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Bridging therapy for oral anticoagulation increases the risk for bleeding-related complications in total joint arthroplasty

BACKGROUND: Patients scheduled for elective surgery with a high risk of thromboembolism require anticoagulation bridging therapy perioperatively. The purpose of this study was to assess the risk of thromboembolic events and bleeding-related complications after total hip and knee arthroplasty in pati...

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Autores principales: Haighton, Martijn, Kempen, Diederik H R, Wolterbeek, Nienke, Marting, Louis N., van Dijk, Martijn, Veen, Remmelt M R
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4573310/
https://www.ncbi.nlm.nih.gov/pubmed/26384316
http://dx.doi.org/10.1186/s13018-015-0285-6
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author Haighton, Martijn
Kempen, Diederik H R
Wolterbeek, Nienke
Marting, Louis N.
van Dijk, Martijn
Veen, Remmelt M R
author_facet Haighton, Martijn
Kempen, Diederik H R
Wolterbeek, Nienke
Marting, Louis N.
van Dijk, Martijn
Veen, Remmelt M R
author_sort Haighton, Martijn
collection PubMed
description BACKGROUND: Patients scheduled for elective surgery with a high risk of thromboembolism require anticoagulation bridging therapy perioperatively. The purpose of this study was to assess the risk of thromboembolic events and bleeding-related complications after total hip and knee arthroplasty in patients requiring bridging therapy for anticoagulants. METHODS: A retrospective cohort study of all patients with primary total hip or total knee replacement in a 4-year period was performed. Outcome measures were blood loss, thromboembolic and bleeding-related complications and hospital stay. RESULTS: Bridged patients had more blood loss and higher complication rates than the control group. Most complications were bleeding-related, and there were no thromboembolic events. Seven of the 14 (50 %) total hip patients bridged with unfractioned heparin required reoperation (three patients with ischial neuropraxia due to hematoma). There were two bleeding-related deaths in total hip patients bridged with low-molecular-weight heparin. Mean hospital stay was significantly longer in unfractioned heparin bridging. CONCLUSION: In this study, there was a significant increase in bleeding-related complications in total joint replacement with bridging therapy compared to prophylaxis. This risk was highest in patients with total hip arthroplasty. There were no thromboembolic events in bridged patients.
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spelling pubmed-45733102015-09-18 Bridging therapy for oral anticoagulation increases the risk for bleeding-related complications in total joint arthroplasty Haighton, Martijn Kempen, Diederik H R Wolterbeek, Nienke Marting, Louis N. van Dijk, Martijn Veen, Remmelt M R J Orthop Surg Res Research Article BACKGROUND: Patients scheduled for elective surgery with a high risk of thromboembolism require anticoagulation bridging therapy perioperatively. The purpose of this study was to assess the risk of thromboembolic events and bleeding-related complications after total hip and knee arthroplasty in patients requiring bridging therapy for anticoagulants. METHODS: A retrospective cohort study of all patients with primary total hip or total knee replacement in a 4-year period was performed. Outcome measures were blood loss, thromboembolic and bleeding-related complications and hospital stay. RESULTS: Bridged patients had more blood loss and higher complication rates than the control group. Most complications were bleeding-related, and there were no thromboembolic events. Seven of the 14 (50 %) total hip patients bridged with unfractioned heparin required reoperation (three patients with ischial neuropraxia due to hematoma). There were two bleeding-related deaths in total hip patients bridged with low-molecular-weight heparin. Mean hospital stay was significantly longer in unfractioned heparin bridging. CONCLUSION: In this study, there was a significant increase in bleeding-related complications in total joint replacement with bridging therapy compared to prophylaxis. This risk was highest in patients with total hip arthroplasty. There were no thromboembolic events in bridged patients. BioMed Central 2015-09-17 /pmc/articles/PMC4573310/ /pubmed/26384316 http://dx.doi.org/10.1186/s13018-015-0285-6 Text en © Haighton et al. 2015 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Haighton, Martijn
Kempen, Diederik H R
Wolterbeek, Nienke
Marting, Louis N.
van Dijk, Martijn
Veen, Remmelt M R
Bridging therapy for oral anticoagulation increases the risk for bleeding-related complications in total joint arthroplasty
title Bridging therapy for oral anticoagulation increases the risk for bleeding-related complications in total joint arthroplasty
title_full Bridging therapy for oral anticoagulation increases the risk for bleeding-related complications in total joint arthroplasty
title_fullStr Bridging therapy for oral anticoagulation increases the risk for bleeding-related complications in total joint arthroplasty
title_full_unstemmed Bridging therapy for oral anticoagulation increases the risk for bleeding-related complications in total joint arthroplasty
title_short Bridging therapy for oral anticoagulation increases the risk for bleeding-related complications in total joint arthroplasty
title_sort bridging therapy for oral anticoagulation increases the risk for bleeding-related complications in total joint arthroplasty
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4573310/
https://www.ncbi.nlm.nih.gov/pubmed/26384316
http://dx.doi.org/10.1186/s13018-015-0285-6
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