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

Transfusion

Volumn 44, Issue 9, 2004, Pages 1293-1299

  Stroncek, David F ^a,b   Byrne, Karen M ^a   Noguchi, Constance T ^a   Schechter, Alan N ^a   Leitman, Susan F ^a  

^a NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES   (United States)

^b NATIONAL INSTITUTES OF HEALTH   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

HEMOGLOBIN; HEMOGLOBIN S; OXYGEN; PLASTIC; POLITEF; POLYVINYLCHLORIDE; TRIMELLITIC ACID TRIS(2 ETHYLHEXYL) ESTER;

ARTICLE; BLOOD DONOR; BLOOD FILTRATION; BLOOD STORAGE; FILTRATION; HEMATOLOGICAL PROCEDURES; HUMAN; HUMAN CELL; LEUKOCYTE COUNT; LEUKOCYTE FUNCTION; MEMBRANE PERMEABILITY; OXIDATION KINETICS; OXYGEN AFFINITY; OXYGEN SATURATION; POLYMERIZATION; SICKLE CELL ANEMIA; STANDARDIZATION; STATISTICAL ANALYSIS;

BENZOATES; BIOPOLYMERS; BLOOD DONORS; BLOOD PRESERVATION; CELL SEPARATION; DIFFUSION; FILTRATION; HEMOGLOBIN, SICKLE; HUMANS; KINETICS; LEUKOCYTES; OXYGEN; OXYHEMOGLOBINS; PARTIAL PRESSURE; PERMEABILITY; POLYTETRAFLUOROETHYLENE; POLYVINYL CHLORIDE; PRODUCT PACKAGING; SICKLE CELL TRAIT; TIME FACTORS;

EID: 4344569694     PISSN: 00411132     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.0041-1132.2004.04086.x     Document Type: Article

References (12)

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