Care for patients with Sickle Cell Disease - Essay Example

Comments (1) Cite this document
Summary
An essay "Care for patients with Sickle Cell Disease" discusses that sickle cell disease (SCD) is a common inherited chronic illness in the United States. According to estimates by the Center for Disease Control and Prevention (CDC), SCD affects 100,000 Americans…
Download full paperFile format: .doc, available for editing
GRAB THE BEST PAPER93.7% of users find it useful
Care for patients with Sickle Cell Disease
Read TextPreview

Extract of sample "Care for patients with Sickle Cell Disease"

Download file to see previous pages Helen Erickson, Evelyn Tomlin, and Mary Ann Swain developed the modeling and role-modeling (MRM) theory. This grand theory of nursing provides holistic care to clients by understanding their needs and providing client-centered interventions to meet the needs. It identifies the nurse as a “facilitator” who uses the modeling and role-modeling processes to help individuals “achieve a perceived optimal state of health and well-being”. Nurses use the process of modeling to develop an “understanding of the client’s world as the client perceives it” by accepting the individual’s belief. While the planning and implementation of client-specific nursing interventions are ongoing, the role-modeling process follows. This theory uses five aims of intervention as a standard in providing individualized care.The MRM theory also integrates Maslow’s theory, Piaget’s theory, and the concept of object attachment. The theory describes many concepts and their relationships in nursing and individuals since its original intentions were to guide the nurse-patient relationship. The nursing concepts include facilitation, nurturance, and unconditional acceptance, while concepts in individuals include similarities and differences in people. The commonness among human beings includes basic needs, holism, lifetime development, and affiliated individuation, while differences include inherent endowment, adaptation to stressors, mind-body relationships, and self-care....
The commonness among human beings include basic needs, holism, lifetime development, and affiliated individuation, while differences include inherent endowment, adaptation to stressors, mind-body relationships, and self-care (Erickson, 2010). There is an interrelationship of these differences and similarities. Following its publishing in 1983, there has been extensive research, examination, and adaptation of the MRM theory in diverse settings. It further guides undergraduate nursing curriculum, weight reduction programs, chronic illness management, and practice in hospitals (Frisch & Bowman, 2011). Strength and Limitations Some general strengths of the MRM theory include clarity, simplicity, and generality (Erickson, 2010). Theorists Erickson, Tomlin, and Swain clearly explained the theory while providing examples of their experiences to give a holistic understanding. The theory has a simple structure since it focuses on two steps of modeling and role-modeling. However, the interactions of its major concepts with the role of nursing add depth and complexity to the theory (Erickson, 2010). Nevertheless, its standard form allows its applicability in many nursing and patient situations by researchers and clinicians. However, its major limitation is that inexperienced nurses find it difficult to apply (Frisch & Bowman, 2011). While clinicians learn to perceive the client’s world by “unconditional acceptance” of the client as a unique individual easily, the theory requires experience and understanding of nursing in order to avoid confusing the role of a “caring professional” with that of a “caring friend” (Frisch & Bowman, 2011, p. 536). The MRM theory’s focus on client-centered care is ...Download file to see next pagesRead More
Cite this document
  • APA
  • MLA
  • CHICAGO
(“Care for patients with Sickle Cell Disease Essay”, n.d.)
Retrieved from https://studentshare.org/nursing/1396214-care-for-patients-with-sickle-cell-disease
(Care for Patients With Sickle Cell Disease Essay)
https://studentshare.org/nursing/1396214-care-for-patients-with-sickle-cell-disease.
“Care for Patients With Sickle Cell Disease Essay”, n.d. https://studentshare.org/nursing/1396214-care-for-patients-with-sickle-cell-disease.
  • Cited: 0 times
Comments (1)
Click to create a comment or rate a document
mm
mmckenzie added comment 11 months ago
Student rated this paper as
This essay was always my weak point. I could never complete it well. Still, after I found this particular paper, I understood how it should be completed. So, I performed my research afterward and completed the essay in several hours, instead of weeks as it was previously.

CHECK THESE SAMPLES OF Care for patients with Sickle Cell Disease

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

Sickle cell disease

...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

Sickle Cell Transition Placement

...(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

Sickle Cell Disease

... 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

Children With Sickle Cell Disease

...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

Sickle cell disease

...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

Sickle cell anemia

...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

Correcting Sickle Cell Disease using Stem Cells

...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

Prenancy woman with sickle cell disease

...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

Sickle cell disease

...(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
sponsored ads
We use cookies to create the best experience for you. Keep on browsing if you are OK with that, or find out how to manage cookies.

Let us find you another Essay on topic Care for patients with Sickle Cell Disease for FREE!

Contact Us