Treatment
What is good kidney disease care?
Effective treatment of kidney disease can prevent the condition from getting worse and can save lives. According to a national review, kidney disease services should:
- identify people at risk of kidney disease, especially people with high blood pressure or diabetes, and treat them as early as possible to maintain their kidney function
- give people access to investigative treatment and follow them up to reduce the risk of the disease getting worse
- give people good-quality information about managing their condition
- provide information about the development of the disease and treatment options
- provide access to a specialist renal (kidney) team
- give people access to dialysis or transplant services if required
Your treatment for kidney disease will need to be reviewed regularly. It may be helpful for you to make a care plan because this can help you manage your day-to-day health. Your kidney disease specialist nurse may be able to help with this.
Treatment
Your treatment will depend on the stage of your chronic kidney disease (CKD). Stages one, two and three CKD can usually be treated by your GP.
Treatment involves making changes to your lifestyle and, in some cases, taking medication to control your blood pressure and lower your blood cholesterol levels. This should help prevent any further damage to your kidneys and circulation.
If you have stage four or stage five CKD, you will usually be referred to a specialist. In addition to the treatments above, you may also be given a number of different medications to control or prevent the symptoms of CKD.
Kidney failure, also called established renal failure or ERF, occurs when you have lost nearly all your kidney function and the condition has become life threatening. About 1% of people with stage three CKD develop ERF.
If you have kidney failure, you will need to decide on the next stage of treatment. Your choice will be whether to have treatment with dialysis (a means of artificially replacing some functions of the kidney), a kidney transplant, or other treatment options that involve less intervention, also known as supportive care.
Lifestyle changes
The following lifestyle changes are known to help reduce your blood pressure and control CKD:
- stopping smoking
- eating a healthy, low-fat, balanced diet
- restricting your salt intake to less than 6g (0.2oz) a day
- not using over-the-counter nonsteroidal anti-inflammatory drugs (NSAIDs), such as ibuprofen, except when advised to by a medical professional
- moderating your alcohol intake so that it is within recommended limits (no more than 3-4 units a day for men and 2-3 units a day for women)
- losing weight if you are overweight or obese
- doing regular exercise for at least 30 minutes a day, five times a week
Find out more about lifestyle changes that can help prevent high blood pressure.
Medications for high blood pressure
One of the most important ways to reduce the progression of kidney damage is to manage high blood pressure. Good control of blood pressure is vital to protect the kidneys. If losing weight, reducing your salt intake and making other lifestyle changes do not control your blood pressure, medication may be needed.
There are many types of blood pressure drug. Medicines called angiotensin converting enzyme (ACE) inhibitors are especially used to control high blood pressure in people with CKD.
As well as reducing blood pressure around the body and reducing the strain on blood vessels, ACE inhibitors give additional protection to the kidney.
ACE inhibitors include:
- ramipril
- enalapril
- lisinopril
- perindopril
Side effects of ACE inhibitors include:
- a persistent, dry cough
- dizziness
- tiredness or weakness
- headaches
Most of these side effects should pass within a few days, although some people continue to have a dry cough.
If the side effects of ACE inhibitors are particularly troublesome, you can be given an alternative medication called an angiotensin-II receptor blocker (ARB). This group of medicines includes candesartan, eprosartan, irbesartan and losartan. The side effects of ARBs are uncommon, but can include dizziness.
Both ACE inhibitors and ARBs can cause a reduction in kidney function and increased levels of potassium in the blood, so blood tests will need to be performed after you start treatment and whenever the dose changes.
Aspirins or statins
Studies have shown that people with CKD have a higher risk of cardiovascular disease, including heart attacks and strokes. This is because some of the risk factors for CKD are the same as those for heart attacks and strokes, including high blood pressure and high levels of cholesterol in the blood (atherosclerosis).
To help reduce your risk of having a heart attack or stroke, you may be given low-dose aspirin or statins.
Statins are a type of medication used to lower cholesterol levels. Cholesterol causes narrowing of the arteries that can lead to blockage of the blood supply to the heart (causing a heart attack) or the brain (causing a stroke). Statins work by blocking the effects of an enzyme in your liver (called HMG-CoA reductase), which is used to make cholesterol.
Statins sometimes have mild side effects, including:
- constipation
- diarrhoea
- headaches
- abdominal pain
Occasionally, statins can cause muscle pain, weakness and tenderness. If you experience any of these symptoms, contact your GP. You may need to have a blood test or change your treatment.
