Abstract

The aim was to reflect on the unexpected finding of persistent pulmonary hypertension of the neonate (PPHN) and pulmonary hypertension in infants born within the Dutch STRIDER trial, its definition and possible pathophysiological mechanisms. The trial randomly assigned pregnant women with severe early-onset fetal growth restriction to sildenafil 25 mg three times a day versus placebo. Sildenafil use did not reduce perinatal mortality and morbidity, but did result in a higher rate of neonatal pulmonary hypertension (PH). The current paper reflects on the used definition, prevalence, and possible pathophysiology of the data on pulmonary hypertension. Twenty infants were diagnosed with pulmonary hypertension (12% of 163 live born infants). Of these, 16 infants had PPHN shortly after birth, and four had pulmonary hypertension associated with sepsis or bronchopulmonary dysplasia. Four infants with PPHN in the early neonatal period subsequently developed pulmonary hypertension associated with bronchopulmonary dysplasia in later life. Infants with pulmonary hypertension were at lower gestational age at delivery, had a lower birth weight and a higher rate of neonatal co-morbidity. The infants in the sildenafil group showed a significant increase in pulmonary hypertension compared to the placebo group (relative risk 3.67; 95% confidence interval 1.28 to 10.51, P = 0.02).Conclusion: Pulmonary hypertension occurred more frequent among infants of mothers allocated to antenatal sildenafil compared with placebo. A possible pathophysiological mechanism could be a “rebound” vasoconstriction after cessation of sildenafil. Additional studies and data are necessary to understand the mechanism of action.What is Known:• In the Dutch STRIDER trial, persistent pulmonary hypertension in the neonate (PPHN) was more frequent among infants after antenatal sildenafil exposure versus placebo.What is New:• The current analysis focuses on the distinction between PPHN and pulmonary hypertension associated with sepsis or bronchopulmonary dysplasia and on timing of diagnosis and aims to identify the infants at risk for developing pulmonary hypertension.• The diagnosis pulmonary hypertension is complex, especially in infants born after severe early-onset fetal growth restriction. The research field could benefit from an unambiguous consensus definition and standardized screening in infants at risk is proposed.

Highlights

  • Fetal growth restriction (FGR) is a condition in which the fetus does not reach its own intrinsic growth potential, most frequently caused by placental insufficiency [1]

  • The current analysis focuses on the distinction between pulmonary hypertension of the neonate (PPHN) and pulmonary hypertension associated with sepsis or bronchopulmonary dysplasia and on timing of diagnosis and aims to identify the infants at risk for developing pulmonary hypertension

  • The diagnosis pulmonary hypertension is complex, especially in infants born after severe early-onset fetal growth restriction

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Summary

Introduction

Fetal growth restriction (FGR) is a condition in which the fetus does not reach its own intrinsic growth potential, most frequently caused by placental insufficiency [1]. Sildenafil prevents formation of guanine monophosphate (GMP) out of cyclic GMP This leads to an increased effect of nitric oxide, leading to vascular smooth muscle relaxation [5]. Previous studies suggested that sildenafil would improve uteroplacental flow, through which a higher gestational age and birth weight could be established. This led to the hypothesis that sildenafil would reduce the risk of perinatal mortality and morbidity. This hypothesis has been investigated in the Dutch STRIDER trial. The primary outcome of the Dutch STRIDER trial was a composite of fetal and neonatal mortality or major neonatal morbidity

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