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Management of choanal atresia in cases of craniofacial malformation
Martin Stieve1, H G Kempf, Th Lenarz
1Department of Otolaryngology, Medical University of Hannover, Hannover, Germany ; Department of Otolaryngology, Medical University of Hannover, Carl-Neuberg-Str. 1, D-30625 Hannover, Germany.
Insights
Endonasal endoscopic surgery effectively treats congenital choanal atresia in infants with craniofacial malformations. This minimally invasive approach reduces surgical trauma and bleeding risk, with restenosis minimized through proper fixation and care.
Area of Science:
- Otolaryngology
- Pediatric Surgery
- Medical Engineering
Background:
- Congenital choanal atresia presents a significant challenge, particularly in infants with complex craniofacial malformations.
- This condition necessitates prompt and effective surgical intervention to ensure adequate respiration and feeding.
Purpose of the Study:
- To detail the methodology and outcomes of the endonasal endoscopic approach for congenital choanal atresia.
- To evaluate the efficacy of this technique in infants and children, including those with severe craniofacial anomalies.
Main Methods:
- Utilized computed tomography (CT) scans for diagnosis and intraoperative endoscopy to assess atresia type (membranous or osseous).
- Employed trocars and diamond drills for atresia plate and osseous portion removal, followed by transnasal silicone tube insertion for several months.
- Surgical intervention was performed immediately after birth for bilateral atresia cases and later for unilateral cases.
Main Results:
- The endonasal endoscopic approach was successful in treating seven pediatric patients with choanal atresia between 1999 and 2006.
- While tube dislodcations required adjustments in bilateral cases, no further stenoses were observed post-tube removal (3-6 months).
- One case of septal perforation was noted, but overall outcomes were positive post-intervention.
Conclusions:
- The transnasal endoscopic approach offers a minimally invasive option for newborns and infants, characterized by low surgical trauma and reduced bleeding risk.
- Effective management of restenosis is achievable through adequate tube fixation and comprehensive inpatient care.
Objective:
To report the method and results of endonasal endoscopic approach in congenital choanal atresia in cases of craniofacial malformation.
Patients:
The pathology of unilateral and bilateral choanal atresia and the treatment results in seven children treated between 1999 and 2006 are presented. 5 infants suffering from bilateral atresia also had severe malformations (Charge syndrome [2 patients], trisomy 18, microcephalus, central cranioschisis, cleft lip and anophthalmia 9). The surgical intervention was carried out immediately after birth. 2 patients with unilateral atresia were treated in their second and sixth year of life respectively. CT scan was the diagnostic procedure of choice. Intraoperative endoscopy showed both membraneous and osseous atresia.
Surgical Procedure:
Trocars of different sizes were used to open the atresia plate, while the osseous parts were removed with diamond drills. Silicone tubes were inserted transnasally and remained in place for several months to improve the infants'ability to breath and drink.
Results:
In all cases of bilateral atresia the tubes either had to be changed repeatedly or replaced with larger tubes due to dislocation and head growth. The septum was perforated in one case. No further stenoses were detected following the removal of the tubes (after 3-6 months).
Conclusion:
The transnasal access is particularly suited to newborns and infants because it induces a minor surgical trauma and carries a low risk of bleeding if endoscopes are used. The results show that the risk of restenoses can be minimised with sufficient fixating and in-patient care.
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