Oedema (fluid retention)
If you have kidney disease, you may be asked to reduce your daily fluid and salt intake. You may develop a build-up of fluid as your kidneys will not be able to get rid of fluid as well as they did before. If you are asked to reduce the amount of fluid you drink, you must also take into account fluid in foods, such as soup and yoghurt. Your GP or dietitian can advise you about this.
The excess fluid that occurs as a result of kidney disease often builds up in your ankles or around your lungs. You may also be given diuretics (water tablets), such as furosemide, which will help get rid of the excess fluid from your body.
If you do not have any fluid retention and you have not been told to reduce your fluid intake, there is no need to do so. In fact, it could be harmful in some circumstances.
Anaemia
Many people with stage three, four and five CKD develop anaemia. Anaemia is a condition in which you do not have enough red blood cells. Symptoms of anaemia include:
- tiredness
- lethargy
- shortness of breath (dyspnoea)
- palpitations (awareness of heartbeat)
Anaemia can occur because of many other conditions and your doctor will investigate to rule out any other possible causes.
Most people with kidney disease will be given iron supplements because iron is needed for the production of red blood cells. To boost iron levels, iron may be given as tablets, such as daily ferrous sulphate tablets, or as occasional intravenous injections.
If this is not enough to treat anaemia, you may given an injection of erythropoietin, a hormone which helps your body produce more red blood cells. These injections are often administered intravenously (into a vein) or subcutaneously (under the skin). Examples of these injections include epoetin alfa, beta and zeta, darbepoetin and methoxy polyethylene glycol-epoetin beta.
Correction of phosphate balance
If you have stage four or five kidney disease, you can get a build-up of phosphate in your body because your kidneys cannot get rid of it. Phosphate is a mineral that, with calcium, makes up most of your bones. Phosphate is obtained through diet, mainly dairy foods. The kidneys usually filter out any excess phosphate. If phosphate levels rise too much, it can upset the normal calcium balance of the body. This can lead to thinning of the bones and furring of the arteries.
You may be asked to limit the amount of phosphate in your diet. Foods that are high in phosphate include red meat, dairy produce, eggs and fish. Your GP or dietitian should be able to advise you about how much phosphate you can eat. However, there is no advantage in reducing your intake of these foods unless you have a raised phosphate level. Always ask a healthcare professional before changing your diet.
If reducing the amount of phosphate in your diet does not lower your phosphate level enough, you may be given medicines called phosphate binders. These medicines bind to the phosphate in the food inside your stomach and stop it from being absorbed into your body.
To work properly, phosphate binders must be taken just before meals. The most commonly used phosphate binders are calcium carbonate and (less commonly) aluminium hydroxide.
The side effects of phosphate binders are uncommon but include:
- nausea
- stomach ache
- constipation
- diarrhoea
- flatulence (wind)
- skin rash
- itchy skin
Vitamin D supplements
People with kidney disease can have low levels of vitamin D, which is needed for healthy bones. This is because the kidneys need to activate the vitamin D from food and from the sun before it can be used by the body.
You may be given a vitamin D supplement called alfacalcidol or calcitriol to help boost vitamin D levels and reduce the risk of bone damage.
Treatment for kidney failure - dialysis or transplant
Many people with kidney failure can continue with treatment using medicines and will have good-functioning kidneys for the rest of their lives.
In a few people, kidney disease will progress to the stage where the kidneys stop working and it becomes life threatening. This is called kidney failure or established renal failure (ERF).
This rarely happens suddenly, and there will be time to plan the next stage of your condition. The decision whether to have dialysis, a kidney transplant or supportive treatment should be discussed with your healthcare team.
Supportive treatment
If you decide not to have dialysis or a transplant for kidney failure, or they are not suitable for you, you will be offered supportive treatment. This is also called palliative care. The aim is to treat and control the symptoms of kidney failure without using dialysis or transplantation. Supportive treatment includes medical, psychological and practical care for both the person with kidney failure and their family, including discussion about how you feel and planning for the end of life.
Many people choose supportive treatment because they:
- do not want to go through the inconvenience of treatment with dialysis or transplantation
- are advised against dialysis because they have other serious illnesses that will shorten their life, and the negative aspects of treatment outweigh any likely benefits
- have been on dialysis but have decided to stop this treatment
- are being treated with dialysis, but have another serious physical illness, especially severe heart disease, that will shorten their life
If you choose to have supportive treatment, your kidney unit will still look after you.
