Interventions For Sickle Cell Anemia Treatment

677 words - 3 pages

Case Study
Sickle Cell Anemia is an autosomal recessive disorder, which increases blood thickness hence affects the smooth flow of blood. This causes by the destruction of red cells where the normal shape of red cell become a stiff sickle shape. As a result, sufficient oxygen does not reach the vital organs. A vaso-occlusive crisis arises from hindrance of blood circulation by sickled blood cells. It is characterized by sturdy pains and in some cases; it may cause permanent organ damage. This paper seeks to formulate a nursing diagnosis, as well as a plan of care that includes nursing interventions and the methods to be used to evaluate whether the interventions are successful (American Sickle Cell Anemia Association).
Nursing diagnosis is a clinical assessment of health problems experienced by a family or an individual and their response to this health problem. It helps in determination of interventions that are to be put in place so as to realize the desired outcome. This diagnosis enables the nurse to come up with a care plan for the patient (National institute of health, 2002).
In this case the nursing diagnosis is probable sickle cell crisis and the possibility of shift in self perception linked to the notion of being different from peers.
Outlined herein, are some of the interventions with their rationale and outcomes.
First, Maya and the family should be encouraged and helped to alternate the intervals of resting and activity. The rationale is that, this will help their bodies to reduce the demand for oxygen and also reduce hypoxia level. Maya should also be assisted in deep breath taking movements and mild body turning exercises. Rationale: this promotes best chest expansion, which boosts the circulation of secretions. In so doing, the risks of blood clotting are reduced (Sickle Cell Disease Association of America).
The outcome is that the patient’s family will know the precautions to be taken and also the actions to be avoided to ensure their well being.
Another intervention is to encourage Maya and the family to take sufficient fluids, like 8 glasses per day. The rationale is, to keep the body well hydrated to prevent or reduce viscosity of blood so as to have proper...

Find Another Essay On Interventions for Sickle Cell Anemia Treatment

Sickle Cell Anemia Essay

544 words - 2 pages Hispanics of Caribbean ancestry. The disease also affects somepeople of Arabian, Greek, Maltese, Sicilian, Sardinian, Turkish, andSouthern Asian ancestry.How transmitted type of gene or chromosomes that causes the disease.Sickle Cell Anemia is a sex linked gene. One way somebody could get thisdisease is if both parents are a carrier for Sickle Cell Anemia. There is one infour chance that a baby will have the disease.How the disease is diagnosed

Sickle Cell Anemia Essay

847 words - 3 pages an iron deficiency in the diet. People with anemia tire easy for lack of oxygen needed for energy. Research study show, without treatment of folic acid supplements daily and a well balanced diet, anemia can cause life threatening complications.Origin …..Sickle cell Anemia is most common in African Americans. According to mamashealth.com/sickle_cell.asp "I out of 400 African Americans have sickle cell". It is also common in people from

Discovering Sickle Cell Anemia

1318 words - 5 pages eye, slow healing sores or ulcers, and even gallstones. When the hemoglobin is low, it is manifested by fatigue and weakness.Currently, there is no cure for Sickle Cell Anemia. But the doctors do offer a treatment that helps control this disease. Pain medication, antibiotics, rest and high fluid intakes are all treatments for aspects of sickle cell anemia. There are also experimental therapies that are available to some patients. The drug

Sickle Cell Anemia

2577 words - 10 pages cure for sickle cell anemia, treatments that are being developed are becoming more effective. Basic treatment for a patient relies solely on oral or intravenous fluids; which help to prevent further complications, and painkillers. Blood transfusions also aid in avoiding serious complications. It properly adjusts the anemia the body acquires from the shortage of red blood cells. The transfusion introduces normal healthy blood cells in blood

Sickle Cell Anemia

1145 words - 5 pages Sickle cell anemia is an inherited, lifelong, blood disorder disease, which is passed down through families. It is described as “sickle-shaped” for the strange appearance of the red blood cells (RBC). The red blood cells, which are normally shaped like a discs, takes on a sickle or crescent shape, therefore called sickle-shaped. Sickle cells have irregular hemoglobin, called sickle hemoglobin or hemoglobin S. Sickle hemoglobin is what causes the

Sickle Cell Anemia

669 words - 3 pages cause spleen and organ damage. Damage to the spleen can eventually have a negative affect on the immune system altering infections. Blockage of blood vessels in the brain can have particularly harsh consequences and can be fatal. Children ages 1-15 are prone to having strokes. There are some minor and some very major affects of sickle cell anemia, but with the write treatment death can be prevented.Although there is no cure for this disease

