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Showing posts with label Kideny Transplant. Show all posts
Showing posts with label Kideny Transplant. Show all posts

Saturday, March 28, 2009

Anaemia

What happens when you suffer from anaemia?

Anaemia is a condition in which the quantity of heamoglobin in the body goes down. Heamoglobin, as we know, is a protein that is very essential to the body. It supplies oxygen to different parts of the body and it does many other functions. If it is low, each and every part of the body gets affected. The first implication would come because there is not sufficient oxygen being transported to different areas. All parts of the body would start feeling weak.

What diet should be prescribed for an anaemic person?

I must clarify that anaemia by itself is not a disease. Anaemia is a manifestation of a particular disease. The real treatment would be to treat the cause. Say, if diet is responsible for anaemia, then taking a good diet could make a difference. There is usually a deficiency of iron or another vitamin. It could be vitamin B12, it could be folic acid or it could be pyridoxine. Deficiency of these things in the diet can lead to anaemia. In case there is iron deficiency, then one has to ensure that whatever food item one takes should contain enough of iron and it should be made available to the body; that means it should get absorbed also.

Should one take supplements or natural forms of iron?

There is no doubt that the natural forms are the best ways of supplementing. But having said it, there are certain problems. Vitamin B12 is not found in vegetarian diet. It is largely a vitamin found in non-vegetarian diet. I would not want any vegetarian to change to a non-vegetarian for the sake of vitamin B12. It is much cheaper, it is more effective and it is more social to supplement with the tablets of B12.

So, basically, if you are not getting it from your daily intake of food, then you have to supplement it with pills. What are the tests to diagnose anaemia?

Anaemia is the reduction of the haemoglobin level in the body. Normally this varies with the age and gender of the individual. According to the WHO criteria, an adult male having the haemoglobin of less than 13, an adult non-pregnant female having a haemoglobin of less than 12 and a pregnant lady having a haemoglobin of less than 11 is diagnosed as anaemic. A simple test is a complete blood count, which gives us a value of haemoglobin and certain other rates and indexes that help us to diagnose a patient as anaemic.

What are the levels of haemoglobin in children?

The values in children tend to vary from the time of birth till about the age of 12 years, though the gender differences do not come till puberty. The value for a newborn is round 13. They vary from the age of six months to one year, two years to six years and again 12 years. So, these are the criteria, which decide whether the child is anaemic or not.

How does a newborn supplement iron? Does it come entirely from the mother’s milk?

When a child is born his haemoglobin is more than the adult’s hemoglobin. Milk that he consumes is deficient in iron, just remember milk is deficient in iron, and that goes on for the whole first year of his life. That is the time by end of first year his haemoglobin drops down to as low as 11, that is normal for them. What we have to remember is that during this time he should be given iron supplementation.

Are only women affected by anaemia?

Not at all, this is a wrong notion that women are the only ones to get affected. However, women have a regular monthly blood loss. In addition to that, married women also might have blood loss during pregnancy or might even have to give away some of their iron and essential elements to the child. This is the reason why women tend to have more prevalence of anaemia as compared to men.

Is there a reserve of iron in the body?

If body needs about 100 mg of iron on a day-to-day basis, 99% of it is recycled and one milligram is taken from the diet. Now, that one milligram is sufficient to manage the requirement of 100 mg because the rest is recycled. Since it is such an essential element in the human body, nature has created a separate reserve for it. So even if somebody does not take iron for a month it should not affect him because he can fall back upon that reserve. By the time anaemia develops, these reserves would have been used up altogether.

Is it true that vegetarians are more likely to be anaemic than non-vegetarians?

The risk of a vegetarian getting into an anaemic state occurs only because of B12 deficiency. We have a large population in our country that is vegetarian. In our clinical practice, we see that most of them do not become deficient in this essential vitamin. So, a healthy person is not likely to get anaemic but there are chances that a vegetarian might get deficient in B12, which may or may not lead to anaemia.

How is thalassaemia related to anaemia?

