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Congenital Anomalies of the Ossicular Chain: Surgical and Audiological Outcomes

OBJECTIVES: In this study, we aim to analyze audiometric outcomes of middle ear surgery in patients with congenital middle ear anomalies. METHODS: In this single center retrospective cohort study, audiological outcomes were extracted from patient files. Patients with a congenital middle ear anomaly...

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Autores principales: Henkemans, Sara E., Smit, Adriana L., Stokroos, Robert J., Thomeer, Hans G.X.M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8899814/
https://www.ncbi.nlm.nih.gov/pubmed/34116598
http://dx.doi.org/10.1177/00034894211025405
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author Henkemans, Sara E.
Smit, Adriana L.
Stokroos, Robert J.
Thomeer, Hans G.X.M.
author_facet Henkemans, Sara E.
Smit, Adriana L.
Stokroos, Robert J.
Thomeer, Hans G.X.M.
author_sort Henkemans, Sara E.
collection PubMed
description OBJECTIVES: In this study, we aim to analyze audiometric outcomes of middle ear surgery in patients with congenital middle ear anomalies. METHODS: In this single center retrospective cohort study, audiological outcomes were extracted from patient files. Patients with a congenital middle ear anomaly treated surgically in a tertiary referral center between June 2015 and December 2020 were included. Pre- and postoperative short- and long-term audiometric data (at ≥3 and ≥10 months respectively) were compared to analyze hearing outcomes. RESULTS: Eighteen ears (15 patients) were treated surgically with an exploratory tympanotomy. At short term follow up statistically significant improvements in air conduction thresholds and air-bone gaps were found. Hearing improved in 94.4% (17/18) of operated ears. Successful outcome, defined as an air-bone gap closure to within 20 dB after surgery, was reached in 44.4% (8/18). Serviceable hearing (air conduction ≤30 dB) was reached in 55.6% (10/18). Negative outcome (any significant deterioration in hearing) occurred in 1 patient: in this ear otitis media occurred during the postoperative course. At long term follow up, available for 50% of the cohort, hearing remained stable in 5 ears, improved in 1 ear and deteriorated in 3, all of which underwent revision surgery. Sensorineural hearing loss due to surgery, or other complications, were not encountered. CONCLUSION: middle ear surgery was found to be an effective treatment option to improve hearing in this cohort of patients with congenital middle ear anomalies. Surgical goals of obtained gain in air conduction thresholds and serviceable hearing levels were met by most patients without the occurrence of any iatrogenic sensorineural hearing loss.
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spelling pubmed-88998142022-03-08 Congenital Anomalies of the Ossicular Chain: Surgical and Audiological Outcomes Henkemans, Sara E. Smit, Adriana L. Stokroos, Robert J. Thomeer, Hans G.X.M. Ann Otol Rhinol Laryngol Original Articles OBJECTIVES: In this study, we aim to analyze audiometric outcomes of middle ear surgery in patients with congenital middle ear anomalies. METHODS: In this single center retrospective cohort study, audiological outcomes were extracted from patient files. Patients with a congenital middle ear anomaly treated surgically in a tertiary referral center between June 2015 and December 2020 were included. Pre- and postoperative short- and long-term audiometric data (at ≥3 and ≥10 months respectively) were compared to analyze hearing outcomes. RESULTS: Eighteen ears (15 patients) were treated surgically with an exploratory tympanotomy. At short term follow up statistically significant improvements in air conduction thresholds and air-bone gaps were found. Hearing improved in 94.4% (17/18) of operated ears. Successful outcome, defined as an air-bone gap closure to within 20 dB after surgery, was reached in 44.4% (8/18). Serviceable hearing (air conduction ≤30 dB) was reached in 55.6% (10/18). Negative outcome (any significant deterioration in hearing) occurred in 1 patient: in this ear otitis media occurred during the postoperative course. At long term follow up, available for 50% of the cohort, hearing remained stable in 5 ears, improved in 1 ear and deteriorated in 3, all of which underwent revision surgery. Sensorineural hearing loss due to surgery, or other complications, were not encountered. CONCLUSION: middle ear surgery was found to be an effective treatment option to improve hearing in this cohort of patients with congenital middle ear anomalies. Surgical goals of obtained gain in air conduction thresholds and serviceable hearing levels were met by most patients without the occurrence of any iatrogenic sensorineural hearing loss. SAGE Publications 2021-06-11 2022-04 /pmc/articles/PMC8899814/ /pubmed/34116598 http://dx.doi.org/10.1177/00034894211025405 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution 4.0 License (https://creativecommons.org/licenses/by/4.0/) which permits any use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Original Articles
Henkemans, Sara E.
Smit, Adriana L.
Stokroos, Robert J.
Thomeer, Hans G.X.M.
Congenital Anomalies of the Ossicular Chain: Surgical and Audiological Outcomes
title Congenital Anomalies of the Ossicular Chain: Surgical and Audiological Outcomes
title_full Congenital Anomalies of the Ossicular Chain: Surgical and Audiological Outcomes
title_fullStr Congenital Anomalies of the Ossicular Chain: Surgical and Audiological Outcomes
title_full_unstemmed Congenital Anomalies of the Ossicular Chain: Surgical and Audiological Outcomes
title_short Congenital Anomalies of the Ossicular Chain: Surgical and Audiological Outcomes
title_sort congenital anomalies of the ossicular chain: surgical and audiological outcomes
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8899814/
https://www.ncbi.nlm.nih.gov/pubmed/34116598
http://dx.doi.org/10.1177/00034894211025405
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