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I had step 1 last October, with loop ileo, infections and complications and leaks in the j pouch, problems with the loop ileo - forever leaking, high output stoma, and he latter has been a big problem - I have been on restricted fluids - 1 litre, increased to 1.5 litres - but tended not to stick to it rigidly. My output though is just watery, if I drink 2 litres - my output will be twice that. However. today I noticed that my meal came through in less than an hour (I don't feel ill by the way) I feel every drop/gush of my output - it can feel 'torrential', and I sleep only odd hours as I have alarms going off every two hours for fear of leaking and making a mess - that happens several times a week. The first four months post op - I spent 14 weeks in hospital - at times in and out, dehydrated, infections etc. I'm always thirsty - and never no what to do for the best - quench my thirst or leave it, my output is horrendous at the moment, I am emptying bag every twenty to thirty minutes as it suddenly fills up
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I think the key is slowing the gut. If Imodium (loperamide) or lomotil does not do it, then you need opiates to slow it down. Failing that, there is Sandostatin injections. Usually, restricting fluids for a high output ileostomy is the opposite of what you are supposed to do, as you are supposed to drink more than your output. However, if you have something like "dumping syndrome" fluid restriction can be necessary. Usually though, it is just hypotonic fluids that are restricted (like water). When you drink, you should be sipping all day, not chugging a Big Gulp quickly. You probably need to increase your salt intake too.

Products like fiber supplements will help thicken the output, reducing the leaking, but will not alter your fluid loss. Also be sure to eat small, frequent meals, as this reduces gastric "dumping."

One last thing, with all our talk about C. difficile infections in the pouch and small bowel these days, I should mention that if it has not been ruled out, you should be tested for this as a possible cause of your high output.
http://jcp.bmj.com/content/62/10/951.abstract

Jan Smiler
Please try a bagel and marshmallows. Metamucil in caplet form where it is in clear gel caps is easier to take than stirring in water, for me. Plus it is better for us to drink less water than is suggested. I was taking these 3-4 times a day, 3-5 each time and they really worked.

I did not get out of the hospital after my first surgery for 16 days as I kept getting dehydrated or everything was running into my bag faster than the nurses and I could empty it. One of the ostomy nurses hooked up a catheter bag beneath the regular bag once. After a walk around the ward as I was getting back into bed it fell off and smashed making a horrible mess all over the floor, IV stand, me, etc. That was one of the worst experiences, and it wasn't even half full. Everyone was so nice about it and I cried like a waterfall. The point of this story is to tell you I feel your pain. Take down surgery was one of the best days ever for me!

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