Support and useful information

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These organisations and charities provide reliable, up to date information and support for patients and families living with a haematological conditions and cancer. If you need help to identify the ones which might be most helpful to you the specialist nurses can help you.

Blood Cancer UK

Cancer Research UK

Leukaemia Care

Lymphoma Action

Macmillan Cancer Support

MDS UK Patient Support Group

MPN Voice

  • MPN Voice’s mission is to provide clear and accurate information and emotional support to everyone who has been diagnosed with a myeloproliferative neoplasm (MPN) and their families/friends.
  • MPN Voice – mpnvoice.org.uk
  • Phone 07934 689 354 

Myeloma UK

  • Provides information and support to anyone affected by myeloma.  Offers support groups, discussion forums and Infoline. Includes related disorders including AL amyloidosis, Monoclonal Gammopathy of Undetermined Significance (MGUS) and Plasmacytoma.
  • Homepage - Myeloma UK
  • Info line: 0800 980 3332 

Penny Brohn

NHS website

Details of support groups and websites correct August 2024 

Clinical Haematology

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Clinical Haematology Service 

The clinical haematology service looks after patients with a range of blood and bone marrow disorders, including haematology cancers. We provide out-patient and day case treatment in our clinics and Chemotherapy Suite in Gate 5b in the Brunel building, Southmead Hospital. We also have a small number of inpatient beds on Gate 27b, and support and advise staff and patients in other areas around the hospital. 

We care for patients with haematological cancers including:

  • Lymphomas.
  • Leukaemias.
  • Multiple Myeloma.
  • Myelodysplastic Syndrome.
  • Myeloproliferative neoplasms. 

The treatments we offer include:

  • Chemotherapy.
  • Immunotherapies.
  • Targeted therapies.
  • Supportive care including blood and platelet transfusions.

We work closely with Medical Day Care, The Macmillan Wellbeing Centre, Acute Oncology, Palliative Care teams, and many others around the trust. We can refer you to dietitians, physiotherapy, psychology, wigs, and financial and benefits support. 

Certain treatments like radiotherapy, stem cell transplants, and more intensive chemotherapy can only be given at the Bristol Haematology and Oncology Centre in Bristol. We have good links with our colleagues there to ensure our patients have access to the most appropriate treatments. 

Haematology clinics take place in Gate 5 every morning (except Thursday) and on Tuesday afternoons. We encourage you to bring someone with you to the clinic, especially if you are expecting to discuss significant test results or a treatment plan.  

Certain specialist clinics take place at the same time every week but you may be asked to come on a different day sometimes depending on appointment availability. The specialist nurses may also offer you appointments at other times, often in the afternoon.  

When you come to clinic it is very likely you will be asked to have a blood test. Sometimes (particularly in the myeloma clinic) it is useful to arrange to have the tests done at your GP surgery a few days before so that all the results are ready you see us.  

In some cases you may be offered a phone appointment, which usually requires a blood test at your GP surgery. A phone appointment is similar way to a face-to-face clinic appointment and you need to be available for us to call you as close as possible to the appointment time. 

Questions to ask

When you come to your haematology appointment, you may have a lot of questions. It is normal to find it difficult to remember things at the time of and after your appointment so here are some tips to help you.  

Before your appointment

  • Write down your most important questions.
  • List or bring all your medicines and pills – including vitamins and supplements.
  • Write down details of your symptoms, including when they started and what makes them better or worse.
  • Ask your CNS team for an interpreter or communication support if needed.
  • Ask a friend or family member to come with you, if you like. 

During your appointment

  • Don't be afraid to ask if you don't understand. For example, 'can you say that again? I still don't understand.'?
  • If you don't understand any words, ask for them to be written down and explained.
  • Write things down or ask a family member or friend to take notes.

Ideas of questions to ask at the time of your appointment

  • 'what's happening if I'm not sent my appointment details,' and 'can I have the results of any tests?'
  • If you don't get the results when you expect – ask for them.
  • Ask what the results mean.

Before you leave your appointment

  • Ask who to contact if you have any more problems or questions.
  • About support groups and where to go for reliable information. 

After your appointment - don't forget the following

  • Write down what you discussed and what happens next.
  • Keep your notes.

