TRANSPLANT
Overview
Once a patient has reached the stage of
kidney failure, the options available to
them are:
•
Dialysis
•
Transplantation
Kidney failure can be managed for many years
with dialysis, but there is a general agreement, supported by
recent studies in both adults and children, that patients who
receive transplants enjoy a better quality of life than those who
remain on dialysis.
Unfortunately, transplantation isn’t the best option for everyone
and transplantation also has its advantages and disadvantages:
Advantages
• Freedom from
dialysis
• Less fluid and dietary restrictions
• Increased energy and well-being
• A less restricted life-style
• A possible return to work
• Improved fertility in women
• Increased life expectancy
Disadvantages
• Initially lots of hospital visits
• Outcomes are less predictable
• Taking drugs for life
• Risk of long-term complications
• Loss of some social welfare benefits
The final decision to be on the transplant
waiting lists is yours.
A major
undertaking
A transplant is a major undertaking – one
that involves a considerable amount of clinical evaluation. Before
the search for a suitable kidney begins, your doctors will
determine if you are a suitable recipient. Not all
dialysis
patients are suitable for transplant.
The standard review procedures for major
operations apply to transplant candidates – for example, your
heart and lung function must be sufficient that you will survive
the operation. Clinical conditions such as obesity and cancer may
affect your suitability for a transplant, as would non-clinical
conditions such as current drug abuse.
If you are having treatment for an infection
or other serious medical condition, you may temporarily be taken
off the transplant list until your body has recovered sufficiently
to undergo such a major operation.
Waiting List
If you decide to opt for a kidney transplant
you may be lucky enough to have a
living donor
offer you a kidney.
However, if you need to wait for a cadaveric
(deceased) donor, you will be put on to the waiting list. Your
details, including blood group and tissue type, will be put into
the national computer at UK Transplant (UKT).
When kidneys become available, the UKT
searches for the most suitable candidate for
transplantation.
The waiting list is not a 'queue' but operates by finding the
right kidney for the right patient.
The average waiting time for an adult kidney
transplant is 506 days.
For children, the average wait is 203 days.
For the latest statistics on transplants in
the UK visit:
Assessment
When you have decided that you want to have
a transplant, and before you are put on the list as a suitable
candidate, you will be seen by the transplant surgeon, after which
you will find yourself taking many tests.
These will help the transplant team to find
any potential problems before they occur, and determine if a
transplant is the best option for you.
These tests are often called the
“pre-transplant workup”.
One of the most important set of tests for a
transplant candidate is the blood and tissue type, [see finding a
suitable donor] but there are many other
tests that you might have pre-transplantation
depending on your clinical needs.
|
Blood and tissue tests |
Your blood count, blood and tissue type,
blood chemistries and immune system will all be checked.
These will help to prepare a suitable donor profile for you.
In addition, your blood will be checked for certain
infectious diseases |
|
Chest x-ray |
To see whether your lungs and lower
respiratory tract are healthy |
|
Pulmonary
function test |
To check how well you lungs are working |
|
Electrocardiogram
(ECG) or Echocardiogram |
To reveal how well your heart is working.
An ECG may show up heart damage that was previously
unsuspected |
|
Stress test |
This is an exercise test that measures
the strength of your heart |
|
Ultrasound |
To create a picture of your kidneys and
the surrounding body structures |
Finding a
donor
There are 3 possible sources for your new
kidney:
• a kidney donated by a living blood relative
• a kidney donated by a living non-relative
• a kidney from a deceased donor (a cadaveric donor)
The living
donor
Living donors are usually your immediate
family – your mother, father, sisters, brothers or children may
offer to donate a kidney. Cousins, aunts and uncles are also
possible blood-related donors. However, if tests prove that their
kidney is compatible, an unrelated person such as a friend or
spouse can become a donor. Regardless of whether the donor is a
blood relation or not, as long as they are healthy, the procedure
is relatively safe and recovery can be rapid (a few weeks).
