The role of Entocort in UC and Crohn's

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Zizzle
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The role of Entocort in UC and Crohn's

Post by Zizzle »

This Medscape article about treatment options for the 2 big IBDs (apparently the only IBDs :roll:), explains why Entocort is not used more frequently. Wonder why it works so well in MC and not at all in UC? Do we have "right-sided" colitis? Back before the diet, I certainly felt most of the pain and bloating in the right side. This may help some of you seeking prescriptions for it, since it is being recognized lately for use in Crohn's.

http://www.medscape.com/viewarticle/744686_3
Because of the high risk of undesirable side effects associated with systemic corticosteroids, there have been trials with oral budesonide, a corticosteroid with high topical activity and a much lower profile of adverse events. A recently published Cochrane meta-analysis of randomized controlled trials of oral budesonide in inducing clinical remission of ulcerative colitis determined that treatment with this agent had significantly lower efficacy than oral mesalamine (RR = 0.72, 95% CI 0.57–0.91) given for 8 weeks and was equally effective to placebo (RR = 1.41, 95% CI 0.59–3.39) given for 4 weeks.[39] Although one small study observed comparable efficacy of oral budesonide to prednisolone in inducing endoscopic remission (RR = 0.75, 95% CI 0.23–2.42), the small size and lack of power precluded assessment of clinical remission.[39,40] In light of currently available evidence, therapy with oral budesonide is not recommended in the treatment of active ulcerative colitis.

On the contrary, budesonide is recommended for the treatment of mild to moderately active ileocecal Crohn's disease as one of the first-line treatment options.[41,42] The most recent randomized, double-blind, double-dummy 8-week multicenter trial comparing budesonide (9 or 3 mg 3 times daily) with mesalamine (4.5 gm) for the treatment of mild-to-moderate active Crohn's disease confirmed that budesonide was numerically but not statistically more effective than mesalamine.[43] The Cochrane systemic review of randomized trials evaluating the efficacy of budesonide at a dose of 9 mg daily demonstrated budesonide to be more effective than placebo (RR 1.96, 95% CI 1.19–3.23) or mesalamine (RR 1.63; 95% CI 1.23–2.16) in inducing remission of mild-to-moderate active ileocecal Crohn's disease after 8 weeks of treatment.[44] Even though some clinical trials demonstrated comparable efficacy in inducing clinical remission between budesonide and prednisolone,[45] the recent Cochrane systematic review of nine randomized controlled trials demonstrated that budesonide at daily dose of 9 mg was inferior to conventional corticosteroids in inducing remission of Crohn's disease (RR 0.85, 95% CI 0.75–0.97).[44] On the contrary, the safety analysis of six trials revealed that budesonide was associated with significant reduction in adverse events related to corticosteroid use with a relative risk of 0.64 (95% CI 0.54–0.76).[44] Despite these results, budesonide has a limited target population for active Crohn's disease. It is not effective in approximately 20% of patients with active Crohn's disease (in particular, patients with extensive diseases who do not have ileocecal involvement or those with left-sided colitis).[46] There is also no supportive evidence for the efficacy of budesonide in fistulizing disease because all patients with fistulas were excluded from entering the trials, which evaluated the efficacy of budesonide. Therefore, in the light of the recent data, budesonide is not recommended as a maintenance treatment of Crohn's disease.
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tex
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Post by tex »

Zizzle wrote:Do we have "right-sided" colitis?
Yes, actually, we do. MC is usually much more widespread in the terminal ileum and ascending colon, and less prominent in the transverse and descending colon.
Third, because both the density of intraepithelial lymphocytes and the thickness of the collagenous band tend to be patchy, it is essential to do multiple biopsies throughout the colon.19 Involvement of the left colon seems to be less intense than that of the right, and biopsy specimens from the left part miss about 10% of the cases.
http://www.med.upenn.edu/gastro/documen ... olitis.pdf

Also, regarding that Medscape article:

While budesonide is indeed a systemic corticosteroid, when it is administered as Entocort EC, (in enteric-coated form), is only 10 to 15% systemic. That research apparently involved the use of budesonide in fully systemic form.

Tex
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It is suspected that some of the hardest material known to science can be found in the skulls of GI specialists who insist that diet has nothing to do with the treatment of microscopic colitis.
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Post by sarkin »

I don't know what side my MC is on (but would guess by the time my symptoms tipped over into overwhelm, it was pretty widespread). I know that it was originally found by biopsy during sigmoidoscopy, so it must have been in the sigmoid colon (so left, in my case - at least back then).

This is really interesting, because it's yet another interesting case where MC has something in common with Crohn's but not UC. (Maybe they should throw UC out of the club instead of us, if they really want to get somewhere... JUST kidding.)

