What Happens When You Have Your Colon Removed?

A colectomy is the surgical removal of all or part of the colon, typically performed to treat serious conditions affecting the large intestine. Common reasons for this surgery include colon cancer, severe inflammatory bowel diseases like Ulcerative Colitis or Crohn’s disease, and complications from severe diverticulitis. Since the colon performs important functions in the digestive process, its removal necessitates a profound change in the body’s digestive physiology and subsequent lifestyle. This article examines the resulting anatomical changes, the functional shifts in digestion, and the practical adjustments required for life after the procedure.

Understanding the Different Procedures and Anatomical Outcomes

The physical result of a colectomy varies significantly based on the extent of the disease and how the surgeon reconnects the remaining digestive tract. A partial colectomy, also called a segmental resection or hemicolectomy, involves removing only the diseased section. The remaining healthy ends of the colon are then surgically joined (anastomosis), allowing waste to continue passing through the rectum and anus.

When the entire colon is removed, two primary anatomical outcomes manage waste. The first is a total proctocolectomy resulting in a permanent ileostomy. Here, the end of the small intestine (ileum) is brought through a surgically created opening in the abdominal wall, called a stoma. Waste exits the body into an external collection appliance.

The second common outcome is a total colectomy with ileoanal anastomosis, often called a J-pouch procedure. The surgeon removes the colon and rectum but uses the end of the small intestine to construct an internal pouch, shaped like the letter ‘J.’ This internal reservoir is connected to the anal canal, allowing bowel movements to pass through the anus and avoiding a permanent external stoma.

Functional Changes to Digestion

The colon’s primary role is to absorb the majority of water and electrolytes from the liquid contents delivered by the small intestine. When the colon is removed, this crucial absorption mechanism is eliminated, causing a significant and permanent functional change to the digestive process.

The most noticeable consequence is an immediate increase in the liquidity and frequency of bowel movements. The small intestine, now the final processing organ, attempts to compensate by absorbing more water and salt over time. However, this compensatory function is rarely complete, meaning stool output remains considerably looser and higher in volume than before the procedure.

A specific concern arises if the terminal ileum, the last section of the small intestine, is removed. This segment absorbs Vitamin B12 and bile acids, and its loss can lead to malabsorption issues. Without the terminal ileum, bile acids may pass into the remaining pouch, stimulating water secretion and increasing diarrhea. B12 deficiency may require lifelong supplementation via injection. Even without terminal ileum removal, the body’s handling of water and electrolytes can be subtly altered, requiring careful monitoring.

Adapting to Life with a Stoma or Internal Pouch

For those with an ileostomy, the stoma is a pink, moist piece of the small intestine visible on the abdomen. It is insensitive to touch and continuously passes waste into a discreet, external appliance. Learning to manage the collection system involves emptying the pouch several times daily and changing the adhesive wafer and bag every few days, a process that becomes routine with practice. Modern appliances are designed to be odor-proof and secure, eliminating the misconception that a stoma is noticeable through clothing or prone to leakage.

Individuals with a J-pouch also face a period of adjustment as the internal reservoir adapts. Immediately after surgery, the small pouch capacity results in frequent and urgent bathroom trips, sometimes 10 or more times per day. Over six to twelve months, the pouch capacity gradually increases. Frequency typically settles to a more manageable four to eight bowel movements daily, often including nighttime awakenings.

A potential complication for J-pouch patients is pouchitis, an inflammation of the internal pouch often related to bacterial overgrowth. Symptoms resemble a flare-up of the original inflammatory bowel disease, including increased stool frequency, urgency, and sometimes fever or pelvic discomfort. Pouchitis is usually treated with a course of antibiotics and requires ongoing management.

Long-Term Dietary and Hydration Management

The loss of the colon’s water-absorbing capacity makes hydration a lifelong consideration for all colectomy patients. The body loses more fluid and electrolytes through the digestive tract, making dehydration a constant risk. Patients must consciously increase their fluid intake, often aiming for eight to ten glasses of non-caffeinated fluid daily to keep urine pale yellow.

Managing electrolytes like sodium is also important to ensure the body retains fluid. Adding extra salt to meals or drinking oral rehydration solutions helps replace the sodium lost through higher-output stool. Certain foods can modulate output consistency, acting as natural thickening agents:

  • Applesauce
  • Bananas
  • Rice
  • White bread

Conversely, high-fiber, tough, or stringy foods can increase output volume and looseness. These foods also pose a risk of intestinal blockage, especially for those with an ileostomy. Examples of foods to approach with caution include:

  • Raw vegetables
  • Nuts
  • Popcorn
  • Citrus fruits

Chewing food thoroughly is necessary, as it aids digestion and reduces the risk of obstruction. Long-term management involves learning how specific foods affect individual output and tailoring the diet to maintain hydration and comfortable bowel function.