Loading…
Ophthalmic complications in patients with nonvalvular atrial fibrillation and type 2 diabetes prescribed rivaroxaban or warfarin
Abstract Funding Acknowledgements Type of funding sources: Private company. Main funding source(s): Bayer AG Berlin, Germany INTRODUCTION Patients with type 2 diabetes (T2D) are at an increased risk of ophthalmic complications compared to those without. Ophthalmic complications in T2D patients with...
Saved in:
Published in: | Europace (London, England) England), 2021-05, Vol.23 (Supplement_3) |
---|---|
Main Authors: | , , , , , , |
Format: | Article |
Language: | English |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Summary: | Abstract
Funding Acknowledgements
Type of funding sources: Private company. Main funding source(s): Bayer AG Berlin, Germany
INTRODUCTION
Patients with type 2 diabetes (T2D) are at an increased risk of ophthalmic complications compared to those without. Ophthalmic complications in T2D patients with comorbid nonvalvular atrial fibrillation (NVAF) may include ophthalmic bleeding and/or diabetic retinopathy.
PURPOSE
We sought to evaluate ophthalmic complications in patients with NVAF and T2D prescribed rivaroxaban or warfarin for stroke prevention.
METHODS
Optum® de-identified electronic health record (EHR) data from 11/2010-3/2020 were utilized. Adults with NVAF and T2D, newly started on rivaroxaban or warfarin and with ≥12 months of prior EHR activity were included. Patients were excluded if they received any oral anticoagulation in the prior 12 months, had valvular disease or pre-existing diabetic retinopathy. Our primary outcome was the incidence rate of any ophthalmic complication including non-traumatic bleeding (choroidal, intraocular, retinal, vitreous) or diabetic retinopathy. Ophthalmic bleeds typically associated with trauma (hyphema, orbital) were excluded from our outcomes. Hazard ratios (HR) with 95% confidence intervals (CIs) were calculated using propensity score-overlap weighted Cox regression.
RESULTS
We included 26,537 rivaroxaban and 61,690 warfarin patients. The average age of patients was 69 ± 9 years, CHA2DS2VASc score was 4.1 ± 1.5 and HASBLED 1.5 ± 0.9. Thirty-two percent of patients had an a1c ≥7.0 and 16% an a1c≥8.0. Rivaroxaban was associated with a 15% (95%CI = 8-21%) relative hazard reduction of any ophthalmic complication (incidence rate = 1.25 vs. 1.46%/year) (Table), driven by reductions in both ophthalmic bleeding (HR = 0.80) and diabetic retinopathy (HR = 0.85).
CONCLUSIONS
Rivaroxaban was associated with a reduction in ophthalmic complications compared to warfarin.
Table. Ophthalmic Complications
Outcome
Rivaroxaban, %/yearN = 26,537
Warfarin, %/yearN = 61,690
PS OLW HR (95%CI)
Any Ophthalmic Complication
1.25
1.46
0.85 (0.79-0.92)
Any Ophthalmic Bleed
0.15
0.19
0.80 (0.63-1.00)
Choroidal Bleed
0.003
0.005
0.59 (0.11-3.17)
Intraocular Bleed
0.01
0.01
0.75 (0.26-2.13)
Retinal Bleed
0.08
0.09
0.93 (0.68-1.28)
Vitreous Bleed
0.07
0.10
0.66 (0.47-0.92)
Any Type of Diabetic Retinopathy
1.15
1.34
0.85 (0.79-0.93)
Diabetic Retinopathy, non-proliferative
0.35
0.44
0.80 (0.69-0.93)
Diabetic Retinopathy, proliferative
0.09
0.12
0.7 |
---|---|
ISSN: | 1099-5129 1532-2092 |
DOI: | 10.1093/europace/euab116.280 |