Sickle Cell Anemia - 637 words

637 words - 3 pages I think a very good report Well done...your best work yet!Sickle Cell AnemiaSickle Cell Anemia is the most common hematologic hereditary disorder knowtoman. It is a condition where the red blood cells (RBC) sometimes assume astrange,sickle©like shape. Observations date back to Herrick in 1910, but themolecularera for the study of Sickle Cell Anemia did not begin until the identificationofHemoglobin S (Hb S), by Linus Pauling in 1949. It is

Sickle Cell Anemia - 890 words

890 words - 4 pages , carriers do not have symptoms, but their red blood cells contain some hemoglobin S.A child who inherits the sickle cell trait from both parents will have a 25% possibility, if both parents are carriers they will develop sickle cell anemia. These cells have a decreased life span in comparison to normal red blood cells. Normal red blood cells survive for approximately 120 days in the bloodstream; sickle cells last only 10-12 days. As a result, the

Sickle Cell Anemia - 4118 words

4118 words - 17 pages also wanted everyone to know that we need their help to make sure families and their children are getting the right treatment and help they need. I wanted to build this website, because the other ones I seen don’t really seem for young adults and their families. The characteristics of my project is to inform others about this disease and let them know that there is a cure for sickle cell anemia. Also I want to let them know that we are here for

Sickle Cell Patient Treatment

1397 words - 6 pages disease in North America. Pediatric Anesthesia [Internet]. [cited 2011 Jan 28]; 21 (1):43-49 Modi Avani C et al. 2009. Barriers to treatment adherence for pediatric patients with sickle cell disease and their families. Children Health Care [Internet]. [cited 2011 Jan 29]; 38 (2): 107-122 [NHBLI]National Heart Blood and Lung Institute. 2011. What is sickle cell anemia? [Internet]. [cited 2011 Jan 22] Available from: http://www.nhlbi.nih.gov

The Differences Betweet Sickle Cell Trait and Sickle Cell Anemia

780 words - 4 pages the disease later, there is no medical treatment necessary, and the person will lead a normal life. Sickle cell anemia occurs when a person gets one gene for sickle (S) hemoglobin from one parent and a sickle (S) hemoglobin gene from the other parent. There is little or no hemoglobin A. When red blood cells carrying hemoglobin S release their oxygen to the tissue, they change from round to sickle shaped (XXXX). Hence the name sickle cell anemia

Similar Essays

Sickle Cell Anemia Essay

1210 words - 5 pages be fatal.Stroke - Occurs when sickled cells create a blockage within the brain. Signs include seizure, weakness in the arms and legs, speech problems, and loss of consciousness.Treatment? Cure? Fatal? - There is no cure for sickle cell anemia but there are however treatments that can increase the life expectancy of a patient. There is a few new treatments still being unleashed like the anticancer drug Hydroxyurea treatment that triggers

Sickle Cell Anemia Essay 833 Words

833 words - 3 pages hemoglobin AS on the hemoglobin electrophoresis. This will not cause sickle cell disease. Other hemoglobin traits common in the United States are AC and AE traits."What are the complications of having Sickle Cell Anemia? There are many complications that go along with having sickle cell for instance, sudden pain episodes, strokes, increased infection rates, leg ulcers, bone damage, lung blockage, kidney damage, blood blockage, eye damage and delayed

Sickle Cell Anemia Essay 1109 Words

1109 words - 4 pages the role red blood cells play in everyday life, and what hemogloben is. As many might already know, the red blood cells carry oxygen to every part of the body, because the body need oxygen to perform their duties. Within the capillaries, hemogloben exchanges oxygen for carbon dioxide in order for us to breath. Sickle cell anemia refers to defective hemogloben that is supposed to distribute oxygen. Normal, healthy adults have Hemogloben A. The "A

Sickle Cell Anemia Essay 1328 Words

1328 words - 5 pages there are treatments available. Most rely heavily on painkilling drugs, both oral and intravenous. Blood transfusions are used to treat and prevent some of the sickle cell complications. The infusions of the correct anemia increase the normal red blood cell count, and treat spleen enlargement. Regular transfusions can prevent recurring strokes in children The first effective drug treatment for adults was reported in 1995: the anticancer drug