Ulcerative Colitis

Condition: Inflammatory Bowel Disease – Ulcerative Colitis

Overview (“What is it?”)

  • Definition:  Ulcerative colitis is a chronic inflammatory disease of the colon (large intestine), where the mucosa, or lining of the bowel, becomes inflamed and develops ulcers. Ulcerative colitis (UC) is thought to be due to the body’s immune system over-reacting against the intestine. This results in bleeding and damage to the cells of the colon. The colon becomes less effective in its function of absorbing water and salt.

Figure 1.
  • Epidemiology:  Ulcerative colitis affects girls and boys equally and is most commonly diagnosed in adulthood (age 30s). However, UC can be diagnosed at any age and occurs in about 2-4 out of every 100,000 people. In children, the inflammation is more likely to affect the entire colon. 

Signs and Symptoms (“What symptoms will my child have?”)

  • Early signs:  Ulcerative colitis usually presents diarrhea—frequent loose bowel movements that may have blood, mucus and/or pus. The child may have of a constant feeling of needing to move his or her bowels and cramping. Many children have loss of appetite and energy, partly because of a low blood count because of bleeding in the stool. A minority of children will have more severe disease at the time of original diagnosis with fevers, severe abdominal pain and bloody diarrhea. These children have “fulminant colitis” and need more urgent medical, and sometimes surgical, treatment. 
  • Later signs/symptoms:  Many children experience a loss of appetite over time with associated weight loss and decreased energy levels. They may also have trouble sleeping due to frequent bowel movements at night. Additional symptoms that some children experience include delay in bone development and puberty, joint pain, kidney stones, eye irritation and skin lesions.

Diagnosis (“What tests are done to find out what my child has?”)

  • Labs and tests: The diagnosis of UC is usually suspected based on a combination of history and physical exam findings. It is important for your doctor to try to distinguish between inflammatory bowel disease (Crohn’s and ulcerative colitis) and an infectious cause of diarrhea. Blood tests should be done to check blood count, electrolytes and nutritional markers. 
    • Plain abdominal X-rays can see the pattern of gas within the intestines.
    • Computed tomography (CT) scan may be obtained, depending on the symptoms that the child has.
    • Colonoscopy:  In this procedure, a flexible lighted telescope is introduced in the anal opening. The doctor is able to see the inner lining of the colon and take pieces (biopsy) of tissue that can be looked at under the microscope. This is how diagnosis is established.
  • Conditions that mimic this condition:  Crohn’s disease, indeterminate colitis, infectious colitis (Clostridium difficile, Salmonella, Shigella, E.coli and Campylobacter)

Treatment (“What will be done to make my child better?”)

  • Medicine:  The goal of therapy is to improve symptoms and prevent flare-ups in the future. 
    • The most common first line therapy for treating UC is steroids, which are used to reduce inflammation. Most children treated with steroids will go into remission, however if steroids are taken for a prolonged period of time there can be significant side effects. If the ulcerative colitis is mostly affecting the rectum and last part of the colon, steroid enemas can be used with much fewer sides effects.
    • Other non-steroidal medications, including sulfasalazine, 5-aminosaliciliates (5-ASA) and mesalamine can be used to achieve remission when mild to moderate symptoms are present.
    • Azathioprine can be used once remission has been achieved to prevent long-term steroid use
    • Infliximab, an antibody against TNF-alpha, has been used in children in both the short and long term to try to reduce the need for steroids.
    • Regardless of the medications that are chosen, it is very important to continue to take them to prevent symptom recurrence.
  • Surgery
    • Preoperative preparation:  Ulcerative colitis can be cured by removing the entire colon and rectum, therefore any child with recurrent and severe symptoms should be considered for surgery. Sometimes surgery will need to be performed urgently if there is significant bleeding or severe abdominal distension and fevers. However, usually the surgery can be planned and scheduled non-urgently. Before surgery, the family will meet with the surgeon and often an enterostomal (ostomy) therapist to discuss the best location for a stoma and to answer any questions. If the child is anemic or malnourished this may need to be corrected before surgery with a blood transfusion or additional nutritional support. Sometimes the child will need to have a “bowel prep” before surgery where a hyperosmolar solution is given to clean out the colon. 
    • Surgery:  The goal of the surgery is to remove the diseased colon (colectomy), reconnect the small intestine with the anus (ileoanal anastomosis), and protect the intestine/anus connection from poop as it is healing (ileostomy). Once the colon is removed, there are a variety of ways to pull the small bowel through to the rectum including creating a “pouch” with the small bowel (J pouch vs. S pouch) vs. a straight pull-through. The details of each of these options will be discussed with your child’s surgeon. Most children will have a temporary ileostomy. The child’s stool will be diverted into the ileostomy (bag) to allow the pouch and the connection between the small intestine and the anus to heal.
    • There are two approaches to this operation.
      • Open laparotomy:  The appendix is removed through a midline vertical incision.
      • Laparoscopy:  In laparoscopic appendectomy, several small cuts (incisions) are made. Through one of the cuts, a video camera is placed. The surgery itself is done using small instruments placed through the other incisions. The usual number of incisions (cuts) for laparoscopic surgery vary from one (single port umbilical) to several.
    • Postoperative care:  Most children will stay in the hospital for about a week after surgery. Diet will be slowly reintroduced, and if the child is on steroids they will be tapered over a few weeks. The family will be taught how to care for the ileostomy. Usually a second surgery is planned in 2-3 months to close the ileostomy. 

