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ILAE SUDEP 工作组关于全球可穿戴式癫痫发作检测设备使用的国家建议和实践报告:全球调查。

Report of the ILAE SUDEP Task Force on national recommendations and practices around the world regarding the use of wearable seizure detection devices: A global survey.

机构信息

Institute of Neuroscience and Physiology, Department of Clinical Neuroscience, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.

Department of Neurology, Sahlgrenska University Hospital, Gothenburg, Sweden.

出版信息

Epilepsia Open. 2023 Dec;8(4):1271-1278. doi: 10.1002/epi4.12801. Epub 2023 Aug 22.

Abstract

Wearable seizure detection devices have the potential to address unmet needs of people with epilepsy. A recently published evidence-based international guideline recommends using such devices for safety indications in patients with tonic-clonic seizures (TCS). Our objective was to map existing guidelines and clinical practices at national level. We conducted a survey of the International League Against Epilepsy (ILAE) chapters regarding national recommendations and practical circumstances for prescribing seizure detection devices, and another survey of physicians in the ILAE constituency anywhere in the world, concerning their views and practices regarding recommendations for and prescription of such devices. Fifty-eight ILAE chapters (response rate 48%) and 157 physicians completed the surveys. More than two-thirds of responding countries do not have standards on wearables for seizure detection, although they indicated availability of such devices. The most often recognized indications were safety and objective seizure quantification. In nearly half of countries, devices are purchased by patients or caregivers, and either lack a uniform reimbursement scheme (41%) or patients pay the full cost for the device (48%). Tonic-clonic seizure frequency, nocturnal seizures, and previous injuries were the main factors that influenced the surveyed physicians to recommend wearable seizure detection devices. Our results document the need to implement international clinical practice guidelines at national level and to consider these when deciding upon reimbursement of seizure detection devices.

摘要

可穿戴式癫痫发作检测设备有可能满足癫痫患者的未满足需求。最近发布的一项基于证据的国际指南建议将此类设备用于强直-阵挛性发作(TCS)患者的安全指征。我们的目标是在国家层面上绘制现有指南和临床实践图。我们对国际抗癫痫联盟(ILAE)各分会进行了一项调查,了解有关国家对癫痫发作检测设备的建议和开具处方的实际情况,以及对世界任何地方的 ILAE 选区的医生进行了另一项调查,了解他们对这些设备的建议和开具处方的看法和做法。有 58 个 ILAE 分会(响应率为 48%)和 157 名医生完成了调查。超过三分之二的回应国家没有针对癫痫发作检测的可穿戴设备标准,尽管他们表示有这些设备。最常被认可的指征是安全性和客观的癫痫发作量化。在近一半的国家中,设备由患者或护理人员购买,并且要么缺乏统一的报销计划(41%),要么患者为设备支付全部费用(48%)。强直-阵挛性发作频率、夜间发作和以前的损伤是影响调查医生推荐可穿戴式癫痫发作检测设备的主要因素。我们的研究结果表明,需要在国家层面实施国际临床实践指南,并在决定癫痫发作检测设备的报销时考虑这些指南。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d4e9/10690692/d35e39a8e52b/EPI4-8-1271-g003.jpg

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