A heart transplant is an operation performed to replace a diseased heart with a healthy one from another person.
A heart transplant is recommended for children who have serious heart dysfunction and will not be able to live without having the heart replaced. Some of the illnesses that affect the heart in this way include complex congenital (present at birth) heart disease and cardiomyopathy (disease of the heart muscle in which the heart loses its ability to pump blood effectively).
The number of children who need heart transplants varies from year-to-year.Visit the United Network for Organ Sharing (UNOS) website for statistics of patients awaiting a heart transplant, and the number of patients who underwent a transplant this year.
Hearts that are transplanted come from organ donors. Organ donors are adults or children who have become critically ill (often due to an accidental injury) and will not live as a result of their illness or injury. If the donor is an adult, he/she may have agreed to be an organ donor before becoming ill. Parents or spouses can also agree to donate a relative's organs. Donors can come from any part of the United States. This type of transplant is called a cadaveric transplant.
The United Network for Organ Sharing (UNOS) is responsible for transplant organ distribution in the United States. UNOS oversees the allocation of many different types of transplants, including liver, kidney, pancreas, heart, lung, and cornea.
UNOS receives data from hospitals and medical centers throughout the country regarding adults and children who need organ transplants. The medical team that currently follows your child is responsible for sending information to UNOS and updating them as your child's condition changes.
Criteria have been developed to ensure that all people on the waiting list are judged fairly as to the severity of their illness and the urgency of receiving a transplant. Once UNOS receives the data from local hospitals, people waiting for a transplant are placed on a waiting list and given a "status" code. The people in most urgent need of a transplant are placed highest on the status list and are given first priority when a donor heart becomes available.
When a donor organ becomes available, a computer searches all the people on the waiting list for a heart and sets aside those who are not good matches for the available heart. A new list is made from the remaining candidates. The person at the top of the specialized list is considered for the transplant. If he or she is not a good candidate, for whatever reason, the next person is considered, and so forth. Some reasons that people lower on the list might be considered before a person at the top include the size of the donor organ and the geographical distance between the donor and the recipient.
An extensive evaluation must be completed before your child can be placed on the transplant list. Testing includes:
Tests are done to gather information that will help determine how urgent it is that your child be placed on the transplant list, as well as to ensure the child receives a donor organ that is a good match. These tests include those to analyze the general health of the body, including the child's heart, lung, and kidney function, the child's nutritional status, and the presence of infection.
Blood tests will help improve the chances that the donor organ will not be rejected. These tests may include:
The diagnostic tests that are performed are extensive, but necessary to understand the complete medical status of your child. The following are some of the other tests that may be performed, although many of the tests are decided on an individual basis:
The transplant team will consider all information from interviews, your child's medical history, physical examination, and diagnostic tests in determining whether your child can be a candidate for heart transplantation.
After the evaluation, if your child is considered a good candidate for a heart transplant, he or she will be placed on the UNOS list.
The group of specialists involved in the care of children who are undergoing a transplant procedure is often referred to as the "transplant team." Team members work together to provide the best chance for a successful transplant. The heart transplant team consists of:
There is no definite answer to this question. Sometimes, children wait only a few days or weeks before receiving a donor organ. It may also take months or years on the waiting list before a suitable donor organ is available. During this time, your child will receive close follow-up from his or her doctor and the transplant team. Various support groups are also available to assist you during this waiting time.
A major problem affecting the availability of hearts for transplant is that these organs cannot come from living donors. Kidney transplants often come from a living donor; both the person who donated a kidney and the recipient are able to live with just one remaining kidney. New techniques are making it possible for some people in need of a liver transplant to receive part of an organ from a living donor; both the recipient and the donor may be able to live successfully with just a segment of a liver. However, an entire heart is needed for a human to live. Neither donor nor recipient can live with only a segment of a heart. Therefore, people in need of a heart transplant must wait for the death of a person who generously decided to share his or her organs.
