Cardiac morphology in children at 2 and 10 years of age after congenital diaphragmatic hernia repair: a comparative MRI-based analysis of ECMO and non-ECMO patients - Report - MDSpire
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Cardiac Structure in Pediatric Patients at Ages 2 and 10 Following Repair of Congenital Diaphragmatic Hernia: A Comparative MRI Study of ECMO and Non-ECMO Cases

  • By

  • Schanas Jawhar

  • Greta Thater

  • Stefan Appelhaus

  • Michael Boettcher

  • Julia Elrod

  • Frank G. Zoellner

  • Florian Kipfmueller

  • Marcia Matos-Karaorman

  • Stefan O. Schoenberg

  • Meike Weis

  • September 9, 2026

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Clinical Report: Cardiac Structure in Pediatric Patients Following CDH Repair

Overview

This study investigates long-term cardiac alterations in pediatric patients with congenital diaphragmatic hernia (CDH) who underwent repair, comparing those who required extracorporeal membrane oxygenation (ECMO) with those who did not. MRI-derived parameters were evaluated at ages 2 and 10 to assess cardiac morphology and function.

Background

Congenital diaphragmatic hernia (CDH) is a significant congenital anomaly that can lead to severe pulmonary complications and long-term morbidity. Advances in treatment have improved survival rates, but many patients experience ongoing cardiopulmonary issues, particularly those who required ECMO.

Data Highlights

ParameterECMO Group (n=31)Non-ECMO Group (n=26)
PA/Ao RatioData not providedData not provided
RV/LV RatioData not providedData not provided
Eccentricity IndexData not providedData not provided

Key Findings

  • CDH affects approximately 1 in 2000–5000 live births.
  • PAH is a significant determinant of outcomes in CDH patients.
  • Patients requiring ECMO face a higher risk of long-term complications.
  • Postnatal ventricular disproportion is linked to increased mortality and ECMO requirement.
  • The study utilized MRI to assess cardiac morphology and function at ages 2 and 10.

Clinical Implications

The findings highlight the need for ongoing cardiopulmonary surveillance in CDH patients, particularly those who required ECMO. Clinicians should consider the long-term cardiac assessments as part of the follow-up care for these patients.

Conclusion

This study underscores the importance of understanding cardiac changes in pediatric CDH patients, particularly in those who underwent ECMO, to inform long-term management strategies.

Related Resources & Content

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  5. American Academy of Pediatrics, Pediatrics, 2026 -- Postdischarge Follow-Up of Infants With Congenital Diaphragmatic Hernia
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  7. Postdischarge Follow-Up of Infants With Congenital Diaphragmatic Hernia: Clinical Report | Pediatrics | American Academy of Pediatrics
  8. Early postnatal echocardiographic characteristics impact survival and extracorporeal life support in congenital diaphragmatic hernia | Pediatric Research

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