Kidneys are vital organs that filter blood to remove waste, extra fluid, and salt
from the body. If they stop working, it's called kidney failure. Someone with kidney
failure must go on
or get a kidney transplant.
A kidney transplant is an operation where doctors put a new kidney
in the body of someone whose own kidneys no longer work. One healthy kidney will do
the work of two failed kidneys.
Because people can survive with just one kidney, a living person can give a healthy
kidney to someone with kidney failure. This is called being a donor.
A kidney also can come from a donor who has recently died, but the wait for this kind
of donated kidney can take a year or more.
Most kidney transplants are successful. People who have kidney transplants will
take medicines for the rest of their lives to prevent the body from rejecting the
kidney. Rejecting means that the body's immune cells destroy the new kidney because
they sense that it's foreign.
But aside from that, many kids and teens who have kidney transplants go on to live
normal, healthy lives after they recover from surgery.
What Are the Different Types of Kidney Transplants?
There are two kinds of kidney transplants depending on who donates the new kidney.
A living-donor transplant is when someone gets a kidney from a
person who is still alive and well. It's usually from a relative or close friend,
but sometimes strangers donate.
A deceased-donor transplant is when people donate their kidneys
for transplant after they die. This requires people who need kidneys to put their
names on a waiting list until a donor is found.
What Happens Before a Kidney Transplant?
If your child needs a kidney transplant, your first step is to visit a transplant
center. The health care team will check to make sure that your child is healthy enough
to have surgery and take the medicines needed after the transplant. This will include
blood tests, X-rays, and other tests, and can take a few weeks or months.
If the transplant team decides your child is a good candidate, the next step is
to find a kidney. In most cases for living donor transplants, a kidney comes from
a close relative or friend who has a compatible blood type.
If a living donor isn't found, your child's name will go on a waiting list until
a kidney from a deceased donor is matched to your child. The need for new kidneys
is far greater than the number donated, so this can take a long time.
You'll stay in close touch with the doctors and the rest of the health care team.
Make sure they know how to reach you at all times. When a kidney is located, you'll
need to go to the transplant center at a moment's notice.
While you wait for a transplant, keep your child as healthy as possible. That way,
he or she will be ready for transplant surgery when the time comes. Help your child:
eat healthy foods and follow any special diet recommendations from the doctor,
nurse, or dietitian
take all medicines as directed
keep all medical appointments
Tell your doctor and the transplant center right away if is any change in your
What Happens During a Kidney Transplant?
The doctors will take a blood sample so they can do an antibody cross-match
test. This is done to find out if your child's immune system will accept
the new kidney. If the test comes back negative, the kidney is acceptable. Other blood
test and imaging studies are done before the transplant.
In the operating room, your child will get general anesthesia
to sleep through the operation. Then the surgeon makes a small cut in the lower belly,
just above your child's hips. The new kidney is placed, and the surgeon attaches its
blood vessels (artery and vein) to blood vessels in the lower body. Then the new kidney's
(a tube that carries pee from the kidney to the bladder) is connected
to the bladder.
In most cases, the old kidneys stay in place. Failed kidneys aren't removed unless
they cause problems like high
blood pressure or an infection. Kidney transplant surgery usually takes about
3 to 4 hours. If your child needs more than one organ (such as a combined kidney–liver
transplant), the surgery time will be longer.
What Happens After a Kidney Transplant?
After kidney transplant surgery, your child will spend a few days (or up to a week)
in the hospital to recover. The health care team will watch closely to make sure there
are no complications from the surgery, such as bleeding or infection.
You and your child will learn about the medicines needed to keep the body from
rejecting the new kidney. These are called immunosuppressants. Taking
them can make your child more likely to get infections, especially in the days right
after surgery. So keep your child away from sick people, and have everyone at home
wash their hands well and often.
For the first couple of months after surgery, you'll see the doctor often to make
sure the new kidney is working well. If your child gets a fever or soreness
in the area of the transplant, tell a doctor right away. These could be signs
that the body isn't accepting the new kidney or that your child has an infection.
How Can I Help My Child?
Having a chronic condition can be hard for kids. Dialysis, surgery, and immunosuppressant
therapy can add to the stress. Talk to your child about these changes and how you
will work them into your routine. Make sure to find time to do fun things together
with family and friends.
For teens, immunosuppressant therapy can be a challenge. These medicines can cause:
getting acne or having acne that gets worse
mood swings and anxiety
trouble sleeping at night
problems with increased blood sugars (or diabetes), sometimes requiring insulin
high blood pressure
increased risk of infection
These side effects are a major reason why teens are at risk for not taking their
medicines after a transplant. This can be dangerous and even lead to rejection of
the new kidney. Do not change or stop any medicines without talking to your doctor
or nurse. In some cases, medicines can be changed to ease the side effects and still
be effective and safe. Talk to about the importance of taking all medicines as directed,
and help your child to do so.
Be there for your child to talk to.
If your child needs more support, make an appointment with a therapist
for yourself too. It can be a huge relief to talk about your feelings with other people
who know what you're going through. Ask the transplant care team if they know of support
groups for families.