Diabetic kidney disease is also known as diabetic nephropathy. Diabetic nephropathy is kidney damage that results from having diabetes. Having high blood glucose levels due to diabetes can damage the part of the kidneys that filters your blood. The damaged filter becomes ‘leaky’ and lets protein into your urine. If this goes untreated/ poorly managed for too long it can severely increase your risks of chronic kidney disease progression and further increasing the likelihood of needing to start dialysis.

Florida Kidney Physicians is proud to announce that we are actively involved in clinical research. Our goal is to provide better access to more advanced treatment therapies within the local communities.

What does clinical research mean for patients within our communities?  

Our nephrologists are specifically trained to be leading experts in preventative and proactive treatments for diabetic kidney disease. However, in some instances, the default standard of care may not be enough. That is why our nephrologists are at the forefront of advanced therapies targeted at the most effective treatment protocols for attenuating the long term effects of diabetic kidney disease. Our Nephrologists conduct clinical research in all facets of Kidney health. Access to such advanced treatment protocols is usually something only available through University based Hospitals- At FKP we strive to bridge that gap; Florida Kidney Physicians is a complex, multi-center clinical research facility.

How do I know if I would be considered eligible to participate in a clinical trial?

Identifying diabetic kidney disease is difficult to do without proper laboratory assessments. If you are aware of any current kidney related issues or someone in your family has a history of dialysis, schedule an appointment to come see us for a consultation or give us a call.

If you are interested in learning more, please contact:

Neal A. Patel Director of Clinical Research


Phone: (561) 351-7822.


We are very grateful to everyone that came to the Pig Jig event this past weekend 🐖. Florida Kidney Physicians was proud to be one of the sponsors supporting this event that raises money for Nephcure, a non-profit organization committed to supporting research, improving treatment and finding a cure for the debilitating kidney disease, FSGS.

We would like to thank you all for helping FKP support Tampa Pig Jig 2018. 🐽 ❤️

Tampa Nephrologists at Pig Gig


By Doctor Alberto Casaretto.

What do my Kidneys Do?

  1. Clean your blood of waste and toxins.
  2. Regulates the extracellular fluid volume, the kidneys work to ensure an adequate quantity of plasma to keep blood flowing to vital organs.
  3. Regulation of osmolality of blood.
  4. Production of Hormones. Erythropoietin – is made in the kidney and is an important hormone in the production of blood in your bones.
  5. Regulates the concentration of important electrolytes like Potassium, Sodium, and Calcium.

How do I Know if I have Kidney disease?

If you have been to your Primary care doctor recently and had blood work, you have probably had your kidney function checked. The two blood tests that check for Kidney disease is Blood Urea Nitrogen (BUN) and Creatinine. Blood Urea nitrogen is a waste product that your Liver makes when it breaks down protein and Creatinine is a waste product made in your Muscles. When your BUN and Creatinine are elevated, we say you have a kidney problem since the Kidney is the organ that removes these two waste products from your body. Another test that is used to evaluate your kidneys filtering ability is Estimated Glomerular Filtration rate (eGFR).

When do I need to see a Nephrologist (Kidney Doctor)?

Since Kidney disease is typically a silent disease- there are no symptoms until kidney disease is severe, the only way to know if you have kidney disease is to check your blood work- specifically BUN and creatinine. Also if you have blood or protein in your Urine- these are signs that you may have damage to some of your filters in the Kidney. You should also consider seeing a Kidney doctor if your eGFR is less than 60.

What can I do to protect my Kidneys?

  1. Stay Hydrated-One of the easiest ways to keep your kidney healthy is to drink enough water. It is recommended that you drink at least 1 1/2 liters of water per day.
  2. Eat Healthy- Avoid High Salt diets.
  3. Watch your Blood Pressure
  4. Exercise regularly
  5. Stop smoking

Are there medications that could be harmful for my Kidneys?

