Kidney Dialysis | In Depth
We understand that you may have a lot of questions when dialysis is being considered as a treatment option for your child.
- What is it?
- How long will it take?
- How will it help my child get better?
We’ve tried to provide some answers to those questions here, and when you meet with our experts, we can explain your child’s options fully.
It’s important to remember that filtering blood is one of several roles the kidneys play in your child’s body. Dialysis takes over that function, but your child may also need to follow a special diet and take medicines to compensate for the other things that a fully functioning kidney may do, such as regulating certain vitamins and minerals.
Does my child have to go to the hospital for dialysis?
Not necessarily. There are two types of dialysis: peritoneal dialysis, which is performed at home; and hemodialysis, which is performed at the hospital or at a dialysis center.
What’s the difference between peritoneal dialysis and hemodialysis?
Peritoneal dialysis and hemodialysis use two different methods to reach the same goal: cleaning your child’s blood. Neither has been scientifically proven to be more effective than the other.
Which type of dialysis is right for my child?
Both types of dialysis are effective treatments. In most cases, you can choose the type of dialysis that works best for your child’s and your family’s specific situation. Your child’s doctor will be happy to discuss your options with you.
Regardless of which option you choose, our staff will make sure that you have all the information and training you need to take care of your child.
Peritoneal dialysis
Peritoneal dialysis can be performed at home. Most families who choose this option do continuous cyclic peritoneal dialysis (CCPD), an automatic process that uses a special dialysis machine. CCPD can be done while your child is asleep.
How does peritoneal dialysis work?
Peritoneal dialysis works by filling your child’s abdomen with a special solution called dialysate. The dialysate absorbs waste from your child’s blood the way water absorbs powdered iced tea mix. After the dialysate has absorbed the waste from your child’s blood, it drains out of the abdomen.
The process of filling your child’s abdomen with dialysate, giving it time to absorb the waste from the blood, and draining out of their body is known as an “exchange.”
How is peritoneal dialysis performed?
First, your child’s surgeon will insert a soft, hollow tube (catheter) into your child's abdomen, near the navel. This is a permanent tube that will carry the dialysate in and out of the abdomen. It is not uncomfortable and easily concealed under clothes.
Each night, as your child sleeps, the dialysis machine will automatically:
- measure out the correct amount of dialysate
- bring it to the correct temperature
- transfer it to your child's abdomen through the catheter
The dialysate will stay in the abdomen, cleaning and filtering blood, for a period of time determined by your child's doctor. Then it will drain back out through the catheter into a sterile drainage bag that is emptied each morning.
This constitutes one exchange, and usually takes about an hour. Generally, around 10 exchanges are performed automatically each night.
Hemodialysis
Hemodialysis is performed in a hospital or in a dialysis center.
Your child is connected to a large machine called a dialyzer that takes blood out of the body in a continuous process, cleans and filters it, and returns it to your child's bloodstream. Only a very small amount of their blood is filtered at a time.
Several weeks before your child’s first treatment, their doctor or another dialysis specialist will create an “access point." This is an opening though which blood is transported to the dialyzer and then back into your child’s body after it has been cleaned.
Depending on your child’s age and how long the course of dialysis is likely to be, the access point might be:
- a catheter: a small, soft tube inserted into one of your child’s main blood vessels, often under their collarbone or in their neck
- an arteriovenous (AV) fistula: a surgeon will connect two blood vessels in your child’s arm. This access point may be used for longer-term dialysis. This requires that the hemodialysis be performed through two tubes connected to needles that must be placed into the fistula. This reduces the risk of infection that comes with using a catheter.
How often will my child need to have hemodialysis performed?
Hemodialysis is generally performed three times per week, and younger children may need it four times per week.
How long does each session take?
Each hemodialysis session lasts between three and four hours. If you are going to a dialysis center, it can be helpful to bring games or reading materials for your child. At Boston Children's Hospital, our Child Life specialists and other dialysis staff members help make sure your child is comfortable and can take part in constructive play and/or provide tutoring as appropriate.
Hemodialysis is much more efficient than peritoneal dialysis, and therefore does not need to be performed every day.
Long-term outlook
What’s the long-term outlook for my child?
Unfortunately, chronic kidney disease is irreversible, and most children on dialysis will need a kidney transplant. at some point. Thanks to efforts on the part of Boston Children's and other institutions, children under 18 are automatically placed at the top of the waiting list for donor kidneys.
FAQ
Q: Does my child have to go to the hospital for dialysis?
A: Not necessarily. There are two types of dialysis: peritoneal dialysis is performed at home; and hemodialysis is performed at the hospital or at a dialysis center.
Q: Which type of dialysis is right for my child?
A: Both types are effective treatments. In most cases, you can choose the type of dialysis that works best for your child’s and your family’s specific situation. Your child’s doctor will be happy to discuss your options with you.
Please be assured that regardless of which option you choose, our staff will make sure that you have all the information and training you need to take care of your child.
Q: What’s the long-term outlook for my child?
A: Unfortunately, chronic kidney disease is irreversible, and most children on dialysis will need a kidney transplant at some point. Thanks to efforts on the part of Boston Children’s and other institutions, children under 18 are automatically moved to the top of the waiting list for donor kidneys.
Questions to ask your doctor
Lots of parents find it helpful to jot down questions before their visit with their child’s doctors to be sure all of their concerns are addressed.
If your child is old enough, you may want to suggest that they write down questions for their doctors too.
Some of the questions you may want to ask include:
- What factors should I take into consideration when choosing between peritoneal dialysis and hemodialysis?
- What nutritional concerns should I be aware of when my child is on dialysis?
- What are my child’s options if they need to go to college or want to travel?
Emergency preparedness
Despite the best planning, an emergency can still occur. If so, knowing what to do can make a stressful situation much easier to deal with.
If you cannot leave your home, call Boston Children’s Dialysis Unit at 617-355-5997 for instructions.
Explore these online resources for helpful information and checklists about:
- meal planning
- infection control for dialysis patients after a disaster
More in-depth, detailed information is available here:
- Preparing for emergencies (Centers for Medicare and Medicaid Services)
Boston Children's Hospital contact numbers:
- Dialysis Unit: 617-355-5997
- Operator: 617-355-6000 and ask for the renal fellow on call
END STAGE RENAL DISEASE ACT |
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In 1972, Congress passed the End Stage Renal Disease Act, ensuring that Medicare will cover dialysis and kidney transplants for anyone who with end stage renal disease who is eligible for Social Security. |
Kidney Dialysis | Research
Boston Children’s Hospital is home to the world’s most extensive research enterprise at a pediatric hospital. In our End Stage Renal Disease Program — which includes the dialysis unit and our Kidney Transplant Program — our treatment is informed by our research.
We also have a great number of partnerships with top research, biotech and health care organizations and we work together to improve kids’ health.
Our Transplant Research Program provides a rich environment for collaboration of scientists and physicians in the areas of transplantation and immunology. We currently participate in more NIH-sponsored pediatric kidney transplant research studies than any other program in the nation.
If your child has end-stage renal disease, dialysis can filter their blood, but not take over the other roles of the kidney, such as regulating the amounts of some important vitamins and minerals released into the bloodstream and controlling blood pressure. For that, your child needs to take medication and follow a special diet. Our researchers are currently involved in several clinical trials to assess the safety and efficacy of medications aimed at fulfilling this pharmaceutical component of treating end-stage renal disease.
We’re committed to developing better anti-rejection medication with the goal of more successful transplants and fewer side effects.