腕带血氧仪的性能准确性及其自动输出参数筛选儿童阻塞性睡眠呼吸暂停

M. Ohn, K. Maddison, J. Nguyen, Daisy Evans, N. Bear, R. N. Khan, P. R. Eastwood, B. S. Ungern-Sternberg, Andrew C Wilson, Jennifer H. Walsh
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引用次数: 0

摘要

目的:阻塞性睡眠呼吸暂停(OSA)增加儿童围手术期不良事件的风险。虽然多导睡眠图(PSG)仍然是OSA诊断的参考标准,但血氧测定法是一种有价值的筛查工具。传统的做法是使用麦吉尔血氧计评分对桌面设备得出的去饱和簇进行人工分析。然而,可穿戴式血氧仪数据的自动分析也是一种选择。本研究探讨了腕带血氧仪与自动分析作为术前OSA筛查工具的准确性。方法:计划行腺扁桃体切除术的健康儿童同时进行夜间PSG和腕带血氧测定。PSG测定阻塞性呼吸暂停低通气指数(OAHI)。自动分析氧饱和度数据以确定3%氧去饱和指数(ODI3),并根据McGill标准进行视觉评分。在调整协变量后,logistic回归模型评估ODI3检测OSA存在和严重程度的预测性能。结果:76名儿童(34名女性),年龄(平均±标准差)5.7±1.6岁,根据psg衍生的OAHI分为无OSA (n=31)、轻度OSA (n=31)和中重度OSA (n=14)。氧饱和度ODI3被确定为中重度OSA (OAHI≥5个事件/小时)的唯一预测因子(优势比1.38,95%可信区间1.15,1.65,p=0.001)。在ODI3=5个事件/h时诊断效果最佳(敏感性78.6%,特异性75.8%[受试者工作特征曲线下面积{ROC-AUC}=0.857])。ODI3在诊断中重度OSA方面也比McGill血氧饱和度评分更敏感(ODI3为78.6%,McGill为33.0%)。对于任何OSA水平(OAHI≥1 event/h),该方法的表现都不理想(敏感性75.6%,特异性61.3% [ROC-AUC=0.709])。结论:腕戴式血氧仪衍生的自动ODI3可以可靠地识别接受腺扁桃体切除术的儿童中重度OSA,使其成为潜在有用的术前OSA筛查工具。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Performance Accuracy of Wrist-Worn Oximetry and Its Automated Output Parameters for Screening Obstructive Sleep Apnea in Children
Objectives: Obstructive sleep apnea (OSA) increases the risk of perioperative adverse events in children. While polysomnography (PSG) remains the reference standard for OSA diagnosis, oximetry is a valuable screening tool. The traditional practice is the manual analysis of desaturation clusters derived from a tabletop device using the McGill oximetry score. However, automated analysis of wearable oximetry data can be an alternative. This study investigated the accuracy of wrist-worn oximetry with automated analysis as a preoperative OSA screening tool. Methods: Healthy children scheduled for adenotonsillectomy underwent concurrent overnight PSG and wrist-worn oximetry. PSG determined the obstructive apnea-hypopnea index (OAHI). Oximetry data were auto-analyzed to determine 3% oxygen desaturation index (ODI3) and visually scored as per McGill criteria. The logistic regression model assessed the predictive performance of ODI3 for detecting the presence and severity of OSA after adjusting for covariates. Results: Seventy-six children (34 females), aged (mean±standard deviation) 5.7±1.6 years were classified, based on PSG-derived OAHI, as no OSA (n=31), mild (n=31), and moderate-severe OSA (n=14). Oximetric ODI3 was identified as the sole predictor of moderate-severe OSA (OAHI≥5 events/h) (odds ratio 1.38, 95% confidence interval 1.15, 1.65, p=0.001). The best diagnostic performance was at ODI3=5 events/h (78.6% sensitivity, 75.8% specificity [receiver operating characteristic-area under the curve {ROC-AUC}=0.857]). ODI3 was also more sensitive than the McGill oximetry score in diagnosing moderate-severe OSA (78.6% by ODI3 vs. 33.0% by McGill). The performance was suboptimal for any level of OSA (OAHI≥1 event/h) (75.6% sensitivity, 61.3% specificity [ROC-AUC=0.709]). Conclusions: Wrist-worn oximetry-derived automated ODI3 can reliably identify moderate-severe OSA in children undergoing adenotonsillectomy, making it a potentially useful preoperative OSA screening tool.
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