Sickle Cell Anemia

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Abstract

Sickle Cell Anemia is a hereditary disease that changes the smallest and most important components of the body. A gene causes the bone marrow in the body to make sickled shapes, when this happens; it causes the red blood cell to die faster. This is what causes Hemolytic Anemia. Older children and adults with sickle cell disease may experience a few complications, or have a pattern of ongoing problems that shorten their lives. The most common and serious complications of sickle cell disease are anemia, pain, fatigue, and organ failure. Today there are many alternatives and opportunities that a sickle cell patient may consider. One outlined in this paper is the Hydroxyurea method.

Sickle Cell Anemia

Sickle Cell Anemia takes place in the bloodstream of the body. The 'Sickle' reference is in relation to the disordered shape red blood cells take. The way the disease is acquired is through hereditary genes. The disease is primarily characterized by chronic anemia, and frequent episodes of pain. Hemoglobin, an important element in the red blood cell is found to be defective.

The job of hemoglobin molecules is to transfer oxygen from the lungs throughout the body, and then transfer carbon dioxide from the body back to the lungs, then finally out of the body altogether. Since the hemoglobin in the defected body is abnormal, after it gives up the oxygen, the molecules cluster together and form long rod-like structures. These formations cause the red blood cells to become stiff; they then assume a sickle shape. Normal red blood cells appear to be donut-shaped and smooth in texture, these cells pass through any blood vessel with ease. Sickled cells don't flow through blood vessels as easily, and usually cause blockage. This results in deprivation of oxygen rich blood to organs and tissues that need it. This causes the painful episodes that associate with the disease. This pain can seriously damage vital organs such as the heart, lungs, kidneys, spleen, pelvic bones and even the brain. Certain tissues can become infected and can cause other serious complications. The cycle of a normal functioning red blood cell is about 120 days. Sickle cells differ in that they last 10-20 days long. Since the body cannot replace them fast enough, the red blood cell supply shortens and creates a condition called Anemia.

Sickle cell anemia is caused by a mistake in t...

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... Pennsylvania Press. 1999

Health Newswire reporters “It's in the blood: dealing with sickle cell anemia” HMG

Worldwide Jul 18, 2003 Medical News. Lexis Nexis St. Francis College McGarry Library http:// www.Lexis-Nexis.com

Davies, Sally C., Oni, Lola "Management of Patients with Sickle Cell Disease" British

Medical Journal Vol.315 Iss.7109 Sep 13, 1997 Pg.656, 5 pgs.

Rehyn, Marsha, Resnik, David, Rich, Ben A. “Pain and Sickle Cell Anemia”/

Commentary Hastings Center Report Vol. 3 1, Iss.3 May/June 2001 Pg.29, 2pgs.

Hurtig, Anita L., Viera, Carol T. Sickle Cell Disease: Psychological and Psychosocial

Issues University of Illinois Press, 1986

Anonymous, “Straightening Things Out” The Economist Vol.340, Iss.7979 Aug 17, 1996

Pg.66, 1pg(s)

Edelstein, Stuart J. The Sickled Cell: From Myths to Molecules Harvard University

Press, 1986

Carlson, Robert "Two Sickle Cell Therapies May Change Practice" Medical Post Vol. 39,

Iss.2 San 14,2003 Pg.59

National Institutes of health National Head, Lung, and Blood Institute

http://www.nhlbi.nih.gov/health/public/blood/sickle/sca-fact.txt

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