective and safe treatment for venous thromboembolism in a real-world setting?
Real-world use of rivaroxaban for VTE shows low rates of recurrence and major bleeding, consistent with pivotal clinical trials.
Answers are grounded in this paper and cite their sources.
Real-world rivaroxaban data in VTE support feasibility; leaves open need for randomized confirmation before practice change.
The clinical profile, evolution and complications of treatment with rivaroxaban in a cohort of patients presenting with venous thromboembolism (VTE) were analyzed in an observational, non-interventional and prospective study.A total of 111 patients were included in the study. Clinical data were collected from the medical history of the patients and recorded in a specific database.Mean age was 63.8 ± 17.4 years, 53.2% of patients were men, 55.9% had at least another concomitant condition, and 40.9% at least 1 VTE risk factor. 54.1% of patients presented with deep venous thrombosis, 32.4% with pulmonary embolism and 13.5% with both conditions simultaneously. The 61% of patients were admitted to hospital and mean hospital length-of-stay was 8.8 ± 9.9 days. After a mean follow-up 530 ± 464 days (median follow-up of 405 days), 3.9% of patients died and VTE recurrence occurred in 2.9% of patients. While receiving rivaroxaban, a first bleeding complication occurred in 8.1%; all events were minor bleeding.Our study supports the current literature data and confirms the similar results of real-life VTE patients with those enrolled in the rivaroxaban pivotal clinical trials. Rivaroxaban may facilitate outpatient treatment and might be considered as a first-line therapy for the management of VTE patients.
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Demelo‐Rodríguez et al. (2019) studied this question.
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