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Role of Famotidine and Other Acid Reflux Medications for SARS-CoV-2: A Pilot Study
Infection with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is responsible for the coronavirus-19 disease (COVID-19) pandemic. The H-2 blocker famotidine has been suggested as an FDA-approved drug that could potentially be repurposed for treatment of COVID-19. Famotidine has since be...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Voice Foundation. Published by Elsevier Inc.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7817459/ https://www.ncbi.nlm.nih.gov/pubmed/33516648 http://dx.doi.org/10.1016/j.jvoice.2021.01.007 |
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author | Balouch, Bailey Vontela, Swetha Yeakel, Heather Alnouri, Ghiath Sataloff, Robert T. |
author_facet | Balouch, Bailey Vontela, Swetha Yeakel, Heather Alnouri, Ghiath Sataloff, Robert T. |
author_sort | Balouch, Bailey |
collection | PubMed |
description | Infection with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is responsible for the coronavirus-19 disease (COVID-19) pandemic. The H-2 blocker famotidine has been suggested as an FDA-approved drug that could potentially be repurposed for treatment of COVID-19. Famotidine has since been shown to improve patient outcomes and reduce symptom severity in patients acutely ill with COVID-19. Other studies have suggested that proton pump inhibitors (PPIs) might have an association with COVID-19. OBJECTIVE: The purpose of the present study was to determine whether famotidine or any other antireflux medications have a prophylactic or detrimental effect for SARS-CoV-2 infection when taken regularly for the management of acid reflux. METHODS: An anonymous, web-based survey was distributed via email to adult otolaryngology patients to collect demographic data, past medical history, medication history, incidence of symptoms associated with COVID-19, potential exposure to SARS-CoV-2, and results of any PCR or serological testing. Associations between reflux medications and incidence of COVID-19 cases were analyzed. Statistical analysis was performed using SPSS. Chi-square with Fisher's exact test, Point-Biserial correlation, Kendall's-tau-b, independent samples t test, and the Mann-Whitney U test were used as appropriate. A binary logistic regression model was fit to determine probability of COVID-19 cases after adjustment for other risk factors. RESULTS: There were 307 patients who responded to the survey. The average age of respondents was 52.63 ± 17.03. Famotidine use was not associated with incidence of laboratory-confirmed (P= 0.717) or symptomatically suspected (P= 0.876) COVID-19. No other reflux medications were found to be significant predictors for laboratory-confirmed or suspected COVID-19 (P> 0.05). Younger age (odds ratio [OR] = 1.043, 95% CI: 1.020–1.065, P< 0.001), high risk obesity (OR = 4.005, 95% CI: 1.449–11.069, P= 0.007), and use of a corticosteroid nasal spray (OR = 3.529, 95% CI: 1.352–9.211, P= 0.010) were significant predictors for symptomatically suspected COVID-19 cases. CONCLUSIONS: There was no association between incidence of COVID-19 and use of reflux medications, including famotidine at doses used orally to manage reflux and high dose PPIs. Reflux medications did not protect against or increase the risk of COVID-19. |
format | Online Article Text |
id | pubmed-7817459 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | The Voice Foundation. Published by Elsevier Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-78174592021-01-21 Role of Famotidine and Other Acid Reflux Medications for SARS-CoV-2: A Pilot Study Balouch, Bailey Vontela, Swetha Yeakel, Heather Alnouri, Ghiath Sataloff, Robert T. J Voice Article Infection with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is responsible for the coronavirus-19 disease (COVID-19) pandemic. The H-2 blocker famotidine has been suggested as an FDA-approved drug that could potentially be repurposed for treatment of COVID-19. Famotidine has since been shown to improve patient outcomes and reduce symptom severity in patients acutely ill with COVID-19. Other studies have suggested that proton pump inhibitors (PPIs) might have an association with COVID-19. OBJECTIVE: The purpose of the present study was to determine whether famotidine or any other antireflux medications have a prophylactic or detrimental effect for SARS-CoV-2 infection when taken regularly for the management of acid reflux. METHODS: An anonymous, web-based survey was distributed via email to adult otolaryngology patients to collect demographic data, past medical history, medication history, incidence of symptoms associated with COVID-19, potential exposure to SARS-CoV-2, and results of any PCR or serological testing. Associations between reflux medications and incidence of COVID-19 cases were analyzed. Statistical analysis was performed using SPSS. Chi-square with Fisher's exact test, Point-Biserial correlation, Kendall's-tau-b, independent samples t test, and the Mann-Whitney U test were used as appropriate. A binary logistic regression model was fit to determine probability of COVID-19 cases after adjustment for other risk factors. RESULTS: There were 307 patients who responded to the survey. The average age of respondents was 52.63 ± 17.03. Famotidine use was not associated with incidence of laboratory-confirmed (P= 0.717) or symptomatically suspected (P= 0.876) COVID-19. No other reflux medications were found to be significant predictors for laboratory-confirmed or suspected COVID-19 (P> 0.05). Younger age (odds ratio [OR] = 1.043, 95% CI: 1.020–1.065, P< 0.001), high risk obesity (OR = 4.005, 95% CI: 1.449–11.069, P= 0.007), and use of a corticosteroid nasal spray (OR = 3.529, 95% CI: 1.352–9.211, P= 0.010) were significant predictors for symptomatically suspected COVID-19 cases. CONCLUSIONS: There was no association between incidence of COVID-19 and use of reflux medications, including famotidine at doses used orally to manage reflux and high dose PPIs. Reflux medications did not protect against or increase the risk of COVID-19. The Voice Foundation. Published by Elsevier Inc. 2023-05 2021-01-20 /pmc/articles/PMC7817459/ /pubmed/33516648 http://dx.doi.org/10.1016/j.jvoice.2021.01.007 Text en © 2021 The Voice Foundation. Published by Elsevier Inc. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Article Balouch, Bailey Vontela, Swetha Yeakel, Heather Alnouri, Ghiath Sataloff, Robert T. Role of Famotidine and Other Acid Reflux Medications for SARS-CoV-2: A Pilot Study |
title | Role of Famotidine and Other Acid Reflux Medications for SARS-CoV-2: A Pilot Study |
title_full | Role of Famotidine and Other Acid Reflux Medications for SARS-CoV-2: A Pilot Study |
title_fullStr | Role of Famotidine and Other Acid Reflux Medications for SARS-CoV-2: A Pilot Study |
title_full_unstemmed | Role of Famotidine and Other Acid Reflux Medications for SARS-CoV-2: A Pilot Study |
title_short | Role of Famotidine and Other Acid Reflux Medications for SARS-CoV-2: A Pilot Study |
title_sort | role of famotidine and other acid reflux medications for sars-cov-2: a pilot study |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7817459/ https://www.ncbi.nlm.nih.gov/pubmed/33516648 http://dx.doi.org/10.1016/j.jvoice.2021.01.007 |
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