{"title":"Red blood cell transfusion in brain injury: Is it solely a matter of hemoglobin threshold?","authors":"Lamamri Myriam, Arnaud Foucrier, Emmanuel Weiss","doi":"10.1186/s13054-024-05226-1","DOIUrl":null,"url":null,"abstract":"<p>To the editor, </p><p>The optimal transfusion strategy for patients with acute brain injury remains a topic of intense debate. Recent large scale randomized controlled trials, such as HEMOTION study, have compared restrictive versus liberal transfusion thresholds [1]. While the TRA4IN study suggested that a more liberal threshold (9 g/dL) was associated with better neurological outcomes, HEMOTION study, focusing specifically on moderate-to-severe traumatic brain injury, failed to demonstrate a significant difference between liberal (10 g/dL) and restrictive (7 g/dL) strategies [2].</p><p>However, these studies primarily focused on the hemoglobin threshold, neglecting a potentially critical factor: the age of transfused red blood cells (RBC). Accumulating evidence suggests that the storage time of RBC can significantly impact their functional properties, including oxygen carrying capacity and ability to modulate inflammation [3] [4]. Storage lesions of red blood cell are proportional to storage duration [5]. Additionally, the number of days beyond which a RBC unit is considered old differs among studies.</p><p>Large meta-analyses of medical patients have yielded inconsistent results regarding the impact of fresh blood component transfusion on in-hospital mortality, failing to provide conclusive evidence of a survival benefit [6]. Yet, limited clinical data exists specifically linking RBC age to neurological outcomes in acute brain injury. Although a few smaller studies have explored this relationship, the results have not been conclusive in small numbers of patients [7] [8].</p><p>The evidence regarding this question is heterogeneous, with studies reporting conflicting findings in diverse population. Considering the susceptibility of the injured brain to hypoxic damage and given the lack of a universal threshold for significantly impaired oxygen carrying capacity, the age of RBC remains a critical variable.</p><p>The discrepancy between the TRAIN and HEMOTION studies may be partially explained by differences in the age of transfused RBC despite differences between inclusion criteria. It is plausible that the beneficial effects observed in the TRAIN study were not solely due to the higher hemoglobin threshold but also to the use of younger RBC with potentially superior oxygen carrying capacity.</p><p>Therefore, future studies should collect data on RBC age and explore its potential impact on neurological outcomes in acute brain injury. Randomized controlled trials specifically designed to evaluate the effects of RBC age, in combination with different hemoglobin thresholds, are needed to provide more definitive evidence.</p><p>No datasets were generated or analysed during the current study.</p><ol data-track-component=\"outbound reference\" data-track-context=\"references section\"><li data-counter=\"1.\"><p>Turgeon AF, Fergusson DA, Clayton L, et al. Liberal or restrictive transfusion strategy in patients with traumatic brain injury. N Engl J Med. 2024;391(8):722–35. https://doi.org/10.1056/NEJMoa2404360.</p><p>Article CAS PubMed Google Scholar </p></li><li data-counter=\"2.\"><p>Taccone FS, Rynkowski Bittencourt C, Møller K, et al. Restrictive vs liberal transfusion strategy in patients with acute brain injury: the TRAIN randomized clinical trial. JAMA. 2024;332(19):1623–33. https://doi.org/10.1001/jama.2024.20424.</p><p>Article CAS PubMed Google Scholar </p></li><li data-counter=\"3.\"><p>Tinmouth A, Fergusson D, Yee IC, Hebert PC. Clinical consequences of red cell storage in the critically ill. Transfusion. 2006;46(11):2014–27.</p><p>Article PubMed Google Scholar </p></li><li data-counter=\"4.\"><p>Stapley R, Owusu B, Brandon A, Cusick M, Rodriguez C, Marques M, et al. Erythrocyte storage increases rates of NO and nitrite scavenging: implications for transfusion-related toxicity. Biochem J. 2012;446(3):499–508.</p><p>Article CAS PubMed Google Scholar </p></li><li data-counter=\"5.\"><p>Marik PE, Sibbald WJ. Effect of stored-blood transfusion on oxygen delivery in patients with sepsis. JAMA. 1993;269(23):3024–9.</p><p>Article CAS PubMed Google Scholar </p></li><li data-counter=\"6.\"><p>Wang D, Sun J, Solomon SB, Klein HG, Natanson C. Transfusion of older stored blood and risk of death: a meta-analysis. Transfusion. 2012;52(6):1184–95. https://doi.org/10.1111/j.1537-2995.2011.03466.x.</p><p>Article PubMed Google Scholar </p></li><li data-counter=\"7.\"><p>Yamal JM, Benoit JS, Doshi P, et al. Association of transfusion red blood cell storage age and blood oxygenation, long-term neurologic outcome, and mortality in traumatic brain injury. J Trauma Acute Care Surg. 2015;79(5):843–9. https://doi.org/10.1097/TA.0000000000000834.</p><p>Article CAS PubMed PubMed Central Google Scholar </p></li><li data-counter=\"8.