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Learning about Stem Cell Transplant in Children

What is it?

A stem cell transplant replaces damaged stem cells with healthy ones. Stem cells are special cells made in the bone marrow. They become red blood cells, white blood cells, platelets, and more stem cells. The procedure is sometimes called a bone marrow transplant.

A stem cell transplant may be needed if your child has a disease such as leukemia, lymphoma, or some kinds of blood or bone marrow diseases.

Having the transplant is a serious decision that you and your child's treatment team will make. The procedure is risky. It's a long and often painful process. Success depends on the type and stage of your child's disease and your child's age and general health. A transplant doesn't work for every child who gets one. But when it works, it can increase the chances of remission or cure of the disease.

How is it done?

The stem cell transplant procedure has several stages. Parts of the treatment may be done in a hospital. Others may be done in an outpatient centre. How long your child's treatment takes will depend on your child's disease, how your child responds to the treatment, and any problems he or she may have from the treatment. The doctor can tell you more about this.

Testing

Your child will first have tests to make sure that his or her health is good enough for the chemotherapy (chemo) and radiation that are part of the procedure. This may take a few days to several weeks.

Deciding on treatment

You and the doctor will look at your child's test results and discuss the physical and emotional challenges your child will face. Based on these things, you might go ahead with the transplant. Or you might choose some other treatment instead.

There are three types of stem cell transplants:

  • The stem cells come from your child's own body (autologous). Your child's blood is sent through a machine that separates stem cells from the blood. The cells are stored until your child needs them for transplant.
  • The stem cells come from a donor (allogeneic). The donor may take medicine to help make more stem cells. Then the stem cells are taken from the donor's blood or bone marrow and given to your child.
  • The stem cells come from umbilical cord blood. The umbilical cord is usually thrown away after birth. But the blood inside the cord can be saved, or banked, to be used later if needed. The cord blood can come from one or more donors. Or it can come from your child if you banked the cord blood when your child was born.

Conditioning

Your child will have chemo and radiation to kill any remaining cancer or bone marrow cells and to prepare his or her body for the new stem cells. This can take 1 to 2 weeks. Your child may have side effects, such as mouth sores, nausea, hair loss, and poor appetite. The side effects may last several weeks to months. But the doctor can give your child medicine to help ease them.

Transplant

After the bone marrow cells are killed, the healthy stem cells are put into your child's bloodstream. This is called infusion. It usually takes about an hour. The stem cells travel through the blood to your child's bone marrow. The infused stem cells will start to make new stem cells in 1 to 4 weeks. These cells will then take over the job of making new blood cells.

Your child may spend up to 4 weeks or longer in the hospital after the transplant.

The chemo and radiation destroy your child's white blood cells. Without them, your child's body can't fight infection. The doctor may give your child medicine to help protect your child from getting an infection while the body is making new white blood cells. Caregivers, family, and other visitors may need to take extra steps during this time to protect your child from infection.

What can you expect afterward?

Your child's immune system will need time to get back to normal. It may take several years.

Your child will need constant care after going home. Your child may need to stay near the transplant centre for the first 3 months. For the next year, your child will see the doctor and have his or her blood tested often. During this time, the doctor may restrict your child from some activities, such as going to school or being in public places, until concerns about infection go away.

Your child may get blood transfusions until your child's body can make enough blood cells on its own. If the stem cells came from a donor, the doctor will check for signs that your child's body is rejecting the cells or that the new cells are attacking other cells in the body (graft-versus-host disease). The doctor will want to see your child if there's any sign of an infection.

Follow-up care is a key part of your child's treatment and safety. Be sure to make and go to all appointments, and call your doctor or nurse call line if your child is having problems. It's also a good idea to know your child's test results and keep a list of the medicines your child takes.

Where can you learn more?

Go to https://www.healthwise.net/patientEd

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