Lung function tests (Breathing tests)

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What is a lung function test?

A “lung function test” is a procedure performed to give us accurate information about your breathing and how your lungs work. 

Why do I need to have this test?

This test provides detailed information about your lungs to your clinical team. This will enable them to provide you with the most appropriate plan. 

What happens during the test?

Before the test starts the Physiologist will explain the test to you in detail and will answer any questions you may have.

The lung function test is painless. It involves a series of breathing tests consisting of breathing and blowing through a mouthpiece connected to special equipment.

The test will take approximately half an hour to one hour depending on the information required.

Important instructions

  • If you are currently taking any inhalers, please stop taking them four hours before the appointment time.
  • Please do not smoke for four hours before the test.
  • Please do not drink alcohol for four hours before the test.
  • Please do not do any vigorous exercise 30 minutes before the test.
  • Please eat and drink as normal.
  • Please do not wear lipstick or nail varnish to the appointment.

Thank you for your cooperation. This will assist us in obtaining accurate information and enable us to provide you with the most appropriate treatment.

Frequently asked questions 

Will I experience any discomfort or side effects?

Some of the breathing tests are tiring, but you will be given time to recover between tests and there are no known side effects associated with this test.

When will I be told the results of my test?

You will usually be told your results at your next clinic appointment, or a letter may be sent to your GP or the doctor who referred you for the test.

What should I wear when I attend for my test?

You should wear normal comfortable clothing.

What will happen if I do not want to have this test?

If you do not attend for this test we will not be able to pass important diagnostic information to the doctors. This may affect the medical treatment that you receive. You can choose to have the test or not.

Reference

Cooper, B, Evans, A, Kendrick, A and Newall, C (2005) Practical Handbook of Respiratory Function Testing: Part 1. Association for Respiratory Technology and Physiology.

© North Bristol NHS Trust. This edition published July 2024. Review due July 2027. NBT002296.

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Hyperventilation provocation study

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Important information

  • Do not consume any alcohol on the day of the test.
  • Wear comfortable clothes; you will need to remove coats and jumpers for this test.
  • Take all medication as usual.
  • Do not wear nail varnish on the day of the test.

Thank you for your cooperation. This will assist us in obtaining accurate information and enable us to provide you with the most appropriate treatment.

What is a hyperventilation provocation test?

A hyperventilation provocation test is designed to assess your breathing pattern.

Why do I need to have this test?

This test is used to check that your breathing pattern, and that your body maintains the correct levels of gases in your blood.

What happens during the test?

The Physiologist will explain the test to you and answer any queries that you may have regarding it. You will fill out some questionnaires about symptoms that you may be experiencing. Your breathing will be assessed at rest and you will then be asked to breathe hard and fast for 60 seconds whilst measurements are taken of gases in the air you breathe out.

Frequently asked questions

Will I experience any discomfort or side effects?

You may experience some short-term symptoms during the test. There are no long-term side effects of performing this test

When will I be told the results of my test?

You are usually told your results at your next clinic appointment, or a letter may be sent to your GP or the healthcare professional who referred you for the test.

What will happen if I do not want to have this test?

If you do not have this test we will not be able to pass important diagnostic information to your clinical team. This may affect the medical treatment that you receive.

Reference

Rafferty GF, Saisch SGN, Gardner WN. Relation of hypocapnic symptoms to rate of fall of end-tidal PCO2 in normal subjects. Respir Med 1992;86:335–340.

© North Bristol NHS Trust. This edition published February 2025. Review due February 2028. NBT002268. 

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Exercise induced asthma test

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Important information

Please do not use your inhalers for one week prior to the appointment.

Salbutamol (Ventolin) and Bricanyl can be used up to 8 hours prior to the appointment.

Please stop taking the following medications prior to the test:

  • Sodium cromoglycate (8 hours)
  • Nedocromil (48 hours)
  • Theophyllines (12 to 48 hours)
  • Leukotrienes (24 hours)
  • Antihistamines (48 hours)

Take all other medication as normal and please bring a list of all medication with you.

  • Please do not smoke, consume alcohol, eat a heavy meal or perform heavy exercise within four hours of the test.
  • Please do not consume coffee, tea, cola drinks or chocolate on the day of the test.
  • Please wear comfortable clothes and shoes suitable for exercise.
  • Please do not wear nail varnish or false nails.