Thalassaemia is a hereditary disorder, which presents itself as anaemia. It is a very frequent problem in India because we have a large gene pool of beta thalassaemics in India. And it presents itself, in a fashion, in a laboratory very similar to iron deficient anaemia, but there are simple tests which are available which help us distinguish between a thalassaemic and an iron deficient individual. A simple estimation of haemoglobin A2 levels and a fetal hemoglobin level estimation with the examination of the complete blood count should by and large be able to give the diagnosis.

What is bone marrow biopsy and does it help in determining anaemia?

A bone marrow biopsy is an investigative technique in which a small needle is inserted into the bone and a piece of the marrow tissue is taken out. As far as the diagnosis of anaemia is concerned, this is rarely restored to, even though staining of the bone marrow iron is supposed to be the most definitive test for iron deficiency. If a patient’s bone marrow does not stain positive for iron it means the patient is completely depleted of iron. But being an invasive technique and with the presence of so many more simple techniques available to us, we do not resort to it. However, it is an important investigation as part of the diagnosis of a patient who is having unexplained anaemia in which he would like to rule out the secondary causes of anaemia, like cancers, like leukaemia or myelodysplastic syndromes in an elderly individual.

Are chemotherapy patients more likely to be anaemic?

Certain groups of anticancer drugs, which act against the folate metabolism can cause anaemia.

By and large all anticancer drugs would have some affect on the bone marrow. Bone marrow is a factory for the production of haemoglobin. Whenever there is anaemia, it is important to check the factory, whether it is working or not. All anticancer drugs can have an affect on this bone marrow.

Is there any way to prevent anaemia?

Yes, and I think that is the best strategy. We have preventive strategies for both kind of anaemias - the hereditary type of anaemia and those that are acquired. I will take the acquired one first because they are more common. Acquired, they are from the deficiency of iron or one of the vitamins such as — B12 or deficiency of protein. It is very easy for anybody to take a healthy diet, a nutritious diet and a balanced diet. Highly processed foods destroy folic acid resulting in anaemia. One should avoid taking tea; one can take some lemon or vitamin C that helps absorb iron. When it comes to the hereditary causes, like thalassaemia: one can prevent it; in fact, some of the countries are going to eradicate thalassaemia by genetic conunselling, which is a preventive and curative measure.

Tuesday, March 10, 2009

World kidney Day

Kidney Disease is common, harmful & treatable

World Kidney Day

When?

· The second Thursday in March every year

· Thursday 12 March 2009 this year

Why?

· To raise awareness of the
importance of healthy kidneys

Who?

· People with kidney disease

· Relatives and friends of people
with kidney disease

· People at risk of kidney disease

· Healthcare professionals

· Researchers

· Health policy makers &
healthcare commissioners

· Governments

Where?

· Everywhere!

Our Kidneys are amazing!

Download a concise guide to help you keep your kidneys healthy

Languages available

English Bengali Gujarati
Hindi Urdu Vietnamese


Are your Kidneys Healthy?
To check your Risk click here

Kidney disease is often ‘silent’, causing few symptoms, especially in the early stages. If left unchecked the disease can progress or lead to kidney failure. It can severely impact on quality of life and ultimately can cost lives. Very often it comes along with other health threatening conditions, such as cardiovascular disease and diabetes.

If kidney disease is detected early, appropriate treatment can delay or even stop chronic kidney disease. It is easy to detect early signs of kidney problems by using simple tests performed by your GP.

Download copies of the Healthy Kidneys Flyer
A4 Format A3 Format

World Kidney Day on 12 March 2009

AMAZING KIDNEYS ARE YOURS HEALTHY?

World Kidney Day (WKD) is a global health awareness campaign focusing on the importance of our kidneys and reducing the frequency and impact of kidney disease and its associated health problems worldwide. The campaign is celebrated every year on the second Thursday of March in more than 100 countries on 6 continents.

World Kidney Day will be held on 12 March 2009.

"Keep the pressure down"

The 2009 campaign highlights the importance of high blood pressure as one of the key symptoms and causes of Chronic Kidney Disease (CKD).

