What Is a Heart Transplant?
A heart transplant is surgery to remove a person's
diseased heart and replace it with a healthy heart from a deceased donor.
Ninety percent of heart transplants are done on patients who have end-stage
heart
failure.
Heart failure is a condition in which the heart is
damaged or weakened and can't pump enough blood to meet the body's needs.
"End-stage" means the condition has become so severe that all treatments, other
than heart transplant, have failed.
Overview
Heart transplants are done as a life-saving measure
for end-stage heart failure when medical treatment and less drastic surgery
have failed.
Because donor hearts are in short supply, patients
who need a heart transplant go through a careful selection process. They need
to be sick enough to need a new heart, yet healthy enough to receive it.
Survival rates for people receiving heart
transplants have improved over the past 5 to 10 years, especially
in the first year after the transplant.
About 88 percent of patients survive the first year
after transplant surgery, and 72 percent survive for 5
years. The 10-year survival rate is close to 50 percent, and 16
percent of heart transplant patients survive 20 years.
After the surgery, most heart transplant recipients
(about 90 percent) can come close to resuming their normal lifestyles. However,
fewer than 40 percent return to work for many different reasons.
The Heart Transplant Process
The heart transplant process starts when doctors
refer patients who have end-stage heart failure to a heart transplant center
for evaluation. Patients found to be eligible for a heart transplant are placed
on a waiting list for a donor heart.
Heart transplant surgery is done in a hospital when
a suitable donor heart is found. After the transplant, patients are started on
a lifelong health care plan. The plan involves multiple medicines and frequent
medical checkups.
Who Needs a Heart Transplant?
Who Is Referred to a Heart Transplant Center?
Most patients referred to a heart transplant center
have end-stage
heart
failure. Of these patients, close to half have heart failure as a result of
coronary
heart disease (also called coronary artery disease).
Others have heart failure caused by hereditary
conditions, viral infections of the heart, or damaged heart valves and muscles.
(Some medicines, alcohol, and pregnancy can damage the heart valves and
muscles.)
Most patients considered for a heart transplant have
tried other, less drastic treatments and have been hospitalized a number of
times for heart failure.
Who Is Eligible for a Heart Transplant?
The heart transplant specialists at the heart
transplant center will determine whether a patient is eligible for a
transplant. Specialists often include a:
- Cardiologist (a doctor who specializes in
diagnosing and treating heart problems)
- Cardiovascular surgeon (a doctor who does the
transplant surgery)
- Transplant coordinator (a person who makes
arrangements for the surgery, such as transportation of the donor heart)
- Social worker
- Dietitian
- Psychiatrist
In general, patients selected for heart transplants
have severe end-stage heart failure, but are healthy enough to have the
transplant. Heart failure is considered end stage when all possible
treatmentssuch as medicine, implanted devices, and surgeryhave
failed.
Patients who have the following conditions might not
be candidates for heart transplant surgery because the procedure is less likely
to be successful.
- Advanced age. Although there's no widely accepted
upper age limit for a heart transplant, most transplant surgery is done on
patients younger than 70 years old.
- Poor blood circulation throughout the body,
including the brain.
- Kidney, lung, or liver diseases that can't be
reversed.
- History of cancer or malignant tumors.
- Inability or unwillingness to follow lifelong
medical instructions after a transplant.
- Pulmonary
hypertension (high blood pressure in the lungs) that can't be reversed.
- Active infection throughout the body.
What To Expect Before a Heart Transplant
The Heart Transplant Waiting List
Patients who are eligible for a heart transplant are
placed on a waiting list for a donor heart. This waiting list is part of a
national allocation system for donor organs run by the
Organ Procurement and
Transplantation Network (OPTN).
OPTN has policies in place to make sure donor hearts
are given out fairly. These policies are based on urgency of need, the organs
that are available for transplant, and the location of the patient who is
receiving the heart (the recipient).
Organs are matched for blood type and size of donor
and recipient.
The Donor Heart
Guidelines on how a donor heart is selected require
that the donor meet the legal requirement for brain death and that the
appropriate consent forms are signed.
Guidelines suggest that the donor be younger than 65
years old, have little or no history of heart disease or trauma to the chest,
and not be exposed to hepatitis or HIV. The guidelines also recommend that the
donor heart not be without blood circulation for more than 4 hours.
