Bilateral hypoglossal nerve stimulation for treatment of adult obstructive sleep apnoea

P. Eastwood, M. Barnes, S. MacKay, J. Wheatley, D. Hillman, Xuân-Lan Nguyên, R. Lewis, M. Campbell, B. Pételle, J. Walsh, A. Jones, C. Palme, A. Bizon, N. Meslier, C. Bertolus, K. Maddison, L. Laccourreye, G. Raux, K. Denoncin, V. Attali, F. Gagnadoux, S. Launois
{"title":"Bilateral hypoglossal nerve stimulation for treatment of adult obstructive sleep apnoea","authors":"P. Eastwood, M. Barnes, S. MacKay, J. Wheatley, D. Hillman, Xuân-Lan Nguyên, R. Lewis, M. Campbell, B. Pételle, J. Walsh, A. Jones, C. Palme, A. Bizon, N. Meslier, C. Bertolus, K. Maddison, L. Laccourreye, G. Raux, K. Denoncin, V. Attali, F. Gagnadoux, S. Launois","doi":"10.1183/13993003.01320-2019","DOIUrl":null,"url":null,"abstract":"Background and aim Hypoglossal nerve stimulation (HNS) decreases obstructive sleep apnoea (OSA) severity via genioglossus muscle activation and decreased upper airway collapsibility. This study assessed the safety and effectiveness at 6 months post-implantation of a novel device delivering bilateral HNS via a small implanted electrode activated by a unit worn externally, to treat OSA: the Genio™ system. Methods This prospective, open-label, non-randomised, single-arm treatment study was conducted at eight centres in three countries (Australia, France and the UK). Primary outcomes were incidence of device-related serious adverse events and change in the apnoea–hypopnoea index (AHI). The secondary outcome was the change in the 4% oxygen desaturation index (ODI). Additional outcomes included measures of sleepiness, quality of life, snoring and device use. This trial was registered with ClinicalTrials.gov, number NCT03048604. Results 22 out of 27 implanted participants (63% male, aged 55.9±12.0 years, body mass index (BMI) 27.4±3.0 kg·m−2) completed the protocol. At 6 months BMI was unchanged (p=0.85); AHI decreased from 23.7±12.2 to 12.9±10.1 events·h−1, a mean change of 10.8 events·h−1 (p<0.001); and ODI decreased from 19.1±11.2 to 9.8±6.9 events·h−1, a mean change of 9.3 events·h−1 (p<0.001). Daytime sleepiness (Epworth Sleepiness Scale; p=0.01) and sleep-related quality of life (Functional Outcomes of Sleep Questionnaire-10; p=0.02) both improved significantly. The number of bed partners reporting loud, very intense snoring, or leaving the bedroom due to participant snoring decreased from 96% to 35%. 91% of participants reported device use >5 days per week, and 77% reported use for >5 h per night. No device-related serious adverse events occurred during the 6-month post-implantation period. Conclusions Bilateral HNS using the Genio™ system reduces OSA severity and improves quality of life without device-related complications. The results are comparable with previously published HNS systems despite minimal implanted components and a simple stimulation algorithm. A new method of hypoglossal nerve stimulation to treat sleep apnoea does so bilaterally via an implanted neurostimulator activated externally. Its simplicity and relative non-invasiveness have not compromised its effectiveness relative to older methods. http://bit.ly/2lDCeif","PeriodicalId":77419,"journal":{"name":"The European respiratory journal. Supplement","volume":"17 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2019-10-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"65","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"The European respiratory journal. Supplement","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1183/13993003.01320-2019","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 65

Abstract

Background and aim Hypoglossal nerve stimulation (HNS) decreases obstructive sleep apnoea (OSA) severity via genioglossus muscle activation and decreased upper airway collapsibility. This study assessed the safety and effectiveness at 6 months post-implantation of a novel device delivering bilateral HNS via a small implanted electrode activated by a unit worn externally, to treat OSA: the Genio™ system. Methods This prospective, open-label, non-randomised, single-arm treatment study was conducted at eight centres in three countries (Australia, France and the UK). Primary outcomes were incidence of device-related serious adverse events and change in the apnoea–hypopnoea index (AHI). The secondary outcome was the change in the 4% oxygen desaturation index (ODI). Additional outcomes included measures of sleepiness, quality of life, snoring and device use. This trial was registered with ClinicalTrials.gov, number NCT03048604. Results 22 out of 27 implanted participants (63% male, aged 55.9±12.0 years, body mass index (BMI) 27.4±3.0 kg·m−2) completed the protocol. At 6 months BMI was unchanged (p=0.85); AHI decreased from 23.7±12.2 to 12.9±10.1 events·h−1, a mean change of 10.8 events·h−1 (p<0.001); and ODI decreased from 19.1±11.2 to 9.8±6.9 events·h−1, a mean change of 9.3 events·h−1 (p<0.001). Daytime sleepiness (Epworth Sleepiness Scale; p=0.01) and sleep-related quality of life (Functional Outcomes of Sleep Questionnaire-10; p=0.02) both improved significantly. The number of bed partners reporting loud, very intense snoring, or leaving the bedroom due to participant snoring decreased from 96% to 35%. 91% of participants reported device use >5 days per week, and 77% reported use for >5 h per night. No device-related serious adverse events occurred during the 6-month post-implantation period. Conclusions Bilateral HNS using the Genio™ system reduces OSA severity and improves quality of life without device-related complications. The results are comparable with previously published HNS systems despite minimal implanted components and a simple stimulation algorithm. A new method of hypoglossal nerve stimulation to treat sleep apnoea does so bilaterally via an implanted neurostimulator activated externally. Its simplicity and relative non-invasiveness have not compromised its effectiveness relative to older methods. http://bit.ly/2lDCeif
双侧舌下神经刺激治疗成人阻塞性睡眠呼吸暂停
背景与目的舌下神经刺激(HNS)通过激活舌下肌和降低上呼吸道塌陷来降低阻塞性睡眠呼吸暂停(OSA)的严重程度。该研究评估了Genio™系统植入6个月后的安全性和有效性,该设备通过外部佩戴的单元激活的小型植入电极提供双侧HNS,用于治疗OSA。该前瞻性、开放标签、非随机、单臂治疗研究在三个国家(澳大利亚、法国和英国)的8个中心进行。主要结局是器械相关严重不良事件的发生率和呼吸暂停-低通气指数(AHI)的变化。次要终点是4%氧去饱和指数(ODI)的变化。其他结果包括嗜睡、生活质量、打鼾和设备使用情况。该试验已在ClinicalTrials.gov注册,注册号为NCT03048604。结果27例植入术患者中有22例完成手术,其中男性63%,年龄55.9±12.0岁,体重指数(BMI) 27.4±3.0 kg·m−2。6个月时BMI不变(p=0.85);AHI从23.7±12.2下降到12.9±10.1事件·h−1,平均变化10.8事件·h−1(每周5天),77%报告每晚使用>5小时。植入后6个月无器械相关严重不良事件发生。结论:使用Genio™系统的双侧HNS可降低OSA严重程度,改善生活质量,无设备相关并发症。结果与之前发表的HNS系统相当,尽管植入的组件很少,刺激算法也很简单。一种新的舌下神经刺激治疗睡眠呼吸暂停的方法是通过植入外部激活的神经刺激器来治疗双侧睡眠呼吸暂停。它的简单性和相对非侵入性并没有损害其相对于旧方法的有效性。http://bit.ly/2lDCeif
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信