Evidence shows that by having only one kidney the donor can lead a
normal life, but all parties involved must consider the
psychological effects associated with this procedure. Discussion
with prospective donors at the beginning of the process is
important to ensure that they are fully aware of all the
implications.
Tests will be carried out to check for
compatibility between you and the donor’s kidney. These include:
Blood typing
This is important in
transplantation
because your donor needs to be of a blood group that you can
accept.
You can be one of four blood types; O, A, B,
AB.
The table below shows how blood typing works:
|
Blood
type |
Can
receive a kidney from: |
Can usually
donate a kidney to: |
|
O |
O |
O, A, B, AB |
|
A |
A, O |
A, AB |
|
B |
B, O |
B, AB |
|
AB |
O, A, B, AB |
AB |
Tissue typing
Each of us carries a set of 6 inherited
markers (Human Leukocyte Antigens or HLAs) on the surface of our
cells. They play a vital role in the recognition of cells by the
immune system and this test is used to determine the match between
the kidney donor and recipient.
The deceased
donor
More than half of all kidney recipients
receive organs from deceased (cadaveric) donors. Kidneys suitable
for
transplantation
tend to come from people who have had strokes or a car crash and
are transferred to a hospital intensive care unit and die whilst
attached to a
ventilator.
The kidney will only be removed from the body when the donor has
been declared brain dead after a series of tests.
When a kidney becomes available, it is logged onto the national
computer at the UK Transplant (UKT) which searches for the most
suitable candidate for transplant.
Certain patients will receive priority:
•children
•those who have the highest level of compatibility with the donor
•those who have been waiting the longest
Donor
Issues
Issues and background
information about donors
Donation is the key to all transplant
activities.
In the UK there are far more recipients than
donors, and this section of the website explores some of the types
of donation available, and some of the issues surrounding the
different types of donation possible.
One of the most common misconceptions about
donation is that you have to have died to be able to donate!
The vast majority of donors are cadaveric
(from deceased individuals) but there are other options.
Techniques have been discovered that allow kidneys and lungs to be
donated from living donors, normally close relatives. For more
information, see our live donor section.
Each day about 8 people receive an organ
transplant.
Anyone, regardless of age, can express a wish to be a donor.
Medical suitability for donation is determined at the time of
death.
Keep in touch
The time you may have to wait for your organ
transplant can vary from a few days to several years.
During this time, it is important to keep in
touch with the transplant centre. Make sure you keep them up to
date with:
• Your ‘round the clock’ contact details for
home, work, school and holidays
• Phone numbers of your friends and family
• Your medical history. Let them know if you have any infections
or if any of your medication is changed.
You may have a mobile/pager that you can
carry with you at all times. Make sure that you have it turned on,
and charged up!
Be prepared
Your call may come at any time, day or
night, so it’s best to be prepared. Make a list and pack ahead of
time, so that you’re ready to go straight to the transplant
centre.
• Pack your hospital bag: clothing, toiletries, books, etc
• Prepare a list of people who should be contacted when you get
‘the call’
• Give the list to a family member or friend so that they can make
phone calls for you and bring any forgotten items to the hospital
• DON'T forget to bring your medicines with you
Get informed
You are about to undergo major surgery, and
enter a new phase of your life. Fear of the unknown is always a
stressful situation, but it is important that you manage your
stress and keep concerns to a minimum whilst you are waiting for
your transplant.
• Learn as much as you can about your
operation and what to expect from your transplant.
• Find out as much as you can about the
lifestyle changes you will have to make to get the most out of
your new organ. (see
lifestyle section)
• Visit the transplant centre and
familiarise yourself with the surroundings
• Information groups and patient education
sessions are run by many centres and can provide you with further
written information
• Your transplant team will be happy to
answer any questions you may have, and will have some useful
leaflets for you to read.
• They may also put you in touch with
patients who have already had a similar operation to the one you
are about to undergo.
