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Plasma Exchange for COVID-19 Thrombo-Inflammatory Disease
Introduction Severe COVID-19 disease is associated with a hyperinflammatory, pro-thrombotic state and a high mortality. A thrombotic phenotype rather than a coagulopathy is suggested and we undertook plasma exchange to determine its effects on organ function and thrombo-inflammatory markers. Methods...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society of Hematology
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8330172/ http://dx.doi.org/10.1182/blood-2020-138851 |
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author | Thomas, Mari Arulkumaran, Nishkantha Brearley, David Alwan, Ferras Singh, Deepak Lunn, Michael P Welch, Anna Clark, Samuel Raith, Eamon Reddy, Ugan Low, Ryan Leverett, David Singer, Mervyn Scully, Marie |
author_facet | Thomas, Mari Arulkumaran, Nishkantha Brearley, David Alwan, Ferras Singh, Deepak Lunn, Michael P Welch, Anna Clark, Samuel Raith, Eamon Reddy, Ugan Low, Ryan Leverett, David Singer, Mervyn Scully, Marie |
author_sort | Thomas, Mari |
collection | PubMed |
description | Introduction Severe COVID-19 disease is associated with a hyperinflammatory, pro-thrombotic state and a high mortality. A thrombotic phenotype rather than a coagulopathy is suggested and we undertook plasma exchange to determine its effects on organ function and thrombo-inflammatory markers. Methods Plasma exchange was carried out in seven critically ill adults with severe COVID-19 respiratory failure (PaO(2):FiO(2) ratio <200 mmHg) requiring invasive or non-invasive ventilatory support and elevated thrombo-inflammatory markers (LDH>800 IU/L and D dimer>1000 µg/L (or doubling from baseline). Patients received a daily single volume 3 litre plasma exchange for a minimum of five days. No other immunomodulatory medications were initiated during this period. Effects on organ function, thrombo-inflammatory markers and complications were monitored. Seven patients matched for age and baseline biochemistry were a comparator group. Results 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 five days of plasma exchange, plasma levels of all the above, and ferritin levels, were significantly reduced (p<0.05, Figure 1) while lymphocyte count normalized (p<0.05). The P(a)O(2):FiO(2) ratio increased from a median(IQR) of 11.6 (10.8- 19.7) kPa to 18.1 (16.0-25.9) kPa (p<0.05). Similar improvements were not observed in controls. Acute kidney injury (AKI) occurred among 5 patients in the control arm but not in patients who underwent plasma exchange. Conclusion Plasma exchange was associated with an improvement in oxygenation, decreased incidence of AKI, normalisation of lymphocytes and reduction in circulating thrombo-inflammatory markers including D-Dimer and VWF Ag:ADAMTS13 ratio. [Figure: see text] DISCLOSURES: Thomas:Ablynx: Honoraria, Other: Advisory Board; Bayer: Honoraria, Speakers Bureau; Sanofi: Honoraria, Other: Advisory Board. Scully:Takeda: Consultancy, Speakers Bureau; Alexion: Consultancy, Speakers Bureau; Sanofi: Consultancy, Speakers Bureau; Shire/Takeda: Other: Advisory Board, Research Funding, Speakers Bureau; Novartis: Other: Advisory Board, Speakers Bureau; Takeda: Speakers Bureau; Ablynx/Sanofi: Consultancy, Other: Advisory Board, Speakers Bureau. |
format | Online Article Text |
id | pubmed-8330172 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | American Society of Hematology |
record_format | MEDLINE/PubMed |
spelling | pubmed-83301722021-08-03 Plasma Exchange for COVID-19 Thrombo-Inflammatory Disease Thomas, Mari Arulkumaran, Nishkantha Brearley, David Alwan, Ferras Singh, Deepak Lunn, Michael P Welch, Anna Clark, Samuel Raith, Eamon Reddy, Ugan Low, Ryan Leverett, David Singer, Mervyn Scully, Marie Blood 322.Disorders of Coagulation or Fibrinolysis Introduction Severe COVID-19 disease is associated with a hyperinflammatory, pro-thrombotic state and a high mortality. A thrombotic phenotype rather than a coagulopathy is suggested and we undertook plasma exchange to determine its effects on organ function and thrombo-inflammatory markers. Methods Plasma exchange was carried out in seven critically ill adults with severe COVID-19 respiratory failure (PaO(2):FiO(2) ratio <200 mmHg) requiring invasive or non-invasive ventilatory support and elevated thrombo-inflammatory markers (LDH>800 IU/L and D dimer>1000 µg/L (or doubling from baseline). Patients received a daily single volume 3 litre plasma exchange for a minimum of five days. No other immunomodulatory medications were initiated during this period. Effects on organ function, thrombo-inflammatory markers and complications were monitored. Seven patients matched for age and baseline biochemistry were a comparator group. Results 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 five days of plasma exchange, plasma levels of all the above, and ferritin levels, were significantly reduced (p<0.05, Figure 1) while lymphocyte count normalized (p<0.05). The P(a)O(2):FiO(2) ratio increased from a median(IQR) of 11.6 (10.8- 19.7) kPa to 18.1 (16.0-25.9) kPa (p<0.05). Similar improvements were not observed in controls. Acute kidney injury (AKI) occurred among 5 patients in the control arm but not in patients who underwent plasma exchange. Conclusion Plasma exchange was associated with an improvement in oxygenation, decreased incidence of AKI, normalisation of lymphocytes and reduction in circulating thrombo-inflammatory markers including D-Dimer and VWF Ag:ADAMTS13 ratio. [Figure: see text] DISCLOSURES: Thomas:Ablynx: Honoraria, Other: Advisory Board; Bayer: Honoraria, Speakers Bureau; Sanofi: Honoraria, Other: Advisory Board. Scully:Takeda: Consultancy, Speakers Bureau; Alexion: Consultancy, Speakers Bureau; Sanofi: Consultancy, Speakers Bureau; Shire/Takeda: Other: Advisory Board, Research Funding, Speakers Bureau; Novartis: Other: Advisory Board, Speakers Bureau; Takeda: Speakers Bureau; Ablynx/Sanofi: Consultancy, Other: Advisory Board, Speakers Bureau. American Society of Hematology 2020-11-05 2021-08-03 /pmc/articles/PMC8330172/ http://dx.doi.org/10.1182/blood-2020-138851 Text en Copyright © 2020 American Society of Hematology. 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 | 322.Disorders of Coagulation or Fibrinolysis Thomas, Mari Arulkumaran, Nishkantha Brearley, David Alwan, Ferras Singh, Deepak Lunn, Michael P 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 | 322.Disorders of Coagulation or Fibrinolysis |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8330172/ http://dx.doi.org/10.1182/blood-2020-138851 |
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