Heart Transplant

What is a heart transplant?

A heart transplant is surgery to remove the diseased heart from a person and replace it with a healthy one from an organ donor. To remove the heart from the donor, two or more healthcare providers must declare the donor brain-dead.

Before you can be put on a waiting list for a heart transplant, a healthcare provider makes the decision that this is the best treatment choice for your heart failure. A healthcare team also makes sure you are otherwise healthy enough to go through the transplant process.

Why might I need a heart transplant?

You may need a heart transplant if your heart is failing and other treatments are not effective.

End-stage heart failure is the
final stage of heart failure. The heart muscle is failing severely in its attempt to
pump blood through the body. Other treatments are no longer working. Despite its name, a
diagnosis of heart failure does not mean
the heart is about to stop beating. The term failure means the heart muscle is failing
to pump blood normally because it is damaged, very weak, or both.

Some causes of heart failure include:

  • Heart attack (myocardial infarction or MI)
  • Viral infection of the heart muscle
  • High blood pressure
  • Heart valve disease
  • Heart defects present at birth (congenital)
  • Irregular heartbeats (arrhythmias)
  • High blood pressure in the lungs (pulmonary hypertension)
  • Alcoholism or substance abuse
  • Chronic lung diseases, such as emphysema or chronic obstructive pulmonary disease (COPD)
  • Enlarged, thick, and stiff heart
    muscle (cardiomyopathy)
  • Low red blood cell count (anemia)

Your healthcare provider may have other reasons to recommend a heart transplant.

What are the risks of a heart transplant?

As with any surgery, complications
may occur. Potential risks of a heart transplant may include:

  • Infection
  • Bleeding during or after the
  • Blood clots that can cause heart
    attack, stroke, or lung problems
  • Breathing problems
  • Kidney failure
  • Coronary allograft vasculopathy (CAV).
    This is a problem with the blood vessels that carry blood to the heart muscle itself.
    They become thick and hard. This can cause serious heart muscle damage.
  • Rejection or failure of the donor
  • Death

Your body’s immune system may
reject the new heart. Rejection is your body’s normal reaction to a foreign object or
tissue. When you get a new heart, your immune system reacts to what it sees as a foreign
threat and attacks the new organ. To allow the transplanted organ to survive in a new
body, you will need to take anti-rejection medicines. The medicines will trick the
immune system into accepting the transplanted organ and keep the immune system from
attacking it.

You will need to take the medicines
to prevent or treat rejection for the rest of your life. These drugs have side effects
too. The side effects will depend on the specific medicines you take. It’s important
that you continue to take these medicines as prescribed by your healthcare provider. You
also need to keep up with regular follow-up appointments to monitor the heart
transplant and reduce your chances for rejection.

Other risks may include:

  • Current or repeated infections that do
    not get better with treatment
  • Poor blood circulation throughout the
    body, including the brain
  • Metastatic cancer. This is when cancer
    has spread from the place it started to one or more other places in the body.
  • Severe health problems that would make
    you unable to tolerate the surgery
  • Serious health problems other than
    heart disease that would not get better after transplant
  • Substance or alcohol abuse

There may be other risks depending
on your specific health condition. Be sure to discuss any concerns with your healthcare
provider before the surgery.

How do I get ready for a heart transplant?

Not everyone is a candidate for
heart transplant. A wide range of information is needed to determine if a person is
eligible for transplant. A transplant team will evaluate the information. The team
includes a transplant surgeon, a transplant cardiologist (doctor specializing in the
treatment of the heart), nurse practitioners or physician assistants, one or more
transplant nurses, a social worker, and a psychiatrist or psychologist. Other team
members may include a dietitian, a chaplain, hospital administrator, and an
anesthesiologist (doctor who uses medicines to keep you asleep during surgery).

The transplant evaluation process will include:

  • Psychological and social evaluation. Some psychological and social issues that are involved in organ transplant include stress, financial issues, and support from family or significant others. These factors can greatly affect how you do after the transplant.
  • Blood tests. You will need blood tests to help find a good donor match and help improve the chances that the donor heart will not be rejected.
  • Diagnostic tests. You will need tests
    to assess your lungs as well as your overall health. These tests may include X-rays,
    ultrasounds, CT scan, pulmonary function tests (PFTs), right heart catheterization,
    and dental exams. Women may need a Pap test, gynecology evaluation, and a
  • Other preparations. You will get several vaccines to decrease the chances of developing infections that can affect the transplanted heart.

