From the Departments of Neurology (G.B., V.A., J.N., A.O.R.) and Intensive Care Medicine (M.O.), Centre Hospitalier Universitaire Vaudois (CHUV) and University of Lausanne, Switzerland; Neurology Unit (G.B.), San Gerardo Hospital, Monza; School of Medicine and Surgery and Milan Center for Neuroscience (NeuroMI), University of Milano-Bicocca, Italy; Department of Neurology (J.W.L., L.B.), Brigham and Women's Hospital, Harvard Medical School, Boston, MA; and Department of Neurology (V.A.), Hôpital du Valais, Sion, Switzerland.
Neurology. 2020 Apr 21;94(16):e1675-e1683. doi: 10.1212/WNL.0000000000009283. Epub 2020 Mar 25.
After cardiac arrest (CA), epileptiform EEG, occurring in about 1/3 of patients, often but not invariably heralds poor prognosis. We tested the hypothesis that a combination of specific EEG features identifies patients who may regain consciousness despite early epileptiform patterns.
We retrospectively analyzed a registry of comatose patients post-CA (2 Swiss centers), including those with epileptiform EEG. Background and epileptiform features in EEGs 12-36 hours or 36-72 hours from CA were scored according to the American Clinical Neurophysiology Society nomenclature. Best Cerebral Performance Category (CPC) score within 3 months (CPC 1-3 vs 4-5) was the primary outcome. Significant EEG variables were combined in a score assessed with receiver operating characteristic curves, and independently validated in a US cohort; its correlation with serum neuron-specific enolase (NSE) was also tested.
Of 488 patients, 107 (21.9%) had epileptiform EEG <72 hours; 18 (17%) reached CPC 1-3. EEG 12-36 hours background continuity ≥50%, absence of epileptiform abnormalities ( < 0.00001 each), 12-36 and 36-72 hours reactivity ( < 0.0001 each), 36-72 hours normal background amplitude ( = 0.0004), and stimulus-induced discharges ( = 0.0001) correlated with favorable outcome. The combined 6-point score cutoff ≥2 was 100% sensitive (95% confidence interval [CI], 78%-100%) and 70% specific (95% CI, 59%-80%) for CPC 1-3 (area under the curve [AUC], 0.98; 95% CI, 0.94-1.00). Increasing score correlated with NSE (ρ = -0.46, = 0.0001). In the validation cohort (41 patients), the score was 100% sensitive (95% CI, 60%-100%) and 88% specific (95% CI, 73%-97%) for CPC 1-3 (AUC, 0.96; 95% CI, 0.91-1.00).
Prognostic value of early epileptiform EEG after CA can be estimated combining timing, continuity, reactivity, and amplitude features in a score that correlates with neuronal damage.
心脏骤停(CA)后,约 1/3 的患者出现癫痫样 EEG,通常但并非总是预示预后不良。我们检验了这样一个假设,即特定 EEG 特征的组合可识别出尽管早期存在癫痫样模式但可能恢复意识的患者。
我们回顾性分析了瑞士 2 个中心的昏迷后 CA 患者的登记处(包括有癫痫样 EEG 的患者)。根据美国临床神经生理学会命名法,对 CA 后 12-36 小时或 36-72 小时的 EEG 中的背景和癫痫样特征进行评分。主要结局是 3 个月内最佳大脑表现类别(CPC)评分(CPC 1-3 与 4-5)。通过受试者工作特征曲线评估具有显著意义的 EEG 变量的组合评分,并在美国队列中进行独立验证;还测试了其与神经元特异性烯醇化酶(NSE)的相关性。
488 例患者中,107 例(21.9%)在 72 小时内出现癫痫样 EEG;18 例(17%)达到 CPC 1-3。EEG 12-36 小时背景连续性≥50%、无癫痫样异常(均<0.00001)、12-36 小时和 36-72 小时反应性(均<0.0001)、36-72 小时正常背景振幅(=0.0004)和刺激诱导放电(=0.0001)与良好结局相关。6 分组合评分≥2 的截断值对 CPC 1-3 的敏感性为 100%(95%置信区间 [CI],78%-100%),特异性为 70%(95% CI,59%-80%)(曲线下面积 [AUC],0.98;95% CI,0.94-1.00)。评分增加与 NSE 相关(ρ=-0.46,=0.0001)。在验证队列(41 例)中,该评分对 CPC 1-3 的敏感性为 100%(95% CI,60%-100%),特异性为 88%(95% CI,73%-97%)(AUC,0.96;95% CI,0.91-1.00)。
结合时间、连续性、反应性和振幅特征的评分可以估计 CA 后早期癫痫样 EEG 的预后价值,该评分与神经元损伤相关。