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Life threating conditions for sickle cell anemia
Life threating conditions for sickle cell anemia
Life threating conditions for sickle cell anemia
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Sickle cell anemia is a genetically inherited and is a lifelong disease. Sickle cell anemia affects the red blood cells because it causes the cells to be crescent shape instead of how a normal cell looks like: an oval disk. This causes the circulation of the blood flow throughout the body to be clogged more often because people with sickle cell tend to have more blood clots. This also exhausts the body a lot more and people with this particular disease are more likely to get winded by a short physical activity. Sickle cell disease is caused by a mutation in the beta-globin gene. The main symptoms of sickle cell are shortness of breath, fatigue, difficulty breathing, deterioration of athletic performance, weakness, headaches, and dizziness. Another set of key features that …show more content…
could also indicate that a person has anemia by having them go through a physical exam, checking if their skin is pale, cracked lips, brittle fingernails, and a rapid pulse. These symptoms are signs of someone having or even developing iron deficiency anemia. Fortunately, there are tests that can determine whether you may or may not have sickle cell anemia. This test is called hematocrit which is a series of lab tests used to diagnose anemia. The test calculates the percentage of whole blood volume that is due to red blood cells. To begin this test, the phlebologist must draw blood into the capillary tube with clay sealed at the bottom. After that, the capillary tube is centrifuged, forcing the red blood cells to the bottom. Once the centrifuged is done, the phlebologist calculates the total blood volume after they finished the calculations and you receive a low hematocrit score then it is viewed that you have anemia. However, there are various factors that contribute to the test, for example, your age, gender, and if you are pregnant. The next test procedure is to determine the hemoglobin in the blood. Hemoglobin is essential for our red blood cells, it is an oxygen-carrying protein that gives red blood cells their color. The hemoglobin test is one of the most widely used tests to screen for anemia. When you have been diagnosed with anemia, it is necessary to assess the situation and treat it.
Medications involve hydroxyurea that stimulates the production of the fetal hemoglobin which is a short-term treatment and causes new blood cells to not be sickled and folic acid increases folate stores responsible for the production of red blood cells. Other treatment options involve a bone marrow transplant which is more likely to cause the patient to get sick and are prone to infection more or blood transfusions to have normal red blood cells to carry out the blood cells’ function. However, it can not be done often because it causes high iron levels. Upon being diagnosed with sickle cell anemia, life may get a lot harder because you can get pain crisis, which can be sudden outbreaks and it can be mild or severe which may lead to necrosis, edema, and increased in pressure. You must also be more conscious of your health because your body cannot handle normal physical activity as others and is more prone to pain in joints, blockages in blood vessels which can lead to heart attacks and stroke and you must take your medications in time to ensure that you will not endanger yourself and be at risk of
death.
Under hypoxic conditions, the abnormal hemoglobin start to change shape. They become sickled, stiff, and have greater difficulty moving though the blood vessels. As a result they begin to stick together and eventually block the tissues from receiving nutrients and oxygen. This causes the tissue to become infarcted and leads to pain. In a hypoxic states the cells are forced to make energy also known as adenosine triphosphate (ATP) without oxygen. This is called anaerobic glycolysis and results in the production of lactic acid as a byproduct (citation). The presence of lactic acid lowers the pH of the environment, the cells must recycle lactic acid back into the cells, and ATP production is significantly slowed. The cells
1. Sickle Cell Disease is life-threatening and has a risk of of causing depression. In this study I examine the experiences that Sickle Cell patients go through specifically at emergency healthcare facilities to find out if there are any negative stigmatizations surrounding this disease. There may be judgments that are made about these patients from healthcare professionals when they seek drugs for their pain relief that may cause the stigmatization to occur. I will also investigate why individuals that have Sickle Cell Disease experience longer waiting times at emergency healthcare facilities and the lack of control they may have over their care regime.
Sickle cell disease is a group of disorders that affects the blood, specifically, a molecule called hemoglobin in red blood cells (“sickle cell disease”, 2016). Hemoglobin is a molecule that facilitates the delivery of oxygen throughout the body (“sickle cell disease”, 2016). A mutant form of the hemoglobin molecule causes red blood cells to become crescent shaped or “sickled shaped” (Lonergan et. al. 2001). This distorted shape of red blood cells causes rigidity of the blood cells and vaso-occulusion (or the blood vessels to become clogged) (Rees et.al., 2010). This often leads to a low number of red blood cells (anemia), repeated infections and episodes of pain that are periodic (“Sickle cell disease”, 2016). Although sickle cell disease
Symptoms of a sickle cell are shortness of breath or fatigue and delayed growth in the development of children. Severe pain can be caused as a symptom when the blood gets stopped up in the vessel and causes the patient 's heart to pump slower, so people begin to feel pain in the body and feel out of breath.
Blood serves as the body transport system; blood carries oxygen to the lungs and cells throughout the body. It takes carbon dioxide or toxins from out the body. The components of the blood fight off different diseases by recognizing engulfing microorganisms and molecules from overseas that doctors found in the blood. The other components support the transports through the kidneys, hormones in the body, and the digestive system to help pass the nutrients through the body.