Every year millions die prematurely of kidney failure or heart attacks and strokes linked to chronic kidney disease (CKD). WKD encourages everyone to learn more about their amazing kidneys and to raise awareness of the fact that that kidney disease is common, harmful and treatable

Take the test and see if you are at risk

Tick the box next to the questions, if your answer to them is yes.












Via: http://www.worldkidneyday.org/

Tuesday, December 16, 2008

FAQ for Kidney Patients

Q. Can I develop kidney disease?
A. Persons who are diabetic, have long-standing or severe hypertension, or have diseases involving the immune system like systemic lupus erythematosus are at risk of developing kidney disease. In addition there are some kidney diseases that run in the family. Therefore presence of family members with kidney diseases may also be an indicator of future renal disease.


Q. How do I know if I have a kidney disease?
A. The symptoms of kidney diseases depend on the nature of the disease. The most common symptoms are swelling of the feet or the face (especially on waking up), a decrease in the amount of urine passed or passage of blood or increased frothiness of urine. If the renal disease is advanced then decrease in appetite and repeated vomiting occur. It is also a good idea to find out if you have a renal disease you are under the age of 40 and have to consistently get up 2-3 times to pass urine in the night. Some patients develop aches and pains in their bones. An increase in BP could also be a manifestation of a kidney disease.


Q. What test should I undergo to find out if I have a renal disease?
A. You should undergo a thorough evaluation by your physician. Among other things, your blood pressure will be checked. Your urine should be looked at for protein as well as for pus cells or blood cells. Your blood urea and creatinine levels should also be checked.


Q. Are both of my kidneys affected?
A. Most diseases affect both the kidneys simultaneously and to the same extent. There are some diseases like stones, cancer and hypertension due to narrowing of the blood supply to kidneys where only one kidney might be affected or the two kidneys may not be involved to the same degree.


Q. I have a kidney disease. What should I do?
A. The treatment of kidney diseases depends on the nature of the kidney disease. The best method to go about it is to consult your nearest Nephrologist. As a broad principle, control of your BP and blood sugar (if high) will be important. Also, many renal diseases are chronic which means they cannot be completely cured but can be controlled with the help of medications. This means regular visits to a nephrologist. Also, many over-the-counter medicines especially commonly available pain remedies can adversely affect kidney function and you should not take any new medicine without consulting and revealing the nature of your illness to a doctor.


Q. How do I find out if there is a Nephrologist in my area?
A. The best method is to contact your physician who can guide you to a nephrologist. The other option is to get in touch with us and we shall inform you.


Q. What happens if my kidneys fail?
A. Mild kidney failure can be managed with medicines. But many kidney diseases will progress to severe kidney failure that will require kidney replacement therapy – either dialysis or kidney transplantation. In general, a person requires renal replacement therapy once the serum creatinine value is consistently above 8 mg/dl, or if symptoms of severe renal failure (loss of appetite, nausea, vomiting, loss of weight, extreme weakness, change in level of consciousness, drastic reduction in urine volume, breathlessness due to accumulation of fluid in the lungs or elevation of potassium levels in blood) appear.


Q. What is dialysis?
A. Toxic wastes and fluid generated constantly in the body as a result of the metabolic processes are normally excreted by the kidneys. Patients with kidney failure are unable to excrete them and hence they accumulate in the bloodstream and adversely affect the functioning of several organ systems. Dialysis is a process by which the blood is cleared of these substances. There are two forms of dialysis – hemodialysis and peritoneal dialysis.


Q. Can dialysis restore the function of my kidneys?
A. Dialysis acts to substitute the excretory function of the kidneys. By itself, it does not have any effect on the function of the kidneys. In some situations the kidney function can recover either spontaneously or with help of drugs, and patients require dialysis only for a short period of time. This is called acute kidney failure. The recovery may be complete or partial depending upon the type and severity of damage. In contrast to this, the kidney function does not recover in patients with chronic kidney failure and dialysis is required indefinitely or until kidney transplant is done.


