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Effectiveness and Controversy of Convalescent Plasma Therapy for Coronavirus Disease 2019 Patients
Since the coronavirus disease 2019 (COVID-19) began to spread, it remains pandemic worldwide. The European Medicines Agency's human medicines committee and Food and Drug Administration have only granted a conditional marketing authorization for remdesivir to treat COVID-19. It is essential to a...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Lippincott Williams & Wilkins
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8772051/ https://www.ncbi.nlm.nih.gov/pubmed/37521156 http://dx.doi.org/10.1097/ID9.0000000000000033 |
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author | Shu, Zhanjun Wu, Peipei Qian, Qianqian Zhou, Li Du, Dandan Ding, Mengxuan Peng, Tao Fang, Ke |
author_facet | Shu, Zhanjun Wu, Peipei Qian, Qianqian Zhou, Li Du, Dandan Ding, Mengxuan Peng, Tao Fang, Ke |
author_sort | Shu, Zhanjun |
collection | PubMed |
description | Since the coronavirus disease 2019 (COVID-19) began to spread, it remains pandemic worldwide. The European Medicines Agency's human medicines committee and Food and Drug Administration have only granted a conditional marketing authorization for remdesivir to treat COVID-19. It is essential to apply other valuable treatments. Convalescent plasma (CP), donated by persons who have recovered from COVID-19, is the cellular component of blood that contains specific antibodies. Therefore, to determine the feasibility of CP for COVID-19, the effectiveness and controversy are discussed in depth here. It is suggested that CP plays a certain role in the treatment of COVID-19. As a treatment, it may have its own indications and contraindications, which need to be further discussed. Meanwhile, it is critical to establish a standard procedure for treatment from CP collection, preservation, transport, to transfusion, and conduct some large sample randomized controlled trials to confirm the transfusion dosage, appropriate time, frequency, and actively prevent adverse outcomes that may occur. |
format | Online Article Text |
id | pubmed-8772051 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Lippincott Williams & Wilkins |
record_format | MEDLINE/PubMed |
spelling | pubmed-87720512022-01-20 Effectiveness and Controversy of Convalescent Plasma Therapy for Coronavirus Disease 2019 Patients Shu, Zhanjun Wu, Peipei Qian, Qianqian Zhou, Li Du, Dandan Ding, Mengxuan Peng, Tao Fang, Ke Infectious Diseases & Immunity Review Since the coronavirus disease 2019 (COVID-19) began to spread, it remains pandemic worldwide. The European Medicines Agency's human medicines committee and Food and Drug Administration have only granted a conditional marketing authorization for remdesivir to treat COVID-19. It is essential to apply other valuable treatments. Convalescent plasma (CP), donated by persons who have recovered from COVID-19, is the cellular component of blood that contains specific antibodies. Therefore, to determine the feasibility of CP for COVID-19, the effectiveness and controversy are discussed in depth here. It is suggested that CP plays a certain role in the treatment of COVID-19. As a treatment, it may have its own indications and contraindications, which need to be further discussed. Meanwhile, it is critical to establish a standard procedure for treatment from CP collection, preservation, transport, to transfusion, and conduct some large sample randomized controlled trials to confirm the transfusion dosage, appropriate time, frequency, and actively prevent adverse outcomes that may occur. Lippincott Williams & Wilkins 2021-12-02 /pmc/articles/PMC8772051/ /pubmed/37521156 http://dx.doi.org/10.1097/ID9.0000000000000033 Text en Copyright © 2022 The Chinese Medical Association, 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), 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. http://creativecommons.org/licenses/by-nc-nd/4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) This article is made available via the PMC Open Access Subset for unrestricted re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the COVID-19 pandemic or until permissions are revoked in writing. Upon expiration of these permissions, PMC is granted a perpetual license to make this article available via PMC and Europe PMC, consistent with existing copyright protections. |
spellingShingle | Review Shu, Zhanjun Wu, Peipei Qian, Qianqian Zhou, Li Du, Dandan Ding, Mengxuan Peng, Tao Fang, Ke Effectiveness and Controversy of Convalescent Plasma Therapy for Coronavirus Disease 2019 Patients |
title | Effectiveness and Controversy of Convalescent Plasma Therapy for Coronavirus Disease 2019 Patients |
title_full | Effectiveness and Controversy of Convalescent Plasma Therapy for Coronavirus Disease 2019 Patients |
title_fullStr | Effectiveness and Controversy of Convalescent Plasma Therapy for Coronavirus Disease 2019 Patients |
title_full_unstemmed | Effectiveness and Controversy of Convalescent Plasma Therapy for Coronavirus Disease 2019 Patients |
title_short | Effectiveness and Controversy of Convalescent Plasma Therapy for Coronavirus Disease 2019 Patients |
title_sort | effectiveness and controversy of convalescent plasma therapy for coronavirus disease 2019 patients |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8772051/ https://www.ncbi.nlm.nih.gov/pubmed/37521156 http://dx.doi.org/10.1097/ID9.0000000000000033 |
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