Tracheomalacia and tracheomegaly in infants and children with congenital diaphragmatic hernia managed with and without fetoscopic endoluminal tracheal occlusion (FETO): a multicentre, retrospective cohort study
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- FETO increases tracheomalacia risk by 5% in CDH infants, but most cases resolve spontaneously within 55 months without long-term sequelae.
- Tracheal occlusion results in 31% wider tracheal diameter (tracheomegaly), a structural change that persists after the intervention.
- 37% of FETO patients retain metallic balloon fragments, though no significant complications from retained material were reported in this cohort.
- Despite higher tracheomalacia rates, FETO remains effective for promoting lung growth in severe CDH without apparent long-term airway morbidity.
- Pediatric surgeons should anticipate transient tracheomalacia in FETO patients and counsel families on expected resolution timeline.
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Could tracheal occlusion for diaphragmatic hernia introduce hidden risks that pediatric surgeons should know about? I'm Carlos Colunga for Stay Current, and this is an article you should know about. Researchers from this multi-center cohort study examined the outcomes from infants with congenital diaphragmatic hernia, with or without tracheal occlusion, to assess its impact on tracheomalacia prevalence and its related complications. And what did they find? First, tracheomalacia was 5% more common in tracheal occluded infants with 4% more cases. Although, These symptoms typically receded within 55 months. Second, these infants typically showed a larger trachea, which was around 31% wider, and finally, 37% of trachealally occluded cases retained metallic balloon components, although no significant complications were reported. In conclusion, while tracheal occlusion is effective in promoting long growth, it is associated with a higher risk of tracheomalacia, although most cases resolve and they do not appear to have long-term effects. So let us know, what do you think?