Clinical validity of systemic arterial steal among extremely preterm infants with persistent patent ductus arteriosus

Lieke Keusters1, Jyotsna Purna1, Poorva Deshpande1,2

  • 1Department of Paediatrics, Mount Sinai Hospital, Toronto, ON, Canada.

Insights

Abnormal diastolic flow in the middle cerebral artery (aMCA) is linked to adverse outcomes in preterm infants with persistent hemodynamically significant patent ductus arteriosus (phsPDA). Celiac trunk abnormalities (aCT) showed less relevance.

Area of Science:

  • Neonatal Medicine
  • Pediatric Cardiology
  • Medical Imaging

Background:

  • Persistent hemodynamically significant patent ductus arteriosus (phsPDA) is common in preterm infants.
  • Assessing phsPDA severity is crucial for clinical management and predicting outcomes.
  • Diastolic flow abnormalities in specific arteries may indicate clinical significance.

Purpose of the Study:

  • To investigate the relevance of diastolic flow abnormalities in the celiac trunk (aCT) and middle cerebral artery (aMCA) in preterm neonates with phsPDA.
  • To determine if aCT or aMCA can serve as markers for phsPDA severity and associated morbidities.

Main Methods:

  • Retrospective analysis of 515 echocardiograms from 156 preterm neonates (<28 weeks gestation).
  • Comparison of infants with and without aCT or aMCA.
  • Logistic regression analysis adjusted for confounders to assess the primary outcome (death, CLD, or NEC ≥ stage 2).

Main Results:

  • Abnormalities in the middle cerebral artery (aMCA) were significantly associated with the primary composite outcome (adjusted OR 2.17) and chronic lung disease (CLD) (adjusted OR 2.20).
  • Abnormalities in the celiac trunk (aCT) were not significantly associated with the primary outcome or CLD.
  • Mean gestational age was 25.2 weeks and birth weight was 820g.

Conclusions:

  • Abnormal middle cerebral artery (aMCA) diastolic flow may be a valuable marker for identifying clinically significant phsPDA in preterm infants.
  • Celiac trunk abnormalities (aCT) appear to have limited value in selecting preterm neonates with phsPDA for treatment.
  • Further research may refine the use of vascular flow patterns in managing phsPDA.
Abstract

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