Guest guest Posted December 20, 2002 Report Share Posted December 20, 2002 Date: Fri, 20 Dec 2002 06:27:44 -0500 Subject: Re: Sphincter of Oddi? Lily, could you explain a little more about what the pain is like from Sphincter of Oddi. I asked my GI about this and she said you would not have chronic pain with it but severe episodes of pain. And how is it diagnosed? By ERCP or what? My pain got really bad 6 weeks post gallbladder surgery and is now pretty constant everyday although I tolerate it with no pain meds I don't know how much longer I will be able to stand it. I don't notice a difference in my pain when I eat (but I still take enzymes & try to stick to a low fat diet). I feel better at night when I am resting (I sleep with a heating pad on) and I feel pretty good in the morning but after being up and moving around the pain starts circulating my upper body. I just had an endoscopic ultrasound yesterday which revealed a healthy looking pancreas - so I am wondering now if the pain could be caused by the sphincter of Oddi or would that show up on the EUS also? I would appreciate comments from anyone who wants to share information on this topic. Thanks so much & A Peaceful, Meaningful, Painfree Christmas to All of YOU!!! Debbie in Mich Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 27, 2003 Report Share Posted February 27, 2003 Debbie: I am searching back older posts as I have not been " on line " for quite a while due to not having a computer. I just wanted to give you some feedback on the SOD problem. Yes, SOD is associated with SEVERE episodes of pain. I have always called them the " pain from the sky! " When I get them, they start for no apparent reason and just seem to come from nowhere. In my own case most of the time they start in my jaw and ear. Fortunately I don't have too many of them anymore. The problem with SOD is the longer it goes untreated, the more likely it is to turn into chronic pancreatitis. In my case that is what happened. It took from 1983 until 1997 to be diagnosed with pancreatitis and it took awhile to figure out the SOD and the horrible pain were one in the same. The way to find SOD is through biliary mannometry...they measure the pressures in the bile duct itself to see if they are elevated. If so, they then treat withe one or all of several treatments including: Balloon dilatation Stent placement Sphincterotomy (cutting the duct) nasobiliary drainage. In my own case I wound up having 4 stents, several dilatations, a sphincterotomy and nasobiliary drainge before the sphincter got straigtend out. But, I have chronic pancreatitis as a result of all of it. SOD, doesn't always if ever show up on ultrasounds, or MRCPs, CTs, EUS or anything else. That is what is so mind boggling. SOD and pancreatitis are two different disorders but hte SOD is what causes the pancreatitis. Early detection and treatment of SOD is the they key to preventing pancreatitis! I can tell you in my own case,until they treated the SOD, nothing would stop the SOD pain, not diet, not enzymes, not anything. It spasmed when it felt like it. SOD most of the time has a mind of its own! I hope this helps you some. Take care Kaye Asheville, NC Quote Link to comment Share on other sites More sharing options...
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