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Published on: November 20, 2015
Oxygenation Instability and Short-Term Morbidities Among Very-Low-Birthweight Premature Infants
Viktoria Leikin Zach1,2, Arieh Riskin1,3, Irina Raizberg2
1Technion-Israel Institute of Technology, Rappaport Faculty of Medicine, Haifa, Israel.
Insights
Oxygenation instability in very-low-birthweight infants is common. Early instability in the first week of life predicts higher risk of bronchopulmonary dysplasia or death.
Area of Science:
- Neonatology
- Pediatric Respiratory Medicine
- Critical Care Medicine
Background:
- Oxygenation instability is a frequent issue in very-low-birthweight (VLBW) infants.
- This instability is linked to significant morbidities associated with prematurity.
Purpose of the Study:
- To investigate the association between oxygenation instability in VLBW infants during the first week of life and short-term neonatal morbidities.
- To analyze oxygenation patterns using SpO2 histograms.
Main Methods:
- Included VLBW infants requiring respiratory support.
- Recorded 24-hour SpO2 histograms daily.
- Classified histograms into stable/unstable categories using a distribution-based system.
Main Results:
- 77 VLBW infants (mean gestational age 28.5 weeks) were studied.
- 38% of infants experienced oxygenation instability, with 52% entering this phase within the first week.
- Instability during the first week significantly increased the risk of bronchopulmonary dysplasia (BPD)/death (aOR 32.4).
Conclusions:
- VLBW infants exhibit a specific oxygenation instability pattern.
- Early entry into an unstable phase within the first week of life is a predictor for BPD/death.
- Hypoxemia burden in the first week correlates with BPD/death; iatrogenic hyperoxemia does not.
Aim:
Oxygenation instability is common among very-low-birthweight premature infants (VLBW) and is correlated with morbidities of prematurity. We aimed to study the association of oxygenation instability of VLBW premature infants during the first week of life, as documented by the SpO2 histogram, with short-term neonatal morbidities.
Methods:
VLBW infants requiring respiratory support were included. 24-h SpO2 histograms were documented once daily. A classification system, based on the distribution of the histogram, was used to classify the histograms into stable/unstable categories.
Results:
Seventy-seven infants with mean (SD) gestational age-28.5 (2.1) weeks and birth weight-1040 (243) g were included in our study. 2063 histograms were recorded. Mean (SD) length of follow-up-27.5 (20.1) days per infant. 62% of infants remained stable during the follow-up period, while 38% experienced instability. 52% entered the unstable period during the first week of life. These infants had a higher risk of bronchopulmonary dysplasia (BPD)/death after adjusting for gestational age (OR [95% CI] 17.5 [4.0, 77.2]; p < 0.001), and for a variety of demographic and clinical variables (OR [95% CI] 32.4 [2.5, 418.5]; p = 0.008).
Conclusion:
VLBW premature infants demonstrate a distinct instability pattern. Entry into the unstable phase during the first week of life is associated with BPD/death, making it a potential predictive tool. Hypoxemia burden during the first week of life is correlated with BPD or death, while iatrogenic hyperoxemia is not.
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