Literature DB >> 30442461

Use of prostaglandin E1 to treat pulmonary hypertension in congenital diaphragmatic hernia.

Kendall M Lawrence1, Kelsey Berger1, Lisa Herkert1, Christine Franciscovich1, Carol Lynn H O'Dea2, Lindsay N Waqar1, Emily Partridge1, Brian D Hanna3, William H Peranteau4, Catherine M Avitabile3, Rachel K Hopper5, Natalie E Rintoul3, Holly L Hedrick6.   

Abstract

BACKGROUND/
PURPOSE: Prostaglandin E1 (PGE) has been used to maintain ductus arteriosus patency and unload the suprasystemic right ventricle (RV) in neonates with congenital diaphragmatic hernia (CDH) and severe pulmonary hypertension (PH). Here we evaluate the PH response in neonates with CDH and severe PH treated with PGE.
METHODS: We performed a retrospective chart review of CDH infants treated at our center between 2011 and 2016. In a subset, PGE was initiated for echocardiographic evidence of severe PH, metabolic acidosis, or hypoxemia. To assess PH response, we evaluated laboratory data, including B-type natriuretic peptide (BNP) and echocardiograms before and after PGE treatment. Categorical and continuous data were analyzed with Fisher's exact tests and Mann-Whitney t-tests, respectively.
RESULTS: Fifty-seven infants were treated with PGE a mean 17 ± 2 days. BNP levels declined after 1.4 ± 0.2 days of treatment and again after 5.2 ± 0.6 days. After 6 ± 0.8 days of treatment, echocardiographic estimates of severe PH by tricuspid regurgitation jet velocity, ductus arteriosus direction, and ventricular septum position also improved significantly. Treatment was not associated with postductal hypoxemia or systemic hypoperfusion.
CONCLUSIONS: In patients with CDH and severe PH, PGE is well tolerated and associated with improved BNP and echocardiographic indices of PH, suggesting successful unloading of the RV. TYPE OF STUDY: Treatment study. LEVEL OF EVIDENCE: Level III.
Copyright © 2018. Published by Elsevier Inc.

Entities:  

Keywords:  Congenital diaphragmatic hernia; Prostaglandin E1; Pulmonary hypertension

Mesh:

Substances:

Year:  2018        PMID: 30442461     DOI: 10.1016/j.jpedsurg.2018.10.039

Source DB:  PubMed          Journal:  J Pediatr Surg        ISSN: 0022-3468            Impact factor:   2.545


  6 in total

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

Authors:  Ruth B Seabrook; Theresa R Grover; Natalie Rintoul; Mark Weems; Sarah Keene; Beverly Brozanski; Robert DiGeronimo; Beth Haberman; Holly Hedrick; Jason Gien; Noorjahan Ali; Rachel Chapman; John Daniel; H Allen Harrison; Yvette Johnson; Nicolas F M Porta; Michael Uhing; Isabella Zaniletti; Karna Murthy
Journal:  J Perinatol       Date:  2021-03-01       Impact factor: 2.521

Review 2.  Use of Prostaglandin E1 in the Management of Congenital Diaphragmatic Hernia-A Review.

Authors:  Srirupa Hari Gopal; Neil Patel; Caraciolo J Fernandes
Journal:  Front Pediatr       Date:  2022-07-01       Impact factor: 3.569

Review 3.  Emerging antenatal therapies for congenital diaphragmatic hernia-induced pulmonary hypertension in preclinical models.

Authors:  Kathleen Marulanda; Nick D Tsihlis; Sean E McLean; Melina R Kibbe
Journal:  Pediatr Res       Date:  2020-10-10       Impact factor: 3.756

Review 4.  The heart in congenital diaphragmatic hernia: Knowns, unknowns, and future priorities.

Authors:  Neil Patel; Anna C Massolo; Ulrike S Kraemer; Florian Kipfmueller
Journal:  Front Pediatr       Date:  2022-08-16       Impact factor: 3.569

Review 5.  Life-threatening PPHN refractory to nitric oxide: proposal for a rational therapeutic algorithm.

Authors:  Feriel Fortas; Matteo Di Nardo; Nadya Yousef; Marc Humbert; Daniele De Luca
Journal:  Eur J Pediatr       Date:  2021-06-06       Impact factor: 3.183

Review 6.  Congenital diaphragmatic hernia: a narrative review of controversies in neonatal management.

Authors:  Michelle J Yang; Katie W Russell; Bradley A Yoder; Stephen J Fenton
Journal:  Transl Pediatr       Date:  2021-05
  6 in total

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