The Effects Of Sickle Cell Disease On Daily Life - 2454 Words

Effects of Sickle Cell Disease on Daily Life Alyssa Bodnar NSG 401-Pediatric Nursing University of North Carolina Wilmington Abstract Sickle Cell disease is a genetic disorder found primarily in minority descents throughout the world. Because of recent accomplishments in medical research, those diagnosed with Sickle Cell disease are able to lead much more fulfilling lives instead of lives filled with excruciating pain. Though crises caused by the disease process may be unavoidable, comfort can be achieved through proper nursing care. This paper will explain the obstacles caused by sickle cell disease in a patient currently consumed by crisis. Effects of Sickle Cell Disease on Daily Life Chief Complaint and Diagnosis On October 27, 2014, client presented with mother to emergency department with a temperature of 101.5 ºF. Mother gave child Tylenol and was unable to break the fever. Labs were drawn with the following results: WBC- 9.9, Hgb- 11.6, and reticulocytes- 1.6, UA-normal, negative blood culture, and flu and strep negative. Client was give one dose of Rocephin and discharged. On November 3, 2014, client, JL, presented to the emergency department. The mother of the client reported increased â€Å"fussiness† and refusal to bear weight on right leg that started over the weekend. Client has history of Sickle Cell Disease which called for a routine complete blood count with differential to be conducted. Results were as follows: WBC-Show MoreRelatedSickle Cell Disease : African Americans1378 Words   |  6 PagesSickle Cell Disease on African Americans Cristina Martinez Nova Southeastern University Sickle Cell Disease on African Americans Sickle cell anemia is an autosomal recessive hereditary blood disorder which causes damage to the cerebrovascular system including important organs such as the spleen and liver due to abnormal red blood cells (Scott Scott, 1999). Sickle cell disorder is caused by mutations in the HBB gene then hemoglobin S and other abnormal beta-globin chains create a rigid consistencyRead MoreA Short Note On Opioid And Opioid Analgesics1182 Words   |  5 Pagesand preventing further prognosis of the disease rather than curing the disease. These medications listed below are commonly used pharmacological medications (Nadine Matthie, 2015). Generic name: acetaminophen, trade name: Tylenol. Acetaminophen is an antipyretic, and nonopioid analgesic used as pain reliever. It suppresses the synthesis of prostaglandins which controls the pain and fever receptors primarily in CNS (Vallerand Deglin, 2017). Common side effects are, increase agitation in children,Read MoreSickle Cell Disease : A Life Long Illness1370 Words   |  6 PagesSickle Cell Sickle cell disease is a life-long illness. The severity of the disease varies widely from person to person. In high-income countries like the United States, the life expectancy of a person with SCD is now about 40–60 years. In 1973, the average lifespan of a person with SCD in the United States was only 14 years. Advances in the diagnosis and care of SCD have made this improvement possible. Sickle Cell disease affects mostly African, Mediterranean and related ancestries it is passedRead MoreCritical Care Nursing: Sickle Cell Anemia2832 Words   |  12 PagesCritical Care Nursing: Sickle Cell Anemia Critical Care Nursing 10/15/2009 Sickle cell anemia affects millions of people worldwide. Sickle cell anemia is a disease in which your body produces abnormally shaped red blood cells. They dont last as long as normal, round red blood cells, which leads to anemia. Sickle cells contain abnormal hemoglobin that causes the cells to have a sickle shape. Sickle-shaped cells don’t move easily through your blood vessels. They’reRead MoreA Research Study On Sickle Cell Disease Essay1765 Words   |  8 PagesSickle Cell Disease, also known as SCD, is a group of genetic red blood cell disorders marked by abnormalities in the hemoglobin. Hemoglobin is a protein in red blood cells made up of alpha and beta chains that helps to deliver oxygen throughout the body. Unlike normal red blood cells that have a circular, biconcave shape, sickle red blood cells have hemoglobin S which causes them to become stiff, sticky and shaped like sickles. Usually normal red blood cells would move smoothly through small bloodRe ad MoreSickle Cell Anemia Is The Most Common Disease Among African Mediterranean Dissent4388 Words   |  18 PagesSickle cell anemia is the most common disease among African Mediterranean dissent; sickle cell anemia affects millions of people worldwide. There are 5 different types of Sickle Cell Disease which are Sickle Cell Anemia, Sickle-Hemoglobin C Disease, Sickle Beta Thalassemia Disease, Sickle-Hemoglobin D Disease, and Sickle-Hemoglobin O Disease. Sickle Cell Anemia is when a child inherits the Sickle Cell Disease gene from both parents in which they may gain the symptoms of Sickle Cell Disease, SickleRead MoreLiving With Sickle Cell Anemia Essay2158 Words   |  9 PagesLiving With Sickle Cell Anemia Introduction According to the 2016 edition of the Oxford dictionary, to define someone or a group of people as vulnerable means that they are susceptible to physical or emotional harm (Vulnerable, 2016). One of the most recognized populations of vulnerable people are children; furthermore, by adding an inherited disease process, that decreases the immune system, would only increase the vulnerability of the population. Children with sickle cell anemia are highly susceptibleRead MoreExplain the Potential Effects of Five Different Life Factors on the Development of an Individual.3226 Words   |  13 PagesRachel Fry - P2- Explain the potential effects of five different life factors on the development of an individual. Life Factors There are five life factors that can effect a person’s growth and development, these are; †¢ Genetic †¢ Biological †¢ Environmental †¢ Socioeconomic †¢ Lifestyle Genetic Factors Determinism/Choice and Interaction Determinism is the belief that your future is fixed or determined, either by what you have genetically inherited or by your social environmentRead MoreEssay on Sickle Cell Anemia2581 Words   |  11 PagesAbstract 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 areRead MoreSickle Of Sickle Cell Disease2167 Words   |  9 PagesSickle cell disease is an ailment that specifically targets red blood cells, causing them to sickle into a cone shape and hinders the transfer of oxygen to other parts of the body. Lack of oxygen can damage tissues and cause major problems for the person affected. As a black male, I am very familiar with sickle cell disease. I have family members with the disease, such as my uncle who was very susceptible to illness as a child due to the disease. I remember him telling me how his body would ache