Tests, such as blood tests or scans

  • What are the tests for?
  • How and when will I get the results?
  • Who do I contact if I don't get the results? 

What next?

  • What happens next?
  • Do I need to come and see you?
  • Who do I contact if things get worse?
  • Do you have and written information?
  • Where can I go for more information?
  • Are there any support groups or other sources of help? 
Haematology for clinicians

Neuropathology Laboratory Services

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For guidelines on how to send diagnostic samples to the Neuropathology Department, download:

To make a referral to the department, download:

For general guidelines for sending a muscle or nerve biopsy to the department, download the guidelines below

For a list of the diagnostic tests performed within the Neuropathology Department, download:

The department works with the Severn Pathology Genetics Department to offer a fully integrated report service for surgical patients. To see full details of this please visit the Severn Pathology webpage.

Contact Neuropathology

Haemorrhoid banding

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This page describes what haemorrhoids are and what causes them. It discusses lifestyle changes to avoid them and details of haemorrhoid banding including risks, benefits, and aftercare.

Haemorrhoids (piles) 

Haemorrhoids (piles) are enlarged blood vessels in the lining of the bottom (anus/lower rectum/back passage). These can get irritated causing bleeding, itching, discomfort, and can sometimes stick out from the bottom. Haemorrhoids are often small and symptoms settle down without treatment, but there are times when treatment is required.

What causes them?

About half of people in the UK get one or more haemorrhoids. Certain situations increase the chance of them developing:

  • Constipation: passing large poos (stool/faeces) and straining on the toilet. These increase the pressure in and around the veins in the bottom causing haemorrhoids to develop.
  • Pregnancy: haemorrhoids are common during pregnancy. This is probably because of the pressure from the baby lying above the rectum and anus, and the effect that changes in hormones during pregnancy have on the veins.
  • Aging: the tissue in the lining of the bottom may become less supportive as we get older.
  • Hereditary factors: some people may inherit a weakness of the walls of the veins in the anal area.

How to avoid haemorrhoids?

Keep poo (sometimes called stool/faeces/motions) soft and don’t strain on the toilet. The following can help with this:

  • Eat plenty of fibre such as fruit, vegetables, cereals, and wholemeal bread.
  • Have lots to drink. Adults should aim to drink at least two litres (10-12 cups) per day. You will pass much of this fluid as urine, but some will be passed out in the gut and softens poo. Most drinks will do this, but alcoholic or caffeinated drinks can be dehydrating and may not be as good.
  • Avoid painkillers that contain codeine such as co-codamol as they are a common cause of constipation.
  • Going to the toilet: go to the toilet as soon as possible after feeling the need. Some people try to put off the feeling and plan to get to a toilet later. This may cause bigger harder poo to form which is more difficult to pass. 
    Avoid straining and sitting on the toilet for more than five minutes at a time. 

Banding treatment

Banding is a common treatment for haemorrhoids. It may be used to treat haemorrhoids which have not settled with the things above (like increasing fibre). 

A surgeon in the outpatient clinic usually does the procedure. A suction device holds each haemorrhoid and a rubber band is placed at the base. The band cuts off the blood supply to the haemorrhoid. This causes the haemorrhoid to shrink, leaving the dead tissue to drop off over a period of up to 10 days. Up to three haemorrhoids can be treated at one time. 

Banding of internal haemorrhoids is usually painless as the base of the haemorrhoid is above the anal opening where there are no pain sensors.

Benefits 

In about 8 in 10 cases the haemorrhoids are ‘cured’ by this technique. In about 2 in 10 cases the haemorrhoids come back at some point. You can have further banding treatment if this happens. Haemorrhoids are less likely to come back after banding if you do not get constipated and do not strain on the toilet as described earlier.

Risks 

A small number of people have complications following banding such as bleeding, urinary problems, infection, or ulcers where the haemorrhoid was treated. If you see lot of fresh, bright-red blood or pass clots you should seek urgent medical attention.

What to expect with haemorrhoid banding recovery

When haemorrhoid banding is finished, expect to feel:

  • Discomfort for anywhere from 24-48 hours.
  • The feeling of fullness in the lower abdomen (tummy).
  • That you need to have a bowel movement (poo).