Thank you for your co-operation. This will assist us in obtaining accurate information and enable us to provide you with the most appropriate treatment.

What is an exercise induced asthma test?

An exercise induced asthma test involves some simple breathing tests and exercising on a treadmill to assess whether this causes your airways to become narrower.

Why do I need to have this test?

This test will help us understand if your airways become narrow in response to exercise. This will help us to provide advice on your ongoing treatment.

Who will perform my test?

The test will be performed by two respiratory physiologists. Respiratory physiologists are staff who have extensive training and knowledge in respiratory physiology and performing lung function tests.

What will happen during the test?

Before the test begins the physiologist will explain the test to you in detail and answer any questions that you have.

To begin with you will be asked to perform some breathing tests through a mouthpiece. You will then have ECG stickers attached to your chest to monitor your heart. You will then be asked to exercise on the treadmill for about six minutes. At particular time periods after you have finished exercising you will be asked to repeat the breathing test.

The whole test will last for approximately one hour. 

Frequently asked questions

Will there be any discomfort or side effects of this test?

Sometimes the test can cause a mild spasm of the airways, which may make you cough or feel tight-chested. This is easily reversed by a common medication (Salbutamol) that is given routinely at the end of the test.

Is there a different test I could have?

There is no other basic test that would give us this information about the sensitivity of your airways.

When will I be told the results of my test?

The results will be sent to the professional that requested the test. They will then discuss the results with you at your next appointment.

© North Bristol NHS Trust. This edition published February 2025. Review due February 2028. NBT002877

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Chest drain

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What is a chest drain?

A chest drain is a narrow tube that is inserted between the ribs and sits in the space between the lung and the chest wall. This space is lined on both sides by a membrane called the pleura and is known as the pleural cavity or pleural space.

A chest drain is inserted when air, fluid, blood or pus has collected in the pleural space.

The external end of the chest drain tube is attached to a bottle which acts as a seal to prevent anything from leaking back into the pleural space.

What is a chest drain for?

You need a chest drain if you have an air leak (pneumothorax), a collection of fluid (pleural effusion), pus (empyema) or blood (haemothorax) in the pleural space. Any of these can cause problems with breathing and can stop the lungs from working properly. The chest drain will allow the fluid or air to leave the body and allow your lung to re-expand.

How does a chest drain work?

Once a chest drain has been inserted the external end is connected to a bottle. The fluid or air travels down the tube, into the bottle.

There are 2 types of chest drain bottle. The first type contains a small amount of water, which acts as a seal preventing air or fluid coming back up the tube into your chest. Alternatively, an electronic chest drainage device may be used (a Thopaz machine), which can deliver suction (to help the lung re-expand) and allows the doctors to measure if there is any ongoing air leak between the lung and pleural cavity.

Before the chest drain is inserted

Before the chest drain is inserted, the doctor will discuss the procedure with you and you will have an opportunity to ask questions. You will then need to sign a consent form.

Blood tests may be needed before the procedure.

If you are on blood thinning medication, they may need to be stopped before the chest drain is inserted, to minimise the risk of bleeding during the procedure.

Please let the doctor know if and why you take blood thinning medication and they will make a plan with you about when it should be stopped.

There are potential rare complications of stopping blood thinning medications but these are generally very rare and the risk is lower than the possible bleeding risk if they are continued.

How will the chest drain be put in?

  • You will either sit with your head and arms resting on a pillow on a table or lie on your bed with your arm above your head. The drain is usually put into the side of your chest below the armpit.
  • Before the procedure starts, an ultrasound may be performed to choose the best place to insert the drain. An ultrasound is painless and a cool gel is used on the skin to ensure good contact for the ultrasound tip. You may be offered painkillers to take before the procedure starts.
  • The procedure is performed using an aseptic technique to minimise the risk of infection. Your skin is cleaned with an alcohol-based liquid to kill any bacteria. A local anaesthetic is then injected into the skin to numb the area where the tubeis to be inserted, which can ‘sting’ temporarily but resolves quickly. A small cut (approximately 2-3mm) is then made in the anaesthetised area. It is normal to feel a sensation of pressure and tugging as the drain is gently eased into the chest, but this should not be painful.
  • The chest drain is held in place with stitches and the exit site is covered with a waterproof dressing. The end of the tubing is connected to a drainage bottle.
  • Your chest drain will be monitored regularly. You may be asked to cough, or take a deep breath. This enables the doctor or nurse to ensure the drain is still functioning. You will be given regular pain relief while the drain is in place. Pain may impair your movement and breathing which may prolong the time your lung takes to expand therefore it is important to report any pain and keep it under control.

