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Plasma exchange for COVID‐19 thrombo‐inflammatory disease
Severe COVID‐19 disease is a hyperinflammatory, pro‐thrombotic state. We undertook plasma exchange (PEX) to determine its effects on organ function and thrombo‐inflammatory markers. Seven critically ill adults with severe COVID‐19 respiratory failure (PaO(2):FiO(2) ratio < 200 mm Hg) requiring in...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7754560/ https://www.ncbi.nlm.nih.gov/pubmed/33363289 http://dx.doi.org/10.1002/jha2.140 |
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author | Arulkumaran, Nishkantha Thomas, Mari Brealey, David Alwan, Ferras Singh, Deepak Lunn, Michael Welch, Anna Clark, Samuel Raith, Eamon Reddy, Ugan Low, Ryan Leverett, David Singer, Mervyn Scully, Marie |
author_facet | Arulkumaran, Nishkantha Thomas, Mari Brealey, David Alwan, Ferras Singh, Deepak Lunn, Michael Welch, Anna Clark, Samuel Raith, Eamon Reddy, Ugan Low, Ryan Leverett, David Singer, Mervyn Scully, Marie |
author_sort | Arulkumaran, Nishkantha |
collection | PubMed |
description | Severe COVID‐19 disease is a hyperinflammatory, pro‐thrombotic state. We undertook plasma exchange (PEX) to determine its effects on organ function and thrombo‐inflammatory markers. Seven critically ill adults with severe COVID‐19 respiratory failure (PaO(2):FiO(2) ratio < 200 mm Hg) requiring invasive or noninvasive ventilatory support and elevated thrombo‐inflammatory markers (LDH >800 IU/L and D‐dimer >1000 μg/L (or doubling from baseline) received PEX, daily, for a minimum of 5 days. No other immunomodulatory medications were initiated during this period. Seven patients matched for age and baseline biochemistry were a comparator group. Coagulation screening revealed no evidence of coagulopathy. However, von Willebrand Factor (VWF) activity, antigen and VWF antigen: ADAMTS13 ratio, Factor VIII and D‐dimers were all elevated. Following 5 days of PEX, plasma levels of all the above, and ferritin levels, were significantly reduced (P < .05) while lymphocyte counts normalized (P < .05). The P(a)O(2):FiO(2) ratio increased from a median interquartile range (IQR) of 11.6 (10.8‐19.7) kPa to 18.1 (16.0‐25.9) kPa (P < .05). Similar improvements were not observed in controls. Acute kidney injury (AKI) occurred among five patients in the control arm but not in patients receiving PEX. PEX improved oxygenation, decreased the incidence of AKI, normalized lymphocyte counts and reduced circulating thrombo‐inflammatory markers including D‐Dimer and VWF Ag:ADAMTS13 ratio. |
format | Online Article Text |
id | pubmed-7754560 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-77545602020-12-22 Plasma exchange for COVID‐19 thrombo‐inflammatory disease Arulkumaran, Nishkantha Thomas, Mari Brealey, David Alwan, Ferras Singh, Deepak Lunn, Michael Welch, Anna Clark, Samuel Raith, Eamon Reddy, Ugan Low, Ryan Leverett, David Singer, Mervyn Scully, Marie EJHaem Sickle Cell, Thrombosis, and Haematology Severe COVID‐19 disease is a hyperinflammatory, pro‐thrombotic state. We undertook plasma exchange (PEX) to determine its effects on organ function and thrombo‐inflammatory markers. Seven critically ill adults with severe COVID‐19 respiratory failure (PaO(2):FiO(2) ratio < 200 mm Hg) requiring invasive or noninvasive ventilatory support and elevated thrombo‐inflammatory markers (LDH >800 IU/L and D‐dimer >1000 μg/L (or doubling from baseline) received PEX, daily, for a minimum of 5 days. No other immunomodulatory medications were initiated during this period. Seven patients matched for age and baseline biochemistry were a comparator group. Coagulation screening revealed no evidence of coagulopathy. However, von Willebrand Factor (VWF) activity, antigen and VWF antigen: ADAMTS13 ratio, Factor VIII and D‐dimers were all elevated. Following 5 days of PEX, plasma levels of all the above, and ferritin levels, were significantly reduced (P < .05) while lymphocyte counts normalized (P < .05). The P(a)O(2):FiO(2) ratio increased from a median interquartile range (IQR) of 11.6 (10.8‐19.7) kPa to 18.1 (16.0‐25.9) kPa (P < .05). Similar improvements were not observed in controls. Acute kidney injury (AKI) occurred among five patients in the control arm but not in patients receiving PEX. PEX improved oxygenation, decreased the incidence of AKI, normalized lymphocyte counts and reduced circulating thrombo‐inflammatory markers including D‐Dimer and VWF Ag:ADAMTS13 ratio. John Wiley and Sons Inc. 2020-11-30 /pmc/articles/PMC7754560/ /pubmed/33363289 http://dx.doi.org/10.1002/jha2.140 Text en © 2020 The Authors. eJHaem published by British Society for Haematology and John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Sickle Cell, Thrombosis, and Haematology Arulkumaran, Nishkantha Thomas, Mari Brealey, David Alwan, Ferras Singh, Deepak Lunn, Michael Welch, Anna Clark, Samuel Raith, Eamon Reddy, Ugan Low, Ryan Leverett, David Singer, Mervyn Scully, Marie Plasma exchange for COVID‐19 thrombo‐inflammatory disease |
title | Plasma exchange for COVID‐19 thrombo‐inflammatory disease |
title_full | Plasma exchange for COVID‐19 thrombo‐inflammatory disease |
title_fullStr | Plasma exchange for COVID‐19 thrombo‐inflammatory disease |
title_full_unstemmed | Plasma exchange for COVID‐19 thrombo‐inflammatory disease |
title_short | Plasma exchange for COVID‐19 thrombo‐inflammatory disease |
title_sort | plasma exchange for covid‐19 thrombo‐inflammatory disease |
topic | Sickle Cell, Thrombosis, and Haematology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7754560/ https://www.ncbi.nlm.nih.gov/pubmed/33363289 http://dx.doi.org/10.1002/jha2.140 |
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