Inborn Versus Outborn Delivery in Neonates With Congenital Diaphragmatic Hernia.


Journal

The Journal of surgical research
ISSN: 1095-8673
Titre abrégé: J Surg Res
Pays: United States
ID NLM: 0376340

Informations de publication

Date de publication:
02 2022
Historique:
received: 15 04 2021
revised: 25 08 2021
accepted: 13 09 2021
pubmed: 29 10 2021
medline: 7 4 2022
entrez: 28 10 2021
Statut: ppublish

Résumé

Congenital diaphragmatic hernia (CDH) is a morbid and potentially fatal condition that challenges providers. The aim of this study is to compare outcomes in neonates with prenatally diagnosed CDH that are inborn (delivered in the institution where definitive care for CDH is provided) versus outborn. Prenatally diagnosed CDH cases were identified from the Congenital Diaphragmatic Hernia Study Group (CDHSG) database between 2007 and 2019. Using risk adjustment based on disease severity, we compared inborn versus outborn status using baseline risk and multivariable logistic regression models. The primary endpoint was mortality and the secondary endpoint was need for extracorporeal life support (ECLS). Of 4195 neonates with prenatally diagnosed CDH, 3087 (73.6%) were inborn and 1108 (26.4%) were outborn. There was no significant difference in birth weight, gestational age, or presence of additional congenital anomalies. There was no difference in mortality between inborn and outborn infants (32.6% versus 33.8%, P = 0.44) or ECLS requirement (30.9% versus 31.5%, P = 0.73). Among neonates requiring ECLS, outborn status was a risk factor for mortality (OR 1.51, 95% CI 1.13-2.01, P = 0.006). After adjusting for post-surgical defect size, which is not known prenatally, outborn status was no longer a risk factor for mortality for infants requiring ECLS. Risk of mortality and need for ECLS for inborn CDH patients is not different to outborn infants. Future studies should be directed to establishing whether highest risk infants are at risk for worse outcomes based on center of birth.

Sections du résumé

BACKGROUND
Congenital diaphragmatic hernia (CDH) is a morbid and potentially fatal condition that challenges providers. The aim of this study is to compare outcomes in neonates with prenatally diagnosed CDH that are inborn (delivered in the institution where definitive care for CDH is provided) versus outborn.
METHODS
Prenatally diagnosed CDH cases were identified from the Congenital Diaphragmatic Hernia Study Group (CDHSG) database between 2007 and 2019. Using risk adjustment based on disease severity, we compared inborn versus outborn status using baseline risk and multivariable logistic regression models. The primary endpoint was mortality and the secondary endpoint was need for extracorporeal life support (ECLS).
RESULTS
Of 4195 neonates with prenatally diagnosed CDH, 3087 (73.6%) were inborn and 1108 (26.4%) were outborn. There was no significant difference in birth weight, gestational age, or presence of additional congenital anomalies. There was no difference in mortality between inborn and outborn infants (32.6% versus 33.8%, P = 0.44) or ECLS requirement (30.9% versus 31.5%, P = 0.73). Among neonates requiring ECLS, outborn status was a risk factor for mortality (OR 1.51, 95% CI 1.13-2.01, P = 0.006). After adjusting for post-surgical defect size, which is not known prenatally, outborn status was no longer a risk factor for mortality for infants requiring ECLS.
CONCLUSIONS
Risk of mortality and need for ECLS for inborn CDH patients is not different to outborn infants. Future studies should be directed to establishing whether highest risk infants are at risk for worse outcomes based on center of birth.

Identifiants

pubmed: 34710705
pii: S0022-4804(21)00572-2
doi: 10.1016/j.jss.2021.09.004
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

245-251

Informations de copyright

Copyright © 2021. Published by Elsevier Inc.

Auteurs

Stephen Stopenski (S)

Department of Surgery, University of California Irvine, Orange, California. Electronic address: sstopens@hs.uci.edu.

Yigit S Guner (YS)

Department of Surgery, University of California Irvine, Orange, California; Division of Pediatric Surgery, Children's Hospital of Orange County, Orange, California.

Jennifer Jolley (J)

Department of Obstetrics and Gynecology, University of California Irvine, Orange, California.

Carol Major (C)

Department of Obstetrics and Gynecology, University of California Irvine, Orange, California.

Tamera Hatfield (T)

Department of Obstetrics and Gynecology, University of California Irvine, Orange, California.

Ashley H Ebanks (AH)

Department of Pediatric Surgery, University of Texas McGovern Medical School and Children's Memorial Hermann Hospital, Houston, Texas.

Danh V Nguyen (DV)

Department of Medicine, University of California Irvine, Orange, California.

Tim Jancelewicz (T)

Division of Pediatric Surgery, Le Bonheur Children's Hospital, University of Tennessee Health Science Center, Memphis, Tennessee.

Matthew T Harting (MT)

Department of Pediatric Surgery, University of Texas McGovern Medical School and Children's Memorial Hermann Hospital, Houston, Texas.

Peter T Yu (PT)

Department of Surgery, University of California Irvine, Orange, California; Division of Pediatric Surgery, Children's Hospital of Orange County, Orange, California.

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