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华法林相关性颅内出血后重新开始抗凝治疗与死亡率风险:颅内出血后重新开始抗凝治疗的最佳实践(BRAIN)研究。

Reinitiation of anticoagulation after warfarin-associated intracranial hemorrhage and mortality risk: the Best Practice for Reinitiating Anticoagulation Therapy After Intracranial Bleeding (BRAIN) study.

机构信息

Division of Cardiology, University of Toronto, Toronto, Ontario, Canada.

出版信息

Can J Cardiol. 2012 Jan-Feb;28(1):33-9. doi: 10.1016/j.cjca.2011.10.002. Epub 2011 Dec 7.

Abstract

BACKGROUND

While warfarin-related intracranial hemorrhage (ICH) occurs in 0.25%-1.1% patients per year, little is known about the practice and outcomes of anticoagulant reinitiation.

METHODS

We studied a cohort of consecutive patients with warfarin-related ICH (intracerebral or subarachnoid) admitted to 13 stroke centres in the Registry of the Canadian Stroke Network between July 2003 and March 2008. We examined patterns of warfarin reinitiation and variables associated with 30-day and 1-year outcomes.

RESULTS

Among the 284 patients studied (mean age 74 ± 12 years), warfarin was restarted in-hospital in 91 patients (32%). Factors associated with restarting warfarin were lower stroke severity (adjusted odds ratio [aOR] 2.07, 95% confidence interval [CI]; 1.20-3.57, P = 0.009) or presence of valve prosthesis (aOR 3.07, 95% CI; 1.29-7.27, P = 0.011). Mortality rates were not higher in those who restarted warfarin in-hospital: 31.9% vs 54.4% (30-day, P < 0.001) and 48% vs 61% (1-year, P = 0.04), and bleeding was not increased. Multivariable predictors of mortality included initial international normalized ratio > 3.0 (aOR, 3.28 [30-day, P < 0.001] and 3.32 [1-year, P = 0.003]), greater stroke severity (aOR, 6.04 [30-day] and 4.22 [1-year]; both P < 0.001), and intraventricular hemorrhage (aOR, 2.19 [30-day; P = 0.03] and 2.04 [1-year; P = 0.04]). In selected patients who reinitiated warfarin, there was no increase in 30-day (aOR, 0.49; P = 0.03) or 1-year mortality (aOR, 0.79; P = 0.43).

CONCLUSIONS

In selected patients at high thrombosis risk, reinitiation of warfarin after ICH did not confer increased mortality or bleeding events.

摘要

背景

华法林相关性颅内出血(ICH)每年在 0.25%-1.1%的患者中发生,但对于抗凝药物重新使用的实践和结果知之甚少。

方法

我们研究了 2003 年 7 月至 2008 年 3 月期间在加拿大卒中网络注册中心的 13 个卒中中心连续收治的 284 例因华法林相关性 ICH(脑内或蛛网膜下腔)而入院的患者队列。我们研究了华法林重新使用的模式以及与 30 天和 1 年结局相关的变量。

结果

在研究的 284 例患者中(平均年龄 74±12 岁),91 例(32%)患者在院内重新开始使用华法林。与重新开始使用华法林相关的因素包括较低的卒中严重程度(调整后的优势比[OR] 2.07,95%置信区间[CI]:1.20-3.57,P=0.009)或存在瓣膜假体(OR 3.07,95%CI:1.29-7.27,P=0.011)。在院内重新开始使用华法林的患者中,死亡率并没有更高:31.9%与 54.4%(30 天,P<0.001)和 48%与 61%(1 年,P=0.04),出血也没有增加。死亡的多变量预测因素包括初始国际标准化比值>3.0(OR,3.28[30 天,P<0.001]和 3.32[1 年,P=0.003])、更高的卒中严重程度(OR,6.04[30 天]和 4.22[1 年];均 P<0.001)和脑室内出血(OR,2.19[30 天,P=0.03]和 2.04[1 年,P=0.04])。在重新开始使用华法林的选定患者中,30 天(OR,0.49;P=0.03)或 1 年死亡率(OR,0.79;P=0.43)均无增加。

结论

在血栓形成风险较高的选定患者中,ICH 后重新开始使用华法林不会增加死亡率或出血事件。

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