Interactive Transcript
0:00
Okay, great. So we'll move on to our next
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case. This is also a patient to presented with
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chest pain and an elevated component after vaccination. So
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again, we're again looking at post-covid-19 vaccine
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cases. And again, this was a
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young adult male patient and this patient
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was actually acutely unwell and was admitted to hospital. So
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this Imaging was done in immediate days
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after symptom.
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Again, I'm going to show you the four chamber Sydney SSD here. This
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is I find a really good overview to look at the function of the ventricles
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and get a sense of what's going on. So unlike the
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last case the ventricles are Contracting normally here.
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We have normal Global stock function and the least
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on this view. I know obvious regionality. So
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both ventricles normal injection.
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And now we'll look at our short axis View.
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Short access in ussrp stack rather and one
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thing I haven't mentioned to you. Is that our at our
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Center are short axis ssfps are required after
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contrast. And so you start to get a clue
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that there may be an abnormality again at that basal to Mid
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in for lateral and infra-wall because we're actually
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seeing some enhancement even on the sequence because it was acquire.
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D after so let's go through it and just a reminder kind of a clue to
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look at that same area of The myocardium and I'll pause
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it as we go through so you can see what I'm talking about. So even
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here on this very basal slice, you can
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see that there's increased signal intensity here at that in
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for a wall and again not all centers of are
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there short access facts after contrast, but we do it's on
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time saving measure while you're waiting for to
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acquire like getting the hands images. And again, you
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can start to see here even on the short acts of Stack that there is
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increasingly long time City. The other thing is that there's
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actually reasonable thickening and that's a common finding when
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you have a Dima you can have vocal Regional law
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beginning related to indominus my cardium and although
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the ejection was normal There is mild hypokinesis
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in that area. So that area of my heart is
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not Contracting as well as other areas.
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So now let's go through and see if we need those T1 based
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and T2 based criteria. So we'll start with our
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teaching-based criteria and we'll pull up our teaching map
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and unfortunately on a scanner this patient with scanned on
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it doesn't display the color map but that's fine. Even the gray
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scale you can start to see that there is an abnormality and our
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black blood teaching Imaging which was kind of our traditional sequence
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that we use qualitatively to assess
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The myocardium and here even without much when doing you can
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start to see that there is a marked abnormality again in the
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sub epicardial myocardium at the
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infer wall and in for a lot of wall actually expanding also into
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the antilateral wall, you're running a
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basil spice and as we come more towards the mid ventricle, you
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can see that there's some artifacts as patients as they said was a cute
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and well I was having difficulty holding their breath and had
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some Rhythm disturbance as well. But despite that you can see
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that this subject of cardinal High signal intensity
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extends both
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Basal level into the midterm treatment level.
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And this patient had only a short act with
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midventricular TT map and Visually I
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even know this is a grayscale again areas of high T2,
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which tell us that there is more free water and
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the demon in this case visually we can see that that solved
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epicardial. Myocardium has higher symptom. I'm just
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gonna die very quick Roi just to show you how those
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numbers compare so here in this again very
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quick Roi at that set up a
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cardilateral wall. The teach you value is 61. This was
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a card at one point five. She as you can see well above our
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normal reference range for one point five T teaching mapping
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and just to compare that more normal spectrum of
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the teaching value that's within our normal reference range
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of 43 milliseconds. So again, we have clearly met
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the teaching base criteria in this patients. And now
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I'm gonna pull up our lake under your hands short axis stock
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on the left and we'll show you our team one map again
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native to your map on the right and Visually again,
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even though this is a great scale we can see that there's
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It would mapping values colocalizing again
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with a edema that we saw in The sub-epocardial myocardium and
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has become down on our Lincoln hands damage. We can see that
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there's some artifact here patient again is having difficulty holding
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their breath. Of course, they'll get an enhanced sequences one
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of the last to be acquired at the post contrast sequence.
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And so if patients are struggling in the scanner,
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sometimes you'll see more marked part of facts later in later
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Acquisitions, but again, you can see here that there's solve epicardial
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algae as well as enhancement of that over one
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pericardium. So again, this is another key of the myopericartidus.
