Department of Cerebrovascular Medicine, National Cerebral and Cardiovascular Center.
Department of Neurology, Kobe City Medical Center General Hospital.
Circ J. 2018 Jun 25;82(7):1935-1942. doi: 10.1253/circj.CJ-18-0067. Epub 2018 Jun 1.
We determined the 2-year long-term risk-benefit profile in patients with stroke or transient ischemic attack (TIA) receiving warfarin or direct oral anticoagulants (DOACs) for nonvalvular atrial fibrillation (NVAF) using a prospective, multicenter, observational registry in Japan.
NVAF patients within 7 days after onset of ischemic stroke/TIA were enrolled in 18 stroke centers. Outcome measures included ischemic and bleeding events and death in the 2-year follow-up period. We enrolled 1,116 patients taking either warfarin (650 patients) or DOACs (466 patients) at acute hospital discharge. DOAC users were younger and had lower National Institutes of Health Stroke Scale, CHADSand discharge modified Rankin Scale scores than warfarin users (P<0.0001 each). Incidences of stroke/systemic embolism (adjusted hazard ratio, 1.07; 95% CI, 0.66-1.72), all ischemic events (1.13; 0.72-1.75), and ischemic stroke/TIA (1.58; 0.95-2.62) were similar between groups. Risks of intracranial hemorrhage (0.32; 0.09-0.97) and death (0.41; 0.26-0.63) were significantly lower for DOAC users. Infection was the leading cause of death, accounting for 40% of deaths among warfarin users.
Stroke/TIA patients receiving DOACs for secondary prevention were younger and had lower stroke severity and risk indices than those receiving warfarin. Estimated cumulative incidences of stroke and systemic embolism within 2 years were similar between warfarin and DOACs users, but those of death and intracranial hemorrhage were significantly lower among DOAC users.
我们通过在日本的一个前瞻性、多中心、观察性登记研究,确定了在缺血性卒中和短暂性脑缺血发作(TIA)后 7 天内接受华法林或直接口服抗凝剂(DOAC)治疗的非瓣膜性心房颤动(NVAF)患者的 2 年长期风险-效益概况。
在 18 家卒中中心入组了缺血性卒中和 TIA 发病后 7 天内的 NVAF 患者。主要终点是在 2 年随访期间发生的缺血性和出血性事件以及死亡。我们在急性住院出院时入组了 1116 名接受华法林(650 例)或 DOACs(466 例)治疗的患者。DOAC 使用者比华法林使用者更年轻,具有更低的国立卫生研究院卒中量表(NIHSS)评分、CHADS₂评分和出院改良Rankin 量表(mRS)评分(P<0.0001)。卒中/全身性栓塞(调整后的危险比,1.07;95%可信区间,0.66-1.72)、所有缺血性事件(1.13;0.72-1.75)和缺血性卒中和 TIA(1.58;0.95-2.62)的发生率在两组之间相似。颅内出血(0.32;0.09-0.97)和死亡(0.41;0.26-0.63)的风险明显低于 DOAC 使用者。感染是华法林使用者死亡的主要原因,占华法林使用者死亡人数的 40%。
接受 DOACs 进行二级预防的卒中和 TIA 患者比接受华法林治疗的患者更年轻,且卒中严重程度和风险指数更低。在 2 年内,华法林和 DOACs 使用者的卒中及全身性栓塞累积发生率相似,但 DOACs 使用者的死亡和颅内出血发生率显著降低。