Does diabetes mellitus affect the safety profile of valproic acid for the treatment of status epilepticus? A retrospective cohort study.

Annekatrin Müller, Judith von Hofen-Hohloch, Carolin Awissus, Jens Przybilla, Achmed Mrestani, Joseph Classen
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引用次数: 1

Abstract

Background: In the treatment of status epilepticus less is known about the influence of comorbidities on the safety profile of anticonvulsive drugs. Especially patients with diabetes mellitus may be predisposed to certain adverse events that have been related to therapy with valproic acid. In this single-center retrospective cohort study we examined if the complications of the intravenous treatment with valproic acid is different in patients with or without diabetes.

Methods: Patients who were treated for status epilepticus with intravenous valproic acid between 2008 and 2020 were identified. Primary endpoint was the discontinuation of therapy with valproic acid due to adverse events. Relevant secondary endpoints were the functional status at the time of discharge from hospital in comparison to the premorbid state and the in-hospital mortality. Both groups (patients with or without diabetes) were compared by Mann-Whitney U-Test or Pearson´s Chi2 test. To identify therapy with valproic acid as a risk factor of in-hospital mortality, a binary regression model was used.

Results: During the study period 408 patients and 482 episodes of status epilepticus were treated with intravenous valproic acid. Group comparisons did not reveal a significant difference in the rates of discontinuation of therapy. A difference was found in the rate of thrombocytopenia (p = 0.015), which occurred more often in patients with diabetes. In total, 36 hypoglycemic episodes could be identified, two occurred spontaneously under intravenous valproic acid. After correction for potential confounders, continuous therapy with valproic acid could not be confirmed as an independent risk factor for in-hospital mortality (p = 0.079). In patients with diabetes, the proportion of patients with a good functional state, indicated by the modified Rankin Scale, was significantly lower in both times (premorbid: 55% vs. 69%, p = 0.008; at discharge: 22% vs. 36%, p = 0.004).

Conclusions: Tolerability of the treatment with valproic acid was similar in patients with or without diabetes. Diabetes as a relevant comorbidity can signal a potentially increased risk of a poor outcome after status epilepticus.

Trial registration: The study was registered at the German Clinical Trials Register on 8 April 2022 (DRKS 00,027,836).

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糖尿病会影响丙戊酸治疗癫痫持续状态的安全性吗?回顾性队列研究。
背景:在癫痫持续状态的治疗中,合并症对抗惊厥药物安全性的影响尚不清楚。特别是糖尿病患者可能易发生与丙戊酸治疗相关的某些不良事件。在这项单中心回顾性队列研究中,我们检查了静脉注射丙戊酸治疗糖尿病患者和非糖尿病患者的并发症是否不同。方法:对2008 ~ 2020年间静脉注射丙戊酸治疗癫痫持续状态的患者进行分析。主要终点是由于不良事件而停止丙戊酸治疗。相关的次要终点是出院时的功能状态与发病前状态和住院死亡率的比较。两组(合并或不合并糖尿病)采用Mann-Whitney U-Test或Pearson ' s Chi2检验进行比较。为了确定丙戊酸治疗是住院死亡率的一个危险因素,我们使用了一个二元回归模型。结果:在研究期间,静脉注射丙戊酸治疗408例患者和482次癫痫持续状态。组间比较未发现停药率有显著差异。在血小板减少率方面发现了差异(p = 0.015),糖尿病患者更常发生血小板减少。总共有36例低血糖发作,其中2例在静脉注射丙戊酸后自发发生。在对潜在混杂因素进行校正后,丙戊酸持续治疗不能被证实为院内死亡率的独立危险因素(p = 0.079)。在糖尿病患者中,采用改良Rankin量表显示功能状态良好的患者比例在两种情况下均显著降低(发病前:55% vs. 69%, p = 0.008;出院时:22% vs. 36%, p = 0.004)。结论:有或无糖尿病患者丙戊酸治疗耐受性相似。糖尿病作为一种相关的合并症可能预示着癫痫持续状态后不良预后的潜在风险增加。试验注册:该研究于2022年4月8日在德国临床试验注册中心注册(DRKS 00,027,836)。
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