Blood transfusions in total hip and knee arthroplasty: an analysis of outcomes. Academic Article uri icon

Overview

abstract

  • BACKGROUND: Various studies have raised concern of worse outcomes in patients receiving blood transfusions perioperatively compared to those who do not. In this study we attempted to determine the proportion of perioperative complications in the orthopedic population attributable to the use of a blood transfusion. METHODS: Data from 400 hospitals in the United States were used to identify patients undergoing total hip or knee arthroplasty (THA and TKA) from 2006 to 2010. Patient and health care demographics, as well as comorbidities and perioperative outcomes were compared. Multivariable logistic regression models were fitted to determine associations between transfusion, age, and comorbidities and various perioperative outcomes. Population attributable fraction (PAF) was determined to measure the proportion of outcome attributable to transfusion and other risk factors. RESULTS: Of 530,089 patients, 18.93% received a blood transfusion during their hospitalization. Patients requiring blood transfusion were significantly older and showed a higher comorbidity burden. In addition, these patients had significantly higher rates of major complications and a longer length of hospitalization. The logistic regression models showed that transfused patients were more likely to have adverse health outcomes than nontransfused patients. However, patients who were older or had preexisting diseases carried a higher risk than use of a transfusion for these outcomes. The need for a blood transfusion explained 9.51% (95% CI 9.12-9.90) of all major complications. CONCLUSIONS: Advanced age and high comorbidity may be responsible for a higher proportion of adverse outcomes in THA and TKA patients than blood transfusions.

publication date

  • January 21, 2014

Research

keywords

  • Arthroplasty, Replacement, Hip
  • Arthroplasty, Replacement, Knee
  • Blood Transfusion
  • Postoperative Complications

Identity

PubMed Central ID

  • PMC3918859

Scopus Document Identifier

  • 84893875101

Digital Object Identifier (DOI)

  • 10.1155/2014/623460

PubMed ID

  • 24587736

Additional Document Info

volume

  • 2014