Long-term morbidity of congenital diaphragmatic hernia: A plea for standardization

Francesco Morini1, Laura Valfrè1, Pietro Bagolan1

  • 1Neonatal Surgery Unit, Department of Medical and Surgical Neonatology, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.

Insights

Congenital diaphragmatic hernia (CDH) survivors face long-term health issues affecting multiple systems. This review examines these sequelae, treatment impacts, and follow-up care for CDH patients.

Area of Science:

  • Pediatric Surgery
  • Neonatology
  • Developmental Pediatrics

Background:

  • Congenital diaphragmatic hernia (CDH) is a serious birth defect with significant long-term health implications.
  • CDH survivors experience morbidities across neurodevelopmental, gastrointestinal, pulmonary, and musculoskeletal systems.
  • The long-term consequences of CDH are increasingly recognized, impacting quality of life.

Purpose of the Study:

  • To review the spectrum of long-term sequelae in congenital diaphragmatic hernia survivors.
  • To evaluate the impact of contemporary treatments on CDH outcomes.
  • To analyze the structure and effectiveness of established follow-up programs for CDH patients.

Main Methods:

  • Comprehensive literature review of studies on congenital diaphragmatic hernia survivors.
  • Analysis of data on neurodevelopmental, gastrointestinal, pulmonary, and musculoskeletal outcomes.
  • Evaluation of current treatment modalities and follow-up care protocols.

Main Results:

  • CDH survivors exhibit a wide range of chronic morbidities.
  • Health-related quality of life is often compromised in a significant proportion of patients.
  • Variability exists in the design and consistency of follow-up programs globally.

Conclusions:

  • Long-term sequelae are a critical consideration for congenital diaphragmatic hernia care.
  • Optimized follow-up programs are essential for managing CDH survivors' complex health needs.
  • Further research is needed to standardize and improve long-term management strategies.