The Operation
The Operation
A kidney transplant operation is the second
most common form of all transplants, and the most common solid
organ transplant in the UK.
It requires a general
anaesthetic
and will usually last between 2 - 3 hours. You will be able to
discuss the operation in detail with your transplant team, but
some general details are given here.
Arriving at
the hospital
When a suitable kidney becomes available,
you will be called into the hospital. If you have not already been
advised to do so, you must immediately stop eating or drinking as
you are about to undergo an operation. Further details on
preparing for this moment can be found in
Pre-transplant section.
You will be taken to your ward and soon
afterwards you will undergo a physical examination to check that
it is safe to proceed with the operation. If the doctor considers
that the risk of the operation is too high, for example, if you
have an infection, then unfortunately you will be sent home and
put back onto the waiting list.
You will also undergo what is called a
cross-match with the donor kidney. This is the final test to check
that your body does not contain
antibodies
that would react with the donor kidney. High levels of these
antibodies indicate a high risk that your body will reject the new
kidney even if it seems a good match. Although this may be very
upsetting, it will also mean that the operation will not go ahead.
However, depending on the centre, it is likely that this test will
be performed before you are informed about the transplant.
The
potassium
levels in your blood will also be checked to make sure they are
low enough for an
anaesthetic.
Pre-op prep
You may need to be dialysed or, if on CAPD,
you will continue with your exchanges and then drain out and cap
off just before the operation.
Prior to the operation you will be given
immunosuppressive
or
anti-rejection
drugs and a general
anaesthetic.
An
intravenous
(IV) tube will be put in place to keep you from getting
dehydrated
and to increase your urine flow.
Your
Operation
Whether the donor is live or deceased, an
operation to transplant a kidney lasts about two to three hours.
Once you are asleep, the surgeon will make a diagonal cut about
8-10” in length into your
abdomen,
on the right or left just below your navel.
The blood supply of the donor kidney will be
attached to your own blood supply and the new kidney’s
ureter
(the tube that takes urine to the
bladder)
will be attached to your bladder.
Your own kidneys are usually left in place,
with the new kidney placed in the pelvic region
When you wake up, you may feel some pain and
discomfort and may feel nausea from the
anaesthetic.
This is completely normal, and the nurses will help you to feel
more comfortable. You will be given pain relief and anti-sickness
drugs.
The first few days after the operation are
critical and your blood pressure, fluid intake and urine output
will be closely monitored to see how your body is responding to
the transplant.
For more information see the
post-transplant section.
Living donor
operation
Living donor
transplants in the UK now represent about one in five of all
kidney transplants, and between 2000 and 2001 increased by 3%
(from 347 in 2000 to 358 in 2001 : source transplant UK).
What is the process for a live donation?
The donor will discuss with the transplant team the options
available to him/her in surgery. The donor may be given the choice
of the traditional ‘open
nephrectomy’ (surgical removal of the
kidney) or the newer ‘laparoscopic’
(keyhole) techniques.
For the donor, the procedure requires a
hospital stay of approximately one week and then another two to
three months away from work. Recovery time for the donor is very
dependent on their health and lifestyle.
Whichever option is chosen, after removal,
the donor's kidney is taken directly to the recipient. Following
transplantation
to the recipient, the kidney usually begins to function
immediately after transplant, even before the donor has left the
operating theatre to start their recovery.
Waking Up
When you wake up, you may feel some pain and
discomfort and may feel nausea from the
anaesthetic.
This is completely normal, and the nurses will help you to feel
more comfortable. You will be given pain relief and anti-sickness
drugs.
The first few days after the operation are
critical and your blood pressure, fluid intake and urine output
will be closely monitored to see how your body is responding to
the operation.
Possible
complications
About 10% of live donors will develop an
infection following their operation. These infections are usually
treated with a course of antibiotics.
Because a donor operation is major surgical
procedure, there is a small risk of death (about 1 in 3000). These
deaths are most often associated with heart attacks or blood clots
on the lungs.
