Accuracy of the Albus Home Research Device (RD) for the Non-Contact and Passive Monitoring of Nocturnal Respiratory Rate at Home in an Adult Population

W. Do, C. Wheeler, M. de Vos, R. Russell, M. Bafadhel
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Abstract

RATIONALE: Reliable remote respiratory monitoring that is acceptable to patients is crucial for healthcare systems and clinical research in the post-COVID-19 era. Existing methods (such as peak-flow, diaries, and pulse oximetry) are limited by adherence and technique or confounded by subjectivity and recall bias. Nocturnal periods provide important signs in respiratory disease activity, yet accurate and unobtrusive methods for home monitoring are lacking. Current gold-standard tools - wearable polysomnography (PSG) devices - capture objective signs such as respiratory rate (RR) but require uncomfortable sensors, which are unsuitable for use beyond a few nights. Emerging monitoring solutions must minimize patient-burden to facilitate long-term engagement in clinical care and research. METHODS: In healthy adults, we evaluated accuracy of a passive, non-contact bedside device (Albus Home RD), that uses wireless motion sensors to capture RR, compared to gold-standard, wearable PSG (SOMNOtouch™ RESPIRATORY, Somnomedics). The table-top Albus Home RD was positioned on the bedside adjacent to the participant in their normal home bedroom environment. Participants slept with usual clothing and bedding;sleeping arrangements ranged from single- to king-size beds with single- and co-sleepers. Gold-standard PSG RR data were recorded using manual count of the raw respiratory traces derived from thoracoabdominal respiratory-effort belts. 10-minute periods from each hour of monitoring were chosen, where sufficient data were available and free from confounding movement and artefacts. Data from Albus Home RD were then analyzed using proprietary signal processing algorithms to output corresponding 30-second RR segments (as breaths/minute). RR results for each device for the selected periods were time-synchronized and compared for each 30-second segment. As per previous validation literature, accuracy was reported as proportion of RR measurements within +/-10% or +/-2 breaths/minute of the PSG RR. RESULTS: 16 healthy adults (9 males, 7 females) participated in overnight monitoring;ages and BMI ranged 20-74 years and 19-38 respectively. Albus Home RD RR measurements for 1540 thirty-second segments were compared against the gold-standard with overall accuracy of 92.4%. Mean Absolute Percentage Error was 0.06 (SD=0.07). CONCLUSIONS: Albus Home RD passively measured RR with 92% accuracy in adults compared to gold-standard in 770 minutes of analysis. Using wireless sensors and proprietary signal processing algorithms, the Albus Home RD is a valid bedside, non-contact monitor of RR in real-world environments. The non-touch, passive nature of this monitor can enable low-burden, long-term home nocturnal monitoring. This system provides new possibilities for remote clinical care and objective data gathering in longitudinal research studies. .
阿不思家庭研究装置(RD)用于成人家庭夜间呼吸频率非接触和被动监测的准确性
理由:患者可接受的可靠远程呼吸监测对于后covid -19时代的医疗保健系统和临床研究至关重要。现有的方法(如峰流量、日记和脉搏血氧仪)受到依从性和技术的限制,或受主观性和回忆偏差的影响。夜间活动是呼吸系统疾病活动的重要标志,但缺乏准确和不显眼的家庭监测方法。目前的黄金标准工具——可穿戴式多导睡眠描记仪(PSG)设备——捕捉呼吸频率(RR)等客观信号,但需要不舒服的传感器,不适合使用超过几个晚上。新兴的监测解决方案必须尽量减少患者负担,以促进临床护理和研究的长期参与。方法:在健康成人中,我们评估了使用无线运动传感器捕获RR的被动式非接触式床边设备(Albus Home RD)与金标准可穿戴式PSG (SOMNOtouch™RESPIRATORY, Somnomedics)的准确性。桌面式阿不思家居RD被放置在床边,靠近他们正常的家庭卧室环境中的参与者。参与者穿着平常的衣服和被褥睡觉;睡眠安排从单人床到特大号床,有单人床和双人床。金标准的PSG RR数据是通过手工计数胸腹呼吸努力带的原始呼吸痕迹来记录的。从每小时的监测中选择10分钟,在那里可以获得足够的数据,并且没有混淆的运动和人为因素。然后使用专有的信号处理算法分析来自Albus Home RD的数据,输出相应的30秒RR片段(以呼吸/分钟为单位)。每个设备在选定时间段内的RR结果是时间同步的,并对每30秒段进行比较。根据先前的验证文献,准确度报告为在PSG RR的+/-10%或+/-2次/分钟内RR测量的比例。结果:16名健康成人(男9名,女7名)参加了夜间监测,年龄20 ~ 74岁,BMI 19 ~ 38岁。阿不思之家1540个32秒片段的RD RR测量值与金标准进行了比较,总体准确度为92.4%。平均绝对百分比误差为0.06 (SD=0.07)。结论:与金标准相比,Albus Home RD被动测量成人RR的准确率为92%,分析时间为770分钟。使用无线传感器和专有的信号处理算法,阿不思家庭RD是一种在现实环境中有效的床边、非接触式RR监视器。该监视器的非接触式、被动式特性可以实现低负担、长期的家庭夜间监控。该系统为远程临床护理和纵向研究的客观数据收集提供了新的可能性。
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