From the Department of Neurology, the 2nd Affiliated Hospital of Zhejiang University, School of Medicine, Hangzhou, China.
Stroke. 2019 Oct;50(10):2716-2721. doi: 10.1161/STROKEAHA.119.025711. Epub 2019 Aug 9.
Background and Purpose- We aimed to thoroughly investigate the relationship between early fibrinogen depletion and symptomatic intracranial hemorrhage (sICH) in patients receiving reperfusion therapy including intravenous thrombolysis (IVT) with or without endovascular thrombectomy (EVT). Methods- This study included 1135 stroke patients with baseline and follow-up fibrinogen levels at 2 hours after the beginning of alteplase infusion for those with IVT only or immediately after the end of EVT for those with combined IVT and EVT. Patients received alteplase up to 9 hours after the onset or on awakening based on automated perfusion imaging. sICH was ascertained using ECASS II (The Second European-Australasian Acute Stroke Study) criteria. Δfibrinogen was calculated as follow-up fibrinogen minus baseline fibrinogen. Results- In patients with IVT only, baseline fibrinogen level was 3.36±0.94 g/L and decreased to 2.47±0.80 g/L at 2 hours after the beginning of alteplase infusion. In patients with IVT followed by EVT, baseline fibrinogen level was 3.35±0.82 g/L and decreased to 2.52±0.83 g/L immediately after the end of EVT. sICH was observed in 44 (3.9%) patients. The extent of Δfibrinogen was associated with sICH in patients with IVT only (odds ratio, 1.929; 95% CI, 1.402-2.654; <0.001) and in those with IVT followed by EVT (odds ratio, 1.765; 95% CI, 1.135-2.743; =0.012). Conclusions- An early decrease in fibrinogen levels was related to sICH after reperfusion therapy with alteplase. More fibrin-specific thrombolytic agents are warranted to be tested in acute ischemic stroke patients. Clinical Trial Registration- URL: https://www.clinicaltrials.gov. Unique identifier: NCT03367286.
背景与目的- 我们旨在深入研究接受包括静脉溶栓(IVT)联合或不联合血管内取栓(EVT)在内的再灌注治疗的患者中,早期纤维蛋白原耗竭与症状性颅内出血(sICH)之间的关系。方法- 本研究纳入了 1135 名基线和 2 小时后接受阿替普酶输注的患者进行随访纤维蛋白原水平的卒中患者,对于仅接受 IVT 的患者,该时间点为阿替普酶输注开始后 2 小时;对于接受 IVT 联合 EVT 的患者,该时间点为 EVT 结束后立即。患者根据自动灌注成像在发病后 9 小时内或醒来时接受阿替普酶治疗。sICH 使用 ECASS II(第二次欧洲-澳大利亚急性卒中研究)标准确定。Δ纤维蛋白原的计算方法为:随访纤维蛋白原减去基线纤维蛋白原。结果- 仅接受 IVT 的患者,基线纤维蛋白原水平为 3.36±0.94 g/L,阿替普酶输注开始后 2 小时降至 2.47±0.80 g/L。接受 IVT 联合 EVT 的患者,基线纤维蛋白原水平为 3.35±0.82 g/L,EVT 结束后立即降至 2.52±0.83 g/L。44 例(3.9%)患者发生 sICH。仅接受 IVT 的患者中,Δ纤维蛋白原程度与 sICH 相关(比值比,1.929;95%可信区间,1.402-2.654;<0.001),在接受 IVT 联合 EVT 的患者中也相关(比值比,1.765;95%可信区间,1.135-2.743;=0.012)。结论- 阿替普酶再灌注治疗后,纤维蛋白原水平早期下降与 sICH 相关。需要进一步测试更多纤维蛋白特异性溶栓药物在急性缺血性卒中患者中的应用。
临床试验注册- URL:https://www.clinicaltrials.gov。唯一标识符:NCT03367286。