A subcutaneous port is a type of central venous catheter, or central line, located under the skin. Medicine is given through the subcutaneous port using a Huber needle.
A subcutaneous port is a long, thin tube (catheter) that provides long-term venous (vein) access. It is a type of central venous catheter (central line) that is placed completely under the skin, usually in the chest. The port looks like a small disc with a raised center. A catheter runs from the port into a large vein near your child’s heart.
A port is sometimes known as a port-a-cath, implantable port, or subcutaneous infusaport, subQ port, or implantable venous access device (IVAD). It allows medicines, nutrition, blood products, and fluids to be given to your child. Blood samples can also be taken.
With good care, the port can stay in place for months to years before it needs to be removed. It is important to take care of the port and follow all instructions to prevent infection and keep it working properly.
The care team makes a small incision to place the port and catheter under the skin. They guide the catheter until it reaches a large vein near the heart. The skin is closed over the port.
The center of the port, called a septum, is a raised area made of rubber. Medicines or other fluids are injected into the septum and travel through the central line to the vein. Medicine is given through the port using a special needle, called a Huber needle. A numbing cream can be used over the area before needle sticks.
The port may have 1 or 2 access points (single lumen or double lumen). A lumen is an opening or channel through which medicines and fluids can be given.
Benefits of a subcutaneous port include:
A subcutaneous port is a central venous catheter located completely under the skin. Medicine is given through the port using a special needle, called a Huber needle.
Knowing what to expect can help you and your child feel more comfortable before and during port placement.
Your child will have general anesthesia for port placement. This means your child will not feel pain or be aware during the procedure. It is important to follow NPO instructions about when your child must stop eating and drinking before the procedure. The entire process, including anesthesia and recovery, usually takes about 1–2 hours.
Every medical procedure has some risks, including those that involve anesthesia and surgery. Your child’s care team takes steps to keep these risks as low as possible.
While the port is being placed, possible risks include:
Possible complications include:
Serious problems are rare, but they can happen. Always ask questions if you are unsure about any part of the procedure. Follow all instructions from your child’s care team.
Your care team will teach you how to care for the subcutaneous port. Always follow your care team’s instructions to keep the line working properly and take steps to prevent infection.
The area will be sore for a few days. There will be medical glue where the cut was made. There may be some swelling or bruising in the area. Your child can return to most usual daily activities as they feel up to it.
During treatment (giving medicines), a Huber needle is used to access the port. Your child may feel a “poke” with the needle stick. Numbing cream, freeze spray, Buzzy®, or other pain management strategies may be used. When the port is not in use, the needle is removed, and your child can do most daily activities.
Medicines can be given with a syringe or an IV bag. Let your care team know if your child has any pain or discomfort while getting medicines.
The port must be flushed every 4 weeks with heparin. Heparin is a medicine that keeps the blood from clotting and blocking the line.
Your child will wear a dressing over the area when the needle is in place. The dressing must be kept clean and dry.
Avoid activities such as contact sports or rough play that might cause impact to the port area.
Protect the skin around the port from seat belts by placing a soft pad over your child’s chest.
Your care team may give you a card with information about your port. Keep this card with you at all times. Tell your child’s teachers, school nurses, and caretakers about the port.
Patients with a port are at risk for a serious infection known as central line-associated blood stream infection (CLABSI), which can be life-threatening. To help prevent infection:
Families will learn how to care for the port to keep it working properly and help prevent infection.
Call your care team if you notice any of the following:
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Reviewed: February 2026
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