Q. What does the dialysis not do?
A. Kidneys have other functions apart from the excretion of wastes and water, such as production of a hormone called erythropoietin that regulates production of red blood cells. These cells contain hemoglobin. Patients with kidney failure cannot form these cells and therefore develop a low hemoglobin. Kidneys also help in formation of active form of Vitamin D which is important in maintaining normal architecture of our bones. Dialysis cannot replace these functions and therefore other medications are required to correct these abnormalities. These problems are corrected after kidney transplantation.


Q. I have kidney failure. What kind of diet should I take?
A. Kidney failure patients are commonly advised to restrict dietary protein intake because unlimited protein consumption can worsen kidney function in patients with kidney disease. A minimum protein intake is necessary for body functions and it is important that the protein intake not be stopped completely. It is a myth that total elimination of proteins from the diet is good for these patients. In fact patients whose blood protein levels are low are likely to fare worse than those with normal levels. An average daily protein intake of 35-40 gms (depending upon the eight of the person) is essential. Patients on dialysis lose a lot of proteins, and the intake needs to be increased to approximately 60-80 gms/day once a patient is on dialysis.

The following food items contain approximately 10 gms of protein and should be taken in various combinations to meet the requirement. Cooking different types of pulses (DAL) in combination is better than anyone alone.

* A cup (~50 gms) of pulses (DAL)
* 250-300 ml of milk
* 350 gms of curd
* 60 gms of paneer (cottage cheese)
* 2 eggs (white portion only)
* chicken 40 gms
* fish 50 gms

In addition, a normal intake of calories is essential to ensure optimal utilization of proteins and therefore cereals like rice, bread etc and vegetables should be taken in normal amount.

Food items to be avoided: Green leafy vegetables (e.g. spinach), potassium rich foods (mangoes, lime, lemon, cheekoo, nuts and other dry fruits, watermelon, tomatoes, amla, jaggery, chocolate, coconut water, coffee).

Fruits that can be taken: cucumber, pineapple, apple, ripe papaya, guava, pear.

Patients who are hypertensive need to restrict their salt intake to around 4-5 gm/day. A general rule is not to add any extra salt to food items and to avoid pickles. Patients with a low urine output need to restrict intake of both salt and water.


Q. I have undergone a kidney transplant. How long do I need to take immunosuppressive medications?
A. Our immune system has been designed to protect our bodies against foreign objects such as infectious organisms by killing them. This system perceives the organ transplanted from another individual (like kidney) as a foreign object and tries to kill (reject) it. A well-matched organ such as from a close relative (e.g. parents, children and siblings) is perceived as "less foreign" than the one from a poorly matched (unrelated) donor and has less chances of getting rejected. The immunosuppressive medications (e.g. cyclosporine, azathioprine, mycophenolate and prednisolone) depress your immune system and thus serve to prevent it from rejecting the new kidney. So these drugs need to be taken for the rest of your life. The dosage, however, may need to be modified from time to time. These medicines are not required only if you have received a kidney from an identical twin. Because of financial reasons, some patients find it unable to continue taking all the drugs (especially cyclosporine) forever. In such cases, your nephrologist may allow you to slowly reduce the dose or even stop this drug altogether if he/she feels it to be safe. It is important that the drug is not stopped suddenly. We recommend that it be withdrawn at least over a 12-week period. The risk of rejection increases after withdrawal and therefore close supervision is necessary during and after withdrawal.


Q. What precautions should I take after transplant?
A. Since the immune system is our main protection against infections, patients taking immunosuppressive medications are under threat of developing severe life threatening infections. The risk is especially high in the first 6 months after transplant and in those who require treatment for rejection episodes. The nature of these infections depends upon the dose and duration of these drugs and the infectious organisms prevalent in the environment around you. After transplant, you will be prescribed certain medications that can prevent development of some of these infections. Leading a clean lifestyle is absolutely crucial. You should drink boiled/filtered water, eat clean cooked food, avoid crowded and polluted places and should be in constant touch with your nephrologist. You should also be compliant with the medicines prescribed for you. A good control of your blood pressure is also important.


