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(693) Infection with Covid Variants of Concern in a Lung Transplant Population

PURPOSE: The COVID pandemic has evolved as the SARS-2 Coronavirus (CoV-2) mutated into unique variants of concern (VOC). The clinical approach to COVID has evolved as new therapeutics have become available. Previous reports demonstrate differences in patient outcomes based on VOC, however outcomes i...

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Autores principales: Rosenheck, J.P., Ramsammy, V., Kirkby, S., Ganapathi, A., Mokadam, N., Henn, M., Sarwar, S., Nichols, C., Marschalk, N., Fallah, T., Burcham, P., Sawyer, C., Mohr, J., Hoover, S., Nicholson, K., McLaughlin, B., Brown, R., Carter, S., Maas, K., Bennett, J., Shafner, C., Reilly, M., Whitson, B., Nunley, D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Published by Elsevier Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10068051/
http://dx.doi.org/10.1016/j.healun.2023.02.707
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author Rosenheck, J.P.
Ramsammy, V.
Kirkby, S.
Ganapathi, A.
Mokadam, N.
Henn, M.
Sarwar, S.
Nichols, C.
Marschalk, N.
Fallah, T.
Burcham, P.
Sawyer, C.
Mohr, J.
Hoover, S.
Nicholson, K.
McLaughlin, B.
Brown, R.
Carter, S.
Maas, K.
Bennett, J.
Shafner, C.
Reilly, M.
Whitson, B.
Nunley, D.
author_facet Rosenheck, J.P.
Ramsammy, V.
Kirkby, S.
Ganapathi, A.
Mokadam, N.
Henn, M.
Sarwar, S.
Nichols, C.
Marschalk, N.
Fallah, T.
Burcham, P.
Sawyer, C.
Mohr, J.
Hoover, S.
Nicholson, K.
McLaughlin, B.
Brown, R.
Carter, S.
Maas, K.
Bennett, J.
Shafner, C.
Reilly, M.
Whitson, B.
Nunley, D.
author_sort Rosenheck, J.P.
collection PubMed
description PURPOSE: The COVID pandemic has evolved as the SARS-2 Coronavirus (CoV-2) mutated into unique variants of concern (VOC). The clinical approach to COVID has evolved as new therapeutics have become available. Previous reports demonstrate differences in patient outcomes based on VOC, however outcomes in a lung transplant population have not been described. METHODS: Our lung transplant program follows over 300 transplant recipients. Relevant information including date of first positive test, hospital admission, monoclonal antibody (mAb) or oral anti-viral treatment, CoV-2 vaccination history, tixagevimab/cilgavimab (T/C) and COVID attributed mortality have been tracked for quality improvement purposes. Outcomes were stratified by predominant US VOC at time of positive testing: wild strain 02/2020-02/2021, alpha strain 02/2021-05/2021, delta strain 06/2021-12/2021, omicron strain 01/2022- 09/25/2022. RESULTS: From 03/20/2020 through 09/25/2022, 142 recipients were diagnosed with COVID 152 times, including 9 recipients infected twice and 1 recipient infected 3 times. Most infected recipients tested positive with CoV-2 during the omicron wave. All recurrent infections occurred during the omicron wave. 8 deaths (5.6%) were attributed to COVID: 6 due to COVID respiratory failure, 1 stroke and 1 new restrictive-chronic lung allograft dysfunction. Therapies directed against CoV-2 were more likely administered in delta and omicron waves. Recipients were more likely to require hospital admission in wild type and alpha waves of CoV-2. Most deaths occurred in the wild type and delta waves. Deceased recipients, and those requiring hospital admission received less vaccinations and were less likely to have received T/C. (Table) CONCLUSION: This analysis shows changing trends in management and outcomes over the COVID pandemic. Future research should focus on transplant specific outcomes, including post-infection changes in allograft function and risk of developing chronic lung allograft dysfunction based on likely infecting VOC.
