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Macmillan and Cancerbackup merged in 2008. Together we provide free, high quality information for people affected by cancer through our publications, website and phone service. Find out more| .
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High doses of radiotherapy for bladder or prostate cancer give a risk of bladder changes. This can also happen if you have been treated for cancer of the colon or rectum, but this is rare. The cells lining the walls of the bladder can become permanently damaged. This can make them fragile, so they may bleed. The bladder walls may also become scarred and hardened (fibrosed). If this happens, the bladder holds less urine.
You may find that you have some of the following:
After pelvic radiotherapy, you may have a weak flow of urine and your bladder may not empty completely. You may need to get up often to pass urine in the night.
You may have other symptoms, but these are much less common:
You may have difficulty passing urine, because the radiotherapy can make the tube that drains urine from the bladder (urethra) narrower. This is known as a stricture.
Many of these problems can be dealt with successfully. The appropriate treatment will depend upon which symptoms or side effects you have and how much of a problem they are. Medicines such as antibiotics and painkillers can be prescribed if needed.
If you want to go to the toilet more often, or feel that you can’t wait when you do want to go, you can get a card to show to staff in shops or pubs etc. The card allows you to use their loos, without them asking awkward questions. You can get the cards from the Bladder and Bowel Foundation| or RADAR| .
After radiotherapy, the bladder irritation usually settles down over a few weeks or months once the treatment has ended. The following tips can help reduce bladder irritation:
If you still have problems three months after the treatment has ended, let your doctor or specialist nurse know.
It has been suggested that cranberry juice may help to prevent urinary infections. Some people feel that it helps them, but there is no strong research evidence to back this up. If you are taking medicine to thin your blood, such as warfarin, you should avoid cranberry juice as it can increase the effects of the medicine and may cause potentially harmful side effects. It is also high in sugar so is not suitable for people with diabetes.
If you develop any new bladder problems after your treatment, or if any immediate side effects get worse, your doctors will probably want you to have some tests. Then you can find out what is causing the problem. This may include: blood and urine tests; a cystoscopy; and specialist x-rays of the bladder and kidneys. A cystoscopy allows the doctors to see inside the bladder using a flexible tube with a light and lens at the end which is passed through your urethra (the tube that drains urine out of the bladder). Usually, a cystoscopy is done under a local anaesthetic.
Leakage of urine from the bladder is quite common after pelvic radiotherapy. The chance of leakage depends on the type of cancer and the dose of the radiotherapy. You may find that you only leak urine when you laugh, sneeze or exercise. This is usually because the valve and muscles that keep the bladder closed become weaker after radiotherapy. Some urine then leaks out if pressure is put on the bladder. This is known as stress incontinence. Some of the following may help:
Exercises to retrain the bladder, or pelvic floor exercises, may help relieve incontinence. A brief description of the exercises is given here. However, a physiotherapist or community continence adviser can give you more detailed information. They can also can help you check you are doing the exercises properly – this can make them more effective. You can get details of your nearest continence clinic or adviser from the Continence Foundation| .
First, you need to identify the muscles that need to be exercised. Do this by sitting comfortably with your knees slightly apart. Then imagine that you are trying to stop yourself passing wind from the bowel. To do this, squeeze the muscle around the back passage. Try squeezing and lifting that muscle as tightly as you can. You should be able to feel the muscle move. If you can’t feel a definite squeeze and lift action in your pelvic floor muscles, you can ask to see a physiotherapist or continence adviser. They can help you get your pelvic floor muscles working properly.
When you can feel the muscles working, you can start to exercise them:
Do these exercises – five as hard as you can, five as long as you can and as many quick pull-ups as you can – at least 10 times a day.
While doing the exercises:
Get into the habit of doing the exercises regularly. You can link doing them to some everyday activities – for example, do them after emptying your bladder or whenever you turn on a tap. Try to keep a simple exercise diary (you could have an unlabelled simple tick chart on a kitchen pin board) to help you remember. Practise the exercises when you are lying down, sitting and especially standing. Get into the habit of tightening your pelvic floor before activities that are likely to make you leak – such as getting up from a chair, coughing, sneezing or lifting.
