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Screening for Olfactory Dysfunction in COVID-19 Patients Using Quick Smell Identification Test
Objective: To determine the prevalence of OD in the confirmed case with COVID-19 among our population using quick smell identification test (Q-SIT) as screening tool. Methods: Cross- sectional study carried out in Qatif area—Saudi Arabia among adult hospitalized patient with confirm COVID-19 during...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer India
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8243049/ https://www.ncbi.nlm.nih.gov/pubmed/34226867 http://dx.doi.org/10.1007/s12070-021-02709-3 |
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author | Albaharna, Hussain Abdullali Alhajjaj, Alya Hassan Al Shabeb, Hussain Ali Alghanim, Dhuha Abdulaziz Alkhabbaz, Fatimah Lateef AlJishi, Jumana Mansour |
author_facet | Albaharna, Hussain Abdullali Alhajjaj, Alya Hassan Al Shabeb, Hussain Ali Alghanim, Dhuha Abdulaziz Alkhabbaz, Fatimah Lateef AlJishi, Jumana Mansour |
author_sort | Albaharna, Hussain Abdullali |
collection | PubMed |
description | Objective: To determine the prevalence of OD in the confirmed case with COVID-19 among our population using quick smell identification test (Q-SIT) as screening tool. Methods: Cross- sectional study carried out in Qatif area—Saudi Arabia among adult hospitalized patient with confirm COVID-19 during the period between May and July, 2020. All adults confirmed COVID-19 patients were interviewed for history of current disease and associated symptoms as well as performing Q-SIT. Participants who had history of olfactory dysfunction, and critical cases required ICU admission were excluded. Results: The prevalence of OD among COVID-19 cases was (16.3%) in our population using Q-SIT compared to (27.4%) for self-reported symptom. Females were having higher prevalence in compare to males (30.5% and 11.1%) respectively; which was statistically significant (P < 0.001). The patients reported higher prevalence of ageusia (31.9%) with significant association with OD (P < 0.001). Q-SIT showed high positive and negative predictive value in detecting OD among patients with COVID-19 (84% and 93% respectively). Conclusion: Q-SIT is a useful, validated and easy to apply tool for screening OD among patients with COVID-19. Some patients presented solely with this symptom which can occurs unnoticed in COVID-19 patients, and there for required objective test for detection. |
format | Online Article Text |
id | pubmed-8243049 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Springer India |
record_format | MEDLINE/PubMed |
spelling | pubmed-82430492021-07-01 Screening for Olfactory Dysfunction in COVID-19 Patients Using Quick Smell Identification Test Albaharna, Hussain Abdullali Alhajjaj, Alya Hassan Al Shabeb, Hussain Ali Alghanim, Dhuha Abdulaziz Alkhabbaz, Fatimah Lateef AlJishi, Jumana Mansour Indian J Otolaryngol Head Neck Surg Original Article Objective: To determine the prevalence of OD in the confirmed case with COVID-19 among our population using quick smell identification test (Q-SIT) as screening tool. Methods: Cross- sectional study carried out in Qatif area—Saudi Arabia among adult hospitalized patient with confirm COVID-19 during the period between May and July, 2020. All adults confirmed COVID-19 patients were interviewed for history of current disease and associated symptoms as well as performing Q-SIT. Participants who had history of olfactory dysfunction, and critical cases required ICU admission were excluded. Results: The prevalence of OD among COVID-19 cases was (16.3%) in our population using Q-SIT compared to (27.4%) for self-reported symptom. Females were having higher prevalence in compare to males (30.5% and 11.1%) respectively; which was statistically significant (P < 0.001). The patients reported higher prevalence of ageusia (31.9%) with significant association with OD (P < 0.001). Q-SIT showed high positive and negative predictive value in detecting OD among patients with COVID-19 (84% and 93% respectively). Conclusion: Q-SIT is a useful, validated and easy to apply tool for screening OD among patients with COVID-19. Some patients presented solely with this symptom which can occurs unnoticed in COVID-19 patients, and there for required objective test for detection. Springer India 2021-06-30 2022-10 /pmc/articles/PMC8243049/ /pubmed/34226867 http://dx.doi.org/10.1007/s12070-021-02709-3 Text en © Association of Otolaryngologists of India 2021 |
spellingShingle | Original Article Albaharna, Hussain Abdullali Alhajjaj, Alya Hassan Al Shabeb, Hussain Ali Alghanim, Dhuha Abdulaziz Alkhabbaz, Fatimah Lateef AlJishi, Jumana Mansour Screening for Olfactory Dysfunction in COVID-19 Patients Using Quick Smell Identification Test |
title | Screening for Olfactory Dysfunction in COVID-19 Patients Using Quick Smell Identification Test |
title_full | Screening for Olfactory Dysfunction in COVID-19 Patients Using Quick Smell Identification Test |
title_fullStr | Screening for Olfactory Dysfunction in COVID-19 Patients Using Quick Smell Identification Test |
title_full_unstemmed | Screening for Olfactory Dysfunction in COVID-19 Patients Using Quick Smell Identification Test |
title_short | Screening for Olfactory Dysfunction in COVID-19 Patients Using Quick Smell Identification Test |
title_sort | screening for olfactory dysfunction in covid-19 patients using quick smell identification test |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8243049/ https://www.ncbi.nlm.nih.gov/pubmed/34226867 http://dx.doi.org/10.1007/s12070-021-02709-3 |
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