呼吸暂停、间歇性低氧血症和心动过缓事件可预测极早产儿晚发败血症

Sherry L Kausch, Douglas E Lake, Juliann M Di Fiore, Debra E Weese-Mayer, Nelson Claure, Namasivayam Ambalavanan, Zachary A Vesoulis, Karen D Fairchild, Phyllis A Dennery, Anna Maria Hibbs, Richard J Martin, Premananda Indic, Colm P Travers, Eduardo Bancalari, Aaron Hamvas, James S Kemp, John L Carroll, Randall J Moorman, Brynne A Sullivan
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引用次数: 0

摘要

目的:检测心肺事件的变化,包括呼吸暂停、周期性呼吸、间歇性低氧血症(IH)和心动过缓,可能有助于及早发现败血症。我们的目的是研究极早产儿(胎龄 29 周)使用有创机械通气与不使用有创机械通气时心肺事件与晚发败血症的关系:对参加 Pre-Vent(ClinicalTrials.gov 标识符 NCT03174301)的婴儿数据进行回顾性分析,这是一项在五家四级新生儿重症监护病房进行的观察性研究。研究分析了 737 名婴儿(平均身高 26.4w,SD 1.71)的临床数据。我们获得并分析了 719 名婴儿(47512 个住院日)的监测数据,其中 109 名婴儿发生了 123 例败血症事件。通过连续监测数据,我们对呼吸暂停、周期性呼吸、心动过缓和 IH 进行了量化。我们分析了这些日常指标与晚期败血症(出生后 72 小时血培养呈阳性,且使用抗生素 5 天或等于 5 天)之间的关系:对于未使用呼吸机的婴儿,呼吸暂停、周期性呼吸和心动过缓在败血症确诊前有所增加。在使用呼吸机期间,脓毒症风险的增加与脓毒症前 IH80 事件的时间延长和心动过缓事件增多有关。IH 事件与较高的脓毒症风险相关,但在脓毒症发生前并没有动态增加,与呼吸机状态无关。多变量模型预测脓毒症的AUC为0.783:我们发现了晚期脓毒症的心肺特征。较长的 IH 事件与脓毒症风险增加有关,但在诊断附近的时间上没有变化。心动过缓、呼吸暂停和周期性呼吸的增加先于败血症的临床诊断。
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Apnea, Intermittent Hypoxemia, and Bradycardia Events Predict Late-Onset Sepsis in Extremely Preterm Infants
Objectives: Detection of changes in cardiorespiratory events, including apnea, periodic breathing, intermittent hypoxemia (IH), and bradycardia, may facilitate earlier detection of sepsis. Our objective was to examine the association of cardiorespiratory events with late-onset sepsis for extremely preterm infants (<29 weeks gestational age (GA)) on versus off invasive mechanical ventilation. Study Design: Retrospective analysis of data from infants enrolled in Pre-Vent (ClinicalTrials.gov identifier NCT03174301), an observational study in five level IV neonatal intensive care units. Clinical data were analyzed for 737 infants (mean GA 26.4w, SD 1.71). Monitoring data were available and analyzed for 719 infants (47,512 patient-days), of whom 109 had 123 sepsis events. Using continuous monitoring data, we quantified apnea, periodic breathing, bradycardia, and IH. We analyzed the relationships between these daily measures and late-onset sepsis (positive blood culture >72h after birth and > or equal to 5d antibiotics). Results: For infants not on a ventilator, apnea, periodic breathing, and bradycardia increased before sepsis diagnosis. During times on a ventilator, increased sepsis risk was associated with longer IH80 events and more bradycardia events before sepsis. IH events were associated with higher sepsis risk, but did not dynamically increase before sepsis, regardless of ventilator status. A multivariable model predicted sepsis with an AUC of 0.783. Conclusion: We identified cardiorespiratory signatures of late-onset sepsis. Longer IH events were associated with increased sepsis risk but did not change temporally near diagnosis. Increases in bradycardia, apnea, and periodic breathing preceded the clinical diagnosis of sepsis.
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