Figure 2.
  • Risks/Benefits
    • Immediate risks:  There is always a small risk of injury to the bowel, bladder or other internal organ during the surgery, although this is uncommon. If a small bowel pouch is created there is a risk of leak, but having a temporary ileostomy if thought to minimize this risk.
    • Long-term risks:  One of the most common problems after creation of a small bowel pouch is inflammation of the pouch or “pouchitis”. This can present with crampy abdominal pain, fever, increased bowel movements and fatigue. This can usually be treated with antibiotics. Occasionally children who have problems after surgery with pouchitis or difficulty gaining weight will be found to have Crohn’s disease or “indeterminate colitis” instead of UC. This may require that the child remain on some anti-inflammatory medications to reduce these symptoms. Other potential problems include a bowel obstruction or stricture that may require dilations or further surgery. 
    • One of the major benefits of surgery is that this can cure ulcerative colitis. This is especially important for children who have frequent symptoms and problems with weight gain and growth.

Home Care (“What do I need to do once my child goes home?”)

  • Diet:  There is no specific diet required, however some patients find that avoiding spicy or acidic foods and chocolate helps decrease the number of bowel movements after surgery. Many children have a hard time gaining weight initially after having their colon removed and therefore need a high-calorie diet with a balance of protein, carbohydrate and fat.
    • Since the colon’s main function is to reabsorb water, it is important for the child to replace losses in the stool. Using sports drinks that have salt and other minerals is a good drink to keep on hand to avoid dehdydration.
  • Activity:  Returning to regular activities as soon as possible is encouraged and depending on the type of surgery and the child, this generally ranges from 2-4 weeks.
  • Wound care:  In general, there is minimal wound care required after surgery. The incisions need to be kept dry for 48 hours. If the child has an ileostomy, there will be education on how to care for the stoma prior to discharge from the hospital.
  • Medicines:  Most medications that were used prior to surgery will no longer be needed afterwards, but steroids will need to be slowly tapered over several weeks. Most children will be started on medications to reduce the number of bowel movements (either fiber supplements or Imodium®)
  • What to call the doctor for:  You should seek medical assistance if the child is having persistent fevers, increasing abdominal pain or vomiting, or seems dehydrated (not urinating very often, increased bowel movements, seems very thirsty). It is important to know that DEHYDRATION is the most common reason for readmission in these children.
  • Follow-up care:  A follow-up visit with the surgeon will be arranged, usually within 2-4 weeks of discharge from the hospital. Follow-up will also be arranged with the gastroenterologist to discuss long-term management and recurrence prevention.

Long Term Outcomes (“Are there future conditions to worry about?”)

Children who undergo surgery for ulcerative colitis for the most part have improved quality of life. However, most patients will have loose and more frequent stools after surgery (5-7 stools at best). Some will have urgency and a degree of incontinence (particularly at night). To get a better outcome, children often need a food diary to regulate their stooling pattern. Children will need to be screened every few years with sigmoidoscopy to ensure that the small amount of rectum that remains does not develop any evidence of cancer.

References

Articles and graphics adapted from:
Updated: 11/2016
Author: Hannah G. Piper, MD
Editors: Patricia Lange, MD; Marjorie J. Arca, MD