The Effect of Patient Size and Dose of Recombinant Human Erythropoietin Therapy on Red Blood Cell Volume Expansion in Autologous Blood Donors for Elective Orthopedic Operation

1995 ◽  
Vol 39 (3) ◽  
pp. 164 ◽  
Author(s):  
L. T. GOODNOUGH ◽  
D. VERBRUGGE ◽  
R. E. MARCUS ◽  
V. GOLDBERG
Author(s):  
Reinhard Schmidt ◽  
Dietmar Lerche ◽  
Erhard D�rp ◽  
Roland Winkler ◽  
Horst Klinkmann

1994 ◽  
Vol 86 (1) ◽  
pp. 30-35 ◽  
Author(s):  
D. H. Biesma ◽  
R. J. Kraaijenhagen ◽  
J. Dalmulder ◽  
J. J. M. Marx ◽  
A. van de Wiel

Blood ◽  
1994 ◽  
Vol 83 (7) ◽  
pp. 1952-1957 ◽  
Author(s):  
AJ Mitus ◽  
JH Antin ◽  
CJ Rutherford ◽  
CJ McGarigle ◽  
MA Goldberg

Abstract In an attempt to reduce or eliminate homologous red blood cell transfusion requirements during allogeneic bone marrow transplantation (BMT), we instituted a novel program whereby recombinant human erythropoietin was administered to pairs of BMT donors and recipients. Eleven recipients and their HLA-matched donors were enrolled. Donors treated with recombinant human erythropoietin (rHuEPO) were phlebotomized a median of 6 U (range, 4 to 11 U) of blood over a 5-week period. This donor-derived blood was available to the BMT donor or recipient as needed. Transplant recipients were also treated with rHuEPO post-BMT to hasten erythropoiesis. Five of 11 BMT recipients underwent transplant receiving only donor-derived red blood cell transfusion, compared with 0 of 11 concomitant control recipients (P = .04). In addition, the time to absolute reticulocyte count > or = 10(4)/microL was statistically shorter in the rHuEPO-treated recipient group. This study serves as a paradigm for hematopoietic growth factor use in allogeneic BMT to decrease or eliminate homologous transfusion exposures and to possibly hasten hematopoietic engraftment.


Blood ◽  
1994 ◽  
Vol 83 (7) ◽  
pp. 1952-1957 ◽  
Author(s):  
AJ Mitus ◽  
JH Antin ◽  
CJ Rutherford ◽  
CJ McGarigle ◽  
MA Goldberg

In an attempt to reduce or eliminate homologous red blood cell transfusion requirements during allogeneic bone marrow transplantation (BMT), we instituted a novel program whereby recombinant human erythropoietin was administered to pairs of BMT donors and recipients. Eleven recipients and their HLA-matched donors were enrolled. Donors treated with recombinant human erythropoietin (rHuEPO) were phlebotomized a median of 6 U (range, 4 to 11 U) of blood over a 5-week period. This donor-derived blood was available to the BMT donor or recipient as needed. Transplant recipients were also treated with rHuEPO post-BMT to hasten erythropoiesis. Five of 11 BMT recipients underwent transplant receiving only donor-derived red blood cell transfusion, compared with 0 of 11 concomitant control recipients (P = .04). In addition, the time to absolute reticulocyte count > or = 10(4)/microL was statistically shorter in the rHuEPO-treated recipient group. This study serves as a paradigm for hematopoietic growth factor use in allogeneic BMT to decrease or eliminate homologous transfusion exposures and to possibly hasten hematopoietic engraftment.


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