Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2024 Apr 19;52(5):546-551.
doi: 10.1515/jpm-2023-0425. Print 2024 Jun 25.

Bias in the prenatal lung measurements in fetal congenital diaphragmatic hernia with intrauterine growth restriction

Affiliations

Bias in the prenatal lung measurements in fetal congenital diaphragmatic hernia with intrauterine growth restriction

Emrah Aydın et al. J Perinat Med. .

Abstract

Objectives: The failure of a fetus to develop to its full potential due to maternal or placental factors is known as intrauterine growth restriction (IUGR). Fetal head growth is usually preserved in that situation producing a potential discordance between head and body size. Our goal is to discover if IUGR has an impact on the prenatal ultrasound measurements taken to assess pulmonary development in congenital diaphragmatic hernia (CDH).

Methods: A retrospective chart review (IRB#2017-6361) was performed on all prenatally diagnosed CDH patients from 2007 to 2016. Patient demographics, fetal and neonatal anthropometric measurements, and fetal lung parameters were the main subjects of the data that were gathered. Fetal growth was assessed by the curves based on US data by Olsen et al. and by Peleg et al. Of 147 CDH patients, 19 (12.9 %) patients were diagnosed with IUGR before the 30th gestational week while there were 20 (13.6 %) patients after the 30th gestational week.

Results: Patients with IUGR and the observed-to-expected lung-to-head ratio (O/E LHR) less than 25 % had better survival rates both to discharge and date compared to non IUGR group (p=0.226, OR 2.25 95 % CI 0.60-1.08 and p=0.175, OR 2.40 95 % CI 0.66-1.17, respectively). Moreover, the ECMO need of the patients who had IUGR and O/E LHR less than 25 % was significantly less than the patients without IUGR (38.5 vs. 80.0 %, p=0.005).

Conclusions: This study confirms that the intrauterine measurements to predict pulmonary hypoplasia in CDH patients are misleading in the presence of IUGR and cause an overestimation.

Keywords: congenital diaphragmatic hernia; fetal growth restriction; intrauterine growth restriction; lung-to-head ratio (LHR); observed-to-expected LHR (O/E LHR).

PubMed Disclaimer

References

    1. Colvin, J, Bower, C, Dickinson, JE, Sokol, J. Outcomes of congenital diaphragmatic hernia: a population-based study in Western Australia. Pediatrics 2005;116:e356–63. https://doi.org/10.1542/peds.2004-2845 . - DOI
    1. Salas, GL, Otaño, JC, Cannizzaro, CM, Mazzucchelli, MT, Goldsmit, GS. Congenital diaphragmatic hernia: postnatal predictors of mortality. Arch Argent Pediatr 2020;118:173–9. https://doi.org/10.5546/aap.2020.eng.173 . - DOI
    1. Jani, JC, Peralta, CFA, Nicolaides, KH. Lung-to-head ratio: a need to unify the technique. Ultrasound Obstet Gynecol 2012;39:2–6. https://doi.org/10.1002/uog.11065 . - DOI
    1. Peleg, D, Kennedy, CM, Hunter, SK. Intrauterine growth restriction: identification and management. Am Fam Physician 1998;58:453–60.
    1. Ross, MG. Fetal growth restriction. Medscape 2020. Available from: https://emedicine.medscape.com/article/261226-overview?form=fpf .

LinkOut - more resources