Doctors and nurses will make sure you receive:
- medicines to protect your remaining kidney function for as long as possible
- medicines to treat other symptoms of kidney failure, such as feeling out of breath, anaemia, loss of appetite or itchy skin
- help to plan your home and money affairs
- bereavement support for your family after your death
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Living with
A diagnosis of kidney disease can be worrying for you and your family, but it does not have to take over your life.
Although it is not possible to repair the damage that has already happened to your kidneys, it does not mean your kidney disease will definitely get worse. Less than 1% of people with stage three kidney disease develop kidney failure.
By leading a healthy lifestyle and following your doctor’s advice on treatment for blood pressure and other conditions, it is possible to live without symptoms or further deterioration of your kidney function. At all stages of kidney disease, you can help reduce the chances of your kidneys getting worse and your risk of cardiovascular disease by living a healthier lifestyle.
Looking after your kidneys
The following steps can help keep your kidneys as healthily as possible:
- Do not smoke.
- Maintain a healthy blood pressure (neither too high nor too low). You can do this by eating a healthy diet (particularly avoiding added salt), living a healthy lifestyle (for example, doing gentle exercise and avoiding stress) and taking medication prescribed by your GP.
- Reduce the amount of cholesterol in your diet. Cholesterol increases blood pressure and can impair kidney function.
- People with diabetes should make sure their blood sugar levels are kept under control.
Self care
Self care is an integral part of daily life. It means that you take responsibility for your own health and wellbeing, with support from the people involved in your care. Self care includes the things you do each day to stay fit, maintain good physical and mental health, prevent illness or accidents, and effectively deal with minor ailments and long-term conditions. People living with long-term conditions can benefit enormously if they receive support for self care. They can live longer, have less pain, anxiety, depression and fatigue, have a better quality of life, and be more active and independent.
Regular reviews
Because kidney disease is a long-term condition, you will be in regular contact with your healthcare team. A good relationship with the team means that you can easily discuss your symptoms or concerns. The more the team knows, the more they can help you.
Keeping well
Everyone with a long-term condition such as kidney disease is encouraged to get a flu jab each autumn to protect against flu (influenza). They are also recommended to get an anti-pneumoccocal vaccination. This is a one-off injection that protects against a specific serious chest infection called pneumococcal pneumonia.
Healthy eating and exercise
Regular exercise and a healthy diet are recommended for everyone, not just people with kidney disease. They can help prevent many conditions, including heart disease and some forms of cancer. Exercising regularly can help relieve stress and reduce fatigue. Try to eat a balanced diet, containing all the food groups, to give your body the nutrition it needs. You will be advised by a dietitian if you need to follow a special diet. The advice you are given will depend on how well your kidneys are working, your blood test results and your own preferences about what you normally eat and drink.
Relationships and support
Coming to terms with a condition such as kidney disease can put a strain on you, your family and your friends. It can be difficult to talk to people about your condition, even if they are close to you.
Learning about kidney disease often helps because you and your family will understand more about what to expect and feel more in control of the illness, instead of feeling that your lives are now dominated by kidney disease and its treatment.
Be open about how you feel, and let your family and friends know what they can do to help. However, do not feel shy about telling them that you need some time to yourself, if that is what you need.
Get support
Your GP or nurse can reassure you if you have questions about your kidney disease, or you may find it helpful to talk to a trained counsellor, psychologist or specialist telephone helpline operator. Your GP surgery will have information on these.
Some people find it helpful to talk to other people with kidney disease at a local support group or through an internet chat room.
Money and finances
If you have to stop work or work part time because of your kidney disease, you may find it hard to cope financially. You may be entitled to one or more of the following types of financial support:
- If you have a job but cannot work because of your illness, you are entitled to Statutory Sick Pay from your employer.
- If you do not have a job and cannot work because of your illness, you may be entitled to Employment and Support Allowance.
- If you are aged 64 or under and need help with personal care or have walking difficulties, you may be eligible for Disability Living Allowance.
- If you are aged 65 or over, you may be able to get Attendance Allowance.
- If you are caring for someone with kidney disease, you may be entitled to Carer’s Allowance.
- You may be eligible for other benefits if you have children living at home or if you have a low household income.
Sex and pregnancy
The symptoms of kidney disease and the stress it causes in your life can affect your sexual relationship.
Some couples become closer after a diagnosis of kidney disease, while others find that their loved ones are affected by worries about how they will cope with the effects of the illness. Both men and women may experience issues about body image and self-esteem, and this can affect the relationship.
Try to share your feelings with your partner. If you have problems with sex that do not get better with time, you can speak to a counsellor or sex therapist.
