Parenteral nutrition (feeding through a vein) and cancer

Parenteral nutrition (PN) means giving nutrients and fluid into the bloodstream through a tube.

About parenteral nutrition (PN)

Parenteral nutrition (PN) means having nutrients and fluid directly into the bloodstream. It is a type of tube feeding for nutrition support.

It is usually used when a person cannot take nutrients in through their digestive system. For example, this may be because:

PN is sometimes called TPN, which means total parenteral nutrition. But it is not always possible to provide total nutrition through the bloodstream.

How PN is given

PN is usually given through a thin tube. A healthcare professional inserts it into a large vein in the neck or chest. The tube is called a central line. Sometimes you have it through a thin tube inserted into a vein in the arm that goes up into a larger vein in the chest. This is called a PICC line (peripherally inserted central catheter). 

Parenteral nutrition

Liquid feed travels from a bag at head height, down a thin tube and into a central line tube fed into a blood vessel near the heart.
Image: The diagram shows someone being fed through parenteral nutrition. Liquid feed is stored in a bag hanging at head height. From there it travels down a thin tube, and through one of two tubes hanging down from the upper chest. The upper end of these tubes is labelled as the central line and runs under the skin, into a blood vessel and towards the heart.

Sometimes, a smaller vein in the arm is used, but this is less common. It may be used if you only need feeding for a short time, usually less than 10 days. It is also only possible if the amount of fluid you can have is not restricted. This is because PN needs to be more dilute if an arm vein is used. The doctors will decide the best type of feeding for you.

PN is usually started slowly. Your feed will be reduced over a few days when you no longer need it.

You usually have PN in hospital, but it may sometimes be possible to have it at home.

Benefits of PN

PN can give you nutrition even when the digestive tract is not working. It can allow the digestive tract to rest so that it can heal – for example, after surgery to the stomach or bowel. You may also have PN if you have severe vomiting, diarrhoea or a sore mouth, and cannot have enteral feeding.

Possible problems with PN

Rarely, an infection may develop either inside the line or where it comes out (the exit site). You should tell your doctor if:

  • the skin around the exit site becomes red or darker, depending on your skin type
  • the surrounding area becomes swollen or sore
  • you notice fluid coming from the exit site
  • you develop a high temperature (fever) or feel unwell.

You may be given antibiotics. If the infection is serious, the tube may need to be removed.

It is possible for a blood clot (thrombosis) to form at the tip of the central line. If this happens, the tube may have to be removed. You may be given some anti-clotting medicines to stop this from happening. These are usually added to the feed.

You will have regular blood tests while having PN. This is to check your levels of sugar, minerals and other substances. Your dietitian will plan the feed you have. Some people may need to have their feed specially prepared for them, taking into account any specific nutritional needs.

More information and support

If you are being fed with a feeding tube, you may find it helpful to contact the following organisations:

  • PINNT – a support group for people having EN or PN at home.
  • Tubefed – a source of information for anyone having tube feeding.

About our information

This information has been written, revised and edited by Macmillan Cancer Support’s Cancer Information Development team. It has been reviewed by expert medical and health professionals and people living with cancer.

Date reviewed

Reviewed: 01 April 2025
|
Next review: 01 April 2028
Trusted Information Creator - Patient Information Forum
Trusted Information Creator - Patient Information Forum

Our cancer information meets the PIF TICK quality mark.

This means it is easy to use, up-to-date and based on the latest evidence. Learn more about how we produce our information.

The language we use


We want everyone affected by cancer to feel our information is written for them.


We want our information to be as clear as possible. To do this, we try to:

  • use plain English
  • explain medical words
  • use short sentences
  • use illustrations to explain text
  • structure the information clearly
  • make sure important points are clear.

We use gender-inclusive language and talk to our readers as ‘you’ so that everyone feels included. Where clinically necessary we use the terms ‘men’ and ‘women’ or ‘male’ and ‘female’. For example, we do so when talking about parts of the body or mentioning statistics or research about who is affected.


You can read more about how we produce our information here.