16815Torrecárdenas Hospital, Almería, Spain.
J Child Neurol. 2022 Jan;37(1):89-97. doi: 10.1177/08830738211056780. Epub 2021 Nov 24.
To determine the long-term probability of remission without antiepileptic treatment of common epileptic syndromes and of children without a specific syndromic diagnosis.
All children less than 14 years old with 2 or more unprovoked seizures seen at our hospital between June 1, 1994, and March 1, 2011 (n = 680), were included and prospectively followed up until August 15, 2020. Syndromic diagnosis was made retrospectively but blinded to subsequent evolution, employing the data available at 6 months after diagnosis and under predefined operational criteria.
The Kaplan-Meier estimate of the probability of achieving a remission period of at least 5 years, with neither seizures nor antiepileptic treatment at 14 years was 97% for well-defined childhood epilepsy with centrotemporal spikes, 82% for uncertain childhood epilepsy with centrotemporal spikes, 85% for well-defined Panayiotopoulos syndrome, 88% for uncertain Panayiotopoulos syndrome, 93% for nonfamilial self-limited infantile epilepsy, 100% for familial self-limited infantile epilepsy, 86% for absence epilepsy, 6% for juvenile myoclonic epilepsy, 71% for cryptogenic West syndrome, 72% for patients with no associated neurologic deficits and no specific syndromic diagnosis, 65% for symptomatic West syndrome, and 40% for patients with associated neurologic deficits and no specific syndromic diagnosis.
The study results highlight the long-term outcomes of the main epileptic syndromes and also of the patients with no syndromic diagnosis.
确定常见癫痫综合征和无特定综合征诊断的儿童在不进行抗癫痫治疗情况下的长期缓解概率。
本研究纳入了 1994 年 6 月 1 日至 2011 年 3 月 1 日期间在我院就诊的年龄小于 14 岁且有 2 次或以上无诱因发作的所有儿童(n=680),并对其进行前瞻性随访,随访时间截至 2020 年 8 月 15 日。采用 6 个月后诊断时及预定义操作标准下的可用数据进行回顾性综合征诊断,但对后续演变情况设盲。
Kaplan-Meier 估计在 14 岁时无癫痫发作且无抗癫痫治疗的情况下,至少 5 年缓解期的概率分别为:明确的儿童中央颞区棘波灶癫痫为 97%、不确定的儿童中央颞区棘波灶癫痫为 82%、明确的 Panayiotopoulos 综合征为 85%、不确定的 Panayiotopoulos 综合征为 88%、非家族性自限性婴儿癫痫为 93%、家族性自限性婴儿癫痫为 100%、失神癫痫为 86%、青少年肌阵挛癫痫为 6%、隐源性 West 综合征为 71%、无相关神经功能缺损且无特定综合征诊断的患者为 72%、症状性 West 综合征为 65%、有相关神经功能缺损且无特定综合征诊断的患者为 40%。
本研究结果突出了主要癫痫综合征患者以及无综合征诊断患者的长期预后。