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Bilateral Lung Transplantation for End-Stage Respiratory Failure from COVID-19 Pneumonia

INTRODUCTION: The SARS-CoV-2 virus is causing severe end-stage fibrosis and respiratory failure in otherwise healthy individuals. Lung transplant (LTX) has been performed internationally in select patients for this indication, but there is limited evidence on its role in COVID-19. We describe a pati...

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Autores principales: Maniar, N., Coster, J., Li, G., Segraves, J., Hemmersbach-Miller, M., Shafii, A., Liao, K., Matar, A., Loor, G., Garcha, P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Published by Elsevier Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7979380/
http://dx.doi.org/10.1016/j.healun.2021.01.2034
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author Maniar, N.
Coster, J.
Li, G.
Segraves, J.
Hemmersbach-Miller, M.
Shafii, A.
Liao, K.
Matar, A.
Loor, G.
Garcha, P.
author_facet Maniar, N.
Coster, J.
Li, G.
Segraves, J.
Hemmersbach-Miller, M.
Shafii, A.
Liao, K.
Matar, A.
Loor, G.
Garcha, P.
author_sort Maniar, N.
collection PubMed
description INTRODUCTION: The SARS-CoV-2 virus is causing severe end-stage fibrosis and respiratory failure in otherwise healthy individuals. Lung transplant (LTX) has been performed internationally in select patients for this indication, but there is limited evidence on its role in COVID-19. We describe a patient who received a bilateral LTX 12 weeks after an initial diagnosis of COVID-19 pneumonia. CASE REPORT: A 51-year-old male with hypertension and presented to an outlying hospital with dyspnea, fever and exposure to SARS-CoV-2. He was hypoxic and a diagnosis of COVID-19 pneumonia was made by nasopharyngeal swab. He was treated with dexamethasone, remdesivir, and convalescent plasma, mechanical ventilation and eventually femoral VV-ECMO cannulation to maintain oxygenation. He was extubated and was transitioned to a left subclavian dual-limb 30 Fr VV-ECMO cannula for improved rehabilitation. He was then transferred to our center for LTX consideration given refractory ARDS. Evaluation for LTX revealed pulmonary hypertension, negative SARS-CoV-2 PCR and deconditioning but no absolute contraindications. He participated in intensive rehabilitation and progressed to assisted steps despite severe deconditioning and hypoxia. He was listed for a bilateral lung transplant with a lung allocation score of 90 and received a donor offer 7 days after listing and after 82 days on ECMO. He underwent bilateral LTX via clamshell exposure with central VA ECMO support. Intraoperatively, the lungs were densely consolidated with severe hilar adenopathy without peripheral adhesions. Post-operatively, he was transitioned back to his original VV ECMO circuit and then decannulated on post-op day 3. Standard induction with basiliximab and immunosuppression with IV methylprednisolone, mycophenolate and tacrolimus was administered. He had a transient elevation of liver enzymes on post-operative day 1 and an early planned tracheostomy was performed due to deconditioning. He has since, been progressing well on oxygen via tracheostomy collar and is able to speak with a one-way valve and participate in rehabilitation. SUMMARY: For patients with irreversible end-stage lung disease after COVID-19 pneumonia, LTX is a viable option. Timely transfer to a lung transplant center and intensive rehabilitation are essential. Standard established immunosuppression and post-transplant protocols should be followed.
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spelling pubmed-79793802021-03-23 Bilateral Lung Transplantation for End-Stage Respiratory Failure from COVID-19 Pneumonia Maniar, N. Coster, J. Li, G. Segraves, J. Hemmersbach-Miller, M. Shafii, A. Liao, K. Matar, A. Loor, G. Garcha, P. J Heart Lung Transplant (1266) INTRODUCTION: The SARS-CoV-2 virus is causing severe end-stage fibrosis and respiratory failure in otherwise healthy individuals. Lung transplant (LTX) has been performed internationally in select patients for this indication, but there is limited evidence on its role in COVID-19. We describe a patient who received a bilateral LTX 12 weeks after an initial diagnosis of COVID-19 pneumonia. CASE REPORT: A 51-year-old male with hypertension and presented to an outlying hospital with dyspnea, fever and exposure to SARS-CoV-2. He was hypoxic and a diagnosis of COVID-19 pneumonia was made by nasopharyngeal swab. He was treated with dexamethasone, remdesivir, and convalescent plasma, mechanical ventilation and eventually femoral VV-ECMO cannulation to maintain oxygenation. He was extubated and was transitioned to a left subclavian dual-limb 30 Fr VV-ECMO cannula for improved rehabilitation. He was then transferred to our center for LTX consideration given refractory ARDS. Evaluation for LTX revealed pulmonary hypertension, negative SARS-CoV-2 PCR and deconditioning but no absolute contraindications. He participated in intensive rehabilitation and progressed to assisted steps despite severe deconditioning and hypoxia. He was listed for a bilateral lung transplant with a lung allocation score of 90 and received a donor offer 7 days after listing and after 82 days on ECMO. He underwent bilateral LTX via clamshell exposure with central VA ECMO support. Intraoperatively, the lungs were densely consolidated with severe hilar adenopathy without peripheral adhesions. Post-operatively, he was transitioned back to his original VV ECMO circuit and then decannulated on post-op day 3. Standard induction with basiliximab and immunosuppression with IV methylprednisolone, mycophenolate and tacrolimus was administered. He had a transient elevation of liver enzymes on post-operative day 1 and an early planned tracheostomy was performed due to deconditioning. He has since, been progressing well on oxygen via tracheostomy collar and is able to speak with a one-way valve and participate in rehabilitation. SUMMARY: For patients with irreversible end-stage lung disease after COVID-19 pneumonia, LTX is a viable option. Timely transfer to a lung transplant center and intensive rehabilitation are essential. Standard established immunosuppression and post-transplant protocols should be followed. Published by Elsevier Inc. 2021-04 2021-03-20 /pmc/articles/PMC7979380/ http://dx.doi.org/10.1016/j.healun.2021.01.2034 Text en Copyright © 2021 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 (1266)
Maniar, N.
Coster, J.
Li, G.
Segraves, J.
Hemmersbach-Miller, M.
Shafii, A.
Liao, K.
Matar, A.
Loor, G.
Garcha, P.
Bilateral Lung Transplantation for End-Stage Respiratory Failure from COVID-19 Pneumonia
title Bilateral Lung Transplantation for End-Stage Respiratory Failure from COVID-19 Pneumonia
title_full Bilateral Lung Transplantation for End-Stage Respiratory Failure from COVID-19 Pneumonia
title_fullStr Bilateral Lung Transplantation for End-Stage Respiratory Failure from COVID-19 Pneumonia
title_full_unstemmed Bilateral Lung Transplantation for End-Stage Respiratory Failure from COVID-19 Pneumonia
title_short Bilateral Lung Transplantation for End-Stage Respiratory Failure from COVID-19 Pneumonia
title_sort bilateral lung transplantation for end-stage respiratory failure from covid-19 pneumonia
topic (1266)
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7979380/
http://dx.doi.org/10.1016/j.healun.2021.01.2034
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