Q. I wish to come to PGI Nephrology Department. How do I go about it?
A. The Nephrology department runs Renal Clinics thrice a week; on Mondays, Wednesdays and Saturdays (9 AM to 1 PM). A separate clinic is held for Renal Transplant patients on Thursdays at 2 PM. You have to first come to Medical OPD and will be referred to the Renal Clinic by the Medical OPD doctors.

Kidney Transplant - Q. & Ans.

The following will help answer questions you may have about kidney transplants.

1. What is a kidney transplant?

A kidney transplant is an operation performed by a transplant surgeon in which a healthy kidney from another person is placed into your body. Normally the non-working kidneys remain. However, in rare cases, they are removed to control infection or high blood pressure. A kidney transplant is the treatment option which is most like normal kidney function.

The new kidney performs the functions of your own non-working kidneys. Because the time spent waiting for a transplant may be lengthy, dialysis is usually required while you are waiting for your transplant.

Additionally, transplanted kidneys may not work immediately and a short period of dialysis may be required after the operation.


2. Where does a donor kidney come from?

A donor kidney may come from any of these sources:

  • Living related donors: A member of your family can donate one of their kidneys if your tissue and their tissue match. Family members who are related by birth are the most likely to have matching tissue.
  • Living unrelated donors: Sometimes people who are not related by birth are willing to donate a kidney. Usually people who are not related will not have tissue that matches yours, but it is possible.
  • Cadaver organs: A cadaver donor is a person who has recently died (usually accidentally.) These people have indicated that they would like to donate their organs when they die.
  • In most instances, donors must be adults, age 18 or older.

3. Do I have the right to refuse a transplant if a kidney becomes available?

Yes. If for any reason you are uncertain about accepting a kidney for transplant, you may decline the offer without jeopardizing your ability to receive another offer. You should discuss your concerns with your doctor.


4. How do we find a kidney that "matches" mine?

The best match for a kidney transplant is an identical twin because identical twins have perfectly matching kidneys. Brothers and sisters (by birth), or your mother or father, may also have a kidney that is compatible. The relative who wishes to donate must talk with the doctor about additional tests, the surgery, and possible risks. Tests include a complete medical evaluation, blood and urine tests, an EKG (electrocardiogram) and x-rays. To determine a good, healthy match, the following steps are done:

  • The donor's blood is tested to rule out hepatitis or AIDS
  • The blood type and tissue type are tested to see if they match (Tissue typing is done on a sample of blood and does not require taking any tissue from your skin or body.



5. What does the kidney donor have to go through? Is it dangerous?

The person who wishes to donate must talk with their doctor. The suitability of the donor depends on: 1) the donor wanting to donate a kidney, 2) normal kidneys in the donor, and 3) the kidney match being good (based on the test results) and his or her medical evaluation.

The hospital stay for the donor is usually 5-7 days. Like any major operation, there is some pain afterwards. The donor should plan for 1-2 weeks at home and 1-2 months with no heavy lifting or labor.

Many people worry donating a kidney will leave the donor in a dangerous situation. The living donor of the kidney is left with one healthy functioning kidney, which should be more than enough for the rest of the donor's life. His or her activities are not usually limited.


6. How many people have successful kidney transplants?

As of 1997, there were over 76,000 people living in the U.S. with a functioning kidney transplant. That same year, there were over 8,000 kidney transplants performed in the U.S. About a third of the patients with renal failure are eligible for a transplant.

7. How will the kidney transplant affect my lifestyle?

The transplanted kidney works 24 hours a day, doing the work of normal kidneys. This often gives the person who has the new kidney more energy than he or she had while on dialysis. Also, a working kidney keeps you healthier overall. Once you have had a kidney transplant, you can resume a fairly normal lifestyle. The kidney will react to chemical and fluid changes in the body immediately. Multiple medications will be required on a strict schedule for the rest of your life.

