Apnea, Intermittent Hypoxemia, and Bradycardia Events Predict Late-Onset Sepsis in Extremely Preterm Infants.

Apnea Bradycardia Intermittent hypoxia Neonatal Late-Onset Sepsis Prematurity

Journal

The Journal of pediatrics
ISSN: 1097-6833
Titre abrégé: J Pediatr
Pays: United States
ID NLM: 0375410

Informations de publication

Date de publication:
01 Apr 2024
Historique:
received: 10 11 2023
revised: 21 03 2024
accepted: 26 03 2024
medline: 4 4 2024
pubmed: 4 4 2024
entrez: 3 4 2024
Statut: aheadofprint

Résumé

To examine the association of cardiorespiratory events, including apnea, periodic breathing, intermittent hypoxemia (IH), and bradycardia, with late-onset sepsis for extremely preterm infants (<29 weeks' gestational age [GA]) on versus off invasive mechanical ventilation. This is a 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 26.4 weeks, 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 >72 hours after birth and ≥5d antibiotics). 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 events with oxygen saturation <80% (IH80) 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 including post menstrual age, cardiorespiratory variables (apnea, periodic breathing, IH80, and bradycardia), and ventilator status predicted sepsis with an AUC of 0.783. 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.

Identifiants

pubmed: 38570031
pii: S0022-3476(24)00145-8
doi: 10.1016/j.jpeds.2024.114042
pii:
doi:

Banques de données

ClinicalTrials.gov
['NCT03174301']

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

114042

Informations de copyright

Copyright © 2024 Elsevier Inc. All rights reserved.

Auteurs

Sherry L Kausch (SL)

Department of Pediatrics, Division of Neonatology, University of Virginia School of Medicine, Charlottesville, VA. Electronic address: Slk7s@virginia.edu.

Douglas E Lake (DE)

Department of Medicine, Division of Cardiology, University of Virginia School of Medicine, Charlottesville, VA.

Juliann M Di Fiore (JM)

Department of Pediatrics, Case Western Reserve University School of Medicine, University Hospitals Cleveland Medical Center, Rainbow Babies and Children's Hospital, Cleveland, OH.

Debra E Weese-Mayer (DE)

Department of Pediatrics, Division of Autonomic Medicine, Northwestern University Feinberg School of Medicine, Chicago, IL.

Nelson Claure (N)

Department of Pediatrics, Division of Neonatology, University of Miami Miller School of Medicine, Miami, FL.

Namasivayam Ambalavanan (N)

Department of Pediatrics, Division of Neonatology, University of Alabama at Birmingham, Birmingham, AL.

Zachary A Vesoulis (ZA)

Department of Pediatrics, Division of Newborn Medicine, Washington University School of Medicine, St. Louis, MO.

Karen D Fairchild (KD)

Department of Pediatrics, Division of Neonatology, University of Virginia School of Medicine, Charlottesville, VA.

Phyllis A Dennery (PA)

Department of Pediatrics, Brown University School of Medicine, Department of Pediatrics, Providence, RI.

Anna Maria Hibbs (AM)

Department of Pediatrics, Case Western Reserve University School of Medicine, University Hospitals Cleveland Medical Center, Rainbow Babies and Children's Hospital, Cleveland, OH.

Richard J Martin (RJ)

Department of Pediatrics, Case Western Reserve University School of Medicine, University Hospitals Cleveland Medical Center, Rainbow Babies and Children's Hospital, Cleveland, OH.

Indic Premananda (I)

Department of Electrical Engineering, University of Texas at Tyler, Tyler, TX.

Colm P Travers (CP)

Department of Pediatrics, Division of Neonatology, University of Alabama at Birmingham, Birmingham, AL.

Eduardo Bancalari (E)

Department of Pediatrics, Division of Neonatology, University of Miami Miller School of Medicine, Miami, FL.

Aaron Hamvas (A)

Department of Pediatrics, Division of Neonatology, Northwestern University Feinberg School of Medicine, Chicago, IL.

James S Kemp (JS)

Department of Pediatrics, Division of Pediatric Pulmonology, Washington University School of Medicine, St. Louis, MO.

John L Carroll (JL)

Department of Pediatrics, University of Arkansas for Medical Sciences and Arkansas Children's Hospital, Little Rock, AK.

J Randall Moorman (JR)

Department of Medicine, Division of Cardiology, University of Virginia School of Medicine, Charlottesville, VA.

Brynne A Sullivan (BA)

Department of Pediatrics, Division of Neonatology, University of Virginia School of Medicine, Charlottesville, VA.

Classifications MeSH