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Anesth Analg ; 125(5): 1597-1599, 2017 11.
Article in English | MEDLINE | ID: mdl-28514321

ABSTRACT

Erythropoietin (EPO) is proposed preoperatively to reduce blood transfusion in anemic patients (hemoglobin < 13 g/dL) scheduled for a major orthopedic surgery. New intravenous iron formulations allow infusion of higher doses, increasing EPO response. In that context, we evaluated in a before-after study (n = 62 and 65 patients for each period) a new EPO administration protocol (2 injections 4 and 3 weeks before surgery, and a third if hemoglobin <13 g/dL instead of <15 g/dL 2 weeks before surgery). After this protocol implementation, the mean (standard deviation) number of EPO injections decreased from 2.8 (0.5) to 2.2 (0.4)/patient (P < .0001) without changing transfusion rates (3% in the 2 periods).


Subject(s)
Anemia/drug therapy , Arthroplasty, Replacement, Hip/adverse effects , Arthroplasty, Replacement, Knee/adverse effects , Blood Loss, Surgical/prevention & control , Erythropoietin/administration & dosage , Ferric Compounds/administration & dosage , Hematinics/administration & dosage , Maltose/analogs & derivatives , Aged , Aged, 80 and over , Anemia/blood , Anemia/complications , Anemia/diagnosis , Biomarkers/blood , Blood Transfusion , Drug Administration Schedule , Drug Compounding , Erythropoietin/adverse effects , Female , Ferric Compounds/adverse effects , Ferric Compounds/chemistry , Hematinics/adverse effects , Hematinics/chemistry , Hemoglobins/metabolism , Humans , Infusions, Intravenous , Injections, Subcutaneous , Male , Maltose/administration & dosage , Maltose/adverse effects , Maltose/chemistry , Middle Aged , Program Evaluation , Retrospective Studies , Risk Factors , Time Factors , Treatment Outcome
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