• Home Page
  • Research Paper On Sickle Cell Anemia

Research Paper On Sickle Cell Anemia

Great Essays
Show More
Sickle Cell Anemia
Dakoda Howard
Indiana State University
Pathophysiology
11/10/2016

Abstract
The aim of this paper is to help individuals who do not understand or want to better their knowledge in Sickle Cell Anemia (SCA). SCA is commonly referred to as Sickle Cell Disease or SDA. The area of target is a general overview of that SCA, along with the various amounts of complications that can arise when someone has the disease. The paper will go over some of the more life threatening conditions as well as showing signs, symptoms, diagnosis, treatment, and lastly prognosis. Many resources were used when compiling evidence for the paper.

Sickle Cell Anemia or Sickle Cell Disease
Sickle Cell Disease is a life long illness …show more content…
Data & Statistics. Centers for Disease Control and Prevention. http://www.cdc.gov/ncbddd/sicklecell/data.html. Published 2016. Accessed November 12, 2016.
4. How Is Sickle Cell Disease Treated? - NHLBI, NIH. U.S National Library of Medicine. https://www.nhlbi.nih.gov/health/health-topics/topics/sca/treatment. Accessed November 12, 2016.
5. O 'Connor DP, Fincher AL. Clinical Pathology for Athletic Trainers: Recognizing Systemic Disease. Thorofare, NJ: SLACK Incorporated; 2015.
6. Sickle cell anemia. Tests and diagnosis. http://www.mayoclinic.org/diseases-conditions/sickle-cell-anemia/basics/tests-diagnosis/con-20019348. Accessed November 12, 2016.
7. Press D. Management of sickle cell disease: challenges and risks of transfusion | IJCTM. Management of sickle cell disease: challenges and risks of transfusion | IJCTM. https://www.dovepress.com/management-of-sickle-cell-disease-challenges-and-risks-of-transfusion-peer-reviewed-article-ijctm. Accessed November 12, 2016.
8. Sickle Cell Research: Symptoms, Diagnosis, Treatment and Recent Developments | NIH MedlinePlus the Magazine. Sickle Cell Research: Symptoms, Diagnosis, Treatment and Recent Developments | NIH MedlinePlus the Magazine. https://medlineplus.gov/magazine/issues/winter11/articles/winter11pg18.html. Accessed November 12,

Related Documents

  • Improved Essays

    Chi Square Test Lab Report
    • 2147 Words
    • 9 Pages

    Chi Square Test Lab Report

    Sickle cell disease is an inherited disorder that is caused by a mutation in the DNA sequences that codes for the beta chain of the hemoglobin protein. Red blood cells are, normally, flexible and round, but with the sickle cell anemia the red blood cells become sticky, rigid, and crescent shaped. The Hemoglobin protein carries oxygen in the red blood cells throughout the body. With the disease, the blood cell’s shape can cause them to get lodged in the blood vessels resulting in the obstruction of blood flow, especially in the smaller arterial vessels in the body This occurrence not only reduces oxygen content to the area of concern, but can be a very painful experience for the victim. People who inherit this disease have two abnormal hemoglobin…

    • 2147 Words
    • 9 Pages
    Improved Essays
    Read More
  • Improved Essays

    Unit 3 Assignment 1 Task 1 For Health And Social Care
    • 800 Words
    • 4 Pages

    Unit 3 Assignment 1 Task 1 For Health And Social Care

    Secondary prevention will help to decrease medical expenses, and save money. Providing outreach programs in high risk community to educate, provide support, and provide counseling for affected individuals, who may not have the appropriate resources to go to a doctor. By increasing support in high risk communities, individuals would be less reluctant to seek information about their health status, and become more active in their health. By educating parents of children who have sickle cell disease about preventing complication that can lead to hospitalization of their child, children will be less likely to miss school due to a Sickle Cell crisis. Information that is given in an easy to understand format will also empower the parents to be active in their child’s health, which will decrease hospitalization due to preventable Sickle Cell complications, and reduced…

    • 800 Words
    • 4 Pages
    Improved Essays
    Read More
  • Improved Essays

    Gel Electrophoresis Lab Report
    • 1612 Words
    • 7 Pages

    Gel Electrophoresis Lab Report

    The hypothesis that was proposed was accepted based on the clear results that we gained after the experiment was finished. The hypothesis proposed if the child’s parents are both carriers, child will likely have sickle cell anemia. Both parents were carriers for sickle cell anemia (HbAHbS), which gave the child small chance of acquiring sickle cell anemia. The chance of acquiring sickle cell anemia was relatively low as compared being a carrier. The chance for the child to have sickle cell were ¼ only 25%, as opposed to being a carrier 2/4 50%, and being normal ¼ 25%.…

    • 1612 Words
    • 7 Pages
    Improved Essays
    Read More
  • Decent Essays

    What Is Renal Damage Inevitable In Sickle-Cell Disease?
    • 317 Words
    • 2 Pages

    What Is Renal Damage Inevitable In Sickle-Cell Disease?

