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now because you just watched the first video on seizures you know what a seizure is

and how we diagnose them and hopefully you've been applying your clinical skills in the NICU.

However that isn't really that helpful unless you know how to figure out what caused the seizure

because most seizures are provoked and how we treat them.

So that's what we're going to be covering today.

Hi, I'm Dr. Tala and I've been a neonatologist for 17 years now.

And today in our follow-up video, we are going to be discussing what causes the seizures, how do we find the underlying cause, how do we treat seizures,

and what the prognosis is for infants that actually have had a seizure.

Let's start with one.

What causes seizures?

Well, as you can imagine, anything that messes with a baby's brain has a potential to cause seizures.

The other important thing that you should realize in neonates, as opposed to older kids and adults, is that the vast majority of the seizures are provoked.

That most of the time something is causing the seizure to happen and it is a short occurrence.

And if we get rid of whatever caused it to happen, then hopefully the baby won't have any more seizures.

This differs from epilepsy.

And remember that epilepsy is when somebody has at least two or more unprovoked seizures with no obvious underlying cause.

So for example, if a baby has meningitis and then has a seizure, even if they have two or three seizures,

then this doesn't count as epilepsy because the baby is getting seizures because of the meningitis.

Relatively few of the seizures that are actually diagnosed are idiopathic, which means that we don't really know why they happen.

or considered neonatal epilepsy syndromes.

And this is where there are actual structural or genetic abnormalities or an inborn error of metabolism

that is causing the baby to actually have these seizures.

Obviously, even though it is quite rare as a cause of seizure, it is very important to pick up on them, not just for treatment, but also for prognosis.

What are the most common causes of seizures?

Well, in term babies, it's HIE or hypoxic ischemic encephalopathy.

And normally these seizures happen six to eight hours after the insult.

So basically six to eight hours after birth and can happen up to about 24 hours of life.

They can also happen as the baby's being rewarmed if the baby's being cooled.

So that's also another aside.

When the baby has a seizure can also help you kind of figure out what's causing that seizure.

In preterm babies, as you can guess, the highest cause for having a seizure would be a bleed, specifically an IVH.

Overall though, anything that messes up with the functioning of the brain, whether it's a mass, a bleed,

a metabolic abnormality, anything really can actually end up causing a seizure.

Look at this pie chart from the New England Journal of Medicine, and you can see like the relative causes of each etiology causing the seizure.

Obviously, these are kind of like broad categories

and it doesn't go into the minute details of all the tiny different things that can cause a seizure.

And in reality, there's probably a bit of overlapping in the seizure etiology.

So check out this chart from Pediatrics in Review

and you can see all the different large groups of causes of things that cause seizures.

You can see that the percentages are actually a little bit different from the New England Journal of Medicine one.

And you have to realize that in your unit, there's going to be different percentages of what's causing seizures.

If you don't have any preemies in your unit, then you are not going to have a lot of IVHs causing seizures.

Let's cover a few more of those etiologies, just kind of like in a very broad context.

So like we already said, in a premature baby, they're more likely to have an IVH.

But an older baby could also have, or a preemie baby could have a bleed elsewhere as well.

For example, a subdural hematoma, if there's trauma at the time of delivery, also a subarachnoid hemorrhage.

Both of these can end up in seizures in babies.

Perinatal arterial ischemic stroke can happen usually from an embolism.

So like a little clot travels up through the blood vessels and then ends up in an artery in the brain.

So that area of the brain onwards doesn't get all the blood that it needs.

Often that embolism can come from like the placenta or the umbilical cord, or really just about anywhere in the body.

If a baby does have a stroke, the most common finding that they actually have is a seizure.

Often it is like a focal seizure as well, a focal clonic seizure, now that you know those words.

And normally it will happen kind of 24 to 72 hours after birth.

A perinatal stroke should be considered in this situation, especially if there are these risk factors.

So if the mother has oligohydramnios, choryoamnionitis, premature rupture of the membranes, preeclampsia, diabetes, or a smoking history.

