Nasogastric/nasojejunal tube insertion

Regular Off On Imaging Patient Information NG or NJ tube insertion

This information is for patients whose doctor has requested you have a nasogastric/nasojejunal tube inserted.

What is a nasogastric/ nasojejunal tube?

A nasogastric (NG) tube is a narrow feeding tube which is placed through your nose down into your stomach. 

A nasojejunal (NJ) tube is also a narrow feeding tube placed through the nose, but it is positioned in the small bowel beyond stomach (the jejunum).  

These feeding tubes can be used to give you fluids, medications and liquid food complete with nutrients directly into your stomach or small bowel, as appropriate.

Why do I need to have an NG/ NJ feeding tube inserted?

NG/ NJ tubes can provide you with the fluids, medications and nutrition your body needs while you are unable to eat or drink adequate amounts. 

This may be because you have swallowing problems or need access for specific medications such as Duodopa, or need additional nutritional support.  

Are there any risks?

NG/ NJ tube insertion is a safe procedure.

On the day of the procedure

Please inform us if you are allergic to anything or you are diabetic.

  • You should not eat for 4 hours before your appointment. 
  • You may drink water and take any prescribed medications until the time of your appointment. 
  • If you are an outpatient, you will arrive at the Imaging Department, Gate 19 of the Brunel building and be accompanied into our day case area. 
  • If you are an inpatient, you will come to the Imaging Department from the ward you have been admitted to.
  • A doctor will discuss the procedure with you. You will be given an opportunity to ask any questions you may have. 
  • Once all the checks have been performed, you will be taken to the procedure room. 
  • There will be a doctor, nurse and radiographer with you throughout the procedure.
  • You will be given a local anaesthetic throat spray to help numb the throat.
  • Some lubricant jelly will be put on the tube to help it into position.
  • The narrow feeding tube will be passed through a nostril, down into your stomach/ small bowel guided by an x-ray machine. You will be asked to swallow a few times to help the tube into position. 
  • The tube will then be secured using a dressing or nasal tape.

What happens after the procedure?

You will be taken back to the day case area or your ward, so that nursing staff may monitor you closely.

We hope this information is helpful. If you have any questions before or after the procedure, please phone the Imaging Department using the number on your appointment letter.

© North Bristol NHS Trust.  This edition published December 2022. Review due December 2025. NBT003519

Medial branch blocks (Imaging)

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What is a medial branch block? 

This procedure is for diagnosis only and is not for permanent pain relief. Your pain is likely to return a few hours after the procedure.

Facet joints are found between each of the spinal bones and allow the spine to move. The medial branches are nerves that carry information, including pain, from the facet joints to the brain. Sometimes back pain arises from these joints. 

A medial branch block uses local anaesthetic to numb these small nerves. 

If the pain is coming from the joints the pain may be reduced for some hours following these injections.

Following this procedure we can determine whether the facet joints are the cause of your pain.

Depending on the results, your consultant may offer a longer-lasting treatment that could be done after your follow up call or visit.

How do I prepare for the medial branch blocks?

We would advise you not to take any pain relief medication for 6 hours before your appointment.  This is so we can accurately assess if the local anaesthetic changes your back pain. You can eat and drink on the day as normal. You are advised not to drive following the procedure.

Please tell us before attending for the procedure if you take any blood thinning medication such as:

  • Warfarin.
  • Clopidogrel.
  • Rivaroxaban.
  • Dipyridamole.
  • Dabigatran.


Please note this list is not exhaustive. 

The number for the Imaging department is on your appointment letter.

What will happen during the procedure?

  • You will arrive at Gate 18 where a member of the Imaging team will take you through to the fluoroscopy waiting room.
  • Following confirmation of your details and history you will be shown into the X-ray room and introduced to the staff performing the procedure.
  • You will be cared for by a small team including a radiologist (X-ray doctor) and/or radiographer and an imaging support worker.
  • Before the examination begins the radiologist or specialist radiographer will explain what they are going to do. You will be given the opportunity to ask any questions you may have. If you are happy to proceed you will be asked to sign a consent form. We will also ask you to score you back pain out of 10 before we begin. 
  • You will then be asked to lie on your front on the X-ray couch. The skin will be cleaned and a small amount of local anaesthetic will be injected under the skin. This stings for a few seconds and the area then goes numb.
  • A very fine needle will be directed to the medial branches using the X-ray machine.
  • When the radiologist or specialist radiographer is satisfied with the needle position, the local anaesthetic will be injected. Following the procedure we will ask you again to score your pain out of 10. 
  • Afterwards you will be asked to sit in our waiting room for 20 - 30 minutes so that we can ensure you are feeling well before you go home.

Will it hurt?

You may have some discomfort during the procedure. If you feel uncomfortable, let one of the members of the team know and they will try to make you more comfortable.

How long will it take?

You will be awake throughout the procedure, which lasts about 15 – 30 minutes.

How will I feel after the injections? 

Remember that medial branch blocks are not a treatment.  They are done to help us diagnose the source of your pain.
Immediately after the injections you may feel less pain but it will probably return after a few hours.

Are there any risks or side effects?

Generally it is a very safe procedure, but as with any treatment there are risks or side effects:

  • An increase in your pain in the first 24 hours following injection. Should this occur, take your usual or prescribed pain medication and seek advice from your pharmacist or GP if necessary.  
  • Bleeding or haematoma (a bruise under the skin) – this should settle down by itself.
  • Infection developing at the injection site. This will happen to less than 1 in 5000 people. Contact your GP if you experience any redness or tenderness at the injection site.  
  • The procedure is performed under X-ray to confirm the needle is in the correct place. Patients who are or may be pregnant should inform the department before attending their appointment.

Who should I contact if I have any concerns?

If you have any concerns please contact the Imaging Department using the number on your appointment letter.

© North Bristol NHS Trust.  This edition published February 2024. Review due February 2027. NBT003581.

Bleomycin sclerotherapy

Regular Off On Imaging Patient Information Sclerotherapy (with bleomycin)

This information is for patients whose doctor has requested you have bleomycin sclerotherapy. 

