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Fetal haemoglobin and oxygen requirement in preterm infants: an observational study
Tommy Ulinder1,2, William Hellström3, Christian Gadsbøll4
1Department of Clinical Sciences Lund, Paediatrics, Lund University, Lund, Sweden tommy.ulinder@med.lu.se.
Insights
Lower fetal hemoglobin (HbF) levels in preterm infants correlate with higher oxygen needs, indicated by increased fraction of inspired oxygen (FiO2) and alveolar-arterial gradient (A-a gradient). This suggests a potential link to bronchopulmonary dysplasia (BPD).
Area of Science:
- Neonatal Medicine
- Respiratory Physiology
- Pediatric Cardiology
Background:
- Bronchopulmonary dysplasia (BPD) is a significant complication in very preterm infants.
- Fetal hemoglobin (HbF) plays a crucial role in oxygen transport in utero.
- Reduced HbF levels have been anecdotally linked to BPD development.
Purpose of the Study:
- To investigate the relationship between fetal hemoglobin fraction (HbF(%)) and oxygen requirements in very preterm infants.
- To determine if HbF levels correlate with the fraction of inspired oxygen (FiO2) and alveolar-arterial gradient (A-a gradient).
- To explore the potential role of increased oxygen exposure in the association between decreased HbF and BPD.
Main Methods:
- A longitudinal, retrospective, observational study was conducted.
- Data from 440 very preterm infants (born before 30 weeks gestation) were analyzed.
- Fraction of inspired oxygen (FiO2) and alveolar-arterial gradient (A-a gradient) were measured using arterial blood gas analyses during the first postnatal week.
Main Results:
- A significant inverse relationship was found between HbF(%) and both FiO2 and A-a gradient.
- These associations remained statistically significant after adjusting for factors like gestational age, postnatal age, pH, pCO2, and sex.
- Lower HbF levels were associated with increased oxygen requirements in the early neonatal period.
Conclusions:
- Decreased HbF(%) in the first postnatal week is significantly associated with higher oxygen requirements (increased FiO2 and A-a gradient) in very preterm infants.
- Increased alveolar oxygen exposure, potentially driven by lower HbF, may contribute to oxidative stress.
- This oxidative stress could partially explain the link between reduced HbF, blood transfusions, and the development of BPD in preterm infants.
Objective:
To investigate the relationship between the fraction of fetal haemoglobin (HbF(%)) and oxygen requirement as determined by the fraction of inspired oxygen (FiO2) and alveolar-arterial gradient (A-a gradient). Increased alveolar exposure to oxygen may explain the association between decreased HbF(%) and the development of bronchopulmonary dysplasia (BPD).
Design:
Longitudinal, retrospective, observational study.
Setting:
Tertiary-level neonatal intensive care unit, referral centre for southern Sweden.
Patients:
Four hundred forty very preterm infants born before gestational week 30, 2009-2015.
Intervention:
Regular clinical practice.
Main Outcome Measures:
The FiO2 and A-a gradient were determined at the time-point of 10 015 arterial blood gas analyses obtained during postnatal days 1-7. The relationship between HbF(%) and FiO2 and A-a gradient and the modifying influence of other factors affecting haemoglobin oxygen affinity were evaluated.
Results:
We found a significant relationship between a low fraction of HbF and an increase in FiO2 and A-a gradient, respectively. These relationships remained significant after adjusting for pH, pCO2, postnatal age, gestational age and sex.
Conclusion:
These high-resolution data show that decreased HbF(%) during the first postnatal week is associated with increased FiO2 and A-a gradient in very preterm infants. Increased alveolar exposure to oxygen and resulting oxidative stress may, at least partly, explain the previously reported associations between decreased HbF, blood transfusions and the development of BPD in preterm infants.
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