Efficacy of oral sodium chloride in reducing the incidence of hyponatremia in children with epilepsy receiving oxcarbazepine monotherapy: A randomized controlled trial (SCHO Trial)

IF 2.3 3区 医学 Q2 BEHAVIORAL SCIENCES Epilepsy & Behavior Pub Date : 2024-07-12 DOI:10.1016/j.yebeh.2024.109939
KC Neha , Prateek Kumar Panda , Anissa Atif Mirza , Puneet Dhamija , Indar Kumar Sharawat
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Abstract

Introduction

Hyponatremia is a well-documented adverse effect of oxcarbazepine treatment, but no clinical trial has yet been conducted to explore any intervention for reducing the incidence of hyponatremia.

Materials and Methods

This open-label trial evaluated the efficacy of add-on daily oral sodium chloride supplementation of 1–2 g/day for 12 weeks in reducing the incidence of hyponatremia in children receiving oxcarbazepine monotherapy aged 1–18 years. Apart from comparing the incidence of symptomatic and severe hyponatremia, serum and urine sodium levels, serum and urine osmolality, changes in behavior and cognition, and the number of participants with recurrence of seizures and requiring additional antiseizure medication (ASM) were also compared.

Results

A total of 120 children (60 in each group) were enrolled. The serum sodium level at 12 weeks in the intervention group was higher than that of the control group (136.5 ± 2.6 vs 135.4 ± 2.5 mEq/L, p = 0.01). The number of patients with hyponatremia was significantly lower in the intervention group (4/60vs14/60, p = 0.01). However, the incidence of symptomatic and severe hyponatremia (0/60vs1/60, p = 0.67 for both), changes in social quotient and child behavior checklist total score (0.6 ± 0.8 vs 0.7 ± 0.5, p = 0.41 and 0.9 ± 1.2 vs 1.1 ± 0.9, p = 0.30 respectively), the number of patients with breakthrough seizures (9/60vs10/60, p = 0.89), and the number of patients requiring additional ASMs (8/60vs10/60, p = 0.79) were comparable in both groups.

Conclusions

Daily oral sodium chloride supplementation is safe and efficacious in reducing the incidence of hyponatremia in children with epilepsy receiving oxcarbazepine monotherapy. However, sodium chloride supplementation does not significantly reduce more clinically meaningful outcome measures like symptomatic and severe hyponatremia.

Trial registry No. CTRI/2021/12/038388.

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口服氯化钠对降低接受奥卡西平单药治疗的癫痫患儿低钠血症发生率的疗效:随机对照试验(SCHO 试验)。
简介:低钠血症是奥卡西平治疗的一种不良反应,但目前尚未开展任何临床试验来探索降低低钠血症发生率的干预措施:这项开放标签试验评估了在接受奥卡西平单药治疗的1-18岁儿童中,每日口服氯化钠1-2克,持续12周,对降低低钠血症发生率的疗效。除了比较症状性低钠血症和严重低钠血症的发生率外,还比较了血清和尿钠水平、血清和尿渗透压、行为和认知能力的变化以及癫痫复发和需要额外服用抗癫痫药物(ASM)的参与者人数:共有 120 名儿童(每组 60 名)参加了治疗。干预组 12 周时的血清钠水平高于对照组(136.5 ± 2.6 vs 135.4 ± 2.5 mEq/L,p = 0.01)。干预组出现低钠血症的人数明显少于对照组(4/60 对 14/60,p = 0.01)。然而,无症状和严重低钠血症的发生率(0/60 对 1/60,两者的 p = 0.67)、社会商数和儿童行为检查表总分的变化(分别为 0.6 ± 0.8 对 0.7 ± 0.5,p = 0.41 和 0.9 ± 1.2 对 1.1 ± 0.9,p = 0.30)和儿童行为检查表总分的变化(分别为 0.6 ± 0.8 对 0.7 ± 0.5,p = 0.41 和 0.9 ± 1.2 对 1.1 ± 0.9,p = 0.30)均低于干预组。9,p = 0.30),两组中出现突破性癫痫发作的患者人数(9/60 vs 10/60,p = 0.89)和需要额外ASMs的患者人数(8/60 vs 10/60,p = 0.79)相当:结论:每日口服氯化钠补充剂可安全有效地降低接受奥卡西平单药治疗的癫痫患儿的低钠血症发生率。然而,氯化钠补充剂并不能显著降低症状性和严重低钠血症等更具临床意义的结果指标。试验登记号:CTRI/2021/12/038388。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Epilepsy & Behavior
Epilepsy & Behavior 医学-行为科学
CiteScore
5.40
自引率
15.40%
发文量
385
审稿时长
43 days
期刊介绍: Epilepsy & Behavior is the fastest-growing international journal uniquely devoted to the rapid dissemination of the most current information available on the behavioral aspects of seizures and epilepsy. Epilepsy & Behavior presents original peer-reviewed articles based on laboratory and clinical research. Topics are drawn from a variety of fields, including clinical neurology, neurosurgery, neuropsychiatry, neuropsychology, neurophysiology, neuropharmacology, and neuroimaging. From September 2012 Epilepsy & Behavior stopped accepting Case Reports for publication in the journal. From this date authors who submit to Epilepsy & Behavior will be offered a transfer or asked to resubmit their Case Reports to its new sister journal, Epilepsy & Behavior Case Reports.
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