We hope that the following information will answer some of the questions you may have about this procedure.

What is bleomycin sclerotherapy and why is it needed?

Bleomycin sclerotherapy is used to treat vascular and lymphatic malformations. It is usually suggested as a treatment for some kinds of malformations e.g:

  • Microcystic lymphatic malformations.
  • Venous malformations with a larger solid part.
  • A second form of treatment of standard sclerotherapy has failed.
  • Malformations on the surface of the skin where the skin is directly involved as it is less likely to cause skin blistering or scarring.
  • Treatment of malformations in areas where the doctors are keen to avoid swelling.

Sclerotherapy is carried out in the Imaging Department by a doctor (radiologist) who specialises in doing procedures under imaging guidance with X-rays or ultrasound.

What is a lymphatic malformation?

A lymphatic malformation is an abnormality of the lymphatic system that results in a collection of fluid filled spaces. These malformations are congenital (they were present when you were born). The cysts are filled with a clear fluid, similar to the fluid in a blister. Lymphatic malformations are not dangerous but can cause pain and swelling. 

Microcystic malformations contain lots of tiny cysts and usually cause problems because they are bulky, unsightly, or get infected. Sclerotherapy is a way of trying to reduce the size of the cysts so that they are smaller and less troublesome.
 

What is a venous vascular malformation?

A venous vascular malformation is a collection of abnormal venous vascular spaces. These spaces will have some connections to nearby normal veins. 

Venous malformations are congenital (they were present when you were born). They contain vascular spaces with slow flowing blood and solid tissue.

Like lymphatic malformations venous vascular malformations are not usually dangerous, but can cause pain and swelling, particularly when blood clots form within the lesion. 

What is bleomycin?

Bleomycin is a medicine that has been used for many years to treat other conditions such as cancer. More recently small doses of bleomycin have been found to be useful for treating vascular and lymphatic malformations. 

When it has been used in higher doses in cancer treatment and has been injected straight into the bloodstream, bleomycin can cause damage and changes to the lungs and how they function. This can happen during the treatment or afterwards. This is extremely unlikely to happen when bleomycin is being used in sclerotherapy, as the doses are much lower, and the medicine is not given in the same way.

However, always tell your doctor if after treatment with bleomycin you: 

  • Develop a wheeze.
  • Develop a cough.
  • Have a fever.
  • Feel breathless.

You should also let them know if any existing breathing problems get worse.

What happens before the sclerotherapy?

Before you attend for bleomycin sclerotherapy we will send you a clinic appointment to meet with the radiologist. Here they will assess your suitability for the procedure.

If necessary, we will arrange for you to have some breathing tests before you have bleomycin treatment.

You will need to have a blood test a few days before the procedure to check that you are not at increased risk of bleeding and that it will be safe to take to proceed with the bleomycin treatment. This may be arranged to take place at your GP surgery. 

You can continue taking your normal medication. If you are on any medication which thins the blood (e.g., aspirin, clopidogrel, warfarin, rivaroxaban, dabigatran, apixaban) please call the Imaging Department using the number on your appointment letter as we may need to adjust your medication.  

On the day of the procedure

  • You should not eat anything from midnight the night before the procedure. You may drink clear fluids until 7am on the day of the procedure.
  • You will arrive at the Imaging Department, Gate 19, and be accompanied into our day case area.
  • You may take your normal medication unless instructed otherwise.
  • Please inform us if you are allergic to anything.
  • The radiologist will discuss the procedure with you. You will be given an opportunity to ask questions. If you want to go ahead with the procedure you will be asked to sign a consent form.
  • You will be asked to change into a hospital gown and a small plastic tube (cannula) may be put into your arm.
  • Once all the checks have been performed and consent signed, you will be taken to the X-ray room on the trolley. There will be a radiologist, nurses and a radiographer with you throughout the procedure.
  • The radiologist will use an ultrasound machine to look at the malformation to find the correct area to be treated.
  • Your skin will be cleaned with an antiseptic solution and covered with sterile drapes.
  • The radiologist will then inject local anaesthetic into the area selected, which will briefly sting and then go numb. The radiologist may then inject X-ray dye into the malformation to confirm the needle position and that it is safe to inject bleomycin. The bleomycin will then be injected through one or several small needles into the malformation under ultrasound and sometimes X-ray guidance.
  • The procedure is likely to take about 30 minutes.
  • Once the procedure is complete the needle(s) will be removed, and the radiologist will apply a dressing if necessary. 

What happens after the procedure?

  • You will be taken back to the day case area, so that nursing staff may monitor you closely.
  • If you are in pain, tell the nursing staff so you can be given appropriate painkillers.
  • You will be advised to stay in our day case area for up to 4 hours.
  • You will be able to eat and drink as normal.
  • If everything is satisfactory, you will be free to go home. 

What are the risks associated with sclerotherapy?

Bleomycin sclerotherapy is usually a safe procedure. Potential complications include:

  • In the first 24 hours following bleomycin sclerotherapy, the area is likely to be swollen. You may take over the counter pain medication as necessary to keep the inevitable associated pain under control. The pain will resolve within a few days, but it may take several weeks for the swelling to settle completely.
  • There is a slight risk of the malformation developing an infection after the treatment. You will need a short course of oral antibiotics if this happens.
  • Very rarely, bleomycin can cause some discolouration of the skin or nails or make some hair fall out. This usually gets better with time. We think that the skin is more likely to be affected if there are monitoring leads or plasters stuck to the skin at the time of treatment. We will try to put these on parts of the skin that are less noticeable.
  • In some cases, when bleomycin has been used in much higher doses straight into the bloodstream for treating cancers, patients have developed scarring of their lungs, causing breathing problems. This has only been reported for high dose treatment with bleomycin, not at the doses used for sclerotherapy of vascular malformations.
  • If the bleomycin spreads beyond the malformation it may cause damage to nearby normal tissues. 
    This is a rare complication but can cause permanent damage to the affected tissues. One example could be damage to the overlying skin which may ulcerate and cause scarring of the area. Other structures that could be affected depend on where in the body the malformation is, but could include muscle or nerve damage which may be permanent. 