You may also find it difficult to pee and control gas or bowel movements for up to 14 days after treatment. The bleeding may get worse at 7-10 days when the haemorrhoid drops off. 

The wound normally takes about two weeks to heal. After this time you should have no more itching, pain, or bleeding.

Aftercare

You can bath or shower as normal. You should be able to get back to your normal routine within 1-2 days. You may find it useful to take paracetamol regularly for the first 24 hours.

If you need a follow-up appointment in clinic it will be arranged during your appointment, or often you will be referred back to your GP.

You may be placed on a Time Limited Patient Initiated Follow-up Pathway. This means you will be discharged from our Colorectal service, but if your symptoms return, get worse, or don’t improve in the next 6 months, you can contact us to request a follow-up. You will need to ring the secretarial team and we can only book a follow-up for the same condition. If you have new problems, or your symptoms return after 6 months, please contact your GP.

References

Haemorrhoids. Clinical Knowledge Summaries. Available at Scenario: Management | Management | Haemorrhoids | CKS | NICE [Accessed June 2009]

Acheson, AG and Scholfield, JH 2008. Management of haemorrhoids. BMJ. Feb 16: 336 (7640) 380-3

Brsinda G. 200. Prevention is best; haemorrhoidectomy needs skilled operators. BMJ. Sep 9; 321 (726) 852-3 

NICE 2007 Haemorrhoid- stapled haemorrhoidopexy. Available at Overview | Stapled haemorrhoidopexy for the treatment of haemorrhoids | Guidance | NICE [Accessed June 2009]

© North Bristol NHS Trust. This edition published February 2025. Review due February 2028. NBT002106

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Diet to help reduce the risk of kidney and ureteric stones

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This advice is for people forming mixed calcium kidney and ureteric stones, and people who do not know what their stones are made of. It contains information on diet and lifestyle to help reduce your risk of forming more stones.  

If you form calcium oxalate stones, please read this page and then follow the link at the end to more advice that is specific to calcium oxalate stones.

Healthy eating and drinking

The most important message is to drink plenty and follow a balanced, healthy diet such as that shown in the Eat well Guide: Eat well - NHS

Drinking

Not drinking enough can increase your risk of kidney stones. You can try to avoid this by aiming to go through 2.5-3 litres each day (5-6 pints). 

Try to spread drinks evenly through the day. Drink more when it is hot, and during and after exercise. 

Drinks to include: 

  • Water (ideal).
  • Dilute squash or cordial.
  • Carbonated water, carbonated drinks (not sugar sweetened).
  • Tea and coffee (limit to 4 mugs day due to caffeine content).
  • Fruit tea. 

Drinks to limit: 

  • Sugar sweetened drinks.
  • Dark carbonated drinks (like cola).
  • Large volumes of fruit juices (high fructose content). 

You can get an idea of how big your cups/mugs/glasses by using a measuring jug to measure how much they hold. It may be useful to write this down. 

Am I drinking enough

If you are drinking enough, you will make over 2 litres of urine each day. Your urine urine should be colourless to pale straw coloured (1-3 on the chart below). 

Chart of gradient of urine colours with numbers 1-7

Salt

Eating too much salt (or sodium) can increase calcium in your urine, and having higher amounts of calcium in your urine may increase your risk of kidney stones. Too much salt in the diet can also reduce something called citrate in your urine, and low citrate may increase your risk of forming stones. It is recommended that you limit salt in your diet to less than 6g each day (about 1 level teaspoon, or about 6 “pinches” of table salt).

Salt in the diet comes in the form of “added salt” and “hidden salt”. Added salt is what we add at the table or in cooking, and hidden salt is what is found in many shop-bought, processed/ manufactured foods. Around 75% of the salt we eat comes hidden in food, so reading food labels is important when trying to limit the amount we eat. Please see our diet sheet on how to reduce salt in the diet (How to eat less salt | North Bristol NHS Trust). 

Calcium

Although there may be calcium in your stone, it is important that you have calcium in your diet. If you are not getting enough calcium from your diet, your body will take calcium from your bones. Over time this can weaken your bones. 

