Interactive Transcript
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Okay, so imaging modality.
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So in the neonate, um, we often start with head ultrasound
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because it's, um, you know, there's no ionizing radiation.
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It's fast bedside exam.
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And so, uh, they can go through various fontanels,
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which are essentially these know, like open, uh, you know,
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non ossified, uh, fibrous things, um, in the skull, uh,
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that actually the sutures and fontanels are there
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because they can mold as the baby goes
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through the birth canal, right?
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So you have some level of plasticity,
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and then as the brain grows, it keeps the sutures open
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and they start to, uh, narrow
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and fuse over time, depending on age.
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So the anterior fontanel actually stays open, you know,
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till about 14, 18 months of age.
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So obviously throughout the infancy you can
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still intonate through it.
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And so you can see in the coronal
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and the satchel plane, um, the ventricles,
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nice gray white distinction here, the corpus callosum, uh,
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the cerebellum, if you're lucky as well.
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We don't typically do ct, you know,
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because of the ionizing radiation,
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but let's say if there's a trauma, right?
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Accidental or, um, non-accidental, um, any concern for, um,
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you know, uh, hemorrhage, for fracture, um, rapid screening,
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if, uh, MR is not immediately available,
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that might be within the risk benefit ratio.
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And so here, uh, you can see that the neonates have, uh,
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water or brains in adults, right?
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Because they're not myelinated yet.
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And so it is, uh,
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a little bit more hypodense here, and that's normal.
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And the overall volumes are fuller too, right?
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So unlike the, the atrophy you see the adult brain, right?
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You, you actually have a relatively smaller, uh,
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ventricle subarachnoid spaces for, for much
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of the infancy childhood.
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Now you can have the, uh, so-called benign enlargement
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of subarachnoid spaces, transiently in around nine months
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or so in self resolving around two or three years,
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but, uh, not in the neonate.
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And then you have these sutures, right, the sutures
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and fontanels that I mentioned.
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So these are gonna, um, gonna be pretty open and,
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and maybe a little overlapping if, uh,
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they had a vaginal burst, right, going
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through the canal there.
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Uh, and then they, they actually narrow pretty rapidly in
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the first like month or so.
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So then you have like a couple millimeters,
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and then they steadily, uh, narrow over time
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and have different, uh, age related times of closure.
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So for example, the atopic suture in the frontier, uh,
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closes earliest, uh, it can be, you know, four months
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or sometimes even a little bit earlier.
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And then we have mr, which is really the workhorse
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for all of our problem solving.
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So I wanna show you this, uh,
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because this is what a normal, uh,
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term neonatal Mr should look like, right?
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So I have these arrows here on
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what are called the posterior limbs of internal capsules.
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If you've got the, you know, anterior limb,
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the Gen U, the posterior limb.
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And so you see that that's pretty much the only part
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of the neonatal brain that's myelinated, right?
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Because what do you have to do when you're born?
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You have to cry and reach out for mom,
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and that's pretty much it.
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So, uh, this T one shortening myelin is fat
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and protein, right?
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So you're gonna get T one bright,
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T two dark, uh, kind of signal here.
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And so it's pretty much that, uh, posterior third
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to posterior half of the IC
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or the click, uh, should be myelinated.
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If you're a full term infant.
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Obviously if you're preterm, it might be a little less,
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but if you're not seeing it at all or barely, then
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You, you have to be suspicious that maybe there's
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something obscuring it, right?
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Like, um, maybe an edema from an, uh,
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hypoxic ischemic injury.
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And so here, this is the,
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the apparent diffusion coefficient map from the diffusion.
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Um, and so there's nothing restricted
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that's as it should be, right?
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This is a perfusion, uh,
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what we call arterial spin labeling.
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And so you see that again, right?
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The basal ganglia are the most robust, um,
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and the corticospinal tract.
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So they have good flow
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because they're actively developing as a result
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because they have more flow.
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Normally, if you have a hypoxic ischemic insult,
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they will be selectively vulnerable to a severe, um, HII
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because they are taking more blood flow baseline,
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but still the rest of the brain does have,
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you know, a reasonable flow.
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It's just not as much as the actively
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developing myelinating areas.
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So that's important too. And then Mr.
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Spectroscopy another advanced tool, right?
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So we can do voxels,
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usually they'll do one over the basal ganglia,
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like a single voxel one over the, uh, white matter.
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Um, and then you can basically get
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the different metabolites.
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This here is a long echo MRS,
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and so we're just cleaning up the baseline here.
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Essentially just looking at the major metabolites.
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And so again, in contradistinction to adults where they have
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that hunter angle that's supposed to go up, right?
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So your NAA from your neurons is higher than your
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choline from your cell membranes.
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Well, the infants are still, you know,
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they have some anaerobic metabolism, even more
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of their preterm, but basically at term age, right,
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they still are undergoing a combination
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of aerobic and anaerobic.
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So the NAAP, uh, area under the curve of the NAA peak,
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right, is around like two thirds of the choline.
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And that's actually normal to have that slight down slope.
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They can have a little bit of lactate
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and lipid again because of that.
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Um, some of that physiologic immature in heric metabolism.
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So that's actually what a normal MRS looks like,
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and that'll be important for us later on.