Sickle Cell Disease (SCD) (also known as Sickle Cell Disorder or Sickle Cell Anemia) is an inherited blood disorder where the red blood cells have abnormal sickle-shaped hemoglobin S (HbS) called sickle haemoglobin (National Heart Lungs and Blood Institute (NHLBI), 2015). The disease, according to medical sciences, is inherited from both parents as part of their genetic makeup and is usually caused by some abnormalities in haemoglobin which is a protein in red blood cells that conveys oxygen through the body. Whereas normal red blood cells are round, in people with sickle cell anemia, a defective substance in red blood cells changes the shape of the cells. The normal haemoglobin called haemoglobin A (HbA) is replaced by HbS which later becomes …show more content…
Onwujekwe , Chima, and Okonkwo (2000) showed that the average expenditure of each household per month on malaria treatment was $1.84, which accounted for 49.87% of curative health care costs incurred by the households. In a similar study, Russell (2004) found that direct malaria cost burden was 2.9% of household income per month. Studies in Africa also showed that indirect cost based on travel time, lost labour time for adults with malaria attack or those who have to stay off work to care for children among others, make up more than 75% of total household malaria costs. Malaria tends to reduce education funds capability and has effects on school attendance (Malaney, Spielman, & Sachs, …show more content…
SCD has major social and economic implications for the affected child and the families. Recurrent sickle-cell crises interfere with the patient’s life, especially with regard to education, work and psychosocial development (WHO). Sickle cell anemia, specifically, is a serious disease that can require frequent hospital stays. Repeated hospitalization for intravenous pain medication, antibiotic therapy and blood transfusions is undertaken to treat medical problems as about 1 in every 10 children with sickle cell disease. People with SCD may suffer abdominal pain, breathlessness, delayed growth and puberty, fatigue, fever, ulcers, among others. These patients often die early of overwhelming infection or as a consequence of acute or chronic damage to the body organs. Those with sickle cell disorder often suffer neglect and
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
...nt of patients with sickle cell anemia. However, the choice of interventions should be done carefully so as to realize the desired outcome otherwise it may not be successful. Key among the innervations listed here, is counseling. This may help the patients to have hope and this may aid in the quick recovery.
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.
What is Sickle cell disease? Sickle cell affects a disease; that disease is called which affects the hemoglobin when the red blood cells that send oxygen through the body are killed off and weakened. Sickle cells can be found in every 1 and 1000 African Americans, it is affecting about 70,000 to 80,000 Americans in the United States. Sickle cell is a death threatening disease, and the severity of symptoms can vary from person to person (Sickle cell disease (SCD), 2015). Some people have light conditions, but others can have severe conditions, which, mean they could be hospitalized. Characteristics of this disease are caused by a minimum of low blood cells, which is called anemia.
The name of this patient is Davon; he is a five-year-old African-American male whom just moved from Chicago. The patient was visiting his pediatrician for a physical to enter kindergarten. The patient mother gave her history about confirming that she has the sickle cell trait and would like to know if her son is also a carrier for sickle cell. ("Sickle Cell Disease", 2015) “Sickle cell trait inherited from both hemoglobin A and S, in the red blood cells”. Those with this disease are still capable of having a healthy life. For instance, if one parent has sickle cell trait, and the other parent does not will only lead to the child having sickle cell trait or nothing. If both parents have the trait, then the child will genetically develop sickle cell disease inside the mother’s womb. Sickle cell trait is a transmitted disease that travels through the red blood cells. The symptoms of sickle cell trait is that when the skin gets pale, always cold, or even tired then that is a sign of having this disease. The patient cannot prevent this disease, due to this is something that is passed on from the womb and birth. Daily doses of penicillin can control the infection; on the other hand, it is not preventable. The only way to make sure that it does not get worse is the person must eat foods with high iron and even
Sickle cell anemia is a genetic disorder that erythrocytes tolerate sickle shape red blood cells. These red blood cells are easy to damage, which leads to hemolytic anemia. Abnormal hemoglobin is fragile to low oxygen conditions within the body. It loses the blood solubility, and then forms thick strands called polymers. This gives the abnormal shape, called Sickle cell.
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.
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.
“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 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.
Malaria is a disease that is caused by parasites. It is transferred from one person to another by the infected female Anopheles mosquito. Malaria has been a serious health problem nowadays. WHO has provided the information that approximately 660,000 people died from malaria globally during 2010. Also, after estimating, there are 219 million cases of malaria infection in 2010 worldwide. In sub-Saharan Africa, being one the country that has the high rate of HIV, AIDS, malaria, and tuberculosis, had 90% of the people that...
Malaria (also called biduoterian fever, blackwater fever, falciparum malaria, plasmodium, Quartan malaria, and tertian malaria) is one of the most infectious and most common diseases in the world. This serious, sometimes-fatal disease is caused by a parasite that is carried by a certain species of mosquito called the Anopheles. It claims more lives every year than any other transmissible disease except tuberculosis. Every year, five hundred million adults and children (around nine percent of the world’s population) contract the disease and of these, one hundred million people die. Children are more susceptible to the disease than adults, and in Africa, where ninety percent of the world’s cases occur and where eighty percent of the cases are treated at home, one in twenty children die of the disease before they reach the age of five. Pregnant women are also more vulnerable to disease and in certain parts of Africa, they are four times as likely to contract the disease and only half as likely to survive it.
...at researchers are doing to try to eradicate malaria in underdeveloped countries such as Africa.