Department of Neurology, Innsbruck Medical University, Innsbruck, Austria.
Neurology. 2013 Mar 26;80(13):1216-24. doi: 10.1212/WNL.0b013e3182897015. Epub 2013 Mar 13.
Prominent fibrinogen cleavage by recombinant tissue plasminogen activator and formation of fibrinogen degradation products with anticoagulant properties was proposed to amplify the risk of thrombolysis-related bleeding complications, but supportive evidence mainly derived from studies on myocardial infarction.
This study included 547 consecutive stroke patients treated with recombinant tissue plasminogen activator, who underwent repeated assessment of fibrinogen levels before and 6 hours after thrombolysis. Symptomatic intracranial hemorrhages were ascertained using National Institute of Neurological Disorders and Stroke criteria.
Intracranial hemorrhage or systemic bleeding events manifested in 47 patients (8.6%). A decrease ≥200 mg/dL in the fibrinogen level 6 hours after thrombolysis emerged as a significant and independent predictor for bleeding risk (multivariable odds ratio [95% confidence interval] 4.53 [2.39-8.60], p < 0.001). The population-attributable risk was 39.9% (95% confidence interval, 19.0-60.2) for any major bleeding, causality assumed, and surpassed 50% in patients with less severe strokes (NIH Stroke Scale score ≤16). Quantification of fibrinogen depletion after stroke thrombolysis significantly improved routine risk prediction of bleeding complications as indicated by an increase in the C-statistics from 0.712 to 0.798 (p = 0.015) and a net reclassification index of 0.341 (p < 0.001). A prospective bicenter validation sample (n = 148) corroborates the key findings of this study and suggests positive and negative predictive values of fibrinogen depletion for any major bleeding of 29.2% and 93.5%.
This study lends strong support to the concept that prominent fibrinogen turnover after IV stroke thrombolysis-a condition termed "early fibrinogen degradation coagulopathy"-is a relevant cause of major bleeding complications. Rigorous testing of more fibrin-specific thrombolytic agents in the setting of acute stroke is warranted.
重组组织型纤溶酶原激活剂(rt-PA)显著切割纤维蛋白原,并形成具有抗凝特性的纤维蛋白原降解产物,据推测这会放大溶栓相关出血并发症的风险,但支持这一观点的证据主要来自心肌梗死研究。
本研究纳入了 547 例接受重组组织型纤溶酶原激活剂治疗的连续卒中患者,这些患者在溶栓前和溶栓后 6 小时重复评估纤维蛋白原水平。采用国立卫生研究院卒中量表(NIHSS)确定症状性颅内出血。
47 例患者(8.6%)出现颅内出血或全身性出血事件。溶栓后 6 小时纤维蛋白原水平下降≥200mg/dL 是出血风险的显著独立预测因素(多变量比值比[95%置信区间]4.53[2.39-8.60],p<0.001)。假设因果关系,人群归因风险为 39.9%(95%置信区间,19.0-60.2),用于任何大出血;假设因果关系,在 NIHSS 评分≤16 的轻度卒中患者中超过 50%。卒中溶栓后纤维蛋白原耗竭的量化显著改善了出血并发症的常规风险预测,C 统计量从 0.712 增加到 0.798(p=0.015),净重新分类指数为 0.341(p<0.001)。一项前瞻性的 2 中心验证样本(n=148)证实了本研究的主要发现,并提示纤维蛋白原耗竭对任何大出血的阳性和阴性预测值分别为 29.2%和 93.5%。
本研究有力支持这样一种观点,即 IV 卒中溶栓后显著的纤维蛋白原转化(称为“早期纤维蛋白原降解性凝血障碍”)是导致大出血并发症的一个相关原因。有必要在急性卒中中对更具纤维蛋白特异性的溶栓剂进行严格测试。