Aim to include 3-4 of the following high calcium foods each day (700g-1200g calcium per day): 

  • Milk: a third of a pint or 200ml.
  • Cheese, including cream cheese: 1oz or 30g.
  • Yoghurt: 1 individual size pot.

For healthier options, choose lower fat alternatives.

If you use non-dairy alternatives, make sure they contain 120mg calcium per 100g/100ml. 

Fruits and vegetables

Eating plenty of fruits and vegetables is good for our health, and people that eat plenty of fruits and vegetables appear to have lower risk of forming kidney stones.

Aim to eat at least 5 portions of fruit and vegetables each day (this does not include potato). 

What is a portion? 

  • Fruit: what you can hold in your hand (for example 2 satsumas or 1 apple).
  • Vegetables: 2-3 heaped tablespoons.
  • Salad: the amount to fill a breakfast bowl. 

Citrus 

Lemons are high something called citrate, and including lemons in your diet may increase the amount of citrate in your urine. Having good amounts of citrate in your urine is linked with a reduced risk of forming kidney stones. 

Ideas to include more citrus fruit: 

  • Try squeezing lemon juice onto food (like Mexican, Thai, fish dishes, and salads).
  • Squeeze lemon juice into water to make it more interesting to drink. 

Eating plenty of fruits and vegetables can also increase the amount of citrate in your urine, so it is another reason to reach for at least 5 portions of fruit and vegetables each day. 

Protein

Eating too much protein has been linked with an increased risk of forming kidney stones.

Animal proteins include: 

  • Meat (like beef, lamb, pork, minced meat, ham, burgers, sausages).
  • Poultry (like chicken and turkey).
  • Fish (like cod, tinned tuna, prawns, fish fingers).
  • Eggs and cheese. 

Try to limit your proteins of animal protein to healthy eating amounts for example: 

  • 60g or 2oz at a snack meal (cold meat/1 large egg in a sandwich).
  • 115g or 4oz at a main meal. This amount is about the size of a packet of playing cards. 

Animal protein from cow's milk and yoghurt does not need to be limited unless you eat large amounts (more than 4 high calcium foods each day). 

Plant based proteins do not seem to increase the risk of kidney stones. Here are some ideas to include more plant-based proteins: 

  • Use lentils and beans as the protein source for meals.
  • Reduce meat portion and pad meals out with beans or pulses.
  • Include meat free days in the week.

Vitamins

If you buy over the counter vitamins, do not take more than the reference nutrient intake (RNI) or dietary reference value (DRV). The label on the the bottle will will you what percentage of RNI or DRV the vitamin will give you. 

Try to avoid any that give you more than 100%. 

Healthy weight

Losing weight if you are overweight may reduce your risk of forming kidney stones. Eating healthily and having smaller portions can help with weight loss. Being more active is also important. 

If you have diabetes

Keeping good control of your blood sugar levels may help you to reduce your risk of forming kidney stones. Make sure you attend your diabetes appointments at your surgery or hospital. 

If you form calcium oxalate stones, please follow this link to specific advice:

© North Bristol NHS Trust. This edition published March 2025. Review due March 2028. NBT003781.


 

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Find out about shared decision making at NBT. 

Options for Kidney Care Clinic at Cossham Hospital

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What is the Options for Kidney Care Clinic?

This is a specialist clinic for people whose kidneys are not working well, including:

  • People whose kidneys are working at 20% or less.
  • People who have recently been found to have advanced kidney disease.
  • People who have started dialysis recently after a new problem with their kidney function.

Why am I coming to the clinic? 

  • To treat the side effects of kidney disease and improve your symptoms.
  • To provide education and advice so you can make decisions about your treatment including dialysis and transplantation.
  • To support you and provide appropriate care if you decide you do not want dialysis or a transplant.

Who will I see at the clinic? 

  • Kidney specialist doctor: a consultant nephrologist who will assess your kidney function and symptoms, and suggest treatments.
  • Kidney education nurse: who specialises in giving information and support about kidney disease. They work with you, your relatives, and the medical team to help you manage your treatment and make decisions about the future.
  • Kidney dietitian: who will give you specialist advice about food and drink to help you reduce the effect of kidney disease on your general health. 

