Small bowel resection is surgery done to take out a diseased part of your small intestine. Your small intestine is a long tube with three parts:
A small bowel resection may be used to treat some cancers and precancerous conditions, such as polyps. It may also be used to treat benign (non-cancerous) conditions such as bleeding, infections, severe ulcers, Crohn’s disease, regional ileitis and enteritis, bowel obstruction (blockage), birth defects, and small intestine injury.
There are three types of small bowel resection, depending on which part of the bowel is removed:
There are different ways of doing a small bowel resection, such as laparoscopic (small incisions or cuts in the skin) and open procedures (a bigger incision or cut in the skin).
An ileostomy (an opening to the outside of the body) may be needed for stool to exit your body after a small bowel resection. If an ileostomy is not needed, the parts of the bowel that are cut are reattached to each other so that bowel movements can happen.
The need for an ileostomy depends on if the surgeon can join the ends of the small bowel. If the ends can be reconnected, stitches or staples will be used to form an anastomosis (connection). At times this can't be done. In these cases, a temporary (short-term) or permanent (long-term) ileostomy is needed.
There are risks and side effects of having a small bowel resection. Risks and side effects may be:
Recovery from a small bowel resection depends on the type of procedure you had. At times, a week-long hospital stay is needed. During surgery, a urinary catheter and a nasogastric (NG) tube will be placed. The urinary catheter will drain pee into a collection bag outside of your body. The nasogastric tube will drain the contents of your stomach. You will not be able to eat to let the bowel heal. At times, IV (into a vein) nutrition may also be needed. These will be removed when you no longer need them.
You will be told how to care for your incisions and stoma (if you have one) and any other instructions before leaving the hospital. Full instructions on caring for your stoma will be given to you by a trained stoma nurse/therapist. Your medical team will talk to you about the medications you will be taking, such as those to prevent pain, blood clots, infection, constipation, or other conditions.
Your provider will tell you what you should and should not do when you go home. This will often include:
You may be able to return to work in 2-3 weeks, based on the type of surgery and your type of job. Talk with your provider about showering, getting your surgical incisions wet, diet recommendations, and sexual activity.
You may need a family member or friend to help you with your daily tasks until you are feeling better. It may take some time before your team tells you that it is ok to go back to your normal activity.
Be sure to take your prescribed medications as directed to prevent pain, infection, and/or constipation. Call your team with any new or worsening symptoms.
There are ways to manage constipation after your surgery. You can change your diet, drink more fluids, and take over-the-counter medications. Talk with your care team before taking any medications for constipation.
Taking deep breaths and resting can help manage pain, keep your lungs healthy after anesthesia, and promote good drainage of lymphatic fluid. Try to do deep breathing and relaxation exercises a few times a day in the first week, or when you notice you are extra tense.
This article contains general information. Please be sure to talk to your care team about your specific plan and recovery.
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