\"><p>Ruel-Laliberté J, Lessard Bonaventure P, Fergusson D, et al. Effect of age of transfused red blood cells on neurologic outcome following traumatic brain injury (ABLE-tbi Study): a nested study of the Age of Blood Evaluation (ABLE) trial. Can J Anaesth. 2019;66(6):696–705. https://doi.org/10.1007/s12630-019-01326-7.</p><p>Article PubMed Google Scholar </p></li></ol><p>Download references<svg aria-hidden=\"true\" focusable=\"false\" height=\"16\" role=\"img\" width=\"16\"><use xlink:href=\"#icon-eds-i-download-medium\" xmlns:xlink=\"http://www.w3.org/1999/xlink\"></use></svg></p><p>No funding.</p><h3>Authors and Affiliations</h3><ol><li><p>Département d’anesthésie Réanimationéanimation, DMU PARABOL, AP-HP, Hôpital Beaujon, Clichy, France</p><p>Lamamri Myriam, Arnaud Foucrier & Emmanuel Weiss</p></li><li><p>Department of Anesthesiology and Critical Care, Beaujon University Hospital, 100 Boulevard du General Leclerc, 92110, Clichy, France</p><p>Lamamri Myriam</p></li></ol><span>Authors</span><ol><li><span>Lamamri Myriam</span>View author publications<p>You can also search for this author in <span>PubMed<span> </span>Google Scholar</span></p></li><li><span>Arnaud Foucrier</span>View author publications<p>You can also search for this author in <span>PubMed<span> </span>Google Scholar</span></p></li><li><span>Emmanuel Weiss</span>View author publications<p>You can also search for this author in <span>PubMed<span> </span>Google Scholar</span></p></li></ol><h3>Contributions</h3><p>ML, AF, EW wrote and approved the manuscript.</p><h3>Corresponding author</h3><p>Correspondence to Lamamri Myriam.</p><h3>Ethics approval and consent to participate</h3>\n<p>Not applicable.</p>\n<h3>Competing interests</h3>\n<p>The authors declare no competing interests.</p><h3>Publisher's Note</h3><p>Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.</p><p><b>Open Access</b> This article is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License, which permits any non-commercial use, sharing, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if you modified the licensed material. You do not have permission under this licence to share adapted material derived from this article or parts of it. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by-nc-nd/4.0/.</p>\n<p>Reprints and permissions</p><img alt=\"Check for updates. 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Red blood cell transfusion in brain injury: Is it solely a matter of hemoglobin threshold?. <i>Crit Care</i> <b>28</b>, 430 (2024). https://doi.org/10.1186/s13054-024-05226-1</p><p>Download citation<svg aria-hidden=\"true\" focusable=\"false\" height=\"16\" role=\"img\" width=\"16\"><use xlink:href=\"#icon-eds-i-download-medium\" xmlns:xlink=\"http://www.w3.org/1999/xlink\"></use></svg></p><ul data-test=\"publication-history\"><li><p>Received<span>: </span><span><time datetime=\"2024-12-13\">13 December 2024</time></span></p></li><li><p>Accepted<span>: </span><span><time datetime=\"2024-12-19\">19 December 2024</time></span></p></li><li><p>Published<span>: </span><span><time datetime=\"2024-12-22\">22 December 2024</time></span></p></li><li><p>DOI</abbr><span>: </span><span>https://doi.org/10.1186/s13054-024-05226-1</span></p></li></ul><h3>Share this article</h3><p>Anyone you share the following link with will be able to read this content:</p><button data-track=\"click\" data-track-action=\"get shareable link\" data-track-external=\"\" data-track-label=\"button\" type=\"button\">Get shareable link</button><p>Sorry, a shareable link is not currently available for this article.</p><p data-track=\"click\" data-track-action=\"select share url\" data-track-label=\"button\"></p><button data-track=\"click\" data-track-action=\"copy share url\" data-track-external=\"\" data-track-label=\"button\" type=\"button\">Copy to clipboard</button><p> Provided by the Springer Nature SharedIt content-sharing initiative </p>","PeriodicalId":10811,"journal":{"name":"Critical Care","volume":"82 1","pages":""},"PeriodicalIF":8.8000,"publicationDate":"2024-12-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Critical Care","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1186/s13054-024-05226-1","RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CRITICAL CARE MEDICINE","Score":null,"Total":0}
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Abstract
To the editor,
The optimal transfusion strategy for patients with acute brain injury remains a topic of intense debate. Recent large scale randomized controlled trials, such as HEMOTION study, have compared restrictive versus liberal transfusion thresholds [1]. While the TRA4IN study suggested that a more liberal threshold (9 g/dL) was associated with better neurological outcomes, HEMOTION study, focusing specifically on moderate-to-severe traumatic brain injury, failed to demonstrate a significant difference between liberal (10 g/dL) and restrictive (7 g/dL) strategies [2].