And the infant has risk factors as well.

All the infant has risk factors such as congenital heart disease, an infection, coagulopathy.

Also, boys are more likely to have an ischemic stroke than girls.

Since most of the strokes are most likely to happen in the middle cerebral artery, which also covers the area of the motor cortex,

these babies are most likely to present with like a clonic focal seizure.

So again, pretty easy to pick up.

And if you see it, then you can be pretty certain the baby is having a seizure.

Also acute metabolic disturbances can cause seizures.

So for example, having abnormal electrolytes.

So as you all know, if you have hypoglycemia, if you have hypocalcemia,

hyponatremia, or hypernatremia, so low or high sodium, or a hypomagnesemia, these can all cause neonatal seizures.

Realize that even if a baby does have a seizure, if you then correct the metabolic abnormality, then the seizures should stop.

And these are babies that don't need to be on anti-seizure medications.

And of course, acute symptomatic seizures can also be caused by infections.

So for example, a group B strep meningitis or a harpy simplex virus encephalitis.

And this is obviously one of the important things to think about.

As we've all gotten so much better at preventing and treating these babies, this cause as a cause of seizures is definitely going down.

And then there are so many brain abnormalities that can end up with seizures, whether it's a congenital brain malformation,

for example, a schizencephaly or lysencephaly, or whether there is a tumor in the brain or a bleed in the brain of uncertain etiology,

whether it's hydrocephalus.

So there are a lot of structural abnormalities that can end up presenting because a baby does have a seizure.

Two, how do we go about finding the underlying cause for the seizure?

Before we get to the diagnostic algorithm, I just want to talk briefly about the importance of getting a good family history,

birth history, perinatal history, as well as doing a good physical exam

to make sure that you're not missing any other reasons for why the baby might be having a seizure.

We'll start with a family history.

Obviously, if the mother tells you that she has generations of her family that have had epilepsy,

then there's a high chance that there is a genetic reason for why this baby might end up having a seizure.

And it really is epilepsy in this situation, as in not an acute reason for provoking the seizure.

Some seizures, for example, those due to non-ketotic hyperglycinemia, an inborn error of metabolism, may start in utero.

And the mother may report that she had these frequent episodes of like this rhythmic jerking by the baby.

Sometimes the mothers think that the babies are hiccuping and really after the baby's born, we figure out that the baby's actually having seizures.

I don't want anybody to watch this thinking when their baby's hiccuping that they're really seizuring.

Babies hiccup a lot, so don't freak out.

I'm just saying it's easy to look the other way.

Now let's move on to the physical exam.

Obviously, you should be doing a really good physical exam

because it can also reveal things for why the baby might be having a seizure.

So if the baby has microcephaly or a really small head, then maybe the baby has cerebral dysgenesis or has a genetic abnormality

or baby has an infection like a torch infection that's causing the seizure.

Macrocephaly or like a huge head, often that's associated with hydrocephalus, that can be associated with a structural abnormality or a genetic abnormality.

For example, babies, especially baby boys because it's X-linked, can be born with an aqueductal stenosis.

Really, anytime a baby has any abnormal dysmorphic features, then you should be concerned that something is going on with the brain.

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This is especially true when the abnormal features are like central.

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So for example, if there is something abnormal with the nose, or you have a central incisor, or for example, you have seizures and a cleft palate,

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I would be very worried that there is something abnormal with the brain.

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Other things that you should be looking at is like hyper or hypotelerism, if the eyes are too close or too far apart from each other.

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So really take a very good look at the baby for dysmorphic features.

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Then take a very good look at the baby's skin because abnormalities you find may suggest a neurocutaneous syndrome.

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For example, in neurofibromatosis, you might see cafe au lait patches, which are actually very difficult to see in the newborn period.

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In tuberous sclerosis, you may see ash leaf spots.

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Actually, tuberous sclerosis is one of the few neurocutaneous syndromes where the babies may start having seizures in the neonatal period.

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So again, you're looking for ash leaf spots in tuberous sclerosis.

