Department of Neurology, the Second Affiliated Hospital of Zhejiang University, School of Medicine, 88# Jiefang Road, Hangzhou, 310009, China.
Department of Neurology, the Fourth Affiliated Hospital of Zhejiang University, School of Medicine, Yiwu, China.
Transl Stroke Res. 2020 Apr;11(2):195-203. doi: 10.1007/s12975-019-00723-w. Epub 2019 Aug 28.
Early neurological deterioration (END) after thrombolysis occurs in 10% acute ischemic stroke (AIS) patients, and its mechanism remains unclear in majority of cases, named as unexplained END. We tested the hypothesis that penumbra/infarct growth beyond the initial penumbra might be the cause of unexplained END. We reviewed the database of AIS patients who received reperfusion therapy. Unexplained END was defined as ≥ 2-point increase of NIHSS from baseline to 24 h, without straightforward causes. For each unexplained END patient, we extracted 2 matched controls based on 4 clinical and radiological characteristics which were strongly associated with unexplained END. We defined extra-penumbra and extra-infarct as penumbra and infarct growth at 24 h beyond baseline penumbral tissue and then investigated the relationship between extra-penumbra and extra-infarct and the presence of unexplained END. Finally, 44 unexplained END patients and 88 matched controls were included. The volume of both extra-infarct (OR, 1.032 per 1-mL increase; p = 0.018) and extra-penumbra (OR, 1.070 per 1-mL increase; p < 0.001) were associated with the presence of unexplained END, while the absence of recanalization was associated with the presence of either extra-infarct or extra-penumbra (OR, 3.291; p = 0.001). Moreover, 51.4% cases with extra-penumbra at 24 h finally progressed to infarct at 7 days, and they underwent higher increase of NIHSS from 24 h to 7 days than those that did not progress to infarct at 7 days (4.0 vs 1.0; p = 0.017). Penumbra/infarct growth beyond the initial penumbra is involved in the unexplained END in AIS patients receiving reperfusion therapy.
早期神经功能恶化(END)发生在 10%的急性缺血性脑卒中(AIS)患者中,但其机制在大多数情况下仍不清楚,称为不明原因的 END。我们检验了这样一个假设,即初始缺血半影区以外的缺血半影区/梗死体积的增加可能是不明原因 END 的原因。我们回顾了接受再灌注治疗的 AIS 患者的数据库。不明原因的 END 定义为 NIHSS 基线至 24 小时增加≥2 分,无明显原因。对于每个不明原因的 END 患者,我们根据 4 个与不明原因 END 强烈相关的临床和影像学特征提取了 2 个匹配的对照。我们将额外的缺血半影区和额外的梗死区定义为基线缺血半影区组织 24 小时后缺血半影区和梗死区的生长,并研究了额外的缺血半影区和额外的梗死区与不明原因 END 的关系。最后,纳入 44 例不明原因 END 患者和 88 例匹配对照。额外梗死区(OR,每增加 1ml 增加 1.032;p=0.018)和额外缺血半影区(OR,每增加 1ml 增加 1.070;p<0.001)的体积与不明原因 END 的发生相关,而无再通与额外梗死区或额外缺血半影区的存在相关(OR,3.291;p=0.001)。此外,24 小时后有 51.4%的患者有额外的缺血半影区最终在 7 天进展为梗死,与没有进展为梗死的患者相比,他们从 24 小时到 7 天 NIHSS 的增加更大(4.0 与 1.0;p=0.017)。接受再灌注治疗的 AIS 患者中,初始缺血半影区以外的缺血半影区/梗死体积的增加与不明原因的 END 有关。