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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...

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Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2021
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.
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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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