If you experience any symptoms you are concerned about, please contact the Imaging Department directly on the number on your appointment letter or alternatively contact your GP or the Emergency Department.

Are there any alternatives to sclerotherapy?

Sclerotherapy is the best treatment option for many malformations as it can be an effective treatment and usually carries lower risks than open surgery. However, as every malformation is different, sclerotherapy may not always be the best option. 

Alternative options may include having no treatment, surgery or a combination of surgery and sclerotherapy. Your doctor will explain the options for treatment suitable for you.

Am I likely to need more than one treatment session?

You might need several sclerotherapy procedures to reduce the malformation. Sclerotherapy will not ‘cure’ the malformation, but it should shrink it significantly. 

We will also review you at an outpatient clinic appointment around 2 - 3 months after treatment.

Again, if you experience any symptoms you are concerned about, please contact the Imaging Department directly on the number on your appointment letter or alternatively contact your GP or the Emergency Department.

Finally, we hope this information is helpful. If you have any questions either before or after the procedure the staff in the Imaging Department will be happy to answer them.

© North Bristol NHS Trust.  This edition published July 2023. Review due July 2026. NBT003584

Imaging Department Contact Centre

If you are unable to attend your appointment please let us know as soon as possible. You can also contact the Imaging Department Contact Centre if you wish to change or discuss your appointment.

Telephone: 0117 414 8989

Dr Stephen West - Intensive Care and Nephrology

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GMC Number: 7020691

Year of first qualification: 2008 Imperial College London

Specialty: Intensive Care and Nephrology

Clinical interest: Acute kidney injury, Spinal Cord Injury, Hospital Acquired Infections, Critical Care Echocardiography

Secretary: Eleanor Hucker (Nephrology), Intensive Care (Anaesthetic Secretaries)

Telephone: 0117 414 7701 (Nephrology), 0117 414 5114 (Intensive Care)

Email: mailto: Stephen.west@nbt.nhs.uk

Professional Bodies:

  • MRCP (Neph, London).
  • FFICM.
  • Intensive Care Society.
  • MDDUS.
  • ESICM.
West

Dr Stephen West - Intensive Care and Nephrology

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GMC Number: 7020691

Year of first qualification: 2008 Imperial College London

Specialty: Intensive Care and Nephrology

Clinical interest: Acute kidney injury, Spinal Cord Injury, Hospital Acquired Infections, Critical Care Echocardiography

Secretary: Eleanor Hucker (Nephrology), Intensive Care (Anaesthetic Secretaries)

Telephone: 0117 414 7701 (Nephrology), 0117 414 5114 (Intensive Care)

Email address: Stephen.west@nbt.nhs.uk

Professional memberships:

  • MRCP (Neph, London)
  • FFICM
  • Intensive Care Society
  • MDDUS
  • ESICM
Related links

Breathing Pattern Disorder - Physiotherapy appointment

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This page is for patients who have been referred to see a specialist physiotherapist, because it has been identified that some of your breathlessness could be due to a change in your breathing pattern from the 'normal'. 

This often triggers your symptoms earlier and they last longer, making your lung condition symptoms appear worse.

A breathing pattern disorder is when your body has adapted to a particular way of breathing due to stressors or triggers, which means your body has lost its natural rhythm.

You may be using the upper chest rather than your diaphragm (muscles below the lungs), or breathing using your mouth rather than your nose.

This can lead to over breathing which can cause a chemical imbalance in the blood, causing feelings like

  • Feeling you can’t fill your lungs up enough.
  • Breathlessness when doing minimal exercise.
  • Frequent sighing and yawning. 
  • Palpitations. 
  • ‘Pins and needles’ in hands/mouth. 
  • Feeling permanently exhausted. 
  • Throat symptoms including coughing. 
  • Light headedness.

Over breathing is a normal reaction to any stressful situation, including colds/upper airway viruses. However sometimes due to a prolonged trigger or increased stress, the breathing does not return to normal.

It is possible to re-train your breathing pattern, initially learning to control the symptoms when resting, before progressing onto maintaining the correct pattern of breathing during your day-to-day life. This in turn allows you to keep a greater sense of control over your breathing.

What to expect in your first appointment

The first appointment will be around 60 minutes. Don’t worry, you won’t be exercising on your first appointment and the exercises you will be given initially will be starting to retrain your breathing while resting.

Attendance

If you are unable to attend your appointment, please phone us to rearrange as soon as you can so we can fill the appointment slot (phone number on back of leaflet). If you have any other questions, please get in contact. 

Websites for more information: 

Physiotherapy for breathing pattern disorders 

Breathing Freely (breathetrain.co.uk)

© North Bristol NHS Trust. This edition published May 2024. Review due May 2027. NBT003695.

Contact us

Respiratory Specialist Team
Gate 18, Brunel building
Southmead Hospital
Westbury-on-Trym
Bristol
BS10 5NB

0117 414 2011

respiratoryspecialistteam@nbt.nhs.uk 

Eating well on peritoneal dialysis

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This information will help you choose foods to keep you well on dialysis. You may also be given some extra information if needed. Your dietitian may change the advice in the future if your health, blood tests, or appetite changes. 

You will be able to talk to your dietitian regularly about your eating. You can contact your dietitian any time. see the end of the page for contact details. 

What can I eat? 

Beans, lentils, fish, eggs, meat, and other protein foods

These are high protein foods. They are essential:

  • For strong muscles.
  • To fight off infections.
  • For healthy skin and blood.

Before starting dialysis, you may have been advised to eat smaller portions of protein foods. Now your body is losing some protein during dialysis. You need to eat extra protein foods to replace what you are losing.