Waiting Times
Approximately 3,000 people in the United States are
on the waiting list for a heart transplant on any given day. About 2,000 donor
hearts are available each year. Wait times vary from days to several months and
will depend on a recipient's blood type and condition.
A person may be taken off the list for some time if
he or she has a serious medical event such as a stroke, infection, or kidney
failure.
Time spent on the waiting list plays a part in who
receives a donor heart. For example, if a donor heart becomes available and two
recipients have equal need, the recipient who has been waiting longer usually
will get the heart.
Ongoing Medical Treatment
Patients on the waiting list for a donor heart
receive ongoing treatment for
heart
failure and other medical conditions.
Treating
arrhythmias
(irregular heartbeats), for example, is very important because they can cause
sudden
cardiac arrest in people who have heart failure.
As a result, many transplant centers will place
implantable
cardioverter defibrillators (ICDs) in patients before surgery. An ICD is a
small device that's placed in the chest or abdomen to help control
life-threatening arrhythmias.
Another treatment that may be recommended to waiting
list patients is an implanted mechanical pump called a
ventricular assist device (VAD). This device
helps the heart pump blood.
Regular outpatient care for waiting list patients
may include frequent exercise testing, assessing the strength of the heartbeat,
and right
cardiac
catheterization (a test to measure blood pressure in the right side of the
heart).
Contact With the Transplant Center During the Wait
People on the waiting list often are in close
contact with their transplant centers. Most donor hearts must be transplanted
within 4 hours after removal from the donor.
At some heart transplant centers, recipients get a
pager so the center can contact them at any time. They're asked to tell the
transplant center staff if they're going out of town. Recipients often need to
be prepared to arrive at the hospital within 2 hours of being notified about a
donor heart.
Not all patients who are called to the hospital will
get a heart transplant. Sometimes, at the last minute, doctors find that a
donor heart isn't suitable for a patient. Other times, patients from the
waiting list are called to come in as possible substitutes, in case something
happens with the selected recipient.
What To Expect During a Heart Transplant
Just before the heart transplant surgery, patients
will get general anesthesia (AN-es-THE-ze-a). The term "anesthesia" refers to a
loss of feeling and awareness. General anesthesia temporarily puts you to
sleep.
A bypass machine is hooked up to the arteries and
veins of the heart. The machine pumps blood through the patient's lungs and
body while the diseased heart is removed and the donor heart is sewn into
place.
Heart Transplant
Figure A shows where
the diseased heart is cut for removal. Figure B shows where the transplanted
healthy heart is sutured (stitched) to the recipient's arteries and veins.
Heart transplant surgery usually takes about 4
hours. Patients often spend the first days after surgery in the intensive care
unit of the hospital.
What To Expect After a Heart Transplant
In the Hospital
The amount of time a heart transplant recipient
spends in the hospital will vary with each person. It often involves 1 to 2
weeks in the hospital and 3 months of monitoring by the transplant team at the
heart transplant center.
Monitoring may include frequent
blood
tests,
lung
function tests,
EKGs
(electrocardiograms),
echocardiograms,
and biopsies of the heart tissue.
A heart biopsy is a standard test used to see
whether your body is rejecting the new heart. It might be done often in the
weeks after a transplant.
During a heart biopsy, a tiny grabbing device is
inserted into a vein in the neck or groin (upper thigh). The device is threaded
through the vein to the right atrium of the new heart to take a small tissue
sample. The tissue sample is checked for signs of rejection.
While in the hospital, your health care team may
recommend that you start a
cardiac
rehabilitation (rehab) program. Cardiac rehab is a medically supervised
program that helps improve the health and well-being of people who have heart
problems.
Cardiac rehab includes counseling, education, and
exercise training to help you recover. Rehab may start with a member of the
rehab team helping you sit up in a chair or take a few steps. Over time, you'll
increase your activity level.
Watching for Signs of Rejection
The new heart is a foreign body that
your immune system may attack if you're not getting enough medicine to suppress
your immune system after the surgery.
You and the transplant team will work together to
protect the new heart by watching for signs of rejection. These signs include:
- Shortness of breath
- Fever
- Fatigue (tiredness)
- Weight gain (retaining fluid in the body)
- Reduced amounts of urine (problems in the kidneys
can cause this)
You and the team also will work together to manage
the transplant medicines and their side effects, prevent infections, and
continue treatment of ongoing medical conditions.
