BLOOD-TRANSFUSION STRATEGIES FOR TOTAL KNEE ARTHROPLASTY - MINIMIZINGAUTOLOGOUS BLOOD WASTAGE, RISK OF HOMOLOGOUS BLOOD-TRANSFUSION, AND TRANSFUSION COST

In this nonrandomized study, alternative strategies were suggested to 10 orthopaedic surgeons to minimize autologous blood wastage, the risk of homologous blood transfusion, and cost associated with blood produ ct usage after total knee arthroplasty (TKA). One hundred fifty-five p atients with 177 consecutive TKAs over a 2-year period were studied. G roup 1 patients had undergone unilateral TKA and did not predonate; 1A patients (n = 19) were drained with a Hemovac, and 1B patients (n = 2 8) with a postoperative blood recovery system. Group 2 patients (n = 4 7) predonated one packed red blood cell (pRBC) unit. Group 3 patients (n = 20) predonated 2 pRBC units. Group 4 patients had undergone bilat eral sequential TKAs (n = 21) and had predonated 2 pRBC units. Group 5 patients (n = 14) had undergone revision TKA procedures and their blo od requirements were individualized. Group 6 patients (n = 6) had pree xisting anemia and were excluded from the study. There was no signific ant difference in total blood loss (909 mL) between groups. Female sex was associated with significantly lower admission hematocrit. Homolog ous blood was required for 4% of patients in the entire study and the percentage was not statistically different between groups. Twenty-five percent of patients who predonated autologous pRBCs did not use all o r some of it. In group 1, the postoperative blood recovery system had a significant effect on reducing postoperative hematocrit drop (P = .0 001), but it was not a significant factor if autologous pRBCs were ava ilable. The costs associated with group 1A were significantly less (P = .0001) compared with the other groups; group 1A had the highest admi ssion hematocrit (43.2). Transfusion with autologous pRBCs was related to lower admission hematocrit rather than to increased postoperative blood loss. An algorithm is presented to provide cost-effective manage ment of blood products after TKA.