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So it defines unrepresented as someone who lacks decisional capacity to provide informedconsent to a particular medical treatment. But like, if you look at a surrogate document, it walks you through step by step, the hierarchy of decision makers, but also, like, how that surrogate should be making decisions. Because if you.
Eric: Just for the aging population, what about long-termcare? I have to do them where I work, but I use them as an opportunity for informedconsent. Katie: Because I have to, and I’ll use it for an opportunity for informedconsent, and then urine drug test screen. Katie: Absolutely.
And yet, I think for everyone who’s elderly, which is anyone who’s my age or older, I would say it’s very important and ought to be part of an annual exam that we ought to be asking that, and documenting it in the chart. I think Bob also noted documenting it. Eric: Anybody else’s thoughts on that?
But at the same time, we’re saving a lot of moral distress of the longtermcare staff in terms of having to bear watching people not have thirst needs addressed. Who do you give informedconsent to? And so I think of it as more like the patient who’s on document dialysis, who.
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