Literature DB >> 15318851

Increasing hemoglobin oxygen saturation levels in sickle trait donor whole blood prevents hemoglobin S polymerization and allows effective white blood cell reduction by filtration.

David F Stroncek1, Karen M Byrne, Constance T Noguchi, Alan N Schechter, Susan F Leitman.   

Abstract

UNLABELLED: BACKGROUND Red blood cell (RBC) components from donors with sickle cell trait (Hb AS) often occlude white blood cell (WBC) reduction filters. Techniques were investigated to successfully filter Hb AS donor blood by increasing the Hb oxygen saturation with storage bags and conditions suitable for transfusion products. STUDY DESIGN AND METHODS: Oxygenation kinetics were measured over 3 days in whole-blood units stored in standard-sized 600-mL polyvinylchloride (PVC) bags and whole-blood units divided into three equal parts and stored in standard-sized blood bags made from PVC, tri-2-(ethylhexyl)trimellitate (CLX) plastic, or Teflon. The filterability of Hb AS blood stored for 3 days was tested with whole-blood filters.
RESULTS: Oxygen saturation levels did not increase in full whole-blood units from donors without sickle cell trait during 3 days of storage in 600-mL PVC bags. In divided Hb AS whole-blood units stored for 3 days, oxygen saturation levels increased from baseline levels of 45 to 56, 66, and 94 percent after storage in 600-mL PVC, CLX, and Teflon bags, respectively (n = 5, p < 0.02), and all components filtered completely. When full Hb AS whole-blood units from eight donors were stored for 3 days in 1.5-L CLX bags, all units filtered completely, but one had a high residual WBC count.
CONCLUSION: Storage of Hb AS whole blood in large-capacity oxygen-permeable bags increases oxygen tension and allows more effective WBC reduction by filtration.

Entities:  

Mesh:

Substances:

Year:  2004        PMID: 15318851     DOI: 10.1111/j.0041-1132.2004.04086.x

Source DB:  PubMed          Journal:  Transfusion        ISSN: 0041-1132            Impact factor:   3.157


  4 in total

1.  Anaerobic storage of red blood cells: the need for caution regarding donor red cells with sickle cell trait.

Authors:  Sagir G Ahmed
Journal:  Blood Transfus       Date:  2011-04-27       Impact factor: 3.443

2.  Assessment of leucoreduction of sickle cell trait blood: quality of the filtered product.

Authors:  Karim Ould Amar; Olivier Bourdonné; Sylvie Bruneau; Fatiha Sellami; Pascale Richard
Journal:  Blood Transfus       Date:  2012-10-30       Impact factor: 3.443

3.  Prevalence of glucose-6-phosphate dehydrogenase deficiency and sickle cell trait among blood donors in Riyadh.

Authors:  Mohammed K Alabdulaali; Khaled M Alayed; Abdulaziz F Alshaikh; Shihab A Almashhadani
Journal:  Asian J Transfus Sci       Date:  2010-01

4.  Sporadic leukoreduction filter failure during red blood cell component preparation: beware of rapid filtration.

Authors:  Jeanne K Wang; Sherry L Sheldon; Harvey G Klein; Susan F Leitman; David F Stroncek
Journal:  Transfusion       Date:  2008-08       Impact factor: 3.157

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.