Sclerotherapy information sheet

 

Contact details

Email: schn-V-TAC@health.nsw.gov.au | Questions/requests will be forwarded to the appropriate team member. We aim to reply within 3 business days. 

Phone: (02) 9382 1749 | Monday-Friday 8:00am-4:00pm | Booking appointments for the V-TAC clinic, referrals, and general enquiries. 

Clinical Nurse Consultant: 0408 722 869 | Call or text Monday-Friday 8:00am-4:00pm | Non-urgent clinical questions and advice.

Location: High Street entrance - Sydney Children's Hospital, Randwick

For assistance out of hours, please contact our team via the Sydney Children’s Hospital Switchboard on (02) 9382 1111 and ask for the on-call doctor for surgery. In an emergency: call an ambulance on 000 or attend your closest emergency department.

Introduction

This information sheet explains sclerotherapy treatment, why it might be suggested for your child, and what to expect when your child comes to Sydney Children’s Hospital at Randwick for sclerotherapy treatment.

This information is not meant to replace discussions with your child’s vascular anomalies team and not all of it may apply to your child. Please feel free to ask the team any questions or raise any concerns you may have about your child and their treatment.

About sclerotherapy

Sclerotherapy is a procedure where a medication, or ‘sclerosant,’ is injected into the malformation to obliterate all or part of it. It is used to treat some types of vascular malformations. 

Sclerotherapy is carried out in the Department of Radiology by an interventional radiologist, a doctor who specialises in image guided procedures.

Most of the time, sclerotherapy is an elective procedure. If the V-TAC team believe it is more necessary or urgent they will discuss this with you.

Vascular malformations that can be treated with sclerotherapy

Vascular malformations that can be treated with sclerotherapy include:

  • Lymphatic malformations
  • Venous malformations
  • Some arteriovenous malformations
  • A combination of vascular malformations.

Reasons to have sclerotherapy

Reasons to have sclerotherapy will be discussed with you and may include:

  • Risks that the malformation will affect vital structures such as the airway or eyes
  • Risk of infection, bleeding or clotting in the malformation
  • The effect of a venous malformation on the blood clotting system, which creates a risk of bleeding and clotting elsewhere in the body
  • The effect of the malformation on functions such as walking, running, playing sport, hand function
  • Pain and discomfort
  • Disfigurement
  • To try and prevent possible future problems

Other considerations

  • Occasionally the radiologist will decide not to go ahead with the sclerotherapy if they think the risk of it getting out of the treatment area is too high. The details of what is planned will be explained to you before you give your consent.
  • Sometimes, a tissue biopsy would be helpful in guiding future treatment. This is done at the same time as the sclerotherapy under the same general anaesthetic. This would be discussed with you prior to arranging the sclerotherapy treatment.

Sclerotherapy factsheet

For more detailed information on sclerotherapy including XXX please see the sclerotherapy factsheet.

Read the sclerotherapy factsheet

Before treatment

You child will usually have had an ultrasound or MRI. The results are then discussed with the multidisciplinary Vascular Tumours and Anomalies Centre (V-TAC) team. Sclerotherapy is recommended by the team, based on your child’s symptoms and test results. 

We will book your child in for up to three or four treatments 4 to 8 weeks apart. More or less treatments may be required, and we will re-assess this regularly. Our V-TAC nurse will be in touch with you to confirm the treatment dates. The doctors will discuss with you what sclerosant/medication would be best to be used and if any other methods will be used to treat the malformation. 

If the area to be treated is in an area where compression can be applied, we will arrange for the physiotherapist to measure your child for a custom-made compression garment that is to be worn after treatment. These garments can take up to three weeks to arrive so make sure you have this done in time for your child’s first treatment. 

In children with a venous malformation, we will do a blood test to check for any clotting abnormalities, and to make sure the biochemistry is normal. If any abnormality is found, treatment of this may be required before the sclerotherapy to reduce the risk of clotting complications. This will be discussed and arranged when you see the V-TAC team. 

You will receive information about how to prepare your child for the procedure in your admission letter. If required, arrangements will be made for you to come to the hospital a few days or weeks before the procedure for a preadmission check by the anaesthetist. You will also receive a call in the week before to make sure your child is well and to confirm the arrangements for treatment. If your child or their accompanying adult are not well, the treatment will have to be rescheduled.

On the day of treatment

Does my child need to fast for the procedure?