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After covid-19 vaccination and I'll
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just draw your attention on the T1 mapping slice. You
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can see that there is also a small pericardial effusion mostly initially
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as well as
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and just I see that there are the question how
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soon does myocarditis appear after vaccination? That's
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a really great question. We'll cover that as well in the
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slide at the end. But this is a great question typically
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within a couple days some patients. We have
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a fairly large case series which we published
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on and continue to follow and most of the patients in
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our case series presented within three days some patient
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even later on the same day after vaccination, but typically
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within a week and that's consistent with other
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reports as well.
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This patient I'm going to show you the follow-up Imaging so gives this
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patient was accumulian. Well was an inpatient
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we recommended follow-up to see what happens. And so
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the dates here are just gonna anonymize them.
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They're not reflective of the actual Imaging. Of course, everything is anonymized. What
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I'm going to do is try to show you the corresponding images top
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and bottom. So we have our Baseline Imaging
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on the top and what I'll do is I'll show you our LGE and
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we can show you that.
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edema Imaging on the
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So again top row here is our Baseline Imaging and I'm going to
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show you the follow-up which was on about three months later on the
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bottom. So you can see kind of the typical trajectory in typical
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change that we would expect.
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So let's start with our T2. So again bottom right that I'm
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highlighting now is our edema Imaging and there is
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no longer a demon. So three months later the patient symptoms
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had resolved proponent had a normalized and there
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was no longer any detectable edema,
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either on black blood T2 with imaging event showing you here or on
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our teaching map. The values were normal and on
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our Lake I'm enhance damage. You can see that there is some residual
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algae. So I'm just gonna get a little bit larger, so
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please
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Sure to see and then pointing to
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hear there's some residual sub epicardial algae at
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that infer wall. And this is important at our
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Center. We typically do follow patients back who have acute macroditis
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in three to six months.
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What you're looking for is to see that the edema has resolved
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which is happens in the vast majority of patients typically
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within weeks and you want to look for
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residual algae. So the extent of LG has decreased essentially
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compared to Baseline. So all of this LG that
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we saw on the initial a study in
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acute and phase most of that at
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the lateral wall has resolved in no longer detecting but
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there is some residual stuff at the Cardinal LG an
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inferol and when you have algae without edema in this
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clinical setting that tells us that there's like the fibrosis there
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and that's important, you know from other causes of
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my heart that is large key series as well as cardiopathies that
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fibrosis and algae specifically indicating
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fibrosis is a marker or can pay
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plays patients at risk of arrhythmia. So important to just
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I see a couple other questions that popped
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up. Do you encounter mismatch between
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Teaching images and teaching mapping for example hyperintensity on
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trm or teaching Imaging
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and normal values on teaching math. And how do
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you approach that? I think this is a great question. Certainly we
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have seen cases where there can be mismatched it
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our Center as they said our routine
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protocol is only a single midventricular short access teaching
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map. And so one of the reasons that you might not detect an
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elevated teaching mapping value in that case is because
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you haven't gone through the area of normality or the area of
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the worst normality. So just to keep in mind, you
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know, if you haven't imaged with a particular sequence at the
8:18
specific area Melody, you might miss it.
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and
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the other thing I think is important to keep in mind is that if you're using
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the revive like Louise criteria, which most Centers do
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you only need to meet one of them. So if you
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have a clear focal of
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a cardinal hyperintensity on your black blood take the weighted
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Imaging whatever it is at your scanner based on
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the vendor you have that would meet criteria for your teaching-based
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criteria wouldn't need to have an abnormality on
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your teaching map. I have to say generally of
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course they do go together. So hopefully that answers your
8:53
question that if you've met your teacher-based criteria on
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one or either sequence that's sufficient and
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call myocardial edema.
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Okay, are there risk factors to get myocarditis at
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post-covid-19 vaccination where we
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will talk about a little bit about the demographics and the slides. I'm just going to leave that
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one. I'll try to just answer any case specific questions now,
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we'll leave the more general questions to the end
9:18
and any cases which
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had edema on T2. But no LG that's a
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great question. You can see that very
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we have very few cases at least in our case
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series if you have very mild edema.
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That has not resulted in sufficient or extensive
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enough damage to you know
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have such a large area of myocardial injury
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that it's holding on to contrast that you can see visually it is certainly
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possible. So that is when possibility not just
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close vaccination but in any cause of myocarditis that's
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quite mild you could have edema particularly if edema
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is intracellular and don't yet have cellular
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destruction or extracellular edema.
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It is possible.