Department of Neurology, Massachusetts General Hospital, Boston, MA.
Department of Emergency Neurology and Neurocritical Care, Massachusetts General Hospital, Boston, MA.
Ann Neurol. 2018 Apr;83(4):858-862. doi: 10.1002/ana.25211. Epub 2018 Apr 10.
We hypothesize that epileptiform abnormalities (EAs) in the electroencephalogram (EEG) during the acute period following traumatic brain injury (TBI) independently predict first-year post-traumatic epilepsy (PTE ). We analyze PTE risk factors in two cohorts matched for TBI severity and age (n = 50). EAs independently predict risk for PTE (odds ratio [OR], 3.16 [0.99, 11.68]); subdural hematoma is another independent risk factor (OR, 4.13 [1.18, 39.33]). Differences in EA rates are apparent within 5 days following TBI. Our results suggest that increased EA prevalence identifies patients at increased risk for PTE , and that EAs acutely post-TBI can identify patients most likely to benefit from antiepileptogenesis drug trials. Ann Neurol 2018;83:858-862.
我们假设创伤性脑损伤 (TBI) 后急性期脑电图 (EEG) 中的癫痫样异常 (EAs) 可独立预测创伤后第一年癫痫 (PTE)。我们分析了两个队列的 PTE 风险因素,这些队列在 TBI 严重程度和年龄方面相匹配 (n=50)。EAs 可独立预测 PTE 风险 (比值比 [OR],3.16 [0.99, 11.68]);硬膜下血肿是另一个独立的危险因素 (OR,4.13 [1.18, 39.33])。TBI 后 5 天内 EAs 的发生率差异明显。我们的研究结果表明,EAs 发生率的增加可识别出 PTE 风险增加的患者,而 TBI 后急性 EAs 可识别出最有可能从抗癫痫发生药物试验中获益的患者。神经病学年鉴 2018;83:858-862.