Pain Relief
Having an open procedure is potentially
painful, however transplant centres are very attentive to pain
relief post-op. You may be hooked up to an I.V. or receive an
epidural for the first couple of days before moving on to regular
painkillers for as long as required.
Life after donation
The only physical reminder to the donor of
the operation will be a scar, as life with one healthy kidney
should be no different from life with two.
·
Open nephrectomy
·
Laparoscopy
Open
nephrectomy
This is the traditional operation to remove
the kidney, which usually takes two to three hours, followed by a
period in the recovery area.
An incision is made into the side, and
sometimes the smallest rib is removed to gain access to the
kidney.
This is a major operation, and the donor is usually in hospital
for about 10 days, although the scar may remain sensitive for
several weeks.
The donor will need to attend a check-up
four to six weeks after discharge, and annual check-ups to monitor
long-term health.
The risks to both the donor and the function of the kidney after
the operation are well established with this procedure.
Laparoscopy
("Keyhole" surgery)
Laparoscopy
is a technique where three or four small incisions are made,
through which the surgeon does most of the operation, and the
kidney is then removed through a larger incision in the navel.
There are several advantages of this
procedure to the donor. There is a reduction in the length of the
hospital stay and recovery is more rapid.
However, there are still some concerns over
the function of the kidney through this procedure, although there
is no difference in function between kidneys from this procedure
or open
nephrectomy.
The transplant team should discuss both of
the procedures with the donor and recipient so that they can make
an agreed choice of operation.
Post-transplant
Overview
After the transplant operation, you are
likely to stay in hospital for up to 10 days, depending on how
well your new kidney functions.
You will already have started to take drugs
to prevent
rejection
and there will be many daily blood tests and urine measuring to
closely monitor your new kidney.
Immediately
after your transplant
When you wake up, you may feel some pain and
discomfort and also may feel nausea from the
anaesthetic.
This is completely normal, and the nurses will help you to feel
more comfortable. You will be given pain relief and anti sickness
drugs.
Central Line
You will also be given fluids via a 'central
line' which is a tube inserted in one side of the neck during your
operation. This line is also used to give you drugs that help
kidney function and prevent infection.
Urinary
Catheter
A urinary
catheter
is a tube that passes the urine from your
bladder
into a bag. This allows the medical staff to accurately measure
the amount of urine you pass. The tube usually stays in for
approximately 5 days after the transplant. Once the catheter has
been removed you should measure your urine and record it on your
chart.
Drinking
The hospital staff will tell you when you
may start drinking and how much to drink each day. You should
record everything you drink on your chart.
How will the
new kidney function
Some kidneys function immediately after the
operation, others don't. If this is the case it doesn't mean it
will never work - just that it needs time to recover.
You will already have started to take drugs
to prevent
rejection,
but about 20 - 30% of patients will experience some form of
rejection in the first few weeks after a transplant. Fortunately,
in most cases this can be overcome with extra drugs. You may find
it difficult coming to grips with the (sometimes) constant change
of drug regime. Some patients report feeling a loss of control.
Unfortunately there may be many changes to regimes on an on-going
basis.
·
Immediate function
·
Primary non-function
·
Hyper-acute rejection
Immediate
function
In this case, the transplanted kidney starts
to work immediately, making urine and filtering out waste
materials from your blood. This is measured by a decrease in the
levels of the chemical
creatinine
in your blood.
Immediate function after transplant occurs
in approximately 70% of patients who receive a kidney from a
deceased donor, and 95% of those who receive a kidney from a
living donor.
Primary
non-function (delayed)
In about 20-40% of those who receive a
kidney from a deceased donor, and 5-10% of those who receive a
kidney from a
living donor,
the kidney takes some time to start working properly.
This may be because of the time the donated
kidney is outside of a body without blood flow. The kidney is,
however, kept on ice and perfused with special fluid to preserve
it until it can be transplanted. Shock to the kidney due to being
removed could offer another explanation for delayed function.
