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Serial Convalescent Plasma Infusions for the Initial COVID-19 Infections in the Appalachian Region of West Virginia
PURPOSE: The rapid spread of SARS-CoV-2, the virus that is responsible for causing COVID-19, has presented the medical community with another example of when convalescent plasma (CP) is still used today. The ability to standardize CP at the onset of a pandemic is unlikely to exist in a reliable and...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9252015/ https://www.ncbi.nlm.nih.gov/pubmed/35795339 http://dx.doi.org/10.1177/21526575221110488 |
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author | Peppers, Brian P. Shmookler, Aaron Stanley, Johnathan Giblin Sutton, Lisa Perrotta, Peter L. Kieffer, Theodore Skoner, David Mahady, Stacey Lewandrowski, Callum Damron, Heath Horspool, Alexander Sakhjua, Ankit McCarthy, Paul Hostoffer, Robert W. |
author_facet | Peppers, Brian P. Shmookler, Aaron Stanley, Johnathan Giblin Sutton, Lisa Perrotta, Peter L. Kieffer, Theodore Skoner, David Mahady, Stacey Lewandrowski, Callum Damron, Heath Horspool, Alexander Sakhjua, Ankit McCarthy, Paul Hostoffer, Robert W. |
author_sort | Peppers, Brian P. |
collection | PubMed |
description | PURPOSE: The rapid spread of SARS-CoV-2, the virus that is responsible for causing COVID-19, has presented the medical community with another example of when convalescent plasma (CP) is still used today. The ability to standardize CP at the onset of a pandemic is unlikely to exist in a reliable and uniformly reproducible way. We hypothesized that CP of unknown strength given in a serial manner will promote health and reduce mortality in those inflicted with COVID-19. METHODS: Participants were given up to 8 CP-units depending on their condition upon entry into the study and their response. RESULTS: 102 out of 117 participants were given CP. The earlier a participant received CP corelated with survival (p = 0.0004). The number of CP-units given, throughout all the clinical severities, was not significant with outcomes, p = 0.3947. A higher number of CP-units given to the severe/critical participants (without biological immunosuppressants or restrictive lung disease) did correlate with survival p = 0.0116 (2.8 vs. 2 units). Lower platelets on admission corelated with mortality. Platelet levels increase correlated with CP infusions p < 0.0001. CONCLUSION: This study supports the serial use of CP of unknown strength based on clinical response for those infected with COVID-19. The use of 3–4 units of CP was found to be statistically significant for survival for severe and critical participants without restrictive lung disease and chronic biological immunosuppression. Increased platelet levels after CP infusions supports that CP is promoting overall health regardless of outcomes. |
format | Online Article Text |
id | pubmed-9252015 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-92520152022-07-05 Serial Convalescent Plasma Infusions for the Initial COVID-19 Infections in the Appalachian Region of West Virginia Peppers, Brian P. Shmookler, Aaron Stanley, Johnathan Giblin Sutton, Lisa Perrotta, Peter L. Kieffer, Theodore Skoner, David Mahady, Stacey Lewandrowski, Callum Damron, Heath Horspool, Alexander Sakhjua, Ankit McCarthy, Paul Hostoffer, Robert W. Allergy Rhinol (Providence) Clinical Trial PURPOSE: The rapid spread of SARS-CoV-2, the virus that is responsible for causing COVID-19, has presented the medical community with another example of when convalescent plasma (CP) is still used today. The ability to standardize CP at the onset of a pandemic is unlikely to exist in a reliable and uniformly reproducible way. We hypothesized that CP of unknown strength given in a serial manner will promote health and reduce mortality in those inflicted with COVID-19. METHODS: Participants were given up to 8 CP-units depending on their condition upon entry into the study and their response. RESULTS: 102 out of 117 participants were given CP. The earlier a participant received CP corelated with survival (p = 0.0004). The number of CP-units given, throughout all the clinical severities, was not significant with outcomes, p = 0.3947. A higher number of CP-units given to the severe/critical participants (without biological immunosuppressants or restrictive lung disease) did correlate with survival p = 0.0116 (2.8 vs. 2 units). Lower platelets on admission corelated with mortality. Platelet levels increase correlated with CP infusions p < 0.0001. CONCLUSION: This study supports the serial use of CP of unknown strength based on clinical response for those infected with COVID-19. The use of 3–4 units of CP was found to be statistically significant for survival for severe and critical participants without restrictive lung disease and chronic biological immunosuppression. Increased platelet levels after CP infusions supports that CP is promoting overall health regardless of outcomes. SAGE Publications 2022-06-30 /pmc/articles/PMC9252015/ /pubmed/35795339 http://dx.doi.org/10.1177/21526575221110488 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Clinical Trial Peppers, Brian P. Shmookler, Aaron Stanley, Johnathan Giblin Sutton, Lisa Perrotta, Peter L. Kieffer, Theodore Skoner, David Mahady, Stacey Lewandrowski, Callum Damron, Heath Horspool, Alexander Sakhjua, Ankit McCarthy, Paul Hostoffer, Robert W. Serial Convalescent Plasma Infusions for the Initial COVID-19 Infections in the Appalachian Region of West Virginia |
title | Serial Convalescent Plasma Infusions for the Initial COVID-19 Infections in the Appalachian Region of West Virginia |
title_full | Serial Convalescent Plasma Infusions for the Initial COVID-19 Infections in the Appalachian Region of West Virginia |
title_fullStr | Serial Convalescent Plasma Infusions for the Initial COVID-19 Infections in the Appalachian Region of West Virginia |
title_full_unstemmed | Serial Convalescent Plasma Infusions for the Initial COVID-19 Infections in the Appalachian Region of West Virginia |
title_short | Serial Convalescent Plasma Infusions for the Initial COVID-19 Infections in the Appalachian Region of West Virginia |
title_sort | serial convalescent plasma infusions for the initial covid-19 infections in the appalachian region of west virginia |
topic | Clinical Trial |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9252015/ https://www.ncbi.nlm.nih.gov/pubmed/35795339 http://dx.doi.org/10.1177/21526575221110488 |
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