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Published on: December 22, 2023
Superior vena cava flow and intraventricular haemorrhage in extremely preterm infants
Sarah Bates1, David Odd1,2, Karen Luyt2
1a Neonatal Intensive Care Unit , Southmead Hospital, North Bristol NHS Trust , Bristol , UK , and.
Insights
Early superior vena cava flow (SVCF) in extremely preterm infants correlates with ductal shunting. However, SVCF measurements within 24 hours of birth are not a reliable predictor for developing intraventricular haemorrhage (IVH).
Area of Science:
- Neonatal physiology
- Pediatric cardiology
- Neonatal neurology
Background:
- Intraventricular haemorrhage (IVH) is a significant complication in extremely preterm infants.
- Early physiological markers may help predict IVH development.
- Superior vena cava flow (SVCF) is a potential indicator of circulatory status in neonates.
Purpose of the Study:
- To investigate the association between early superior vena cava flow (SVCF) measurements and the incidence of intraventricular haemorrhage (IVH).
- To determine if SVCF can serve as a predictive marker for IVH in extremely preterm infants.
Main Methods:
- Retrospective cohort study including 108 infants born before 28 weeks' gestation.
- SVCF was measured within the first 24 hours of life.
- The primary outcome was the degree of IVH assessed at 7 days postnatal age.
Main Results:
- Infants who developed IVH had a lower mean SVCF (75 ml/kg/min) compared to those without IVH (87.7 ml/kg/min, p=0.055).
- SVCF showed an inverse association with patent ductus arteriosus diameter and reversal of flow in the descending aorta.
- Sensitivity analysis did not confirm an independent association between SVCF and IVH development (OR 0.990, p=0.115).
Conclusions:
- Early SVCF in extremely preterm infants is linked to the degree of ductal shunting.
- SVCF measurements in the first 24 hours are insensitive for predicting IVH in this population.
Objective:
To evaluate the relationship between superior vena cava flow (SVCF) measurements within the first 24 h of life, and development of intraventricular haemorrhage (IVH) in extremely preterm infants.
Study Design:
Single centre retrospective cohort study of 108 preterm infants born less than 28 weeks' gestation. Main outcome measure was degree of IVH at day 7 postnatal age.
Results:
The mean GA of the study group was 25.4 weeks. Mean SVCF was lower (75 ml/kg/min) in infants later diagnosed with IVH (n = 46) compared to infants, who did not develop IVH (87.7 ml/kg/min, p = 0.055). PDA diameter was inversely associated with SVCF (p = 0.024) and reversal of flow in the descending aorta (p = 0.001). Sensitivity analysis did not confirm an independent association of SVCF with development of IVH [OR 0.990 (0.978-1.002), p = 0.115].
Conclusion:
Our study describes early SVCF in extremely preterm infants is associated with the extent of ductal shunting, but insensitive in predicting IVH.
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