Pressing urine out of the bladder Some urine may be left in the bladder after you have finished passing water. This can be pushed out by pressing up behind the scrotum and massaging the base of the penis with your thumb.
Acupuncture may also help some people to improve bladder control. Your doctor may be able to refer you for acupuncture or you can contact the British Medical Acupuncture Society| .
Anti-spasm medicines You may be prescribed a type of medicine known as an antimuscarine. These include oxybutynin, tolterodine, trospium chloride, propiverine, and solifenacin. These medicines also have different brand names. They work by blocking certain nerve impulses to the bladder. The bladder muscle then relaxes and the bladder can hold more urine.
Pads are available from your doctor. Continence advisers, specialist nurses and Cancerbackup| can advise you on caring for your skin if it gets sore.
You may have to pass urine very often after pelvic radiotherapy. The bladder can be more sensitive and might feel like is full of urine when there is not much urine there. This is known as an overactive bladder. Several things can help:
Anti-spasm medicines can help with frequency and urgency.
Pelvic floor exercises
Bladder retraining Bladder retraining means training yourself to ignore the feeling of needing to pass urine, so that your bladder gets used to feeling more full. This can mean that you do not need to go to the toilet so often and it also reduces the chance of leaking urine. Bladder training can be difficult, but gets easier with time if you practice. It works best if you also have advice and support from a continence adviser, nurse, or doctor.
You will need to keep a diary. In the diary make a note of the times you pass urine, and the amount (volume) that you pass each time. Also make a note of the times you leak urine. Your doctor, nurse or continence adviser may have some diary-charts you can use.
When you first start, go to the toilet as usual for 2–3 days at first. You can see how often you go to the toilet and how much urine you normally pass each time. If you have an overactive bladder you may be going to the toilet every hour or so. Each time you may pass less than 100–200 ml.
After the 2–3 days, the aim is to 'hold on' for as long as possible before you go to the toilet. This will seem difficult at first. It may be quite uncomfortable and difficult to stop going to the toilet when you feel you want to. When you are trying to hold on, you can distract yourself by:
After a while it should get easier, as your bladder gradually gets used to holding larger amounts of urine. The idea is to gradually extend the time before you go to the toilet. It may take several weeks, but the aim is to pass urine only 5–6 times in 24 hours and to pass up to 250–300 mls each time. After several months you may find that you just have the normal feelings of needing to go to the toilet and can easily put them off for a reasonable time until it is convenient to go.
It can help to fill in your diary for a 24 hour period every week or so while doing the bladder training. This will record your progress. Make sure you drink a normal amount of fluids when you do bladder training.
The urethra (the tube that drains urine from the bladder) can get narrower after pelvic radiotherapy. This is known as a urethral stricture. It can usually be treated with a small operation. The stricture can be stretched or dilated when you are under a general anaesthetic. Usually this operation is successful but it may need to be repeated.
If you are passing blood in your urine, you will need to have a cystoscopy to find out why the bleeding is happening. If the bleeding is caused by radiation damage to the walls of the bladder and is only slight or occasional, no treatment may be needed. If the bleeding occurs often or is heavier, or is making you anaemic, taking tranexamic acid tablets can sometimes help. Your doctor may prescribe these for you. They are usually taken three times a day and have few side effects.
It may also be possible to stop the bleeding by putting a particular liquid into the bladder through a catheter. This can be uncomfortable, but should not be painful. If the bleeding continues or if you are passing blood clots, you may need to have a catheter so that a liquid can be passed into the bladder to flush out the clots. This procedure is known as a bladder wash-out.
If these treatments don’t stop the bleeding, the areas within the bladder that are bleeding can be cauterised during a minor operation using a cystoscope. Intense heat is applied to the area using an electrical current or laser.
If the bleeding carries on, other treatments such as blood transfusions| or hyperbaric oxygen therapy| may be needed, but this is very rare. We can give you information about both of these treatments.
If the problems continue or do not respond to initial treatments, your doctor or nurse will be able to explain the other treatments that are available. Surgery may be needed. In extreme circumstances it may be necessary to remove the bladder, but this is extremely rare.
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