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Orofacial Mycoses in Coronavirus Disease-2019 (COVID-19): A Systematic Review

OBJECTIVES: Studies reviewing orofacial mycoses in coronavirus disease-2019 (COVID-19) caused by severe acute respiratory syndrome 2 (SARS-CoV-2) infection are sparse. Here we review the major oral and maxillofacial mycoses of COVID-19, the associated comorbidities, and the probable precipitating fa...

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Autores principales: Samaranayake, Lakshman P., Fakhruddin, Kausar S., Ngo, Hien C., Bandara, H.M.N.M., Leung, Y.Y.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8885299/
https://www.ncbi.nlm.nih.gov/pubmed/35367044
http://dx.doi.org/10.1016/j.identj.2022.02.010
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author Samaranayake, Lakshman P.
Fakhruddin, Kausar S.
Ngo, Hien C.
Bandara, H.M.N.M.
Leung, Y.Y.
author_facet Samaranayake, Lakshman P.
Fakhruddin, Kausar S.
Ngo, Hien C.
Bandara, H.M.N.M.
Leung, Y.Y.
author_sort Samaranayake, Lakshman P.
collection PubMed
description OBJECTIVES: Studies reviewing orofacial mycoses in coronavirus disease-2019 (COVID-19) caused by severe acute respiratory syndrome 2 (SARS-CoV-2) infection are sparse. Here we review the major oral and maxillofacial mycoses of COVID-19, the associated comorbidities, and the probable precipitating factors. METHODS: English-language manuscripts published between March 2020 and October 2021 were searched using PubMed, OVID, SCOPUS, and Web of Science databases, using appropriate keywords. RESULTS: We identified 30 articles across 14 countries, which met the inclusion criteria of PRISMA guidelines. These yielded a total of 292 patients with laboratory-confirmed COVID-19, 51.4% (n = 150) of whom presented with oral and maxillofacial fungal infections, mainly comprising candidosis, mucormycosis, and aspergillosis. Candida infections were the most prevalent, present in 64% (n = 96), followed by mucormycosis, and only a single case of aspergillosis was noted. Oral and maxillofacial mycoses were predominantly seen in those with comorbidities, especially in those with diabetes (52.4%). Oral mucormycosis was noted in 8.6% (n = 13) and mainly manifested on the hard palate. An overall event rate of oral/maxillofacial mucormycosis manifestation in patients with COVID-19 with diabetes mellitus type 1/2 was about 94% (49/52; 95% confidence interval, 0.73%-0.89%), implying a very high association between diabetes mellitus and the latter condition. All fungal infections appeared either concurrently with COVID-19 symptoms or during the immediate recovery period. CONCLUSIONS: SARS-CoV-2 infection–related immunosuppression, steroid therapy, as well as comorbidities such as diabetic hyperglycemia appear to be the major predisposing factors for the onset of oral and maxillofacial mycoses in patients with COVID-19 across all age groups.
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spelling pubmed-88852992022-03-01 Orofacial Mycoses in Coronavirus Disease-2019 (COVID-19): A Systematic Review Samaranayake, Lakshman P. Fakhruddin, Kausar S. Ngo, Hien C. Bandara, H.M.N.M. Leung, Y.Y. Int Dent J Scientific Research Report OBJECTIVES: Studies reviewing orofacial mycoses in coronavirus disease-2019 (COVID-19) caused by severe acute respiratory syndrome 2 (SARS-CoV-2) infection are sparse. Here we review the major oral and maxillofacial mycoses of COVID-19, the associated comorbidities, and the probable precipitating factors. METHODS: English-language manuscripts published between March 2020 and October 2021 were searched using PubMed, OVID, SCOPUS, and Web of Science databases, using appropriate keywords. RESULTS: We identified 30 articles across 14 countries, which met the inclusion criteria of PRISMA guidelines. These yielded a total of 292 patients with laboratory-confirmed COVID-19, 51.4% (n = 150) of whom presented with oral and maxillofacial fungal infections, mainly comprising candidosis, mucormycosis, and aspergillosis. Candida infections were the most prevalent, present in 64% (n = 96), followed by mucormycosis, and only a single case of aspergillosis was noted. Oral and maxillofacial mycoses were predominantly seen in those with comorbidities, especially in those with diabetes (52.4%). Oral mucormycosis was noted in 8.6% (n = 13) and mainly manifested on the hard palate. An overall event rate of oral/maxillofacial mucormycosis manifestation in patients with COVID-19 with diabetes mellitus type 1/2 was about 94% (49/52; 95% confidence interval, 0.73%-0.89%), implying a very high association between diabetes mellitus and the latter condition. All fungal infections appeared either concurrently with COVID-19 symptoms or during the immediate recovery period. CONCLUSIONS: SARS-CoV-2 infection–related immunosuppression, steroid therapy, as well as comorbidities such as diabetic hyperglycemia appear to be the major predisposing factors for the onset of oral and maxillofacial mycoses in patients with COVID-19 across all age groups. Elsevier 2022-03-01 /pmc/articles/PMC8885299/ /pubmed/35367044 http://dx.doi.org/10.1016/j.identj.2022.02.010 Text en © 2022 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Scientific Research Report
Samaranayake, Lakshman P.
Fakhruddin, Kausar S.
Ngo, Hien C.
Bandara, H.M.N.M.
Leung, Y.Y.
Orofacial Mycoses in Coronavirus Disease-2019 (COVID-19): A Systematic Review
title Orofacial Mycoses in Coronavirus Disease-2019 (COVID-19): A Systematic Review
title_full Orofacial Mycoses in Coronavirus Disease-2019 (COVID-19): A Systematic Review
title_fullStr Orofacial Mycoses in Coronavirus Disease-2019 (COVID-19): A Systematic Review
title_full_unstemmed Orofacial Mycoses in Coronavirus Disease-2019 (COVID-19): A Systematic Review
title_short Orofacial Mycoses in Coronavirus Disease-2019 (COVID-19): A Systematic Review
title_sort orofacial mycoses in coronavirus disease-2019 (covid-19): a systematic review
topic Scientific Research Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8885299/
https://www.ncbi.nlm.nih.gov/pubmed/35367044
http://dx.doi.org/10.1016/j.identj.2022.02.010
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