8. Can I travel?

Transplant patients are free to travel as long as they follow treatment guidelines. Patients should always make sure they have enough medication with them, and should always make sure to take their doctor's phone number with them.

9. Are there any diet restrictions?

Medications to prevent rejection make soMedications to prevent rejection make some patients very hungry. Since it is easy to gain weight after a transplant, you may need to watch calories closely. Some patients find it difficult to manage this weight gain, which can affect a patient's body image, or the way they feel about themselves. In addition, if you have high blood pressure, you may also need to limit the amount of sodium (salt) you eat. Protein and phosphorus are not limited as they are when you are on dialysis. A dietitian or a member of your health care team will be able to help you with any special diet recommended by your doctor. They will help you and your family select the right foods

10. Can people tell that I've had a kidney transplant?

Other than the scar that remains after a kidney transplant, there is little evidence to indicate that the surgery ever took place. However, the medications that your doctor prescribes to keep you from rejecting your transplant may result in some changes in your physical appearance. Some of these may include:

  • Weight gain
  • Increased sweating
  • Acne
  • Muscle weakness
  • Puffiness of the face and abdomen
  • Gum problems
  • Hand tremors
  • An increase in the amount of hair

Not all patients suffer from all of these side effects.


11. Will I be able to keep working and/or go to school?

Once you have received a kidney transplant and have recovered completely from the surgery, you may return to work or school outside the home as long as your health remains stable.


12. What should I know about exercise?

There are some activities you may be asked to avoid after a kidney transplant. You should discuss this with your doctor. You will be urged to pace yourself and do as much as you feel able to do. Keep busy with activities at work, at home, with family and friends, or within the community. This will help you both physically and emotionally.


13. Are kidney transplants expensive? How can I afford one?

Costs associated with a transplant can add up quickly. Few patients are able to pay all the costs from one single source. Most likely, you will have to rely on several sources. These might include: private insurance, Medicare, the Veterans Administration (VA), and prescription drugs assistance programs.

There are also costs associated with a transplant after surgery, including the cost of the anti-rejection drugs, which must be taken for as long as you have your transplanted kidney.

Ask your transplant financial team, your insurance provider, and your employee benefits officer for the latest information or help.


14. My doctor said there are medications to take after the transplant. What do they do?

As a transplant patient, you will need to take immunosuppressive medications to stop your body from rejecting the donor kidney. These medications protect the kidney from attack by your immune system. These oral medications must be taken daily for as long as you have the transplanted kidney.

Immunosuppressive medications lower your ability to fight off illness. To stay healthy, you should stay away from people who have contagious conditions such as colds, flu, or chicken pox. After you go home from the hospital, it is important that you take the correct dose of medicine, and that you visit your doctor on a regular basis. Your doctor will then be able to routinely check your kidney function and adjust your medicine as needed.

Using immunosuppressive medications has been associated with mild to severe side effects. Some of the side effects are temporary, and some are related to the dose and can be prevented by adjusting the dose. It is important to note that not everyone has all of these side effects. Some of the most common side effects include:

  • Weight gain
  • Increased sweating
  • Elevated blood pressure
  • Acne
  • Muscle weakness
  • Puffiness of the face and abdomen
  • Gum problems
  • Upset stomach
  • Hand tremors
  • Mood swings

15. What happens if my body rejects the kidney transplant?

Rejection is the major problem with kidney transplants. This means your body is trying to get rid of something that doesn't belong there. The body's immune system, which normally protects us from illness by recognizing and attacking foreign bodies such as bacteria and viruses, can also recognize a transplanted kidney as something foreign. When this happens, it tries to attack it the same way as it would with a virus. Rejection stops the transplanted kidney from working. Rejection episodes are relatively common in at least half the people in the first 3 months. Treatment for rejection includes increasing the dose of your current medications and possibly taking steroids. Of the rejection episodes, 90 to 95% occurring in the first 3 months can be reversed. However, 10 to 15% of all transplants are still lost to rejection in the first year. If the transplanted kidney is rejected totally by the body, a patient will need to return to dialysis and await another transplant. It is up to you to take your medication every day for as long as you have your new kidney. You should take it at the same time every day. The success of the kidney transplant is directly related to taking this medication.

