Bleeding Risk of Direct Oral Anticoagulants in Patients With Heart Failure And Atrial Fibrillation

被引:27
作者
Jackevicius, Cynthia A. [1 ,4 ,5 ,6 ,7 ]
Lu, Lingyun [1 ]
Ghaznavi, Zunera [2 ,8 ]
Warner, Alberta L. [2 ,3 ]
机构
[1] Vet Affairs Greater Angeles Healthcare Syst, Dept Pharm, Los Angeles, CA USA
[2] Vet Affairs Greater Angeles Healthcare Syst, Dept Cardiol, Los Angeles, CA USA
[3] UCLA, David Gef Fen Sch Med, Los Angeles, CA USA
[4] Western Univ Hlth Sci, Coll Pharm, Dept Pharm Practice & Adm, Pomona, CA 91766 USA
[5] ICES, Toronto, ON, Canada
[6] Univ Toronto, Inst Hlth Policy Management & Evaluat, Toronto, ON, Canada
[7] Univ Hlth Network, Dept Pharm, Toronto, ON, Canada
[8] Univ Southern Calif, Dept Preventat Med, Los Angeles, CA USA
来源
CIRCULATION-CARDIOVASCULAR QUALITY AND OUTCOMES | 2021年 / 14卷 / 02期
关键词
anticoagulation; atrial fibrillation; heart failure; hemorrhage; observational study; renal insufficiency; chronic; warfarin; RENAL-FUNCTION; WARFARIN; DABIGATRAN; EFFICACY; THERAPY; SAFETY; APIXABAN; IMPAIRMENT; INSIGHTS; DISEASE;
D O I
10.1161/CIRCOUTCOMES.120.007230
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Patients with heart failure and atrial fibrillation are an important atrial fibrillation subgroup in which direct oral anticoagulants (DOACs) have not been adequately studied in real-world settings. Since DOACs rely on renal elimination and renal dysfunction is prevalent in patients with heart failure, their use may increase bleeding risk, negating some of their advantage over warfarin. Methods: We conducted a retrospective cohort study using linked Veterans Administration databases of patients with heart failure newly started on warfarin or DOACs for atrial fibrillation from October 2010 to August 2017 (23 635 warfarin, 25 823 DOAC). Outcomes included time to first bleeding, stroke, and death using Cox proportional hazards models with inverse probability of treatment weighting. Results: Total bleeding (hazard ratio, 0.62 [95% CI, 0.56-0.68]), major bleeding (hazard ratio, 0.49 [95% CI, 0.40-0.61]), and death (hazard ratio, 0.74 [95% CI, 0.71-0.78]) were lower with DOAC than warfarin, and with apixaban and dabigatran, but not rivaroxaban. Moderate/severe chronic kidney disease was common (48.7%); moderate chronic kidney disease was associated with increased bleeding with DOACs but not warfarin. However, death and bleeding remained lower with DOACs than warfarin across all renal function levels and clinical subgroups. A >20% transient/persistent decline in renal function occurred in 53% of DOAC-treated patients at some point during follow-up, would have required dose reduction in 10.5% of patients, and was associated with increased bleeding. Dose adjustments were made more often, and bleeding and death were lower in patients seen by pharmacists or anticoagulation clinics. There were significant between-site variations in DOAC dosing. Conclusions: DOACs overall, apixaban, and dabigatran, but not rivaroxaban, were associated with less total bleeding and death than warfarin in patients with heart failure and atrial fibrillation at all levels of renal function. Renal function decline resulted in increased bleeding in patients with DOACs. DOAC dose adjustment was often indicated, associated with increased bleeding when not adjusted, emphasizing the need for closer monitoring in these patients.
引用
收藏
页码:155 / 168
页数:14
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