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早产儿心肺控制系统与阻塞性睡眠呼吸暂停风险

Cardioventilatory Control in Preterm-born Children and the Risk of Obstructive Sleep Apnea.

机构信息

1 Division of Pulmonary Medicine.

2 Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.

出版信息

Am J Respir Crit Care Med. 2018 Jun 15;197(12):1596-1603. doi: 10.1164/rccm.201708-1700OC.

Abstract

RATIONALE

The contribution of ventilatory control to the pathogenesis of obstructive sleep apnea (OSA) in preterm-born children is unknown.

OBJECTIVES

To characterize phenotypes of ventilatory control that are associated with the presence of OSA in preterm-born children during early childhood.

METHODS

Preterm- and term-born children without comorbid conditions were enrolled. They were categorized into an OSA group and a non-OSA group on the basis of polysomnography.

MEASUREMENTS AND MAIN RESULTS

Loop gain, controller gain, and plant gain, reflecting ventilatory instability, chemoreceptor sensitivity, and blood gas response to a change in ventilation, respectively, were estimated from spontaneous sighs identified during polysomnography. Cardiorespiratory coupling, a measure of brainstem maturation, was estimated by measuring the interval between inspiration and the preceding electrocardiogram R-wave. Cluster analysis was performed to develop phenotypes based on controller gain, plant gain, cardiorespiratory coupling, and gestational age. The study included 92 children, 63 of whom were born preterm (41% OSA) and 29 of whom were born at term (48% OSA). Three phenotypes of ventilatory control were derived with risks for OSA being 8%, 47%, and 77% in clusters 1, 2, and 3, respectively. There was a stepwise decrease in controller gain and an increase in plant gain from clusters 1 to 3. Children in cluster 1 had significantly higher cardiorespiratory coupling and gestational age than clusters 2 and 3. No difference in loop gain was found between clusters.

CONCLUSIONS

The risk for OSA could be stratified according to controller gain, plant gain, cardiorespiratory coupling, and gestational age. These findings could guide personalized care for children at risk for OSA.

摘要

背景

通气控制对早产儿阻塞性睡眠呼吸暂停(OSA)发病机制的影响尚不清楚。

目的

描述与早产儿早期 OSA 相关的通气控制表型。

方法

招募无合并症的早产儿和足月儿。根据多导睡眠图将其分为 OSA 组和非 OSA 组。

测量和主要结果

从多导睡眠图中识别的自发性叹息中分别估计反映通气不稳定、化学感受器敏感性和血气对通气变化反应的环路增益、控制器增益和植物增益。通过测量吸气与前一个心电图 R 波之间的间隔来估计反映脑干成熟度的心肺耦联。基于控制器增益、植物增益、心肺耦联和胎龄进行聚类分析,以开发表型。研究纳入了 92 名儿童,其中 63 名早产儿(41%为 OSA),29 名足月儿(48%为 OSA)。从聚类 1 到聚类 3,分别得到了三种通气控制表型,其 OSA 风险分别为 8%、47%和 77%。从聚类 1 到聚类 3,控制器增益逐渐降低,植物增益逐渐增加。聚类 1 的儿童的心肺耦联和胎龄明显高于聚类 2 和聚类 3。聚类之间的环路增益没有差异。

结论

根据控制器增益、植物增益、心肺耦联和胎龄,可以对 OSA 的风险进行分层。这些发现可以为有 OSA 风险的儿童提供个性化的护理。

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