School of Engineering, College of Science Engineering and Technology, University of Tasmania, Hobart, Tasmania, Australia.
Department of Paediatrics, Royal Hobart Hospital, Hobart, Tasmania, Australia.
Pediatr Pulmonol. 2019 Nov;54(11):1712-1721. doi: 10.1002/ppul.24451. Epub 2019 Jul 16.
The factors influencing the severity of apnea-related hypoxemia and bradycardia are incompletely characterized, especially in infants receiving noninvasive respiratory support.
To identify the frequency and predictors of physiological instability (hypoxemia-oxygen saturation (SpO ) <80%, or bradycardia-heart rate (HR) < 100 bpm) following respiratory pauses in infants receiving noninvasive respiratory support.
Respiratory pause duration, derived from capsule pneumography, was measured in 30 preterm infants of gestation 30 (24-32) weeks [median (interquartile range)] receiving noninvasive respiratory support and supplemental oxygen. For identified pauses of 5 to 29 seconds duration, we measured the magnitude and duration of SpO and HR reductions over a period starting at the pause onset and ending 60 seconds after resumption of breathing. Temporally clustered pauses (<60 seconds separation) were analyzed separately. The relative contribution of respiratory pauses to overall physiological instability was determined, and predictors of instability were sought in regression analysis, including demographic, clinical and situational variables as inputs.
In total, 17 105 isolated and 9180 clustered pauses were identified. Hypoxemia and bradycardia were more likely after longer duration and temporally-clustered pauses. However, the majority of such episodes occurred after 5 to 9 second pauses given their numerical preponderance, and short-lived pauses made a substantial contribution to physiological instability overall. Birth gestation, hemoglobin concentration, form of respiratory support, caffeine treatment, respiratory pause duration and temporal clustering were identified as predictors of instability.
Brief respiratory pauses, especially when clustered, contribute substantially to hypoxemia and bradycardia in preterm infants.
影响与呼吸暂停相关的低氧血症和心动过缓严重程度的因素尚未完全明确,尤其是在接受无创呼吸支持的婴儿中。
确定接受无创呼吸支持的婴儿发生呼吸暂停后出现生理不稳定(氧饱和度(SpO )<80%或心率(HR)<100 bpm)的频率和预测因素。
使用胶囊测压法测量 30 例胎龄 30 周(24-32 周)[中位数(四分位距)]接受无创呼吸支持和补充氧气的早产儿的呼吸暂停持续时间。对于持续时间为 5 至 29 秒的暂停,我们测量了 SpO 和 HR 降低的幅度和持续时间,测量从暂停开始到恢复呼吸后 60 秒结束。对时间上聚集的暂停(间隔时间<60 秒)进行单独分析。确定呼吸暂停对整体生理不稳定的相对贡献,并通过回归分析寻找不稳定的预测因素,包括人口统计学、临床和情况变量作为输入。
共识别出 17105 个孤立暂停和 9180 个聚集暂停。持续时间较长和时间上聚集的暂停更可能导致低氧血症和心动过缓。然而,由于其数量上的优势,大多数此类事件发生在 5 至 9 秒的暂停之后,而短暂的暂停对整体生理不稳定有很大的贡献。胎龄、血红蛋白浓度、呼吸支持形式、咖啡因治疗、呼吸暂停持续时间和时间聚集被确定为不稳定的预测因素。
短暂的呼吸暂停,尤其是聚集性的呼吸暂停,会导致早产儿严重的低氧血症和心动过缓。