Interactive Transcript
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So let's take a moment to talk about perfusion.
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You know, what I showed you so far was just a single phase
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of perfusion, and that's often all you get
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with a coronary CT
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because you're just looking at one, uh, point in time,
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which is the, the time which happens
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to enhance the arteries best.
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Um, but if we looked broadly at a set of myocardium, um,
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and injected contrast
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and had a magical, uh, device
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that could keep taking CT scans repeatedly,
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or if you're doing a nuclear scan, you can run that
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and image the radio tracer repeatedly,
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or an MRI you can image, uh, repeatedly.
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You would see that as we inject contrast at first pass, um,
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you would have relatively normal
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and, uh, rapid enhancement of healthy myocardium.
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What we saw in the example
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of the LAD profusion abnormality on that MRI, we saw
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that there was an area of regional hypoperfusion
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and we weren't really sure whether
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that was ischemic myocardium.
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Were infarcted myocardium.
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The fact is there'll be a hypo enhancement
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and the one will look worse than the other,
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but you won't know until you get another time point.
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So, um, one time point tells you
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that there's some abnormality, a second time point,
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and with MRI, you look between seven and 40 minutes later
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and a ct it's maybe five
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to eight minutes as your sweet spot.
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But what you're seeing is
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that there is extracellular accumulation of contrast
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and I'll give you an example of that, um, in a moment.
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But what you would see is
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that there's a late enhancement phenomenon.
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The fibrous tissue
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and the intracellular spaces start to enhance.
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So if you give two time points,
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you'll know there's a relative abnormality
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and you look late, you'll see
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that there's a hyper enhancement relatively in an infarcted
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myocardial segment, whereas there'll be deen enhancement
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just like normal myocardium in the live
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but ischemic myocardium.
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So, um, first pass
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and delayed images can help differentiate.
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So let's illustrate that.
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So scar enhances late
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and that would be if you just have a late enhancement image,
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then you wouldn't know whether there's a,
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a relative hypoperfusion,
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but just late accumulation of contrast.
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Here's an MRI of that.
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So this is on the left, a normal patient
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with normal healthy inferior wall
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and on the right an infarct.
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So this is somebody with a pretty much
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transmural inferior wall infarct.
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And it's also a nice chance to review our segmental anatomy.
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So there's an anterior lateral inferior septal
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and this does look like the mid myocardial segment.
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I don't see two papillary muscles
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'cause I think they were just a little high
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and also one of them may be infarcted in this case.
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So, um, whether you're looking at an MRI
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or a CT scan, we're injecting small molecules,
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whether it's gadolinium or iodine.
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So I've just illustrated iodine here. Tightly packed.
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Normal healthy myocytes don't have a lot
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of intracellular space.
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Infarcted, fibrous, uh, infiltrated myocytes
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that have now died and been replaced by fiber.
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Um, they have lots of extracellular space,
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so a late phenomenon would, would allow for accumulation
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of those small molecules and that can happen with CT or mri.
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The reference here is just a CT paper we did comparing
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to mr, but the idea
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Is those small molecules arrive late and stay late
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because they're not well perfused.
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And that's a good way on those late images
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to differentiate infarct from ischemia.
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The same thing happens in the nuclear lab,
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but you might do a 24 hour delayed image
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to let thallium accumulate, which is rarely done these days.
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And just so that you can see
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what this would look like in the pathology lab, um, this is,
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uh, one of the first papers of delayed enhancement.
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MRI kind of a fundamental in the field.
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And you can see this is a, uh, a specimen
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where there is fibro fatty infiltration.
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In an LED infarct, there's the interseptal wall.
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This is a pathology, uh, specimen.
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And right before that was taken, uh, and
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before the, uh, I think it's a dog was sacrificed,
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this is an MRI of that same segment
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and you can see that there was a late
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enhancement phenomenon.
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So, um, very exquisite detail
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and really perfect matching of the gadolinium, uh,
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infiltrating to that extracellular space outlining the
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fibrous tissue.