If you have Chronic Kidney disease you should be careful with Non- steroidal -Anti-inflammatory medications (such as Ibuprofen and Naproxen). Some Antibiotics can also damage the Kidney- especially if the duration of the antibiotics is extended.
Some of the contrast dyes that are used for radiologic test can also be toxic to the Kidney such as the contrast used for CAT scans and Cardiac catheterizations. If you have kidney disease – talk to your doctor before doing these tests.


Diabetes, like many chronic diseases, may co-exist with mental health conditions like depression. For some patients with diabetes that can lead to a third problem.

Researchers from the University of Toronto found that people with diabetes, who were also depressed, had an increased risk of developing chronic kidney disease (CKD).

Diabetes affects every cell in the body. When your blood sugar is too high–especially over a period of time–it can cause significant cellular damage.

The longer a patient has diabetes the more likely he or she is to develop complications like heart disease, eye damage, skin problems, nerve damage, kidney damage, and even kidney failure.

Marta Novak, MD, Ph.D., of the University of Toronto, led the study of more than 933,000 patients who also had diabetes. The patients were selected from a larger group of more than three million US veterans who had signs of kidney disease.

Researchers used the glomerular filtration rate (GFR) to determine kidney damage. The GFR is is an indication of how well the kidneys can filter urine. A normal GFR is 90 or above. Patients in the study had a GFR of 60 or above.

At the time they enrolled in the study 340,806 of the patients had been diagnosed with depression.

Dr. Novak and her colleagues found that patients who had diabetes and were depressed were younger, had a higher GFR and were more likely to have other problems–known as comorbidities.

180,343 of the patients developed chronic kidney disease (CKD). Patients who were depressed were more likely to develop CKD and having depression was also linked to all causes of death.

The research does not indicate depression causes CKD in people with diabetes, only that there is a link between the two.

The study was published in the June issue of Diabetes Care.

Information on study funding and conflict of interest was not available.


  • HealthDay, “Depression linked to CKD in patients with diabetes”
  • Diabetes Care, “Increased Risk of Incident Chronic Kidney Disease, Cardiovascular Disease, and Mortality in Diabetic Patients Wi
  • Mayo Clinic, “Diabetes”
  • National Kidney Foundation, “Glomerular Filtration Rate”
  • Image Courtesy of Tyler Olson |

Promote superior care for patients, provide exceptional services to physicians, and create a fulfilling environment for teammates!  That is the Lifeline mission statement.

At Lifeline Vascular Access Center Fort Lauderdale, the physicians and clinical care team take pride in delivering dedicated, compassionate and highly specialized procedures for those in need of vascular services. Our patients receive proactive care, early intervention, and are able to maintain a quality of life that is all too often compromised by disease.

Through this early detection and timely resolution of access dysfunction, the physicians at our outpatient center are better able to ensure the best possible outcomes for every patient we treat, resulting in fewer missed dialysis treatments and a lower frequency of complications which may lead to hospitalization*.

Since opening in 2014, Lifeline Vascular Access Center Fort Lauderdale has had over 3,500 patient encounters, and has sustained an impressive 99% overall procedure success rate.  Under the new physician leadership of FKP Nephrologist, Dr. Reinaldo Rosario, M.D., our continuing goal is to serve the patients within the community in a dedicated, positive, environment and provide them with superior care.

We are committed to ensuring that that with each and every visit, our patients can expect to be treated the same: as the most important patient in our center!

Lifeline Vascular Access Center Ft. Lauderdale, as part of the Lifeline Vascular Access system of centers, is accredited by The Joint Commission is located 2283 SW 2ndStreet, Pompano Beach, FL, 33069. For more information about the facility and our services, call 954-978-7932 or visit us on the web at

*Based on a study conducted by Dobson | DaVanzo & Associates, published in Seminars in Dialysis 26.5 (2013), “Clinical and Economic Value of Performing Dialysis Vascular Access Procedures in a Freestanding Office-Based Center as Compared with the Hospital Outpatient Department among Medicare ESRD Beneficiaries”.