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Or as you would definitely not miss, you may see a port wine stain in Sturge Weber syndrome.

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Or you could see a rash suggestive of incontinentia pigmenti, which honestly I've never seen, but I've had to study.

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And it's a very rare disease.

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It's X-linked dominant.

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And it starts off looking like a blistering rash, and then it devolves into kind of like wart-like lesions.

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This can be associated with neurological abnormalities including seizures.

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Obviously do a good cardiac exam.

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If the baby does have congenital heart disease then the baby is at increased risk of having a stroke.

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So that's the board answer with a congenital heart disease and focal seizures.

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The baby had a stroke.

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And then overall what does the baby look like?

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Does the baby seem to have some sort of encephalopathy?

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So something actually affecting the underlying functioning of the brain Is the baby sleepy and lethargic?

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Is there decreased tone?

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Is there increased tone?

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What are the reflexes like?

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What's the suck like?

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What are the pupillary reactions like?

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So you can have an overlying feel of whether this is something very specific in the brain

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or whether the whole body seems to be affected.

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After you take a good history and perform a good physical exam, you can start going down the diagnostic algorithm.

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So for now, what I'm going to follow is the diagnostic algorithm put forward by Dr. Jozawicz in the New England Journal Medicine article.

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Let's go through this beautiful diagnostic algorithm.

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The first thing is, if you think the baby is having a seizure, then do some blood work immediately.

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Obviously, the easiest things to rule out would be some electrolyte abnormalities.

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So send a set of electrolytes, so you're checking the sodium, the calcium, the glucose, the magnesium, making sure that those aren't the obvious causes for the seizure.

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They also recommend just getting a CBC, even though it's not a great screening test for an infection, it's not sensitive or specific,

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it's very easy to get and it's a bedside.

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So get that as well.

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And then if you are suspecting a seizure, then try to start setting up an EEG.

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Obviously, it is well acknowledged that actually getting the EEG in place does take some time.

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Obviously, if the baby had a seizure because of an abnormal electrolyte issue, then you need to correct that.

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Or if you think the baby has an infection, then obviously treat for the infection.

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If the baby, like we already said, did have a seizure because of an abnormal electrolyte issue, it is very unlikely that that baby is going to need an anti-seizure medication.

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Just correct the electrolyte issue.

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If those previous studies didn't reveal the underlying cause, then we have to broaden the differential.

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So one of the first things that you then get is a blood gas

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or preferably an arterial blood gas to check for acidosis

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if the baby does have severe acidosis then maybe it was just the hypoxemia

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and the acidosis that caused the baby to have a seizure just like in a baby with hie

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but also it's important to know just how sick the baby is

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or how acidotic the baby is because if the baby is acidotic and the brain already isn't getting enough oxygen,

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then anything else that the baby might be going through, like a borderline low sugar or something else, is a lot more likely to cause a seizure.

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Like a lot of things in medicine, if two things are bad, not just one, then you're much more likely to have that worse outcome.

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Then evaluate for infection.

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At this point, you're doing definitely more than just sending a CBC.

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You're probably sending cultures, probably a blood culture, a urine culture, depending on how old the baby is.

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And then at this point, you're probably also doing some sort of screening for torch infections.

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So for toxoplasmosis, for rubella, CMV, herpes simplex virus, HIV, hepatitis, syphilis, the whole nine yards,

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all of these can cause seizures.

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You should be performing a lumbar puncture or a spinal tap.

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I was actually taught that literally any time a baby has a seizure, unless there is a very clear, obvious reason for it.

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So baby, a preemie baby has like a massive head bleed

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or a baby has a sugar of five for like three days, then we should be doing a spinal tap.

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Remember that if you do a spinal tap, then make sure that you try to keep extra CSF.

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So keep an extra bottle with extra fluid in it because

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if we don't have an infectious reason or the tests that you send don't actually give us the answer,

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then neurology may come back and ask for all these like metabolic labs

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that they want to send on the CSF to make weird diagnoses of inborn errors of metabolism.

