๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Problems of chronic transfusion in sickle cell disease

โœ Scribed by Dr. Armando R. Orlina; Steven D. Sosler; Mabel Koshy


Publisher
John Wiley and Sons
Year
1991
Tongue
English
Weight
674 KB
Volume
6
Category
Article
ISSN
0733-2459

No coin nor oath required. For personal study only.


๐Ÿ“œ SIMILAR VOLUMES


Modified method of exchange transfusion
โœ Carol A. Talacki; Samir K. Ballas ๐Ÿ“‚ Article ๐Ÿ“… 1990 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 423 KB

The treatment of various complications of sickle cell disease has included red cell exchange in the past, and the development of automated pheresis equipment has greatly simplified such exchanges. Traditionally, the patient's red cells have been exchanged while their plasma was returned to them. Rec

Post-transfusion alloimmunization in pat
โœ Armando R. Orlina; Phyllis J. Unger; Mabel Koshy ๐Ÿ“‚ Article ๐Ÿ“… 1978 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 339 KB ๐Ÿ‘ 2 views

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

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

Erythrocytapheresis limits iron accumula
โœ Hilliard, Lee M.; Williams, Bonita F.; Lounsbury, Amy E.; Howard, Thomas H. ๐Ÿ“‚ Article ๐Ÿ“… 1998 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 671 KB

Cerebrovascular accidents (CVA) as a complication of sickle cell disease occur most frequently in childhood. Life-long transfusion prevents recurrent stroke, but inevitably leads to iron overload. Although effective chelation exists, many patients are not compliant. Erythrocytapheresis, an automated