Otolaryngological Disease Clinical Trial
Official title:
Stentless Endoscopic Transnasal Transseptal Choanoplasty
Congenital choanal atresia is an abnormality of the posterior nasal passages resulting in
complete or partial obstruction of the nasal airways. It has an incidence of 1: 5000 to 8000
live births, with a female predominance. 41% - 72% occur in conjunction with non-syndromic
facial abnormalities such as arched palate, cleft lip, and auricular deformities. About 4%
present as a component of chromosomally-based syndromes such as (coloboma, heart defect,
atresia choanae, retarded growth, genital abnormality, and ear abnormality" and Treacher
Collins syndromes.
Previous reports have described the ratio of bony to membranous choanal atresia as 9:1.
However, a detailed review of computed tomography study combined with histopathological
studies has shown mixed bony-membranous atresia in about 70% of cases and purely bony
atresia in 30% of cases.
Common choanal atresia repair techniques include puncture and dilatation of the atretic
area. Endoscopic drilling combined with dissection of the atretic plate and its surrounding
structures has been introduced more recently. The approaches have been through transnasal,
transpalatal, and transseptal routes. Each of which have experienced varying popularity
through time. Regardless of the access route and repair technique used, re-stenosis is a
common postoperative complication. To prevent re-stenosis and subsequent re-operation, many
authors advocate meticulous preservation of mucosa for use as flaps, which in most cases are
combined with postoperative stenting. However, stenting, is controversial
The surgical procedure is performed under general anesthesia. Preoperatively, cotton
pledgets soaked in a solution of topical vasoconstrictors are placed against the nasal
mucosa for topical decongestion. Local anesthesia is infiltrated into the nasal septum, the
atretic plate, the middle turbinate, and the superolateral nasal wall. An endoscopic view of
the surgical field is maintained at all times during the procedure using a 4-mm nasal
endoscope with 0-degree or 30-degree visual angulation. Firstly, mucosa is elevated
bilaterally from the underlying cartilaginous and bony septum on both sides. Then the
posterior half of the septum including the vomer is removed using Blakesley forceps and a
1-mm or 2.5-mm diamond burr. After that, the flaps are fashioned using the preserved mucosa.
At last, the flaps are secured in position with a thin layer of fibrin glue or gel foam. No
packing or stenting is used. The patient is extubated immediately following the procedure
and early oral feeding encouraged. The intended length of stay is overnight.
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