Department of Neuroscience, Central Clinical School, Monash University, Melbourne, Victoria, Australia.
Epilepsy Unit, Alfred Hospital, Melbourne, Victoria, Australia.
JAMA Neurol. 2022 Apr 1;79(4):334-341. doi: 10.1001/jamaneurol.2021.5420.
Early posttraumatic seizures (EPS) that may occur following a traumatic brain injury (TBI) are associated with poorer outcomes and development of posttraumatic epilepsy (PTE).
To evaluate risk factors for EPS, associated morbidity and mortality, and contribution to PTE.
DESIGN, SETTING, AND PARTICIPANTS: Data were collected from an Australian registry-based cohort study of adults (age ≥18 years) with moderate to severe TBI from January 2005 to December 2019, with 2-year follow-up. The statewide trauma registry, conducted on an opt-out basis in Victoria (population 6.5 million), had 15 152 patients with moderate to severe TBI identified via Abbreviated Injury Scale (AIS) head severity score, with an opt-out rate less than 0.5% (opt-out n = 136).
EPS were identified via International Statistical Classification of Diseases, Tenth Revision, Australian Modification (ICD-10-AM) codes recorded after the acute admission. Outcome measures also included in-hospital metrics, 2-year outcomes including PTE, and post-discharge mortality. Adaptive least absolute shrinkage and selection operator (LASSO) regression was used to build a prediction model for risk factors of EPS.
Among the 15 152 participants (10 457 [69%] male; median [IQR] age, 60 [35-79] y), 416 (2.7%) were identified with EPS, including 27 (0.2%) with status epilepticus. Significant risk factors on multivariable analysis for developing EPS were younger age, higher Charlson Comorbidity Index, TBI sustained from a low fall, subdural hemorrhage, subarachnoid hemorrhage, higher Injury Severity Score, and greater head injury severity, measured using the AIS and Glasgow Coma Score. After adjustment for confounders, EPS were associated with increased ICU admission and ICU length of stay, ventilation and duration, hospital length of stay, and discharge to inpatient rehabilitation rather than home, but not in-hospital mortality. Outcomes in TBI admission survivors at 24 months, including mortality (relative risk [RR] = 2.14; 95% CI, 1.32-3.46; P = .002), development of PTE (RR = 2.91; 95% CI, 2.22-3.81; P < .001), and use of antiseizure medications (RR = 2.44; 95% CI, 1.98-3.02; P < .001), were poorer for cases with EPS after adjustment for confounders. The prediction model for EPS had an area under the receiver operating characteristic curve of 0.72 (95% CI, 0.66-0.79), sensitivity of 66%, and specificity of 73% in the validation set.
We identified important risk factors for EPS following moderate to severe TBI. Early posttraumatic seizures were associated with longer ICU and hospital admissions, ICU ventilation, and poorer 24-month outcomes including mortality and development of PTE.
创伤性脑损伤(TBI)后可能发生的早期创伤后癫痫(EPS)与较差的预后和创伤后癫痫(PTE)的发展有关。
评估 EPS 的风险因素、相关发病率和死亡率以及对 PTE 的贡献。
设计、地点和参与者:数据来自澳大利亚基于登记的队列研究,纳入 2005 年 1 月至 2019 年 12 月期间年龄≥18 岁的中度至重度 TBI 成人患者,随访 2 年。全州创伤登记处(维多利亚州,人口 650 万)采用基于选择退出的方法进行,通过损伤严重程度评分的简明损伤量表(AIS)头部严重程度评分识别出 15152 例中度至重度 TBI 患者,选择退出率低于 0.5%(选择退出 n=136)。
通过国际疾病分类、第十次修订版、澳大利亚修正版(ICD-10-AM)在急性入院后记录的代码识别 EPS。其他测量指标还包括住院指标、包括 PTE 在内的 2 年结局以及出院后死亡率。自适应最小绝对收缩和选择算子(LASSO)回归用于建立 EPS 风险因素的预测模型。
在 15152 名参与者中(10457 [69%] 为男性;中位数[IQR]年龄为 60 [35-79] 岁),416 名(2.7%)被确定患有 EPS,包括 27 名(0.2%)患有癫痫持续状态。多变量分析中发生 EPS 的显著风险因素包括年龄较小、Charlson 合并症指数较高、由低坠落引起的 TBI、硬膜下血肿、蛛网膜下腔出血、损伤严重程度评分较高以及头部损伤严重程度较高,分别使用 AIS 和格拉斯哥昏迷评分进行测量。在调整混杂因素后,EPS 与 ICU 入院和 ICU 住院时间延长、通气和持续时间、住院时间延长以及出院至住院康复而不是出院回家有关,但与住院期间死亡率无关。在 24 个月时 TBI 幸存者的预后,包括死亡率(相对风险 [RR] =2.14;95%CI,1.32-3.46;P=0.002)、PTE 发展(RR=2.91;95%CI,2.22-3.81;P<0.001)和抗癫痫药物的使用(RR=2.44;95%CI,1.98-3.02;P<0.001),在调整混杂因素后,EPS 病例的预后更差。预测模型在验证组中的受试者工作特征曲线下面积为 0.72(95%CI,0.66-0.79),敏感性为 66%,特异性为 73%。
我们确定了中度至重度 TBI 后发生 EPS 的重要风险因素。早期创伤后癫痫与 ICU 和住院时间延长、ICU 通气以及 24 个月预后较差(包括死亡率和 PTE 发展)有关。