The transplant team will consider all the information from interviews, your health history, the findings from your physical exam, and your diagnostic test results when deciding if you are eligible for a heart transplant.

Once you have been accepted as a transplant candidate, you will be placed on the United Network for Organ Sharing list. When a donor organ becomes available, candidates are selected based on the severity of their condition, body size, and blood type. If the heart is to be yours, you will need to go to the hospital right away so you can get ready for the transplant. (Most hearts must be transplanted within 4 hours after they’ve been removed from the donor.)

These things will need to be done before the transplant:

  • Your healthcare provider will explain the procedure and let you ask questions.
  • You will be asked to sign a consent form that gives your permission to do the surgery. Read the form carefully and ask questions if anything is unclear.
  • You should not eat or drink anything (fast) as soon as you have been told that a heart has become available.
  • You may be given medicine to help you relax (sedative).
  • Based on your health condition, your healthcare provider may request other specific preparation.

What happens during a heart transplant?

A heart transplant requires open heart surgery and a stay in a hospital. Procedures may vary depending on your condition and your healthcare provider’s practice.

Generally, a heart transplant follows this process:

  1. You will be asked to remove any jewelry or other objects that may interfere with the procedure.
  2. You will change into a hospital gown.
  3. A healthcare professional will start
    an IV (intravenous) line in your hand or arm to inject medicine and to give IV
    fluids. Additional catheters will be put into the blood vessels in your neck and
    wrist to monitor the status of your heart and blood pressure, and to take blood
    samples. Other sites may be used for additional catheters, including under the
    collarbone and the groin.
  4. A soft, flexible tube (Foley catheter) will be put into your bladder to drain urine.
  5. A tube will be put through your mouth or nose into your stomach to drain stomach fluids.
  6. If there is a lot of hair on your
    chest, it may be clipped or shaved.
  7. You will be given general anesthesia
    to put you in a deep sleep during surgery. . Once you are asleep, a breathing tube
    will be put through your mouth into your lungs. The tube will be attached to a
    machine (ventilator) that will breathe for you during the surgery.
  8. The anesthesiologist will watch your heart rate, blood pressure, and blood oxygen level during the surgery.
  9. The skin over your chest will be cleaned with an antiseptic solution.
  10. The surgeon will make a cut (incision) down the center of your chest from just below the Adam’s apple to just above the navel.
  11. The surgeon will cut the breastbone
    (sternum) in half. Once cut, the surgeon will separate the two halves of the
    breastbone and spread them apart to reach your heart.
  12. The surgeon will put tubes into your chest so that your blood can be pumped through your body by a heart-lung (cardiopulmonary bypass) machine while your heart is stopped and replaced.
  13. Once the blood has been completely
    diverted into the bypass machine and is being pumped by the machine, your surgeon
    will remove the diseased heart.
  14. The surgeon will sew the donor heart
    into place. Once your new heart is in place, they will connect the blood vessels
    carefully so there are no leaks.
  15. When your new heart is fully connected, the blood circulating through the bypass machine will be allowed back into the heart and the tubes to the machine are removed. Your surgeon will shock the heart with small paddles to restart the heartbeat.
  16. Once your new heart starts to beat, the healthcare team will watch the heart to see how it’s working and make sure there are no leaks.
  17. Wires for pacing may be put into the heart. Your surgeon can attach these wires to a pacemaker outside your body for a short time to pace your new heart, if needed, during the initial recovery period.
  18. The surgeon will rejoin the sternum and sew it together with small wires.
  19. The surgeon will sew the skin over the
    sternum back together using stitches or surgical staples to close the incision.
  20. Tubes will be put into your chest to drain blood and other fluids from around the heart. These tubes will be connected to a suction device to drain fluids away from the heart as it heals.
  21. A sterile bandage or dressing will be applied.