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Prednisolone does not improve olfactory function after COVID-19: a randomized, double-blind, placebo-controlled trial

BACKGROUND: Prednisolone has been suggested as a treatment for olfactory disorders after COVID-19, but evidence is scarce. Hence, we aimed to determine the efficacy of a short oral prednisolone treatment on patients with persistent olfactory disorders after COVID-19. METHODS: We performed a randomiz...

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Autores principales: Schepens, Emma J. A., Blijleven, Esther E., Boek, Wilbert M., Boesveldt, Sanne, Stokroos, Robert J., Stegeman, Inge, Kamalski, Digna M. A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9667850/
https://www.ncbi.nlm.nih.gov/pubmed/36384737
http://dx.doi.org/10.1186/s12916-022-02625-5
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author Schepens, Emma J. A.
Blijleven, Esther E.
Boek, Wilbert M.
Boesveldt, Sanne
Stokroos, Robert J.
Stegeman, Inge
Kamalski, Digna M. A.
author_facet Schepens, Emma J. A.
Blijleven, Esther E.
Boek, Wilbert M.
Boesveldt, Sanne
Stokroos, Robert J.
Stegeman, Inge
Kamalski, Digna M. A.
author_sort Schepens, Emma J. A.
collection PubMed
description BACKGROUND: Prednisolone has been suggested as a treatment for olfactory disorders after COVID-19, but evidence is scarce. Hence, we aimed to determine the efficacy of a short oral prednisolone treatment on patients with persistent olfactory disorders after COVID-19. METHODS: We performed a randomized, double-blind, placebo-controlled, single-centered trial in the Netherlands. Patients were included if they were > 18 years old and if they had persistent (> 4 weeks) olfactory disorders within 12 weeks after a confirmed COVID-19 test. The treatment group received oral prednisolone 40 mg once daily for 10 days and the placebo group received matching placebo. In addition, all patients performed olfactory training. The primary outcome was the objective olfactory function on Sniffin’ Sticks Test (SST) 12 weeks after the start of treatment, measured in Threshold-Discrimination-Identification (TDI) score. Secondary outcomes were objective gustatory function assessed by the Taste Strip Test (TST) and subjective self-reported outcomes on questionnaires about olfactory, gustatory and trigeminal function, quality of life, and nasal symptoms. The CONSORT 2010 guideline was performed. RESULTS: Between November 2021 and February 2022, we included 115 eligible patients, randomly assigned to the treatment (n = 58) or placebo group (n = 57). No difference in olfactory function between groups was obtained after 12 weeks. Median TDI score on SST was 26.8 (IQR 23.6–29.3) in the placebo group and 28.8 (IQR 24.0–30.9) in the prednisolone group, with a median difference of 2.0 (95% CI 0.75 to 1.5). There was similar improvement on olfactory function in both groups after 12 weeks. Furthermore, on secondary outcomes, we obtained no differences between groups. CONCLUSIONS: This trial shows that prednisolone does not improve olfactory function after COVID-19. Therefore, we recommend not prescribing prednisolone for patients with persistent olfactory disorders after COVID-19. TRIAL REGISTRATION: This trial is registered on the ISRCTN registry with trial ID ISRCTN70794078.
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spelling pubmed-96678502022-11-16 Prednisolone does not improve olfactory function after COVID-19: a randomized, double-blind, placebo-controlled trial Schepens, Emma J. A. Blijleven, Esther E. Boek, Wilbert M. Boesveldt, Sanne Stokroos, Robert J. Stegeman, Inge Kamalski, Digna M. A. BMC Med Research Article BACKGROUND: Prednisolone has been suggested as a treatment for olfactory disorders after COVID-19, but evidence is scarce. Hence, we aimed to determine the efficacy of a short oral prednisolone treatment on patients with persistent olfactory disorders after COVID-19. METHODS: We performed a randomized, double-blind, placebo-controlled, single-centered trial in the Netherlands. Patients were included if they were > 18 years old and if they had persistent (> 4 weeks) olfactory disorders within 12 weeks after a confirmed COVID-19 test. The treatment group received oral prednisolone 40 mg once daily for 10 days and the placebo group received matching placebo. In addition, all patients performed olfactory training. The primary outcome was the objective olfactory function on Sniffin’ Sticks Test (SST) 12 weeks after the start of treatment, measured in Threshold-Discrimination-Identification (TDI) score. Secondary outcomes were objective gustatory function assessed by the Taste Strip Test (TST) and subjective self-reported outcomes on questionnaires about olfactory, gustatory and trigeminal function, quality of life, and nasal symptoms. The CONSORT 2010 guideline was performed. RESULTS: Between November 2021 and February 2022, we included 115 eligible patients, randomly assigned to the treatment (n = 58) or placebo group (n = 57). No difference in olfactory function between groups was obtained after 12 weeks. Median TDI score on SST was 26.8 (IQR 23.6–29.3) in the placebo group and 28.8 (IQR 24.0–30.9) in the prednisolone group, with a median difference of 2.0 (95% CI 0.75 to 1.5). There was similar improvement on olfactory function in both groups after 12 weeks. Furthermore, on secondary outcomes, we obtained no differences between groups. CONCLUSIONS: This trial shows that prednisolone does not improve olfactory function after COVID-19. Therefore, we recommend not prescribing prednisolone for patients with persistent olfactory disorders after COVID-19. TRIAL REGISTRATION: This trial is registered on the ISRCTN registry with trial ID ISRCTN70794078. BioMed Central 2022-11-16 /pmc/articles/PMC9667850/ /pubmed/36384737 http://dx.doi.org/10.1186/s12916-022-02625-5 Text en © The Author(s) 2022 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/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research Article
Schepens, Emma J. A.
Blijleven, Esther E.
Boek, Wilbert M.
Boesveldt, Sanne
Stokroos, Robert J.
Stegeman, Inge
Kamalski, Digna M. A.
Prednisolone does not improve olfactory function after COVID-19: a randomized, double-blind, placebo-controlled trial
title Prednisolone does not improve olfactory function after COVID-19: a randomized, double-blind, placebo-controlled trial
title_full Prednisolone does not improve olfactory function after COVID-19: a randomized, double-blind, placebo-controlled trial
title_fullStr Prednisolone does not improve olfactory function after COVID-19: a randomized, double-blind, placebo-controlled trial
title_full_unstemmed Prednisolone does not improve olfactory function after COVID-19: a randomized, double-blind, placebo-controlled trial
title_short Prednisolone does not improve olfactory function after COVID-19: a randomized, double-blind, placebo-controlled trial
title_sort prednisolone does not improve olfactory function after covid-19: a randomized, double-blind, placebo-controlled trial
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9667850/
https://www.ncbi.nlm.nih.gov/pubmed/36384737
http://dx.doi.org/10.1186/s12916-022-02625-5
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