You will need to continue
dialysis
until the kidney starts to function properly, which may take
several weeks.
Hyper-acute
rejection
In less than 5% of kidney transplants, the
kidney does not work immediately, and your body immediately
rejects it. This
rejection
is because your body’s immune system recognises the transplanted
kidney is ‘foreign’ and tries to remove it.
Hyper-acute
rejection is very difficult to
treat, and unfortunately usually results in a loss of the kidney,
and a return to
dialysis
and the waiting list.
What
complications might there be?
The majority of complications can be split
into the five main categories below. Before your operation, your
transplant team will discuss with you the likelihood that you will
suffer from any of these or other complications following
transplant.
·
Problems with the transplanted kidney
·
Infections
·
High blood pressure and high cholesterol
·
Diabetes
·
Nephrotoxicity
·
Hospital infection
Problems
with the transplanted kidney
Your immune system fights foreign bodies or
invaders such as
bacteria
or germs. There are two kinds of natural defences used by the
body:
white blood cells
and
antibodies.
Before you undergo the transplant operation,
a cross-match with the donor kidney is carried out to see that you
do not have a high level of antibodies that would react with the
donor kidney. However, some antibodies remain undetected and your
body is able to recognise that the transplanted kidney is
‘foreign’.
The
rejection
process then starts – the severity varies from patient to patient
– and may be
acute or
chronic.
[link to acute and link to chronic]
Infections
The drugs that you take to prevent
rejection
make it more likely that you will be affected by bacterial, viral
and fungal infections.
Although you are surrounded by germs it is
not necessary to become a recluse.
Follow these few simple points and you will reduce the risk of
infection:
• Eat a healthy diet and get enough sleep
• Exercise regulary and maintain a normal weight
• Wash your hands thoroughly after using the toilet and before
meals
• Wear gloves when gardening or handling rubbish
• Avoid contact with people with viral infections
In your physical review pre-transplant, your
doctors will assess the likelihood that you could suffer from
viral infections such as
hepatitis
B and C or
cytomegalovirus
(CMV). The donor kidney will also be checked for any bacterial or
viral infection before transplant. You may be given medications to
prevent any suspected infections.
• Bacterial infections tend to occur within
one month after the operation and
urinary tract
infections are the most common. The majority of these can be
prevented by the use of antibiotics after the transplant.
• Viral infections usually occur between the
first and sixth month after
transplantation.
The most common viral problem is called cytomegalovirus (CMV), but
there is a very effective treatment for this, given orally or as
an
intravenous
infusion.
High blood
pressure and high cholesterol
Circulation problems are important
complications after
transplantation,
and these can be caused by high blood pressure (hypertension)
or high levels of fats in the blood (hyperlipidaemia)
• Hypertension is common in people with
kidney disease, but after transplant can be increased as a side
effect of some of the
immunosuppressant
drugs. At least half of kidney transplant patients have high blood
pressure.
• Hyperlipidaemia is high levels of certain
fats (cholesterol and triglycerides) in the blood. Again, high
cholesterol levels are a side effect of some of the
immunosuppressant drugs.
Both conditions can be treated effectively with lifestyle changes,
such as giving up smoking and taking up exercise, dietary changes
and drugs. [link to lifestyle section]
Diabetes
There are several reasons why
diabetes
can be a problem after a transplant. Diabetes is a disease that
affects blood sugar levels.
High blood
sugar (hyperglycaemia)
• When the blood sugar level is too high, it
passes into the urine. This high level of sugar makes your kidney
produce more and more urine, dehydrating the rest of the body.
After a transplant, this dehydration caused by high blood sugars
can sometimes result in kidney failure.
• High blood sugar prevents your body’s
defences from working properly, so you may get an infection
• A major problem with continued high blood
sugar levels in
diabetes
is a narrowing of the arteries. This may cause heart attacks and
strokes.
