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Management of Blood Loss in Hip Arthroplasty: Korean Hip Society Current Consensus
The volume of hip arthroplasty is stiffly increasing because of excellent clinical outcomes, however it has not been shown to decrease the incidence of transfusions due to bleeding related to this surgery. This is an important consideration since there are concerns about the side effects and social...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Korean Hip Society
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5465399/ https://www.ncbi.nlm.nih.gov/pubmed/28611958 http://dx.doi.org/10.5371/hp.2017.29.2.81 |
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author | Song, Joo-Hyoun Park, Jang Won Lee, Young-Kyun Kim, In-Sung Nho, Jae-Hwi Lee, Kyung-Jae Park, Kwan Kyu Kim, Yeesuk Park, Jai Hyung Han, Seung Beom |
author_facet | Song, Joo-Hyoun Park, Jang Won Lee, Young-Kyun Kim, In-Sung Nho, Jae-Hwi Lee, Kyung-Jae Park, Kwan Kyu Kim, Yeesuk Park, Jai Hyung Han, Seung Beom |
author_sort | Song, Joo-Hyoun |
collection | PubMed |
description | The volume of hip arthroplasty is stiffly increasing because of excellent clinical outcomes, however it has not been shown to decrease the incidence of transfusions due to bleeding related to this surgery. This is an important consideration since there are concerns about the side effects and social costs of transfusions. First, anemia should be assessed at least 30 days before elective hip arthroplasty, and if the subject is diagnosed as having anemia, an additional examination of the cause of the anemia should be carried and steps taken to address the anemia. Available iron treatments for anemia take 7 to 10 days to facilitate erythropoiesis, and preoperative iron supplementation, either oral or intravenous, is recommended. When using oral supplements for iron storage, administer elemental iron 100 mg daily for 2 to 6 weeks before surgery, and calculate the dose using intravenous supplement. Tranexamic acid (TXA) is a synthetic derivative of the lysine component, which reduces blood loss by inhibiting fibrinolysis and clot degradation. TXA is known to be an effective agent for reducing postoperative bleeding and reducing the need for transfusions in primary and revision total hip arthroplasties. Patient blood management has improved the clinical outcome after hip arthroplasty through the introduction and research of various agents, thereby reducing the need for allogeneic blood transfusions and reducing the risk of transfusion-related infections and the duration of hospitalizations. |
format | Online Article Text |
id | pubmed-5465399 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Korean Hip Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-54653992017-06-13 Management of Blood Loss in Hip Arthroplasty: Korean Hip Society Current Consensus Song, Joo-Hyoun Park, Jang Won Lee, Young-Kyun Kim, In-Sung Nho, Jae-Hwi Lee, Kyung-Jae Park, Kwan Kyu Kim, Yeesuk Park, Jai Hyung Han, Seung Beom Hip Pelvis Review Article The volume of hip arthroplasty is stiffly increasing because of excellent clinical outcomes, however it has not been shown to decrease the incidence of transfusions due to bleeding related to this surgery. This is an important consideration since there are concerns about the side effects and social costs of transfusions. First, anemia should be assessed at least 30 days before elective hip arthroplasty, and if the subject is diagnosed as having anemia, an additional examination of the cause of the anemia should be carried and steps taken to address the anemia. Available iron treatments for anemia take 7 to 10 days to facilitate erythropoiesis, and preoperative iron supplementation, either oral or intravenous, is recommended. When using oral supplements for iron storage, administer elemental iron 100 mg daily for 2 to 6 weeks before surgery, and calculate the dose using intravenous supplement. Tranexamic acid (TXA) is a synthetic derivative of the lysine component, which reduces blood loss by inhibiting fibrinolysis and clot degradation. TXA is known to be an effective agent for reducing postoperative bleeding and reducing the need for transfusions in primary and revision total hip arthroplasties. Patient blood management has improved the clinical outcome after hip arthroplasty through the introduction and research of various agents, thereby reducing the need for allogeneic blood transfusions and reducing the risk of transfusion-related infections and the duration of hospitalizations. Korean Hip Society 2017-06 2017-06-02 /pmc/articles/PMC5465399/ /pubmed/28611958 http://dx.doi.org/10.5371/hp.2017.29.2.81 Text en Copyright © 2017 by Korean Hip Society http://creativecommons.org/licenses/by-nc/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Review Article Song, Joo-Hyoun Park, Jang Won Lee, Young-Kyun Kim, In-Sung Nho, Jae-Hwi Lee, Kyung-Jae Park, Kwan Kyu Kim, Yeesuk Park, Jai Hyung Han, Seung Beom Management of Blood Loss in Hip Arthroplasty: Korean Hip Society Current Consensus |
title | Management of Blood Loss in Hip Arthroplasty: Korean Hip Society Current Consensus |
title_full | Management of Blood Loss in Hip Arthroplasty: Korean Hip Society Current Consensus |
title_fullStr | Management of Blood Loss in Hip Arthroplasty: Korean Hip Society Current Consensus |
title_full_unstemmed | Management of Blood Loss in Hip Arthroplasty: Korean Hip Society Current Consensus |
title_short | Management of Blood Loss in Hip Arthroplasty: Korean Hip Society Current Consensus |
title_sort | management of blood loss in hip arthroplasty: korean hip society current consensus |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5465399/ https://www.ncbi.nlm.nih.gov/pubmed/28611958 http://dx.doi.org/10.5371/hp.2017.29.2.81 |
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