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Another caveat here, if you think that the baby is having seizures because of an infection, but the baby is too unstable to actually tap,

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do not stop from treating before you get the tap.

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Obviously, anytime that you're worried that a baby is really sick from an infection, you want to get those antibiotics or those antivirals in as quickly as possible.

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In this algorithm, it actually says at this point to perform genetic testing.

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This is a bit interesting to me because it is kind of quite early on.

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Other references suggest actually sending genetic testing if the initial evaluations come back negative and the imaging and everything is negative,

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or if there's a strong family history of having epilepsy.

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There are genetic panels that you can send.

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So you can send the specific study for epilepsy, all the different genes that are involved in possible epilepsy syndromes.

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So just be sure that if you are sending that panel at this point, you really should have a neurologist or a geneticist involved, just to make sure that you're sending the right one.

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Obviously, at some point, we need to be doing neuroimaging.

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If a baby has a seizure, even if you think it is from meningitis, then you should be getting some sort of neuroimaging to make sure

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that nothing else is going on structurally or the baby doesn't have a bleed or something else abnormal as well.

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As you all know, the ultrasonography or an ultrasound of the brain is always kind of like our first line step.

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And we can do it because the babies have the anterior fontanelle.

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So we have a window into their brain.

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They are quick.

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They are easy to use.

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We can do it at bedside so we don't have to transport a sick kid.

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And we can get the results very, very quickly and

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because of the ease of access it is recommended at this step just to get the ultrasound first

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and ultrasounds are still really good at detecting bleeds especially the

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larger bleed they might miss some tiny ones maybe would miss a tiny subarachnoid hemorrhage or a tiny subdural

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hemorrhage they are not as good at getting stuff in the posterior aspect of the brain

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and you may miss some avms or vein of gallon malformations

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and stuff like that but overall as an initial screening test to look at the brain, they're fantastic.

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The other slight caveat that you have to realize is that ultrasounds are user dependent.

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So the pictures are only as good as the images that are obtained by the ultrasound technician.

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As part of this step, we should be monitoring the EEG.

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Obviously, at this point that we don't have an obvious reason for the seizures, we're still trying to figure out what's going on, we're still worried about the seizures,

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we really should be monitoring the electrical activity of the brain at this point.

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And like we already said,

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this EEG should be monitored continuously even as we start the baby on the anti-epileptic medication because sometimes the electrical activity,

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the electrical seizures continue even if the baby clinically doesn't look like it's having a seizure any longer.

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So make sure that you're continuing to monitor the baby on the EEG.

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We should also be monitoring the baby on an EKG or the electrocardiogram, just monitoring the baby's heart rate and the SATs and everything.

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If a neonate is seizing, hopefully you've already moved them to the NICU and you are actually putting them on a monitor and watching that.

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Sometimes, very rarely, arrhythmias can actually cause seizures.

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But really why this is more important is

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that we can see the autonomic signs of seizures on the EKG

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and make sure that the baby is stable even if the baby is having seizures.

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So yes, definitely be monitoring these babies.

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Obviously, at this point, if you found out what's causing the seizure, then you should be trying to actually treat that cause if you can.

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So if it is hyperglycemia or if it is herpes encephalitis, then make sure that you do start acyclovir,

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whatever it is that you think is causing it, as well as actually treating the seizures.

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If the baby is still having seizures and you still don't know what caused it,

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then we have to start going down more diagnostic pathways into kind of like even more rare stuff that could be happening.

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One of the next steps is to perform an MRI.

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I would argue that really, anytime a baby has a seizure, you're probably going to end up with an MRI.

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Even if you don't actually have the, even if you have an etiology for it, even if you see a bleed on an ultrasound,

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as you all know, an MRI can give much more details of the structure of the brain, the extent of the bleed,

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the amount of hypoxic ischemic damage that occurred, lots of other things that could be missed on an ultrasound.

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So really, most of the time that a baby is having a seizure, we would want to get an MRI, but especially if we don't have a reason for it.

