[Operative technique and follow-up effect of endoscopic congenital choanal atresia and dilatation]

Insights

Endoscopic dilatation and plasty effectively treat infant choanal atresia. Prolonged nasal stenting (over 6 months) is crucial to prevent restenosis and ensure good nasal ventilation post-surgery.

Area of Science:

  • Otolaryngology
  • Pediatric Surgery
  • Endoscopic Surgery

Background:

  • Congenital choanal atresia is a rare condition affecting newborns.
  • Surgical intervention is necessary to restore nasal breathing in affected infants.

Purpose of the Study:

  • To evaluate the operative technique and outcomes of endoscopic dilatation and plasty for congenital choanal atresia.
  • To determine the optimal duration for nasal stenting to prevent restenosis.

Main Methods:

  • Retrospective analysis of 7 infants with congenital choanal atresia treated between September 2016 and January 2018.
  • Diagnosis confirmed using electronic nasopharyngoscopy and nasal CT scans.
  • Surgical procedures involved endoscopic dilatation and plasty, with varying durations of nasal stenting.

Main Results:

  • All 7 patients successfully underwent endoscopic surgery.
  • Postoperative follow-up (8-23 months) showed good nasal ventilation in most cases.
  • One patient required reoperation due to early stent removal, highlighting the importance of prolonged stenting.

Conclusions:

  • Endoscopic techniques are accurate and effective for diagnosing and treating choanal atresia.
  • Maintaining nasal stenting for over 6 months is recommended to avoid re-constriction and ensure long-term success.

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