Evidence of a substantial heritability of diabetic kidney disease (DKD) exists but the genetic background is poorly understood.
Diabetes and kidneys
New data confirm that renal complications in type 1 diabetes mellitus (T1DM) are highly heritable and provide insights into the biological mechanisms of DKD.basics diabetic nephropaty
To comprehensively study the genetic architecture of DKD in T1DM, Niina Sandholm and colleagues — on behalf of the SUMMIT consortium — performed a meta-analysis of genome-wide association studies, which included data from 12,540 individuals. They also used whole-exome sequencing to investigate the effects of low-frequency and rare genetic variants in 997 patients with T1DM.
“We found strong heritability estimates for DKD; additive genetic factors were estimated to explain 35% of the phenotypic variance and even higher heritability estimates werobtained for more extreme phenotypic definitions,” says Sandholm. The analyses did not, however, identify novel susceptibility loci with robust evidence or confirm many previously published associations. The findings suggest that there are no low-frequency variants with a major effect on DKD risk.
Using data from their meta-analysis, the researchers show thabasics diabetic nephropatyt sets of alleles thaincrease body mass index and genetic risk scores for type 2 diabetes are associated with an increased risk of DKD, whereas smoking cessation might have a protective effect.
In addition, they identified potential roles of ascorbate and aldarate metabolism and pentose and glucuronate interconversion pathways in the pathogenesis of DKD.
The researchers are now performing a meta-analysis of data from nearly 18,000 patients with T1DM in the JDRF-DNCRI consortium to identify common and low-frequency genetic variation. They hope thathisanalysis will identify novel susceptibility loci for DKD and provide biological information in relation to other traits and diseases.
ORIGINAL ARTICLE Sandholm, N. etal. The geneticlandscape of renal complications in type 1 diabetes. J. Am. Soc. Nephrol.


Why is Monitoring Phosphorus Important in Chronic Kidney Disease (CKD), End Stage Renal Disease (ESRD) and Dialysis?

10 Things ESRD CKD and Dialysis patients need to know about Phosphorus:

1.     Phosphorus is a very common and important mineral element in the body, symbol P.

2.     Phosphorus is found in meat, dairy products, dark cola (non translucent), beans, nuts, and in some food additives, especially in processed foods.

3.     Phosphorus is important in bone metabolism and in maintaining the proper pH (acidity) of the blood stream.

4.     When Phosphorus is combined with oxygen, it is called phosphate.

5.     Healthy kidneys maintain a proper level of blood Phosphorus by eliminating excessive Phosphorus in the urine.

6.     Patients with ESRD and CKD can retain too much phosphorus, called hyperphosphatemia.

7.     High levels of phosphorus combine (bind) with Calcium. Calcium can come out of the bones and lead to weak bones (renal osteodystrophy). The Phosphorus-Calcium complexes can also be deposited into organs and blood vessels, leading to hardening of these organs.

8.     CKD, ESRD, Dialysis, and Hemodialysis patients are counseled to follow a diet that limits the amount of phosphorous-containing foods they eat.

9.     CKD, ESRD, Dialysis and Hemodialysis patients are often prescribed phosphorus-binding medications. Phosphorus-binding medications are usually taken before meals to help prevent phosphorus from being absorbed from the intestines.
Dialysis patients have their blood level of phosphorus measured every month to keep the phosphorus level in the appropriate range.

If you are a CKD, ESRD, Dialysis, and Hemodialysis, talk to your FKP Physicians.



Peritoneal Dialysis

What do I Need to Know?


With peritoneal dialysis (PD), you have some choices in treating advanced and permanent kidney failure. Since the 1980s, when PD first became a practical and widespread treatment for kidney failure, much has been learned about how to make PD more effective and minimize side effects. Since you don’t have to schedule dialysis sessions at a center, PD gives you more control. You can give yourself treatments at home, at work, or on trips. But this independence makes it especially important that you work closely with your healthcare team: your nephrologist, dialysis nurse, dialysis technician, dietitian, and social worker. But the most important members of your health care team are you and your family. By learning about your treatment, you can work with your health care team to give yourself the best possible results, and you can lead a full, active life.