Low blood
sugar (hypoglycaemia)
• If the level of sugar in your blood is too
low, your brain does not receive enough to function effectively
and you may suffer from a
hypoglycaemic
attack, which may lead to a coma.
Managing
diabetes
Some of the most important drugs used after
a transplant – a
steroid
and some of the
immunosuppressive
drugs – can cause
diabetes.
However, there is currently no alternative to these – so even if
they cause diabetes, you may have to keep using them to prevent
kidney
rejection.
The management of diabetes is very clearly understood and you may
receive medications to control the levels of sugar in your blood.
Diet, exercise and lifestyle changes such as giving up smoking are
also effective in the management of diabetes. [link to lifestyle]
Nephrotoxicity
This is when your kidney cells are destroyed
by a toxin or antibody. Unfortunately a side effect of some of the
important
immunosuppressive
drugs is nephrotoxicity. Nephrotoxicity can be
acute or
chronic.
• Acute nephrotoxicity is reversible by
lowering the dose of the drug.
• Chronic nephrotoxicity can only be diagnosed once tissue
scarring is already present (by a kidney
biopsy).
Once scarring exists, the disease is usually irreversible, but the
kidney can continue to work successfully for several more years .
Hospital
infection
Hospital aquired infections (such as MRSA),
are a hazard to a newly transplanted patient. Hospitals are alert
to this potential problem, however, and will take every precaution
to prevent such a thing from happening.
Follow-up
clinics
During the first few months after a
transplant, you may feel your life dominated by all the medicines
you have to take, and the frequent visits you need to make to the
hospital. You will get used to taking the drugs and the hospital
visits will become less frequent. Above all, it is important to
return to the transplant unit every week for your follow up
visits.
During these visits your kidney will be
checked to make sure everything is working well, and you will be
checked for signs of
rejection
or infection.
Biopsy
If your kidney function changes or is not as
good as it should be, you may be required to have a
biopsy.
The biopsy will show up any signs of
rejection.
Most kidney transplant patients will have a biopsy at some stage
during their recovery.
Ultrasound
scan
An
ultrasound
scan is sometimes used to check the kidney, the
bladder
and the blood supply to the kidney.
Medication
The main drugs that you will have to take
for the rest of your life are the
immunosuppressant
drugs.
These are also called
anti-rejection
drugs, as they help your body to accept the new kidney and prevent
it from trying to destroy it.
One of the biggest causes of transplant
failure is not taking the immunosuppressant drugs. This is called
non-compliance.
You must take the correct amount of your
immunosuppressive
drugs at the right time without missing a single dose
• If you are unable to do this or forget at
any time, call your transplant coordinator or doctor straight away
to ask what to do.
• Do not stop taking your drugs if you
experience any side effects, but call your transplant coordinator
or doctor straight away. They will decide the best course of
action
For more information on drugs go to the
Medication section.
Long term
The majority of long term problems after
transplantation
result from the
anti-rejection
drugs and not from the transplant itself.
Being healthy will help you to reduce the risks.
Infection
Transplant patients are vulnerable to viral
infections, chicken pox, cold sores and shingles in particular. If
you suspect you have these, or have come into contact with them,
you should contact your transplant unit immediately.
Rejection
Rejection
of a new kidney is a common complication. Rejection is usually
treated easily with
anti-rejection
drugs and should not be a cause for great anxiety.
Skin Cancer
The risk of kidney transplant patients
developing skin cancer is increased to 70% because of the
immunosuppressive
drugs. You must therefore take great care to protect your skin
from the sun.
• Use a Factor 30 sun block in the summer
• Wear clothing that covers the skin when outside
• Avoid the midday sun
Other
Cancers
The risk of other cancers is only slightly
increased after
transplantation
with the exception of:
• Skin Cancer - see above
• Cervical cancer - have annual cervical screening
• Lymph glands - These abnormal cells caused by the glandular
fever
virus
effect approx 1 in 100 patients and can usually be treated with a
reduction in the
immunosuppressive
drugs.
|