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2700. Reducing the Dose of Mycophenolate in Solid Organ Transplant Recipients Diagnosed with SARS-CoV-2 Infection Increases the Risk of Severe COVID-19
BACKGROUND: Most of the available COVID-19 outcome data in solid organ transplant (SOT) recipients does not suggest a higher mortality rate in the SOT population. Though theoretically immunosuppressive medications might be associated with worse outcome, its immunomodulatory effect might be beneficia...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10678438/ http://dx.doi.org/10.1093/ofid/ofad500.2311 |
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author | Gillcrist, Marion Waller, Stephen Taylor, Ryan M Bahr, Nathan C Cibrik, Diane M Shah, Zubair Eid, Albert |
author_facet | Gillcrist, Marion Waller, Stephen Taylor, Ryan M Bahr, Nathan C Cibrik, Diane M Shah, Zubair Eid, Albert |
author_sort | Gillcrist, Marion |
collection | PubMed |
description | BACKGROUND: Most of the available COVID-19 outcome data in solid organ transplant (SOT) recipients does not suggest a higher mortality rate in the SOT population. Though theoretically immunosuppressive medications might be associated with worse outcome, its immunomodulatory effect might be beneficial. METHODS: We retrospectively analyzed the effect of dose-reduction of mycophenolate, tacrolimus, and prednisone on the severity of COVID-19 in SOT recipients diagnosed with COVID-19 at the University of Kansas Medical Center between January 1, 2020 and December 31, 2022. Severe COVID-19 was defined by development of hypoxia while the patient was on room air during a 21-day period following COVID-19 diagnosis. To evaluate the effect of dose changes after the diagnosis of COVID-19 on the odds of developing severe COVID-19, we subset our data based on whether patients were taking mycophenolate (n = 449), tacrolimus (n = 537) or prednisone (n = 386) at the time of diagnosis. Within each subgroup, we fit a logistic regression model with severe COVID-19 as the response variable and adjusted for the relevant immunosuppressant and a set of covariates (age, sex, race, body mass index, hypertension, diabetes mellitus, prespecified time period of COVID-19 diagnosis during the pandemic, chronic heart disease, chronic lung disease, malignancy, end stage renal disease, cirrhosis, smoking, receipt of COVID-19 vaccine, and receipt of SARS-CoV-2 monoclonal antibodies). RESULTS: In our SOT population, 570 patients were diagnosed with COVID-19 (458 kidney, 73 liver, 54 heart, 43 pancreas, and 8 lung recipients). The median patient age was 54 years, 59% were male, and 70% were white. After adjusting for other covariates, a mycophenolate dose-reduction of < 50% was associated with an odds ratio of 2.01 (95% CI: 1.03 - 3.90; p = 0.04) for developing severe COVID-19. Similarly, decreasing the dose of mycophenolate by ≥ 50% was associated with an odds ratio of 2.65 (95% CI: 1.09 - 6.41, p = 0.03) for developing severe disease. Tacrolimus dose reduction did not increase the risk of severe COVID-19, nor did a dose increase or decrease of prednisone. CONCLUSION: A mycophenolate dose reduction when a SOT patient is diagnosed with COVID-19 should be discouraged, especially if the patient has mild disease. DISCLOSURES: All Authors: No reported disclosures |
format | Online Article Text |