The bottle to which the chest drain tubing is attached

The bottle contains a small amount of water, which acts as a seal preventing air or fluid coming back up the tube into your chest.

A clear bottle with a blue lid which the chest drain tubing is attached to. There is pink/orange liquid in the bottle.

 

 

 

 

 

 

 

 

 

The bottle to which the chest drain tubing is attached

The bottle must be kept below the level of the waist at all times.

Patient sitting in a chair with the chest drain tubing attached to a chest drain bottle on the floor.

 

 

 

 

 

 

 

 

 

 

 

 

Insertion site of the drain into the chest

It is secured with a stitch and a waterproof dressing is placed over the top.

Close up view of a patient's chest drain (small blue wire) with a stitch and waterproof dressing.

 

 

 

 

 

 

 

 

 

 

 

 

Thopaz machine (an electronic chest drain device)

Your drain may be attached to this machine, rather than to a bottle, if you have a pneumothorax (air leak into the pleural space). This allows the air leak to be accurately measured and can be used to apply gentle suction to the drain.

Thopaz machine (electronic chest drain device) which has white casing and a black screen on the top of the device.

 

 

 

 

 

 

 

 

 

 

 

 

Looking after your chest drain

As the fluid or air around the lung drains you should be able to move more easily. There are a few simple rules that you can follow to minimise any problems:

  • You can move and walk around with a chest drain but you must remember to carry the drainage bottle with you.
  • Always carry the bottle below the level of your waist. If it is lifted above your waist level fluid from the bottle may flow back into the pleural space.
  • Whilst in bed keep the drainage bottle on the floor.
  • Don’t pull on your chest drain or tangle it around your bed.
  • Do not swing the bottle by the tube.
  • Try not to knock the bottle over.
  • If your chest is painful please tell your nurse.
  • If you feel your tube may have moved or may be coming out please tell your nurse.
  • Inform your nurse if you feel any increased shortness of breath.

When is the drain taken out?

How long the chest drain will be needed depends on your condition and how well you respond to treatment.

Removing the drain is a simple procedure. Once all the dressings are removed, the stitch is cut and the drain is gently pulled out. The doctor or nurse may ask you to breathe in a particular way while the drain is removed. Removal of the drain can feel a little uncomfortable but only lasts a few seconds. You will have a chest X-ray once the drain has been removed.

In some cases a stitch is left where the drain has been. This needs to be removed after 7 to 10 days.

If you experience discomfort after the drain has been taken out you can take simple painkillers. If you develop any other worsening symptoms (lots of pain, difficulty breathing or a temperature) you must tell the doctors and nurses.

Are there any risks with chest drains?

In most cases the insertion of a chest drain is a routine and safe procedure. Most people find their breathing is much easier once the chest drain is in place. However, like all medical procedures, chest drains can cause some problems:

  • Chest drains sometimes fall out and may need to be replaced (this happens in less than 1 in 10 drains). This risk is minimised by stitching the drain in place and covering it with a secure dressing. You can also help by following the suggestions above (‘Looking after your chest drain’).
  • Fewer than 1 in 10 drains may become blocked, which stops them working effectively.
  • You may feel temporarily dizzy or light-headed when the drain is inserted. This occurs in about 1 in 50 patients. It is usually short-lived, but please let your doctor know if you experience this.
  • Pain: most people (1 in 2 people having a drain) experience some discomfort from their chest drain but painkiller medication should control this.
  • Infection: sometimes chest drains can become infected but this is uncommon (about 1 in 50 patients). Thorough cleaning of the skin before putting in the chest drain and a good aseptic technique will help to reduce this risk. If you feel feverish or notice any increase in pain or redness around the chest drain, inform your nurse or doctor.
  • Bleeding: a bruise at the site of insertion occurs commonly. Rarely (less than 1 in 250 patients), the chest drain may accidentally damage a blood vessel and cause bleeding into the pleural cavity. Often it stops by itself but occasionally it might require an operation or other intervention to stop the bleeding.
  • Subcutaneous emphysema: sometimes air can collect under the skin near the chest drain, causing swelling or a ‘crackly’ feeling (less than 1 in 25). Usually this resolves by itself, but occasionally may require a larger drain to be inserted.
  • Re-expansion pulmonary oedema: if the lung re-expands quickly, there is a risk of fluid collecting in the lung itself, which can occur in around 1 in 200 patients. This can cause a cough or worsening breathlessness. If you experience these symptoms, please let the nursing or medical team know as soon as possible as it may help if the fluid is drained more slowly.
  • Chest drain wrongly positioned: if the drain is being inserted for fluid in the pleural cavity, an ultrasound will be used to guide where the drain is placed to help position the drain correctly. However in about 1 in 50 patients, the tip of the drain is not placed in the pleural cavity and instead sits in the tissues of the chest wall. If this is the case, a new drain may need to be inserted.
  • A very rare complication of a drain insertion (about 1 in 200) is puncture of another organ. This could include other structures in the chest (e.g. the lung, heart, diaphragm or major blood vessel) or abdominal organs (e.g. stomach, liver or spleen). If the drain punctures the underlying lung, it may require the drain to stay in place longer. If organ puncture were to happen, another procedure or operation may be needed.
  • Death: less than 1 in 1000 risk.

