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Blood transfusion after total shoulder arthroplasty: Which patients are at high risk?

PURPOSE: There are multiple reported risk factors and a wide range of reported blood transfusion rates for total shoulder arthroplasty (TSA). There are no evidence-based guidelines for blood transfusions in TSA patients. MATERIALS AND METHODS: We utilized the Nationwide Inpatient Sample to analyze 5...

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Autores principales: Kandil, Abdurrahman, Griffin, Justin W., Novicoff, Wendy M., Brockmeier, Stephen F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4857534/
https://www.ncbi.nlm.nih.gov/pubmed/27186059
http://dx.doi.org/10.4103/0973-6042.180719
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author Kandil, Abdurrahman
Griffin, Justin W.
Novicoff, Wendy M.
Brockmeier, Stephen F.
author_facet Kandil, Abdurrahman
Griffin, Justin W.
Novicoff, Wendy M.
Brockmeier, Stephen F.
author_sort Kandil, Abdurrahman
collection PubMed
description PURPOSE: There are multiple reported risk factors and a wide range of reported blood transfusion rates for total shoulder arthroplasty (TSA). There are no evidence-based guidelines for blood transfusions in TSA patients. MATERIALS AND METHODS: We utilized the Nationwide Inpatient Sample to analyze 51,191 patients undergoing TSA between 1998 and 2011. The purpose was to describe the incidence and identify the preoperative factors that are independently associated with blood transfusion after TSA. In addition, we studied the association of blood transfusions with certain variables such as length of stay (LOS), total charges, and payer status. RESULTS: The blood transfusion rate in our study was 6.1%. There was no difference in the rate of blood transfusions over the study period (P < 0.001). In our logistic regression model, significant associations were found with increased age (odds ratio [OR] =1.03), white race (OR = 1.05), higher Charlson-Deyo score (OR = 1.12), presence of ischemic heart disease (OR = 1.24), blood loss anemia (OR = 1.65), female gender (OR = 1.94), presence of coagulation disorders (OR = 2.25), and presence of deficiency anemia (OR = 3.5). Patients receiving a blood transfusion had higher total charges, a longer hospital LOS, and were more likely to be Medicare payers (P < 0.001). CONCLUSIONS: Our study found five clinically significant risk factors for blood transfusions for TSA: female gender, ischemic heart disease, deficiency anemia, coagulation disorder, and blood loss anemia. Patients with these risk factors should be considered higher risk for requiring a blood transfusion after TSA and counseled appropriately. LEVEL OF EVIDENCE: Level II, retrospective cohort study, prognostic study.
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spelling pubmed-48575342016-05-16 Blood transfusion after total shoulder arthroplasty: Which patients are at high risk? Kandil, Abdurrahman Griffin, Justin W. Novicoff, Wendy M. Brockmeier, Stephen F. Int J Shoulder Surg Original Article PURPOSE: There are multiple reported risk factors and a wide range of reported blood transfusion rates for total shoulder arthroplasty (TSA). There are no evidence-based guidelines for blood transfusions in TSA patients. MATERIALS AND METHODS: We utilized the Nationwide Inpatient Sample to analyze 51,191 patients undergoing TSA between 1998 and 2011. The purpose was to describe the incidence and identify the preoperative factors that are independently associated with blood transfusion after TSA. In addition, we studied the association of blood transfusions with certain variables such as length of stay (LOS), total charges, and payer status. RESULTS: The blood transfusion rate in our study was 6.1%. There was no difference in the rate of blood transfusions over the study period (P < 0.001). In our logistic regression model, significant associations were found with increased age (odds ratio [OR] =1.03), white race (OR = 1.05), higher Charlson-Deyo score (OR = 1.12), presence of ischemic heart disease (OR = 1.24), blood loss anemia (OR = 1.65), female gender (OR = 1.94), presence of coagulation disorders (OR = 2.25), and presence of deficiency anemia (OR = 3.5). Patients receiving a blood transfusion had higher total charges, a longer hospital LOS, and were more likely to be Medicare payers (P < 0.001). CONCLUSIONS: Our study found five clinically significant risk factors for blood transfusions for TSA: female gender, ischemic heart disease, deficiency anemia, coagulation disorder, and blood loss anemia. Patients with these risk factors should be considered higher risk for requiring a blood transfusion after TSA and counseled appropriately. LEVEL OF EVIDENCE: Level II, retrospective cohort study, prognostic study. Medknow Publications & Media Pvt Ltd 2016 /pmc/articles/PMC4857534/ /pubmed/27186059 http://dx.doi.org/10.4103/0973-6042.180719 Text en Copyright: © 2016 International Journal of Shoulder Surgery http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms.
spellingShingle Original Article
Kandil, Abdurrahman
Griffin, Justin W.
Novicoff, Wendy M.
Brockmeier, Stephen F.
Blood transfusion after total shoulder arthroplasty: Which patients are at high risk?
title Blood transfusion after total shoulder arthroplasty: Which patients are at high risk?
title_full Blood transfusion after total shoulder arthroplasty: Which patients are at high risk?
title_fullStr Blood transfusion after total shoulder arthroplasty: Which patients are at high risk?
title_full_unstemmed Blood transfusion after total shoulder arthroplasty: Which patients are at high risk?
title_short Blood transfusion after total shoulder arthroplasty: Which patients are at high risk?
title_sort blood transfusion after total shoulder arthroplasty: which patients are at high risk?
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4857534/
https://www.ncbi.nlm.nih.gov/pubmed/27186059
http://dx.doi.org/10.4103/0973-6042.180719
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