You will see each member of the team in one appointment for about 20 minutes each, so you will spend at least one hour in the clinic. You may also need blood tests at the end of the clinic. 

How many times will I come to the clinic? 

Most people will come to the Options for Kidney Care Clinic for a maximum of three appointments. We will then refer you back to your original consultant, and they will be kept informed of all the discussions at this clinic. 

What should I bring to my appointment? 

  • A list of your current medications.
  • A record of your blood pressure readings (if you have them).

Can I bring someone with me? 

Yes, it can be helpful to bring a friend or relative with you, as they can support you listen to the information being discussed, and talk about your treatment decisions with you afterwards.

Both you and your GP will also receive a letter with details of your appointments.

© North Bristol NHS Trust. This edition published February 2025. Review due February 2028. NBT003779

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Contrast enhanced ultrasound

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This information is about a contrast enhanced ultrasound examination. It will answer most questions, however if after reading it you have any concerns or need further explanation, please do ask a member of the Imaging team. The number for the Imaging Department can be found on your appointment letter.

What is a contrast enhanced ultrasound scan?

Your doctor has requested that you undergo an ultrasound examination with contrast. This examination is usually performed to provide more information about a lesion or blood flow in part of your body.

The procedure involves using an ultrasound machine to view images of the inside of your body. Contrast enhanced ultrasound is like a regular ultrasound, with the addition of the use of small, gas filled bubbles, that are slightly smaller than a cell in the blood. These “microbubbles” are non-toxic and help us to see cavities in the body, large vessels and blood flow to organs. The microbubbles dissolve rapidly and harmlessly in your blood stream.

This type of procedures is safe and easy to perform with no radiation and no risk to the kidneys.

Are there any risks?

There is a very low risk of minor side effects, including:

  • Headache (less than 5%).
  • Nausea (0.5%).
  • Feeling hot (0.3%).
  • Injection site pain (0.3%).

These side effects should settle on the same day as your scan. 

Rarely there have been reactions to the contrast with certain heart diseases such as shunts. We will check your allergies before the procedure to minimise this risk. The doctor may give you medicine if you do have an allergy and we will monitor you after the procedure. 

The only severe side effects have occurred in patients with pulmonary hypertension or serious heart and lungs conditions. You should let us know if you have a severe heart condition, are pregnant or have had a severe allergic reaction in the past.

Do I need to prepare in advance?

No special preparation is needed in most cases. However, if you need to starve or fill your bladder, we will inform you of this on your appointment letter.

Can I bring somebody with me?

Yes, you may bring a friend or relative with you. It may not always be possible for them to accompany you into the scanning room but if it is necessary, please do ask and we will try to accommodate your request.

What will happen when I arrive?

Please go to the Gate 18 reception desk and follow the check-in process in your appointment letter. You will be shown where to wait until a member of staff comes to collect you.

Who will I see?

You will be seen by a radiologist (a doctor who specialises in X-rays) or a sonographer (a radiographer who specialises in ultrasound). 

North Bristol NHS Trust is a teaching hospital; there may be a trainee present for some examinations. They will be introduced at the beginning of the examination. If you would prefer them not to be present, please feel free to say to the radiologist or sonographer.

Will I need to undress?

We will tell you if you need to remove any clothes covering the area being examined before your examination. Private cubicles are available if you need to take off your outer garments or put on a hospital gown.

What happens during the scan?

  • A member of the team will place an intravenous (IV) catheter for microbubble contrast in one of your arm veins before the scan. A small plastic tube (cannula) may be put into a vein in your arm to allow us to administer during the procedure.
  • After this, we will dim the lights so that the images on the screen can be seen more clearly.
  • You may be asked to take deep breaths and to hold your breath for a few moments.
  • The radiologist or sonographer will move the ultrasound probe over your skin while viewing the images on a screen.
  • Ultrasound images will be taken before and after the injection, so that they can be viewed later.
  • Occasionally a patient might experience a bitter taste in the mouth or burning or cold sensation in the arm after the injection. The cold sensation is usually the result of the saline (salted water) used to flush the cannula, not the contrast itself.
  • After the scan we might ask you to stay in the department for 10-20 minutes to ensure you are well before you leave the department. Before you leave, a member of the team will remove the cannula.

