Institute of Public Health, Charité - Universitätsmedizin Berlin, Berlin, Germany.
Department of Neurology with Experimental Neurology, Charité - Universitätsmedizin Berlin, Berlin, Germany.
BMC Health Serv Res. 2024 Aug 27;24(1):994. doi: 10.1186/s12913-024-11076-y.
Epilepsy and other seizure disorders account for a high disease burden in Germany. As a timely diagnosis and accurate treatment are crucial, improving the management of these disorders is important. Outside of Germany, outpatient long-term video EEGs (ALVEEGs) have demonstrated the potential to support the diagnosis and management of epilepsy and other seizure disorders. This study aims to evaluate the implementation of ALVEEGs as a new diagnostic pathway in eastern parts of Germany to diagnose epilepsy and other seizure disorders and to assess if ALVEEGs are equally effective as the current inpatient-monitoring gold standard, which is currently only available at a limited number of specialized centers in Germany.
ALVEEG is a prospective, multicenter, randomized controlled equivalence trial, involving five epilepsy centers in the eastern states of Germany. Patients will be randomized into either intervention (IG) or control group (CG), using a permuted block randomization. The sample size targeted is 688 patients, continuously recruited over the trial. The IG will complete an ALVEEG in a home setting, including getting access to a smartphone app to document seizure activity. The CG will receive care as usual, i.e., inpatient long-term video-EEG monitoring. The primary outcome is the proportion of clinical questions being solved in the IG compared to the CG. Secondary outcomes include hospital stays, time until video EEG, time until diagnosis and result discussion, patients' health status, quality of life and health competence, and number and form of epilepsy-related events and epileptiform activity. Alongside the trial, a process implementation and health economic evaluation will be conducted.
The extensive evaluation of this study, including an implementation and health economic evaluation, will provide valuable information for health policy decision-makers to optimize future delivery of neurological care to patients affected by epilepsy and other seizure disorders and on the uptake of ALVEEG into standard care in Germany.
German Clinical Trials Register (DRKS00032220), date registered: December 11, 2023.
癫痫和其他发作性疾病在德国造成了很高的疾病负担。由于及时诊断和准确治疗至关重要,因此改善这些疾病的管理非常重要。在德国以外,门诊长程视频脑电图(ALVEEG)已证明有助于支持癫痫和其他发作性疾病的诊断和管理。本研究旨在评估在德国东部地区实施 ALVEEG 作为新的诊断途径,以诊断癫痫和其他发作性疾病,并评估其是否与目前仅在德国少数专门中心提供的住院监测黄金标准同样有效。
ALVEEG 是一项前瞻性、多中心、随机对照等效性试验,涉及德国东部的五个癫痫中心。患者将被随机分为干预组(IG)或对照组(CG),采用随机分组。试验的目标样本量为 688 名连续招募的患者。IG 将在家中进行 ALVEEG,包括使用智能手机应用程序记录发作活动。CG 将接受常规护理,即住院长程视频脑电图监测。主要结局是 IG 中解决临床问题的比例与 CG 相比。次要结局包括住院时间、视频 EEG 时间、诊断和结果讨论时间、患者健康状况、生活质量和健康能力、癫痫相关事件和癫痫样活动的数量和形式。在试验的同时,还将进行实施过程和健康经济学评估。
该研究的广泛评估,包括实施和健康经济学评估,将为卫生政策决策者提供有价值的信息,以优化未来为受癫痫和其他发作性疾病影响的患者提供神经科护理,并将 ALVEEG 纳入德国标准护理。
德国临床试验注册(DRKS00032220),注册日期:2023 年 12 月 11 日。