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Choice of treatment evaluated after trial periods with bone conduction devices and contralateral routing of sound systems in patients with single‐sided deafness

OBJECTIVES: Patients with single‐sided deafness (SSD) may experience difficulties with speech perception in noise, sound localization, have tinnitus and experience a reduced quality of life (QoL). contralateral routing of sound hearing aids (CROS) or bone conduction devices (BCD) may partly improve...

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Autores principales: Wendrich, Anne W., van Heteren, Jan A. A., Peters, Jeroen P. M., Cattani, Guido, Stokroos, Robert J., Versnel, Huib, Smit, Adriana L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9948587/
https://www.ncbi.nlm.nih.gov/pubmed/36846432
http://dx.doi.org/10.1002/lio2.1002
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author Wendrich, Anne W.
van Heteren, Jan A. A.
Peters, Jeroen P. M.
Cattani, Guido
Stokroos, Robert J.
Versnel, Huib
Smit, Adriana L.
author_facet Wendrich, Anne W.
van Heteren, Jan A. A.
Peters, Jeroen P. M.
Cattani, Guido
Stokroos, Robert J.
Versnel, Huib
Smit, Adriana L.
author_sort Wendrich, Anne W.
collection PubMed
description OBJECTIVES: Patients with single‐sided deafness (SSD) may experience difficulties with speech perception in noise, sound localization, have tinnitus and experience a reduced quality of life (QoL). contralateral routing of sound hearing aids (CROS) or bone conduction devices (BCD) may partly improve subjective speech communication and QoL in SSD patients. A trial period with these devices can help in making a well‐informed choice of treatment. Our aim was to evaluate factors influencing the choice of treatment made after a BCD and CROS trial period in adult SSD patients. METHODS: Patients were randomized in the: “first BCD, then CROS” or “first CROS, then BCD” trial period group. After the BCD on headband and CROS were tested for 6 weeks each, patients choose for BCD, CROS or no treatment. Primary outcome was the distribution of choice of treatment. Secondary outcomes included the association between the choice of treatment and patient characteristics, reasons for treatment acceptance or rejection, device usage during the trial periods, and disease‐specific QoL outcomes. RESULTS: Of 91 patients randomized, 84 completed both trial periods and made their choice of treatment: 25 (30%) BCD, 34 (40%) CROS, and 25 (30%) no treatment. No characteristics were found to be related to choice of treatment. Top three reasons for acceptance or rejection were: device (dis)comfort, sound quality and (dis)advantage of subjective hearing. Average daily device use during the trial periods was higher for CROS than for BCD. Choice of treatment was significantly related with both duration of device usage and greater improvement of QoL after the corresponding trial period. CONCLUSION: The majority of SSD patients preferred BCD or CROS over no treatment. Evaluating device usage, discussing treatment (dis)advantages and disease‐specific QoL outcomes after trial periods are to be considered during patient counseling and could facilitate whether to choose one of these treatments. LEVEL OF EVIDENCE: 1B.
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spelling pubmed-99485872023-02-24 Choice of treatment evaluated after trial periods with bone conduction devices and contralateral routing of sound systems in patients with single‐sided deafness Wendrich, Anne W. van Heteren, Jan A. A. Peters, Jeroen P. M. Cattani, Guido Stokroos, Robert J. Versnel, Huib Smit, Adriana L. Laryngoscope Investig Otolaryngol Otology, Neurotology, and Neuroscience OBJECTIVES: Patients with single‐sided deafness (SSD) may experience difficulties with speech perception in noise, sound localization, have tinnitus and experience a reduced quality of life (QoL). contralateral routing of sound hearing aids (CROS) or bone conduction devices (BCD) may partly improve subjective speech communication and QoL in SSD patients. A trial period with these devices can help in making a well‐informed choice of treatment. Our aim was to evaluate factors influencing the choice of treatment made after a BCD and CROS trial period in adult SSD patients. METHODS: Patients were randomized in the: “first BCD, then CROS” or “first CROS, then BCD” trial period group. After the BCD on headband and CROS were tested for 6 weeks each, patients choose for BCD, CROS or no treatment. Primary outcome was the distribution of choice of treatment. Secondary outcomes included the association between the choice of treatment and patient characteristics, reasons for treatment acceptance or rejection, device usage during the trial periods, and disease‐specific QoL outcomes. RESULTS: Of 91 patients randomized, 84 completed both trial periods and made their choice of treatment: 25 (30%) BCD, 34 (40%) CROS, and 25 (30%) no treatment. No characteristics were found to be related to choice of treatment. Top three reasons for acceptance or rejection were: device (dis)comfort, sound quality and (dis)advantage of subjective hearing. Average daily device use during the trial periods was higher for CROS than for BCD. Choice of treatment was significantly related with both duration of device usage and greater improvement of QoL after the corresponding trial period. CONCLUSION: The majority of SSD patients preferred BCD or CROS over no treatment. Evaluating device usage, discussing treatment (dis)advantages and disease‐specific QoL outcomes after trial periods are to be considered during patient counseling and could facilitate whether to choose one of these treatments. LEVEL OF EVIDENCE: 1B. John Wiley & Sons, Inc. 2022-12-27 /pmc/articles/PMC9948587/ /pubmed/36846432 http://dx.doi.org/10.1002/lio2.1002 Text en © 2022 The Authors. Laryngoscope Investigative Otolaryngology published by Wiley Periodicals LLC on behalf of The Triological Society. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Otology, Neurotology, and Neuroscience
Wendrich, Anne W.
van Heteren, Jan A. A.
Peters, Jeroen P. M.
Cattani, Guido
Stokroos, Robert J.
Versnel, Huib
Smit, Adriana L.
Choice of treatment evaluated after trial periods with bone conduction devices and contralateral routing of sound systems in patients with single‐sided deafness
title Choice of treatment evaluated after trial periods with bone conduction devices and contralateral routing of sound systems in patients with single‐sided deafness
title_full Choice of treatment evaluated after trial periods with bone conduction devices and contralateral routing of sound systems in patients with single‐sided deafness
title_fullStr Choice of treatment evaluated after trial periods with bone conduction devices and contralateral routing of sound systems in patients with single‐sided deafness
title_full_unstemmed Choice of treatment evaluated after trial periods with bone conduction devices and contralateral routing of sound systems in patients with single‐sided deafness
title_short Choice of treatment evaluated after trial periods with bone conduction devices and contralateral routing of sound systems in patients with single‐sided deafness
title_sort choice of treatment evaluated after trial periods with bone conduction devices and contralateral routing of sound systems in patients with single‐sided deafness
topic Otology, Neurotology, and Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9948587/
https://www.ncbi.nlm.nih.gov/pubmed/36846432
http://dx.doi.org/10.1002/lio2.1002
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