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Bilateral choanal atresia: key to success with the transnasal approach

Published online by Cambridge University Press:  29 June 2007

Bharath Singh*
Affiliation:
Durban, Republic of South Africa
*
Dr B. Singh, Dept. of Otohinolaryngology, Faculty of Medicine, P.O. Box 17039, Congella, 4013South Africa.

Abstract

The intranasal approach is generally accepted as the route of choice in the correction of bilateral choanal atresia but unfortunately it is associated with a significant incidence of stenosis.

Over a five-year period, we have diagnosed bilateral choanal atresia in 30 neonates. Trans-nasal surgery was performed on 27 of them. All belonged to the Black race group. The incidence was 1:8,300 live births. There was a female predominance of 5:1. Four (13 per cent) had other associated anomalies. One was a twin.

Various factors were analysed to determine the cause of the stenosis. These were:

1. Drilling compared with curettage of the bony atretic plate. 2. Stenting versus non-stenting. 3. Soft versus hard Portex tube stenting. 4. Variation of stenting period—six, eight and twelve weeks. 5. The use of prophylactic broad spectrum antibiotic for the whole of the stenting period.

The conclusion derived from this study is that curettage of bony atresia, stenting with soft Portex tube for a period of six weeks and the use of broad spectrum antibiotic for the entire stenting period eliminates the problem of stenosis associated with the trans-nasal approach for the correction of bilateral choanal atresia.

Type
Main Articles
Copyright
Copyright © JLO (1984) Limited 1990

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References

Carpenter, R. J., Neel, H. B. (1977) Correction of congenital choanal atresia in children and adults. Laryngoscope, 87: 13041311.CrossRefGoogle ScholarPubMed
Evans, J. N. G., Maclachlan, R. F. (1971) Choanal atresia. Journal of Laryngoscope and Otology, 85: 903929.CrossRefGoogle Scholar
Feuerstein, S. S., Krepsi, Y. P., Sachdev, R. K. (1980) Transnasal correction of choanal atresia. Head and Neck Surgery, 3: 97104.CrossRefGoogle ScholarPubMed
Flake, C. G., Ferguson, C. F. (1964) Congenital choanal atresia in infants and children. Annals of Otology, Rhinology and Laryngology, 73: 458473.CrossRefGoogle ScholarPubMed
Lantz, H. J., Birck, H. G. (1981) Surgical correction of choanal atresia in neonates. Laryngoscope, 81: 16291634.CrossRefGoogle Scholar
Wright, W. K., Shambaugh, G. E., Green, L. (1947) Congenital choanal atresia: A new surgical approach. Annals of Otology, Rhinology and Laryngology, 56: 120126.Google ScholarPubMed