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耐药性癫痫患者的迷走神经刺激疗法(CORE-VNS):真实世界上市后综合结局登记的原理与设计

Vagus nerve stimulation therapy in people with drug-resistant epilepsy (CORE-VNS): rationale and design of a real-world post-market comprehensive outcomes registry.

作者信息

Sen Arjune, Verner Ryan, Valeriano James P, Lee Ricky, Zafar Muhammad, Thomas Rhys, Kotulska Katarzyna, Jespers Ellen, Dibué Maxine, Kwan Patrick

机构信息

Nuffield Department of Clinical Neurosciences, John Radcliffe Hospital, Oxford, Oxfordshire, UK.

Clinical and Medical Affairs, LivaNova Plc, London, UK.

出版信息

BMJ Neurol Open. 2021 Dec 23;3(2):e000218. doi: 10.1136/bmjno-2021-000218. eCollection 2021.

Abstract

INTRODUCTION

The Vagus Nerve Stimulation Therapy System (VNS Therapy) is an adjunctive neuromodulatory therapy that can be efficacious in reducing the frequency and severity of seizures in people with drug-resistant epilepsy (DRE). CORE-VNS aims to examine the long-term safety and clinical outcomes of VNS in people with DRE.

METHODS AND ANALYSIS

The CORE-VNS study is an international, multicentre, prospective, observational, all-comers, post-market registry. People with DRE receiving VNS Therapy for the first time as well as people being reimplanted with VNS Therapy are eligible. Participants have a baseline visit (prior to device implant). They will be followed for a minimum of 36 months and a maximum of 60 months after implant. Analysis endpoints include seizure frequency (average number of events per month), seizure severity (individual-rated categorical outcome including very mild, mild, moderate, severe or very severe) as well as non-seizure outcomes such as adverse events, use of antiseizure medications, use of other non-pharmacological therapies, quality of life, validated measures of quality of sleep (Pittsburgh Sleep Quality Index or Children's Sleep Habit Questionnaire) and healthcare resource utilisation. While the CORE-VNS registry was not expressly designed to test hypotheses, subgroup analyses and exploratory analysis that require hypothesis testing will be conducted across propensity score matched treatment groups, where possible based on sampling.

ETHICS AND DISSEMINATION

The CORE-VNS registry has already enrolled 823 participants from 61 centres across 15 countries. Once complete, CORE-VNS will represent one of the largest real-world clinical data sets to allow a more comprehensive understanding of the management of DRE with adjunctive VNS. Manuscripts derived from this database will shed important new light on the characteristics of people receiving VNS Therapy; the practical use of VNS across different countries, and factors influencing long-term response.

TRAIL REGISTRATION NUMBER

NCT03529045.

摘要

简介

迷走神经刺激疗法系统(VNS疗法)是一种辅助神经调节疗法,对降低耐药性癫痫(DRE)患者的癫痫发作频率和严重程度可能有效。CORE-VNS旨在研究VNS在DRE患者中的长期安全性和临床疗效。

方法与分析

CORE-VNS研究是一项国际性、多中心、前瞻性、观察性、面向所有患者的上市后注册研究。首次接受VNS疗法的DRE患者以及接受VNS疗法再次植入的患者均符合条件。参与者有一次基线访视(在设备植入前)。植入后将对他们进行至少36个月、最长60个月的随访。分析终点包括癫痫发作频率(每月发作事件的平均数量)、癫痫发作严重程度(个体评定的分类结果,包括非常轻微、轻微、中度、重度或非常严重)以及非癫痫发作结果,如不良事件、抗癫痫药物的使用、其他非药物疗法的使用、生活质量、经过验证的睡眠质量测量指标(匹兹堡睡眠质量指数或儿童睡眠习惯问卷)和医疗资源利用情况。虽然CORE-VNS注册研究并非专门设计用于检验假设,但将在倾向评分匹配的治疗组中进行需要假设检验的亚组分析和探索性分析,尽可能基于抽样。

伦理与传播

CORE-VNS注册研究已招募了来自15个国家61个中心的823名参与者。一旦完成,CORE-VNS将代表最大的真实世界临床数据集之一,以便更全面地了解辅助VNS治疗DRE的情况。从该数据库得出的手稿将为接受VNS疗法的患者特征、VNS在不同国家的实际应用以及影响长期反应的因素提供重要的新见解。

试验注册号

NCT03529045。

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