Sickle cell anemia occurs when an abnormal form of hemoglobin (HbS) is produced. HbS molecules tend to clump together, making red blood cells sticky, stiff, and more fragile, and causing them to form into a curved, sickle shape. Red blood cells containing HbS can go back and forth between being shaped normally and being sickle shaped until they eventually become sickle shaped permanently. Instead of moving through the bloodstream easily, these sickle cells can clog blood vessels and deprive the body's tissues and organs of the oxygen they need to stay healthy.
Sickle-cell anemia is a genetic disorder that makes your body produce red blood cells that are abnormal in shape. This disease is also widely known as hemoglobin SS disease. Unlike normal red blood cells, sickle cells are rigid and tenacious. Due to their shape and rigidness, they can block blood flow. In turn, this could cause organ damage to the body. Sickle cells are also fragile and die very easily due to the fact sickle cells have a lifespan of twenty days instead of the normal one hundred and twenty days for normal red blood cells.This causes the body to have a lower blood cell count, hence the name anemia in sickle cell anemia.
“In the United States, it's estimated that sickle cell anemia affects 70,000–100,000 people, mainly African Americans” (NHLBI, NIH, Who is at risk for sickle cell anemia). SCD is a disease that is a serious disorder in which the body can make normal blood cells and sickle shape cells. Sickle shape cells can block the blood flow in your vessels and cause pain or organ damage also put you in risk for infections. SCD has no cure available but there are many treatments out there to deal with the complications of it. From over years treatments did get better from way back in the day doctors have learned. Sickle cell disease has lack of attention and funding because it’s only affecting African American the most.
Sickle cell anemia is an inherited disease of red blood cells. Normally red blood cells contain a protein called hemoglobin A, which carries oxygen to all the organs in the body. With sickle cell anemia, however, the body makes a different kind of protein, called hemoglobin S.
Many people can prove to the fact that sickle cell originated in Africa. Going by different names related to tribal languages but in 1910 a young dental student came to the office of Doctor James B. Herrick, a cardiologists complaining of black problems Herrick wanted nothing to do with young kids. So he referred him to Dr.Ernest Irons after drawing flood and examines it. Dr.Irons notice that the red blood cells had a sickle shape at that moment he immediately informed Dr. Herrick and he later wrote many medical journals able the sickle shaped cell. In 1927 Hahn and Gillespie realized removing oxygen individuals that were inflected red blood cells could form the sickle shape. So they came up with the term trait but,
Sickle cell anemia is a blood disorder that is inherited from both parents in which the body produces abnormally shaped red blood cells. In sickle cell anemia, the hemoglobin in red blood cells links together; resulting in the red blood cells to become rigid and a C-shaped. These deformed cells block blood and oxygen flow in blood vessels. Sickle cells deteriorate quicker than normal red blood cells, which results in anemia.
Sickle cell disease is an inherited disease where the red blood cells in the body are produced abnormally by bone marrow as crescent shaped red blood cells. Unlike normal red blood cells, sickle shaped cells are unable to deliver much oxygen to other parts of the body due to the abnormal hemoglobin. Sickle cell’s are stiff and sticky and tend to clump together between blood vessels that can cause pain, damage to the organs, and infections. If a child inherits this disease they can be healthy throughout their life or need special care. “In the United States, SCD is most common among blacks and Hispanics. SCD affects about 1 in 500 black births and about 1 in 36,000 Hispanic births in this country. SCD is also common among people with family from Africa, the Caribbean, Greece, India, Italy, Malta, Sardinia, Saudi Arabia, Turkey or South or Central America (March of Dimes)”.
Sickle cell anemia is a disease that reforms the patient’s red blood cells, which makes the red blood cells has an abnormal shape like a sickle. Sickled red blood cells can result to severe anemia; decrease causes numerous painful symptoms in patients. A defective protein called hemoglobin is what cause the abnormal shape of the red blood cells in the sickle cell patients.
Sickle Cell is a disease that affects many people in the world today. It is the number one genetic disorder in the United States. Sickle Cell is deficient hemoglobin. Hemoglobin is what functions in providing oxygen to the cells in the body. The sickle shape comes from the atypical hemoglobin s molecules. Hemoglobin molecules are composed of two different parts called the alpha and beta. The beta subunit of the hemoglobin molecule has a mutation in gene, on chromosome 11 which produces the change in the red blood cell shape causing them to die and not reproduce accurately. The change in shape causes the red blood cells to get stuck in the blood vessels and block the effectiveness of oxygen transport causing pain and organ damage to the body. This disease does not have a cure and some common treatments are used to help patients live with the disease. Some treatment options are antibiotics (penicillin) to prevent infections, blood transfusions, folic acid that help produces new blood cells. These are just some of the current treatments for Sickle Cell.
Sickle Cell Anemia is an inherited blood disorder that is extremely challenging to live with. Its symptoms are many, with the most prominent being severe pain that can become unbearable to the point where hospitalization is required. Because sickle cell is a genetic disorder, a person is born with it and it is usually permanent. Unfortunately, there are risks and complications associated with this disease. However there are various treatment options for a patient with sickle cell and also support to help people understand and cope with this challenging disease.