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Effectiveness and safety of PRP on persistent olfactory dysfunction related to COVID-19
INTRODUCTION: Olfactory dysfunction (OD) is a well know symptom of coronavirus disease 2019 (COVID-19), accounting for 48 to 85% of patients. In 1 to 10% of cases, patients develop a chronic olfactory dysfunction (COD), lasting more than 6 months. Recently, platelet-rich plasma (PRP) was used in pat...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Springer Berlin Heidelberg
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9336533/ https://www.ncbi.nlm.nih.gov/pubmed/35904632 http://dx.doi.org/10.1007/s00405-022-07560-y |
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author | Steffens, Younès Le Bon, Serge-Daniel Lechien, Jerome Prunier, Léa Rodriguez, Alexandra Saussez, Sven Horoi, Mihaela |
author_facet | Steffens, Younès Le Bon, Serge-Daniel Lechien, Jerome Prunier, Léa Rodriguez, Alexandra Saussez, Sven Horoi, Mihaela |
author_sort | Steffens, Younès |
collection | PubMed |
description | INTRODUCTION: Olfactory dysfunction (OD) is a well know symptom of coronavirus disease 2019 (COVID-19), accounting for 48 to 85% of patients. In 1 to 10% of cases, patients develop a chronic olfactory dysfunction (COD), lasting more than 6 months. Recently, platelet-rich plasma (PRP) was used in patients with non-COVID-19 COD and authors reported encouraging results. METHODS: In the present study, we investigated the usefulness and safety of PRP injection in 56 patients with COVID-19 COD by the Sniffing Stick test (TDI score) and a linker-scale from 0 (none) to 3 (strong) and we compare the result to a control group. RESULTS: At 1 month post-PRP injection, the mean TDI scores significantly improved by 6.7 points in the PRP group (p < 0,001), the mean self-assessment of improvement in smell function was 1.8 (mild-to-moderate) in the PRP group, which was significantly higher than the score (0.3) in the control group (p < 0,001). CONCLUSION: Our results showed that PRP in the olfactory cleft can increase the olfactory threshold 1 month after the injection. Moreover, our results suggest that timing of treatment may be an important factor and that PRP is a safe treatment, because no adverse effects were reported throughout the study. Trial registration number: NCT05226546. |
format | Online Article Text |
id | pubmed-9336533 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-93365332022-08-01 Effectiveness and safety of PRP on persistent olfactory dysfunction related to COVID-19 Steffens, Younès Le Bon, Serge-Daniel Lechien, Jerome Prunier, Léa Rodriguez, Alexandra Saussez, Sven Horoi, Mihaela Eur Arch Otorhinolaryngol Short Communication INTRODUCTION: Olfactory dysfunction (OD) is a well know symptom of coronavirus disease 2019 (COVID-19), accounting for 48 to 85% of patients. In 1 to 10% of cases, patients develop a chronic olfactory dysfunction (COD), lasting more than 6 months. Recently, platelet-rich plasma (PRP) was used in patients with non-COVID-19 COD and authors reported encouraging results. METHODS: In the present study, we investigated the usefulness and safety of PRP injection in 56 patients with COVID-19 COD by the Sniffing Stick test (TDI score) and a linker-scale from 0 (none) to 3 (strong) and we compare the result to a control group. RESULTS: At 1 month post-PRP injection, the mean TDI scores significantly improved by 6.7 points in the PRP group (p < 0,001), the mean self-assessment of improvement in smell function was 1.8 (mild-to-moderate) in the PRP group, which was significantly higher than the score (0.3) in the control group (p < 0,001). CONCLUSION: Our results showed that PRP in the olfactory cleft can increase the olfactory threshold 1 month after the injection. Moreover, our results suggest that timing of treatment may be an important factor and that PRP is a safe treatment, because no adverse effects were reported throughout the study. Trial registration number: NCT05226546. Springer Berlin Heidelberg 2022-07-29 2022 /pmc/articles/PMC9336533/ /pubmed/35904632 http://dx.doi.org/10.1007/s00405-022-07560-y Text en © The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature 2022 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic. |
spellingShingle | Short Communication Steffens, Younès Le Bon, Serge-Daniel Lechien, Jerome Prunier, Léa Rodriguez, Alexandra Saussez, Sven Horoi, Mihaela Effectiveness and safety of PRP on persistent olfactory dysfunction related to COVID-19 |
title | Effectiveness and safety of PRP on persistent olfactory dysfunction related to COVID-19 |
title_full | Effectiveness and safety of PRP on persistent olfactory dysfunction related to COVID-19 |
title_fullStr | Effectiveness and safety of PRP on persistent olfactory dysfunction related to COVID-19 |
title_full_unstemmed | Effectiveness and safety of PRP on persistent olfactory dysfunction related to COVID-19 |
title_short | Effectiveness and safety of PRP on persistent olfactory dysfunction related to COVID-19 |
title_sort | effectiveness and safety of prp on persistent olfactory dysfunction related to covid-19 |
topic | Short Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9336533/ https://www.ncbi.nlm.nih.gov/pubmed/35904632 http://dx.doi.org/10.1007/s00405-022-07560-y |
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