However, these studies primarily focused on the hemoglobin threshold, neglecting a potentially critical factor: the age of transfused red blood cells (RBC). Accumulating evidence suggests that the storage time of RBC can significantly impact their functional properties, including oxygen carrying capacity and ability to modulate inflammation [3] [4]. Storage lesions of red blood cell are proportional to storage duration [5]. Additionally, the number of days beyond which a RBC unit is considered old differs among studies.
Large meta-analyses of medical patients have yielded inconsistent results regarding the impact of fresh blood component transfusion on in-hospital mortality, failing to provide conclusive evidence of a survival benefit [6]. Yet, limited clinical data exists specifically linking RBC age to neurological outcomes in acute brain injury. Although a few smaller studies have explored this relationship, the results have not been conclusive in small numbers of patients [7] [8].
The evidence regarding this question is heterogeneous, with studies reporting conflicting findings in diverse population. Considering the susceptibility of the injured brain to hypoxic damage and given the lack of a universal threshold for significantly impaired oxygen carrying capacity, the age of RBC remains a critical variable.
The discrepancy between the TRAIN and HEMOTION studies may be partially explained by differences in the age of transfused RBC despite differences between inclusion criteria. It is plausible that the beneficial effects observed in the TRAIN study were not solely due to the higher hemoglobin threshold but also to the use of younger RBC with potentially superior oxygen carrying capacity.
Therefore, future studies should collect data on RBC age and explore its potential impact on neurological outcomes in acute brain injury. Randomized controlled trials specifically designed to evaluate the effects of RBC age, in combination with different hemoglobin thresholds, are needed to provide more definitive evidence.
No datasets were generated or analysed during the current study.
Turgeon AF, Fergusson DA, Clayton L, et al. Liberal or restrictive transfusion strategy in patients with traumatic brain injury. N Engl J Med. 2024;391(8):722–35. https://doi.org/10.1056/NEJMoa2404360.
Article CAS PubMed Google Scholar
Taccone FS, Rynkowski Bittencourt C, Møller K, et al. Restrictive vs liberal transfusion strategy in patients with acute brain injury: the TRAIN randomized clinical trial. JAMA. 2024;332(19):1623–33. https://doi.org/10.1001/jama.2024.20424.
Article CAS PubMed Google Scholar
Tinmouth A, Fergusson D, Yee IC, Hebert PC. Clinical consequences of red cell storage in the critically ill. Transfusion. 2006;46(11):2014–27.
Article PubMed Google Scholar
Stapley R, Owusu B, Brandon A, Cusick M, Rodriguez C, Marques M, et al. Erythrocyte storage increases rates of NO and nitrite scavenging: implications for transfusion-related toxicity. Biochem J. 2012;446(3):499–508.
Article CAS PubMed Google Scholar
Marik PE, Sibbald WJ. Effect of stored-blood transfusion on oxygen delivery in patients with sepsis. JAMA. 1993;269(23):3024–9.
Article CAS PubMed Google Scholar
Wang D, Sun J, Solomon SB, Klein HG, Natanson C. Transfusion of older stored blood and risk of death: a meta-analysis. Transfusion. 2012;52(6):1184–95. https://doi.org/10.1111/j.1537-2995.2011.03466.x.
Article PubMed Google Scholar
Yamal JM, Benoit JS, Doshi P, et al. Association of transfusion red blood cell storage age and blood oxygenation, long-term neurologic outcome, and mortality in traumatic brain injury. J Trauma Acute Care Surg. 2015;79(5):843–9. https://doi.org/10.1097/TA.0000000000000834.
Article CAS PubMed PubMed Central Google Scholar
Ruel-Laliberté J, Lessard Bonaventure P, Fergusson D, et al. Effect of age of transfused red blood cells on neurologic outcome following traumatic brain injury (ABLE-tbi Study): a nested study of the Age of Blood Evaluation (ABLE) trial. Can J Anaesth. 2019;66(6):696–705. https://doi.org/10.1007/s12630-019-01326-7.
Article PubMed Google Scholar
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Authors and Affiliations
Département d’anesthésie Réanimationéanimation, DMU PARABOL, AP-HP, Hôpital Beaujon, Clichy, France
Lamamri Myriam, Arnaud Foucrier & Emmanuel Weiss
Department of Anesthesiology and Critical Care, Beaujon University Hospital, 100 Boulevard du General Leclerc, 92110, Clichy, France
Lamamri Myriam
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ML, AF, EW wrote and approved the manuscript.
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Correspondence to Lamamri Myriam.
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Myriam, L., Foucrier, A. & Weiss, E. Red blood cell transfusion in brain injury: Is it solely a matter of hemoglobin threshold?. Crit Care28, 430 (2024). https://doi.org/10.1186/s13054-024-05226-1
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DOI: https://doi.org/10.1186/s13054-024-05226-1
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期刊介绍:
Critical Care is an esteemed international medical journal that undergoes a rigorous peer-review process to maintain its high quality standards. Its primary objective is to enhance the healthcare services offered to critically ill patients. To achieve this, the journal focuses on gathering, exchanging, disseminating, and endorsing evidence-based information that is highly relevant to intensivists. By doing so, Critical Care seeks to provide a thorough and inclusive examination of the intensive care field.