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Outcomes of COVID-19 in Heart Transplant Recipients

PURPOSE: Data on outcomes after Covid-19 in heart transplant recipients are scarce and inconsistent. We sought to evaluate the early and late post-discharge outcomes in this patient population. METHODS: This case series includes 19 consecutive adult heart transplant recipients hospitalized for Covid...

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Autores principales: Poglajen, G., Frljak, S., Kokošar, B., Kotar, T., Nadrah, K., Rojko, T., Cerar, A., Zemljič, G., Okrajšek, R., Šebeštjen, M., Vrtovec, B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Published by Elsevier Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8988599/
http://dx.doi.org/10.1016/j.healun.2022.01.814
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author Poglajen, G.
Frljak, S.
Kokošar, B.
Kotar, T.
Nadrah, K.
Rojko, T.
Cerar, A.
Zemljič, G.
Okrajšek, R.
Šebeštjen, M.
Vrtovec, B.
author_facet Poglajen, G.
Frljak, S.
Kokošar, B.
Kotar, T.
Nadrah, K.
Rojko, T.
Cerar, A.
Zemljič, G.
Okrajšek, R.
Šebeštjen, M.
Vrtovec, B.
author_sort Poglajen, G.
collection PubMed
description PURPOSE: Data on outcomes after Covid-19 in heart transplant recipients are scarce and inconsistent. We sought to evaluate the early and late post-discharge outcomes in this patient population. METHODS: This case series includes 19 consecutive adult heart transplant recipients hospitalized for Covid-19 at our tertiary center between March 1, 2020 and April 30, 2021. After discharge, all patients were followed per standard post-transplant protocol for 6 months. Significant allograft dysfunction was defined as a decrease in LVEF ≥ 10% and myocardial damage was defined as at least 30% increase in troponin or NT-proBNP serum levels. CMV reactivation was defined as any positive PCR CMV requiring virostatic therapy. RESULTS: Of 19 recipients 15 (79%) were male with a mean age of 62±8 years and a mean time from transplantation of 4.5±3.4 years. 14 (73%) and 5 (26%) recipients had hypertension and diabetes, respectively. Immunosupressive (IS) regimen at the time of infection consisted of tacrolimus (TAC; mean C0 level 7.5±2.1 μg/mL), mycophenolate mofetil (MMF; mean dose 2052±359 mg) and steroids (mean dose 4.6±4.7 mg). During hospital management IS was reduced in 6 (31%) patients with a maintenence of TAC serum levels (mean C0 7.7±1.9 μg/mL pre-infection vs. 7.5±2.2 μg/mL during infection, P=0.75) and a decrease of MMF dose (2052±359 mg vs. 1906±657 mg, P= 0.01). In 11 (58%) patients we applied oxygen supplementation; however none required non-invasive or invasive forms of ventilation. During hospitalisation 12 (63%) recipients received hyperimmune plasma, 13 (68%) were treated with remdesivir (cumulative dose 600 mg), and 11 (58%) received steroid therapy (mean methylprednisolone dose 29±21 mg). All recipients survived to discharge (mean hospitalization time of 17.4±12.6 days) and to 6-month follow-up. We found no evidence of allograft dysfunction (LVEF 67±6% at baseline vs 68±7% at follow-up; P=0.88) or persistent myocardial damage (troponin: 22±28 pg/mL vs. 14±21 pg/mL; P=0.41 and NT-proBNP: 829±823 pg/mL vs. 817±940 pg/mL; P=0.96). CMV reactivation occured in 3 (16%) recipients and in 1 (5%) recipient a thrombotic event was noted. CONCLUSION: Covid-19 outcomes in heart transplant recipients appear to be acceptable when managed in a tertiary center with dedicated heart transplant and Covid-19 facilities. Further data is needed to establish optimal Covid-19 management algorithms for this patient population.