It is important for anyone having an anaesthetic to have an empty stomach. If the stomach is full, there is a chance that during the anaesthetic whatever is in there could end up somewhere else like the lungs. 

Before the day of the operation, the day surgery staff will call and give you times to stop eating and drinking. Generally, this will mean: 

  • No solid food or milk (including formula) for six hours before anaesthesia. 
  • For breastfeeding children, we usually request 4 hours with no breast-feeds before anaesthesia. Formula feeds are thicker, so they are considered as “solids” for fasting. •
  • Clear fluids (things you can see through) up to 1 hour before anaesthesia.

Who will we see on the day?

On the day of the procedure, the V-TAC nurse will come and see you. 

You will meet the interventional radiologist, who will explain the procedure in more detail, discuss any questions you may have and ask you to sign a consent form giving permission for your child to have the sclerotherapy. 

If your child has any medical problems, please tell the doctors. An anaesthetist will visit to talk to you about your child’s anaesthetic, and make sure they are fit and well on the day.

How long will my child need to stay in hospital?

Sclerotherapy is usually a day stay procedure. Your child will come into hospital on the day and be discharged once awake and comfortable after the procedure. 

The exceptions are treatment of some larger vascular malformations or those in the head and neck region. These children need to stay the night and may need to be observed in intensive care unit.

After treatment

Your child will return to the ward after they have recovered from the anaesthetic. 

The treated area may become quite swollen. This should subside after a few days and resolve almost completely over two-three weeks. 

If the treatment has been in the neck or another vital area, your child may be monitored in the intensive care unit. In that case, they may need to be on a breathing machine until the swelling settles. This is to prevent any unexpected breathing problems. This will be discussed with you and planned before the treatment. 

If your child has a compression garment, they need to have it on as soon as possible after the treatment. Otherwise, the area may be bandaged or have a dressing on it.

General anaesthetic side effects

Some children feel sick and vomit after a general anaesthetic. Your child may have a headache or sore throat or feel dizzy, but these side effects are usually short-lived and not severe. Your child can start eating and drinking as normal once they feel like it.

Going home

You will be able to take your child home once the doctors/nurses are happy that your child is recovering well. 

Any bruising and swelling of the malformation will only last for a few days. Some parents say that the discomfort or swelling is more noticeable on day 3 or 4 rather than straight after the procedure. This is normal. Children’s pain relief medicine such as paracetamol or ibuprofen is usually enough to deal with any pain. 

Depending on the area treated, your child should be able to go back to childcare/preschool/school within a few days. Any compression garment or bandages should be worn until the next treatment or 4 to 6 weeks following treaments. They can play sport after three weeks if they feel comfortable. 

The doctors/nurses will tell you if your child needs further sclerotherapy procedures and if so, when. 

Your child may be booked for a series of treatments, or it may be a single treatment. After your booked treatments have been completed, we will arrange to review your child at the V-TAC Clinic in 4 to 6 months. This is so the doctors can check on your child’s progress and decide whether the treatment has worked or more treatments may be required

After going home, you should seek medical attention if:

  • Your child is in a lot of pain and pain relief medicine does not seem to help 
  • The treated area is unusually hot, red and painful or your child is generally unwell with a high temperature or not eating or drinking as usual 
  • A clot or swelling develops in another part of the malformation
  • You have any other concerns that things are not progressing as expected

The future

Your child might need several sclerotherapy procedures to reduce the size and effect of malformation. As sclerotherapy causes swelling and discomfort, it is safer to carry out several smaller treatments, limiting these effects each time. 

Sclerotherapy will not ‘cure’ the malformation, but it should shrink it significantly. Children may need to have further sclerotherapy as they get older and, in some, surgery may be suggested to improve the result. 

Your doctor will explain the options for treatment suitable for your child. These recommendations may change as time goes on. 

Important things to remember:

  • Treatment with sclerotherapy aims to reduce the size and symptoms of your child’s vascular malformation. 
  • The method of sclerotherapy is tailored for each child, and this will be discussed with you before going ahead. 
  • Most sclerotherapy can be done as a day stay procedure, although some children need to stay in hospital for a day or two while the swelling goes down.
  • Sclerotherapy is not a cure, but we hope it will help your child by shrinking the malformation and helping to improve any symptoms they may have. 

If you have any questions about your child’s treatment, please feel free to ask the V-TAC Team at any time.