When Your Kidneys Fail
Healthy kidneys clean your blood by removing excess fluid, minerals, and wastes. They also make hormones that keep your bones strong and your blood healthy. When your kidneys fail, harmful wastes build up in your body, your blood pressure may rise, and your body may retain excess fluid and not make enough red blood cells. When this happens, you need treatment to replace the work of your failed kidneys.
How PD Works

In PD, a soft tube called a catheter is used to fill your abdomen with a cleansing liquid called dialysis solution. The walls of your abdominal cavity are lined with a membrane called the peritoneum, which allows waste products and extra fluid to pass from your blood into the dialysis solution. The solution contains a sugar called dextrose that will pull wastes and extra fluid into the abdominal cavity. These wastes and fluid then leave your body when the dialysis solution is drained. The used solution, containing wastes and extra fluid, is then thrown away. The process of draining and filling is called an exchange and takes about 30 to 40 minutes. The period the dialysis solution is in your abdomen is called the dwell time. A typical schedule calls for four exchanges a day, each with a dwell time of 4 to 6 hours. Different types of PD have different schedules of daily exchanges.

One form of PD, continuous ambulatory peritoneal dialysis (CAPD), doesn’t require a machine. As the word ambulatory suggests, you can walk around with the dialysis solution in your abdomen. Another form of PD, continuous cycler-assisted peritoneal dialysis (CCPD), requires a machine called a cycler to fill and drain your abdomen, usually while you sleep. CCPD is also sometimes called automated peritoneal dialysis (APD).

Peritoneal dialysis.Getting Ready for PD

Whether you choose an ambulatory or automated form of PD, you’ll need to have a soft catheter placed in your abdomen. The catheter is the tube that carries the dialysis solution into and out of your abdomen. If your doctor uses open surgery to insert your catheter, you will be placed under general anesthesia. Another technique requires only local anesthetic. Your doctor will make a small cut, often below and a little to the side of your navel (belly button), and then guide the catheter through the slit into the peritoneal cavity. As soon as the catheter is in place, you can start to receive solution through it, although you probably won’t begin a full schedule of exchanges for 2 to 3 weeks. This break-in period lets you build up scar tissue that will hold the catheter in place.
The standard catheter for PD is made of soft tubing for comfort. It has cuffs made of a polyester material, called Dacron, that merge with your scar tissue to keep it in place. The end of the tubing that is inside your abdomen has many holes to allow the free flow of solution in and out.

Types of PD
The type of PD you choose will depend on the schedule of exchanges you would like to follow, as well as other factors. You may start with one type of PD and switch to another, or you may find that a combination of automated and nonautomated exchanges suits you best. Work with your health care team to find the best schedule and techniques to meet your lifestyle and health needs.
Continuous Ambulatory Peritoneal Dialysis (CAPD)

If you choose CAPD, you’ll drain a fresh bag of dialysis solution into your abdomen. After 4 to 6 or more hours of dwell time, you’ll drain the solution, which now contains wastes, into the bag. You then repeat the cycle with a fresh bag of solution. You don’t need a machine for CAPD; all you need is gravity to fill and empty your abdomen. Your doctor will prescribe the number of exchanges you’ll need, typically three or four exchanges during the day and one evening exchange with a long overnight dwell time while you sleep.
Continuous Cycler-Assisted Peritoneal Dialysis (CCPD)
CCPD uses an automated cycler to perform three to five exchanges during the night while you sleep. In the morning, you begin one exchange with a dwell time that lasts the entire day.