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As you all know, generally, we're taking babies It's too radiology to get an MRI.

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There are a few portable MRI machines.

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So generally, the baby has to be stable enough to actually transport them to MRI.

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By the way, if you are suspecting a stroke based on clinical features, so for example, like we said, we're seeing that focal clonic jerking or the focal clonic seizures,

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then not just an MRI would be recommended, but an MRA and MRV, which is magnetic resonance angiography and venography.

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So that's where they're actually putting the dye into the arteries and the veins, and you can get a really good idea about whether there was a stroke

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or whether there was an embolus or something in those areas.

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So consider that if you think that the baby has a stroke

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or if the MRI actually is indicative that the baby did have a stroke.

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If the baby is still having seizures and you've already tried the conventional anti-seizure medications and nothing seems to be working,

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then at this point, it's recommended to give trials of pyridoxine,

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pyridoxal phosphate, folinic acid, and biotin to correct uncommon vitamin-responsive epilepsies.

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Again, very rare, but if you're having these unresponsive seizures, then you really should be trying this.

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Continuing down the algorithm, then realize that this baby should be on EEG monitoring until the baby is seizure-free, so at least for 12 to 24 hours.

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You should also be considering inborn errors and metabolites at this point.

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Like I said, we're getting into the more and more rare causes of the seizures.

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So if you haven't already sent it, then send an ammonia, a lactate, make sure obviously that the glucose is okay.

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The acid is okay.

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At this point, also consider sending the urine organic acids and serum amino acids.

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Then I'm sure the neurologist will also want some weird metabolites in the CSF,

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but at least you should be sending glucose and glycine in the CSF.

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And that's where that extra CSF from the tubes comes in.

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Other things that you should consider if you haven't done it yet.

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Again, we said screening for infection.

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Again, with the emphasis on torch infections and other weird infections that you may be missing.

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Was anybody in the family sick?

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Again, we're reaching like rarer, rarer stages here at this point.

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If you haven't sent any genetic studies, then at this point you should definitely be sending some epileptic genetic panels,

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or you could do a microarray if that's what you have in your unit, or the whole exome sequencing.

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Again, I recommend that if you are actually sending genetic testing, then get a neurologist or a geneticist involved just so that you do end up sending the right thing.

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Other things that you could do is get an ophthalmologist to come and look at the eyes, see if that gives any clues,

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whether it's a torch infection or anything abnormal with the retina or anything else.

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Some weird inborn errors in metabolism can present that way.

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And another thing that you could do is actually look at the placental pathology.

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That can sometimes give clues like with a torch infection or some sort of embolism or something like that.

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In all, lots of diagnostic steps.

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Realize you shouldn't just be throwing the sink at the baby immediately when the baby first has a seizure, especially if it was just because of hyperglycemia.

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So it's important, go step by step as you're also trying to stop the seizures from happening.

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We don't want the baby to be in status just while you're waiting to send genetic panels or whatever.

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Three, how do we manage and treat seizures?

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Well, like every emergency in medicine, we have to take care of the ABCs.

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So take care of airway, breathing, and circulation for the babies first.

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Make sure that the baby is stable and breathing.

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Then, like we said, the beginning of the algorithm is to immediately send labs, make sure that we're not missing obvious reversible causes of the seizures,

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the electrolyte disturbances, send a CBC as well, and start antibiotics if that's what you need to do.

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The goal of treatment of neonatal seizures is to reduce the seizure burden,

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but also to try to prevent any poor neurodevelopmental outcomes that we would expect if loads of seizures went untreated.

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Neuronal apoptosis, which is where the neurons, the cells in the brain, undergo a pre-programmed cell death.

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And poor neurodevelopmental outcomes have been associated with untreated seizures, both in animal as well as human models.

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So we know that having prolonged untreated seizures is bad.

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Having said that, there is no high quality data from randomized trials to suggest that actually treating seizures actually helps neurodevelopmental outcomes.

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And you can imagine just how difficult of a study that is to do.

