Types of Ileostomies and Pouching Systems

Temporary ileostomies

Certain bowel problems may be treated by giving part of the bowel a rest or with surgery to remove the damaged part. The bowel must be kept empty so it can heal. To keep stool from getting to the bowel, a short-term (temporary) ileostomy is created. Healing may take a few weeks, months, or even years. In time, the ileostomy will be surgically reversed (removed) and the bowel will work much like it did before. A temporary ileostomy can also be done as the first stage in forming an ileo-anal reservoir (or J-pouch).

Permanent ileostomies

When part of the bowel becomes diseased, a long-term (permanent) ileostomy must be made. The diseased part of the bowel and anus are removed or permanently rested. In this case, the ileostomy is not ever expected to be closed (removed).

Three major types of ileostomies may be made when all of the colon must be removed or rested. You and your surgeon should talk about your choices and together decide on the best surgery for you. Some of the things to think about when planning an ileostomy are the disease process, your age, your general health, and your preference.

Standard or Brooke ileostomy

Reasons for the surgery:

Ulcerative colitis

Crohn’s disease

Familial polyposis

Cancer-related problems

Output:

Liquid or paste-like constant drainage that contains digestive enzymes

Management:

Skin protection is needed; use an open-ended pouch that can be emptied

Illustration showing a standard or Brooke ileostomy where the end of the ileum is pulled through the abdominal wall and is turned back and sutured to the skin, leaving the smooth, rounded, inside-out ileum as the stoma.

The standard or Brooke ileostomy surgery is done most often. The end of the ileum is pulled through the abdominal wall and is turned back and sutured to the skin, leaving the smooth, rounded, inside-out ileum as the stoma.

The stoma is usually in the right lower part of the abdomen, on a flat surface of normal, smooth skin. The fecal output is not controlled. This means you’ll need to wear a collection pouch all the time, and empty it regularly.

Continent ileostomy (abdominal pouch)

Reasons for surgery:

Ulcerative colitis

Familial polyposis

Cancer-related problems

Output:

Liquid or paste-like drainage

Management:

Drain fairly often with a small tube (catheter) and use a stoma cover

Illustration showing a continent ileostomy made by looping part of the ileum back on itself so that a reservoir or pocket is formed inside the belly (abdomen).

A continent ileostomy is a different type of standard ileostomy. You don’t need to wear an external pouch with this kind of ileostomy.

It’s made by looping part of the ileum back on itself so that a reservoir or pocket is formed inside the belly (abdomen). A nipple valve is made from part of the ileum. A few times each day you put in a thin, soft tube called a catheter to drain the waste out of the reservoir inside your belly.

Ileo-anal reservoir (J-pouch or pelvic pouch)

Reasons for surgery:

Ulcerative colitis

Familial polyposis

Output:

Soft, formed stool

Management:

Natural bowel movements take place, but you need to protect the skin around the anus

Illustration of an ileo-anal reservoir (or pelvic pouch) made from the ileum and the rectum and placed inside the body in the pelvis.

The ileo-anal reservoir or pelvic pouch is a pouch made from the ileum and the rectum and placed inside the body in the pelvis. Other names for this include J-pouch, W-pouch, and S-pouch depending on the surgical procedure.

The pouch is connected to the anus. Waste passes into the pouch, where it’s stored. When an “urge” is felt, the stool is passed through the anus, out of the body. The sphincter muscle around the anal opening must be intact to keep the pouch from leaking. The consistency of the output of the pelvic pouch depends on what you eat and drink, and may be managed with medicines. In most cases at least 2 surgeries are needed to make the ileo-anal reservoir or pelvic pouch.

Types of pouching systems

A pouching system is needed to collect ileostomy output. Pouches come in many styles and sizes, but they all have a collection pouch to collect stool drainage that comes out of the stoma and an adhesive part (called a flange, skin barrier, or wafer) that protects the surrounding skin. There are 2 main types of systems available:

  • One-piece pouches are attached to the skin barrier
  • Two-piece systems are made up of a skin barrier and a pouch that can be taken off and put back on the barrier

Depending on the design of the skin barrier or wafer of the pouch, you may need to cut a hole out for your stoma, or it may be sized and pre-cut. It’s designed to protect the skin from the stoma output and be as gentle to the skin as possible.

Pouches for one- and two-piece systems are drained through an opening at the bottom. They are made from odor-resistant materials and vary in cost. Pouches are either clear or opaque and come in different lengths.

 

illustration showing a one-piece drainable pouch with skin barrier, two-piece drainable pouch, flange for two-piece system and drainable pouch clip

After surgery, the stoma may be swollen for about 6 to 8 weeks. During this time the stoma should be measured about once a week. A measuring card may be included in boxes of pouches, or you can make your own template to match your stoma shape. The opening on the skin barrier should be no more than 1/8 inch larger than the stoma.

Belts and tape

 

Illustration of an adjustable ostomy belt

Wearing a belt to help hold the pouch in place is a personal choice. Some people with ileostomies wear a belt because it makes them feel more secure and it supports the pouching system. Others find a belt awkward and use tape instead. Tape can be put around the outside edge of the skin barrier like a frame.

If you choose to wear a belt, adjust it so that you can get 2 fingers between the belt and your waist. This helps to keep you from getting a deep groove or cut in the skin around the stoma which can cause serious damage to the stoma and sores (pressure ulcers) on the nearby skin. If a belt is used, it shouldn’t ride above or below the level of the belt tabs on the pouching system. People in wheelchairs may need special belts. Supply companies often carry these special belts or an ostomy nurse can talk to you about making one yourself.

 

In its original form this document was written by the United Ostomy Association, Inc. (1962-2005) and reviewed by Jan Clark, RNET, CWOCN and Peg Grover, RNET. It has since been modified and updated by:

The American Cancer Society medical and editorial content team
Our team is made up of doctors and master’s-prepared nurses with deep knowledge of cancer care as well as journalists, editors, and translators with extensive experience in medical writing.

Last Medical Review: June 2, 2017 Last Revised: June 12, 2017

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