Customizing Your PD
If you’ve chosen CAPD, you may have a problem with the long overnight dwell time. It’s normal for some of the dextrose in the solution to cross into your body and become glucose. The absorbed dextrose doesn’t create a problem during short dwell times. But overnight, some people absorb so much dextrose that it starts to draw fluid from the peritoneal cavity back into the body, reducing the efficiency of the exchange. If you have this problem, you may be able to use a minicycler (a small version of a machine that automatically fills and drains your abdomen) to exchange your solution once or several times overnight while you sleep. These additional, shorter exchanges will minimize solution absorption and give you added clearance of wastes and excess fluid.
If you’ve chosen CCPD, you may have a solution absorption problem with the daytime exchange, which has a long dwell time. You may find you need an additional exchange in the mid-afternoon to increase the amount of waste removed and to prevent excessive absorption of solution.

Preventing Problems
Infection is the most common problem for people on PD. Your health care team will show you how to keep your catheter bacteria-free to avoid peritonitis, which is an infection of the peritoneum. Improved catheter designs protect against the spread of bacteria, but peritonitis is still a common problem that sometimes makes continuing PD impossible. You should follow your health care team’s instructions carefully, but here are some general rules:
-Store supplies in a cool, clean, dry place.
-Inspect each bag of solution for signs of contamination before you use it.
-Find a clean, dry, well-lit space to perform your exchanges.
-Wash your hands every time you need to handle your catheter.
-Clean the exit site with antiseptic every day.
-Wear a surgical mask when performing exchanges.

Keep a close watch for any signs of infection and report them so they can be treated promptly. Here are some signs to watch for:
-Nausea or vomiting
-Redness or pain around the catheter
-Unusual color or cloudiness in used dialysis solution

Equipment and Supplies for PD
Transfer Set
A transfer set is tubing that connects the bag of dialysis solution to the catheter. When your catheter is first placed, the exposed end of the tube will be securely capped to prevent infection. Under the cap is a universal connector.

When you start dialysis training, your dialysis nurse will provide a transfer set. The type of transfer set you receive depends on the company that supplies your dialysis solution. Different companies have different systems for connecting to your catheter.

Connecting the transfer set requires sterile technique. You and your nurse will wear surgical masks. Your nurse will soak the transfer set and the end of your catheter in an antiseptic solution for 5 minutes before making the connection. The nurse will wear rubber gloves while making the connection.

Depending on the company that supplies your solution, your transfer set may require a new cap each time you disconnect from the bag after an exchange. With a different system, the tubing that connects to the transfer set includes a piece that can be clamped at the end of an exchange and then broken off from the tubing so that it stays on the transfer set as a cap until it is removed for the next exchange. Your dialysis nurse will train you in the aseptic (germ-free) technique for connecting at the beginning of an exchange and disconnecting at the end. Follow instructions carefully to avoid infection.

Transfer set. Between exchanges, you can keep your catheter and transfer set hidden inside your clothing. At the beginning of an exchange, you will remove the disposable cap from the transfer set and connect it to a Y-tube. The branches of the Y-tube connect to the drain bag and the bag of fresh dialysis solution. Always wash your hands before handling your catheter and transfer set, and wear a surgical mask whenever you connect or disconnect.

During an exchange, you can read, talk, watch television, or sleep.

The first step of an exchange is to drain the used dialysis solution from the peritoneal cavity into the drain bag. Near the end of the drain, you may feel a mild “tugging” sensation that tells you most of your fluid is gone.

After the used solution is removed from your abdomen, you will close or clamp the transfer set and let some of the fresh solution flow directly into the drain bag. This flushing step removes air from the tubes.

The final step of the exchange is to refill the peritoneal cavity with fresh dialysis solution from the hanging bag.

Dialysis Solution
Dialysis solution comes in 1.5-, 2-, 2.5-, or 3-liter bags. A liter is slightly more than 1 quart. The dialysis dose can be increased by using a larger bag, but only within the limit of the amount your abdomen can hold. The solution contains a sugar called dextrose, which pulls extra fluid from your blood. Your doctor will prescribe a formula that fits your needs.
You’ll need a clean space to store your bags of solution and other supplies. You may also need a special heating device to warm each bag of solution to body temperature before use. Most solution bags come in a protective outer wrapper that allows for microwave heating. Do not microwave a bag of solution after it has been removed from its wrapper because microwaving can change the chemical makeup of the solution.