You may be asked to check your temperature, blood
pressure, and pulse when you go home.
Preventing Rejection
You'll need to take medicine to suppress your immune
system so that it doesn't reject the new heart.
These transplant medicines are called
immunosuppressants. They're a combination of medicines that are tailored to
your situation. Often, they include cyclosporine, tacrolimus, MMF
(mycophenolate mofetil), and steroids such as prednisone.
Your doctors may need to change or adjust your
transplant medicines if they aren't working well or if you have too many side
effects.
Managing Transplant Medicines and Their Side
Effects
You'll have to manage multiple medicines. It's
helpful to set up a routine for taking medicines at the same time each day and
for refilling prescriptions. It's crucial to never run out of medicine. Always
using the same pharmacy may help.
Keep a list of all your medicines with you at all
times in case of an accident. When traveling, keep extra doses of medicine with
you, not packed in your luggage. Bring your medicines with you to all doctor
visits.
Side effects from medicines can be serious. Side
effects include risk of infection, diabetes, osteoporosis (thinning of the
bones),
high
blood pressure, kidney disease, and cancerespecially lymphoma and
skin cancer.
Discuss any side effects of the medicines with your
transplant team. Your doctors may change or adjust your medicines if you're
having problems. Make sure your doctors know all of the medicines you're
taking.
Preventing Infection
Some transplant medicines can increase your risk of
infection. You may be asked to watch for signs of infection, including fever,
sore throat, cold sores, and flu-like symptoms.
Signs of possible chest or lung infections could
include shortness of breath,
cough,
and a change in the color of sputum (spit).
The incision (cut) from your surgery must be checked
for redness, swelling, or drainage. It's especially important to look for signs
of infection because transplant medicines often can mask these signs.
Talk to your doctor about what steps you should take
to reduce your risk of infection. For example, your doctor may recommend that
you avoid contact with animals or crowds of people in the first few months
after your transplant.
Regular dental care also is important. Your doctor
may prescribe antibiotics before any dental work to prevent infections.
Pregnancy
Many successful pregnancies have occurred after
heart transplant surgeries; however, special care is important. If you've had a
heart transplant, talk with your doctor before planning a pregnancy.
Emotional Issues and Support
Having a heart transplant may cause fear, anxiety,
and stress. While you're waiting for a heart transplant, you may worry that you
won't live long enough to get a new heart. After surgery, you may feel
overwhelmed, depressed, or worried about complications.
All of these feelings are normal for someone going
through major heart surgery. It's important to talk about how you feel with
your health care team. Talking to a professional counselor also can help. If
you're feeling very depressed, your health care team or counselor may prescribe
medicines to make you feel better.
Support from family and friends also can help
relieve stress and anxiety. Let your loved ones know how you feel and what they
can do to help you.
What Are the Risks of a Heart Transplant?
Although heart transplant surgery is a life-saving
measure, it has many risks. Careful monitoring, treatment, and regular medical
care can prevent or help manage some of these risks.
Risks of heart transplant include:
- Failure of the donor heart
- Complications from medicines
- Infection
- Cancer
- Problems that arise from not following a lifelong
health care plan
Failure of the Donor Heart
Over time, the new heart may fail due to the same
reasons that caused the original heart to fail. Failure of the donor heart also
can occur if your body rejects the donor heart or if cardiac allograft
vasculopathy (CAV) develops. CAV is a blood vessel disease.
Patients who have a heart transplant that fails can
be considered for another transplant (called a retransplant).
Primary Graft Dysfunction
The most frequent cause of death in the first 30
days after transplant is primary graft dysfunction. This occurs if the new
donor heart fails and isn't able to function.
Factors such as shock or trauma to the donor heart
or narrowed blood vessels in the recipient's lungs can cause primary graft
dysfunction. Medicines (for example, inhaled nitric oxide and intravenous
nitrates) may be used to treat this condition.
Rejection of the Donor Heart
Rejection is one of the leading causes of death in
the first year after transplant. The recipient's immune system sees the new
heart as a "foreign body" and attacks it.
During the first year, 25 percent of heart
transplant patients have signs of a possible rejection at least once. Half of
all possible rejections happen in the first 6 weeks after surgery, and most
happen within 6 months of surgery.