--Sara
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TooManyHats
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Post by TooManyHats »

Three biopsies were taken during my colonoscopy. They showed active (mild-hahahahahaha) colitis in the ascending, transverse, and descending colon.

I landed a full time job today. I now have no choice. I've made an appointment for next Tuesday with the Doc who did the colonoscopy and plan to ask for a prescription for Endocort. I'm not happy, but feel I have no choice. I simply cannot work full-time like this.
Arlene

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sarkin
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Post by sarkin »

Arlene,

Congratulations on the job. I'm sorry it forces your hand into a medication you prefer not to take. I hope you have success with it, and that it helps you on this rough MC/mast-cell road. I am lucky to be working part-time, with a flexible schedule, and am grateful I've been able to come along as much as I have without an Rx. If my circumstances were different I would do just what you're doing (and it may yet come to that). I hope if I reach that point, that it will feel more like a choice than is your experience. You've had it enough feeling like you're running out of diet options, without feeling this as well. I'm sorry.

Sara
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coryhub
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entocorte

Post by coryhub »

It's interesting you mention using the Entocorte for work. Myself I can only afford 10 pills at a time ($50 a shot) and I am saving them for the month of September when my job gets ultra stressful and I can't afford to be running to the bathroom 10 X's a day like happened last September. Come on retirement!
CoryGut
Age 71
Diagnosed with Lymphocytic Colitis Sept. 2010
On and off Entocort(Currently Off)
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dgshelton
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Post by dgshelton »

My pain was always right sided. I was checked for an appendicitis several times because if right side pain.

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Denise

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Post by Gloria »

Cory,

Great picture! It's nice to "see" you!

Gloria
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Post by Gloria »

Arlene,

I was going to suggest that you consider Entocort. It stabilized my symptoms for 4 years. The only time I had real issues was when I went off of it. I've still left open the possibility of going back on it for no other reason than to expand my diet. Dee, of Dee's Kitchen fame, is on a maintenance dose of 2 pills per day, and you can see that she's eating a wide variety of foods. I'm not considering resuming it at the moment, but I haven't completely ruled it out.

Ginny, I know that you are still taking Entocort 2x daily. I was taking it 3x daily last year from March to December, and that was after I'd already been taking various doses of it for the prior 3 years. It feels like we're admitting defeat when we resume or increase it, but we've given it our all. It's apparent that the three of us (and a few more here) have extraordinary sensitivities to foods. We can only dream about the diets some others have.

What keeps me going is knowing that Tex went through a similar ordeal when he was reacting, but he didn't have any support group or Entocort. His healing diet was also very limited. Granted, he could eat eggs and potatoes, but it was still a pretty limited diet with no fruit and little sugar, and it worked for him. He stayed with the diet for 4 years, I believe, and would have healed sooner except he kept testing foods. (Tex, if I've stated it incorrectly, please correct me.)

Mast cells certainly complicate our recovery. The diagnosis and treatment for mast cell issues is still in the embryonic stage. I don't have faith that I can find a doctor who will help me. Arlene's recent experience says it all. We are pretty much on our own, and that means OTC drugs and a low-histamine diet for now. I do have faith that things will get better and they already have for me. I'm off Entocort and I don't have symptoms beyond my control. That is a major step forward for me. I'm sure it is in your futures also.

Gloria
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tex
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Post by tex »

Gloria,

You're pretty close - but actually, even though I cut out gluten 100%, (and never tried it again), for the first year and a half, I experimented with avoiding various other foods for varying periods of time, (usually 2 or 3 weeks), before finally deciding that I wasn't getting anywhere, so I completely cut all those suspect foods out of my diet at that point. You're right that I never stopped eating eggs and potatoes, (except for a couple of short trials), and most weeks, I ate no vegetables at all, (other than the potatoes), but now and then, I would eat 2 or 3 small servings of other veggies per week, (such as squash, green beans, or broccoli). I ate no fruit at all, (not even bananas). After only a couple of weeks on that diet, I was pretty much in remission, and about 5 months later, I stumbled upon Sally's old board, (and many of the awesome people who are still posting here, today), and I made the amazing, (to me), discovery that I wasn't the only one in the world dealing with this "rare" disease. It was truly an epiphany.

I stayed on that very restricted diet for a few days short of 2 years, at which point I discovered that I could begin to reintroduce a few foods back into my diet, and eventually, I was able to eat a wide variety of foods. Actually, though, I don't eat a wide variety of foods, (even though I could, if I wanted), I typically stick with a very limited diet. It seems to make life a lot easier. :shrug: Maybe I'm just lazy. :grin:

Tex
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It is suspected that some of the hardest material known to science can be found in the skulls of GI specialists who insist that diet has nothing to do with the treatment of microscopic colitis.
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