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Encouragement for Further Study of Tranexamic Acid Administration for Sacroiliac Joint Fusion Surgery

TO THE EDITOR: We read with great interest the article by Huynh et al.regarding the association between tranexamic acid (TXA) and blood loss in patients undergoing surgical treatment for hip fracture (Huynh PAN, Miller M, Will R. Intravenous Tranexamic Acid Decreases Blood Transfusions and Blood Los...

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Autores principales: Beyer, Ryan S., Hatter, Matthew J., Streetman, Daniel, Brown, Nolan, Gendreau, Julian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9087243/
https://www.ncbi.nlm.nih.gov/pubmed/35557600
http://dx.doi.org/10.1177/21514593221098606
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author Beyer, Ryan S.
Hatter, Matthew J.
Streetman, Daniel
Brown, Nolan
Gendreau, Julian
author_facet Beyer, Ryan S.
Hatter, Matthew J.
Streetman, Daniel
Brown, Nolan
Gendreau, Julian
author_sort Beyer, Ryan S.
collection PubMed
description TO THE EDITOR: We read with great interest the article by Huynh et al.regarding the association between tranexamic acid (TXA) and blood loss in patients undergoing surgical treatment for hip fracture (Huynh PAN, Miller M, Will R. Intravenous Tranexamic Acid Decreases Blood Transfusions and Blood Loss for Patients with Surgically Treated Hip Fractures. Geriatric Orthopedic Surg Rehabil. 2021). The authors illustrated, via retrospective chart review of 505 patients who were surgically treated for hip fractures, that patients administered TXA had statistically significant decreases in perioperative blood loss and reduced relative risk of transfusion. Huynh et al. reported no statistically significant increases in thromboembolic events in patients given TXA. Mechanistically, TXA is a synthetic anti-fibrinolytic that competitively inhibits the plasminogen activation pathway. By preventing activated plasmin from de-stabilizing the fibrin matrix, TXA promotes clot formation. Given the anti-fibrinolytic effects of TXA, concerns in the literature exist regarding its use being associated with increased risk for thromboembolic events. However, it is important to note the complication profile associated with TXA is minimal, as elucidated by Brown et al., specifically finding that no patients who were administered TXA perioperatively experienced a thromboembolic event (or at least, there were no reports of thromboembolism or any other adverse events). While administration of TXA may theoretically increase the risk for thrombosis, Brown et al. showed this does not seem to occur in spinal laminectomy and fusion with posterior instrumentation. Similarly, in a systematic review of the literature describing TXA use in intracranial tumor resection, this study revealed a statistically significant reduction in the need for intraoperative blood transfusion in patients administered TXA. Upon consideration of postoperative outcomes, no significant increase in complication rate was found. This evidence in the existing literature on TXA use in orthopedic, spinal, and cranial neurosurgery exemplifies the wide potential of TXA for reducing blood loss with minimal complications in surgical procedures, especially involving the craniospinal axis.
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spelling pubmed-90872432022-05-11 Encouragement for Further Study of Tranexamic Acid Administration for Sacroiliac Joint Fusion Surgery Beyer, Ryan S. Hatter, Matthew J. Streetman, Daniel Brown, Nolan Gendreau, Julian Geriatr Orthop Surg Rehabil Letter to the Editor TO THE EDITOR: We read with great interest the article by Huynh et al.regarding the association between tranexamic acid (TXA) and blood loss in patients undergoing surgical treatment for hip fracture (Huynh PAN, Miller M, Will R. Intravenous Tranexamic Acid Decreases Blood Transfusions and Blood Loss for Patients with Surgically Treated Hip Fractures. Geriatric Orthopedic Surg Rehabil. 2021). The authors illustrated, via retrospective chart review of 505 patients who were surgically treated for hip fractures, that patients administered TXA had statistically significant decreases in perioperative blood loss and reduced relative risk of transfusion. Huynh et al. reported no statistically significant increases in thromboembolic events in patients given TXA. Mechanistically, TXA is a synthetic anti-fibrinolytic that competitively inhibits the plasminogen activation pathway. By preventing activated plasmin from de-stabilizing the fibrin matrix, TXA promotes clot formation. Given the anti-fibrinolytic effects of TXA, concerns in the literature exist regarding its use being associated with increased risk for thromboembolic events. However, it is important to note the complication profile associated with TXA is minimal, as elucidated by Brown et al., specifically finding that no patients who were administered TXA perioperatively experienced a thromboembolic event (or at least, there were no reports of thromboembolism or any other adverse events). While administration of TXA may theoretically increase the risk for thrombosis, Brown et al. showed this does not seem to occur in spinal laminectomy and fusion with posterior instrumentation. Similarly, in a systematic review of the literature describing TXA use in intracranial tumor resection, this study revealed a statistically significant reduction in the need for intraoperative blood transfusion in patients administered TXA. Upon consideration of postoperative outcomes, no significant increase in complication rate was found. This evidence in the existing literature on TXA use in orthopedic, spinal, and cranial neurosurgery exemplifies the wide potential of TXA for reducing blood loss with minimal complications in surgical procedures, especially involving the craniospinal axis. SAGE Publications 2022-04-29 /pmc/articles/PMC9087243/ /pubmed/35557600 http://dx.doi.org/10.1177/21514593221098606 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 pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Letter to the Editor
Beyer, Ryan S.
Hatter, Matthew J.
Streetman, Daniel
Brown, Nolan
Gendreau, Julian
Encouragement for Further Study of Tranexamic Acid Administration for Sacroiliac Joint Fusion Surgery
title Encouragement for Further Study of Tranexamic Acid Administration for Sacroiliac Joint Fusion Surgery
title_full Encouragement for Further Study of Tranexamic Acid Administration for Sacroiliac Joint Fusion Surgery
title_fullStr Encouragement for Further Study of Tranexamic Acid Administration for Sacroiliac Joint Fusion Surgery
title_full_unstemmed Encouragement for Further Study of Tranexamic Acid Administration for Sacroiliac Joint Fusion Surgery
title_short Encouragement for Further Study of Tranexamic Acid Administration for Sacroiliac Joint Fusion Surgery
title_sort encouragement for further study of tranexamic acid administration for sacroiliac joint fusion surgery
topic Letter to the Editor
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9087243/
https://www.ncbi.nlm.nih.gov/pubmed/35557600
http://dx.doi.org/10.1177/21514593221098606
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