Port – Implantable venous access device factsheet

Introduction 

Your child’s doctor may advise if your child needs a device called a ‘port’. 

A port is a type of central venous access device that lies completely underneath the skin and may be inserted for: 

  • certain medications 
  • small/difficult veins 
  • long term treatment

Ports are long term devices that can stay in place for up to 2 years or more if they are still working and required for your childs treatment. 

 About the device

A port has two main parts. There is an injection chamber that is within a solid case of titanium or plastic which is covered by a special thick silicone membrane or top that seals itself after injection. Attached to the injection chamber is a narrow soft tube called a catheter. This catheter is placed into one of the large veins of the neck or chest, with the catheter tip ending in a big vein close to the heart. 

Two small incisions (cuts) are made in the skin. The first at the neck, is where the catheter is inserted into a vein (entry site). The second incision is made on the chest or upper abdomen, where the chamber of the port is placed underneath the skin. 

The two incisions are stitched closed. In older children there may be only one incision site. Rarely, the port may be inserted into another area, such as the groin, or the inside of the upper arm. The surgeon will discuss the site of the chamber prior to the operation. 

 Care of the device

How to access the port

A port is accessed using a special needle called a non-coring needle. A local anaesthetic cream is first applied to the skin. The needle is inserted through the skin into the soft silicone chamber/top of the port and a clear dressing will be applied over the top to prevent the needle from becoming accidentally removed. 

Once the needle is in and the port is accessed, the non-coring needle can remain in place for up to 7 days. Fluids and medication can then be administered through the port. Ports can be used to obtain blood tests. Please speak to you child’s doctor for further information. 

Flushing and locking

Flushing of the port occurs when a normal saline (salt water) solution is injected into the port to prevent it from blocking. This is typically done after medications or blood collection has taken place. It may feel cold or they may taste salt, this is normal

Locking refers to when a solution made out of anti-blood clotting agent (heparin or citrate) and sometimes an added antibacterial agent (taurolidine/Taurolock) is left in the line when it is not being used. This is typically done when the port does not need to be accessed for a period of time and should be done monthly when not in use

Removal

Removal of the port is done as soon as it is no longer needed, (such as on completion of treatment) or if it is not functioning well (such as an unresolved complication). Removal of the port is done by a surgeon in the operating theatre. Your child will require a general anaesthetic

When to seek help

It is expected that a port can last many years and serious complications are very rare. Most of the time a port is the best choice for your child. However, it’s important to know of the risks involved before you consent to the procedure. 

Bleeding 

  • like most operations, there is a risk of bleeding during the insertion 
  • there is a risk of bleeding or oozing around the insertion site in the neck and the exit site on the chest. This usually settles within the first few days

Infection 

  • as with any procedure there is a risk of infection, although we do our best to avoid this by making sure everything is clean and sterile in the operating theatre
  • signs to look for include redness, pain, heat and swelling over the site where the port is inserted
  • your child might also have a fever or feel unwell. Your child needs to present to the Emergency Department if they have a temperature of 38°C or more, as the port is a possible source for infection
  • if the port is thought to be the reason for the infection, there may be ways for us to clear the infection. Sometimes the port may need to be removed

Blockage 

  • a common complication is blockage of the catheter
  • this happens if blood or medication gets stuck in the port
  • to prevent blockages the port will either have fluid running through it or be locked
  • a blocked port can sometimes be fixed using a type of anti-clotting medication. Sometimes the port is too blocked and needs to be removed

Air bubbles 

  • there is a small risk of air bubbles entering the port
  • we make sure that there is no air in the syringes and IV tubing used to inject into the port
  • if there is a break or a leak in the non-coring needle extension set, it is important to clamp it immediately to prevent air from entering

Blood clots 

A blood clot could develop around the catheter in the vein. There is always a little bit of clotting but this rarely causes problems. If the clot is large or spreading, medicine may be needed to dissolve the clot and the catheter may need to be removed. 

Needle and port catheter positioning 

  • It is important that the port needle is placed in the correct position with the tip of the needle making contact with the back of the port chamber
  • If the port needle is moved out of place or becomes blocked, it will need to be changed
  • The tip of the catheter may move into an incorrect position. This may be indicated by inability to take blood from the port or flush. If this is suspected, further investigations (such as an X-ray) may be needed

It is important that you discuss these possible complications with your child’s doctor, as well as all the risks and benefits of the port before you consent to the procedure. 

Please feel free to talk to your team doctor about any concerns you have. Being informed will help you make the best choice for your child. 

 Management

Pain management

  • local anaesthetic may be injected into the surrounding area to numb the area and reduce pain
  • oral pain relief medicine may be needed for a short period after insertion, usually not lasting more than 4-5 days
  • for about a week after insertion, the two incision sites where the port was inserted will be a little sore. Once these have healed, your child should not feel any pain. If there is still pain after a week, please speak to your doctor or nurse 

Problem with insertion

Pneumothorax - very rarely the lung may be punctured during the insertion. This may require the placement of a second tube or drain into the chest cavity to drain the air. The drain will need to stay in until the leak seals, which can take a few days or occasionally longer. 

Very rarely there can be serious complications. These can be life-threatening. 

  • the catheter could damage or puncture the walls of the blood vessels or of the heart. Fluid from the catheter or blood could collect around the heart (This is called cardiac tamponade) or in the chest (this is called haemothorax)
  • if either of these things happen, emergency treatment to drain the fluid or blood and fix the hole may be required

Childs activities

  • Your child will be able to resume most activities including day care and school once the port has been inserted it is recommended that the dressings stay dry and intact for at least 7 days following insertion
  • Your child is able to swim with the port, as long as it is not accessed. When the port is accessed with the non-coring needle, it is recommended that your child’s catheter is not submerged in water. For example swimming or bathing are to be avoided. However, your child is able to sit in a bath or have a shower, as long as the catheter is covered with a plastic taped bag to prevent it getting wet 
  • If your child currently plays a contact sport, please speak to you doctor for further advice

Resources and more information

Healthdirect provides free, trusted health information and advice, 24 hours a day, 7 days a week online or via telephone 1800 022 022. 

Last updated Monday 20th May 2024

Disclaimer

This factsheet is provided for general information only. It does not constitute health advice and should not be used to diagnose or treat any health condition.

Please consult with your doctor or other health professional to make sure this information is right for you and/or your child.

The Sydney Children’s Hospitals Network does not accept responsibility for inaccuracies or omissions, the interpretation of the information, or for success or appropriateness of any treatment described in the factsheet.

© Sydney Children’s Hospitals Network 2024


This factsheet was produced with support from John Hunter Children's Hospital.