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有抗凝治疗史的缺血性脑卒中患者的预后:直接口服抗凝剂与华法林。

Prognosis of Patients With Ischemic Stroke With Prior Anticoagulant Therapy: Direct Oral Anticoagulants Versus Warfarin.

机构信息

Division of Cardiology National Health Insurance Service Ilsan Hospital Goyang Republic of Korea.

Department of Research and Analysis National Health Insurance Service Ilsan Hospital Goyang Korea.

出版信息

J Am Heart Assoc. 2024 Aug 6;13(15):e034698. doi: 10.1161/JAHA.124.034698. Epub 2024 Aug 5.

DOI:10.1161/JAHA.124.034698
PMID:39101509
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11964058/
Abstract

BACKGROUND

Direct oral anticoagulants (DOACs) have been the drug of choice for preventing ischemic stroke in patients with atrial fibrillation since 2014. In previous studies, the stroke risk while taking warfarin was 2 per 100 patient-years and 1.5% per year while taking DOACs. We hypothesized that even if ischemic stroke occurred during anticoagulation therapy with DOACs, the prognosis was likely to be better than that with warfarin.

METHODS AND RESULTS

Data from 2002 to 2019, sourced from a nationwide claims database, were used to identify atrial fibrillation patients using codes. Patients who experienced an ischemic stroke during anticoagulation were categorized by the drugs used (warfarin, dabigatran, apixaban, rivaroxaban, and edoxaban). The primary outcome was mortality within 3 months and 1 year after the ischemic stroke. Among the 9578 patients with ischemic stroke during anticoagulation, 3343 received warfarin, and 6235 received DOACs (965 dabigatran, 2320 apixaban, 1702 rivaroxaban, 1248 edoxaban). The DOACs group demonstrated lower risks of 3-month (adjusted hazard ratio [HR], 0.550, [95% CI, 0.473-0.639]; <0.0001) and 1-year mortality (adjusted HR, 0.596 [95% CI, 0.536-0.663]; <0.0001) than the warfarin group. Apixaban and edoxaban within the DOAC group exhibited particularly reduced 1-year mortality risk compared with other DOACs (<0.0001).

CONCLUSIONS

Our study confirmed that DOACs have a better prognosis than warfarin after ischemic stroke. The apixaban and edoxaban groups had a lower risk of death after ischemic stroke than the other DOAC groups.

摘要

背景

自 2014 年以来,直接口服抗凝剂(DOACs)一直是预防房颤患者缺血性卒中的首选药物。在以前的研究中,华法林治疗时的卒中风险为每 100 患者年 2 例,DOACs 治疗时为每年 1.5%。我们假设,即使在 DOAC 抗凝治疗期间发生缺血性卒中,其预后也可能优于华法林。

方法和结果

使用全国性索赔数据库中的 2002 年至 2019 年的数据,使用代码识别房颤患者。将抗凝期间发生缺血性卒中的患者按所用药物(华法林、达比加群、阿哌沙班、利伐沙班和依度沙班)分类。主要结局是缺血性卒中后 3 个月和 1 年内的死亡率。在 9578 例抗凝期间发生缺血性卒中的患者中,3343 例接受华法林治疗,6235 例接受 DOACs 治疗(965 例达比加群、2320 例阿哌沙班、1702 例利伐沙班、1248 例依度沙班)。DOACs 组的 3 个月(校正后的危险比 [HR],0.550,[95%置信区间,0.473-0.639];<0.0001)和 1 年死亡率(校正 HR,0.596 [95%置信区间,0.536-0.663];<0.0001)的风险低于华法林组。DOAC 组中的阿哌沙班和依度沙班与其他 DOAC 相比,1 年死亡率风险降低尤其明显(<0.0001)。

结论

本研究证实,DOACs 在缺血性卒中后预后优于华法林。与其他 DOAC 组相比,阿哌沙班和依度沙班组缺血性卒中后死亡风险更低。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cd8b/11964058/ecc357ee1f92/JAH3-13-e034698-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cd8b/11964058/f2af208555d3/JAH3-13-e034698-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cd8b/11964058/ecc357ee1f92/JAH3-13-e034698-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cd8b/11964058/f2af208555d3/JAH3-13-e034698-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cd8b/11964058/ecc357ee1f92/JAH3-13-e034698-g001.jpg

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