Ambrose A Chiang, Evin Jerkins, Steven Holfinger, Sharon Schutte-Rodin, Arvind Chandrakantan, Laura Mong, Steve Glinka, Seema Khosla
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To help clinicians comprehend these devices and their functionalities, we meticulously reviewed their operating mechanisms, sensors, algorithms, data output, and related performance evaluation literature.</p><p><strong>Methods: </strong>We collected information from PubMed, United States Food and Drug Administration clearance documents, ClinicalTrials.gov, and web sources, with direct industry input whenever feasible.</p><p><strong>Results: </strong>In this \"device-centered\" review, we broadly categorized these wearables into 2 main groups: those that primarily harness photoplethysmography data and those that do not. The former include the peripheral arterial tonometry-based devices. The latter was further broken down into 2 key subgroups: acoustic-based and respiratory effort-based devices. We provided a performance evaluation literature review and objectively compared device-derived metrics and specifications pertinent to sleep clinicians. Detailed demographics of study populations, exclusion criteria, and pivotal statistical analyses of the key validation studies are summarized.</p><p><strong>Conclusions: </strong>In the foreseeable future, these novel obstructive sleep apnea-detecting wearables may emerge as primary diagnostic tools for patients at risk for moderate-to-severe obstructive sleep apnea without significant comorbidities. While more devices are anticipated to join this category, there remains a critical need for cross-device comparison studies as well as independent performance evaluation and outcome research in diverse populations. Now is the moment for sleep clinicians to immerse themselves in understanding these emerging tools to ensure our patient-centered care is improved through the appropriate implementation and utilization of these novel sleep technologies.</p><p><strong>Citation: </strong>Chiang AA, Jerkins E, Holfinger S, et al. 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引用次数: 0
摘要
研究目标:自 2019 年以来,美国食品和药物管理局(FDA)已经批准了九种新型阻塞性睡眠呼吸暂停(OSA)检测可穿戴设备用于家庭睡眠呼吸暂停测试,其中许多设备现已上市,睡眠临床医生可将其整合到临床实践中。为了帮助临床医生理解这些设备及其功能,我们仔细研究了它们的运行机制、传感器、算法、数据输出以及相关的性能评估文献:方法:我们从 PubMed、FDA 批准文件、ClinicalTrial.gov 和网络资源中收集信息,并在可行的情况下直接听取行业人士的意见:结果:在这篇 "以设备为中心 "的综述中,我们将这些可穿戴设备大致分为两大类:一类主要利用光电血压计 (PPG) 数据,另一类则不利用。前者包括基于外周动脉测压(PAT)的设备。后者又进一步细分为两个关键的子组:基于声学的设备和基于呼吸努力的设备。我们提供了一份性能评估文献综述,并客观比较了与睡眠临床医生相关的设备衍生指标和规格。我们总结了研究人群的详细人口统计学特征、排除标准以及主要验证研究的关键统计分析:在可预见的未来,这些新型 OSA 检测可穿戴设备可能会成为中重度 OSA 高危患者的主要诊断工具。虽然预计会有更多的设备加入这一行列,但仍亟需进行跨设备比较研究以及针对不同人群的独立性能评估和结果研究。现在正是睡眠临床医生深入了解这些新兴工具的大好时机,以确保通过适当实施和利用这些新型睡眠技术,改善我们以患者为中心的护理。
OSA diagnosis goes wearable: are the latest devices ready to shine?
Study objectives: From 2019-2023, the United States Food and Drug Administration has cleared 9 novel obstructive sleep apnea-detecting wearables for home sleep apnea testing, with many now commercially available for sleep clinicians to integrate into their clinical practices. To help clinicians comprehend these devices and their functionalities, we meticulously reviewed their operating mechanisms, sensors, algorithms, data output, and related performance evaluation literature.
Methods: We collected information from PubMed, United States Food and Drug Administration clearance documents, ClinicalTrials.gov, and web sources, with direct industry input whenever feasible.
Results: In this "device-centered" review, we broadly categorized these wearables into 2 main groups: those that primarily harness photoplethysmography data and those that do not. The former include the peripheral arterial tonometry-based devices. The latter was further broken down into 2 key subgroups: acoustic-based and respiratory effort-based devices. We provided a performance evaluation literature review and objectively compared device-derived metrics and specifications pertinent to sleep clinicians. Detailed demographics of study populations, exclusion criteria, and pivotal statistical analyses of the key validation studies are summarized.
Conclusions: In the foreseeable future, these novel obstructive sleep apnea-detecting wearables may emerge as primary diagnostic tools for patients at risk for moderate-to-severe obstructive sleep apnea without significant comorbidities. While more devices are anticipated to join this category, there remains a critical need for cross-device comparison studies as well as independent performance evaluation and outcome research in diverse populations. Now is the moment for sleep clinicians to immerse themselves in understanding these emerging tools to ensure our patient-centered care is improved through the appropriate implementation and utilization of these novel sleep technologies.
Citation: Chiang AA, Jerkins E, Holfinger S, et al. OSA diagnosis goes wearable: are the latest devices ready to shine? J Clin Sleep Med. 2024;20(11):1823-1838.
期刊介绍:
Journal of Clinical Sleep Medicine focuses on clinical sleep medicine. Its emphasis is publication of papers with direct applicability and/or relevance to the clinical practice of sleep medicine. This includes clinical trials, clinical reviews, clinical commentary and debate, medical economic/practice perspectives, case series and novel/interesting case reports. In addition, the journal will publish proceedings from conferences, workshops and symposia sponsored by the American Academy of Sleep Medicine or other organizations related to improving the practice of sleep medicine.