These are high protein foods:

ProteinRecommended portions
Meat, chicken, and turkeyPalm size portion
FishHand size portion 
Eggs2
Beans, lentilsHalf a tin/6 tablespoons
Quorn, tofu, tempeh, soya, proteinPalm size portion

 

Dairy or dairy alternatives (such as soya drinks and yoghurts)

Milk, cheese, yoghurt and fortified soya milk are great sources of protein and calcium. They also contain a lot of phosphate.

Phosphate levels in the blood may be high when the kidneys are not working properly; this can increase your risk of heart disease, cause weak bones and itching. Your dietitian will advise if you need to limit these foods to lower phosphate levels in the blood. See page 10 for more information about phosphate.

Potatoes, yams, cassava, plantain, bread, rice, pasta, cereals, and other starchy carbohydrates

These foods give us energy. 

Try to include one serving at every meal. 

Wholegrain varieties are high in fibre. Fibre helps to keep your bowels healthy and prevent constipation. Constipation can prevent your dialysis from working well.  Try to choose these wholegrain foods:

  • Wholemeal or granary bread.
  • Wholegrain cereals such as shredded wheat or Weetabix.
  • Wholewheat pasta.
  • Brown rice.

You may have been advised to always boil potatoes, yam, cassava and plantain; this reduces the potassium. Your dietitian will advise you if you still need to do this.

Fruit and vegetables

Eat at least five portions of a variety of fruit and vegetables per day. 

You may have been advised not to eat some fruit and vegetables because your potassium levels in the blood have been high.

Your dietitian will advise you if you still need to do this.

Fatty and sugary foods

Foods high in fat and/or sugar include pastry, fried foods, cakes, biscuits and chocolate.  

Dialysis fluid usually contains glucose (a form of sugar). Some of this glucose will get into your blood and give you extra calories which may cause unwanted weight gain.  

If your appetite is good and you want to manage your weight and eat to keep your heart healthy, you could:

  • Eat smaller portions of high fat/high sugar foods.
  • Choose low fat options where possible such as lean meats.
  • Choose lower fat dairy foods such as milks, yoghurts and cheeses.
  • Use smaller amounts of unsaturated fats and oils such as vegetable oil and olive oil spread.

Fluid

Fluid mainly comes from liquids you drink.

When most people start dialysis, they are still passing urine. Fluid is removed from the body by dialysis and by passing urine. Many people find that after a while on dialysis they pass less urine; they begin to rely on dialysis to remove most of the fluid.

If you are drinking more fluid than can be removed, you will become fluid overloaded (oedema).  The extra fluid puts a strain on your heart and lungs. It is often difficult to remove extra fluid by dialysis.

Signs you are overloaded are:

  • Rapid weight gain.
  • Swollen ankles.
  • Feeling breathless.
  • Higher blood pressure.

Weigh yourself daily and this helps you quickly notice rapid weight changes due to fluid.

If you are gaining too much fluid your doctor, dialysis nurse or dietitian may advise you to limit the fluid you drink.

Tips if you need to have less fluid:

  • Try to have fewer drinks and spread your fluid throughout the day.
  • Use a small cup or glass for drinks.
  • If eating sloppy or liquid foods such as such as soup, custard, yoghurt, ice-cream, reduce how much you drink.
  • Spicy and salty foods can make you thirsty so try to reduce these foods.
  • Try using plastic ice cubes in drinks to save extra fluid.
  • Rinsing your mouth, gargling with mouthwash and brushing your teeth can help freshen your mouth.
  • You can quench your thirst with slices of lemon, orange, frozen grapes, pineapple cubes, boiled sweets, sugar free mints and chewing gum.
  • If you have a dry mouth, artificial saliva sprays may help such as Glandosane (available on prescription).
  • Keep a record of all liquids you are having including all drinks, soups, gravies, jelly, yoghurts, and ice-cream.

Your dietitian can give you more ideas to help.

Salt

Eating less salt can help you to feel better. Reducing salt helps your dialysis remove fluid, can improve your blood pressure and make you feel less thirsty. Most of the salt we eat comes from processed and ready prepared foods. Tips to reduce salt:

  • Have more home cooked foods. Cook from scratch where you can.
  • Try to reduce processed foods. Sausages, bacon, ham, ready meals, jars of mustard, sauces, pickles, and table sauces are salty.
  • When shopping, check food labels. Aim to eat mainly foods which have less than 0.3g salt per 100g or with a green traffic light symbol for salt. If you are choosing ready meals, aim for less than 1.8g per portion.
  • Consider having higher salt foods (more than 0.3g salt per serving, or amber or red traffic light) less often and in smaller amounts.
  • Free apps such as FoodSwitch or NHS Food Scanner can help.
  • Flavour your food with herbs, spices, lemon, garlic, vinegar, dry mustard powder.
  • Try to avoid using salt in cooking. Taste food first as you may not need it.  
  • Try not to add any salt at the table.
  • Avoid salt that has ‘low in sodium’ written on the label as these contain potassium. This includes LoSalt, Solo, Saxa So-low.

Your dietitian can give you more help to reduce the salt you eat.

Potassium

Potassium is a mineral found in many foods. It helps our nerves, muscles and heart to work properly. Our kidneys usually control the level of potassium in the blood. Extra potassium is passed out in the urine.  

Dialysis removes potassium but you may still have high levels in the blood, especially if you start to pass less urine or have problems with dialysis. Your levels of potassium in your blood will be checked regularly.  

The target range for potassium in your blood is 3.5 – 5.4mmol/l. A high level of potassium can be dangerous, as it can affect your muscles and heart.  

Your dietitian will advise if you need to eat less potassium to keep your blood levels safe.      

These are foods and drinks higher in potassium:

  • Some fruits such as apricots, avocado, bananas and dried fruit.
  • Some vegetables such as mushrooms, parsnips, spinach and tomatoes.
  • Potatoes which have not been boiled such as chips and jacket potatoes.
  • Snacks such as potato crisps, nuts, chocolate and liquorice.
  • Drinks such as coffee, malted milk drinks and fruit juices.
  • Alcoholic drinks such as cider and strong ales.
  • Soups containing tomatoes and vegetables.
  • Salt substitutes such as Losalt, Saxa So low and Solo.
  • Only limit high potassium foods if you have been advised to.