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I don't know

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if I would be willing to randomize into a study where my baby just didn't get an anti-epileptic medication just

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because we were trying to figure out whether it would affect neurodevelopmental outcome or not.

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And like we talked about in the previous video, we shouldn't be treating anything that even closely resembles a seizure.

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We really should only be treating the seizures with EEG correlation.

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So like if we actually see the seizures on the EEG, unless it is like a clonic seizure that we would expect to see in a stroke or something.

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So we're not treating every abnormal movement in a baby, even if it looks like a seizure.

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But there isn't really a lot of data on exactly how

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or when we should be treating the babies or which medications we should use.

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And honestly, a lot of the medications that we do end up using

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and are actually recommended to be used are actually off-label.

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Then we need to be worried about the actual effects from the anti-seizure medications on the brain.

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So it has been shown in studies that phenobarbital may affect the development of the brain, may actually induce apoptosis by itself,

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and may just affect neurodevelopmental outcome.

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So this is not something that we're just giving very casually.

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Having said that, it's still felt

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that the burden of untreated seizures is a lot worse on the developing brain than actually giving the anti-seizure medication.

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So right now, if there is a documented seizure on the EEG, we should be treating it.

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The New England Journal article that we keep referencing actually suggests that we should speak to the family about treating seizures,

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that it's not just such an obvious decision to be made,

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that we should be weighing the risks and the benefits of giving babies anti-seizure medications and kind of consenting them.

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So which medications?

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The ILAE recommends that phenobarbital should be our starting medication to stop seizures, no matter the cause of the seizure.

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So whether it was HIE or a stroke or IVH, we should be loading babies with phenobarbital first.

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The recommended loading dose is 20 milligrams per kilogram.

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And then if you need to give like another little dose, a bolus loading dose, you can give another 10 to 20 milligrams per kilogram.

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Realize that if you're giving like above 40 milligrams per kilogram in a short period of time,

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that's when you can really start affecting the baby's respiratory status and the blood pressure.

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You can end up with respiratory depression and hypertension, and it can really throw off the baby's neurological exam.

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They can become just really out of it and lethargic just from the medication.

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We went through this phase of sometimes using Keppra or Leveteracetam, I never really used that word, instead of starting with phenobarb,

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Keppra does seem to have fewer side effects, even if it's given in higher quantities.

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And a study from a few years ago showed

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that maybe babies given Keppra had maybe improved neurodevelopmental outcomes versus those that were given phenobarb.

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However, a randomized study, so this was Leveterisatam versus Phenobarb for neonatal seizures,

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the NEOLEV2 study, which was a small 2B randomized controlled trial,

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it showed that Phenobarbital was more effective than Keppra at 24 hours for the treatment of neonatal seizures,

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which means that the Phenobarb was much better at stopping the seizures, and that's exactly our goal, to actually stop the seizures from happening.

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Generally, if the phenobarbital has still not managed to stop the seizures from happening, then we'll give another medication.

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It's really uncertain which medication we should be giving next.

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Often we will give Keppra about 60 milligrams per kilogram or a little bit less than that as a bolus,

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or we'll give phenytoin, which is we give it at a 20 milligram per kilogram ambolus.

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We could also be giving a midazolam, which is a benzodiazepine, or a lidocaine as well to try to stop the seizures.

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Again, not a lot of clear evidence which medication we use as a second line drug.

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This table from the New England Journal article goes over the different medications

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and the doses that we could use after the phenobarbital.

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Again, notice that phenobarbital is the only one that's actually FDA approved to treat neonatal seizures.

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And by the way, all the references are below.

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The other really interesting thing about phenobarbital is that the volume of distribution of phenobarbital is about one liter per kilo.

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So let me tell you why this is helpful.

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Whatever dose we give the baby, so say we give 20 milligrams per kilo of a phenobarbital bolus,

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the level in blood of the phenobarbital will be about 20 micrograms per ml.

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And so we know that a therapeutic dose for a baby is somewhere between 10 and 40 micrograms per ml.

