Service de Pneumologie Infantile, Allergologie et Centre De Référence En Mucoviscidose, Hôpital Femme Mère Enfant, Hospices Civils de Lyon, Bron, France.
Service d'Explorations Fonctionnelles Pédiatriques, Hôpital d'Enfants, Centre Hospitalier Universitaire de Nancy, Nancy, France.
J Clin Sleep Med. 2024 Jul 1;20(7):1059-1067. doi: 10.5664/jcsm.11064.
Sleep laboratory polysomnography is the gold standard for obstructive sleep apnea (OSA) diagnosis in infants, but its access remains limited. Oximetry-capnography is another simple and widely used tool that can provide information on the presence of desaturations and alveolar hypoventilation. However, its reliability is debated. This study aimed at examining its use in determining OSA severity in infants.
This retrospective study was conducted in a sleep unit in a tertiary hospital in infants < 4 months old with clinical signs of OSA or Pierre Robin sequence who underwent a 1-night polysomnography coupled with oximetry-capnography.
Among the 78 infants included (median [interquartile range] age: 61 [45-89] days at polysomnography), 44 presented with Pierre Robin sequence and 34 presented with isolated airway obstruction. The clinical, sleep, and respiratory characteristics were not significantly different between the 2 subgroups. In the entire cohort, 63.5% had severe OSA. The median obstructive apnea-hypopnea index was 14.5 (7.4-5.9) events/h, peripheral oxygen saturation (SpO) was 97.4% (96.5-98.1%), and transcutaneous carbon dioxide pressure (PtcCO) was 41.1 mmHg (38.3-44.9). The optimal threshold to predict an obstructive apnea-hypopnea index > 10 events/h was 6 events/h for an oxygen desaturation index ≥ 3% (sensitivity, 95.7%; specificity, 51.9%) and 2 events/h for an oxygen desaturation index ≥ 4% (sensitivity, 95.7%; specificity, 48.1%).
Whereas transcutaneous capnography does not appear to be sufficient in predicting severe OSA in infants < 4 months old with Pierre Robin sequence or clinical signs of OSA, oximetry may be a useful alternative for the screening of severe OSA in infants in the absence of polysomnography.
Gyapay R, Ioan I, Thieux M, et al. Gas exchange parameters for the prediction of obstructive sleep apnea in infants. . 2024;20(7):1059-1067.
睡眠实验室多导睡眠图是婴儿阻塞性睡眠呼吸暂停(OSA)诊断的金标准,但获得它的途径仍然有限。血氧饱和度-二氧化碳描记法是另一种简单且广泛使用的工具,可提供关于饱和度降低和肺泡通气不足的信息。然而,其可靠性存在争议。本研究旨在检查其在确定婴儿 OSA 严重程度中的应用。
这是一项在一家三级医院的睡眠单位进行的回顾性研究,纳入了 < 4 个月大、有 OSA 临床体征或 Pierre Robin 序列的婴儿,这些婴儿接受了 1 晚多导睡眠图和血氧饱和度-二氧化碳描记法检查。
在纳入的 78 名婴儿中(多导睡眠图时的中位[四分位距]年龄:61[45-89]天),44 名婴儿患有 Pierre Robin 序列,34 名婴儿患有孤立性气道阻塞。两组的临床、睡眠和呼吸特征无显著差异。在整个队列中,63.5%的婴儿患有严重 OSA。中位阻塞性呼吸暂停低通气指数为 14.5(7.4-5.9)次/小时,外周血氧饱和度(SpO₂)为 97.4%(96.5-98.1%),经皮二氧化碳分压(PtcCO)为 41.1mmHg(38.3-44.9)。预测阻塞性呼吸暂停低通气指数 > 10 次/小时的最佳阈值为:氧减饱和度指数≥3%时为 6 次/小时(敏感性 95.7%,特异性 51.9%),氧减饱和度指数≥4%时为 2 次/小时(敏感性 95.7%,特异性 48.1%)。
虽然经皮二氧化碳描记法似乎不足以预测患有 Pierre Robin 序列或 OSA 临床体征的 < 4 个月大婴儿的严重 OSA,但在没有多导睡眠图的情况下,血氧饱和度可能是筛查严重 OSA 的有用替代方法。
Gyapay R, Ioan I, Thieux M, et al. 婴儿阻塞性睡眠呼吸暂停的气体交换参数预测。. 2024;20(7):1059-1067.