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dc.contributor.authorEspetvedt, Annelin
dc.contributor.authorWiig, Siri
dc.contributor.authorMyrnes-Hansen, Kai Victor
dc.contributor.authorBrønnick, Kolbjørn Kallesten
dc.date.accessioned2023-06-27T11:02:26Z
dc.date.available2023-06-27T11:02:26Z
dc.date.created2023-06-22T16:41:14Z
dc.date.issued2023
dc.identifier.citationEspetvedt, A., Wiig, S., Myrnes-Hansen, K. V., & Brønnick, K. K. (2023). The assessment of qualitative olfactory dysfunction in COVID-19 patients: a systematic review of tools and their content validity. Frontiers in Psychology, 14, 1190994.en_US
dc.identifier.issn1664-1078
dc.identifier.urihttps://hdl.handle.net/11250/3073452
dc.description.abstractBackground: There is a lack of overview of the tools used to assess qualitative olfactory dysfunction, including parosmia and phantosmia, following COVID-19 illness. This could have an impact on the diagnosis and treatment offered to patients. Additionally, the formulations of symptoms are inconsistent and often unclear, and consensus around the wording of questions and responses is needed. Aim of study: The aim of this systematic review is to provide an overview of tools used to assess qualitative olfactory dysfunction after COVID-19, in addition to addressing the content validity (i.e., item and response formulations) of these tools. Methods: MEDLINE, Web of Science, and EMBASE were searched 5th of August 2022 and updated on the 25th of April 2023 to identify studies that assess qualitative olfactory dysfunction in COVID-19 patients. Primary outcomes were the tool used (i.e., questionnaire or objective test) and item and response formulations. Secondary outcomes included psychometric properties, study design, and demographic variables. Results: The assessment of qualitative olfactory dysfunction is characterized by heterogeneity, inconsistency, and lack of validated tools to determine the presence and degree of symptoms. Several tools with overlapping and distinct features were identified in this review, of which some were thorough and detailed, while others were merely assessing the presence of symptoms as a binary measure. Item and response formulations are also inconsistent and often used interchangeably, which may lead to confusion, incorrect diagnoses, and inappropriate methods for solving the problem. Conclusions: There is an unmet need for a reliable and validated tool for assessing qualitative olfactory dysfunction, preferably one that also captures quantitative olfactory issues (i.e., loss of smell), to ensure time-effective and specific assessment of the ability to smell. A consensus around the formulation of items and response options is also important to increase the understanding of the problem, both for clinicians, researchers, and the patient, and ultimately to provide the appropriate diagnosis and treatment.en_US
dc.language.isoengen_US
dc.publisherFrontiers Media S.A.en_US
dc.rightsNavngivelse 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/deed.no*
dc.titleThe assessment of qualitative olfactory dysfunction in COVID-19 patients: a systematic review of tools and their content validityen_US
dc.typePeer revieweden_US
dc.typeJournal articleen_US
dc.description.versionpublishedVersionen_US
dc.rights.holderThe authorsen_US
dc.subject.nsiVDP::Medisinske Fag: 700en_US
dc.source.volume14en_US
dc.source.journalFrontiers in Psychologyen_US
dc.identifier.doi10.3389/fpsyg.2023.1190994
dc.identifier.cristin2157268
dc.relation.projectSHARE - Centre for Resilience in Healthcare: 5091en_US
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1


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