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Outcomes of SOT Recipients With COVID-19 in Different Eras of COVID-19 Therapeutics
BACKGROUND. Few reports have focused on newer coronavirus disease 2019 (COVID-19) therapies (remdesivir, dexamethasone, and convalescent plasma) in solid organ transplant recipients; concerns had been raised regarding possible adverse impact on allograft function or secondary infections. METHODS. We...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams & Wilkins
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8710330/ https://www.ncbi.nlm.nih.gov/pubmed/34966840 http://dx.doi.org/10.1097/TXD.0000000000001268 |
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author | Sait, Afrah S. Chiang, Teresa Po-Yu Marr, Kieren A. Massie, Allan B. Cochran, Willa Shah, Pali Brennan, Daniel C. Thomas, Alvin G. Mehta Steinke, Seema Permpalung, Nitipong Shoham, Shmuel Merlo, Christian Jain, Tania Boyarsky, Brian Charnaya, Olga Gurakar, Ahmet Sharma, Kavita Durand, Christine M. Werbel, William A. Huang, Chiung-Yu Ostrander, Darin Desai, Niraj Kim, Min Young Alasfar, Sami Bloch, Evan M. Tobian, Aaron A.R. Garonzik-Wang, Jacqueline Segev, Dorry L. Avery, Robin K. |
author_facet | Sait, Afrah S. Chiang, Teresa Po-Yu Marr, Kieren A. Massie, Allan B. Cochran, Willa Shah, Pali Brennan, Daniel C. Thomas, Alvin G. Mehta Steinke, Seema Permpalung, Nitipong Shoham, Shmuel Merlo, Christian Jain, Tania Boyarsky, Brian Charnaya, Olga Gurakar, Ahmet Sharma, Kavita Durand, Christine M. Werbel, William A. Huang, Chiung-Yu Ostrander, Darin Desai, Niraj Kim, Min Young Alasfar, Sami Bloch, Evan M. Tobian, Aaron A.R. Garonzik-Wang, Jacqueline Segev, Dorry L. Avery, Robin K. |
author_sort | Sait, Afrah S. |
collection | PubMed |
description | BACKGROUND. Few reports have focused on newer coronavirus disease 2019 (COVID-19) therapies (remdesivir, dexamethasone, and convalescent plasma) in solid organ transplant recipients; concerns had been raised regarding possible adverse impact on allograft function or secondary infections. METHODS. We studied 77 solid organ transplant inpatients with COVID-19 during 2 therapeutic eras (Era 1: March–May 2020, 21 patients; and Era 2: June–November 2020, 56 patients) and 52 solid organ transplant outpatients. RESULTS. In Era 1, no patients received remdesivir or dexamethasone, and 4 of 21 (19.4%) received convalescent plasma, whereas in Era 2, remdesivir (24/56, 42.9%), dexamethasone (24/56, 42.9%), and convalescent plasma (40/56, 71.4%) were commonly used. Mortality was low across both eras, 4 of 77 (5.6%), and rejection occurred in only 2 of 77 (2.8%) inpatients; infections were similar in hypoxemic patients with or without dexamethasone. Preexisting graft dysfunction was associated with greater need for hospitalization, higher severity score, and lower survival. Acute kidney injury was present in 37.3% of inpatients; renal function improved more rapidly in patients who received remdesivir and convalescent plasma. Post–COVID-19 renal and liver function were comparable between eras, out to 90 d. CONCLUSIONS. Newer COVID-19 therapies did not appear to have a deleterious effect on allograft function, and infectious complications were comparable. |
format | Online Article Text |
id | pubmed-8710330 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Lippincott Williams & Wilkins |
record_format | MEDLINE/PubMed |
