2017年8月6日星期日

Methods of polycystic kidney examination

Many people do not understand the polycystic kidney disease, once the disease, great harm, great harm to the kidneys. We should pay attention to the development of the disease. Reasonable medication and treatment. After the disease, the patient will feel the waist pain, there will be hematuria, the great harm. So, what is the method of polycystic kidney examination?

A family history

Patient friends, polycystic kidney disease is a family hereditary disease, heritability in 50%, the general male is greater than women, all families have the disease patients, then the family of people need to do an early check.

Second, the clinical manifestations

Polycystic kidney disease; Chronic renal failure symptoms. The cardiovascular system is characterized by high blood pressure, sometimes the first symptom.

Third, physical examination

How to check the polycystic kidney disease, the most simple way, the patient's regular physical examination, the patient can undergo physical examination side or bilateral kidney, was nodular. With tenderness when infected.

Fourth, auxiliary inspection

1, urine routine, early no abnormalities, in the late stage microscopic hematuria, some patients with proteinuria. With stones and infection with white blood cells and pus.
2, urine osmotic pressure determination. Early lesions only a few cysts, renal necrosis can be damaged performance, suggesting that the changes are not completely related to renal structural damage, may be associated with renal adverse diuretic hormone response. Decreased renal function decreased before glomerular filtration rate decreased.
3, serum creatinine with the loss of renal compensatory capacity was a progressive increase. Creatinine clearance is a more sensitive indicator.

PKD patients with small helper

What Treatment Can Improve Kidney Function in PKD
Patients with PKD suffer a lot, back pain, hypertension, immune system disorder and other compliments. How can patients get away from these nettlesome complications? What treatment can improve kidney function in PKD?

To improve kidney function, patients should create a good environment, which means keeping a healthy diet and good mood.
Keep a healthy diet.

Limit salt and spicy food. Salt contains sodium. Too much sodium can lead to hyponatremia, which can do harm to your blood system. Spicy food can irritate to your digestive system, diseases such as gastric ulcer, gastro spasm will be caused.
Limit protein ingestion. Avoid red meat. Our doctor suggests the high-quality low protein diet for PKD patients.
Keep a healthy lifestyle.

Take some exercise with the direction of your health care provider. Keeping a good mood can also help you avoid further damage.
Medical treatment for improving kidney function in PKD
Here we suggest you the Hot Compress Therapy to improve your kidney function.

With the using of the hot compress therapy 2 to 3 times per day, which contains Chinese herbal medicines on bilateral Shenshu Acupoints (BL23), can improve kidney function. The short course is 7 days, and the long course is 49 days.

If you want to know more please click here, Shijiazhuang kidney hospital for you

Learn about polycystic kidney disease



Definition of polycystic kidney
Polycystic kidney disease (PKD) is a genetic disorder characterized by the growth of numerous cysts in the kidneys. When cysts form in the kidneys, they are filled with fluid. PKD cysts can profoundly enlarge the kidneys while replacing much of the normal structure, resulting in reduced kidney function and leading to kidney failure. PKD is the most common inherited kidney disease, affecting an estimated 12.5 million worldwide. 1 in 10 people under 65 on dialysis has it, and 1 in 8 with a kidney transplant has it.
Types of polycystic kidney

● Autosomal dominant PKD is the most common inherited form. Symptoms usually develop between the ages of 30 and 40, but they can begin earlier, even in childhood. About 90 percent of all PKD cases are autosomal dominant PKD. Autosomal dominant PKD is the most common inherited disorder of the kidneys. The phrase "autosomal dominant" means that if one parent has the disease, there is a 50 percent chance that the disease gene will pass to a child. In some cases-perhaps 10 percent-autosomal dominant PKD occurs spontaneously in patients. In these cases, neither of the parents carries a copy of the disease gene.
● Autosomal recessive PKD is a rare inherited form. It appears in infancy or childhood. This form is much less common than autosomal dominant PKS, but it tends to be very serious and gets worse quickly. It can cause serious lung and liver disease, end-stage kidney disease, and it usually causes death in infancy or childhood.
Direct reason for polycystic kidney

Phenotypic cells turn into the cyst wall skin cells, constantly in secretory fluids, makes the cyst growing thus forming the polycystic kidney. A family history of PKD increases your risk for the condition. As many as half people with PKD have cysts on the liver. The typical characteristics of the disease is has a tendency to familial aggregation.


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