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Tissue engineered mastoid air cells' regeneration for intractable otitis media

Presenting Author: Shin-ichi Kanemaru

Published online by Cambridge University Press:  03 June 2016

Shin-ichi Kanemaru
Affiliation:
Medical research institute, Kitano Hospital
Rie Kanai
Affiliation:
Medical research institute, Kitano Hospital
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Abstract

Type
Abstracts
Copyright
Copyright © JLO (1984) Limited 2016 

Learning Objectives: How to regenerate middle ear gas exchange function.

Aim: Most chronic otitis media(OMC) are observed poor development of mastoid air cells(MACs) and poor function of Eustachian tube. In order to a complete recovery from intractable otitis media, regeneration of the MACs' gas exchange functions is thought to be need. In this study, we implanted autologous bone fragments as a scaffold and gelatin sponge soaked in basic-fibroblast growth factor (b-FGF) as a regulatory factor to the newly opened mastoid cavity and assessed whether these promote regeneration of MACs or not.

Material and Method: In this study, 10 cases with severe chronic otitis media(n = 3), cholesteatoma(n = 5), and adhesive otitis media(n = 2) were selected. At the 1st stage of operation, before mastoidectomy, cortex bone lid was harvested. Harvested autologous bone fragments with gelatin sponge soaked in b-FGF were implanted into the newly opened mastoid cavity and they were fixed by fibrin glue. Cortex bone lid was returned to the original position and was fixed by autologous bone pate.

By the images of high resolution computed tomography (HRCT), whether MACs were regenerated or not were estimated. The Eustachian tube function were measured before and 9 to 12 months after the 1st stage operation.

Results: Regeneration of MACs was observed 7 out of 10 cases (70%). In 6 out of 7 cases (86%) in the successful cases of regeneration of MACs in both group, Eustachian tube functions were improved. On the other hand, in the failure cases of regeneration of MACs, Eustachian tube functions were not improved.

Conclusions: Implanted autologous bone fragments and gelatin sponge soaked in b-FGF to the newly opened mastoid cavity contribute to regeneration of MACs in both HRCT images and gas exchange function.