Interactive Transcript
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So when I'm reading a head ultrasound,
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I want to know the history.
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If it's a preterm infant, I'm looking
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for germinal matrix hemorrhage, encephalopathy
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of prematurity, things like that.
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In a term infant, I'm focusing on other findings
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and an infant who's over the age
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of 34 weeks gestational age.
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The likelihood of germinal matrix hemorrhage is much lower
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and so we're looking for typically other, uh, abnormalities
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to, to answer or screen for in those infants.
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So a reminder of the papilla grading
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of germinal matrix hemorrhages in premature infants.
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So a grade one germinal matrix hemorrhage will be hemorrhage
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that is confined to the coth thalamic groove.
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Grade two, you have intraventricular extension without
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ventricular magaly.
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Grade three is where you have intraventricular hemorrhage
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related to germinal matrix hemorrhage plus
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ventricular magaly.
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There can be some confusion
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between post hemorrhagic hydrocephalus
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and grade three germinal matrix hemorrhage,
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especially among my residents.
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So in order to call it a grade three germinal matrix
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hemorrhage, it has to be a at the time
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of presentation of hemorrhage.
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So, um, you have germinal matrix hemorrhage filling the
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ventricles plus ventricular mely at the time of diagnosis
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on follow-up studies.
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We'll talk about post hemorrhagic hydrocephalus in a little
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bit, but the blood itself can cause ventriculitis and lead
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or plugging of, uh, of the cerebral aqueducts.
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And then you can get subsequent, uh, hydrocephalus.
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So grade three is when you have blood plus dilation
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of the ventricles at the time of presentation of hemorrhage.
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Grade four germinal matrix hemorrhage is not called grade
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four germinal matrix hemorrhage anymore
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because they used to think it was blood extending
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through the append of ventricular lining into the
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periventricular white matter.
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And we now know that that's not the case.
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It is a per ventricular hemorrhagic venous infarction,
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so not blood extending through the append lining.
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Most of my NICU colleagues still want us
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to say grade four germinal matrix hemorrhage just so
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that they can kind of fit the, um,
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infant into their carrying algorithms.
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But they also understand
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that it's now a more appropriately called periventricular
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hemorrhagic venous infarction.
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Um, so an example of what that looks like,
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so not grade four germinal matrix hemorrhage,
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it is now periventricular hemorrhagic venous infarction
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where you have that abnormal hyper echogenicity related
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to venous hemorrhagic infarction in the
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periventricular white matter.
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And again, just a reminder of why this happens.
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You have these teeny tiny like thread like venous structures
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that with a little bit of blood pressure
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or heart rate instability, you can get venous stasis
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and that leads to hemorrhagic venous and infarction.
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So, uh, formally known
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as grade four germinal matrix hemorrhage, periventricular,
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hemorrhagic venous infarction is what we call
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that more appropriately these days. It has a
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Typical appearance as that blood ages over time.
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And this patient unfortunately is a nice example
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of us following that, uh, evolution
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of the hemorrhagic venous infarction over time.
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So at the time of, uh, acute presentation,
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the per ventricular white matter will be hyper coic, um,
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at the side of the hemorrhagic venous infarction.
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Over time, encephalomalacia develops
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and that, uh, echogenic focus will turn into a
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hypoechoic focus and then it will become anti coic as
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that blood evolves over time as that evolution occurs.
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Typically that cystic space will communicate
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with the lateral ventricle
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and that's when it's called the po and cephalic cyst.
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So you can see this abnormal, uh,
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cystic structure communicating
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with the frontal horn lateral ventricle
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as a po and cephalic cyst.
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I wanna distinguish that from post
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hemorrhagic hydrocephalus.
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So, uh, post hemorrhagic hydrocephalus results typically
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from germinal matrix hemorrhage.
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The hemorrhage irritates the
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ventricular or epidermal lining.
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It plugs up the arachnoid granulations
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and impedes reabsorption of cerebral spinal fluid.
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And then you might also have hemosiderin
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or clot physically blocking the flow of CSF.
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So a reminder of the normal flow of cerebral spinal fluid.
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Um, it goes from the lateral ventricles
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down into the cerebral aqueduct
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and this is the most common location where blood, uh,
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will physically cause an obstruction
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of the ventricular system.
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So it's kind of a multifocal multifold process going
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on in these infants.
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Um, this is an, uh, an example of an MRI
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where you can actually see
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that low signal hemorrhage blocking that cerebral aqueduct.
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Um, we can see that in infants that ultrasound
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and we will follow the size of ventricles over time.
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Um, a couple of words about encephalopathy of prematurity
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or white matter injury of prematurity.
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Uh, this is, uh, like a watershed type infarct
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that happens in extremely premature infants.
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It's in the per ventricular location.
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The location is classic, so at the frontal
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and posterior aspects of the lateral ventricles,
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the periventricular white matter, um,
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normally your periventricular white matter
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after one week of age will be less echogenic than the
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adjacent choroid plexus.
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Um, I will show you an example on the next slide about
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what we call flaring.
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So prior to one week of life, you may have this, uh,
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normally hyper coic appearance, especially
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of your posterior parietal occipital white matter in the
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per ventricular region.
