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Published on: November 20, 2015
Neonatal outcomes of preterm infants with pulmonary hypertension: clustering based on prenatal risk factors
Seong Phil Bae1,2, Sung Shin Kim3,4, Jungha Yun5
1Department of Pediatrics, Soonchunhyang University Seoul Hospital, Seoul, Republic of Korea.
Insights
Prenatal risk factors like histologic chorioamnionitis and small-for-gestational-age impact preterm infant outcomes. Understanding these clusters aids in managing pulmonary hypertension (PH) and improving neonatal care.
Area of Science:
- Neonatal Medicine
- Perinatal Epidemiology
- Pediatric Cardiology
Background:
- Pulmonary hypertension (PH) is a significant concern in preterm infants, often presenting as hypoxic respiratory failure.
- The etiologies of PH in this population are complex and multifactorial.
- Few studies have classified preterm infants based on distinct prenatal risk factor profiles for PH.
Purpose of the Study:
- To investigate the association between specific prenatal risk factors and neonatal outcomes in preterm infants diagnosed with pulmonary hypertension (PH).
- To classify very-low-birth-weight infants based on a combination of gestational age, small-for-gestational-age status, and prenatal exposures.
- To identify distinct clusters of infants with similar prenatal conditions and predict their neonatal outcomes.
Main Methods:
- A prospective cohort study included very-low-birth-weight infants (22-29 weeks' gestation) requiring PH-specific treatment.
- Infants were categorized into six clusters using a two-step cluster analysis.
- Key classification factors included gestational age, small-for-gestational-age (SGA), antenatal corticosteroid (ACS) exposure, histologic chorioamnionitis (HCA), and oligohydramnios.
Main Results:
- Six distinct infant clusters were identified based on prenatal factors: HCA (Cluster A), oligohydramnios (Cluster B), SGA (Cluster C), no ACS (Cluster D), no dominant parameter (Cluster E), and HCA with oligohydramnios (Cluster F).
- Cluster C (SGA) showed a significantly higher risk of in-hospital mortality compared to the reference group (Cluster A).
- Clusters B (oligohydramnios), D (no ACS), and F (HCA and oligohydramnios) exhibited increased risks of requiring PH-specific treatment within the first week of life.
Conclusions:
- The identified clusters reveal distinct patterns of prenatal conditions and associated neonatal outcomes in preterm infants with PH.
- This classification provides a better understanding of how specific prenatal risk factors contribute to the development of PH.
- These findings can inform targeted interventions and improve the management of pulmonary hypertension in vulnerable preterm populations.
Background:
To investigate association of prenatal risk factors and neonatal outcomes of preterm infants with pulmonary hypertension (PH).
Methods:
A prospective cohort study of very-low-birth-weight infants born at 22-29 weeks' gestation who received PH-specific treatment during hospitalization. Infants were classified using a two-step cluster analysis based on gestational age (GA), small-for-gestational-age (SGA), exposure to antenatal corticosteroids (ACS), histologic chorioamnionitis (HCA), and oligohydramnios.
Results:
Among 910 infants, six clusters were identified: cluster A (HCA, n = 240), cluster B (oligohydramnios, n = 79), cluster C (SGA, n = 74), cluster D (no-ACS, n = 109), cluster E (no dominant parameter, n = 287), and cluster F (HCA and oligohydroamnios, n = 121). Cluster A was used as a reference group for comparisons among clusters. Compared to cluster A, cluster C (aHR: 1.63 [95% CI: 1.17-2.26]) had higher risk of overall in-hospital mortality. Clusters B (aHR: 1.52 [95% CI: 1.09-2.11]), D (aHR: 1.71 [95% CI: 1.28-2.30]), and F (aHR: 1.51 [95% CI: 1.12-2.03]) had higher risks of receiving PH-specific treatment within the first week of birth compared to cluster A.
Conclusion:
These findings may provide a better understanding of prenatal risk factors contributing to the development of PH.
Impact:
Pulmonary hypertension (PH), presenting as hypoxic respiratory failure, has complex etiologies in preterm infants. Although multifactorial risks for the development of PH in preterm infants are known, few studies have classified infants with similar etiologies for PH. Each cluster has distinct patterns of prenatal condition and neonatal outcome.
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