Appropriate blood transfusions can both prevent and treat serious complications related to sickle cell disease (SCD), but inevitably lead to iron overload and its complications in terms of morbidity and mortality. Transfusion history and serial serum ferritin level assessments are convenient and cos
The Management of Sickle Cell Disease
- Book ID
- 127402823
- Year
- 2002
- Tongue
- English
- Weight
- 829 KB
- Edition
- 4
- Category
- Library
No coin nor oath required. For personal study only.
β¦ Synopsis
The fourth edition of The Management of Sickle Cell Disease - developed by physicians, nurses, psychologists, and social workers who specialize in the care of children and adults with sickle cell disease - describes the current approach to counseling and also to management of many of the medical complications of sickle cell disease. It is organized into four parts: Diagnosis and Counseling, Health Maintenance, Treatment of Acute and Chronic Complications, and Special Topics. Multiple new therapies are now available for children and adults with sickle cell disease, and often the options to be chosen present a dilemma for both patients and physicians. This book does not provide answers to many of these newer questions but rather explains the choices available. It is to serve as an adjunct to recent textbooks that delve more deeply into all aspects of the disorder. NIH Publication.
π SIMILAR VOLUMES
Sickle cell disease (SCD) is one of the most common genetic diseases with some 250,000 new births each year. Most patients suffer intermittent pain crises and life-threatening events while life expectancy is considerably reduced. Until the last decade management was purely preventative or supportive