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儿童未经治疗的强直阵挛性发作的临床病程:一项基于医院的前瞻性研究。

Clinical course of untreated tonic-clonic seizures in childhood: prospective, hospital based study.

作者信息

van Donselaar C A, Brouwer O F, Geerts A T, Arts W F, Stroink H, Peters A C

机构信息

Department of Neurology, University Hospital, Rotterdam Dijkzigt, Netherlands.

出版信息

BMJ. 1997 Feb 8;314(7078):401-4. doi: 10.1136/bmj.314.7078.401.

Abstract

OBJECTIVE

To assess decleration and acceleration in the disease process in the initial phase of epilepsy in children with new onset tonic-clonic seizures.

STUDY DESIGN

Hospital based follow up study.

SETTING

Two university hospitals, a general hospital, and a children's hospital in the Netherlands.

PATIENTS

204 children aged 1 month to 16 years with idiopathic or remote symptomatic, newly diagnosed, tonic-clonic seizures, of whom 123 were enrolled at time of their first ever seizure; all children were followed until the start of drug treatment (78 children), the occurrence of the fourth untreated seizure (41 children), or the end of the follow up period of two years (85 untreated children).

MAIN OUTCOME MEASURES

Analysis of disease pattern from first ever seizure. The pattern was categorised as decelerating if the child became free of seizures despite treatment being withheld. In cases with four seizures, the pattern was categorised as decelerating if successive intervals increased or as accelerating if intervals decreased. Patterns in the remaining children were classified as uncertain.

RESULTS

A decelerating pattern was found in 83 of 85 children who became free of seizures without treatment. Three of the 41 children with four or more untreated seizures showed a decelerating pattern and eight an accelerating pattern. In 110 children the disease process could not be classified, mostly because drug treatment was started after the first, second, or third seizure. The proportion of children with a decelerating pattern (42%, 95% confidence interval 35% to 49%) may be a minimum estimate because of the large number of patients with an uncertain disease pattern.

CONCLUSIONS

Though untreated epilepsy is commonly considered to be a progressive disorder with decreasing intervals between seizures, a large proportion of children with newly diagnosed, unprovoked tonic-clonic seizures have a decelerating disease process. The fear that tonic-clonic seizures commonly evolve into a progressive disease should not be used as an argument in favour of early drug treatment in children with epilepsy.

摘要

目的

评估新发性强直阵挛发作儿童癫痫初始阶段疾病进程的减速和加速情况。

研究设计

基于医院的随访研究。

研究地点

荷兰的两家大学医院、一家综合医院和一家儿童医院。

研究对象

204名年龄在1个月至16岁之间,患有特发性或远隔症状性、新诊断的强直阵挛发作的儿童,其中123名在首次发作时被纳入研究;所有儿童均随访至开始药物治疗(78名儿童)、出现第四次未治疗发作(41名儿童)或两年随访期结束(85名未治疗儿童)。

主要观察指标

分析首次发作后的疾病模式。如果儿童在未进行治疗的情况下不再发作,则该模式被分类为减速。在发作四次的病例中,如果连续发作间隔增加,则模式被分类为减速;如果间隔减少,则模式被分类为加速。其余儿童的模式分类为不确定。

结果

85名未治疗即不再发作的儿童中,有83名呈现减速模式。41名有四次或更多次未治疗发作的儿童中,3名呈现减速模式,8名呈现加速模式。110名儿童的疾病进程无法分类,主要是因为在第一次、第二次或第三次发作后开始了药物治疗。由于大量患者的疾病模式不确定,减速模式儿童的比例(42%,95%置信区间35%至49%)可能是最低估计值。

结论

虽然未经治疗的癫痫通常被认为是一种发作间隔逐渐缩短的进行性疾病,但很大一部分新诊断的、无诱因的强直阵挛发作儿童的疾病进程是减速的。不应将强直阵挛发作通常会演变为进行性疾病的担忧作为支持对癫痫儿童进行早期药物治疗的理由。

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