Erythropoietin as adjuvant to pre-operative autologous blood donation in total hip arthroplasty: New algorithm for use
Erythropoietin (rhEPO) has been used in different surgical procedures as a method for saving allogeneic blood, with variable efficacy. Forty consecutive patients entered the pre-operative autologous blood donation (PABD) program, and during donations hemoglobin fell below 115 g/l; they received rhEP...
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Veröffentlicht in: | Transfusion and apheresis science 2005-10, Vol.33 (2), p.91-97 |
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Sprache: | eng |
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Zusammenfassung: | Erythropoietin (rhEPO) has been used in different surgical procedures as a method for saving allogeneic blood, with variable efficacy. Forty consecutive patients entered the pre-operative autologous blood donation (PABD) program, and during donations hemoglobin fell below 115
g/l; they received rhEPO 40,000
U every week for three or four weeks (group 1). As control group, 35 consecutive patients who entered the PABD program were studied; during donations, hemoglobin levels in these patients fell below 115
g/l, but rhEPO was not administered (group 2). Pre-surgery hemoglobin levels were higher in patients who received rhEPO (134
g/l vs. 121
g/l;
p
<
0.0002), and an average of 3.47 doses were administered. The number of transfused autologous units was 1.6 in group 1 and 2.1 in group 2 (
p
<
0.05), while the number of allogeneic units was 0.9 and 0.1, respectively (
p
<
0.0005), so that only 5% of patients treated with rhEPO required some allogeneic unit, as compared to 40% of those who did not receive rhEPO (
p
<
0.0005). There were no relevant adverse effects, but in two patients from group 1, rhEPO treatment had to be discontinued because the level of hemoglobin exceeded 150
g/l. The mean duration of hospital admission was shorter in the patients who received rhEPO than in those who only underwent PABD (8 days vs. 11.8 days; NS). When adequately used, rhEPO is an effective and safe alternative to the use of allogeneic blood. |
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ISSN: | 1473-0502 1878-1683 |
DOI: | 10.1016/j.transci.2005.05.002 |