The first 3 months after receiving a transplant are the most unstable. It is during this time that the patient is most likely to experience rejection. Clinic visits are usually scheduled once a week for the first 3 months. If all goes well during this period, you will have to see your doctor less often after this time.


16. What do I do to take care of my kidney transplant?

To keep a transplanted kidney healthy, you need to take care of it. Following treatment guidelines are key to keeping healthy. You will need to:

  • Take your immunosuppressive medicine as directed by your doctor, for as long as you have the transplanted kidney
  • Visit your doctor as scheduled
  • Follow your doctor's guidelines
  • Control your diet
  • Keep active
  • Watch for and report any problems
  • Once you have your transplanted kidney, you will continue to visit your doctor on a regular basis.
  • Clinic visits are more frequent for the first 3 months. Your doctor will check your kidney function and adjust your immunosuppressive medications.

It is up to you to take your medication for as long as you have the transplant. It is too easy to forget the transplant exists and to forget to take your medication.

Medications to prevent rejection make some patients very hungry. Since it is easy to gain weight after a transplant, you may need to watch calories more closely than on dialysis.


17. How do I know if I'm a candidate for transplant?

You must not be a substance abuser. You should be free from cancer and free from infection. You should be close to your ideal body weight. Remember that you must actively involve yourself in the process if you want to be placed on the waiting list for a transplant.


18. Is the transplant surgery dangerous for the recipient?

Same risk as any major surgery



Dialysis...continue


Benefit
In-center Hemodialysis
Peritoneal dialysis
Can have dialysis sessions at the best time for you each week
NOT ALWAYS
YES
Can easily get to know other patients and see them on a regular basis at centers
YES
NO
Can do treatment at home

NO
YES
Easy to do dialysis while traveling

NOT ALWAYS
YES
Suits someone with this attitude: "I'm independent. I preferred to learn about my treatment and be responsible for it myself."

NO
YES
Suits someone with this attitude:"When it comes to my treatment, I'm more comfortable if someone else is responsible for everything."

YES
NO
Requires a special diet and a special fluid allowance

YES
YES
Can participate in most sports and activities, except for contact sports

YES
YES
Can easily go to school or work full time

NOT ALWAYS
YES

Remember that a kidney transplant may also be options. Click on a link to find out more:
TRANSPLANT


What to ask your doctor
Chances are, this chart has confirmed for you that you should be on peritoneal dialysis. You can use this chart to talk to your doctor about the differences between PD and hemodialysis.

BACK

Dialysis

There are two types of dialysis available today - and both can help you live a healthier life without working kidneys.


Hemodialysis
Peritoneal

Something to remember: no decision is a final decision. Your dialysis needs may change as time goes by. And if you are already living with one type of dialysis, you may be a candidate for another and not know it. Talk to your doctor about any questions or concerns you have.

If you are able to make a dialysis treatment choice, you should weigh your options carefully. Give a lot of thought to your current lifestyle. You will want a dialysis treatment that disrupts your lifestyle as little as possible. This summary of the dialysis treatment options may help you decide.

Hemodialysis
Positives
Possible Negatives
Staff performs treatment (center)
Requires travel to a center
Regular contact with people in the center
Fixed treatment schedule
Three times per week
Requires a partner for home hemodialysis
No external access required
Permanent internal access
No equipment/supplies at home
Two needle sticks for each treatment
Travel not required for home hemodialysis
Diet and fluid restricted

Some risk of infection

Peritoneal Dialysis
Positives
Possible Negatives
Patient involved in self-care
Four exchanges per day
Control over schedule/freedom
Permanent external catheter
Once a month clinic visits
Some risk of infection
No needles
Potential weight gain
More steady physical condition
Supplies stored at home
Less restricted diet
Body image change

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