If you have diabetes, you may have been recommended to eat more fruit, vegetables and nuts. Your dietitian can advise you on appropriate quantities and help you choose lower potassium options. 

Rarely blood potassium levels may be too low. Your dietitian will advise you what to eat to help with this.

Phosphate

Phosphate levels in the blood can be high when the kidneys are not working properly; this can increase your risk of heart disease, weaken your bones and cause itching.  

Dialysis is poor at removing phosphate from the blood. Your levels of phosphate in your blood will be checked regularly.  

The target range for phosphate in your blood is 0.8 – 1.5mmol/l. If your levels are high, eating less phosphate can protect your bones and heart, and help you feel less itchy.  

High phosphate food and drinks include:

  • Cola drinks and other dark coloured fizzy drinks which contain phosphoric acid.
  • Processed foods containing phosphate additives such as ready meals, processed meats and cake mixes. Check the ingredients label for additives with ‘phosphate’ in the name such as diphosphates, triphosphates, sodium phosphate.
  • Nuts and chocolate.
  • Products with raising agents such as muffins and scones.
  • Malted milk drinks, drinking chocolate and cocoa.
  • Evaporated and condensed milk.
  • Fish with edible bones such as sardines, pilchards and whitebait.
  • Shellfish such as fresh crab and scampi.
  • Offal products such as liver, liver sausage and pate.

Other high phosphate foods such as dairy products, milk, fish and meat are good sources of protein and other nutrients.  Some recommended portion sizes are below. 

Your dietitian can guide you on how many servings to have per day or per week. For most people 2 servings per day of dairy foods and up to 6 eggs per week will limit the amount of phosphate you’re eating. 

FoodRecommended portion sizes
Milk200ml
Yoghurt1 small pot
Cheese1 small matchbox size portion
Eggs 6 per week

If you are already following a low phosphate diet your dietitian will advise if you need to continue. Only limit high phosphate foods if you have been advised to.

To help control phosphate levels, some people may be prescribed tablets called phosphate binders. Your dietitian will advise on the best way to take these to make sure they work well.

Peritonitis

If you have peritonitis you will lose more protein than usual through the dialysis process. Eating extra protein foods at this time will help your recovery. Ask your dialysis nurse or renal dietitian for advice. The information below may help if your appetite is reduced.

Small appetite

If you have a small appetite, the following information may help:

  • Eat little and often throughout the day.  Try three meals and 2 - 3 snacks every day.
  • Eat small nourishing snacks between meals such as cereal and milk, cheese and biscuits, cakes, biscuits, desserts, pastries.
  • Have a snack, sandwich or a milky drink if you cannot manage your normal meal.
  • Try easy to prepare high protein meals such as cheese, scrambled egg, poached egg on toast or omelette.
  • Use full fat and full sugar versions of foods and drinks such as full fat milk, full fat yoghurt instead of diet or low fat ones.
  • Try to eat more on days or at times you feel better.
  • Spread butter, margarine, honey, jam and marmalade thickly on bread, croissants, and crumpets.
  • Add honey or sugar to cereals and puddings.

Eating well is important to help you feel better and cope with dialysis.  

Some of these foods are high in salt, sugar, phosphate and potassium which may not be in line with the diet you have previously been advised to follow. If you have diabetes or you are limiting potassium or phosphate speak to your dietitian for more information.

Vitamins

Water soluble vitamins are lost during the dialysis process. 

Your GP can prescribe a multivitamin tablet (Renavit) suitable for people with kidney disease; this helps to replace the vitamins lost during dialysis.  

Renavit contains a beef product so if you are unable to take this, we can recommend an alternative.

You will need to take Renavit once a day.

How can I eat more sustainably?

Many people want to eat food that is more environmentally friendly.

Below are some ideas you could consider:

  • Try some plant food sources of protein such as beans, lentils, soya mince, Quorn, tofu.
  • When buying fish look for the Marine Stewardship Council or Aquaculture Stewardship Council symbols.
  • Try calcium fortified plant milk such as soya or oat instead of cow’s milk.
  • Opt for wholemeal breads and wholegrain versions of pasta and cereals.
  • Choose local and seasonal produce.
  • Avoid chopped, ready prepared and packaged fresh fruit, veg and salads if you can.
  • Reduce food waste, especially of fresh fruit and veg, by choosing tinned and frozen alongside seasonal fresh produce.

Further information

Patients Know Best is an easy-to-use online service that allows you to monitor your own blood test results.
Register to Patients Know Best - Patients Know Best

Information on kidney disease and food written by the kidney dietitians at North Bristol NHS Trust.
Nutrition & Dietetics | North Bristol NHS Trust (nbt.nhs.uk)

Education videos on how to eat less salt presented by the Kidney dietitians at North Bristol NHS Trust.
Educational videos on salt for kidney patients - YouTube 

Diet and lifestyle information including recipe books to download.
Living with kidney disease | Kidney Care UK

Diet information including menus and recipe books to download.
Kidney Patient Guide - Diet

Website of the Edinburgh Renal Unit and contains useful dietary information.
Diet in renal disease – edren.org
 

© North Bristol NHS Trust. This edition published March 2023. Review due March 2026. NBT003497.

Contact Nutrition & Dietetics

Kendon House
Kendon Way
Southmead Hospital
Bristol

Telephone:  0117 414 5428 or 0117 414 5429

How to eat less salt

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Why is eating less salt good?

Eating less salt can improve your blood pressure (if it is high) and may help to slow any decline in your kidney function. If a doctor has asked you to limit how much you drink, eating less salt can help you feel less thirsty, and may help reduce fluid build-up in the body (oedema).  

You should aim to have no more than 6g salt per day (about 1 level teaspoon) or no more than 5g per day if you are on dialysis. 

The average person in the UK eats around 8g of salt per day. Some salt comes from that which you add to food and some salt is found naturally in food, but most of the salt that we eat comes hidden in manufactured food (around 3 quarters or 75%). 

