Objective: Our aim was to confirm whether extreme hyperoxemic events had been associated with excess mortality in our diverse critical care population.
Methods: Retrospective analysis of 9 years of data collected in the pediatric and cardiothoracic ICUs in Children's Hospital Los Angeles was performed. The analysis was limited to those mechanically ventilated for at least 24 h, with at least 1 arterial blood gas measurement. An extreme hyperoxemic event was defined as a PaO of ≥300 torr. Multivariable logistic regression was used to assess the association of extreme hyperoxemia events and mortality, adjusting for confounding variables. Selected a-priori, these were Pediatric Risk of Mortality III predicted mortality, general or cardiothoracic ICU, number of blood gas measurements, as well as an abnormal blood gas measurements (pH < 7.25, pH > 7.45, and PaO < 50 torr).
Results: There were 4,003 admissions included with a predicted mortality of 7.1% and an actual mortality of 9.7%. Their care was associated with 75,129 blood gas measurements, in which abnormal measurements were common. With adjustments for these covariates, any hyperoxemic event was associated with excess mortality ( < 0.001). Excess mortality increased with multiple hyperoxemic events ( < 0.046). Additionally, treatment resulting in SpO > 98% markedly increased the risk of a hyperoxemic event.
Conclusion: Retrospective analysis of critical care admissions showed that extreme hyperoxemic events were associated with higher mortality. Supplemental oxygen levels resulting in SpO > 98% should be avoided.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11322569 | PMC |
http://dx.doi.org/10.3389/fped.2024.1429882 | DOI Listing |
Trials
November 2024
Centre for Pediatric Clinical Studies (CPCS), University Children's Hospital Tübingen, Calwerstr. 7, Tübingen, 72076, Germany.
Background: Extremely low gestational age neonates (ELGANs, i.e. those born before 28 weeks postmenstrual age (PMA)) often require supplemental oxygen and frequently experience intermittent hypo- and hyperoxemic episodes.
View Article and Find Full Text PDFFront Pediatr
July 2024
Department of Anesthesiology Critical Care Medicine, Children's Hospital Los Angeles, University of Southern California Keck School of Medicine, Los Angeles, CA, United States.
Objective: Our aim was to confirm whether extreme hyperoxemic events had been associated with excess mortality in our diverse critical care population.
Methods: Retrospective analysis of 9 years of data collected in the pediatric and cardiothoracic ICUs in Children's Hospital Los Angeles was performed. The analysis was limited to those mechanically ventilated for at least 24 h, with at least 1 arterial blood gas measurement.
Diagnostics (Basel)
October 2023
Faculty of Biomedical Engineering, Czech Technical University in Prague, 272 01 Kladno, Czech Republic.
Unlabelled: The utility of decision tree machine learning in exploring the interactions among the SpO target range, neonatal maturity, and oxemic-risk is demonstrated.
Methods: This observational study used 3 years of paired age-SpO-PaO data from a neonatal ICU. The CHAID decision tree method was used to explore the interaction of postmenstrual age (PMA) on the risk of extreme arterial oxygen levels at six different potential SpO target ranges (88-92%, 89-93%, 90-94%, 91-95%, 92-96% and 93-97%).
Crit Care
March 2023
Department of Clinical Science and Education, Södersjukhuset, Karolinska Institutet, Stockholm, Sweden.
BMC Pediatr
June 2022
Alberta Children's Hospital, Neonatology, Calgary, Canada.
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