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奥卡西平与低钠血症。

Oxcarbazepine and Hyponatremia.

机构信息

Department of Neurology, Medical Academy, Lithuanian University of Health Sciences, A. Mickevičiaus Str. 9, LT 44307 Kaunas, Lithuania.

出版信息

Medicina (Kaunas). 2022 Apr 19;58(5):559. doi: 10.3390/medicina58050559.

Abstract

Background and Objectives: Hyponatremia is one of the most common adverse effects in patients treated with oxcarbazepine (OXC). Different risk factors for OXC-induced hyponatremia have been described as age, female gender, dosage, and combination with other drugs During our clinical practice, we noticed that a longer duration of treatment with OXC could be associated with a higher risk of hyponatremia, therefore, in this study, we aimed to evaluate factors that may increase the risk of OXC-induced hyponatremia. Materials and Methods: Data were retrospectively collected from our clinical database at the Department of Neurology of the Hospital of Lithuanian University of Health Sciences Kaunas Clinics. The sample was divided into three groups: OXC consumers (n = 31), other anti-seizure medications (ASMs) consumers (n = 43), and controls absent ASMs (n = 31). All groups were matched by age and gender. Hyponatremia was defined as <136 mmol/L. Results: The frequency of hyponatremia was significantly higher among OXC patients (61.3%) compared to other ASM patients (5.4%) and controls (3.2%). The mean serum sodium concentration in the OXC group was 133.1 ± 5.1 mmol/L. The frequency of severe hyponatremia among OXC-treated patients was 19.4%; this subgroup was older than patients with moderate hyponatremia and normonatremia and had a longer OXC treatment duration compared to a subgroup of normonatremia. The average duration of OXC therapy was 8.7 ± 5.5 years with a range from 1 to 21 years. Serum sodium concentration and duration of treatment with OXC demonstrated a significant negative correlation (r = −0,427, p = 0.017). Each year of therapy with OXC increased the risk of hyponatremia 1.3 times (OR = 1.326, 95% Cl 1.027−1.712, p = 0.031). Other factors (gender, age, polypharmacy, OXC dosage, and serum concentration) did not show a significant association with the development of hyponatremia. Conclusions: Longer duration of treatment with OXC is an important factor in the development and severity of hyponatremia.

摘要

背景与目的

奥卡西平(OXC)治疗的患者中,低钠血症是最常见的不良反应之一。已描述了不同的 OXC 诱导性低钠血症的危险因素,包括年龄、女性性别、剂量和与其他药物的联合使用。在我们的临床实践中,我们注意到 OXC 治疗时间较长可能与低钠血症风险增加相关,因此,在这项研究中,我们旨在评估可能增加 OXC 诱导性低钠血症风险的因素。

材料与方法

数据从立陶宛健康科学大学考纳斯临床医院神经内科的临床数据库中回顾性收集。样本分为三组:OXC 使用者(n=31)、其他抗癫痫药物(ASM)使用者(n=43)和无 ASM 的对照组(n=31)。所有组均按年龄和性别匹配。低钠血症定义为<136mmol/L。

结果

与其他 ASM 患者(5.4%)和对照组(3.2%)相比,OXC 患者低钠血症的发生率明显更高(61.3%)。OXC 组的平均血清钠浓度为 133.1±5.1mmol/L。OXC 治疗患者中严重低钠血症的发生率为 19.4%;该亚组比中度低钠血症和正常钠血症患者年龄更大,OXC 治疗持续时间也比正常钠血症亚组更长。OXC 治疗的平均持续时间为 8.7±5.5 年,范围为 1 至 21 年。血清钠浓度与 OXC 治疗时间呈显著负相关(r=-0.427,p=0.017)。OXC 治疗每增加一年,低钠血症的风险增加 1.3 倍(OR=1.326,95%CI 1.027-1.712,p=0.031)。其他因素(性别、年龄、多药治疗、OXC 剂量和血清浓度)与低钠血症的发生无显著相关性。

结论

OXC 治疗时间较长是低钠血症发生和严重程度的重要因素。

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