Department of Hematology, Karolinska University Hospital and Karolinska Institute, Stockholm, Sweden.
Stroke. 2010 Dec;41(12):2860-6. doi: 10.1161/STROKEAHA.110.593087. Epub 2010 Oct 28.
The optimum timing of resumption of anticoagulation after warfarin-related intracranial hemorrhage in patients with indication for continued anticoagulation is uncertain. We performed a large retrospective cohort study to obtain more precise risk estimates.
We reviewed charts of 2869 consecutive patients with objectively verified intracranial hemorrhage over 6 years at 3 tertiary centers. We calculated the daily risk of intracranial hemorrhage or ischemic stroke with and without resumption of warfarin; we focused on patients who survived the first week and had cardiac indication for anticoagulation or previous stroke. Using a Cox model, we estimated rates for these 2 adverse events in relation to different time points of resumed anticoagulation. The combined risk of either a new intracranial hemorrhage or an ischemic stroke was calculated for a range of warfarin resumption times.
We identified warfarin-associated intracranial hemorrhage in 234 patients (8.2%), of whom 177 patients (76%) survived the first week and had follow-up information available; the median follow-up time was 69 weeks (interquartile range [IQR] 19-144). Fifty-nine patients resumed warfarin after a median of 5.6 weeks (IQR 2.6-17). The hazard ratio for recurrent intracranial hemorrhage with resumption of warfarin was 5.6 (95% CI, 1.8-17.2), and for ischemic stroke it was 0.11 (95% CI, 0.014-0.89). The combined risk of recurrent intracranial hemorrhage or ischemic stroke reached a nadir if warfarin was resumed after approximately 10 to 30 weeks.
The optimal timing for resumption of warfarin therapy appears to be between 10 and 30 weeks after warfarin-related intracranial hemorrhage.
华法林相关性颅内出血患者,若存在继续抗凝的适应证,其恢复抗凝治疗的最佳时机仍不确定。本研究旨在通过大样本回顾性队列研究获得更精确的风险评估。
研究共纳入 3 家三级医疗中心 6 年期间 2869 例经客观证实的颅内出血患者的病历资料。本研究计算了恢复华法林治疗与不恢复华法林治疗时颅内出血或缺血性卒中的每日风险;研究重点关注生存至第 1 周且存在心脏抗凝适应证或既往卒中的患者。采用 Cox 模型,本研究评估了不同恢复华法林治疗时间点上述 2 种不良事件的发生率。本研究还计算了不同华法林恢复时间范围内发生新发颅内出血或缺血性卒中的联合风险。
共纳入 234 例(8.2%)华法林相关性颅内出血患者,其中 177 例(76%)患者生存至第 1 周且有随访信息,中位随访时间为 69 周(IQR 19-144)。59 例患者于中位时间 5.6 周(IQR 2.6-17)后恢复华法林治疗。恢复华法林治疗后颅内出血再发的风险比(HR)为 5.6(95%CI 1.8-17.2),缺血性卒中的 HR 为 0.11(95%CI 0.014-0.89)。若于华法林相关性颅内出血后 10~30 周恢复华法林治疗,新发颅内出血或缺血性卒中的联合风险最低。
恢复华法林治疗的最佳时机似乎为华法林相关性颅内出血后 10~30 周。