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Hi everyone,

I had an IPAA procedure done in 2009, with a J-pouch. For the first 10 years afterward, I would get occasional blockages that would last about 10 hours from start to finish. Maybe 3 times a year. Extreme pain, no gas/stool passed.

Over the last 5 years, the frequency of blockages has gone down. However, a new symptom has crept in. Low-grade stomach aches that last almost the whole day, during which I have no appetite. This will go on for months at a time, daily.  I can’t force myself to eat because I’ve since learned that if I eat while I am feeling achey, it can turn into a full blown blockage.

a recent CT scan, in conjunction with previous ones, has confirmed that I have a stricture at the location of my ileosteal closure site. This is something I’ve been suspicious of for many years. My surgeon says I can either monitor, or undergo resection surgery. Has anyone has experience with endoscopic balloon dilation, or anything else? I would like to avoid surgery, as I worry that the situation will recur.

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I've had mine dilated endoscopically within the first few years of my surgery. Haven't had a problem since. I was told there are two basic surgical approaches use to take the loop of bowel down from the stoma and reconnect, and either of them can end up with some stricture at the site.

Have you been scoped in a while?  An endoscopist might have a different suggestion than the surgeon.  

Last edited by AMB

Thank you so much for your response. I’ve only ever had pouchoscopies, post 2009. Somewhat frustrating, as I’ve always felt that the stricture was located quite a ways beyond the jpouch. This was confirmed when I had a CT scan that showed the entire small intestine, and the stricture was confirmed to be along the ileum, above the jpouch. Where the stoma was, pre-takedown.
My last pouchoscopy was done about 6 months ago, and maybe 3 or 4 times prior to that over the last 5 years. I asked the surgeon about balloon dilation, and the resident basically told me it was pointless because of rupture risk, and that it might not work. But…there are risks to every procedure. And I’ll take the chances of “it might not work” if it means I can avoid a 4 day stay in a hospital. I’m a mom of 3 young kids, and I’m trying to be practical. I live in Canada, where my experience has been that doctors err on the side of caution, and they aren’t exactly bold in their treatments. They go with what’s maximally guaranteed, and I think they are intimidated by the “intermediate” options.

I’d be cautious about overinterpreting “there are risks to every procedure” to create a false equivalence. Risks can vary enormously between procedures (and practitioners) in both likelihood and severity. That being said, a resident isn’t likely to be qualified to help you navigate this. Perhaps you can get a referral to a well qualified procedure-oriented gastroenterologist who really understands the options and tradeoffs?

@Scott F posted:

I’d be cautious about overinterpreting “there are risks to every procedure” to create a false equivalence. Risks can vary enormously between procedures (and practitioners) in both likelihood and severity. That being said, a resident isn’t likely to be qualified to help you navigate this. Perhaps you can get a referral to a well qualified procedure-oriented gastroenterologist who really understands the options and tradeoffs?

Hey Scott,

Agreed! I did ask them to refer me to someone with experience in this field, so I’m just waiting for that. Could be about 4-6 weeks to hear back, so I just wanted to see if anyone had a bit of experience.

@AMB posted:

I've had mine dilated endoscopically within the first few years of my surgery. Haven't had a problem since. I was told there are two basic surgical approaches use to take the loop of bowel down from the stoma and reconnect, and either of them can end up with some stricture at the site.

Have you been scoped in a while?  An endoscopist might have a different suggestion than the surgeon.  

Hi. Which end did they go from to reach that area?  I had a bad stricture in my stoma closure and was getting bowel obstructions from anything physical and from food. I had a pouch redo and at the time my surgeon also resected the old stoma closure. Pathology noted a severe stricture with dilation of the adjacent bowel in the specimen. Post redo and resection I can tell my stoma closures are still an issue at times. I would want to consider a dilation like you did if they get severe again. Thanks!

@AMB posted:

Mine was balloon dilatation of the pouch inlet during a pouchoscopy by a very experienced gastroenterologist.  

I actually think I underwent the same procedure within the first year of my takedown. I was young, so I don’t remember the details, but the surgeon said there was a narrowing at the pouch-anal junction. And they dilated it a bit. I recall not having any issues at that point, but he insisted I do it anyway. It was definitely not where my current stricture is.

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