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Optimal Target Range of Closed-Loop Inspired Oxygen Support in Preterm Infants: A Randomized Cross-Over Study
Maria Elisabeth Nicoletta van den Heuvel1, Henriette A van Zanten2, Tom E Bachman3
1Department of Neonatology, Emma Children's Hospital, Academic Medical Center Amsterdam, The Netherlands.
Narrowing the target oxygen saturation range for automated fraction of inspired oxygen control in preterm infants significantly reduced time spent in severe hypoxemia. This approach effectively minimized low oxygen levels without increasing the risk of high oxygen levels.
Area of Science:
- Neonatal Medicine
- Pediatric Critical Care
- Respiratory Physiology
Background:
- Oxygen-dependent infants often require precise oxygen monitoring and control.
- Automated fraction of inspired oxygen (A-FiO2) systems aim to maintain target oxygen saturation (SpO2) levels.
- Variability in SpO2 can lead to adverse outcomes in preterm infants.
Purpose of the Study:
- To evaluate the impact of different SpO2 target ranges during A-FiO2 on time spent within alarm limits.
- To determine if narrower SpO2 targets reduce hypoxemia without increasing hyperoxemia in infants.
Main Methods:
- A randomized crossover study involving 41 preterm infants on noninvasive respiratory support.
- Three SpO2 target ranges (86%-94%, 88%-92%, 89%-91%) were applied via A-FiO2 for 24 hours each.
- SpO2 levels were manually controlled during 24-hour washout periods between target range changes.
Main Results:
- All A-FiO2 target ranges resulted in similar time spent within the 86%-94% SpO2 alarm range (74%).
- Time in severe hypoxemia (SpO2 <80%) was significantly reduced with narrower target ranges (88%-92% and 89%-91%) compared to the widest range (86%-94%).
- No significant differences in hyperoxemia were observed between the tested target ranges.
Conclusions:
- Narrowing the A-FiO2 target range to ±2% around the desired median SpO2 effectively reduces time spent in hypoxemia.
- This strategy minimizes hypoxemia without elevating the risk of hyperoxemia in oxygen-dependent preterm infants.
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