Dynamic changes in comorbid conditions following vagus nerve stimulation for epilepsy.

IF 1.2 Q4 CLINICAL NEUROLOGY
Deng Chen, Lina Zhu, Ling Liu, Dong Zhou, Xintong Wu
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引用次数: 0

Abstract

Background: Vagus nerve stimulation (VNS) has been widely used in the clinical treatment of epilepsy, while its effects on comorbidities in epilepsy remain incompletely elucidated. This study aimed to evaluate the impact of VNS on comorbidities and quality of life in adult patients with epilepsy.

Methods: A longitudinal, multicenter cohort study was conducted from 2021 to 2024 among adult patients with epilepsy who underwent VNS implantation. We enrolled 128 participants from 83 hospitals. The inclusion criteria were patients over 18 years old, diagnosed with epilepsy according to the 2014 International League Against Epilepsy guidelines, and having complete data from at least two follow-up visits. Standard assessment tools, including diagnosis according to International Classification of Diseases, 10th Edition (ICD-10), Neurological Disorders Depression Inventory for Epilepsy (NDDI-E), Generalized Anxiexy Disorde-7 (GAD-7), Pittsburgh Sleep Quality Index (PSQI), and Quality of Life in Epilepsy-31 (QOLIE-31) were used to evaluate comorbidities and quality of life. Statistical analysis was performed using SPSS 26.0. The major clinical measurements were changes in the scales above before and after VNS implantation during follow-up. Generalized estimation model was applied to illustrate the effect over time an its relation to seizure control.

Results: A total of 113 participants met the inclusion criteria. Baseline characteristics were comparable between the comorbidity and non-comorbidity groups in terms of gender, seizure onset, age at VNS implantation, seizure types, or the number of antiseizure medications used. Significant improvements were observed from the implantation to the end of follow-up. The PSQI score decreased from 5.43 ± 3.60 to 4.44 ± 3.14 (P < 0.01), indicating better sleep quality. Depressive symptoms (NDDI-E) and anxiety symptoms (GAD-7) decreased significantly, with scores dropping from 6.49 ± 4.67 to 4.83 ± 4.37 (P < 0.01) and from 7.15 ± 5.06 to 4.95 ± 3.69 (P < 0.01), respectively. The QOLIE-31 score increased from 54.40 ± 15.70 to 61.33 ± 16.19 (P < 0.01), suggesting improved quality of life. Further analysis indicated that in the early second postoperative follow-up (1 month after implantation), the scales had already improved significantly (P < 0.001 for PSQI and QOLIE-31, P = 0.006 for NDDI-E and GAD-7). We did not find any statistically significant difference between patients with comorbidity and those without on the efficacy of any scales in this study. The efficacy of VNS on the four scales above was related to follow-up time, with a slightly rebound at the last two follow-ups. The NDDI-E as well as the GAD-7 scores were related to better seizure control according to the GEE model. Higher stimulation currents over 1 mA did not improve the efficacy of VNS on the comorbid conditions.

Conclusions: VNS implantation significantly improved sleep quality, mental health, and overall quality of life in adult patients with epilepsy. Such effects could be observed shortly after the implantation and were mostly long-lasting. Further research is needed to validate its long-term effects.

Abstract Image

迷走神经刺激治疗癫痫后合并症的动态变化。
背景:迷走神经刺激(VNS)已广泛应用于癫痫的临床治疗,但其对癫痫合并症的影响尚不完全清楚。本研究旨在评估VNS对成人癫痫患者合并症和生活质量的影响。方法:对2021 - 2024年接受VNS植入的成年癫痫患者进行纵向、多中心队列研究。我们招募了来自83家医院的128名参与者。纳入标准是18岁以上、根据2014年国际抗癫痫联盟指南诊断为癫痫的患者,并至少有两次随访的完整数据。采用国际疾病分类第十版(ICD-10)诊断、癫痫神经障碍抑郁量表(NDDI-E)、广泛性焦虑障碍-7 (GAD-7)、匹兹堡睡眠质量指数(PSQI)和癫痫生活质量-31 (QOLIE-31)等标准评估工具评估合并症和生活质量。采用SPSS 26.0进行统计学分析。随访期间观察的主要临床指标为VNS植入前后上述指标的变化。应用广义估计模型来说明随时间的影响及其与癫痫发作控制的关系。结果:共有113名受试者符合纳入标准。在性别、癫痫发作、植入VNS时的年龄、癫痫发作类型或使用的抗癫痫药物数量方面,共病组和非共病组的基线特征具有可比性。从植入到随访结束,观察到明显的改善。PSQI评分由5.43±3.60降至4.44±3.14 (P)。结论:VNS植入可显著改善成人癫痫患者的睡眠质量、心理健康及整体生活质量。这种效果可以在植入后不久观察到,并且大多数是持久的。需要进一步的研究来验证其长期影响。
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
Acta Epileptologica
Acta Epileptologica Medicine-Neurology (clinical)
CiteScore
2.00
自引率
0.00%
发文量
38
审稿时长
20 weeks
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