Steroid Treatment in UC
The use of a class of steroids known as “corticosteroids,” is common for the induction of disease remission in IBD. This form of steroid is different from the anabolic type of steroids which receive media attention regarding use among athletes. Corticosteroids have a variety of anti-inflammatory effects which make them useful in the short-term to aid in achieving control of disease. Corticosteroids are produced in topical, oral, and intravenous formulations which can be administered depending on the severity and locations of a patient's disease.
Topical Corticosteroids
UC which is limited to the very bottom portion of the rectum is called ulcerative proctitis or proctosigmoiditis. Patients with mild-moderate forms of ulcerative proctitis limited to the rectum or distal portion of the colon may be candidates for topical corticosteroid therapy. Topical corticosteroids come in enema solution and foam preparations. During periods of active disease, enemas are typically administered at night. Patients should be instructed to use the washroom prior using enema preparations in an attempt to empty the rectum. Ideally, enemas should be retained on the rectum as long as possible (hours to overnight). Many patients note that the foam preparations are easier to retain due to the consistency of the medication. As disease activity subsides, the enemas can be spaced out and tapered. The corticosteroids applied topically are systemically absorbed to some degree, and can result in side effects similar to those of oral steroids. For this reason, they are not recommended for long-term use and topical 5-ASA preparations may supplant them.
Systemic Corticosteroids
For disease that involves more extensive portions of the colon (beyond the left side of the colon) or is of greater severity, oral and/or intravenous corticosteroids may aid in inducing remission of disease. Oral prednisone is commonly prescribed at diagnosis and during flares of disease to quickly abolish the cycle of inflammation. At maximum doses (typically 40mg daily), patients responsive to corticosteroids will note abrupt improvement in symptoms over a period of days to weeks. Once a patient feels well again (1-2 formed bowel movements per day, no blood, no urgency, no nighttime symptoms), the steroids can be gradually tapered. In instances where the colitis is severe, patients may fail to respond to oral steroids. For these forms of severe, acute disease, hospitalization with intravenous corticosteroids is recommended. The vast majority of patients receiving intravenous therapy will note an improvement in symptoms within 5-7 days; a transition is then made to oral steroids with eventual taper.
Side Effects
While corticosteroids have a variety of useful anti-inflammatory properties, the duration of their use is limited by toxicities which are time and dose dependent. As such, corticosteroids are indicated for a limited time (weeks to 3 months) to obtain disease control and then should be safely tapered; their use for maintenance of disease remission is not recommended. Many side effects are dose-dependent and reversible with the exception of osteoporosis, osteonecrosis, and cataracts which are irreversible.
1) High blood pressure - Corticosteroids cause sodium (salt) and water retention which results in swelling and can elevate blood pressure.
2) High blood glucose - Hyperglycemia (a high blood sugar) can occur with steroids. Signs and symptoms of high blood glucose include excessive thirst and urination as well as fatigue. Careful monitoring of blood glucose levels is necessary for diabetics with IBD who require steroid treatment. Other patients exhibiting signs and symptoms of hyperglycemia should have a blood glucose checked.
3) Low potassium levels - Low blood potassium levels can be associated with corticosteroid use and are manifested by musculoskeletal cramps, weakness, nausea, and vomiting
4) Osteoporosis - Long-term corticosteroid use (>3 months) impairs calcium metabolism and can weaken bone mineralization. Patient’s receiving corticosteroids for > 3 months should have a bone density scan performed to assess for changes in bone mineralization.
5) Osteonecrosis - Osteonecrosis is a form of irreversible bone injury resulting from loss of blood flow to bony tissue. It most commonly affects the hip, shoulder joints, leg and foot joints.
6)Cataracts - Cataracts are associated with long-term corticosteroids use. Patient’s utilizing recurrent courses of steroids should have routine eye exams.
7) Fluid retention - As noted above, corticosteroids result in salt and water retention which makes patient’s swell. Many people will note fullness in the cheeks as well as fluid around the ankles.
8) Skin changes - Corticosteroids may thin skin or result in striae, the technical name for stretch marks.
9) Increased appetite - Many patients note a dramatic increase in their appetite after starting steroids.
10) Irritability/Insomnia - High doses of corticosteroids often make people feel jittery or hyperactive. Sleep disturbances may be noted.










Comments
I have been on corticosteroids for about 6 months started at a high dose of 40 mg. I have tapered off to 20 mg but do not seem to be able to get completely off them as the bleeding starts again. Is surgery the only option left or is there some other medical intervention that can be done. I have tried infliximab infusion which help a little but not able to discontinue steroids. I am also taking Imuran 150 mg daily. My Dr. stopped giving me Asacol as she said it was not doing anything.
Posted by: Victor | September 24, 2007 8:40 PM
My brother-in-law was diagnosed with UC a little over a year ago. He initally was placed on the high dose prednisone (40mg) and tried to taper off when his symptoms improved. However the disease has gotten worse and his doctor just keeps upping his daily dose of prednisone. He is currently prescribed 60mg daily and has been at that level for 6 months. His condition has shown little improvement and he was readmitted to the ICU today. I am worried that corticosteroids are the wrong treatment for him and about the damage that they could be doing to his body. He is only 24 years old. Any information that you could provide would be greatly appreciated.
Posted by: Nicole | October 1, 2007 9:55 PM
My daughter (17) has been diagnosed with UC in October. Hospitalized for 3 days, home taking 60 mg prednisone, 9 tables of Asacol = 400 mg per day, and 40 mg potassium. She was down to 5 mg of prednisone, still taking Asacol, and no more potassium pills as of November 22 (Thanksgiving Day). Next day started with diarrhea again, and throughout the last 2 and a half weeks has upped the steroid to 40 mg per day and 12 Asacol. Was prescribed Flagyl in case of infection. Nothing is working to calm the vomiting, diarrhea down. Took her to ER this afternoon. Given IV for dehydration and 40 mg of potassium. Her level of potassium was low again. Could potassium (low levels) cause all of the sypmtoms? Dr's don't seem to know.
Posted by: Brenda | December 10, 2007 12:29 AM
1986 - diagnosed UC as a "tween", began sulfasalazine & prednisone. 2 hospital episodes 1986 and 1988.
early 1990s: off sulfa, changed to Asacol. Still on preds but lower dosage (10 mg/every other day??)
1996: flareup of joints, increased preds for two months, gradual taper to 5 mg every other day
late 1990s: finally off steroids after 10+ years.
2004: no more Asacol, due to IAPT successful surgery
Posted by: Angie | February 29, 2008 12:50 PM
Just wanted to mention something that really has worked for me. I have pan colitis (entire colon affected). I seem to flare up every two years and need a round of steroids to get back in remission. This last time, I flared again when I had tapered down off the prednisone a bit.
For me, what finally got me off the steroids was a probiotic (live bacteria and other helpful "bugs") called Primal defense. I have been almost as colitis free as before I was diagnosed. Primal defense is soil organisms, similar to what you would ingest if you ate fresh vegetables out of a garden. Apparently they crowd out the unhealthy bugs that tend to accumulate in the guts of IBD sufferers.
I can't guarantee it will work for anyone else, but it sure did the trick for me.
Of course, check with your GI Doc before trying anything. Most will say stuff like "well, at least it won't harm you".
Posted by: Kevin | June 21, 2008 11:35 PM