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Caring for the orthopaedic patient with sickle cell disease.
- Source :
-
Orthopedic nursing [Orthop Nurs] 1992 Jan-Feb; Vol. 11 (1), pp. 41-8. - Publication Year :
- 1992
-
Abstract
- Sickle cell disease (SCD) is an inherited, chronic, painful condition seen primarily in blacks and populations from the Mediterranean and Caribbean areas. The crescent or sickle shaped red blood cells have a shorter lifespan causing severe anemia; they are sticky and easily clump together causing intravascular occlusions which eventually damage vital organs. Providing nursing care for patients with sickle cell disease can be very challenging because of the chronic nature of the illness. Understanding the disease phenomena can facilitate nursing assessments and help nurses individualize care for these clients.
- Subjects :
- Adaptation, Psychological
Adolescent
Adult
Anemia, Sickle Cell complications
Anemia, Sickle Cell psychology
Exercise
Female
Health Education
Humans
Male
Mental Processes
Nutritional Physiological Phenomena
Rest
Self Concept
Sexual Dysfunction, Physiological etiology
Social Values
Urologic Diseases prevention & control
Anemia, Sickle Cell nursing
Nursing Assessment
Orthopedic Nursing
Subjects
Details
- Language :
- English
- ISSN :
- 0744-6020
- Volume :
- 11
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Orthopedic nursing
- Publication Type :
- Academic Journal
- Accession number :
- 1741172