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A stoma is an opening on the tummy where the bowel is brought to the skin surface and allows poo to come out. Your baby will need a general anaesthetic and an operation to have a stoma formed. The nurses and the doctors will explain this all to you in more detail. Some stomas are formed using the small bowel allowing the poo to drain out of the stoma instead of going through the large bowel and rectum. These can either be a:
Stomas formed using the large bowel are called a colostomy.
Babies will often have 2 stomas of bowel brought to skin surface. 1 stoma will be where the poo comes out through. This is known as the ‘proximal’ stoma. The other stoma is the distal stoma which is where the bowel goes to the rectum from the stoma. This is also known as the ‘mucous fistula’.
After your baby’s stomas have been formed, they will need to be monitored. A paraffin gauze dressing (Jelonet©) will be applied over the stoma to keep it moist until it starts to work and produce poo.
When the stoma begins to produce poo, a stoma bag will be put on the stoma to collect the poo. The nurses and doctors will monitor, measure and record the amount of poo that drains from the stoma. We call these stoma losses.
The nurses will show you how to put a stoma bag on, and then help you to do this until you are confident to do it on your own.
To put on a stoma bag you will need:
How to put on the stoma bag:
We will measure and monitor your baby’s stoma losses because this will help us to assess how your baby is progressing, help to prevent problems developing and understand what are normal stoma losses for your baby. We will look at the amount of poo your baby produces, the colour and the consistency as this helps us with monitoring your baby.
Sometimes your baby may need medicines because they have a stoma. These can be loperamide and sodium supplements.
Loperamide medicine will help to slow down the amount of poo.
If your baby’s has a lot of stoma losses, they can loose a lot of fluid and minerals like sodium and potassium which are also known as electrolytes. We will check your baby’s wee every week to check their sodium levels. If the sodium levels are low in the wee, we may need to give your baby sodium as a medicine to help replace the sodium that is lost through the stoma losses.
A prolapse of the stoma happens when the bowel pushes through the opening in the skin more than it should do. A small prolapse is okay if the stoma remains red in colour and continues to work.
A small amount of bleeding from the stoma is normal.
Sometimes the skin around the stoma may become very red, sore or broken down.
Dehydration and diarrhoea
If your baby gets diarrhoea, they can become poorly and dehydrated very quickly. They may need to given extra fluids and electrolytes to help replace fluid and minerals that have been lost.
Sometimes your baby may not be able to have a stoma bag put on a stoma. This may be because the skin is sore or the stoma bags will not stick.
If your baby can not have a stoma bag on, they can have creams put on the skin around the stomas to keep the skin healthy, or to help heal the sore or broken skin. There are many types of creams we may use including the following;
Metanium©
This is a thick yellow paste which you can put on the skin around the stoma to protect the skin from the poo and to soothe red and sore skin.
Orabase paste and orahesive powder
This can be used on very sore, wet and broken skin. It helps to heal and protect the skin as it works like a barrier preventing the skin becoming more damaged.
Ilex paste
We can use this paste on broken or non broken skin. It prevents and treats sore, irritated skin. We use soft paraffin with Ilex.
Medi Honey
This can be a wound gel or a honey infused antibacterial dressing. It can used on broken down or sore skin. It helps with healing by protecting the skin. The antibacterial dressing helps by absorbing any fluid coming from the sore skin which helps with healing
If you have any further questions or concerns, please speak to a doctor or nurse caring for your baby.
Please note: this is a generic information sheet relating to care at Sheffield Children’s NHS FT. These details may not reflect treatment at other hospitals. This information is not intended as a substitute for professional medical care. Always follow your healthcare professionals’ instructions. If this resource relates to medicines, please read it alongside the medicine manufacturer’s patient information leaflet. If this information has been translated into another language from English, efforts have been made to maintain accuracy, but there may still be some translation errors. If you are unsure about any of the guidance in this resource or have specific questions about how it relates to your child, always ask your healthcare professional for further advice.
Resource number: NSU20
Resource Type: Article
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