The cycler-which automatically fills and drains your abdomen, usually at night while you sleep-can be programmed to deliver specified volumes of dialysis solution on a specified schedule. Most systems include the following components:

-Solution storage. At the beginning of the session, you connect bags of dialysis solution to tubing that feeds the cycler. Most systems include a separate tube for the last bag because this solution may have a higher dextrose content so that it can work for a day-long dwell time.

-Pump. The pump sends the solution from the storage bags to the heater bag before it enters the body and then sends it to the disposal container or drain line after it’s been used. The pump doesn’t fill and drain your abdomen; gravity performs that job more safely.

-Heater bag. Before the solution enters your abdomen, a measured dose is warmed to body temperature. Once the solution is the right temperature and the previous exchange has been drained, a clamp is released to allow the warmed solution to flow into your abdomen.

-Fluid meter. The cycler’s timer releases a clamp to let the used dialysis solution drain from your abdomen into a disposal container or drain line. As the solution flows through the tube, a fluid meter in the cycler measures and records how much solution has been removed. Some systems compare the amount of solution inserted with the amount drained and display the net difference between the two volumes. This lets you know whether the treatment is removing enough fluid from your body.

-Disposal container or drain line. After the used solution is weighed, it’s pumped to a disposal container that you can throw away in the morning. With some systems, you can dispose of the used fluid directly by stringing a long drain line from the cycler to a toilet or bathtub.

-Alarms. Sensors will trigger an alarm and shut off the machine if there’s a problem with inflow or outflow.

Testing the Effectiveness of Your Dialysis
To see if the exchanges are removing enough waste products, such as urea, your health care team must perform several tests. These tests are especially important during the first weeks of dialysis to determine whether you’re receiving an adequate amount, or dose, of dialysis.
The peritoneal equilibration test (often called the PET) measures how much sugar has been absorbed from a bag of infused dialysis solution and how much urea and creatinine have entered into the solution during a 4-hour exchange. The peritoneal transport rate varies from person to person. If you have a high rate of transport, you absorb sugar from the dialysis solution quickly and should avoid exchanges with a very long dwell time because you’re likely to absorb too much solution from such exchanges.
In the clearance test, samples of used solution drained over a 24-hour period are collected, and a blood sample is obtained during the day when the used solution is collected. The amount of urea in the used solution is compared with the amount in the blood to see how effective the PD schedule is in removing urea from the blood. For the first months or even years of PD treatment, you may still produce small amounts of urine. If your urine output is more than several hundred milliliters per day, urine is also collected during this period to measure its urea concentration.
From the used solution, urine, and blood measurements, your health care team can compute a urea clearance, called Kt/V, and a creatinine clearance rate (adjusted to body surface area). The residual clearance of the kidneys is also considered. These measurements will show whether the PD prescription is adequate.
If the laboratory results show that the dialysis schedule is not removing enough urea and creatinine, the doctor may change the prescription by

-increasing the number of exchanges per day for patients treated with CAPD or per night for patients treated with CCPD
-increasing the volume of each exchange (amount of solution in the bag) in CAPD
-adding an extra, automated middle-of-the-night exchange to the CAPD schedule
-adding an extra middle-of-the-day exchange to the CCPD schedule

One of the big problems with PD is that patients sometimes don’t perform all of the exchanges prescribed by their medical team. They either skip exchanges or sometimes skip entire treatment days when using CCPD. Skipping PD treatments has been shown to increase the risk of hospitalization and death.

Remaining Kidney Function
Normally the PD prescription factors in the amount of residual, or remaining, kidney function. Residual kidney function typically falls, although slowly, over months or even years of PD. This means that more often than not, the number of exchanges prescribed, or the volume of exchanges, needs to increase as residual kidney function falls.

