TY - JOUR
T1 - Fetoscopic Endoluminal Tracheal Occlusion in Congenital Diaphragmatic Hernia
T2 - Unraveling the Impact of Prematurity and Suboptimal Fetal Lung Growth
AU - Holden, Kylie I.
AU - Ebanks, Ashley H.
AU - Bergh, Eric P.
AU - Johnson, Anthony
AU - Tsao, Kuojen
AU - Lally, Kevin P.
AU - Harting, Matthew T.
N1 - Publisher Copyright:
© 2025 S. Karger AG, Basel.
PY - 2025
Y1 - 2025
N2 - Introduction: Congenital diaphragmatic hernia (CDH) poses significant challenges in both prenatal diagnosis and postnatal management. Fetoscopic endoluminal tracheal occlusion (FETO) aimed to enhance survival rates among patients with severe CDH, defined by an observedto- expected lung-to-head ratio (o/e-LHR) of less than 25%. However, issues such as preterm delivery and suboptimal fetal lung growth (SFLG) complicate outcomes. This study examines the effects of these critical risks on FETO results. Methods: Data were retrospectively gathered from the multi-institutional CDH Study Group registry on patients with CDH who underwent FETO between 2015 and 2023. Key metrics included CDH study group stage, gestational age (with preterm defined as <37 weeks), o/e-LHR, FETO details, and survival outcomes. The primary outcome was survival, correlated with lung growth and prematurity. Results: Among 4,524 CDH patients, 106 (2.3%) received FETO; however, 43 patients had o/e-LHR data. Analyses revealed an overall survival rate of 72.1%, though survival for patients delivered preterm with SFLG decreased to 57.1%, while survival among term patients with any increase in fetal lung growth was 90.0%. In univariate analyses, the balloon inflation duration (p = 0.05), the use of extracorporeal life support (p = 0.04), and the post-balloon o/e-LHR (p = 0.04) were associated with survival, while in a multivariable logistic regression, the change in o/e-LHR after FETO (OR = 1.07, p = 0.05) was the only variable found to be significantly associated with survival. Conclusion: Prematurity and SFLG are critical factors linked to decreased survival in FETO, with improved o/ e-LHR correlating with better outcomes. Future research should focus on refining patient selection and procedural protocols, with a particular focus on mitigating known complications such as preterm delivery and SFLG, to enhance survival rates.
AB - Introduction: Congenital diaphragmatic hernia (CDH) poses significant challenges in both prenatal diagnosis and postnatal management. Fetoscopic endoluminal tracheal occlusion (FETO) aimed to enhance survival rates among patients with severe CDH, defined by an observedto- expected lung-to-head ratio (o/e-LHR) of less than 25%. However, issues such as preterm delivery and suboptimal fetal lung growth (SFLG) complicate outcomes. This study examines the effects of these critical risks on FETO results. Methods: Data were retrospectively gathered from the multi-institutional CDH Study Group registry on patients with CDH who underwent FETO between 2015 and 2023. Key metrics included CDH study group stage, gestational age (with preterm defined as <37 weeks), o/e-LHR, FETO details, and survival outcomes. The primary outcome was survival, correlated with lung growth and prematurity. Results: Among 4,524 CDH patients, 106 (2.3%) received FETO; however, 43 patients had o/e-LHR data. Analyses revealed an overall survival rate of 72.1%, though survival for patients delivered preterm with SFLG decreased to 57.1%, while survival among term patients with any increase in fetal lung growth was 90.0%. In univariate analyses, the balloon inflation duration (p = 0.05), the use of extracorporeal life support (p = 0.04), and the post-balloon o/e-LHR (p = 0.04) were associated with survival, while in a multivariable logistic regression, the change in o/e-LHR after FETO (OR = 1.07, p = 0.05) was the only variable found to be significantly associated with survival. Conclusion: Prematurity and SFLG are critical factors linked to decreased survival in FETO, with improved o/ e-LHR correlating with better outcomes. Future research should focus on refining patient selection and procedural protocols, with a particular focus on mitigating known complications such as preterm delivery and SFLG, to enhance survival rates.
KW - Congenital diaphragmatic hernia
KW - Fetoscopic endoluminal tracheal occlusion
KW - Neonatal outcome
KW - Prenatal diagnosis
KW - Preterm delivery
KW - Pulmonary hypoplasia
UR - https://www.scopus.com/pages/publications/105012928092
U2 - 10.1159/000546839
DO - 10.1159/000546839
M3 - Article
C2 - 40532679
AN - SCOPUS:105012928092
SN - 1015-3837
JO - Fetal Diagnosis and Therapy
JF - Fetal Diagnosis and Therapy
ER -