Cardiovascular transition to extrauterine life in growth-restricted neonates: relationship with prenatal Doppler findings

Fetal Diagn Ther. 2013;33(2):103-9. doi: 10.1159/000345092. Epub 2012 Dec 12.

Abstract

Objective: Cardiovascular status in fetal growth restriction (FGR) can be classified by the severity of individual Doppler abnormalities (early and late) or by the rate of clinical progression. We tested the hypothesis that aspects of the fetal cardiovascular status in FGR affect neonatal cardiovascular findings.

Study design: FGR cases [abdominal circumference <5th percentile and an elevated umbilical (MCA) artery (UA) pulsatility index] had UA, middle cerebral artery and ductus venosus (DV) Doppler. Positive UA end-diastolic velocity and/or a low MCA pulsatility index denoted early and absent/reversed UA end-diastolic velocity, whereas an increased DV pulsatility index for veins denoted late responses. The rate of progression was classified into mild, progressive and severe. After delivery, shunt dynamics and blood flow across the patent ductus arteriosus (PDA), foramen ovale and atriaventricular valves, myocardial contractility and pharmacologic pressor requirement were noted at neonatal echocardiography. These findings were related to prenatal Doppler parameters.

Results: In 94 patients, only individual Doppler parameters related to neonatal echocardiographic findings. Absent/reversed UA DV significantly predicted PDA with right to left shunt (p = 0.016). The pressor need for cardiovascular instability was observed in neonates with abnormal prenatal DV Doppler and with lower birth weights delivered at earlier gestational age (p < 0.0001 for both). Pressor need was significantly related to neonatal death (Nagelkerke R² = 0.35, p = 0.002).

Conclusion: A markedly abnormal UA Doppler predisposes growth-restricted neonates to persistence of fetal circulation associated with right to left shunting. Abnormal venous Doppler is a risk factor for cardiovascular instability which in turn significantly contributes to neonatal mortality. Further clarification of the neonatal cardiovascular transition may be helpful in guiding early neonatal assessment and management.

Publication types

  • Multicenter Study

MeSH terms

  • Cardiovascular Diseases / diagnostic imaging
  • Cardiovascular Diseases / embryology
  • Cardiovascular Diseases / etiology*
  • Cardiovascular Diseases / physiopathology
  • Cardiovascular System / diagnostic imaging
  • Cardiovascular System / embryology
  • Cardiovascular System / physiopathology*
  • Female
  • Fetal Growth Retardation / etiology
  • Fetal Growth Retardation / physiopathology*
  • Humans
  • Infant, Newborn
  • Longitudinal Studies
  • Male
  • Middle Cerebral Artery / diagnostic imaging
  • Middle Cerebral Artery / embryology
  • Persistent Fetal Circulation Syndrome / diagnostic imaging
  • Persistent Fetal Circulation Syndrome / embryology
  • Persistent Fetal Circulation Syndrome / etiology*
  • Persistent Fetal Circulation Syndrome / physiopathology
  • Placenta Diseases / physiopathology*
  • Placental Circulation
  • Portal Vein / diagnostic imaging
  • Portal Vein / embryology
  • Pregnancy
  • Retrospective Studies
  • Risk Factors
  • Severity of Illness Index
  • Ultrasonography, Doppler, Color
  • Ultrasonography, Prenatal
  • Umbilical Arteries / diagnostic imaging
  • Umbilical Arteries / embryology