Open AccessSuggestions for shaping tinnitus service provision in Western Europe: Lessons from the COVID‐19 pandemic
Author(s) -
Beukes Eldré W.,
Lourenco Matheus P. C. G.,
Biot Lana,
Andersson Gerhard,
Kaldo Viktor,
Manchaiah Vinaya,
Jacquemin Laure
Publication year - 2021
Publication title -
international journal of clinical practice
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.756
H-Index - 98
eISSN - 1742-1241
pISSN - 1368-5031
DOI - 10.1111/ijcp.14196
Subject(s) - tinnitus , medicine , pandemic , hearing loss , multidisciplinary approach , audiology , covid-19 , disease , pathology , social science , sociology , infectious disease (medical specialty)
Background Tinnitus severity has been exacerbated because of the COVID‐19 pandemic and those with tinnitus require additional support. Such support should be informed by patient preferences and needs. The objective of this study was to gather information from individuals with tinnitus living in Europe to inform stakeholders of the (a) support they needed in relation to changes associated with the COVID‐19 pandemic and (b) suggestions regarding tinnitus care for the future. Methods A cross‐sectional mixed method study design was used using closed and open‐ended questions via an online survey. Data were gathered from 710 adults experiencing tinnitus in Western Europe, with the majority living in The Netherlands, Belgium and Sweden. Data were analysed using qualitative content analysis and descriptive statistics. Results Those with tinnitus indicated the following support needs during the pandemic (a) support for tinnitus, (b) support for hearing‐related difficulties, (c) social support and (d) pandemic‐related support. Five directions for future tinnitus care were provided, namely, (a) need for understanding professional support and access to multidisciplinary experts, (b) greater range of therapies and resources, (c) access to more information about tinnitus, (d) prioritising tinnitus research and (e) more support for hearing protection and hearing loss prevention. Conclusions The findings point to the need for accessible (remote), patient‐centred, suitable and evidence‐based tinnitus care. Insights from the current study can be used by various stakeholders including clinical practitioners and tinnitus support services to ensure those with tinnitus have access to the help and support required in order to reduce service provision insufficiencies.