Effectiveness and safety in non-valvular atrial fibrillation patients switching from warfarin to direct oral anticoagulants in US healthcare claims

被引:0
|
作者
Lip, Gregory Y. H. [1 ,2 ,3 ,8 ]
Noxon, Virginia [4 ]
Kang, Amiee [5 ]
Luo, Xuemei [6 ]
Atreja, Nipun [5 ]
Han, Stella [5 ]
Cheng, Dong [5 ]
Jiang, Jenny [5 ]
Abramovitz, Lisa [4 ]
Deitelzweig, Steven [7 ]
机构
[1] Liverpool John Moores Univ, Univ Liverpool, Liverpool Ctr Cardiovasc Sci, Liverpool, England
[2] Liverpool Heart & Chest Hosp, Liverpool, England
[3] Aalborg Univ, Danish Ctr Clin Hlth Serv Res, Dept Clin Med, Aalborg, Denmark
[4] STATinMED LLC, Dallas, TX USA
[5] Bristol Myers Squibb Co, Manlius, NY USA
[6] Pfizer Inc, New York, NY USA
[7] Ochsner Clin Fdn, Dept Hosp Med, New Orleans, LA USA
[8] Univ Liverpool, Fac Hlth & Life Sci, Fdn Bldg,Brownlow Hill, Liverpool L697TX, England
关键词
Stroke/systemic embolism; Non-valvular atrial fibrillation; Direct oral anticoagulant; Warfarin; Switching; Apixaban; STROKE PREVENTION; RISK; METAANALYSIS; RIVAROXABAN; GUIDELINES; DABIGATRAN; APIXABAN;
D O I
10.1007/s11239-024-02976-1
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction There is a paucity of real-world studies examining the risks of stroke/systemic embolism (SE) and major bleeding (MB) among non-valvular atrial fibrillation (NVAF) patients switching from warfarin to a direct oral anticoagulant (DOAC). This retrospective study was conducted to compare the stroke/SE and MB risks between patients switched from warfarin to apixaban, dabigatran, or rivaroxaban in real-world clinical practice.Materials and methods This study used data from four United States commercial claims databases from January 1, 2012 to June 30, 2019. The study population included NVAF patients initially treated with warfarin and switched to apixaban, dabigatran, or rivaroxaban within 90 days of their warfarin prescription ending. Patients were matched 1:1 between the DOACs in each database using propensity scores and then pooled for the final analysis. Cox proportional hazards models were used to calculate the risk of stroke/SE and MB.Results and conclusions The final population consisted of 2,611 apixaban-dabigatran, 12,165 apixaban-rivaroxaban, and 2,672 dabigatran-rivaroxaban pairs. Apixaban vs. dabigatran was associated with a lower risk of stroke/SE (hazard ratio [HR]: 0.61; 95% confidence interval [CI]: 0.39-0.96) and MB (HR: 0.67; 95% CI: 0.50-0.91). Apixaban vs. rivaroxaban was associated with a similar risk of stroke/SE (HR: 0.88; 95% CI: 0.73-1.07) and a lower risk of MB (HR: 0.60; 95% CI: 0.52-0.68). There was no significant difference in either risk between dabigatran and rivaroxaban. These results provide important insights into how the risks of stroke/SE and MB for NVAF patients vary when switching from warfarin to different DOACs. center dot Patients with NVAF may switch to DOACs for effectiveness, safety, or convenience.center dot Risk of stroke/SE and MB may vary among patients with NVAF who switch to DOACs.center dot Switching to apixaban had a lower risk of MB than dabigatran/rivaroxaban.center dot Results may inform DOAC prescribing decisions after warfarin in patients with NVAF.
引用
收藏
页码:1092 / 1102
页数:11
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