Cardiac Allograft Vasculopathy
CAV is a chronic (ongoing) disease in which the
walls of the coronary arteries in the new heart become thick, hard, and lose
their elasticity. CAV can destroy blood circulation in the new heart and cause
serious damage.
CAV is a leading cause of donor heart failure and
death in the years following transplant surgery. CAV can cause
heart
attack,
heart
failure, dangerous
arrhythmias,
and
sudden
cardiac arrest.
To detect CAV, your doctor may recommend
coronary
angiography yearly and other tests, such as
stress
echocardiography or
intravascular ultrasound.
Complications From Medicines
Taking daily medicines that stop the immune system
from attacking the new heart is absolutely critical, even though the medicine
combinations have serious side effects.
Cyclosporine and other medicines can cause kidney
damage. Kidney damage affects more than 25 percent of patients in the first
year after transplant. Five percent of transplant patients will develop
end-stage kidney disease within 7 years.
Infection
When the immune systemthe body's defense
systemis suppressed, the risk of infection increases. Infection is a
major cause of hospital admission for heart transplant patients and a leading
cause of death in the first year after transplant.
Cancer
Suppressing the immune system leaves patients at
risk of cancers and malignancies. Malignancies are a major cause of late death
in heart transplant patients, accounting for nearly 25 percent of heart
transplant deaths 3 years after transplant.
The most common malignancies are tumors of the skin
and lips (patients at highest risk are older, male, and fair-skinned) and
malignancies in the lymph system, such as non-Hodgkin's lymphoma.
Other Complications
High
blood pressure develops in more than 70 percent of heart transplant
patients in the first year after transplant and in nearly 95 percent of
patients within 5 years.
High levels of cholesterol and triglycerides in the
blood develop in more than 50 percent of heart transplant patients in the first
year after transplant and in 84 percent of patients within 5 years.
Osteoporosis can develop or worsen in heart
transplant patients. This condition thins and weakens the bones.
Complications From Not Following a Lifelong Health
Care Plan
Not following a lifelong health care plan increases
the risk of all heart transplant complications. Heart transplant patients are
asked to closely follow their doctors' instructions and check their own health
status throughout their lives.
Lifelong health care includes taking multiple
medicines on a strict schedule, watching for signs and symptoms of
complications, keeping all medical appointments, and stopping unhealthy
behaviors (such as smoking).
Key Points
- A heart transplant is surgery to remove a
person's diseased heart and replace it with a healthy heart from a deceased
donor.
- Heart transplants are done as a life-saving
measure when medical treatment and less drastic surgery have failed. Most heart
transplants are done on patients who have end-stage
heart
failure.
- Donor hearts are in short supply, so patients who
need a heart transplant go through a careful selection process at a heart
transplant center.
- Patients who are eligible for a heart transplant
are placed on a waiting list for a donor heart. Policies on giving out donor
hearts are based on urgency of need, the organs that are available for
transplant, and the location of the patient who is receiving the heart. Organs
are matched for blood type and size of donor and recipient.
- Waiting times for a donor heart vary from days to
several months.
- Heart transplant surgery usually takes about 4
hours. Patients might spend the first days after surgery in the intensive care
unit of the hospital.
- The amount of time a heart transplant recipient
spends in the hospital will vary with each person. It often involves 1 to 2
weeks in the hospital and 3 months of monitoring by the transplant
team at the heart transplant center.
- Once at home, patients must carefully check and
manage their health status. Patients will work with their transplant teams to
protect their new hearts. The team will watch for signs of rejection, manage
the transplant medicines and their side effects, try to prevent infections, and
continue treatment of ongoing medical conditions.
- Risks of heart transplant include failure of the
donor heart; complications from medicines; infection; cancer; and problems that
arise from not following a lifelong health care plan.
- Lifelong health care includes taking multiple
medicines on a strict schedule, watching for signs and symptoms of
complications, keeping all medical appointments, and stopping unhealthy
behaviors (such as smoking).
- Survival rates for people receiving heart
transplants have improved over the past 5 to 10 years, especially in the first
year after the transplant. About 88 percent of patients survive the first year
after transplant surgery.
- After the surgery, most heart transplant
recipients (about 90 percent) can come close to resuming their normal
lifestyles.
Links to Other Information About Heart
Transplant
NHLBI Resources
Non-NHLBI Resources
Clinical Trials
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