Skip to main content

Penetrating Injuries to the Pancreas

Medically reviewed by Drugs.com. Last updated on Feb 21, 2024.

WHAT YOU SHOULD KNOW:

CARE AGREEMENT:

You have the right to help plan your care. Learn about your health condition and how it may be treated. Discuss treatment options with your caregivers to decide what care you want to receive. You always have the right to refuse treatment.

RISKS:

WHILE YOU ARE HERE:

Informed consent

is a legal document that explains the tests, treatments, or procedures that you may need. Informed consent means you understand what will be done and can make decisions about what you want. You give your permission when you sign the consent form. You can have someone sign this form for you if you are not able to sign it. You have the right to understand your medical care in words you know. Before you sign the consent form, understand the risks and benefits of what will be done. Make sure all your questions are answered.

Central line:

This is a special IV catheter or tube. It is put into a large vein (blood vessel) near your collarbone, in your neck, or in your groin. The groin is the area where your abdomen meets your upper leg. Other central lines, such as a PICC, may be put into your arm. You may need a central line to receive medicines or IV fluids that need to be given through a big vein. You may need a central line if it is hard for caregivers to insert a regular IV. Also, a central line may stay in longer than a regular IV can. Some central lines may also be used to take blood samples.

An IV

is a small tube placed in your vein that is used to give you medicine or liquids.

Drains:

These are thin rubber tubes put into your skin to drain fluid from around your incision. The drains are taken out when the incision stops draining.

A Foley catheter

is a tube put into your bladder to drain urine into a bag. Keep the bag below your waist. This will prevent urine from flowing back into your bladder and causing an infection or other problems. Also, keep the tube free of kinks so the urine will drain properly. Do not pull on the catheter. This can cause pain and bleeding, and may cause the catheter to come out. Caregivers will remove the catheter as soon as possible to help prevent infection.

Jejunostomy tube (J-Tube):

A jejunostomy tube is a small, flexible tube that is put into a small cut in your abdomen. The end of the tube goes into your small intestine (bowel). The tube is used to give you liquids, food, and medicine. You may have a J-tube for a short time, or long-term. If you need it long-term, your tube may need to be replaced with a new one at certain times.

Nasogastric (NG) tube:

An NG tube is put into your nose, and passes down your throat until it reaches your stomach. Food and medicine may be given through an NG tube if you cannot take anything by mouth. The tube may instead be attached to suction if caregivers need to keep your stomach empty.

Medicines:

You may be given the following medicines:

Tests:

One or more of the following tests may be done. Certain tests use a special dye to help organs and structures show up better. Tell caregivers if you are allergic to shellfish (lobster, crab, or shrimp), as you may also be allergic to this dye.

Treatment options:

Vital signs:

Caregivers will check your blood pressure, heart rate, breathing rate, and temperature. They will also ask about your pain. These vital signs give caregivers information about your current health.

Learn more about Penetrating Injuries to the Pancreas

Care guides

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.