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Olfactory dysfunction in COVID-19: a marker of good prognosis?

INTRODUCTION: In May 2020, the World Health Organization recognized olfactory dysfunction as a COVID-19 symptom. The presence of hyposmia/anosmia may be a marker of good prognosis in COVID-19. OBJECTIVE: To associate the presence of olfaction disorder to the clinical condition severity in patients w...

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Autores principales: Mendonça, Cindy Vitalino, Mendes Neto, José Arruda, Suzuki, Fabio Akira, Orth, Marlon Steffens, Machado Neto, Hugo, Nacif, Sérgio Roberto
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7831803/
https://www.ncbi.nlm.nih.gov/pubmed/33441276
http://dx.doi.org/10.1016/j.bjorl.2020.12.002
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author Mendonça, Cindy Vitalino
Mendes Neto, José Arruda
Suzuki, Fabio Akira
Orth, Marlon Steffens
Machado Neto, Hugo
Nacif, Sérgio Roberto
author_facet Mendonça, Cindy Vitalino
Mendes Neto, José Arruda
Suzuki, Fabio Akira
Orth, Marlon Steffens
Machado Neto, Hugo
Nacif, Sérgio Roberto
author_sort Mendonça, Cindy Vitalino
collection PubMed
description INTRODUCTION: In May 2020, the World Health Organization recognized olfactory dysfunction as a COVID-19 symptom. The presence of hyposmia/anosmia may be a marker of good prognosis in COVID-19. OBJECTIVE: To associate the presence of olfaction disorder to the clinical condition severity in patients with COVID-19. METHODS: Individuals with the flu syndrome caused by SARS-CoV-2, diagnosed from March to June 2020, were recruited. They were divided into three groups: mild flu syndrome, severe flu syndrome (admitted to hospital wards) and critical illness (admitted to the ICU). Inpatients were interviewed by telephone contact after hospital discharge and their medical records were also evaluated regarding complementary test results. Outpatients answered an electronic questionnaire containing only clinical information. RESULTS: A total of 261 patients participated in the study: 23.75% with mild flu syndrome, 57.85% with severe flu syndrome and 18.40% with critical illness. A total of 66.28% patients with COVID-19 had olfaction disorders. In approximately 56.58% of the individuals the smell alterations lasted between 9 days and 2 months. There was a significantly higher proportion of individuals with olfactory dysfunction in the group with mild flu syndrome than in the severe flu syndrome group (mild × severe – p < 0.001; Odds Ratio = 4.63; 95% CI [1.87–10.86]). This relationship was also maintained between patients with mild flu syndrome and critically-ill patients (mild × critical – p <  0.001; Odds Ratio = 9.28; 95% CI [3.52–25.53]). CONCLUSION: Olfaction dysfunction was significantly more prevalent in patients with mild flu syndrome in COVID-19. It may be a predictor of a good prognosis for this infection. New population-based studies must be carried out to corroborate these findings.
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spelling pubmed-78318032021-01-26 Olfactory dysfunction in COVID-19: a marker of good prognosis? Mendonça, Cindy Vitalino Mendes Neto, José Arruda Suzuki, Fabio Akira Orth, Marlon Steffens Machado Neto, Hugo Nacif, Sérgio Roberto Braz J Otorhinolaryngol Original Article INTRODUCTION: In May 2020, the World Health Organization recognized olfactory dysfunction as a COVID-19 symptom. The presence of hyposmia/anosmia may be a marker of good prognosis in COVID-19. OBJECTIVE: To associate the presence of olfaction disorder to the clinical condition severity in patients with COVID-19. METHODS: Individuals with the flu syndrome caused by SARS-CoV-2, diagnosed from March to June 2020, were recruited. They were divided into three groups: mild flu syndrome, severe flu syndrome (admitted to hospital wards) and critical illness (admitted to the ICU). Inpatients were interviewed by telephone contact after hospital discharge and their medical records were also evaluated regarding complementary test results. Outpatients answered an electronic questionnaire containing only clinical information. RESULTS: A total of 261 patients participated in the study: 23.75% with mild flu syndrome, 57.85% with severe flu syndrome and 18.40% with critical illness. A total of 66.28% patients with COVID-19 had olfaction disorders. In approximately 56.58% of the individuals the smell alterations lasted between 9 days and 2 months. There was a significantly higher proportion of individuals with olfactory dysfunction in the group with mild flu syndrome than in the severe flu syndrome group (mild × severe – p < 0.001; Odds Ratio = 4.63; 95% CI [1.87–10.86]). This relationship was also maintained between patients with mild flu syndrome and critically-ill patients (mild × critical – p <  0.001; Odds Ratio = 9.28; 95% CI [3.52–25.53]). CONCLUSION: Olfaction dysfunction was significantly more prevalent in patients with mild flu syndrome in COVID-19. It may be a predictor of a good prognosis for this infection. New population-based studies must be carried out to corroborate these findings. Elsevier 2021-01-01 /pmc/articles/PMC7831803/ /pubmed/33441276 http://dx.doi.org/10.1016/j.bjorl.2020.12.002 Text en © 2020 Associação Brasileira de Otorrinolaringologia e Cirurgia Cérvico-Facial. Published by Elsevier Editora Ltda. https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Original Article
Mendonça, Cindy Vitalino
Mendes Neto, José Arruda
Suzuki, Fabio Akira
Orth, Marlon Steffens
Machado Neto, Hugo
Nacif, Sérgio Roberto
Olfactory dysfunction in COVID-19: a marker of good prognosis?
title Olfactory dysfunction in COVID-19: a marker of good prognosis?
title_full Olfactory dysfunction in COVID-19: a marker of good prognosis?
title_fullStr Olfactory dysfunction in COVID-19: a marker of good prognosis?
title_full_unstemmed Olfactory dysfunction in COVID-19: a marker of good prognosis?
title_short Olfactory dysfunction in COVID-19: a marker of good prognosis?
title_sort olfactory dysfunction in covid-19: a marker of good prognosis?
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7831803/
https://www.ncbi.nlm.nih.gov/pubmed/33441276
http://dx.doi.org/10.1016/j.bjorl.2020.12.002
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