Key result
Rivaroxaban was associated with a significantly lower composite risk of stroke and systemic embolism (HR 0.77) compared with warfarin in patients with nonvalvular atrial fibrillation, obesity, and polypharmacy.
Why the study?
There is limited evidence on the impact of polypharmacy in patients with nonvalvular atrial fibrillation and obesity receiving rivaroxaban.
Does rivaroxaban reduce the risk of stroke, systemic embolism, and major bleeding compared to warfarin in patients with nonvalvular atrial fibrillation, obesity, and polypharmacy?
Cohort (n=43,094)
Yes
Does rivaroxaban reduce the risk of stroke, systemic embolism, and major bleeding compared to warfarin in patients with nonvalvular atrial fibrillation, obesity, and polypharmacy?
Hazard Ratio: 0.77 (95% CI 0.7–0.84)
Absolute Event Rate: 4.3% vs 5.6%
p-value: p=<0.001
In patients with nonvalvular atrial fibrillation and obesity, rivaroxaban is associated with a lower risk of stroke and systemic embolism and a similar risk of major bleeding compared to warfarin, regardless of polypharmacy burden.
May inform anticoagulant choice in obese polypharmacy AF; hypothesis-generating and requires randomized confirmation.
BACKGROUND: Current evidence suggests that rivaroxaban may be well tolerated and effective in patients with nonvalvular atrial fibrillation (NVAF) and obesity; however, there is limited evidence on the impact of polypharmacy in this population. This study evaluated real-world clinical outcomes with rivaroxaban versus warfarin in patients with NVAF and obesity according to the number of concurrent medications. METHODS: and the presence of polypharmacy (1-4, 5-9, or ≥ 10 concurrent medications). Outcomes of stroke, systemic embolism, and major bleeding were compared between the rivaroxaban and warfarin cohorts after propensity score matching (PSM). RESULTS: A total of 95,875 patients were identified with one or more claim for either rivaroxaban or warfarin. After PSM, patient characteristics were balanced between cohorts (n = 21,547 in each cohort). The overall composite risk of stroke and systemic embolism was significantly lower in the rivaroxaban cohort compared with the warfarin cohort (hazard ratio [HR] 0.77, 95% confidence interval [CI] 0.70-0.84; p < 0.001). The risks of ischemic stroke, hemorrhagic stroke, and systemic embolism separately were also significantly reduced with rivaroxaban. Major bleeding risk was similar between cohorts (HR 0.93, 95% CI 0.81-1.06; p = 0.2842), and results were consistent across the three polypharmacy groups. CONCLUSIONS: In this real-world study of NVAF patients with obesity, rivaroxaban was associated with lower risks of stroke and systemic embolism and similar risk of major bleeding versus warfarin across polypharmacy categories.
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Alberts et al. (2022) conducted a cohort in Nonvalvular Atrial Fibrillation with Obesity and Polypharmacy (n=43,094). Rivaroxaban vs. Warfarin was evaluated on Composite of stroke and systemic embolism (HR 0.77, 95% CI 0.70-0.84, p=<0.001). Rivaroxaban was associated with a significantly lower composite risk of stroke and systemic embolism (HR 0.77) compared with warfarin in patients with nonvalvular atrial fibrillation, obesity, and polypharmacy.
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