Department of Paediatrics, University of Oxford, Oxford, UK.
Institute of Biomedical Engineering, Department of Engineering Science, University of Oxford, Oxford, UK.
BMJ Open Respir Res. 2021 Dec;8(1). doi: 10.1136/bmjresp-2021-001042.
Respiratory disorders, including apnoea, are common in preterm infants due to their immature respiratory control compared with term-born infants. However, our inability to accurately measure respiratory rate in hospitalised infants results in unreported episodes of apnoea and an incomplete picture of respiratory activity.
We develop, validate and use a novel algorithm to identify interbreath intervals (IBIs) and apnoeas in preterm infants. In 42 preterm infants (1600 hours of recordings), we assess IBIs from the chest electrical impedance pneumograph using an adaptive amplitude threshold for the detection of breaths. The algorithm is refined by comparing its accuracy with clinically observed breaths and pauses in breathing. We develop an automated classifier to differentiate periods of true apnoea from artefactually low amplitude signal. We assess the performance of this algorithm in the detection of morphine-induced respiratory depression. Finally, we use the algorithm to investigate whether retinopathy of prematurity (ROP) screening alters the IBI distribution.
Individual breaths were detected with a false-positive rate of 13% and a false-negative rate of 12%. The classifier identified true apnoeas with an accuracy of 93%. As expected, morphine caused a significant shift in the IBI distribution towards longer IBIs. Following ROP screening, there was a significant increase in pauses in breathing that lasted more than 10 s (t-statistic=1.82, p=0.023). This was not reflected by changes in the monitor-derived respiratory rate and no episodes of apnoea were recorded in the medical records.
We show that our algorithm offers an improved method for the identification of IBIs and apnoeas in preterm infants. Following ROP screening, increased respiratory instability can occur even in the absence of clinically significant apnoeas. Accurate assessment of infant respiratory activity is essential to inform clinical practice.
与足月出生的婴儿相比,早产儿由于呼吸控制不成熟,因此常见呼吸障碍,包括呼吸暂停。然而,我们无法在住院婴儿中准确测量呼吸频率,这导致呼吸暂停事件未被报告,也无法全面了解呼吸活动情况。
我们开发、验证并使用了一种新算法来识别早产儿的呼吸间期(IBI)和呼吸暂停。在 42 名早产儿(1600 小时的记录)中,我们使用自适应幅度阈值从胸部电阻抗描记图中检测呼吸,以检测呼吸。通过将其准确性与临床观察到的呼吸和呼吸暂停进行比较,对算法进行了优化。我们开发了一种自动分类器来区分真正的呼吸暂停期和假信号幅度低的时期。我们评估了该算法在检测吗啡引起的呼吸抑制中的性能。最后,我们使用该算法研究早产儿视网膜病变(ROP)筛查是否会改变 IBI 分布。
个体呼吸的假阳性率为 13%,假阴性率为 12%。分类器识别真正的呼吸暂停的准确率为 93%。正如预期的那样,吗啡导致 IBI 分布向更长的 IBI 显著转移。ROP 筛查后,呼吸暂停时间超过 10 秒的呼吸暂停显著增加(t 统计量=1.82,p=0.023)。这并没有反映在监护仪得出的呼吸率变化中,也没有在医疗记录中记录到呼吸暂停事件。
我们表明,我们的算法为早产儿的 IBI 和呼吸暂停识别提供了一种改进的方法。ROP 筛查后,即使没有临床上显著的呼吸暂停,呼吸也可能变得更加不稳定。准确评估婴儿的呼吸活动对于指导临床实践至关重要。