| Reasons for Procedure
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An ostomy is a surgical procedure that connects an internal organ to the surface of the body. An artificial opening called a stoma is created to allow waste to exit the body and pass into an external bag.
The 2 types of ostomies discussed here include:
- Colostomy—brings the large intestine to the wall of the abdomen
- Ileostomy—brings the small intestine to the wall of the abdomen
Ostomies can be permanent, but they are often temporary in infants and children.
Reasons for Procedure
The intestines create a path for food to be digested and passed out of the body. An ileostomy or colostomy may be needed if the path through the intestines is interrupted. The interruption may be due to injury or illness of the intestine such as:
A temporary ostomy may be done to allow the intestine to rest after surgery, trauma, or illness.
A permanent ostomy may be needed if:
- A large area of intestine needed to be removed
- The remaining lower intestine or rectum cannot be repaired
Problems from the procedure are rare, but all procedures have some risk. Your child’s doctor will review potential problems, like:
- Adverse reaction to anesthesia
- Nausea and vomiting
- Soreness in throat
- Skin irritation
- Excess bleeding
- Wound opening
- Hernia at the incision site
- Damage to nearby organs
- Scar tissue
- Bowel presses out of the stoma
- Heart attack
- Blood clots
- Nutritional deficiencies, particularly low levels of vitamins
Talk to your child’s doctor about ways to manage factors that may increase your child’s risk of complications.
What to Expect
- Your child’s doctor may do the following:
- Physical exam
- Blood and urine tests
- Imaging tests
- Refer you and your child to a nurse who specializes in ostomy patients
- Do give your child anything to eat or drink after midnight the night before the procedure.
- Certain medications may cause complications during the procedure or recovery. These medications may need to be stopped up to one week before the procedure. Talk to your child’s doctor before the procedure about all medications, herbs, and supplements your child is taking.
General anesthesia will be used. It will block pain and keep your child asleep through the procedure. It is given through an IV.
The exact steps will differ based on the specific reason for the surgery. Other work may need to be done before the ostomy is created. The surgery may be:
- Open—a larger incision is made in the abdominal wall so that the surgeon can view inside the abdomen
- Laparoscopic—a few small incisions are made that allow surgical instruments to pass into the abdominal cavity
An opening will be made through the muscle and skin of the abdominal wall.
If the intestine remains intact, a section of the intestine will be placed next to the opening in the abdominal wall. Incisions will be made in the intestine wall to create a second opening. The open area of the intestine will be pulled through the opening of the abdominal wall. The inner lying tissue of the intestine will be visible as the stoma.
If a section of the intestine has been removed, part of the remaining intestine will be pulled through the opening. The intestine end is secured outside the opening with sutures. This creates the stoma.
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After the operation, your child will be taken to the recovery room for observation.
How long the procedure takes depends on the reason your child needs to have the ostomy.
Anesthesia will prevent pain during surgery. Pain and discomfort after the procedure can be managed with medications.
This procedure is done in a hospital setting. The usual length of stay is 3 days-1 week depending on the reason for the procedure. Your doctor may choose to keep your child longer or if complications occur.
At the Hospital
Right after the procedure, your child will be in a recovery room where their blood pressure, pulse, and breathing will be monitored. Care for the remainder of your child’s hospital stay may also include:
- Pain medications
- Antibiotics to prevent infection
- Medication to prevent blood clots
- Learning how to care for the ostomy, stoma, and pouch
- Receiving information about diet and activity
Depending on your child’s age, the hospital staff may ask your child to:
- Walk often after surgery
- Suck on ice chips
- Start with clear fluids and slowly advance to a regular diet
During your stay, the hospital staff will take steps to reduce your child’s chance of infection, such as:
- Washing their hands
- Wearing gloves or masks
- Keeping your child’s incisions covered
There are also steps you and your child can take to reduce the chances of infection, such as:
- Washing your hands often and reminding visitors and healthcare providers to do the same
- Reminding your child’s healthcare providers to wear gloves or masks
- Not allowing others to touch your child’s incisions
It will take about 6-8 weeks for the stoma to fully heal. There will be some changes needed to care for your child’s stoma and ostomy bag, but with practice it should not interfere with daily activities. Regular contact with your child’s medical care team will make sure your child is healing as expected and help manage any complications.
Call Your Doctor
Contact your child's doctor if their recovery is not progressing as expected or they develop complications, such as:
- Nausea and/or vomiting that your child cannot control with the medications that were given
- Signs of infection, including fever and chills
- Skin irritation
- Change in stool consistency
- Not passing any stool
- Blood in your child’s stool, or black, tarry stools
- Severe abdominal pain or cramps
- Change in the appearance of your child’s stoma, including narrowing or changes in color
- Bleeding from the stoma opening or in the pouch
- Blocked or bulging stoma
- New or worsening symptoms
If you think your child has an emergency, call for emergency medical services right away.
Colostomy. Johns Hopkins Medicine website. Available at: http://www.hopkinsmedicine.org/healthlibrary/test_procedures/gastroenterology/colostomy_92,p07727. Accessed December 2, 2014.
For parents of children with colostomies. American Cancer Society website. Available at: http://www.cancer.org/treatment/treatmentsandsideeffects/physicalsideeffects/ostomies/colostomyguide/colostomy-for-parents-of-kids-with-ostomies. Updated March 17, 2011. Accessed December 2, 2014.
A guide for patients with an ileostomy or colostomy. Memorial Sloan Kettering Cancer Center website. Available at: http://www.mskcc.org/cancer-care/patient-education/resources/guide-patients-ileostomy-colostomy. Updated August 4, 2014. Accessed December 2, 2014.
Ostomy. American Society of Colon and Rectal Surgeons website. Available at: https://www.fascrs.org/patients/disease-condition/ostomy-0. Updated October 2012. Accessed December 2, 2014.
Ostomy surgery of the bowel. National Institute of Diabetes and Digestive and Kidney Diseases website. Available at: http://www.niddk.nih.gov/health-information/health-topics/digestive-diseases/ostomy-surgery-bowel/Pages/ez.aspx. Updated August 13, 2014. Accessed December 2, 2014.
Stoma care for children and their families. UCSF Benioff Children’s Hospital website. Available at: https://www.ucsfbenioffchildrens.org/education/stoma_care_for_children_and_their_families/index.html. Accessed December 2, 2014.
What is a colostomy or ileostomy? American College of Surgeons website. Available at: https://www.facs.org/~/media/files/education/patient%20ed/your%20colostomy.ashx. Accessed December 2, 2014.
Last reviewed March 2016 by Daus Mahnke, MD
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