Tips to help you limit salt (sodium chloride)

  • Try to avoid adding salt at the table and into cooking (this includes all salt such as table salt, sea salt, rock salt, Himalayan pink salt and garlic salt).
  • Use herbs and spices, pepper, garlic, ginger, chilli, lemon juice and vinegar to flavour food (ask the dietitian for our herbs and spices leaflet).
  • Taste food before you season it.
  • Limit processed, ready/shop bought foods, jar sauces and takeaway foods as they can be salty. Try to cook from scratch where you can.
  • Different brands of the same food can contain different amounts of salt, so look at labels and compare products.

Reduced sodium salts such as Losalt, Saxa So Low and Solo are made from both sodium chloride and potassium chloride. Because these are high in potassium, they are not suitable for people with kidney disease.

Food labels

Most of the salt we eat comes already hidden in food (¾ or 75%), so it helps to know how to read food labels. 

By reading food labels you will know if a food is low, medium, or high in salt.

How much per 100g?

Food label colourAmount of saltWhen to eat
Green circle

Green

Low salt

0-0.3g

Eat freely.
Amber circle

Amber

Medium salt

0.3g-1.5g

Try to limit to around 2 foods per day.
Red circle

Red

High salt

More than 1.5g

Try to limit. 

How much per portion?

Foods that weigh more than 100g can be labelled per portion. Please check the suggested portion is the same as the amount you plan to eat.

Where possible, try to avoid foods with more than 1.8g of salt per portion.

 

Examples of food labels

Breakfast wheat cereal (40g portion)

NutritionPer 100gPer 40g
Energy (KJ/Kcal)1540/364616/146
Fat (g)1.70.68
Carbohydrate (g)7128
Protein (g)114.4
Salt (g)0.60.24

Salt is 0.6g/100g which is medium (amber). 

Pasta sauce (jar)

NutritionPer 100gPer 40g
Energy (KJ/Kcal)471/114542/131
Fat (g)8.59.8
Carbohydrate (g)78.1
Protein (g)1.41.6
Salt (g)1.511.74

Salt is 1.51g/100g which is high in salt (labelled red). 

Help to reduce the amount of salt you eat

Small changes that can help reduce the amount of salt you eat

Meal/SnackOption 1Option 2 
Breakfast 40g wheat cereal 
1 toast with butter and marmite
2 wheat biscuits
1 toast with margarine and jam
Mid-morning snack2 digestive biscuits2 gingernut biscuits
LunchHam and cheese sandwich 
Crisps 
Orange
Egg salad sandwich
Yoghurt
Orange
Mid-afternoon snackPearPear
Evening mealChicken and vegetable pasta ready mealChicken and vegetable pasta homemade with passata, garlic and Italian herbs
Bedtime snackHot chocolate
2 crackers with hummus
Cup of tea
2 crackers with cream cheese
Total salt content6g salt 3.12 Salt 

What about eating out?

Meals eaten away from the home are often high in salt. If you know you will be eating out, try to choose lower salt options for other meals and snacks eaten that day.

High salt foods to be aware of

  • Feta, halloumi and blue cheese. If you eat a lot of moderately high salt cheese such as cheddar, try lower salt alternatives such as cream cheese and cottage cheese
  • Salted butter (try margarine or unsalted butter).
  • Cured meats such as bacon, ham, gammon, salami, chorizo, Parma ham, serrano ham, salt beef. 
  • Tinned and processed meats such as corned beef, luncheon meat, spam, sausages, black pudding. • Smoked fish (haddock, mackerel, salmon) and shell fish.
  • Tinned vegetables, sundried tomatoes, olives in brine. 
  • Sauces such as soy, oyster, ketchup and ready spice mixes/seasonings – if using, add in smaller amounts. 
  • Salted crisps and nuts. Try unsalted varieties.

Further information

Useful websites 

Action on salt: 
Action on Salt - Action on Salt

British Heart Foundation:
Salt - how much is too much? - BHF

The Eatwell Guide:
The Eatwell Guide - NHS (www.nhs.uk)

A with more information about salt:
What is salt? (youtube.com)

Useful apps

Apps you can use to scan your food and look for lower slat alternatives.

FoodSwitch
FoodSwitch UK

Better Health
Healthier Families - Home - NHS (www.nhs.uk)

 

 

© North Bristol NHS Trust. This edition published March 2023. Review due March 2026. NBT003534.

Contact Nutrition & Dietetics

Kendon House
Kendon Way
Southmead Hospital
Bristol

Telephone:  0117 414 5428 or 0117 414 5429

Pelvic floor exercises for men

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This page contains information for patients about pelvic floor exercises for men. 

Where are my pelvic floor muscles?

They are the layer of muscles that extend from your pubic bone at the front of your pelvis to your tail bone (coccyx) at the back of your pelvis. They are the the muscular support at base of your pelvis.

Illustration of male pelvic floor muscles

What are the functions of your pelvic floor?

  • Bladder control. 
  • Bowel control.
  • Sexual function.  
  • Stabilises the pelvis. 
  • Supports the pelvic organs.

Possible risk factors leading to pelvic floor weakness:

  • Prostate or pelvic surgery (e.g. prostatectomy).
  • Radiation to the pelvis.
  • Straining to poo due to chronic constipation.
  • Certain conditions such as MS, strokes, or uncontrolled diabetes.
  • Being overweight.
  • Chronic coughs.
  • Injury to the perineum. 

What are the symptoms of pelvic floor weakness in men?

Many men experience weakness of the pelvic floor. If this happens you may have a variety of symptoms including:

  • Leaking urine during activity, for example when you sneeze, cough or laugh (known as stress urinary incontinence).
  • A need to go to the toilet often during the day or night (known as frequency or nocturia, respectively).
  • An urgent need to visit the toilet and leaking before you get there (known as urgency incontinence).
  • You are unable to control the passing of wind or stool from your back passage.
  • Erectile dysfunction (the pelvic floor helps you maintain erections).
  • Post micturition dribble (leaking urine immediately after you have finished passing urine).