The doctor should determine your PD dose on the basis of practice standards established by the National Kidney Foundation Dialysis Outcomes Quality Initiative (NKF-DOQI). Work closely with your health care team to ensure that you get the proper dose, and follow instructions carefully to make sure you get the most out of your dialysis exchanges.

Conditions Related to Kidney Failure and Their Treatments
Your kidneys do much more than remove wastes and extra fluid. They also make hormones and balance chemicals in your system. When your kidneys stop working, you may have problems with anemia and conditions that affect your bones, nerves, and skin. Some of the more common conditions caused by kidney failure are fatigue, bone problems, joint problems, itching, and restless legs.

Anemia and Erythropoietin (EPO)
Anemia is a condition in which the volume of red blood cells is low. Red blood cells carry oxygen to cells throughout the body. Without oxygen, cells can’t use the energy from food, so someone with anemia may tire easily and look pale. Anemia can also contribute to heart problems.
Anemia is common in people with kidney disease because the kidneys produce the hormone erythropoietin (EPO), which stimulates the bone marrow to produce red blood cells. Diseased kidneys often don’t make enough EPO, and so the bone marrow makes fewer red blood cells. EPO is available commercially and is commonly given to patients on dialysis.

Renal Osteodystrophy
The term “renal” describes things related to the kidneys. Renal osteodystrophy, or bone disease of kidney failure, affects up to 90 percent of dialysis patients. It causes bones to become thin and weak or malformed and affects both children and adults. Symptoms can be seen in growing children with kidney disease even before they start dialysis. Older patients and women who have gone through menopause are at greater risk for this disease.

Itching (Pruritus)
Many people treated with peritoneal dialysis complain of itchy skin. Itching is common even in people who don’t have kidney disease; with kidney failure, however, itching can be made worse by uremic toxins in the blood that dialysis doesn’t adequately remove. The problem can also be related to high levels of parathyroid hormone (PTH). Some people have found dramatic relief after having their parathyroid glands removed. But a cure that works for everyone has not been found. Phosphate binders seem to help some people; others find relief after exposure to ultraviolet light. Still others improve with EPO shots. A few antihistamines (Benadryl, Atarax, Vistaril) have been found to help; also, capsaicin cream applied to the skin may relieve itching by deadening nerve impulses. In any case, taking care of dry skin is important. Applying creams with lanolin or camphor may help.

Sleep Disorders
Patients on dialysis often have insomnia, and some people have a specific problem called sleep apnea syndrome. Episodes of apnea are breaks in breathing during sleep. Over time, these sleep disturbances can lead to “day-night reversal” (insomnia at night, sleepiness during the day), headache, depression, and decreased alertness. The apnea may be related to the effects of advanced kidney failure on the control of breathing. Treatments that work with people who have sleep apnea, whether they have kidney failure or not, include losing weight, changing sleeping position, and wearing a mask that gently pumps air continuously into the nose, called nasal continuous positive airway pressure (CPAP).
Many people on dialysis have trouble sleeping at night because of aching, uncomfortable, jittery, or restless legs. You may feel a strong impulse to kick or thrash your legs. Kicking may occur during sleep and disturb a bed partner throughout the night. Theories about the causes of this syndrome include nerve damage and chemical imbalances.
Moderate exercise during the day may help, but exercising a few hours before bedtime can make it worse. People with restless leg syndrome should reduce or avoid caffeine, alcohol, and tobacco; some people also find relief with massages or warm baths. A class of drugs called benzodiazepines, often used to treat insomnia or anxiety, may help as well. These prescription drugs include Klonopin, Librium, Valium, and Halcion. A newer and sometimes more effective therapy is levodopa (Sinemet), a drug used to treat Parkinson’s disease.
Sleep disorders may seem unimportant, but they can impair your quality of life. Don’t hesitate to raise these problems with your nurse, doctor, or social worker.

