Key result
Class 1 obesity linked to ~440% higher all-cause mortality versus underweight patients on rivaroxaban.
Why the study?
Real-world prescribing trends and clinical outcomes based on body mass index categorization in patients receiving rivaroxaban therapy had not been sufficiently investigated.
Does body mass index affect the risk of all-cause mortality, bleeding, or thromboembolic events in patients receiving rivaroxaban therapy?
Cohort (n=4,638)
Yes
Does body mass index affect the risk of all-cause mortality, bleeding, or thromboembolic events in patients receiving rivaroxaban therapy?
In a real-world cohort, rivaroxaban prescribing declined in obese patients after 2018, and obesity was associated with significantly higher all-cause mortality but not increased bleeding or thromboembolic events compared to lower BMI categories.
Answers are grounded in this paper and cite their sources.
Obesity may confer higher mortality risk on rivaroxaban; this cohort study leaves open whether BMI should guide therapy or monitoring.
Purpose To investigate real-world prescribing trends and clinical outcomes based on body mass index (BMI) categorization in patients who received rivaroxaban therapy. Methods This was a retrospective cohort study involving all patients who received rivaroxaban therapy across all Hamad Medical Corporation (HMC) hospitals from 2015 to 2020. Results The number of patients initiated on rivaroxaban therapy significantly increased from 152 (3.3%) in 2015 to 1342 (28.9%) in 2020 ( p <0.001). Within BMI categories, a similar increasing trend was observed in underweight, normal, and overweight patients, while from 2018 to 2020, there was a decreasing trend in rivaroxaban prescribing in all obese classes. The prevalence rate of all-cause mortality differed significantly between the BMI groups, with the highest mortality being among morbidly obese patients (BMI ≥ 40 kg/m 2 ) ( p < 0.001). On the other hand, no significant differences were found between the BMI groups in terms of bleeding, pulmonary embolism, deep vein thrombosis and stroke incidences. Multivariate logistic regression analyses showed that the likelihood of all-cause mortality was significantly higher in overweight and all categories of obese patients compared to underweight patients: overweight (OR: 5.3, 95% CI: 2.3–11.9, p < 0.001); obese class 1 (OR: 5.4, 95% CI: 2.3 – 12.2, p < 0.001); obese class 2 (OR: 6.5, 95% CI: 2.7 – 15.6, p < 0.001); and obese class 3 (OR: 3.7, 95% CI: 1.6 – 8.7, p = 0.003). Conclusions Rivaroxaban prescribing has significantly increased over the years across general population, with a noticeable decline in obese population during the last few years (from 2018 onwards). Furthermore, an appreciable association was evident between all-cause mortality and BMI of these patients.
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Alalawneh et al. (2023) conducted a cohort in Thromboembolic disorders (n=4,638). Obesity (Class 1, BMI 30-34.99 kg/m2) vs. Underweight (BMI <18.5 kg/m2) was evaluated on All-cause mortality (OR 5.4, 95% CI 2.3-12.2, p=<0.001). Obesity class 1 was associated with a significantly higher likelihood of all-cause mortality compared to underweight patients receiving rivaroxaban therapy (OR 5.4).
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