Sickle Cell Anemia
Definition
Incidence
Risk Factors
Symptoms
acute chest syndrome
triggers
Evaluation
Treatment
questions for doctor
specialist
Home Care
pain in adults
pain in children
taking control
vomiting in adults
vomiting in children
warning signs
Prevention
Outlook
Complications
Underlying Cause
Anatomy
Genetics
Trusted Sites
Sickle Cell Anemia Outlook
What to expect with sickle cell
anemia
:
There is no cure for sickle cell
anemia
.
The average life expectancy for males with sickle cell
anemia
is 42 years.
The average life expectancy for females with sickle cell
anemia
is 48 years.
Continue to
Sickle Cell Anemia Complications
Related Conditions
Aplastic anemia
Erythroblastosis fetalis
Hemolytic anemia
Iron deficient anemia
Megaloblastic anemia
Pernicious anemia
Thalassemia
Rapid Pulse Checkup
Difficulty breathing
Faintness
Fatigue
Sickle cell anemia with pain
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Last Updated: Jul 29, 2008
References
Authors:
Stephen J. Schueler, MD
;
John H. Beckett, MD
;
D. Scott Gettings, MD
Copyright 1989-2009
DSHI Systems, Inc.
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Sickle Cell Anemia References:
Ander DS, Vallee PA. Diagnostic evaluation for infectious etiology of sickle cell pain crisis. Am J Emerg Med. 1997 May;15(3):290-2.
Fletcher C. Appraisal and coping with vaso-occlusive crisis in adolescents with sickle cell disease. Pediatr Nurs. 2000 May-Jun;26(3):319-24.
Johnson L. Managing acute and chronic pain in sickle cell disease. Nurs Times. 2005 Feb 22-28;101(8):40-3.
Miller JA, Hinrichs CR. Sickle cell crisis in the adult: chest radiographic findings and comparison with pediatric sickle cell disease. J Natl Med Assoc. 2001 Feb;93(2):58-63.
Silbergleit R, Jancis MO, McNamara RM. Management of sickle cell pain crisis in the emergency department at teaching hospitals. J Emerg Med. 1999 Jul-Aug;17(4):625-30.
Yale SH, Nagib N, Guthrie T. Approach to the vaso-occlusive crisis in adults with sickle cell disease. Am Fam Physician. 2000 Mar 1;61(5):1349-56, 1363-4.