id | pubmed-10678438 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-106784382023-11-27 2700. Reducing the Dose of Mycophenolate in Solid Organ Transplant Recipients Diagnosed with SARS-CoV-2 Infection Increases the Risk of Severe COVID-19 Gillcrist, Marion Waller, Stephen Taylor, Ryan M Bahr, Nathan C Cibrik, Diane M Shah, Zubair Eid, Albert Open Forum Infect Dis Abstract BACKGROUND: Most of the available COVID-19 outcome data in solid organ transplant (SOT) recipients does not suggest a higher mortality rate in the SOT population. Though theoretically immunosuppressive medications might be associated with worse outcome, its immunomodulatory effect might be beneficial. METHODS: We retrospectively analyzed the effect of dose-reduction of mycophenolate, tacrolimus, and prednisone on the severity of COVID-19 in SOT recipients diagnosed with COVID-19 at the University of Kansas Medical Center between January 1, 2020 and December 31, 2022. Severe COVID-19 was defined by development of hypoxia while the patient was on room air during a 21-day period following COVID-19 diagnosis. To evaluate the effect of dose changes after the diagnosis of COVID-19 on the odds of developing severe COVID-19, we subset our data based on whether patients were taking mycophenolate (n = 449), tacrolimus (n = 537) or prednisone (n = 386) at the time of diagnosis. Within each subgroup, we fit a logistic regression model with severe COVID-19 as the response variable and adjusted for the relevant immunosuppressant and a set of covariates (age, sex, race, body mass index, hypertension, diabetes mellitus, prespecified time period of COVID-19 diagnosis during the pandemic, chronic heart disease, chronic lung disease, malignancy, end stage renal disease, cirrhosis, smoking, receipt of COVID-19 vaccine, and receipt of SARS-CoV-2 monoclonal antibodies). RESULTS: In our SOT population, 570 patients were diagnosed with COVID-19 (458 kidney, 73 liver, 54 heart, 43 pancreas, and 8 lung recipients). The median patient age was 54 years, 59% were male, and 70% were white. After adjusting for other covariates, a mycophenolate dose-reduction of < 50% was associated with an odds ratio of 2.01 (95% CI: 1.03 - 3.90; p = 0.04) for developing severe COVID-19. Similarly, decreasing the dose of mycophenolate by ≥ 50% was associated with an odds ratio of 2.65 (95% CI: 1.09 - 6.41, p = 0.03) for developing severe disease. Tacrolimus dose reduction did not increase the risk of severe COVID-19, nor did a dose increase or decrease of prednisone. CONCLUSION: A mycophenolate dose reduction when a SOT patient is diagnosed with COVID-19 should be discouraged, especially if the patient has mild disease. DISCLOSURES: All Authors: No reported disclosures Oxford University Press 2023-11-27 /pmc/articles/PMC10678438/ http://dx.doi.org/10.1093/ofid/ofad500.2311 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of Infectious Diseases Society of America. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Abstract Gillcrist, Marion Waller, Stephen Taylor, Ryan M Bahr, Nathan C Cibrik, Diane M Shah, Zubair Eid, Albert 2700. Reducing the Dose of Mycophenolate in Solid Organ Transplant Recipients Diagnosed with SARS-CoV-2 Infection Increases the Risk of Severe COVID-19 |
title | 2700. Reducing the Dose of Mycophenolate in Solid Organ Transplant Recipients Diagnosed with SARS-CoV-2 Infection Increases the Risk of Severe COVID-19 |
title_full | 2700. Reducing the Dose of Mycophenolate in Solid Organ Transplant Recipients Diagnosed with SARS-CoV-2 Infection Increases the Risk of Severe COVID-19 |
title_fullStr | 2700. Reducing the Dose of Mycophenolate in Solid Organ Transplant Recipients Diagnosed with SARS-CoV-2 Infection Increases the Risk of Severe COVID-19 |
title_full_unstemmed | 2700. Reducing the Dose of Mycophenolate in Solid Organ Transplant Recipients Diagnosed with SARS-CoV-2 Infection Increases the Risk of Severe COVID-19 |
title_short | 2700. Reducing the Dose of Mycophenolate in Solid Organ Transplant Recipients Diagnosed with SARS-CoV-2 Infection Increases the Risk of Severe COVID-19 |
title_sort | 2700. reducing the dose of mycophenolate in solid organ transplant recipients diagnosed with sars-cov-2 infection increases the risk of severe covid-19 |
topic | Abstract |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10678438/ http://dx.doi.org/10.1093/ofid/ofad500.2311 |
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