CHECK THESE SAMPLES OF Care for patients with Sickle Cell Disease
...?Sickle Cell Disease: The Various Nursing Intervention Approaches to Decrease Pain among Patients in Kendall Regional Hospital In-Patient Section -Abstract Pain is one of the most important characteristic of sickle cell disease. While prevalent to certain race origins, the treatment of, control and reduction of pain among SCD patients has become an integral approach towards delivery of equitable health care services. The patients with SCD has been identified to be mainly from marginalized groups – poor and ethnic minorities. Pain treatment among SCD...
20 Pages(5000 words)Research Proposal
...to ensure that they do not experience a lot of pain. The first step is for the patient to know the kind of medications that is needed to stop the pain. Make sure that the patient is still and tolerant as this will help the drugs to get well into their systems (Serjeant, 1985). Conclusion Sickle cell is a disease that can be well managed and the pain reduced during the crises times. However, it is important that during these crises times, the cooperation of the patient is important to the doctor and the patient himself. If well taken care of, sickle cell is a...
10 Pages(2500 words)Research Paper
...(2008), any personal confidential information regarding the patient/s and individuals involved in this placement shall not be disclosed. The Trust where I conducted my placement shall also be kept confidential. Body Reflection on the Transition Activity I had my transition placement on sickle cell disease, and initially during my placement, I had a discussion at the hospital with the patients and later visited them in their own homes. In general, the activities during my placement were varied. I met with the multidisciplinary team regarding patients who suffered from sickle cell and how best to...
10 Pages(2500 words)Essay
... haemoglobin formation, this oxygen delivery is affected. The red blood cells also lose their normal functional capacity and acquire a sickle shape and this leads to anaemia in the patient. These individuals are also more prone to infections (Bloom 1995; Govan et al 1995; Ganong 2005). The image above shows the difference between the normal shaped red blood cells and the red blood cells of sickle cell disease (National Heart Lung and Blood Institute 2011). Each parent contributes to the genetic makeup of an individual. Half of the genes are inherited from mother and the other half from father. Some traits are completely governed by the type of genes present in the body like colour of eyes and height while others may be influenced... and...
5 Pages(1250 words)Research Paper
...Quality of life of children with sickle cell diseaseCaring for a child suffering from sickle cell disease needs extra demand on parents both psychologically and practically, which may influence their quality of life. This kind of disease is associated with communities with low socio-economic status. The main objective of the study was to evaluate the quality of life of caregivers of children suffering from sickle cell disease. A total of 700 healthy Dutch females and female caregivers of healthy children with the same ethnic background and...
8 Pages(2000 words)Research Paper
...depend on the family history and family's ethnic background (people from West Africa, Middle east and central India). Abnormal hemoglobin (i.e., sickle hemoglobin) can be detected by hemoglobin electrophoresis, a gel in which various types of hemoglobin move at different speed (Robinson et al., 1957). Genetic testing is rarely required for diagnosis.
Treatment options include zinc supplements which help in stabilizing the RBC membrane. Pain is treated with analgesics, sometimes requiring opioid administration. The first drug approved for treating sickle cell disease is hydroxyurea, was shown to reduce the number and severity of the symptoms. Bone marrow transplantation...
2 Pages(500 words)Essay
...as acute sickle cell crises are most commonly brought on by other forms of infection (Clarke & Higgins, 2000).
There is no current means of ‘curing’ sickle cell anemia. From infancy, children who present with sickle cell disease are treated with a 1 mg dose of folic acid daily for life as a means of reducing their susceptibility to infection. It is also necessary to treat children with daily doses of penicillin until age five again as a means of boosting their immune system and reducing the number of crises they experience in early age. Cyanate introduced through planned dietary measures, has proven somewhat...
5 Pages(1250 words)Essay
...will only possibly manifest if both parents are carrier of hemoglobin A. However, at present, the only available long term treatment for the disease is bone marrow transplant, which is prone to rejection and subsequent immune system reaction. The goals of other treatments, blood transfusion and pain medicines, are only for short-term relief of symptoms (Zieve and Chen, 2011).
Recently, however, researchers from Johns Hopkins have found another plausible long term treatment for sickle cell anemia. By inserting the correct hemoglobin A gene to pluripotent bone marrow cells and removing the defective hemoglobin S, the patient can be able to produce RBCs...
1 Pages(250 words)Essay
...Nursing-family Partnership Plan Nursing and Family partnership plan The role of nursing in the Plan Nursing-Family partnerships enhance nursing care of expectant mothers with sickle-cell anemia. Through families, nurses craft cost-effective plans of data-based visitation programs for pregnant mothers with sickle-cell anemia. The aim of this program is to ensure good health outcomes of babies born from victim mothers through an effective nursing care unit.. Nursing, especially community nursing, is reliable in providing home-based, clinic, and hospital care to mothers with sickle cell anemia. Nurses are adaptable and willing to work in whichever conditions they come across. The impact of this scheme will assist the next generations... ...
2 Pages(500 words)Essay
...(tormenting, delayed erection). It additionally causes harm to the spleen, kidneys and liver. The harm to the spleen makes patients - particularly adolescent youngsters - effectively overpowered by bacterial diseases. An infant conceived with sickle cell infection inherits a gene for the issue from both folks. At the point when both folks/parents have the hereditary imperfection, theres a 25 percent risk that every youngster will be conceived with sickle cell infection (Monroe, 2008).
Most individuals with SCD have a solitary abscond on both duplicates of chromosome 11 that makes them process imperfect hemoglobin atoms, which tie...
5 Pages(1250 words)Research Paper