Why should I do pelvic floor exercises?

The pelvic floor muscles can be strengthened to increase the support of the pelvic organs. This can improve bladder and bowel control and can reduce/cure leakage of urine. It may also improve your ability to maintain an erection. 

Identifying the pelvic floor muscles

It’s important to know where the pelvic floor muscles are, so that you’re sure you’re exercising the correct muscles. To identify the pelvic floor muscles, tighten your back passage as if you’re trying to stop yourself passing wind; at the same time, imagine you’re trying to stop yourself passing urine.
You should have a sense of squeezing, pulling the back passage up and in. You may see the base of your penis retract slightly in your body and your testicles rise a little. Do not tighten your thighs or buttocks and do not hold your breath. After contracting it is important to feel the muscles relaxing and softening as you let go.  

How do I do pelvic floor exercises?

You can exercise your pelvic floor anywhere and anytime. They can be performed lying, sitting or standing  but to start with it may be easier to do the exercises sitting down. Make sure you’ve found the correct muscles and know how it should feel when you tighten them before trying these exercises.

There are two types of exercises, slow and fast, it is important you do both:

Exercise 1: slow pull-ups

  • Take a breath in. 
  • On the breath out, tighten the pelvic floor muscles. 
  • Return to normal breathing but continue to tighten for your length of hold, relax, and feel the muscle let go. 
  • Rest for 5 seconds. 
  • Repeat this 5 times.

As it gets easier, gradually increase length of hold and number of repetitions, aiming for 10 seconds.

Exercise 2: fast pull-ups 

  • Tighten the pelvic floor muscles quickly and then let go straight away. 
  • Repeat this 10 times – approximately 1 contraction per second.

You may find that the muscles are weak initially and that it takes a lot of concentration to exercise them, but this should improve with time

Do not practice stopping the flow of urine midstream as this may interfere with the normal process of emptying your bladder.

How often should I do my exercises?

Do exercises 1 and 2 during each session. As soon as you can, increase to 10 slow and 10 fast pull-ups. 

Aim to repeat these 3 times each day, so in total you will be doing 30 slow and 30 fast pull-ups a day. 

It will take up to 3-6 months of regular exercise to increase the strength in your pelvic floor muscles and hopefully reduce your symptoms.

As your muscles get stronger you may progress to doing the exercises standing up.

To help remind you to do your exercises daily try to combine them with an everyday activity, for example, when brushing your teeth, and after breakfast, lunch, and dinner. 

You can also download an app called Squeezy which is recommended by the NHS. It will send you reminders to do the exercises and you can personalise the programme to suit you.

How long should I continue with the exercises?

Once your symptoms have improved, continue with these exercises once daily for the rest of your life to keep these muscles fit and healthy (e.g., 10 slow and 10 fast pull-ups daily).

Additional tips

  • Being overweight can weaken the pelvic floor muscles so it is important to maintain a healthy BMI. 
  • You may want to try sitting in the correct toilet position to help with constipation like in the image below. (This is sat on a toilet with feet on a foot rest, knees higher than your hips, lean forward with your elbows onto your knees. Bulge out your abdomen and straighten your spine). 
  • You should try to drink 6-8 cups of fluid a day. 
  • Caffeinated drinks, alcohol, acidic drinks (fruit juices) and fizzy drink can irritate your bladder and cause urgency; we suggest avoiding these. 
  • Tighten the pelvic floor muscles before lifting anything heavy or if you are going to sneeze or cough. 
  • If you have urgency, contract your pelvic floor muscles when you have the desire to empty your bladder and only move when the desire has passed.
Diagram of correct position to sit on toilet

Image courtesty of Bladder and Bowel Community:
www.bladderandbowel.org/help-information/resources/toilet-positions/

© North Bristol NHS Trust.  This edition published May 2024. Review due May 2027. NBT002673.

Over 50s and alcohol use

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This information is for people over 50 years old, who are drinking  alcohol above low risk guidelines (14 units most weeks) and are worried about their drinking.

It may also be of use to carers, friends, or health professionals who are worried about an older person’s drinking.

What’s different about alcohol for older people?

Anyone at any age can drink too much. Sometimes health problems can be mistake for conditions related to ageing, rather than our drinking habits. People drink alcohol for many reasons:

  • It might be just a habit or routine; they have always drunk. 
  • Significant changes in life roles - retirement, no longer caring for dependent children, bereavement, separation/divorce - leading to more opportunity/time to drink.
  • Boredom, loss of social contacts, loss of hobbies/interests.
  • Change in social group, revolving around pubs/clubs.

As we get older, our bodies change; we, lose muscle, gain fat and break down alcohol more slowly.

This means that we can become more sensitive to the effects of alcohol. Other health problems can also make us more susceptible to the effects of alcohol.

We sometimes react more slowly and balance may deteriorate with age - even a small amount of alcohol can make us more unsteady and at risk of falls.

So, even if our alcohol routine hasn’t changed it can affect us more and can impact on our quality of life

Lower risk drinking

The Department of Health Guidelines state that there is no safe level of alcohol use. The more you drink, the more likely it is that alcohol will harm your health. Drinking 14 units a week or less, is considered low risk. However, the changes to our bodies as we age, mean that safe drinking levels for older people are probably less than this. 

It is important to know how much alcohol we drink. Drinks containing alcohol show the number of units they contain on the label. There are also unit calculators online e.g. Alcohol Concern UK. 

For example:

  • A pint of ordinary strength beer (4%) or a double whisky (50mls) both contain two units.
  • A 75cl bottle of wine contains 8 - 10 units and so a glass of wine might contain anything from 1 to 3 units depending on its size.

If you drink 10 units daily, you have alcohol in your body for 10 hours. Over time this puts strain on your liver, which is why alcohol free days are so important.

Lower risk drinking advice is:

  • Have two or three alcohol free days each week. 
  • It’s important to spread drinks evenly over a few days.
  • Binge drinking (six or more units) over a matter of hours increases risk of accidental injuries and these risks can increase with age.