People on dialysis often experience specific sexual difficulties. Loss of sex drive in both men and women and impotence in men are commonly reported problems. Treatment is available. However, it may take some time and requires commitment from both partners. The first step is to discuss it with your healthcare team.
Pregnancy
Both men and women with early stage kidney disease will find that their fertility is unaffected. This means it is important to use contraception unless you want to have a baby.
Later stage kidney disease may affect women's periods, which can make pregnancy more difficult. For men, later stage kidney disease can cause a reduction in sperm count. However, having kidney disease does not mean you will not get pregnant or be able to father a child, so both men and women need to use an effective method of contraception unless they want to have a baby.
Women who want to have a baby should talk to their renal specialist or an obstetrician with an interest in kidney disease. Depending on the stage of kidney disease, there can be risks to both the mother and the baby. It is important to minimise any risk with a planned pregnancy. Your healthcare team can advise you about this.
Kidney failure
About 1% of people with stage three CKD develop kidney failure, also called established renal failure or ERF. Kidney failure has a major impact on your life and the lives of those close to you. People diagnosed with kidney failure usually go through shock, grief and denial before they accept their condition.
Choices if you have established renal failure
If you have established renal failure (ERF), you will need to decide whether to have treatment with dialysis (a machine that replicates the functions of the kidneys) or a kidney transplant. You may decide to have neither treatment and to have supportive care. These choices should be made with your healthcare team.
For people who want active treatment for their ERF, a transplant would be the best option. However, a transplant is only suitable for about half of all people with ERF. This is because they may have had recent cancer or they are not physically fit.
Many people who have slowly progressive kidney failure and who have very serious health problems, and who are usually older, may choose to avoid dialysis. Supportive care can still allow you to live for some time with a good quality of life.
Dialysis
Dialysis can take place at home or in hospital. It involves filtering the blood of waste products and excess water. It is not as efficient as a human kidney, so people with kidney failure usually need to restrict their intake of fluid and certain foods. They also require additional medicines such as iron supplements, phosphate binders and antihypertensive medicine (to reduce blood pressure). There are two types of dialysis: peritoneal dialysis and haemodialysis.
Peritoneal dialysis
The abdomen (tummy) has a lining called the peritoneal membrane, which can be used as a filter to remove excess waste and water. If you have opted for peritoneal dialysis, a tube (catheter) will be inserted into your abdomen during an operation. This will allow you to drain dialysis fluid in and out of your tummy yourself. You will not need to go into hospital to be treated, but you will have to spend an hour or two each day draining the fluid. The treatment involves either four exchanges spaced out during the day, each taking half an hour, or attaching yourself to a machine overnight that pumps the fluid in and out for you.
Haemodialysis
Haemodialysis removes waste products and excess fluid that build up in the body when the kidneys stop working. Blood is taken from the body to be cleaned in a filter known as a dialyser. It is effectively an artificial kidney.
The whole process takes about four hours and usually has to be repeated three times a week. Most people go into hospital to have haemodialysis. However, some people choose to have the treatment in their own home.
Home haemodialysis will give you more flexibility, but comes with greater responsibility. You’ll need to have the space in your home for a dedicated machine and, in most cases, a lot of support from a close family member or friend. Some people choose to have their dialysis at night while they are asleep, others during the day. Most people who choose home haemodialysis have it every day, so their fluid intake is not as restricted.
Quality vascular access
During haemodialysis, it is important that large volumes of blood are passed through the machine. This requires special measures to get into large enough blood vessels. For this reason, haemodialysis patients need a minor operation to join one of the deep arteries to a superficial vein (called a fistula). This is carried out in day surgery and should be done at least six weeks before dialysis is required because it needs time to mature before it can be used. Occasionally, there will be insufficient time for a fistula to be created before dialysis is required. In this case, a temporary solution is found, usually involving the use of an indwelling plastic dialysis catheter.
All the issues will be discussed in detail with you by the dialysis team before any decisions are made.
Kidney transplant
A kidney transplant, when suitable, is the best treatment for ERF. The transplanted kidney can be obtained from a deceased or living donor and survival rates are now extremely good. About 90% of transplants still function after five years and many transplants work usefully after 20 years. The main reason people have to wait for a transplant is the shortage of available donors.
One major risk after transplantation is rejection, where the immune system attacks the donated kidney because it mistakes it for a foreign object. This is prevented with the use of strong drugs to suppress the immune system. These drugs need to be taken meticulously. They are usually well tolerated but may have side effects, including an increased susceptibility to infections and some forms of cancer. For this reason, transplant patients are given regular reviews in a specialist transplant clinic.
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