TY - JOUR
T1 - Neonatal pulmonary hypertension after severe early-onset fetal growth restriction
T2 - post hoc reflections on the Dutch STRIDER study
AU - Pels, Anouk
AU - Onland, Wes
AU - Berger, Rolf M. F.
AU - van Heijst, Arno F. J.
AU - Lopriore, Enrico
AU - Reiss, Irwin K. M.
AU - Limpens, Jacqueline
AU - Gordijn, Sanne J.
AU - Ganzevoort, Wessel
N1 - Funding Information: Ethical approval for the Dutch STRIDER trial was given on July 22, 2014 (2014–131) by Amsterdam UMC. The trial was funded by the Netherlands Organization for Health Research and Development (ZonMW project no. 836021023). After discontinuation of the trial and because of the unexpected finding, the study team decided to install a blinded external adjudication committee of neonatologists (WO, AFJvH, EL, IKMR) and a pediatric cardiologist (RMFB) with expertise in PPHN/PH and preterm infants with FGR to review and study all potential cases of PH. In the study database, no distinction was made between PPHN and late-onset PH, associated with (developing) BPD and/or sepsis. Echocardiography was not performed in all infants as outcome in the trial, but based on local protocol of routine care, only on clinical indication at discretion of the treating physician. In the Netherlands, no standard echocardiography is performed in infants born after FGR or prematurity. Therefore, echocardiography is only performed if a suspicion of PPHN or other cardiac problems have been raised. This is in line with the other international STRIDER studies, in which also no routine echocardiography was performed in this population. Publisher Copyright: © 2022, The Author(s).
PY - 2022/4/1
Y1 - 2022/4/1
N2 - 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.
AB - 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.
KW - Fetal growth restriction
KW - Neonatal morbidity
KW - Neonatal mortality
KW - Pulmonary hypertension
KW - Sildenafil
UR - http://www.scopus.com/inward/record.url?scp=85122686066&partnerID=8YFLogxK
U2 - https://doi.org/10.1007/s00431-021-04355-x
DO - https://doi.org/10.1007/s00431-021-04355-x
M3 - Article
C2 - 35018508
SN - 0340-6199
VL - 181
SP - 1709
EP - 1718
JO - European journal of pediatrics
JF - European journal of pediatrics
IS - 4
ER -