Interactive Transcript
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Okay, so term brain imaging, uh,
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there are multiple patterns described.
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So it it depends on the duration, severity of the imaging.
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So you might have just like a few little, you know,
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embolic things or whatever, writes a little punt injury.
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But the two most common are the
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watershed and the central patterns.
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So watershed is just like adults, right?
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It's between like A-C-A-M-C, A PCA
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or the internal, like the recurrent artery of hubner
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and the, you know, lenticular, trites and whatnot.
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Um, posterior choroidal.
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So, um, so those are like more border zone,
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mostly white matter, uh, kind of pattern.
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And that's what you see with your partial asphyxia, right?
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So like, not total, but like partial, like usually shorter,
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but could be prolonged, but still, like they,
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they had some oxygen but it was reduced, right?
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And the central pattern, that's when you
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have like severe, right?
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So, so if you have like a complete anoxia,
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severe prolonged, right?
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Then now the most metabolically active structures
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that are selectively vulnerable, right?
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The basal ganglion thalami,
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the corticospinal tracts, the hippo camp, right?
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Those, the, the ones that require the most oxygen
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and blood flow are gonna be selectively hit
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because you have a complete anoxic situation.
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Uh, there's also infant editorial injury,
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which is usually underestimated
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and that's typically seen with advanced cases.
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And then you could have just diffuse or global injury. Okay?
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So timing wise, right?
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Uh, just like in adult stroke, right, the diffusion
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will peak, you know, usually like two to three days after,
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but it, you know, anywhere from one to four
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as you get toward a week, right?
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You start to have pseudo normalization
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because the restricted diffusion in the swollen dying cell
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membranes, the cell membranes license,
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they release the edema into the, you know, uh,
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interstitial space.
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And so you get that, uh, pseudo normalization of the A DC.
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So then after that you can't really use this.
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So you can use the other things like I mentioned, the T one
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that dys myelination, um, on the watery brain background
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that T one hyperintensity is helpful.
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Often edema on top
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of an already watery brain is hard to appreciate.
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So it's pretty hard in many cases to see the T two
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unless it's in a myelinate area like the clicks.
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So that's usually more helpful late when you start
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to see like the ence laia or the gliosis or whatever.
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So it starts to present, uh, more in the late period.
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Uh, but you can see it's very dependent on
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kind of physiology and timing.
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And then you can also do perfusion to look
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that hyperperfusion response and metabolism.