Risk behaviours

Alcohol can impair your judgement and alter your behaviour. You can misread situations and react in ways that are out of character. Alcohol can increase your vulnerability to financial and sexual exploitation. Arguments can escalate into assault or fights. 

Delay making important decisions if you have been drinking; consider getting advice/support from trusted friends/family/healthcare professions.

Driving

Don’t drink and drive. On average it takes a healthy liver an hour to process one unit of alcohol. An evening drink can mean you still have alcohol in your system the next morning. The safest option is to avoid drinking alcohol altogether when driving.

 

Alcohol and medicine

Alcohol can enhance the effect of some medications, such as painkillers or sleeping tablets, and reduce the effect of others, such as medications to thin the blood (Rivaroxaban) and antidepressants.  

Check with your doctor if it is safe for you to drink with your particular health problems and/or medication. Ask your pharmacist and/or read the leaflet that comes with your prescription, over-the-counter or herbal medicines.

What are the risks of drinking too much?

Alcohol can damage nearly every part of the body:

  • The stomach lining - ulcers or bleeding.
  • The liver - fatty liver, cirrhosis and liver failure.
  • Heart muscle - heart failure produces a build-up of fluid in the lungs which results in shortness of breath.
  • Cancer - 6% of cancers world wide can be linked to alcohol. Mouth, stomach, liver and breast cancers have strong links with alcohol use.
  • Malnutrition - alcohol has lots of calories for energy, but none of the protein, fats, vitamins or minerals you need to keep the body in good repair. People who drink most days are recommended to take Thiamine and Sanatogen.
  • Sense of balance - falls and accidents (even when not intoxicated).
  • Blackouts, seizures or fits.
  • Stroke.
  • Poor sleep - broken sleep, early morning waking and daytime tiredness.
  • Menopause - increase in symptoms.

Not everyone who drinks too much will develop health problems, but the more you drink, the more likely you are to get such problems.

Alcohol and mental health

Anxiety

Alcohol can be a short term fix to relieve anxiety, but the  anxiety will return. It is not a long term solution. So the temptation is to drink again to feel better.

Depression

Alcohol is a depressant. Low mood and depression can lead to a loss of interest in things you used to enjoy. You can feel tired, but have difficulty sleeping. It becomes more difficult to take things in when reading or following a TV programme. Your appetite can be poor, and your body can become depleted of essential nutrition for normal brain function. In extreme cases you may feel life is not worth living.

Hearing voices

This is less common but can happen if you have been drinking heavily for a long time. It starts with vague noises, like leaves rustling, and gradually becomes distinct voices. These can be unpleasant and distracting.

Confusion

Alcohol use plus poor or absent diet can result in low  Thiamine and Magnesium. This can cause confusion and poor memory. If not treated this leads to Alcohol Related Brain Injury, including Korsakoff’s dementia.

Cut down your drinking

Keep a drink diary, this is a good starting point for change. Write down the date, what type of drinks you have, how many units, and add up the total number of units each day. Bottles/cans have information about number of units. 

Have an alcohol reduction plan 

  • Think about hobbies, interests, and social opportunities that don’t involve alcohol. This may be a brand new activity or something that you used to enjoy. 
  • Alcohol can fill a gap when you are bored so don’t leave space. Occupy yourself and get out of the routine/habits that revolve around alcohol.
  • Local Council websites/libraries will have information about volunteering opportunities, wellbeing groups and leisure activities in your local area.
  • Friends and family can support you to make changes.
  • Home measures are usually large ones. Use a measure or a smaller glass, and make sure you keep track. Don’t top-up your glass before it’s empty. Put the bottle away between drinks.
  • Make each drink last longer. Drink a soft drink or water with, or after, each alcoholic drink.
  • Eat something before you drink, this will help slow down the absorption of alcohol into your body.
  • Plan two or three alcohol-free days a week.
  • If you have a lapse or don’t manage to cut down as you had hoped, don’t give up! If it was an easy thing to do you would have done it already.
  • Have a plan and acknowledge your successes.

     

What support and treatments are available?

If you are drinking dependently, it could be unpleasant or even dangerous for you to stop drinking abruptly (cold turkey) as your body is accustomed to alcohol.

Talk to your GP or healthcare professional about alcohol. Each person is different, so speaking to a medical professional about your own circumstances is always a good starting point. Ask about a prescription of Thiamine and Sanatogen A-Z Complete. Your GP may be able to offer a medically supported detox (depending on your alcohol intake, your physical/mental health, and your support at home). You will need a robust plan about how to stay abstinent following detox.

Your GP can offer information about local community alcohol service. They can refer you or you can self-refer.

Community alcohol services, support you to make changes either by a safe/slow reduction or by medically supported detox.

If your goal is abstinence, but cravings for alcohol are a problem, there are medications that might be of use to you, to help reduce these cravings. Ask your GP or local alcohol service.

Discuss with your GP access to Wellbeing support/social prescribing/counselling services. If you are drinking to help manage anxiety, low mood or physical problem, a wellbeing service can help provide alternative strategies, not reliant on alcohol.

Support Groups: Mutual aid organisations AA (Alcoholics Anonymous) and SMART Recovery. These offer abstinence based recovery support. Look at their websites for up to date meeting details.

By making healthier choices about alcohol you can start to see the positive effects on your health and wellbeing.
 

Support organisations

Age UK
Bristol: 0117 929 7537
South Gloucestershire 0145 441 1707

Alcoholics Anonymous
Bristol helpline: 0117 926 5520
Email: help@aamail.org

SMART Recovery
Self-Help Addiction Recovery | UK Smart Recovery

Bristol ROADS/ Bristol DHI
0117 440 0540

BDP 50+ Crowd
0117 440 0540

South Gloucestershire DHI
0800 073 3011

North Somerset We Are With You
01934 427940

Drinkline
0300 123 1110

© North Bristol NHS Trust.  This edition published August 2023. Review due August 2026. NBT003101.