References and further information

If you require further information, please speak to your doctors and nurses.

Hooper et al., Pleural procedures and patient safety: a national BTS audit of practice. Thorax 2015; 70:198-191.

How to contact us

Brunel building

Southmead Hospital

Westbury-on-Trym

Bristol

BS10 5NB

0117 414 6337

If you or the individual you are caring for need support reading this leaflet please ask a member of staff for advice. If you’re an overseas visitor, you may need to pay for your treatment or you could face fraud or bribery charges, so please contact the overseas office:

6 minute walk test

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Important information

  • Please do not wear nail varnish to your appointment.
  • Please bring any walking aids (stick etc.) that you regularly use when walking and any oxygen prescribed to you for use whilst walking outside the home.

Thank you for your cooperation. This will assist us in obtaining accurate information and enable us to provide you with the most appropriate treatment.

What is a 6 minute walk test?

A “6 minute walk” test is a simple procedure performed to give us accurate information about your blood oxygen levels whilst you exercise.

Why do I need to have this test?

This test can be used to determine your exercise capacity and whether you need additional oxygen when you are exercising. In some situations, the 6 minute walk test provides better information of a patient’s ability to perform daily activities.

What happens during the test?

Before the test begins the Physiologist will explain the test to you in detail and will answer any questions that you have.

A probe will be put on your ear. This will provide us with information about your blood oxygen levels. You will then be asked to walk for 6 minutes along a flat corridor.

The test will take approximately half an hour to complete. The length of the test may vary slightly depending on your oxygen levels during the test.

Frequently asked questions

Will I experience any discomfort or side effects?

You may become breathless during the test but there are no long term side effects associated with the test.

Is there a different test I could have?

This is the most basic test that would give us this information about your exercise tolerance and limitations.

When will I be told the results of my test?

You are usually told your results at your next clinic appointment, or a letter may be sent to your GP or the healthcare professional who referred you for the test.

What should I wear when I attend for my test?

You should wear normal comfortable clothing and flat shoes suitable for walking in.

Reference

American Thoracic Society (2002) ATS Statement: Guidelines for the Six-Minute Walk Test American Journal of Respiratory Critical Care Medicine.

© North Bristol NHS Trust. This edition published February 2025. Review due February 2028. NBT002285

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The importance of eating well in hospital - information for kidney patients

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Everyone who comes into hospital is checked for risk of malnutrition. You may have been asked to read this page if you are at risk of malnutrition or have a small appetite at the moment. Eating well can help you to get better.

What is malnutrition?

Malnutrition is when you do not get all the nutrients (e.g. energy or protein) your body needs to function properly.

Malnutrition can occur if you have:

  • A low body weight.
  • Recently lost a lot of weight.
  • Been eating much less than usual.
  • A high need for nutrition due to illness or surgery.

Malnutrition increases the risk of problems such as:

  • Infection.
  • Falls.
  • Pressure ulcers.
  • Tiredness.
  • Heart and breathing problems.
  • Staying in hospital for longer.

Why is it important to eat well in hospital?

Eating well in hospital will reduce your risk of malnutrition and the problems which can happen because of this.

Eating better will help you to:

  • Fight infection.
  • Heal wounds and broken bones.
  • Do more for yourself.
  • Give you more strength to move around and breathe better.
  • Stay in hospital for less time.