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So this is the same infant who was, um, imaged twice,
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once on day of life, one for concerned
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for intracranial hemorrhage,
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and then we image this infant one week later
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and look at the echogenicity
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of the posterior per ventricular white matter on day
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of life one compared to, uh, after one week of age.
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So it's the same echogenicity
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as your choroid plexus prior to one week of life.
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After one week of life it becomes h hypo coic compared to
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that choroid plexus.
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So just be careful calling, uh, white matter injury
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of prematurity prior to one week of life.
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You don't wanna call normal variant flaring, hyper genicity
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a word about the extra axial spaces.
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So especially when we are looking at our mastoid view at the
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posterior fossa or when we are looking at the subarachnoid
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and uh, subdural spaces at the vertex, a reminder
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that the subdural space is a potential space.
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So we don't typically see the subdural space
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unless something is abnormally located in
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that subdural space.
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Our, um, text part of our protocol will get, um,
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magnified images of the extra AAL spaces at the vertex,
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looking at the subarachnoid versus subdural space, looking
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for any abnormal collections to distinguish
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between the subdural space
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and the subarachnoid spaces to look
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for either a subdural collection or subdural hemorrhage.
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Um, we are looking for a couple of things.
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Number one, we don't wanna see any displaced arachnoid
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monitor, so we want to be able to see the, uh,
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bridging veins and arachnoid granulations extending from the
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surface of the brain all the way to the inner table
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of the calvarium.
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We don't wanna see any displacement towards the brain
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parenchyma and we definitely don't wanna see any
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displaced arachnoid matter.
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So here is an example of that.
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So this was an infant who, uh, has subdural collection,
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so pay attention to a couple of things.
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Um, on this ultrasound,
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this white arrow is showing you displaced arachnoid mod.
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So typically this arachnoid mater is pushed all the way up
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to the inner table of the calvarium.
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So we don't actually see this structure.
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So this purple arrow is pointing to the subdural space.
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There's some, an coic fluid pushing
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that arachnoid monitor down towards the brain.
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When if we were to put color doppler imaging on,
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we would see vascular structures extending only
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to the displaced arachnoid matter, not all the way
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to the calvarium, which we would like to see.
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So that's what this blue arrow is pointing to on MRI.
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We can see this, um, on T two weighted sequences,
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but it has to be, uh, like a, a super fluid sensitive
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MRI sequence to be able to see that level of detail.
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So again, the white arrow on the sagittal uh, cysts
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or fiesta super T two weighted sequence, you can see
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that wide arrow is pointing
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to the displaced arachnoid monitor.
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We see, uh, bridging veins displaced towards
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the brain parenchyma.
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Normally they should extend all the way to the inner table
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of the calvarium and the purple arrow is pointing to
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that subdural space.
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So this is a subdural collection in an infant.
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This patient for some reason, the clinicians
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before they got the MRI got a ct,
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which does not give us the level of detail that we need.
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So a reminder that an infant's
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optimal imaging is either ultrasound or MRI.
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Uh, so head ultrasound is for screening, MRI is
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for diagnosing, um, in much greater detail
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'cause we can see much better and we can see signal changes
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of ischemia and hemorrhage, et cetera.
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Um, CT is really not, not great
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unless your only question is,
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is there hyper attenuating hemorrhage And compare
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that example to this case.
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So this is a case of benign macro cranium infancy
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where the extra axial spaces at the vertex are large,
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but we see bridging structures extending all the way
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through these extra axial spaces.
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So this blue arrow is showing you a bridging vein extending
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through that subarachnoid space.
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So we have those structures going all the way from the
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surface of the brain through the inner table
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of the calvarium, and we also don't see any displaced
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arachnoid moderate in this infant.
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I also wanna point out that this is a specific
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patient population.
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So benign macro cran of infancy is a normal finding.
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These patients typically have big heads
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and if you look at mom
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and dad who are in the room with you, um, one
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of them will typically have large head
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circumference size as well.
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So these are infants who are typically six
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to nine months of age.
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They have a totally normal neurological examination.
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If you have an infant in the NICU
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who is younger than six months of age
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who maybe was premature and has been in the NICU feeding
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and growing for their entire life,
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that is not gonna be benign.
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Macro cranium of infancy.
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If you see large subarachnoid spaces in those infants,
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that typically is gonna be a level of atrophy, um, related
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to, um, their prematurity.
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So in summary, uh,
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most germinal matrix hemorrhage occurs
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within one week of life.
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And that is why we typically do screening head ultrasounds
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at one week of life.
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We want to see most of the cases of hemorrhage
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that are gonna occur and then we'll do screening head
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ultrasound again at about four to six weeks of age.
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And then at term equivalent
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or the time of discharge, a reminder that grade four
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germinal matrix hemorrhage is no longer
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actually called grade four germinal matrix hemorrhage.
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The more appropriate term is periventricular
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hemorrhagic venous infarction.
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There are a lot of normal variants
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that we can see at head ultrasound, especially flaring
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and don't call that pathology erroneously.
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Make sure you pay close attention to the extra axial spaces,
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subarachnoid versus subdural space.
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And if you can see a vascular structure,
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make sure you interrogate it with color doppler.
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Or if you have a machine with some sort
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of microvascular imaging, um, like a B flow
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or a superb mi microvascular image, um, make sure you use
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that to ensure vascular patency.
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With that, let's go on to several examples
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to illustrate some of these things that we've just learned.