Tuesday, June 16, 2015

Polycystic Kidney Disease (PKD) Clinic Avoid Dialysis

ADPKD is the most common of all the hereditary cystic kidney diseases. It affects approximately 600,000 people in the U.S. alone and occurs in approximately one in every 400 to 1,000 live births. ADPKD is characterized by progressive cyst development and bilaterally enlarged kidneys with multiple cysts. There are two genetic mutations, PKD1 and PKD2.

Treat infections early to prevent further kidney damage. Individuals with PKD are especially prone to kidney, bladder and urinary tract infections. In order to avoid further damaging the kidneys, it is important for infections to be treated promptly with antibiotics. An untreated infection can lead to further, irreversible damage to the kidneys.

Get regular checkups. Going to the doctor once or twice a year for a checkup and blood work can help your doctor detect complications, infections and massive cysts that can speed up the progression of PKD to end-stage kidney failure. Preventive care can slow the progression of the disease through early treatment intervention.

Undergo kidney dialysis or kidney transplant. According to the National Kidney and Urological Diseases Information Clearinghouse, 50 percent of the 600,000 Americans suffering from PKD will eventually require dialysis, removal of one or both kidneys and a kidney transplant. Once the kidneys are no longer able to function on their own, PKD sufferers will have to prepare themselves for dialysis and the possibility of a kidney transplant. kidneyhospitalabroad@hotmail.com

Patients with ADPKD should avoid long-term exposure to nephrotoxic agents or medications in order to manage their condition including:


  • Caffeine - which may promote renal cyst growth
  • Estrogen - which may be contraindicated in those with associated severe polycystic liver disease
  • Smoking

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