Health Encyclopedia

Ileostomy - changing your pouch

Description

You had an injury or disease in your digestive system and needed an operation called an ileostomy. The operation changed the way your body gets rid of waste (stool, feces, or poop).

Now you have an opening called a stoma in your belly. Waste will pass through the stoma into a pouch that collects it. You will need to take care of the stoma and empty the pouch several times a day.

Alternative Names

Standard ileostomy - pouch change; Brooke ileostomy - pouch change; Continent ileostomy - changing; Abdominal pouch changing; End ileostomy - pouch change; Ostomy - pouch change; Inflammatory bowel disease - ileostomy and your pouch change; Crohn disease - ileostomy and your pouch change; Ulcerative colitis - ileostomy and your pouch change

When to Change Your Pouch

Change your pouch every 5 to 8 days. If you have itching or leakage, change it right away.

If you have a pouch system made of 2 pieces (a pouch and a wafer) you can use 2 different pouches during the week. Wash and rinse the pouch not being used, and let it dry well.

Choose a time of day when there is less stool output from your stoma. Early in the morning before you eat or drink anything (or at least 1 hour after a meal) is best.

You may need to change your pouch more often if:

• You have been sweating more than usual from hot weather or exercise.
• You have oily skin.
• Your stool output is more watery than usual.

Steps for Changing Your Pouch

Wash your hands well and have all equipment ready. Put on a clean pair of medical gloves.

Gently remove the pouch. Push the skin away from the seal. DO NOT pull the ostomy away from your skin.

Wash your stoma and the skin around it carefully with soapy water.

• Use mild soap, such as Ivory, Safeguard, or Dial.
• Do not use a soap that has perfume or lotion added to it.
• Look carefully at your stoma and the skin around it for any changes. Allow your stoma to dry completely before connecting the new pouch.

Trace the shape of your stoma onto the back of the new pouch and barrier or wafer (wafers are part of a 2-piece pouch system).

• Use a stoma guide with different sizes and shapes, if you have one.
• Or, draw the shape of your stoma on a piece of paper. You may want to cut out your drawing and hold it up to your stoma to make sure it is the right size and shape. The edges of the opening should be close to the stoma, but they should not touch the stoma itself.

Trace this shape onto the back of your new pouch or wafer. Then cut the wafer to the shape.

Use skin barrier powder or paste around the stoma, if your health care provider has recommended this.

• If the stoma is at or below the level of your skin, or if the skin around your stoma is uneven, using the paste will help seal it better.
• The skin around your stoma should be dry and smooth. There should be no wrinkles in the skin around the stoma.

Remove the backing from the pouch. Make sure the opening of the new pouch is centered over the stoma and pressed firmly onto your skin.

• Hold your hand over the pouch and barrier for about 30 seconds after you have placed it. This will help seal it better.
• Ask your provider about using tape around the sides of the pouch or wafer to help seal them better.

Fold the bag and secure it.

When to Call the Doctor

Contact your provider if:

• Your stoma is swelling and is more than a half inch (1 centimeter) larger than normal.
• Your stoma is pulling in, below the skin level.
• Your stoma is bleeding more than normal.
• Your stoma has turned purple, black, or white.
• Your stoma is leaking often.
• Your stoma does not seem to fit as well as it did before.
• You have to change the appliance every day or two.
• You have a skin rash, or the skin around your stoma is raw.
• You have a discharge from the stoma that smells bad.
• The skin around your stoma is pushing out.
• You have any kind of sore on the skin around your stoma.
• You have any signs of being dehydrated (there is not enough water in your body). Some signs are dry mouth, urinating less often, and feeling lightheaded or weak.
• You have diarrhea that is not going away.

References

American Cancer Society website. Caring for an ileostomy. www.cancer.org/treatment/treatments-and-side-effects/physical-side-effects/ostomies/ileostomy/management.html. Updated October 16, 2019. Accessed February 3, 2023.

Galandiuk S, Netz U, Morpurgo E, Tosato SM, Abu-Freha N, Ellis CT. Colon and rectum. In: Townsend CM Jr, Beauchamp RD, Evers BM, Mattox KL, eds. Sabiston Textbook of Surgery. 21st ed. St Louis, MO: Elsevier; 2022:chap 52.

Raza A, Araghizadeh F. Ileostomy, colostomy, and pouches. In: Feldman M, Friedman LS, Brandt LJ, eds. Sleisenger and Fordtran's Gastrointestinal and Liver Disease. 11th ed. Philadelphia, PA: Elsevier; 2021:chap 117.

Review Date:10/1/2022
Reviewed By:Debra G. Wechter, MD, FACS, General Surgery Practice Specializing in Breast Cancer, Virginia Mason Medical Center, Seattle, WA. Also reviewed by David C. Dugdale, MD, Medical Director, Brenda Conaway, Editorial Director, and the A.D.A.M. Editorial team.

The Agency for Health Care Administration (Agency) and this website do not claim the information on, or referred to by, this site is error free. This site may include links to websites of other government agencies or private groups. Our Agency and this website do not control such sites and are not responsible for their content. Reference to or links to any other group, product, service, or information does not mean our Agency or this website approves of that group, product, service, or information.

Additionally, while health information provided through this website may be a valuable resource for the public, it is not designed to offer medical advice. Talk with your doctor about medical care questions you may have.