You can’t ignore the noise because we don’t know it’s noise. I know I’m failing to get that idea across, but I honestly don’t know how to articulate it better t

You can’t ignore the noise because we don’t know it’s noise. I know I’m failing to get that idea across, but I honestly don’t know how to articulate it better than I have been. I can tell you’re honestly trying to understand, and I feel the blame is likely on me as a communicator. Possibly what I’ve failed to communicate is this: MRI, CXR, etc are not images of the body. It’s not like getting a photograph of a liver and saying, at least we know this is or isn’t going on in the liver. They’re indirect measures of certain attributes of the body, such as tissue density, which we use - coupled with their medical information, and the mechanisms of likely diseases - to infer what’s happening. That’s why reading radiology is a medical specialty, and not something anyone with an anatomy background can do. (There’s a radiologist currently browsing the thread - he’s very welcome to correct me if I’m wrong about what radiology “is”.) Because of this, every such finding has to be interpreted in a context, and studies tell us how. Completely out of context findings aren’t a big problem if they’re completely unambiguous: hey, that bone is in two pieces and it should be in one. What about the finding that isn’t, though? This is equivalent to not having any information on a test’s false positive / false negative rate, only now it’s open-ended to “every condition that could look like that thing” because the defining characteristic of an incidental finding is that it’s -incidental-. It’s not related to any symptoms. So what do I do with “every disease or non-disease process that could potentially look like a spot on the lung, without any accompanying symptoms of that disease”? What I believe is the responsible answer is: “if I think the pre-test probability isn’t borderline zero, AND the post-test probability would change my course of treatment or diagnosis, order the test. If the pre-test probability is so low that any positive test result would be very likely to be a false positive and thus force me to act in a manner harmful to the patient, don’t order it - it shouldn’t be allowed to change the course of treatment. If the pre-test probability is already so high that any negative result is likely a false negative, don’t order it - it shouldn’t be allowed to change the course of treatment. Only order tests whose results should impact the course of diagnostics or treatment.” What do I do with findings that haven’t been studied in a given context, so I have no clue what their impact on the post-test probability of a diagnosis is? I don’t know. But “test just in case” isn’t the zero-risk option. There aren’t any zero consequence options. Not every test is an RCT because grant funding agencies don’t provide the budget, plus or minus, many RCTs we’d like to do are unethical (if you have good reason to believe one course of therapy is superior to another, you don’t have the clinical uncertainty to ethically allow randomizing people into an inferior therapy), plus or minus many sub-populations are just too uncommon to build an RCT on without a gigantic budget that facilitates long collection periods across multiple institutions.