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Allogeneic blood transfusion reduction by risk-based protocol in total joint arthroplasty.

Canadian journal of anaesthesia = Journal canadien d'anesthesie
April 1, 2010
Saifudin Rashiq et al. (6 authors)
Comparative StudyEvaluation StudyJournal ArticleHuman Study
Study Details

Study Goal

To evaluate the effectiveness of a preoperative protocol using iron and other interventions to reduce the risk of allogeneic blood transfusion in patients undergoing total joint arthroplasty.

Results Summary

The study found that the protocol significantly reduced the risk of allogeneic blood transfusion (relative risk 0.68) and decreased the number of units transfused (35 vs. 104 in the control group). There was no worsening of anemia or its consequences in the study group.

Population

Patients awaiting total joint arthroplasty with varying hemoglobin levels (100-139 g/L).

Effective Dosage

Oral iron and folate supplementation (specific dosage not mentioned).

Duration

Preoperative period (exact duration not specified).

Interactions

None mentioned

Extracted Claims (7)
InterventionDirectionEndpointPopulationDosageImpactClaim #
preoperative protocol triaging patients to one of four strategies based on transfusion risk
decrease
risk of allogeneic blood transfusion (ABT)
patients awaiting total joint arthroplasty
-
effectively targets interventions that mitigate the risk
#1
erythropoietin, dosed by weight
neutral
hemoglobin (Hb) 100-129 g.L(-1)
protocol subjects
-
given
#2
preoperative autologous blood harvest and perioperative re-infusion
neutral
hemoglobin (Hb) 130-139 g.L(-1)
protocol subjects
-
underwent
#3
oral iron and folate supplementation
neutral
hemoglobin (Hb) >139 g.L(-1), aged >70 yr and weighed < 70 kg
protocol subjects
-
received
#4
preoperative protocol
decrease
relative risk of ABT
Study group
0.68 (95% confidence interval 0.54-0.85)
reduced
#5
preoperative protocol
decrease
units of allogeneic blood received
Study group
35 units vs 104 units in Control group (P = 0.0007)
reduced
#6
preoperative protocol
no change
anemia or its consequences
Study group
-
no worsening
#7
Abstract

PURPOSE: To evaluate the effect of a preoperative protocol that triages patients awaiting total joint arthroplasty to one of four strategies designed to mitigate the risk of allogeneic blood transfusion (ABT) based on a priori transfusion risk on perioperative exposure to allogeneic blood. METHODS: We compared the transfusion experiences of a historical control series of 160 subjects with a study group of 160 subjects treated by protocol. Protocol subjects with hemoglobin (Hb) 100-129 g.L(-1) were given erythropoietin, dosed by weight. Subjects with Hb 130-139 g.L(-1) underwent preoperative autologous blood harvest and perioperative re-infusion as deemed clinically necessary. Subjects with Hb >139 g.L(-1) received no special intervention, unless they were aged >70 yr and weighed < 70 kg, in which case they received oral iron and folate supplementation. RESULTS: The relative risk of ABT in the Study group was 0.68 (95% confidence interval 0.54-0.85). The Control group received 104 units of allogeneic blood and the Study group received 35 units (P = 0.0007). These differences cannot be explained by differences in transfusion risk or autologous units transfused. There was no worsening of anemia or its consequences in the Study group. CONCLUSION: A simple protocol based on easily obtained preoperative clinical indices effectively targets interventions that mitigate the risk of ABT.

Medical Subject Headings (MeSH)
AgedArthroplasty, Replacement, HipArthroplasty, Replacement, KneeBlood TransfusionClinical ProtocolsErythropoietinFemaleHemoglobinsHumansLength of StayMaleMiddle AgedReference ValuesTransfusion ReactionTransplantation, AutologousTreatment OutcomeTriage
Study Links
Quality Scores
SafetyNot Assessed
Efficacy85/10
Quality75/10
Citation Metrics
Total Citations8
Citations/Year0.5
Relative Citation Ratio0.31
NIH Percentile16.4%
Research Impact Scores
APT Score0.50
Weight Score1.12
Normalized Score0.69
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