Ways to eat better

If you find you can’t eat very much at meal times, here are some suggestions:

  • Try eating smaller portions and more often.
  • Ask for a glass of hot or cold milk between meals instead of tea or coffee.
  • Have a biscuit or piece of cake with your drink between meals.
  • Ask the nurse looking after you for a slice of toast or bowl of cereal and milk at bedtime. These foods are always available in the ward kitchen.
  • Try to eat the protein portion of your meal first e.g. meat, chicken, fish, egg, cheese, beans.
  • Try to eat a dessert also. Good choices are sponge and custard, crumble and custard, milk pudding, yoghurt or cheese and crackers.
  • You may also be offered a special high energy drink such as Fortisip Compact Protein.

What could my friends and relatives bring in?

Visitors may like to bring in food to help you eat more.

We have to be careful that foods brought in won’t make you ill. For this reason, only foods which can be kept safely in your room may be brought in. Foods such as sandwiches and cream cakes need to be eaten immediately. They should not be kept for later.

Check with your nurse if some foods can be put in the fridge for eating later that day e.g. sealed individual pots of yoghurt, trifle, rice pudding, cheesecake. These should be labelled with your name and the use by date.

Here are some ideas for foods which can be brought in:

  • Biscuits e.g. shortbread, digestives, custard creams, rich tea.
  • Small boxes of breakfast cereals.
  • Cake e.g. sponge, Madeira, blueberry or lemon muffins, flapjacks, doughnuts.
  • Individual pots of long life rice puddings, custard.
  • Breadsticks, popcorn, maize or wheat based crisps e.g. Mini Cheddars, Doritos, Sunbites.

If you usually follow a low potassium diet, it may not be necessary whilst you have a poor appetite. The snacks listed above are suitable for a low potassium diet. You can ask to speak to the dietitian if you are unsure.

If you normally follow a fluid restriction at home, then you will still need to continue with this in hospital, unless the doctor or dietitian advises you otherwise.

Suggested meal plan

Breakfast:

  • Porridge or cereal with milk.
  • Toast with butter and jam or marmalade.

Mid-morning:

  • Cup of hot or cold milk and biscuits.

Mid-day meal:

  • Hot meal or sandwich.
  • Sponge or crumble and custard or milk pudding or yoghurt or cheese and crackers.

Mid-afternoon:

  • Biscuits or cake with a cup of tea.

Evening meal:

  • Sandwich or hot meal.
  • Milk pudding, yoghurt or cheese and crackers.

During evening:

  • Cheese and crackers or a slice of toast and butter or a small bowl of cereal with milk.

Other tips

  • Staff can be busy but they want to help you get better. Don’t be afraid to ask for a drink of milk or if snacks are available. Milk, bread and breakfast cereals are usually available in the ward kitchens.
  • Do ask the nurses if you need any help at mealtimes.
  • If you are concerned you are still not eating enough, speak to your nurse about seeing a dietitian.

If you or the individual you are caring for need support reading this please ask a member of staff for advice.

www.nbt.nhs.uk/nutrition-dietetics

© North Bristol NHS Trust. This edition published January 2023. Review due January 2026. NBT002485.

Looking after yourself whilst you are receiving kidney treatment

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Living with a long term health condition can have an impact on your emotional wellbeing. Looking after your emotional health is just as important as looking after your physical health.

Evidence* suggests there are five steps we can all take to improve our mental wellbeing. If you give them a try, you may feel happier, more positive, and able to get the most from life.

  • Connect – connect with the people around you. Spend time developing supportive relationships with people that have a positive impact on your wellbeing.
  • Be active – you don't have to go to the gym. Take a walk, spend time outside, stretch, or play a game. Find an activity that you enjoy and make it a part of your life. You might need to think creatively about getting more activity into your life in a way that feels manageable.
  • Keep learning – learning new skills can give you a sense of achievement and a new confidence. So why not sign up for that cooking course, start learning to play a musical instrument, learn another language, or figure out how to fix your bike?
  • Give to others – even the smallest act can count, whether it's a smile, a thank you or a kind word. Larger acts, such as volunteering at your local community centre, can improve your mental wellbeing and help you build new social networks.
  • Be mindful – be more aware of the present moment, including your thoughts and feelings, your body and the world around you. Some people call this awareness "mindfulness". It can positively change the way you feel about life and how you approach challenges.

