Apnoea-triggered increase in fraction of inspired oxygen in preterm infants: a randomised cross-over study.

Arch Dis Child Fetal Neonatal Ed

Menzies Institute for Medical Research, College of Health and Medicine, University of Tasmania, Hobart, Tasmania, Australia.

Published: December 2023

Objectives: To investigate the impact of a pre-emptive apnoea triggered oxygen response on oxygen saturation (SpO) targeting following central apnoea in preterm infants.

Design: Interventional crossover study of a 12-hour period of automated oxygen control with an apnoea response (AR) module, nested within a crossover study of a 24-hour period of automated oxygen control compared with aggregated data from two flanking 12-hour periods of manual control.

Setting: Neonatal intensive care unit PATIENTS: Preterm infants receiving non-invasive respiratory support and supplemental oxygen; median (IQR) birth gestation 27 (26-28) weeks, postnatal age 17 (12-23) days.

Intervention: Automated oxygen titration with an automated control algorithm modified to include an AR module. Alterations to inspired oxygen concentration (FiO) were actuated by a motorised blender. Desired SpO range was 90-94%. Apnoea detection was by capsule pneumography.

Main Outcome Measures: Duration, magnitude and area under the curve (AUC) of SpO deviations following apnoea; frequency and duration of apnoeic events. Comparisons between periods of manual, automated and automated control with AR module.

Results: In 60 studies in 35 infants, inclusion of the AR module significantly reduced AUC for SpO deviations below baseline compared with both automated and manual control (manual: 87.1%±107.6% s, automated: 84.6%±102.8% s, AR module: 79.4%±102.7% s). However, there was a coincident increase in SpO overshoot (AUC (SpO>SpO); manual: 44.3±99.9% s, automated: 54.7%±103.4% s, AR module: 65.7%±126.2% s).

Conclusion: Automated control with a pre-emptive apnoea-triggered FiO boost resulted in a modest reduction in post-apnoea hypoxaemia, but was followed by a greater SpO overshoot.

Trial Registration Number: ACTRN12616000300471.

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Source
http://dx.doi.org/10.1136/archdischild-2023-325849DOI Listing

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