spelling | pubmed-87103302021-12-28 Outcomes of SOT Recipients With COVID-19 in Different Eras of COVID-19 Therapeutics Sait, Afrah S. Chiang, Teresa Po-Yu Marr, Kieren A. Massie, Allan B. Cochran, Willa Shah, Pali Brennan, Daniel C. Thomas, Alvin G. Mehta Steinke, Seema Permpalung, Nitipong Shoham, Shmuel Merlo, Christian Jain, Tania Boyarsky, Brian Charnaya, Olga Gurakar, Ahmet Sharma, Kavita Durand, Christine M. Werbel, William A. Huang, Chiung-Yu Ostrander, Darin Desai, Niraj Kim, Min Young Alasfar, Sami Bloch, Evan M. Tobian, Aaron A.R. Garonzik-Wang, Jacqueline Segev, Dorry L. Avery, Robin K. Transplant Direct Infectious Disease BACKGROUND. Few reports have focused on newer coronavirus disease 2019 (COVID-19) therapies (remdesivir, dexamethasone, and convalescent plasma) in solid organ transplant recipients; concerns had been raised regarding possible adverse impact on allograft function or secondary infections. METHODS. We studied 77 solid organ transplant inpatients with COVID-19 during 2 therapeutic eras (Era 1: March–May 2020, 21 patients; and Era 2: June–November 2020, 56 patients) and 52 solid organ transplant outpatients. RESULTS. In Era 1, no patients received remdesivir or dexamethasone, and 4 of 21 (19.4%) received convalescent plasma, whereas in Era 2, remdesivir (24/56, 42.9%), dexamethasone (24/56, 42.9%), and convalescent plasma (40/56, 71.4%) were commonly used. Mortality was low across both eras, 4 of 77 (5.6%), and rejection occurred in only 2 of 77 (2.8%) inpatients; infections were similar in hypoxemic patients with or without dexamethasone. Preexisting graft dysfunction was associated with greater need for hospitalization, higher severity score, and lower survival. Acute kidney injury was present in 37.3% of inpatients; renal function improved more rapidly in patients who received remdesivir and convalescent plasma. Post–COVID-19 renal and liver function were comparable between eras, out to 90 d. CONCLUSIONS. Newer COVID-19 therapies did not appear to have a deleterious effect on allograft function, and infectious complications were comparable. Lippincott Williams & Wilkins 2021-12-23 /pmc/articles/PMC8710330/ /pubmed/34966840 http://dx.doi.org/10.1097/TXD.0000000000001268 Text en Copyright © 2021 The Author(s). Transplantation Direct. Published by Wolters Kluwer Health, Inc. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) , where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal. |
spellingShingle | Infectious Disease Sait, Afrah S. Chiang, Teresa Po-Yu Marr, Kieren A. Massie, Allan B. Cochran, Willa Shah, Pali Brennan, Daniel C. Thomas, Alvin G. Mehta Steinke, Seema Permpalung, Nitipong Shoham, Shmuel Merlo, Christian Jain, Tania Boyarsky, Brian Charnaya, Olga Gurakar, Ahmet Sharma, Kavita Durand, Christine M. Werbel, William A. Huang, Chiung-Yu Ostrander, Darin Desai, Niraj Kim, Min Young Alasfar, Sami Bloch, Evan M. Tobian, Aaron A.R. Garonzik-Wang, Jacqueline Segev, Dorry L. Avery, Robin K. Outcomes of SOT Recipients With COVID-19 in Different Eras of COVID-19 Therapeutics |
title | Outcomes of SOT Recipients With COVID-19 in Different Eras of COVID-19 Therapeutics |
title_full | Outcomes of SOT Recipients With COVID-19 in Different Eras of COVID-19 Therapeutics |
title_fullStr | Outcomes of SOT Recipients With COVID-19 in Different Eras of COVID-19 Therapeutics |
title_full_unstemmed | Outcomes of SOT Recipients With COVID-19 in Different Eras of COVID-19 Therapeutics |
title_short | Outcomes of SOT Recipients With COVID-19 in Different Eras of COVID-19 Therapeutics |
title_sort | outcomes of sot recipients with covid-19 in different eras of covid-19 therapeutics |
topic | Infectious Disease |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8710330/ https://www.ncbi.nlm.nih.gov/pubmed/34966840 http://dx.doi.org/10.1097/TXD.0000000000001268 |
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