    Renal complications Renal damage is almost inevitable in sickle-cell disease. There is a strong tendency for HbS to polymerise in the renal medulla, because of the low partial pressure of oxygen, the low pH, and the high osmolality causing erythrocyte dehydration. The consequent vaso-occlusion causes renal infarction with papillary necrosis, and medullary fibrosis with focal segmental glomerulosclerosis. Other complications include haematuria, renal medullary carcinoma, nocturnal enuresis (bedwetting), and chronic tubulointerstitial nephritis may occur. Neurological complications Complications occur in 25% of patients, Sickle-cell anaemia is one of the most common causes of stroke in children.…

    • 317 Words
    • 2 Pages
    Decent Essays
    Read More
  • Improved Essays

    Sickle Cell Disease Affects The Circulatory System
    • 656 Words
    • 3 Pages

    Sickle Cell Disease Affects The Circulatory System

    Sickle cell is a disease that affects the circulatory system. The circulatory system is in charge of moving nutrients throughout the entire body with the use of the blood stream. According to hopkinsmedicine.org the circulatory system moves nutrients, water, and oxygen to the your billions of body cells and carries away wastes like; carbon dioxide that body cells create. The circulatory system includes; the heart: which keeps the circulatory system working at all times with its constant pumping; the arteries: which carry oxygen-rich blood away from the heart to where it is needed; veins: they carry oxygen-less blood to the lungs where they have their oxygen then replenished; and lastly the blood,it is like the liquid train of the circulatory…

    • 656 Words
    • 3 Pages
    Improved Essays
    Read More
  • Superior Essays

    Survival Of The Sickest Rhetorical Analysis
    • 1478 Words
    • 6 Pages

    Survival Of The Sickest Rhetorical Analysis

    The Gale Encyclopedia of Alternative Medicine stated that the genetic mutation associated with sickle-cell anemia occurred thousands of years ago and continued to pass down through generations. The mutation holders were less likely to be affected by malaria (Kapes, 2009). More research on the effects of sickle-cell anemia and malaria was conducted by Dr. Allison of the British Medical Journal. He found studies in Northern Rhodesia, an area greatly affected by malaria, that indicated a positive connection between sickle-cell anemia and malaria. 9.8 percent of sicklers had…

    • 1478 Words
    • 6 Pages
    Superior Essays
    Read More
  • Improved Essays

    Sickle Cell Disease Process
    • 1703 Words
    • 7 Pages

    Sickle Cell Disease Process

    Identify the disease process presented by the case study as well as the normal structure and function of the organ system and/or physiological process that has the alteration. Shawn, the main character of “The Uniformed Coach” scenario has sickle cell disease (SCD) and is suffering from a sickle cell crisis. Sickle cell disease is a form of hemolytic anemia that is inherited; being caused by an abnormal hemoglobin molecule. There are several forms of SCD but the most severe is simply called sickle cell anemia; the dysfunctional hemoglobin molecule, called hemoglobin S (Hb S), assumes an unusual shape when it is subject to deoxygenation or dehydration (McCance & Huether, 2014). In a normal person, all hemoglobin molecules are shaped like…

    • 1703 Words
    • 7 Pages
    Improved Essays
    Read More
  • Improved Essays

    Sickle Cell Research Paper
    • 1293 Words
    • 6 Pages

    Sickle Cell Research Paper

    Introduction Sickle cell disease is a genetic disorder that can be best described as irregular shaped red blood cells that block blood flow, which cause chronic periodic episodes of pain. Sickle Cells affects over 72,000 Americans and millions throughout the world, Sickle cell most commonly affect African American descent, approximately 1 in 12 African Americans carry the trait for Sickle cell and 1 of every 350 African-American infants born have the disorder and the incidence of the disorder in Africa is ten times higher (AAFP,2000). This paper will highlight background information, causes, diagnosis and discuss several treatment and therapies of Sickle cell disease and why African American are largely affected by this disease. Background…