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spelling pubmed-100680512023-04-03 (693) Infection with Covid Variants of Concern in a Lung Transplant Population Rosenheck, J.P. Ramsammy, V. Kirkby, S. Ganapathi, A. Mokadam, N. Henn, M. Sarwar, S. Nichols, C. Marschalk, N. Fallah, T. Burcham, P. Sawyer, C. Mohr, J. Hoover, S. Nicholson, K. McLaughlin, B. Brown, R. Carter, S. Maas, K. Bennett, J. Shafner, C. Reilly, M. Whitson, B. Nunley, D. J Heart Lung Transplant Article PURPOSE: The COVID pandemic has evolved as the SARS-2 Coronavirus (CoV-2) mutated into unique variants of concern (VOC). The clinical approach to COVID has evolved as new therapeutics have become available. Previous reports demonstrate differences in patient outcomes based on VOC, however outcomes in a lung transplant population have not been described. METHODS: Our lung transplant program follows over 300 transplant recipients. Relevant information including date of first positive test, hospital admission, monoclonal antibody (mAb) or oral anti-viral treatment, CoV-2 vaccination history, tixagevimab/cilgavimab (T/C) and COVID attributed mortality have been tracked for quality improvement purposes. Outcomes were stratified by predominant US VOC at time of positive testing: wild strain 02/2020-02/2021, alpha strain 02/2021-05/2021, delta strain 06/2021-12/2021, omicron strain 01/2022- 09/25/2022. RESULTS: From 03/20/2020 through 09/25/2022, 142 recipients were diagnosed with COVID 152 times, including 9 recipients infected twice and 1 recipient infected 3 times. Most infected recipients tested positive with CoV-2 during the omicron wave. All recurrent infections occurred during the omicron wave. 8 deaths (5.6%) were attributed to COVID: 6 due to COVID respiratory failure, 1 stroke and 1 new restrictive-chronic lung allograft dysfunction. Therapies directed against CoV-2 were more likely administered in delta and omicron waves. Recipients were more likely to require hospital admission in wild type and alpha waves of CoV-2. Most deaths occurred in the wild type and delta waves. Deceased recipients, and those requiring hospital admission received less vaccinations and were less likely to have received T/C. (Table) CONCLUSION: This analysis shows changing trends in management and outcomes over the COVID pandemic. Future research should focus on transplant specific outcomes, including post-infection changes in allograft function and risk of developing chronic lung allograft dysfunction based on likely infecting VOC. Published by Elsevier Inc. 2023-04 2023-04-03 /pmc/articles/PMC10068051/ http://dx.doi.org/10.1016/j.healun.2023.02.707 Text en Copyright © 2023 Published by Elsevier Inc. 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
Rosenheck, J.P.
Ramsammy, V.
Kirkby, S.
Ganapathi, A.
Mokadam, N.
Henn, M.
Sarwar, S.
Nichols, C.
Marschalk, N.
Fallah, T.
Burcham, P.
Sawyer, C.
Mohr, J.
Hoover, S.
Nicholson, K.
McLaughlin, B.
Brown, R.
Carter, S.
Maas, K.
Bennett, J.
Shafner, C.
Reilly, M.
Whitson, B.
Nunley, D.
(693) Infection with Covid Variants of Concern in a Lung Transplant Population
title (693) Infection with Covid Variants of Concern in a Lung Transplant Population
title_full (693) Infection with Covid Variants of Concern in a Lung Transplant Population
title_fullStr (693) Infection with Covid Variants of Concern in a Lung Transplant Population
title_full_unstemmed (693) Infection with Covid Variants of Concern in a Lung Transplant Population
title_short (693) Infection with Covid Variants of Concern in a Lung Transplant Population
title_sort (693) infection with covid variants of concern in a lung transplant population
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10068051/
http://dx.doi.org/10.1016/j.healun.2023.02.707
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