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AAKP Renal Flash
In This Issue
Take Charge of Your Healthcare with My Health
Doubling Frequency of Dialysis May Help Kidney Failure Patients
New Approach May Help Dialysis Patients Fight Anemia
Vitamin C May Improve Resistant Anemia in Hemodialysis Patients
Understanding Sudden Cardiac Death in Dialysis Patients
High Phosphorus Raises Death Risk in Peritoneal Dialysis Patients
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AAKP My Health™ now offers new features to help users take charge of their health care. Users can now:
 
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AAKP My Health™ is a free, unique section of the AAKP website, www.aakp.org, that provides you with online tools to be the leader in your healthcare. With AAKP My Health™, you can:
 
· Track your lab results
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· Test your kidney knowledge
 
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AAKP My Health™ is supported by Amgen, Inc., Astellas Pharma US, and Genzyme
December 2010 
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Doubling Frequency of Dialysis May Help Kidney Failure Patients 
dialysisKidney failure patients who double the number of weekly dialysis treatments typically prescribed had significantly better heart function, overall health and general quality of life, new research indicates. The finding stems from an analysis that compared the impact of the 40-year-old standard of care - three dialysis treatments per week, for three to four hours per session - with a six-day a week treatment regimen involving sessions of 2.5 to three hours per session.

 

The comparison involved 245 dialysis patients assigned to either a standard dialysis schedule or the high-frequency option. All participants underwent MRIs to assess heart muscle structure, and all completed quality-of-life surveys. In addition to improved cardiovascular health and overall health, the analysis further revealed that two concerns faced by most kidney failure patients - blood pressure and phosphate level control - also fared better under the more frequent treatment program.

New Approach May Help Dialysis Patients Fight Anemia
A new drug called FG-2216 can stimulate production of the hormone erythropoietin (EPO) in dialysis patients-possibly offering a new approach to treatment of kidney disease-related anemia, according to a study in the Journal of the American Society of Nephrology (JASN). Anemia is a major problem in patients with kidney disease. It is caused by low production of EPO, which has been assumed to result from damage to the kidney cells that produce EPO. The study shows this may not be the case, and that the kidneys of patients on dialysis retain significant ability to produce erythropoietin. Renal anemia seems to result from not being able to regulate EPO.

The study evaluated an experimental drug called FG-2216. Treatment with FG-2216 significantly increased EPO production in dialysis patients, as well as in healthy people with normal kidneys. The greatest increase in EPO production occurred in dialysis patients whose kidneys were still present, but no longer functioning. FG-2216 also stimulated EPO production in dialysis patients who had no kidneys. The increase in EPO production in patients without kidneys was almost as high as in people with normally functioning kidneys. In the patients without kidneys, FG-2216 apparently stimulated production of EPO by the liver.
Vitamin C May Improve Resistant Anemia in Hemodialysis Patients 
vitaminsA study suggests vitamin C may benefit hemodialysis (HD) patients with anemia resistant to treatment with erythropoietin (EPO). The study included 47 HD patients with hemoglobin (Hb) levels below 11 g/dL and hyperferritinemia (iron levels greater than 300 ng/mL). Group one received standard care; group two received standard care and 500 mg of oral vitamin C per day; and group three received standard care plus 300 mg of IV vitamin C with each dialysis session.

 

After three months, Hb, hematocrit, and TSAT increased significantly in groups two and three, but remained unchanged in group one. EPO dose decreased significantly in groups two and three, but not in group one. The researchers concluded IV and oral vitamin C therapy can improve anemia, hyperferritemia and EPO resistance in HD patients, and the effect of IV and oral vitamin C are similar.

Understanding Sudden Cardiac Death in Dialysis Patients

neph nurseApproximately 500,000 Americans require dialysis to treat kidney disease; of that population nearly half of the deaths that occur are caused by cardiovascular disease. Dialysis patients have extraordinarily high mortality rates with cardiac disease accounting for 43 percent of deaths in this population and approximately 27 percent of the mortalities are due to sudden cardiac death. Patients on dialysis are excluded from clinical trials examining sudden cardiac death because of their kidney disease. The lack of research complicates doctors' ability to understand the connection between renal disease and cardiovascular disease. The risk of cardiac arrest in dialysis patients is related to age and dialysis duration. Longer dialysis duration is associated with higher mortality.

 

By analyzing USRDS data, researchers are beginning to better understand how cardiovascular disease affects renal patients and to develop plans for preventing sudden cardiac death. The best methods for prevention are medicinal options, including beta-blockers, ACE inhibitors and angiotensin type II receptor blockers (ARB), or both external and implantable defibrillators. The research also indicates a connection between potassium levels in a patient's dialysate prescription and sudden cardiac death. Patients who suffered a cardiac arrest during dialysis were twice as likely to be on low-potassium dialysate versus higher levels of potassium, which were associated with the best survival rates.

High Phosphorus Raises Death Risk in Peritoneal Dialysis Patients
Hyperphosphatemia is associated with an increased six-year mortality risk in patients on chronic peritoneal dialysis (CPD), a new study shows. Researchers identified 12,170 CPD patients who underwent PD treatment for at least 90 days in dialysis clinics from July 2001 to June 2006. The researchers divided subjects into eight groups based on serum phosphorus level.

 

Compared with a reference value of 5.0-6.0 mg/dL, a phosphorus level greater than 7.0 was associated with increased six-year mortality risk after adjusting for demographics and co-morbid conditions. Patients with a phosphorus level of 7.0-8.0 had a 30 percent increased death risk. Patients with levels of 8.0-9.0 and 9.0 or higher had a 60 percent increased risk. Lower baseline phosphorus levels (below 5.0) appeared protective. Patients with serum phosphorus levels of 4.0-5.0, 3.0-4.0, and below 3.0 were at 21, 22, and 19 percent decreased risk of death, respectively.