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Maternal hyperoxygenation test in fetuses undergoing FETO for severe isolated congenital diaphragmatic hernia

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Maternal hyperoxygenation test in fetuses undergoing FETO for severe isolated congenital diaphragmatic hernia Elisa Done’ 1, Karel Allegaert2, Paul Lewi1, Jacques Jani1, Leonardo Gucciardo1, Tim Van Mieghem1, Eduardo Gratacos3, Roland Devlieger1, Dominique Van Schoubroeck1, Jan Deprest1 ...

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  • August 26, 2024
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Maternal hyperoxygenation test in fetuses undergoing FETO for severe

isolated congenital diaphragmatic hernia

Elisa Done’ 1 , Karel Allegaert 2 , Paul Lewi1 , Jacques Jani1 , Leonardo Gucciardo1 ,

Tim Van Mieghem1 , Eduardo Gratacos 3 , Roland Devlieger1 , Dominique Van

Schoubroeck1 , Jan Deprest1

From the Division of Woman and Child (Departments 1Obstetrics &

Gynaecology and 2Neonatology) of the University Hospitals Leuven, Leuven,

Belgium and the Department of Obstetrics, Hospital Clinic, Barcelona, Spain.

Corresponding author:

Jan Deprest, MD PhD

Division Woman and Child, Dept. Obstetrics and Gynaecology

UZ Leuven

Herestraat 49 , 3000 Leuven

Tel: + 32 16 344215

Fax: + 32 16 34 4205

Email: jan.deprest@uzleuven.be




This article has been accepted for publication in Ultrasound in Obstetrics &
Gynecology and is currently being edited and typeset. Readers should note that this
article has been fully refereed, but has not been through the technical editing, copy-
editing and proof correction process. Wiley-Blackwell and the International
Society of Ultrasound in Obstetrics and Gynecology cannot be held responsible for
errors or consequences arising from the use of information contained in this
article; nor do the views and opinions expressed necessarily reflect those of Wiley-
Blackwell or the International Society of Ultrasound in Obstetrics and Gynecology


1

,Acknowledgments: The European Commission (EC) supports this work in its 6th Framework

and Marie Curie Fellowship Programme (EuroSTEC; LSHC-CT-2006-037409; MEST CT2005

019707); the Flemish government via its Instituut voor Wetenschap en Technologie (IWT-

070715). E.D. J.J., L.G., T.V.M. are recipients of a grant from the EC. J.D. and K.A. are

recipients of a “Fundamental Clinical Researcher” grant of the Fonds Wetenschappelijk

Onderzoek-Vlaanderen (1801207N and 1800209N).




2

,Abstract



Rationale: Pulmonary hypoplasia and hypertension are the main problems in

newborns with isolated congenital diaphragmatic hernia (CDH). The outcome

can be prenatally predicted by the measurement of contralateral lung size.

Prenatal evaluation of lung vasculature has been much less investigated, and

there are no data on the ability to predict pulmonary hypertension.

Objective: To predict neonatal survival and pulmonary hypertension by

measurement of fetal pulmonary artery reactivity to maternal hyperoxygenation

in fetuses with severe CDH treated by fetoscopic endoluminal tracheal occlusion

(FETO).

Methods: 38 fetuses underwent FETO around 28 wks and the balloon was

removed at 34 weeks. We performed a hyperoxygenation test and measured the

lung-to-head ratio before and after each procedure. Outcome measures were

neonatal survival, occurrence of pulmonary hypertension and its response to

inhaled-NO (iNO)

Results : Fetuses who survived had a larger increase in lung size and decrease of

resistance in the first branch of the main pulmonary artery, than those who died.

Both measures were also predictive of pulmonary hypertension unresponsive to

iNO. The hyperoxygenation test and lung-to-head-ratio were both best predictive

for neonatal survival when measured following balloon removal (p<0.002).

Discriminant analysis confirmed that these two parameters are independent

predictors of outcome.




3

, Conclusions: In fetuses undergoing FETO, pulmonary vascular reactivity in

relation to oxygen and lung size are independent predictors of neonatal survival,

and pulmonary hypertension. The hyperoxygenation test merits further study in

expectantly managed cases.




Key words: Congenital Diaphragmatic Hernia, hyperoxygenation test,

pulmonary hypertension, lung vascular reactivity.




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