NHS Psychological Therapies

Psychological therapies, sometimes called talking therapies, can help with common difficulties like stress, anxiety and low mood. If you are registered with a GP you can refer yourself directly to free services (or you can ask your GP to refer you).

These services are also known as Improving Access to Psychological Therapies (IAPT) services and provide psychological support in a variety of ways including face-to-face, online, over the phone, and courses.

Bristol, North Somerset and South Gloucestershire:

VitaMinds
0333 200 1893
refer.BNSSG@nhs.net

B&NES: B&NES Talking Therapies

01225 675150

Wiltshire: Wiltshire IAPT Service

01380 731335
awp.wilts-iapt@nhs.net

Swindon: LIFT Psychology

01793 836836
lift.psychology@nhs.net

If you have any concerns about your mental wellbeing or physical health you can always contact your GP. If you need urgent help please call 999 or attend A&E.

If you are feeling distressed and would like a confidential listening service, you can contact the Samaritans. They are available 24 hours a day, 7 days a week.

Telephone: 116 123
Email: jo@samaritans.org

Other ways to access free support

Kidney Peer Mentor Service

The Kidney Peer Mentor Service aims to give short term practical and emotional support to people living with kidney disease, their families, and carers. All trained peer mentors are people who have lived with kidney disease themselves, and are allocated to you based on their experiences. If you would like to find out more please email: kidneypeermentorservice@nbt.nhs.uk

Renal Psychology Service for Renal and Transplant Patients

We have two clinical psychologists based within the Renal Team at Southmead to support people with a wide range of issues. Sometimes people experience emotional difficulties as a direct result of adjusting to and living with kidney problems, at other times difficulties may come up independently making it more difficult to cope with the demands of living with kidney problems and treatment. If you would like an appointment with one of the renal psychologists please speak to a member of staff who will be able to refer you.

If you or the individual you are caring for need support reading this please ask a member of staff for advice.

How to contact us:

Clinical Psychology Service
Renal & Transplantation Directorate
Gate 10 Level 6
Southmead Hospital
Westbury on Trym
Bristol
BS10 5NB

0117 414 7696
www.nbt.nhs.uk

Peritoneal dialysis catheter insertion

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Peritoneal dialysis catheter insertion: Placing a Tenckhoff catheter in the abdomen

Why do I need a Tenckhoff catheter? 

Your doctor has recommended you start dialysis treatment for kidney failure because of your blood test results and how you feel. You have chosen peritoneal dialysis.

The peritoneum is a membrane that lines the organs in the abdomen (tummy). Peritoneal dialysis (PD) filters the blood to “clean” it, when your kidneys don’t work well enough to keep you healthy.

A permanent tube called a Tenckhoff catheter is placed in the lower part of your belly. This is used to put in and drain out dialysis fluid. It is a soft, flexible tube, that lies flat against your body. There is a cap on the end of the tube so no opening.

How does it work?

For Peritoneal Dialysis the fluid is left in your abdomen to do the dialysis for several hours, then drained out. This fluid takes away some of the waste products and excess water that are normally removed by the kidneys. Fresh fluid is then put into the abdomen.

This exchange of fluid takes about 30 minutes and you will do it 2 - 4 times a day. The fluid comes in a range of volumes and “strengths”. The type of fluid you use depends on your needs.

The catheter is inserted by a surgeon at Southmead Hospital. The operation will usually be a day case (you will not stay overnight) using general or local anaesthetic.

Where will the catheter be?

There are a few things to think about when choosing the position of your catheter. You will discuss this with your surgeon before the operation and the community dialysis nurse will mark the place you agree on your skin.

Things to think about:

  • Where do the waistbands on your clothes and underwear sit? You may not want these to be on top of your tube or exit site as this could interfere with healing.
  • Do you prefer to sleep on one side? You do not want the tube to come out of the side you sleep most on as it can be uncomfortable and may interfere with healing.
  • Where are your natural skin folds when you are sitting? The exit site should not be in a fold.

Preparing for the procedure

Infection screening

Before the procedure we will take swabs of your nose and groin. This is to check if you are carrying any bacteria on your skin that could cause infection of the catheter.

If the swabs are positive you may need treatment to clear the bacteria before the procedure.

