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Sexual Dimorphism in Hematocrit Response Following Red Blood Cell Transfusion of Critically Ill Surgical Patients

The change in hematocrit (ΔHct) following packed red blood cell (pRBCs) transfusion is a clinically relevant measurement of transfusion efficacy that is influenced by post-transfusion hemolysis. Sexual dimorphism has been observed in critical illness and may be related to gender-specific differences...

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Autores principales: Pieracci, Fredric M., Barnett, Carlton C., Townsend, Nicole, Moore, Ernest E., Johnson, Jeffery, Biffl, Walter, Bensard, Denis D., Burlew, Clay C., Gerber, Andrew, Silliman, Christopher C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Scholarly Research Network 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3320002/
https://www.ncbi.nlm.nih.gov/pubmed/22536521
http://dx.doi.org/10.5402/2012/298345
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author Pieracci, Fredric M.
Barnett, Carlton C.
Townsend, Nicole
Moore, Ernest E.
Johnson, Jeffery
Biffl, Walter
Bensard, Denis D.
Burlew, Clay C.
Gerber, Andrew
Silliman, Christopher C.
author_facet Pieracci, Fredric M.
Barnett, Carlton C.
Townsend, Nicole
Moore, Ernest E.
Johnson, Jeffery
Biffl, Walter
Bensard, Denis D.
Burlew, Clay C.
Gerber, Andrew
Silliman, Christopher C.
author_sort Pieracci, Fredric M.
collection PubMed
description The change in hematocrit (ΔHct) following packed red blood cell (pRBCs) transfusion is a clinically relevant measurement of transfusion efficacy that is influenced by post-transfusion hemolysis. Sexual dimorphism has been observed in critical illness and may be related to gender-specific differences in immune response. We investigated the relationship between both donor and recipient gender and ΔHct in an analysis of all pRBCs transfusions in our surgical intensive care unit (2006–2009). The relationship between both donor and recipient gender and ΔHct (% points) was assessed using both univariate and multivariable analysis. A total of 575 units of pRBCs were given to 342 patients; 289 (49.9%) donors were male. By univariate analysis, ΔHct was significantly greater for female as compared to male recipients (3.81% versus 2.82%, resp., P < 0.01). No association was observed between donor gender and ΔHct, which was 3.02% following receipt of female blood versus 3.23% following receipt of male blood (P = 0.21). By multivariable analysis, recipient gender remained associated significantly with ΔHct (P < 0.01). In conclusion, recipient gender is independently associated with ΔHct following pRBCs transfusion. This association does not appear related to either demographic or anthropomorphic factors, raising the possibility of gender-related differences in recipient immune response to transfusion.
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spelling pubmed-33200022012-04-25 Sexual Dimorphism in Hematocrit Response Following Red Blood Cell Transfusion of Critically Ill Surgical Patients Pieracci, Fredric M. Barnett, Carlton C. Townsend, Nicole Moore, Ernest E. Johnson, Jeffery Biffl, Walter Bensard, Denis D. Burlew, Clay C. Gerber, Andrew Silliman, Christopher C. ISRN Hematol Clinical Study The change in hematocrit (ΔHct) following packed red blood cell (pRBCs) transfusion is a clinically relevant measurement of transfusion efficacy that is influenced by post-transfusion hemolysis. Sexual dimorphism has been observed in critical illness and may be related to gender-specific differences in immune response. We investigated the relationship between both donor and recipient gender and ΔHct in an analysis of all pRBCs transfusions in our surgical intensive care unit (2006–2009). The relationship between both donor and recipient gender and ΔHct (% points) was assessed using both univariate and multivariable analysis. A total of 575 units of pRBCs were given to 342 patients; 289 (49.9%) donors were male. By univariate analysis, ΔHct was significantly greater for female as compared to male recipients (3.81% versus 2.82%, resp., P < 0.01). No association was observed between donor gender and ΔHct, which was 3.02% following receipt of female blood versus 3.23% following receipt of male blood (P = 0.21). By multivariable analysis, recipient gender remained associated significantly with ΔHct (P < 0.01). In conclusion, recipient gender is independently associated with ΔHct following pRBCs transfusion. This association does not appear related to either demographic or anthropomorphic factors, raising the possibility of gender-related differences in recipient immune response to transfusion. International Scholarly Research Network 2012-03-22 /pmc/articles/PMC3320002/ /pubmed/22536521 http://dx.doi.org/10.5402/2012/298345 Text en Copyright © 2012 Fredric M. Pieracci et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Clinical Study
Pieracci, Fredric M.
Barnett, Carlton C.
Townsend, Nicole
Moore, Ernest E.
Johnson, Jeffery
Biffl, Walter
Bensard, Denis D.
Burlew, Clay C.
Gerber, Andrew
Silliman, Christopher C.
Sexual Dimorphism in Hematocrit Response Following Red Blood Cell Transfusion of Critically Ill Surgical Patients
title Sexual Dimorphism in Hematocrit Response Following Red Blood Cell Transfusion of Critically Ill Surgical Patients
title_full Sexual Dimorphism in Hematocrit Response Following Red Blood Cell Transfusion of Critically Ill Surgical Patients
title_fullStr Sexual Dimorphism in Hematocrit Response Following Red Blood Cell Transfusion of Critically Ill Surgical Patients
title_full_unstemmed Sexual Dimorphism in Hematocrit Response Following Red Blood Cell Transfusion of Critically Ill Surgical Patients
title_short Sexual Dimorphism in Hematocrit Response Following Red Blood Cell Transfusion of Critically Ill Surgical Patients
title_sort sexual dimorphism in hematocrit response following red blood cell transfusion of critically ill surgical patients
topic Clinical Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3320002/
https://www.ncbi.nlm.nih.gov/pubmed/22536521
http://dx.doi.org/10.5402/2012/298345
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