Dialysis-related amyloidosis (DRA) is common in people who have been on dialysis for more than 5 years. DRA develops when proteins in the blood deposit on joints and tendons, causing pain, stiffness, and fluid in the joints, as is the case with arthritis. Working kidneys filter out these proteins, but dialysis is not as effective [Top]

Adjusting to Changes
You can do your exchanges in any clean space, and you can take part in many activities with solution in your abdomen. Even though PD gives you more flexibility and freedom than hemodialysis, which requires being connected to a machine for 3 to 5 hours three times a week, you must still stick to a strict schedule of exchanges and keep track of supplies. You may have to cut back on some responsibilities at work or in your home life. Accepting this new reality can be very hard on you and your family. A counselor or social worker can help you cope.

Many patients feel depressed when starting dialysis, or after several months of treatment. Some people can’t get used to the fact that the solution makes their body look larger. If you feel depressed, you should talk with your social worker, nurse, or doctor because depression is a common problem that can often be treated effectively.

How Diet Can Help
Eating the right foods can help improve your dialysis and your health. You may have chosen PD over hemodialysis because the diet is less restrictive. With PD, you’re removing wastes from your body slowly but constantly, while in hemodialysis, wastes may build up for 2 or 3 days between treatments. You still need to be very careful about the foods you eat, however, because PD is much less efficient than working kidneys. Your clinic has a dietitian to help you plan meals. Follow the dietitian’s advice closely to get the most from your dialysis treatments. You can also ask your dietitian for recipes and titles of cookbooks for patients with kidney disease. Following the restrictions of a diet for kidney failure might be hard at first, but with a little creativity, you can make tasty and satisfying meals.


Do you have Symptoms of Kidney Failure? Symptoms occur when your kidney function is less than 15%

Many people may be in the early stages of Kidney Failure and not have any indication something is wrong with their kidneys. There are certain symptoms, however, that could be a sign you have kidney failure, whether it is acute renal failure or hereditary such as Polycystic Kidney Disease. When kidney failure (also called renal failure) is detected in the early stages, there are steps you can take to help slow the progression of kidney disease and improve your quality of life.

Below are lists of kidney failure symptoms that are grouped in categories based on a typical cause. If you have any of these renal failure symptoms, you should make an appointment with your doctor as soon as possible and ask that your kidneys be checked:

-Kidney failure symptoms from buildup of wastes in the body
-A metallic taste in the mouth or ammonia breath
-Protein aversion (no longer wanting to eat meat)
-Nausea and vomiting
-Difficulty concentrating
-Loss of appetite
-Itchiness (pruritis)
-Kidney failure symptoms from buildup of fluid in the body
-Swelling in the face, feet or hands
-Shortness of breath (from fluid in the lungs)
-Kidney failure symptoms from damage to the kidneys
-Making more or less urine than usual
-Blood in the urine (typically only seen through a microscope)
-Urine that is foamy or bubbly (may be seen when protein is in the urine)
-Kidney failure symptoms from anemia
-Shortness of breath
-Mental confusion
-Feeling cold all the time
-Desire to chew ice, clay or laundry starch (called pica)

To determine if the symptoms you have are because of kidney failure, your doctor will perform specific tests:
-Urinalysis – An examination of a sample of your urine to check for protein, blood and white blood cells in the urine
-Blood tests – Particularly a test for creatinine and BUN, waste products that healthy kidneys remove from the bloodstream.
-Take action when you have kidney failure symptoms.

Often, early kidney problems don’t have many symptoms—but if you are experiencing any of the ones mentioned above, you will want to see your doctor to determine if your signs are caused by kidney failure. Write down any of the renal failure symptoms you may have and bring that information with you to your next doctor’s appointment. Whether you discover that your kidneys are okay or if you learn you have kidney problems, knowing about it sooner may ease your mind and allow you to take steps to slow the progress of kidney disease, including delay or prevent dialysis or a kidney transplant.


Copyright by Florida Kidney Physicians.