Sillanpää Matti, Schmidt Dieter
Department of Public Health, University of Turku, Turku, Finland.
Brain. 2009 Apr;132(Pt 4):989-98. doi: 10.1093/brain/awn357. Epub 2009 Jan 19.
In clinical practice, it is important to predict as soon as possible after diagnosis and starting treatment, which children are destined to develop medically intractable seizures and be at risk of increased mortality. In this study, we determined factors predictive of long-term seizure and mortality outcome in a population-based cohort of 102 children. At the end of the 40-year median follow-up, since their first seizure before the age of 16 years, 95 (93%) of 102 patients had entered one or more one-year remissions (1YR). In contrast, 7 (7%) patients never experienced any 1YR and their epilepsy was considered drug-resistant. Two factors present early in the course of treatment were found to be associated with adverse outcome. Having weekly seizures during the first year of treatment carried an 8-fold risk [hazard ratio 8.2 (1.6-43.0), P = 0.0125] of developing drug resistant epilepsy and a 2-fold risk of never entering terminal 1YR [hazard ratio 2.7 (1.5-5.0), P = 0.0010]. Having weekly seizures prior to treatment only slightly increased the risk to never enter terminal 1YR [hazard ratio 1.7 (1.04-2.9), P = 0.0350]. Thirteen of 102 patients (13%) died during follow-up. Long-term mortality was 9-fold higher for patients with symptomatic epilepsy [hazard ratio 9.0 (1.8-44.8), P = 0.0071]. Mortality was not, however, increased by having weekly seizures prior to or during the first year of treatment versus fewer seizures. Early seizure frequency can predict long-term seizure control during antiepileptic drug treatment, but not mortality. Aetiology, however, is predictive of both seizure outcome and mortality in childhood-onset epilepsy. Using these criteria allows early identification of children destined to develop intractable epilepsy and increased mortality.
在临床实践中,在诊断和开始治疗后尽快预测哪些儿童注定会发展为药物难治性癫痫并面临死亡率增加的风险非常重要。在本研究中,我们在一个基于人群的102名儿童队列中确定了预测长期癫痫发作和死亡率结局的因素。在40年的中位随访结束时,自他们16岁之前首次发作以来,102名患者中有95名(93%)进入了一个或多个一年缓解期(1YR)。相比之下,7名(7%)患者从未经历过任何1YR,他们的癫痫被认为是耐药性的。发现治疗过程早期出现的两个因素与不良结局相关。治疗第一年每周发作与发展为耐药性癫痫的风险高8倍[风险比8.2(1.6 - 43.0),P = 0.0125]以及从未进入最终1YR的风险高2倍[风险比2.7(1.5 - 5.0),P = 0.0010]相关。仅在治疗前每周发作只会略微增加从未进入最终1YR的风险[风险比1.7(1.04 - 2.9),P = 0.0350]。102名患者中有13名(13%)在随访期间死亡。症状性癫痫患者的长期死亡率高9倍[风险比9.0(1.8 - 44.8),P = 0.0071]。然而,与发作较少相比,治疗前或治疗第一年每周发作并不会增加死亡率。早期癫痫发作频率可预测抗癫痫药物治疗期间的长期癫痫控制,但不能预测死亡率。然而,病因可预测儿童期癫痫的发作结局和死亡率。使用这些标准可以早期识别注定会发展为难治性癫痫并增加死亡率的儿童。