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Topic:

Polycystic Kidney Disease

Essay Instructions:
Use at least two professional resources to gather information and review Polycystic Kidney Disease. Explain the disease process, nursing interventions associated with the disease process and pertinent patient education. All references must be in APA format.
Essay Sample Content Preview:

POLYCYSTIC KIDNEY DISEASE
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Institution Affiliation
Course
(October 9, 2012)
Polycystic Kidney Disease
Polycystic Kidney Disease is a genetic kidney disorder inherited through family lines, where the kidneys form many cysts making them bloated; this is due to the formation of many cysts in the kidney. There are two types of the disorder which are the autosomal dominant and the autosomal recessive. The autosomal dominant is usually developed at older years such as 30 – 40 but also occurs in children and is the most common; while the autosomal recessive is developed in childhood years and can even start from the womb and is a rare condition (Dakshinamurty, 2009).
Causes
The Polycystic Kidney Disease is inherited from family with the autosomal dominant trait being more prevalent. When one parent has the gene to this disorder then chances are that the child has 50 percent chance to contract the disorder. This disorder is associated with aortic and brain aneurysms, liver, testes, and pancreas cysts, and colon diverticula (Simons & Walz, 2006).
Symptoms
The symptoms include pain in the abdomen and abdominal tenderness; blood in the urine; too much urination at night, and flank pain on the abdominal parts (one or both sides). Other symptoms include pain in the joints, drowsiness, and abnormalities on nails (Dakshinamurty, 2009).
Signs and tests
During examination there may be abdominal tenderness on the upper part of the liver, which may also be enlarged. There also may be heart murmurs; growth of the kidneys and/or abdomen; and high blood pressure (Dakshinamurty, 2009).
The tests done on the patient include a complete blood count (CBC), urinalysis, and a celebral angiography. Through scans on the body the swellings will be identified and hence abdominal CT scans, MRI scans, ultrasound and intravenous pyelogram (IVP) may be done. For persons who identify the disease in other family members it is best to take a genetic test to ascertain their health (Dakshinamurty, 2009).
Treatment
In view of the fact that the disorder is genetic, treatment is aimed at control and preventing further complications of the symptoms. For this reason, medication is taken to treat the given ailments found out such as blood pressure drugs (high blood pressure) and antibio...
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