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So we know that if we've given a 20 mg bolus, 20 mg per kg bolus, and then another 20 mg per kg bolus,

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If we check that level in the baby's blood, most likely it will be very close to 40 micrograms per ml,

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which is the level that we're looking for.

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And when do we stop treatment?

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This is such an age-old question, and if you ask 10 neonatologists, 10 neurologists, you're going to get different replies.

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Some people say as soon as the seizures are controlled, maybe 24 hours after the seizures are controlled.

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That's extremely aggressive.

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Other people say that before the baby leaves the NICU, we can try to come off the anti-seizure medication.

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Or more traditionally, we've kept them on the anti-seizure medication for a few months.

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Four, let's talk about the prognosis of neonatal seizures.

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I'm sure, as you've already gathered, that the prognosis will really depend on what's causing the seizure in the first place,

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how long the seizure lasted untreated, and as well, whether the seizure was responsive to an anti-seizure medication or not.

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Obviously, if you have a horrible brain abnormality, then the seizure is just a very small part of contributing to that poor neurodevelopmental outcome.

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As you can probably guess,

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the ones with the worst prognosis are the ones with a genetic or metabolic abnormality that kind of have this epilepsy syndrome,

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that are basically going to exist for life.

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They're unprovoked, and it's something that's innately abnormal with the baby's brain and with the baby's genes.

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And so developmentally, they easily have the worst outcome.

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It has been well-documented, like we've already said, that untreated seizures can cause neuronal apoptosis as well as hippocampal sclerosis.

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And so that in itself can obviously worsen the outcome.

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But it's difficult to tease out exactly how much of the bad outcome is from the untreated seizures

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or from the seizures versus the original brain injury.

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Data from several case series show that if babies have a long length of seizures in a short period of time,

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then that will worsen outcome.

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For example, we definitely don't want babies to be in status epilepticus.

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So we don't want babies to have seizures for five minutes or longer.

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That's the definition of status.

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Also, another set of studies showed that if babies have more than 12 to 13 minutes of seizures within an hour period,

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then their prognosis is a lot worse as well.

356

So we don't want babies to be like continuously seizing.

357

But there is good news from the other end of the spectrum.

358

And studies show that maybe an isolated provoked seizure, whether it goes away or it's treated with an anti-seizure medication,

359

in animals at least, does not seem to worsen the developmental outcome.

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In fact, animal studies suggest that maybe the immature brain is less likely to be damaged

361

or injured from a seizure than a more mature brain.

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There are also certain EEG patterns, so background EEG patterns.

363

So what the brain looks like

364

when the baby is not having a seizure on the EEG that can be more predictive or prognosis.

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As you can imagine, if the background EEG pattern is normal, then that's more likely to end up with a completely good outcome and a good prognosis.

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If the background activity has background birth suppression or ictal activity, then these are associated with a worse prognosis.

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In one study with HIE, it was found that if the babies had a normal or slightly abnormal background EEG,

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then they were most likely going to end up with a normal development.

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Another good prognostic sign for HIE and seizures is if the seizures are completely controlled by day of life too,

370

then we can also be optimistic about a good developmental outcome.

371

Last thing I want to say about this, and that is that the background activity of the EEG especially can be really affected by the state

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that the baby is in.

373

So literally whether the baby is awake or not, which they can figure out on the EEG, but also just if the baby is being cooled or the baby's on a lot of medication,

374

especially anti-seizure medication or other narcotics or benzodiazepines or whatever, that in itself can affect the background activity of the EEG.

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So sometimes we have to wait until the baby is kind of like in a more normal state

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or at least completely warmed up before we can trust that background activity, the EEG.

377

And that brings us to the end of our seizure videos.

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I really do hope that you learned something.

379

If you're interested in a more neonatal education, then please subscribe to this channel and like this video if you did like it.

380

And if you are interested in telling us which videos you want to see next, then please think about joining our lovely community and our channel membership.

381

Again, thank you so much for being here.

