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The oxyhaemoglobin dissociation curve is generally left‐shifted in COVID‐19 patients at admission to hospital, and this is associated with lower mortality
Lung damage caused by SARS‐Cov‐2 virus results in marked arterial hypoxia, accompanied in many cases by hypocapnia. The literature is inconclusive as to whether these conditions induce alteration of the affinity of haemoglobin for oxygen. We studied the oxyhaemoglobin dissociation curves (ODCs) of 5...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9538192/ https://www.ncbi.nlm.nih.gov/pubmed/35971642 http://dx.doi.org/10.1111/bjh.18431 |
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author | Valle, Andrea Rodriguez, Javier Camiña, Félix Rodriguez‐Segade, Miguel Ortola, Juan B. Rodriguez‐Segade, Santiago |
author_facet | Valle, Andrea Rodriguez, Javier Camiña, Félix Rodriguez‐Segade, Miguel Ortola, Juan B. Rodriguez‐Segade, Santiago |
author_sort | Valle, Andrea |
collection | PubMed |
description | Lung damage caused by SARS‐Cov‐2 virus results in marked arterial hypoxia, accompanied in many cases by hypocapnia. The literature is inconclusive as to whether these conditions induce alteration of the affinity of haemoglobin for oxygen. We studied the oxyhaemoglobin dissociation curves (ODCs) of 517 patients hospitalized with coronavirus disease 2019 (COVID‐19) for whom arterial blood gas analysis (BGA) was performed upon hospitalization (i.e., before treatment). With respect to a conventional normal p50 (pO(2) at 50% saturation of haemoglobin) of 27 mmHg, 76% had a lower standardized p50 (p50s) and 85% a lower in vivo p50 (p50i). In a 33‐patient subgroup with follow‐up BGAs after 3, 6, 9, 12, 15 and 18 days' treatment, p50s and p50i exhibited statistically significant differences between baseline values and values recorded at all these time points. The 30‐day Kaplan–Meier survival curves of COVID‐19 patients stratified by p50i level show a higher probability of survival among patients who at admission had p50 values below 27 mmHg (p = 0.012). Whether the observed alteration of the affinity of haemoglobin for oxygen in COVID‐19 patients is a direct or indirect effect of the virus on haemoglobin is unknown. |
format | Online Article Text |
id | pubmed-9538192 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-95381922022-10-11 The oxyhaemoglobin dissociation curve is generally left‐shifted in COVID‐19 patients at admission to hospital, and this is associated with lower mortality Valle, Andrea Rodriguez, Javier Camiña, Félix Rodriguez‐Segade, Miguel Ortola, Juan B. Rodriguez‐Segade, Santiago Br J Haematol Original Papers Lung damage caused by SARS‐Cov‐2 virus results in marked arterial hypoxia, accompanied in many cases by hypocapnia. The literature is inconclusive as to whether these conditions induce alteration of the affinity of haemoglobin for oxygen. We studied the oxyhaemoglobin dissociation curves (ODCs) of 517 patients hospitalized with coronavirus disease 2019 (COVID‐19) for whom arterial blood gas analysis (BGA) was performed upon hospitalization (i.e., before treatment). With respect to a conventional normal p50 (pO(2) at 50% saturation of haemoglobin) of 27 mmHg, 76% had a lower standardized p50 (p50s) and 85% a lower in vivo p50 (p50i). In a 33‐patient subgroup with follow‐up BGAs after 3, 6, 9, 12, 15 and 18 days' treatment, p50s and p50i exhibited statistically significant differences between baseline values and values recorded at all these time points. The 30‐day Kaplan–Meier survival curves of COVID‐19 patients stratified by p50i level show a higher probability of survival among patients who at admission had p50 values below 27 mmHg (p = 0.012). Whether the observed alteration of the affinity of haemoglobin for oxygen in COVID‐19 patients is a direct or indirect effect of the virus on haemoglobin is unknown. John Wiley and Sons Inc. 2022-08-30 /pmc/articles/PMC9538192/ /pubmed/35971642 http://dx.doi.org/10.1111/bjh.18431 Text en © 2022 The Authors. British Journal of Haematology published by British Society for Haematology and John Wiley & Sons Ltd. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Original Papers Valle, Andrea Rodriguez, Javier Camiña, Félix Rodriguez‐Segade, Miguel Ortola, Juan B. Rodriguez‐Segade, Santiago The oxyhaemoglobin dissociation curve is generally left‐shifted in COVID‐19 patients at admission to hospital, and this is associated with lower mortality |
title | The oxyhaemoglobin dissociation curve is generally left‐shifted in COVID‐19 patients at admission to hospital, and this is associated with lower mortality |
title_full | The oxyhaemoglobin dissociation curve is generally left‐shifted in COVID‐19 patients at admission to hospital, and this is associated with lower mortality |
title_fullStr | The oxyhaemoglobin dissociation curve is generally left‐shifted in COVID‐19 patients at admission to hospital, and this is associated with lower mortality |
title_full_unstemmed | The oxyhaemoglobin dissociation curve is generally left‐shifted in COVID‐19 patients at admission to hospital, and this is associated with lower mortality |
title_short | The oxyhaemoglobin dissociation curve is generally left‐shifted in COVID‐19 patients at admission to hospital, and this is associated with lower mortality |
title_sort | oxyhaemoglobin dissociation curve is generally left‐shifted in covid‐19 patients at admission to hospital, and this is associated with lower mortality |
topic | Original Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9538192/ https://www.ncbi.nlm.nih.gov/pubmed/35971642 http://dx.doi.org/10.1111/bjh.18431 |
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