    • 1293 Words
    • 6 Pages
    Improved Essays
    Read More
  • Improved Essays

    Sickle Cell Disease Benefits
    • 903 Words
    • 4 Pages

    Sickle Cell Disease Benefits

    Sickle Cell Disease (SCD) is an inherited blood disorder, in which people have abnormal hemoglobin. This causes a variety of problems for the person throughout their entire life, but severity of the disease varies. Sickle Cell Disease is not necessarily deadly, but it decreases the average life expectancy of a persson. In countries like the United states, a person with Sickle Cell Disease has a life expectancy of about forty to sixty years. Other than stem cell transplants there is no cure for Sickle Cell Disease currently, but if discovered early regular medical care and treatments can not only prolong the life of a person with the disease, it can also improve their quality of life.…

    • 903 Words
    • 4 Pages
    Improved Essays
    Read More
  • Decent Essays

    Sickle Cell Disease Personal Statement
    • 107 Words
    • 1 Pages

    Sickle Cell Disease Personal Statement

    The goal of the NIH Sickle Cell Disease Branch is to cure sickle cell disease through transplants and gene therapy. I shadow Dr. Courtney FItzhugh in a clinic where she investigates protocols that could aid in minimizing immunosuppression during transplant. From my experience I am able to witness the direct relationship between biomedical research and the development of treatment plans. I have also learned the importance of keeping open communication with patients throughout treatment, which helps to improve patient compliance. I work under the hydroxyurea protocol where I will be testing exosome activity in the recipient's blood as a measure to predict level of possible immune rejection.…

    • 107 Words
    • 1 Pages
    Decent Essays
    Read More
  • Improved Essays

    Sickle Cell Crisis Research Paper
    • 932 Words
    • 4 Pages

    Sickle Cell Crisis Research Paper

    Sickle cell crisis is an acute condition of sickle cell anemia. Sickle cell anemia is a genetic condition. Both parents must be carriers of the gene in order for a baby to be born with sickle cell anemia. In the United States, the gene predominantly affects black people of African decent. Sickle cell anemia is a disease where there is an inadequate number of healthy red blood cell throughout the body.…

    • 932 Words
    • 4 Pages
    Improved Essays
    Read More
  • Improved Essays

    Sickle Cell Research Paper
    • 1038 Words
    • 5 Pages

    Sickle Cell Research Paper

    Sickle Cell Sickle cell is a blood disease that has become a more public disease amongst people. Sickle cell has been prominent since the discovery in 1910 in America. The disease was said to be around for 5000 years before that originating in East Africa. The Disease was discovered in the U.S when a patient from Granada came to Dr. Ernest Irons with anemia symptoms. The disease has a dominant gene and a recessive gene.…

    • 1038 Words
    • 5 Pages
    Improved Essays
    Read More
  • Superior Essays

    Essay On Sickle Cell Anemia
    • 2226 Words
    • 9 Pages

    Essay On Sickle Cell Anemia

    As of today most people with sickle cell anemia are not cured, but with treatment life is much better with relief of pain and other related problems of the disorder. A patient is usually diagnosed…

    • 2226 Words
    • 9 Pages
    Superior Essays
    Read More
  • Improved Essays

    Sickle Cell Anemia Research Papers
    • 1506 Words
    • 7 Pages

    Sickle Cell Anemia Research Papers

    Sickle cell anemia is a genetic blood disorder that causes normal red blood cells to form into an irregular shape, called sickled-cells. The sickle cell gene causes the body to produce abnormal hemoglobin. After a while, the hemoglobin will then cluster together anywhere in the body causing the blockage of blood flow through the blood vessels. This blockage deprives the tissues and blood of oxygen which can lead to many difficulties and problems. SCD becomes life-threatening when the damaged red blood cells begin to breakdown, when the spleen does not work properly or at all, or when it is unable to prevent infections from coming in.…

    • 1506 Words
    • 7 Pages
    Improved Essays
    Read More
  • Superior Essays

    Essay On Sickle Cell
    • 1260 Words
    • 6 Pages

    Essay On Sickle Cell

    Pediatric hematologist in New York, Janet Watson, suggested the insufficiency of sickle cells in the peripheral blood of newborns was due to the fetal hemoglobin in the red blood…

    • 1260 Words
    • 6 Pages
    Superior Essays
    Read More

Related Topics

Ready To Get Started?
Discover
Company
Follow
©2024 Cram.com
Privacy Policy |  About Ads |  Site Map |  Advertise  | 
  • Cookie Settings