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この動画で話す練習をする理由

医療分野の専門用語や論理的な説明が豊富なこの動画は、英語シャドーイングやスピーキングの練習に最適です。ネオナトロジーの専門家が分かりやすく説明する中で、「原因を特定する」「治療法を議論する」といった実用的な会話の流れを学べます。YouTubeで英語学習する際、こうした専門的なコンテンツを使うと、日常会話だけでなく、IELTS スピーキング対策にも役立つ論理的な発話能力が身につきます。シャドーイングを続けると、自然なリズムと語彙力が向上し、実際の会話でも自信を持って話せるようになります。

文脈の中の文法と表現

動画の中で使われている表現をいくつか見てみましょう。

「However that isn't really that helpful unless...」：「～しない限り、それはあまり役に立たない」という条件文で、否定的な前提を示しながら重要な情報を伝えます。シャドーイングでこの構造を覚えると、複雑な関係を明確に表現できるようになります。
「as opposed to older kids and adults」：「年長の子供や成人とは対照的に」という比較表現で、専門的な説明でよく使われます。shadowspeakの練習でこのフレーズを使いこなすと、議論の中で違いを明確に述べることができます。
「for example, if a baby has meningitis and then has a seizure...」：「例えば、赤ちゃんが髄膜炎を患い、そして痙攣を起こした場合...」という例示文で、具体的なケースを挙げながら説明を展開します。IELTS スピーキングでは例を挙げることが重要で、この構造を使うと論述が豊かになります。

発音の注意点

動画の中には発音が難しい単語やアクセントの癖があります。英語の発音を良くするために、注意が必要な箇所をチェックしましょう。

「neonatal」：/ˌniːoʊˈneɪtl/ と発音し、「ネオネイタル」となります。最初の「ne」が長く伸びるのがポイントで、短く発音してしまうと意味が通りにくくなります。
「encephalopathy」：/ɛnˌsɛfəˈlɑːpəθi/ という長い単語で、「エンセファロパチー」と発音します。途中の「pha」の部分が曖昧になりがちなので、シャドーイングで一音ずつ確認しましょう。
「etiology」：/ˌiːtiˈɑːlədʒi/ と発音し、「エティオロジー」となります。アクセントが「ti」の部分にあるので、誤って「エティオロジー」と発音しないように注意します。

これらの単語を正しく発音できるようになると、英語の発音を良くするだけでなく、リスニング能力も向上します。

この動画の文法

話し手がよく使っている文型を、動画の実際の表現とともに紹介します。

文型	動画での表現
現在完了形 have/has + 過去分詞 — 過去の出来事が今も関係している	I've been · have had · I've never seen
受動態 be + 過去分詞 — 誰がするかより、何が起きるかに焦点を当てる	are provoked · are actually diagnosed · being rewarmed
関係詞節 who / which + 節 — 人や物について情報を加える	idiopathic, which means · patches, which are · MRV, which is

シャドーイングとは？英語上達に効果的な理由

シャドーイング（Shadowing）は、もともとプロの通訳者養成プログラムで開発された言語学習法で、多言語習得者として知られるDr. Alexander Arguelles によって広く普及されました。方法はシンプルですが非常に効果的：ネイティブスピーカーの英語を聞きながら、1〜2秒の遅延で声に出してすぐに繰り返す——まるで「影（shadow）」のように話者を追いかけます。文法ドリルや受動的なリスニングと異なり、シャドーイングは脳と口の筋肉が同時にリアルタイムで英語を処理・再現することを強制します。研究により、発音精度、抑揚、リズム、連音、リスニング力、そして会話の流暢さが大幅に向上することが確認されています。IELTSスピーキング対策や自然な英語コミュニケーションを目指す方に特におすすめです。

シャドーイングのやり方: ステップ別の完全ガイドを読む →

シャドーイング練習: NEONATAL seizures! Work-up and TREATMENT!! - 動画で英語スピーキングを学ぶ

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この動画で話す練習をする理由

文脈の中の文法と表現

発音の注意点

この動画の文法

シャドーイングとは？英語上達に効果的な理由