Off label use of contrast ultrasound

The contrast agent used with ultrasound is approved for use in the UK, Europe and North America.

In the UK, it has been approved for use in the heart and liver lesions. We would like to make you aware however, that it is not specifically approved for examinations of the other organs. This may seem unusual as we will be injecting the same material in the same amount that would be used to examine your heart and liver but scanning over your kidney or other organs. This is known as an “off label use of an approved drug” and is a common practice since often drugs are not specifically approved for every possible use. 

Should you have further questions please feel free to ask the radiologist who, along with the experienced sonographer, will be performing the study.

How long will it take?

The process of carrying out a scan usually takes around 20-30 minutes. Unless emergency patients delay you, your total time should be less than an hour.

Are there any side effects?

No. You can drive afterwards and return to work as necessary.

Can I eat and drink afterwards?

Provided no other investigations are needed, you can eat and drink normally after your scan.

When will I get the results?

After the scan, we will examine the images further and prepare a report on our findings. This may take some time to reach your referring doctor but is normally less than 14 days. You could ask the radiologist/sonographer how long it might take to get the results. 

References

This leaflet is based on the NHS England website for Ultrasound scans. Ultrasound scan - NHS (accessed 05.05.2022)

NHS Constitution for England. Information on your rights and responsibilities. NHS Constitution for England - GOV.UK (accessed 05.05.2022)

Guidelines for Professional Ultrasound Practice (2021) Society of Radiographers and British Medical Ultrasound Society, (accessed 05.05.2022)

Sidhu PS, Cantisani V, Dietrich CF, et al (2018) The EFSUMB Guidelines and Recommendations for the Clinical Practice of Contrast-Enhanced Ultrasound (CEUS) in Non-Hepatic Applications: Update 2017 (Long Version). Ultraschall Med 39:e2-e44.

The EFSUMB Guidelines and Recommendations for the Clinical Practice of Contrast-Enhanced Ultrasound (CEUS) in Non-Hepatic Applications: Update 2017 (Long Version) (accessed 05.05.2022)

S.Weinstein et al.; How to set up a contrast enhanced ultrasound service. Abdom Radiol NY (2018) 43:808-818

© North Bristol NHS Trust. This edition published February 2023. Review due February 2026. NBT003509

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

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Sclerotherapy for venous vascular and lymphatic malformations

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This page is patients whose doctor has requested that you have sclerotherapy. We hope that the following information will answer some of the questions you may have about this procedure.

What is a venous vascular malformation?

Venous vascular malformations are abnormal collections of veins. They are present from before birth, but often not noticeable until much later in life. They grow with the person and may not cause any symptoms at all. 

They most commonly appear as a soft lump and are slightly blue in colour. They may cause pain or be cosmetically disfiguring. These symptoms may worsen after trauma, infection or hormonal changes such as puberty or pregnancy.

What is a lymphatic malformation?

Lymphatic malformations are where the lymphatic system (part of the body’s immune system) has failed to form normally in one part of the body and instead forms fluid filled spaces that may occasionally be painful.

Who will be involved in my treatment?

Your initial consultation is likely to be with a consultant radiologist, but at North Bristol there are also vascular surgeons, plastic surgeons, and other specialists with experience in vascular malformation management, allowing a multidisciplinary approach to treatment.

How is a suspected vascular or lymphatic malformation investigated?

Usually, the diagnosis can be made in a clinical examination and by taking a patient history at an outpatient appointment. The area of concern will normally be imaged (scanned) with ultrasound. If the ultrasound does not provide enough information, then an MRI scan may be arranged. 

MRI is particularly useful for assessing larger and deeper malformations, or for providing detail of the anatomy of those malformations near important structures. 

Occasionally imaging cannot provide enough information on its own and then a small piece of tissue (a biopsy) may be needed to analyse the types of cells present in a malformation.

How is a suspected vascular or lymphatic malformation treated?

Venous vascular or lymphatic malformations are not dangerous conditions and often require no treatment at all. Treatment is normally only indicated if the malformation causes pain or limits your activity. 

Non-invasive treatments such as compression stockings can be useful for venous vascular malformations and may be tried first before any invasive interventions such as sclerotherapy are discussed.

