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Development of a diagnostic model to identify patients at high risk for cerebellopontine angle lesions

PURPOSE: To develop a diagnostic model to identify patients at high risk of a CPA lesion. METHODS: A consecutive cohort of patients with AAD referred by a general practitioner, who underwent their first MRI examination of the CPA between 2005 and 2015 was included. Demographics, symptoms, findings d...

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Autores principales: Hentschel, Mayke, Rovers, Maroeska, Steens, Stefan, Hannink, Gerjon, Kunst, Henricus
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8897319/
https://www.ncbi.nlm.nih.gov/pubmed/33813627
http://dx.doi.org/10.1007/s00405-021-06778-6
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author Hentschel, Mayke
Rovers, Maroeska
Steens, Stefan
Hannink, Gerjon
Kunst, Henricus
author_facet Hentschel, Mayke
Rovers, Maroeska
Steens, Stefan
Hannink, Gerjon
Kunst, Henricus
author_sort Hentschel, Mayke
collection PubMed
description PURPOSE: To develop a diagnostic model to identify patients at high risk of a CPA lesion. METHODS: A consecutive cohort of patients with AAD referred by a general practitioner, who underwent their first MRI examination of the CPA between 2005 and 2015 was included. Demographics, symptoms, findings during physical examination, and pure-tone audiometry were used as potential predictors. The presence of a CPA lesion was used as outcome. RESULTS: We analyzed data of 2,214 patients, detecting 73 CPA lesions in 69 (3.1%) patients. The final model contained eleven variables, namely gender [male] [OR 1.055 (95% CI 0.885–1.905)], sudden onset of hearing loss [OR 0.768 (95% CI 0.318–0.992)], gradual onset of hearing loss [OR 1.069 (95% CI 0.500–1.450)], unilateral tinnitus [OR 0.682 (95% CI 0.374–0.999)], complaints of unilateral aural fullness [OR 1.006 (95% CI 0.783–2.155)], instability [OR 1.006 (95% CI 0.580–2.121)], headache [OR 0.959 (95% CI 0.059–1.090)], facial numbness [OR 2.746 (95% CI 0.548–11.085)], facial nerve dysfunction during physical examination [OR 1.024 (95% CI 0.280–3.702)], and asymmetry in BC at 1 kHz [OR 1.013 (95% CI 1.000–1.027)] and 4 kHz [OR 1.008 (95% CI 1.000–1.026)]. CONCLUSION: The proposed diagnostic model is a first step in selecting patients with a high risk of a CPA lesion among those with AAD. It needs to be externally validated prior to its implementation in clinical practice. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00405-021-06778-6.
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spelling pubmed-88973192022-03-08 Development of a diagnostic model to identify patients at high risk for cerebellopontine angle lesions Hentschel, Mayke Rovers, Maroeska Steens, Stefan Hannink, Gerjon Kunst, Henricus Eur Arch Otorhinolaryngol Otology PURPOSE: To develop a diagnostic model to identify patients at high risk of a CPA lesion. METHODS: A consecutive cohort of patients with AAD referred by a general practitioner, who underwent their first MRI examination of the CPA between 2005 and 2015 was included. Demographics, symptoms, findings during physical examination, and pure-tone audiometry were used as potential predictors. The presence of a CPA lesion was used as outcome. RESULTS: We analyzed data of 2,214 patients, detecting 73 CPA lesions in 69 (3.1%) patients. The final model contained eleven variables, namely gender [male] [OR 1.055 (95% CI 0.885–1.905)], sudden onset of hearing loss [OR 0.768 (95% CI 0.318–0.992)], gradual onset of hearing loss [OR 1.069 (95% CI 0.500–1.450)], unilateral tinnitus [OR 0.682 (95% CI 0.374–0.999)], complaints of unilateral aural fullness [OR 1.006 (95% CI 0.783–2.155)], instability [OR 1.006 (95% CI 0.580–2.121)], headache [OR 0.959 (95% CI 0.059–1.090)], facial numbness [OR 2.746 (95% CI 0.548–11.085)], facial nerve dysfunction during physical examination [OR 1.024 (95% CI 0.280–3.702)], and asymmetry in BC at 1 kHz [OR 1.013 (95% CI 1.000–1.027)] and 4 kHz [OR 1.008 (95% CI 1.000–1.026)]. CONCLUSION: The proposed diagnostic model is a first step in selecting patients with a high risk of a CPA lesion among those with AAD. It needs to be externally validated prior to its implementation in clinical practice. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00405-021-06778-6. Springer Berlin Heidelberg 2021-04-03 2022 /pmc/articles/PMC8897319/ /pubmed/33813627 http://dx.doi.org/10.1007/s00405-021-06778-6 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Otology
Hentschel, Mayke
Rovers, Maroeska
Steens, Stefan
Hannink, Gerjon
Kunst, Henricus
Development of a diagnostic model to identify patients at high risk for cerebellopontine angle lesions
title Development of a diagnostic model to identify patients at high risk for cerebellopontine angle lesions
title_full Development of a diagnostic model to identify patients at high risk for cerebellopontine angle lesions
title_fullStr Development of a diagnostic model to identify patients at high risk for cerebellopontine angle lesions
title_full_unstemmed Development of a diagnostic model to identify patients at high risk for cerebellopontine angle lesions
title_short Development of a diagnostic model to identify patients at high risk for cerebellopontine angle lesions
title_sort development of a diagnostic model to identify patients at high risk for cerebellopontine angle lesions
topic Otology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8897319/
https://www.ncbi.nlm.nih.gov/pubmed/33813627
http://dx.doi.org/10.1007/s00405-021-06778-6
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