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Treatment of pulmonary hypertension during initial hospitalization in a multicenter cohort of infants with congenital diaphragmatic hernia (CDH).

Ruth B SeabrookTheresa R GroverNatalie RintoulMark F WeemsSarah KeeneBeverly BrozanskiRobert DiGeronimoBeth HabermanHolly HedrickJason GienNoorjahan AliRachel ChapmanJohn DanielH Allen HarrisonYvette JohnsonNicolas F M PortaMichael UhingIsabella ZanilettiKarna Murthynull null
Published in: Journal of perinatology : official journal of the California Perinatal Association (2021)
PH medication use is common in CDH. Identification of infants at risk for persistent PH may impact ongoing management. Post-discharge follow-up of all CDH infants with echocardiographic evidence of PH is warranted.
Keyphrases
  • pulmonary hypertension
  • pulmonary artery
  • pulmonary arterial hypertension
  • mitral valve
  • cross sectional
  • clinical trial
  • coronary artery
  • double blind
  • smoking cessation