I monitor my inflammation levels with calprotectin tests every 2-3 months. I believe the recommendation is at least once every 6 months but I don't like to wait that long (calprotectin rises in advance of a flare) as I want to catch and treat any flare-up early.
Besides that I'm required to do a colonoscopy at least once every 2 years for cancer screening purposes. I am in Europe and here you can do your scopes unsedated (at least in the few countries i have lived in). I've done it one time under fentanyl only (i.e. strong pain relief but i was still awake), and it was fine, but that was when i was in remission. Another time i tried unsedated when i was flaring (i wanted to watch the tv screen) - it was too painful to proceed so they sedated me. I have friends who did their routine 50-plus colonoscopy without sedation but they don't have IBD.
A calprotectin test will not detect cancer and, depending on where your inflammation, is located, may not accurately represent the inflammation in your colon. I have a "classic" type of UC in that the inflammation begins and is most severe in the rectum. I had a period of many scopes and calprotectin tests in a short time interval so that I know how to correlate my numbers with what's happening in my bowel. I wouldn't ever skip doing scopes completely as there is really no substitute for direct observation and biopsies. The calprotectin is more intended to monitor things in between scopes and give extra insight beyond the symptoms.
Post Edited (poopydoop) : 2/5/2023 9:57:54 AM (GMT-8)