The usual treatment is:

  • Cleaning your skin with antibacterial wash (Hibiscrub or Octenisan) for 5 days before the procedure.
  • Applying antibacterial ointment (Mupirocin or Naseptin) to both nostrils 3 times a day, for 5 days before the procedure.

If for any reason you haven’t had the swab tests done before the procedure, they will be done when you are admitted. If treatment is required it will be started then for at least 5 days.

Medications

If you take warfarin, clopidogrel or any other blood-thinning tablets, you will need to stop taking these before the procedure. Your doctor or pre-operative assessment clinic (POAC) nurse will tell you when to stop taking them.

What happens before the operation?

If you are having general anaesthetic

You will be given a date to attend the pre-operative assessment clinic (POAC). Some blood samples and swabs will be taken, and measurements of your blood pressure, pulse, temperature, and oxygen level.

If you are having local anaesthetic

Blood samples and swabs will be taken at the initial visit to your home. Before your surgery a member of the Renal Community Team will come to your house to go through the details of peritoneal dialysis (PD) including:

  • Storage of dialysis fluids.
  • Ordering stores and delivery.
  • The area where you will do peritoneal dialysis.
  • Handwashing technique and cleanliness.
  • Instructions for how to keep the tube safe when you get home after the operation.

You will be given a date for your surgery. It is important your bowels are empty so you will be asked to take laxatives called sodium docusate and senna 3 days before the operation.

You will continue to take laxatives after the operation to make sure the PD tube won’t move because of constipation.

On the day of the operation

If you are having general anaesthetic

You will go to the medirooms.

If you are having a local anaesthetic

You will go to the renal ward 8b.

  • If your operation is planned for the morning don’t have anything to eat or drink after 00:00 (midnight). If your operation is in the afternoon you will be given an early breakfast at around 06:00 - you won’t have anything to eat or drink after that.
  • If you have diabetes that is treated with medication is it essential that you tell the nurses.
  • You will be given antiseptic solution to shower with and then put on a clean theatre gown and anti-embolism compression socks.
  • We cannot give you an exact time for your operation. Theatre lists need to be flexible in case of any emergencies. Everything possible will be done to make sure you don’t have to stop eating/drinking for any longer than necessary.
  • Please don’t bring any valuables or large amounts of cash as we cannot be responsible for them.
  • A member of the Renal Community Team will see you before the procedure to mark the position of the PD tube exit site.
  • You will be asked to sign a consent form. The surgeon will explain what you should expect, including the reason for inserting the catheter and any possible complications to make sure you are aware of them.

What happens after the operation? 

  • When you have recovered from the anaesthetic you will be given painkillers if you need them. You will be encouraged to eat and drink as soon as you feel like it.
  • If you had general anaesthetic you will have blood tests to check kidney function and haemoglobin level.
  • You will have dressings on your abdomen and a stitch (suture) closing the tube exit site. The stitch is usually dissolvable but if not you will have it removed 10 days later.
  • You are likely to have some bruising on your abdomen.
  • You will be able to go home the same day in most cases.
  • You will have a phone number to ring if you have any problems.

What immediate follow-up care will I have? 

  • The day after your operation a member of the Renal Community Team will phone you to check your recovery. They will give you a date to come for check-up usually 7 days later.
  • We will check your wound and flush the PD tube to check it’s working.
  • 2 - 3 weeks after your operation, you will have PD training which usually takes 3 days.
  • 2 - 3 weeks after training you will come to the PD clinic to check your progress.

Will I need to take time off work?

Most patients are advised to take 7 days of work to recover.

Some people need more than this, particularly if you have a manual job.

What complications might happen?

There are 4 main possible complications that may happen. 

Functional problems

Occasionally the catheter might not work. This might be because the tip of the catheter is in the wrong place or is covered by internal tissue which stops it working. At Southmead this happens in less than 7 in 100. 

Bleeding 

Bleeding can happen, mostly because of bruising around the wound. It usually stops on its own. In rare cases (less than 1 in 100) you may need surgery to stop the bleeding. 

Infection

You will have intravenous (IV) antibiotics when the catheter is inserted to prevent infection. Despite this, some patients develop infection at the catheter exit site which needs further antibiotics. This happens in less than 1 in 100 cases, and very occasionally the catheter may need to be removed.

There is also a risk of infection deeper in the abdomen, causing peritonitis in the first 2 weeks after insertion. This happens in about 3 in 100 cases, and will be treated with different antibiotics.