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spelling pubmed-89885992022-04-11 Outcomes of COVID-19 in Heart Transplant Recipients Poglajen, G. Frljak, S. Kokošar, B. Kotar, T. Nadrah, K. Rojko, T. Cerar, A. Zemljič, G. Okrajšek, R. Šebeštjen, M. Vrtovec, B. J Heart Lung Transplant (793) PURPOSE: Data on outcomes after Covid-19 in heart transplant recipients are scarce and inconsistent. We sought to evaluate the early and late post-discharge outcomes in this patient population. METHODS: This case series includes 19 consecutive adult heart transplant recipients hospitalized for Covid-19 at our tertiary center between March 1, 2020 and April 30, 2021. After discharge, all patients were followed per standard post-transplant protocol for 6 months. Significant allograft dysfunction was defined as a decrease in LVEF ≥ 10% and myocardial damage was defined as at least 30% increase in troponin or NT-proBNP serum levels. CMV reactivation was defined as any positive PCR CMV requiring virostatic therapy. RESULTS: Of 19 recipients 15 (79%) were male with a mean age of 62±8 years and a mean time from transplantation of 4.5±3.4 years. 14 (73%) and 5 (26%) recipients had hypertension and diabetes, respectively. Immunosupressive (IS) regimen at the time of infection consisted of tacrolimus (TAC; mean C0 level 7.5±2.1 μg/mL), mycophenolate mofetil (MMF; mean dose 2052±359 mg) and steroids (mean dose 4.6±4.7 mg). During hospital management IS was reduced in 6 (31%) patients with a maintenence of TAC serum levels (mean C0 7.7±1.9 μg/mL pre-infection vs. 7.5±2.2 μg/mL during infection, P=0.75) and a decrease of MMF dose (2052±359 mg vs. 1906±657 mg, P= 0.01). In 11 (58%) patients we applied oxygen supplementation; however none required non-invasive or invasive forms of ventilation. During hospitalisation 12 (63%) recipients received hyperimmune plasma, 13 (68%) were treated with remdesivir (cumulative dose 600 mg), and 11 (58%) received steroid therapy (mean methylprednisolone dose 29±21 mg). All recipients survived to discharge (mean hospitalization time of 17.4±12.6 days) and to 6-month follow-up. We found no evidence of allograft dysfunction (LVEF 67±6% at baseline vs 68±7% at follow-up; P=0.88) or persistent myocardial damage (troponin: 22±28 pg/mL vs. 14±21 pg/mL; P=0.41 and NT-proBNP: 829±823 pg/mL vs. 817±940 pg/mL; P=0.96). CMV reactivation occured in 3 (16%) recipients and in 1 (5%) recipient a thrombotic event was noted. CONCLUSION: Covid-19 outcomes in heart transplant recipients appear to be acceptable when managed in a tertiary center with dedicated heart transplant and Covid-19 facilities. Further data is needed to establish optimal Covid-19 management algorithms for this patient population. Published by Elsevier Inc. 2022-04 2022-04-07 /pmc/articles/PMC8988599/ http://dx.doi.org/10.1016/j.healun.2022.01.814 Text en Copyright © 2022 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 (793)
Poglajen, G.
Frljak, S.
Kokošar, B.
Kotar, T.
Nadrah, K.
Rojko, T.
Cerar, A.
Zemljič, G.
Okrajšek, R.
Šebeštjen, M.
Vrtovec, B.
Outcomes of COVID-19 in Heart Transplant Recipients
title Outcomes of COVID-19 in Heart Transplant Recipients
title_full Outcomes of COVID-19 in Heart Transplant Recipients
title_fullStr Outcomes of COVID-19 in Heart Transplant Recipients
title_full_unstemmed Outcomes of COVID-19 in Heart Transplant Recipients
title_short Outcomes of COVID-19 in Heart Transplant Recipients
title_sort outcomes of covid-19 in heart transplant recipients
topic (793)
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8988599/
http://dx.doi.org/10.1016/j.healun.2022.01.814
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