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Allogeneic blood transfusion and prognosis following total hip replacement: a population-based follow up study

BACKGROUND: Allogeneic red blood cell transfusion is frequently used in total hip replacement surgery (THR). However, data on the prognosis of transfused patients are sparse. In this study we compared the risk of complications following THR in transfused and non-transfused patients. METHODS: A popul...

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Autores principales: Pedersen, Alma B, Mehnert, Frank, Overgaard, Soren, Johnsen, Soren P
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2805607/
https://www.ncbi.nlm.nih.gov/pubmed/20040083
http://dx.doi.org/10.1186/1471-2474-10-167
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author Pedersen, Alma B
Mehnert, Frank
Overgaard, Soren
Johnsen, Soren P
author_facet Pedersen, Alma B
Mehnert, Frank
Overgaard, Soren
Johnsen, Soren P
author_sort Pedersen, Alma B
collection PubMed
description BACKGROUND: Allogeneic red blood cell transfusion is frequently used in total hip replacement surgery (THR). However, data on the prognosis of transfused patients are sparse. In this study we compared the risk of complications following THR in transfused and non-transfused patients. METHODS: A population-based follow-up study was performed using data from medical databases in Denmark. We identified 28,087 primary THR procedures performed from 1999 to 2007, from which we computed a propensity score for red blood cell transfusion based on detailed data on patient-, procedure-, and hospital-related characteristics. We were able to match 2,254 transfused with 2,254 non-transfused THR patients using the propensity score. RESULTS: Of the 28,087 THR patients, 9,063 (32.3%) received at least one red blood cell transfusion within 8 days of surgery. Transfused patients had higher 90-day mortality compared with matched non-transfused patients: the adjusted OR was 2.2 (95% confidence interval (CI): 1.2-3.8). Blood transfusion was also associated with increased odds of pneumonia (OR 2.1; CI: 1.2-3.8), whereas the associations with cardiovascular or cerebrovascular events (OR 1.4; CI: 0.9-2.2) and venous thromboembolism (OR 1.2; CI: 0.7-2.1) did not reach statistical significance. The adjusted OR of reoperation due to infection was 0.6 (CI: 0.1-2.9). CONCLUSIONS: Red blood cell transfusion was associated with an adverse prognosis following primary THR, in particular with increased odds of death and pneumonia. Although the odds estimates may partly reflect unmeasured bias due to blood loss, they indicate the need for careful assessment of the risk versus benefit of transfusion even in relation to routine THR procedures.
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spelling pubmed-28056072010-01-13 Allogeneic blood transfusion and prognosis following total hip replacement: a population-based follow up study Pedersen, Alma B Mehnert, Frank Overgaard, Soren Johnsen, Soren P BMC Musculoskelet Disord Research article BACKGROUND: Allogeneic red blood cell transfusion is frequently used in total hip replacement surgery (THR). However, data on the prognosis of transfused patients are sparse. In this study we compared the risk of complications following THR in transfused and non-transfused patients. METHODS: A population-based follow-up study was performed using data from medical databases in Denmark. We identified 28,087 primary THR procedures performed from 1999 to 2007, from which we computed a propensity score for red blood cell transfusion based on detailed data on patient-, procedure-, and hospital-related characteristics. We were able to match 2,254 transfused with 2,254 non-transfused THR patients using the propensity score. RESULTS: Of the 28,087 THR patients, 9,063 (32.3%) received at least one red blood cell transfusion within 8 days of surgery. Transfused patients had higher 90-day mortality compared with matched non-transfused patients: the adjusted OR was 2.2 (95% confidence interval (CI): 1.2-3.8). Blood transfusion was also associated with increased odds of pneumonia (OR 2.1; CI: 1.2-3.8), whereas the associations with cardiovascular or cerebrovascular events (OR 1.4; CI: 0.9-2.2) and venous thromboembolism (OR 1.2; CI: 0.7-2.1) did not reach statistical significance. The adjusted OR of reoperation due to infection was 0.6 (CI: 0.1-2.9). CONCLUSIONS: Red blood cell transfusion was associated with an adverse prognosis following primary THR, in particular with increased odds of death and pneumonia. Although the odds estimates may partly reflect unmeasured bias due to blood loss, they indicate the need for careful assessment of the risk versus benefit of transfusion even in relation to routine THR procedures. BioMed Central 2009-12-29 /pmc/articles/PMC2805607/ /pubmed/20040083 http://dx.doi.org/10.1186/1471-2474-10-167 Text en Copyright ©2009 Pedersen et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research article
Pedersen, Alma B
Mehnert, Frank
Overgaard, Soren
Johnsen, Soren P
Allogeneic blood transfusion and prognosis following total hip replacement: a population-based follow up study
title Allogeneic blood transfusion and prognosis following total hip replacement: a population-based follow up study
title_full Allogeneic blood transfusion and prognosis following total hip replacement: a population-based follow up study
title_fullStr Allogeneic blood transfusion and prognosis following total hip replacement: a population-based follow up study
title_full_unstemmed Allogeneic blood transfusion and prognosis following total hip replacement: a population-based follow up study
title_short Allogeneic blood transfusion and prognosis following total hip replacement: a population-based follow up study
title_sort allogeneic blood transfusion and prognosis following total hip replacement: a population-based follow up study
topic Research article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2805607/
https://www.ncbi.nlm.nih.gov/pubmed/20040083
http://dx.doi.org/10.1186/1471-2474-10-167
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