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Natural History of Postnatal Cardiopulmonary Adaptation in Infants Born Extremely Preterm and Risk for Death or
Hussnain Mirza1, Jorge A Garcia2, Elizabeth Crawford3
1Center for Neonatal Care, Florida Hospital for Children/University of Central Florida College of Medicine, Orlando, FL.
Insights
Delayed cardiopulmonary adaptation in extremely preterm infants is common and independently linked to increased death or bronchopulmonary dysplasia (BPD). Understanding this adaptation is crucial for improving outcomes in high-risk newborns.
Area of Science:
- Neonatal Physiology
- Pediatric Cardiology
- Respiratory Medicine
Background:
- Extremely preterm infants (<29 weeks) face significant challenges in postnatal cardiopulmonary adaptation.
- Pulmonary hypertension (PH) is a common complication, impacting morbidity and mortality.
- Understanding the trajectory of cardiopulmonary adaptation is vital for predicting outcomes.
Purpose of the Study:
- To investigate the natural history of postnatal cardiopulmonary adaptation in extremely preterm infants.
- To determine the association between adaptation patterns and the risk of death or bronchopulmonary dysplasia (BPD).
Main Methods:
- Prospective, observational cohort study of infants born <29 weeks gestation.
- Serial echocardiograms performed within 48 hours of birth and every 24-48 hours up to 14 days.
- Classification of adaptation based on pulmonary hypertension (PH) resolution at 72-96 hours and persistence up to 14 days.
Main Results:
- 55% of infants exhibited delayed cardiopulmonary adaptation.
- Delayed adaptation was associated with lower gestational age, birth weight, and increased need for ventilation and oxygen.
- Delayed adaptation independently increased the risk of death or BPD (P<.001).
Conclusions:
- Postnatal cardiopulmonary adaptation in extremely preterm infants can be normal or delayed, with varying degrees of PH.
- Delayed adaptation is a significant independent predictor of death or BPD in this vulnerable population.
- Early identification and management of delayed adaptation are critical for improving survival and reducing BPD rates.
Objective:
To study the natural history of postnatal cardiopulmonary adaptation in infants born extremely preterm and establish its association with death or bronchopulmonary dysplasia (BPD).
Study Design:
This was a prospective, observational, cohort study of infants born extremely preterm (<29 weeks). Initial echocardiogram was performed at <48 hours of life, followed by serial echocardiograms every 24-48 hours until 14 days of life. Resolution or no resolution of pulmonary hypertension (PH) at 72-96 hours was considered normal or delayed postnatal cardiopulmonary adaptation, respectively. PH between 96 hours and 14 days was defined as subsequent PH. Elevated pulmonary artery pressure throughout the 14 days of life was considered persistent PH. BPD was assessed at 36 weeks of postmenstrual age.
Results:
Sixty infants were enrolled; 2 died before a sequential echocardiogram could be done at 72-96 hours. Normal and delayed cardiopulmonary adaptation were noted in 26 (45%) and 32 (55%) infants, respectively. Five patterns of postnatal cardiopulmonary adaptation were recognized: normal without subsequent PH (n = 20), normal with subsequent PH (n = 6), delayed adaptation without subsequent PH (n = 6), delayed adaptation with subsequent PH (n = 16), and persistent PH (n = 10). Infants with delayed cardiopulmonary adaptation were of lower gestation and birth weight and required prolonged ventilation and supplemental oxygen (P < .05). On multivariate analysis, the incidence of death or BPD was significantly greater among infants with delayed adaptation (P < .001).
Conclusion:
Infants born extremely preterm have normal or delayed postnatal cardiopulmonary adaptation that can be complicated by subsequent or persistent PH. Delayed cardiopulmonary adaptation is associated independently with death or BPD.
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