Department of Neurology, University of Rochester, Rochester, New York, USA.
University Teaching Hospitals Children's Hospital, Lusaka, Zambia.
Epilepsia Open. 2024 Apr;9(2):750-757. doi: 10.1002/epi4.12921. Epub 2024 Feb 17.
To determine the long-term outcomes, including mortality and recurrent seizures, among children living with HIV (CLWH) who present with new onset seizure.
Zambian CLWH and new onset seizure were enrolled prospectively to determine the risk of and risk factors for recurrent seizures. Demographic data, clinical profiles, index seizure etiology, and 30-day mortality outcomes were previously reported. After discharge, children were followed quarterly to identify recurrent seizures and death. Given the high risk of early death, risk factors for recurrent seizure were evaluated using a model that adjusted for mortality.
Among 73 children enrolled, 28 died (38%), 22 within 30-days of the index seizure. Median follow-up was 533 days (IQR 18-957) with 5% (4/73) lost to follow-up. Seizure recurrence was 19% among the entire cohort. Among children surviving at least 30-days after the index seizure, 27% had a recurrent seizure. Median time from index seizure to recurrent seizure was 161 days (IQR 86-269). Central nervous system opportunistic infection (CNS OI), as the cause for the index seizure was protective against recurrent seizures and higher functional status was a risk factor for seizure recurrence.
Among CLWH presenting with new onset seizure, mortality risks remain elevated beyond the acute illness period. Recurrent seizures are common and are more likely in children with higher level of functioning even after adjusting for the outcome of death. Newer antiseizure medications appropriate for co-usage with antiretroviral therapies are needed for the care of these children. CNS OI may represent a potentially reversible provocation for the index seizure, while seizures in high functioning CLWH without a CNS OI may be the result of a prior brain injury or susceptibility to seizures unrelated to HIV and thus represent an ongoing predisposition to seizures.
This study followed CLWH who experienced a new onset seizure to find out how many go on to have more seizures and identify any patient characteristics associated with having more seizures. The study found that mortality rates continue to be high beyond the acute clinical presentation with new onset seizure. Children with a CNS OI causing the new onset seizure had a lower risk of later seizures, possibly because the trigger for the seizure can be treated. In contrast, high functioning children without a CNS OI were at higher risk of future seizures.
确定新发病例的 HIV 感染儿童(CLWH)中出现新发癫痫的长期结局,包括死亡率和复发性癫痫。
前瞻性纳入赞比亚 CLWH 和新发癫痫,以确定复发性癫痫的风险和危险因素。先前报道了人口统计学数据、临床特征、指数性癫痫病因和 30 天死亡率结局。出院后,每季度对儿童进行随访,以识别复发性癫痫和死亡。由于早期死亡风险高,因此使用调整死亡率的模型评估了复发性癫痫的危险因素。
73 名患儿中,28 例死亡(38%),22 例死亡发生在指数性癫痫发作后 30 天内。中位随访时间为 533 天(IQR 18-957),有 5%(4/73)失访。整个队列中癫痫复发率为 19%。在至少存活 30 天的指数性癫痫发作的患儿中,27%出现复发性癫痫。从指数性癫痫发作到复发性癫痫发作的中位时间为 161 天(IQR 86-269)。中枢神经系统机会性感染(CNS OI)作为指数性癫痫发作的病因可预防复发性癫痫发作,功能状态较高是癫痫发作复发的危险因素。
在新发病例的 CLWH 中,死亡率在急性疾病期过后仍处于较高水平。即使在考虑到死亡结局后,复发性癫痫也很常见,且在功能状态较高的患儿中更常见。需要新的抗癫痫药物与抗逆转录病毒疗法联合使用,以治疗这些儿童。CNS OI 可能代表指数性癫痫发作的潜在可逆触发因素,而无 CNS OI 的高功能 CLWH 中的癫痫发作可能是先前脑损伤或对与 HIV 无关的癫痫发作易感性的结果,因此代表持续的癫痫发作倾向。