Outcomes of infants with congenital diaphragmatic hernia by side of defect in the FETO era

Kamal Ali, Theodore Dassios, Syed Abdul Khaliq, Emma E. Williams, Kentaro Tamura, Mark Davenport, Anne Greenough*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

21 Citations (Scopus)

Abstract

Purpose: To compare the outcomes of infants with a right (RCDH) versus a left-sided (LCDH) congenital diaphragmatic hernia (CDH) and whether these differed according to whether the infants had undergone fetoscopic tracheal occlusion (FETO). Methods: Demographics, the type of surgical repair, preoperative and postoperative courses and respiratory, gastrointestinal, surgical and skeletal morbidities at follow-up were compared between infants with a RCDH or LCDH. A sub-analysis was undertaken in those who had undergone FETO. Results: During the study period, there were 167 infants with a LCDH and 24 with a RCDH; 106 underwent FETO (15 RCDH). Overall, the need for inhaled nitric oxide (p = 0.036) was higher in the RCDH group and, at follow-up, infants with RCDH were more likely to have a hernia recurrence (p = 0.043), pectus deformity (p = 0.019), scoliosis (p = 0.029) and suffer chronic respiratory morbidity (p = 0.001). There were, however, no significant differences in short term or long term outcomes (hernia recurrence (p = 0.237), pectus deformity (p = 0.322), scoliosis (p = 0.0174) or chronic respiratory morbidity (p = 0.326)) between infants with a right or left sided CDH who had undergone FETO. Conclusion: Overall, infants with a RCDH compared to those with a LCDH had greater long-term morbidity, but not if they had undergone FETO.

Original languageEnglish
Pages (from-to)743-747
Number of pages5
JournalPediatric Surgery International
Volume35
Issue number7
Early online date14 May 2019
DOIs
Publication statusPublished - 8 Jul 2019

Keywords

  • Congenital diaphragmatic hernia
  • Follow-up
  • Hernia recurrence
  • Survival

Fingerprint

Dive into the research topics of 'Outcomes of infants with congenital diaphragmatic hernia by side of defect in the FETO era'. Together they form a unique fingerprint.

Cite this