What is sclerotherapy?

Sclerotherapy is a treatment for venous vascular or lymphatic malformations. A sclerosant is a powerful chemical that is injected into the vascular or lymphatic spaces within a malformation causing scarring. 

This is performed using imaging guidance to ensure the sclerosant does not affect nearby normal structures. The procedure is performed by a team led by a consultant radiologist. A radiologist is a doctor who has specialist training and experience in the use of imaging to guide treatment.

Who has decided that sclerotherapy is appropriate for me?

If sclerotherapy has been proposed for you the consultant radiologist, in agreement with any other doctors involved in your care (consultant surgeon or consultant physician), will have decided that you would be likely to benefit from the treatment. This will have been discussed and agreed with you in clinic. Your opinion will be taken into account and if after discussion with your doctors you do not want the procedure carried out, you can decide against it. 

The procedure uses X-rays and the amount of radiation used is small however if you think you may be pregnant, please inform the Imaging Department before attending the appointment.

What happens before the procedure?

You will need to have a blood test a few days before the procedure to check your kidney function, that you are not at increased risk of bleeding, and that it will be safe to proceed. 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) we ask you to call the Imaging Department using the number on your appointment letter as we may need to adjust your medication before undergoing this procedure.

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 form signed, you will be taken to the procedure room on the trolley. There will be a nurse, radiographer, and a radiologist with you throughout the procedure.
  • The radiologist will use an ultrasound machine to look at the vascular 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 will then inject X-ray dye into the malformation to confirm the needle position and that it is safe to inject sclerosant. The sclerosant will then be injected through one or several small needles into the malformation under ultrasound and X-ray guidance. The procedure is likely to take about 30 minutes.
  • Once the procedure is complete the needles will be removed, and the radiologist will apply a dressing if necessary. If the malformation is in a limb, the limb may be bandaged, and you may be asked to wear a compression garment for a period of 1 week.

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, please tell the nursing staff so you can be given appropriate painkillers.
  • You will be required to stay in our day case area for 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?

Sclerotherapy is usually a safe procedure. Potential complications include:

  • n In the first 24 hours following sclerotherapy, the area is likely to be very swollen. Painkillers will be administered as necessary to keep the pain under control. The pain will resolve within a few days, but it may take several weeks for the swelling to settle completely.
  • You may notice your urine turn red the first time you urinate after the procedure. This is entirely normal after sclerotherapy and should not cause you any concern.
  • You may experience a fever during the first 12 hours after the procedure, though this will resolve without further treatment.
  • The one serious risk associated with sclerotherapy is if the sclerosant spreads beyond the malformation and causes 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 whereabouts 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. 

You should check your travel insurance if you wish to travel within 4 weeks of this procedure.

Am I likely to need more than one treatment session?

The amount of sclerotherapy that can be performed at a single treatment session is limited by the local pain and swelling caused. Whether or not multiple sessions are required depends in part on the size of the malformation, but most people with a vascular malformation require multiple sessions. This may be 2, 3, or 4 for a successful outcome. 

Because it is rare for a patient to be completely cured of a vascular malformation, the malformation may again start to cause symptoms in the future and further treatment session(s) may be required at that time.

How successful is sclerotherapy?

Patients with a vascular malformation suitable for sclerotherapy are likely to have an improved quality of life in the majority of cases following a series of sclerotherapy treatment sessions. However, it would be very unusual for the patient to be completely cured. It is almost never possible to eliminate the malformation completely using sclerotherapy. 

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.

References and Sources of further information

Cabrera J et al (2003) “Treatment of venous malformations with sclerosant in microfoam form”. Archives of Dermatology, 139, 1409-1416 

Donnelly LF et al (1999) “Combined sonographic and fluoroscopic guidance a modified technique for percutaneous sclerosis of low flow vascular malformations”. American Journal of Roentgenology, 173, 655-657 

Ogita S et al (1994) “OK-432 therapy in 64 patients with lymphangioma”. Journal of Pediatric Surgery, 29, 784- 785 

Website available at: Birthmark Support Group [accessed April 2024]

© North Bristol NHS Trust. This edition published June 2024. Review due June 2027. NBT003166