Bowel perforation

Very rarely during the procedure the bowel is cut by mistake. This happens in less that 1 in 100 cases. It is a serious complication that may need another operation and a stay in hospital.

How will I be looked after long-term?

A community nurse will look after your ongoing care, and they will keep in contact with you. This will involve some visits to your home. A follow-up clinic appointment will be arranged with one of the renal doctors after your training.

Hospital transport can be arranged for appointments and training, but this is only for patients who meet certain criteria. We encourage you to make your own arrangements if possible.

© North Bristol NHS Trust. This edition published October 2024. Review due October 2027. NBT002131. 

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Contact Renal Community Team

Renal Community Team
Level 1, Gate 5
Brunel building
Southmead Hospital
BS10 5NB

renalcommunityteam@nbt.nhs.uk

Looking after yourself whilst having kidney treatment (Renal Psychology Service)

Regular Off Off

Living with a long-term health condition can have an impact on your emotional wellbeing. Looking after your emotional health is just as important as your physical health. 

Evidence suggests there are five steps we can all take to improve our emotional wellbeing. If you give them a try you may feel happier, more positive, and able to get the most from life. 

  • Connect - connect with the people around you. Spend time developing supportive relationships with people that have a positive effect on your wellbeing.
  • Be active - you do not have to go to the gym. Take a walk, spend time outside, stretch, or play a game. Find an activity that you enjoy and make it part of your everyday life. You might need to think creatively about getting more activity into your life in a way that feels manageable.
  • Keep learning - learning new skills can give you a sense of achievement and a new confidence. Why not sign up to learn a new skill, pick up a musical instrument, or develop your DIY skills. Is there a new craft you would like to learn?
  • Give to others - even the smallest act can count, whether it’s a smile, a thank you, or a kind word. Larger acts, such as volunteering at your local community centre can improve your emotional wellbeing and help you build new relationships.
  • Be mindful - this can positively change the way you feel about life and how we approach challenges. This means learning to focus on the present, for example, what are we thinking, feeling, and noticing about the world around us?

Further support for emotional wellbeing available 

NHS Psychological Therapies 

Psychological therapies, sometimes called talking therapies, can help with common difficulties like stress, anxiety, and low mood. If you are registered with a GP you can refer yourself directly to services, or ask your GP to refer you. These services used to be known as Improving Access to Psychological Therapies (IAPT) services. They provide psychological support in a variety of ways including face-to-face, online, over the phone, and courses.

Find NHS Psychological Therapies in your area

Bristol North Somerset an South Gloucestershire 

Bath and North East Somerset 

Wiltshire Talking Therapies

Swindon Talking Therapies 

If you have any concerns about your emotional wellbeing or physical health, you can always contact your GP. If you need urgent help please call 999 or go to A&E. 

If you are feeling distressed and would like a confidential listening service, you can contact the Samaritans by phoning 116 123. They are available 24 hours a day, 7 days a week.

Other ways to access free support

Social prescribing

Social prescribing is available through all GP practices. It aims to help people improve their health, emotional wellbeing, and social networking by connecting them to community activities and resources. For example, social prescribers can discuss your interests with you and help find local activities that you might want to get involved in.

Kidney Peer Mentor Service 

The Kidney Peer Mentor Service aims to give short-term practical and emotional support to people living with kidney disease, their families, and carers. All trained peer mentors are people who have lived with kidney disease themselves, and are allocated to you based on their experiences. If you would like to find out more please email: kidneypeermentorservices@nbt.nhs.uk

Renal Psychology Service for Renal and Transplant patients

We have two clinical psychologists based in the Renal Team at Southmead to support people with a wide range of issues. Sometimes people experience emotional difficulties as a direct result of adjusting to and living with kidney problems. At other times difficulties may come up independently, making it more difficult to cope with the demands of living with kidney problems and treatment.

If you would like an appointment with one of the renal psychologists, please speak to a member of staff who will be able to refer you.

How to contact us

  • Clinical Psychology Service, Renal and Transplant, Gate 10 level 6, Brunel building, Southmead Hospital, BS10 5NB
  • 0117 414 7698

© North Bristol NHS Trust. This edition published January 2025. Review due January 2028. NBT003225

Support your local hospital charity

Southmead Hospital Charity logo

See the impact we make across our hospitals and how you can be a part of it. 

It's okay to ask

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