๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Post-transfusion alloimmunization in patients with sickle cell disease

โœ Scribed by Armando R. Orlina; Phyllis J. Unger; Mabel Koshy


Publisher
John Wiley and Sons
Year
1978
Tongue
English
Weight
339 KB
Volume
5
Category
Article
ISSN
0361-8609

No coin nor oath required. For personal study only.

โœฆ Synopsis


The transfusion histories over a 33-month period of 50 patients with sickle cell disease were reviewed to determine the frequency of alloimmunization to red cell antigens following transfusion in these patients. There were 30 females and 20 males, aged 19--49 years. Eighteen (36%) were immunized of which thirteen were females. Five of the patients have formed only one antibody so far, while the other 13 have formed two or more. Thirty-six antibodies were identified: 16 against various Rh antigens, 12 anti-Lewis, 5 anti-Kell and one each of anti-Jka, -Fya and -M. The immunized patients received, on the average, more transfusions although there was a considerable degree of overlap between the immunized and nonimmunized groups. An approach to the hemotherapy of patients with sickle cell disease (SCD) is discussed.


๐Ÿ“œ SIMILAR VOLUMES


A simple, practical model for reducing a
โœ Dr. Steven D. Sosler; Bernard J. Jilly; Catherine Saporito; Mabel Koshy ๐Ÿ“‚ Article ๐Ÿ“… 1993 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 350 KB ๐Ÿ‘ 1 views

Patients with sickle cell disease (SCD) form immune alloantibodies more frequently than other transfused populations because red cells (RBCs) from white donors (with a higher incidence of certain Rh, Duffy, Kell, and Kidd blood group antigens) are transfused to black patients often lacking these ant

Malignancy in patients with sickle cell
โœ William H. Schultz; for the International Association of Sickle Cell Nurses; Phy ๐Ÿ“‚ Article ๐Ÿ“… 2003 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 66 KB ๐Ÿ‘ 2 views
Patterns of hepatic iron distribution in
โœ Nilesh R. Ghugre; Ignacio Gonzalez-Gomez; Ellen Butensky; Leila Noetzli; Roland ๐Ÿ“‚ Article ๐Ÿ“… 2009 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 190 KB ๐Ÿ‘ 2 views

## Abstract Patients with sickle cell disease (SCD) appear to be at lower risk of endocrinopathies and cardiac dysfunction than those with thalassemia major (TM). Circulating redox active iron is lower in these patients, possibly due to increased systemic inflammation and circulating cytokines. Hep