A condition being an exclusion criterion in a trial does not mean the treatment is contraindicated. It frequently means the trialists wanted a cleaner population.
Hepatic steatosis: what the MASH trial evidence supports
Checked the hepatic steatosis claim against the primary source this morning. It survives, with a narrower scope than the version quoted here. Posting the narrower scope.
Registry and observational data covering excluded populations is accumulating and is weaker evidence than a trial and better than nothing.
The conclusion is tentative; the arithmetic underneath it is not.
Coming back to post #36, because the follow-up matters more than the original answer.
Bariatric surgery history: altered anatomy after surgery affects absorption. That matters for oral medications and for reconstituted solutions. Discussing specific medications and doses with a clinician familiar with bariatric surgery is prudent.
The short version is the first sentence; the rest is why.
Adding a reference point for hepatic steatosis. Mine is a single case, collected without controls, and I am posting the method alongside it so it can be discounted appropriately.
Post #56 is the version of this I will quote in future. One addition.
Type 2 diabetes: the population with the largest evidence base for these compounds. The SURPASS and SUSTAIN programmes established glycaemic benefit. The renal and cardiovascular benefit evidence is separate from the glycaemic benefit evidence.
I have said this before in a thread nobody could find, so it is worth repeating.
Post-authorisation safety studies are the place where under-studied populations eventually appear, and they are public.
The short answer was in the first line; everything after is the working.
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