Availability of donors for heart transplantation is also affected by the size of the child needing the transplant. For instance, an adult donor heart cannot be transplanted into an infant because the infant's chest is simply too small to accommodate the large organ. Children must wait for an appropriately sized organ to become available. However, as of May 15, 2000, new UNOS guidelines were established to give preference to children under 18 on the waiting list before adults whenever a heart from an adolescent donor (ages 11 to 17) becomes available.
Each transplant team has its own specific guidelines regarding waiting on the transplant list and being notified when a donor organ is available. In most instances, you will notified by phone or pager that an organ is available. You will be told to come to the hospital immediately so your child can be prepared for the transplant.
Once an organ becomes available to your child, you and your child will be immediately called to the hospital. This call can occur at any time, so you should always be prepared to go to the hospital, if needed. Once at the hospital, the child will have some more final blood work and tests to confirm the match of the organ.
The child will then go to the operating room. The transplant surgery may require several hours, but will vary greatly depending on each individual case. During the surgery, a member of the transplant team will keep you informed on the progress of the transplant.
After the surgery, your child will go to the intensive care unit (ICU) to be monitored closely. The length of time your child will spend in the ICU will vary based on your child's unique condition. After your child is stable, he or she will be sent to the special unit in the hospital that cares for heart transplant patients. Your child will continue to be monitored closely. You will be educated on all aspects of caring for your child during this time. This will include information about medications, activity, follow-up, diet, and any other specific instructions from your child's transplant team.
Rejection is a normal reaction of the body to a foreign object. When a new heart is placed in your child's body, the body sees the transplanted organ as a threat and tries to attack it. The immune system makes antibodies to try to destroy the new organ, not realizing that the transplanted heart is beneficial. To allow the organ to successfully live in a new body, medications must be given to trick the immune system into accepting the transplant and not thinking it is a foreign object.
The following are the most common signs and symptoms of rejection. However, each child may experience symptoms differently. Symptoms may include:
Your child's transplant team will instruct you on who to call immediately if any of these symptoms occur.
Medications must be given for the rest of the child's life to fight rejection. Each child is unique, and each transplant team has preferences for different medications. Some of the antirejection medications most commonly used include the following:
Because antirejection medications affect the immune system, children who receive a transplant will be at higher risk for infections. A balance must be maintained between preventing rejection and making your child very susceptible to infection. Blood tests are performed periodically to measure the amount of medication in the body to ensure your child does not get too much or too little of the medication. White blood cell counts are also an important indicator of how much medication your child needs.
This risk of infection is especially great in the first few months because higher doses of antirejection medicines are given during this time. Your child will most likely need to take medications to prevent other infections from occurring. Some of the infections your child will be especially susceptible to include oral yeast infections (thrush), herpes, and respiratory viruses.
Your child will have very close follow-up with the transplant team after leaving the hospital. This will allow for close monitoring of your child and the function of the transplanted heart. Follow-up visits may include the following:
Children who have received a heart transplant will need lifelong follow-up with doctors who are specialized in transplant medicine. Keeping appointments with your child's transplant doctor, as well as maintaining contact with the transplant team when symptoms of rejection occur is vital. Parents (and the recipient, when old enough) are the first line of defense; they must understand and recognize the signs and symptoms of rejection and report them as soon as possible to the transplant team.
Living with a transplant is a lifelong process. Medications must be given that trick the immune system so it will not attack the transplanted organ. Other medications must be given to prevent side effects of the antirejection medications, such as infection. Frequent visits to and contact with the transplant team are essential. Knowing the symptoms of organ rejection (and watching for them on a daily basis) is critical. When the child becomes old enough, he or she will need to learn about antirejection medications (what they do and the signs of rejection), so he or she can eventually care for himself or herself independently.
Every child is unique and every transplant is different. Results continually improve as doctors and scientists learn more about how the body deals with transplanted organs and search for ways to improve transplantation.
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