Interactive Transcript
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Hello and welcome to Noon Conference, hosted by modality
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Noon Conference connects the global radiology community
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through free live educational webinars that are accessible
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for all and is an opportunity
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to learn alongside top radiologists from around the world.
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Today we are honored to welcome Dr.
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Dane for a lecture entitled Photon Counting,
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CT Physics and Applications.
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Dr. Dane completed her radiology residency
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and body MRI fellowship at NYU Langone Health
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where she also served as chief resident.
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She's now an abdominal radiologist at NYU
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where she also serves as director of CT
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and the director of Quality and Safety
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for Maine Campus Outpatient Imaging.
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At the end of the lecture, please join her in a Q
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and A session where she will address questions you may
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have on today's topic.
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Please remember to use that q
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and a feature to submit your questions so we can get to
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as many as we can before our time is up.
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With that, we're ready to begin today's lecture. Dr.
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Dane, please take it from here.
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Alright, thank you for having me.
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So I'm excited to talk to you about photon counting ct.
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So this is the general breakdown for
1:08
what we'll talk about today.
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We'll start by talking about the detector basics.
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So that really covers the physics
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and really what's important,
1:14
what plays out into the clinical applications.
1:16
So I am a clinical abdominal radiologist, so a lot of
1:19
what we talk about will be clinical work today
1:21
and then at the end we'll conclude
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with some PACS considerations.
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So first, the detector basics.
1:28
So here's a schematic
1:29
of a conventional energy integrating CT detector.
1:32
So most of the scanners on the market
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that are not photon counting ct, you can see
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that it has a scintillator.
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So when the x-ray photon comes in, it gets converted
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to light in that scintillator,
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then the light gets converted to current.
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So it's a two step conversion using light,
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there are a number of consequences of using light
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and one is that like a flashlight light can travel
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in any direction.
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So you need these opaque SEPTA in order to avoid crosstalk
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between the adjacent detector elements, which in doing so,
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does limit the spatial resolution
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and dose efficiency of conventional ct.
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And here's why. You can see with decreasing pixel size,
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you have more and more opaque SEPTA
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and more and more dead space.
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Eventually it becomes too dose inefficient
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to get smaller pixels
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and that limit for most
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of the conventional scanners in the market is about
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0.6 millimeters.
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So there are other consequences of using light
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and one is that light is really fast.
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So even the fastest detectors in the market cannot separate
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the signal from different light pulses.
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So instead it'll create a cumulative measure of all
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of the energy in that detector.
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But in essence that down weights, low energy photons,
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unfortunately the low energy photons are the ones we wanna
2:42
see more of Those are closer to the K edge of iodine,
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which means that iodine looks brighter on those.
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The low energy photons are the ones that contribute most
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to iodine image contrast.
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So to give you an analogy, if I think
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of conventional detectors, I think of them
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as a bag of change.
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It has some combination of coins, pennies,
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nickels, dimes or quarters.
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We have no idea what combination is in the bag for ct.
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We hope there's a lot of low energy photons
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because it increases iodine contrast to noise.
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But we don't know. But we know this bag has 77 cents.
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Now let's move on and we'll talk about this is the
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clinically available photon counting detector.
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So now you see it has a semiconductor
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instead of that scintillator.
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So when the x-ray photon comes in,
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it now gets directly converted
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to current in a single step conversion.
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So without the scintillator there's no light.
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Without the light, you don't need the septa.
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Without the septa there's better dose
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efficiency and spatial resolution.
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So that we talked about less dead space.
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So in addition, something else exciting about this is
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that each x-ray will produce a
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charge proportional to its energy.
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So what does that mean? It means
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that we can measure the energy
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of every photon of the detector.
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So let's go back to our analogy for conventional detectors.
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We can think they're like a bag of change.
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There's some combination of change in the bag.
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You don't know if you have quarters or pennies,
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but you know that there's 77 cents in the bag.
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Whereas photon counting CT can tell you you have seven
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pennies, five nickels, two dimes and a quarter.
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So every coin is counted, every photon is counted.
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So in this example we can see that we have seven coins
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or that are pennies which account for 47% of the coins.
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Whereas if you were to look at their energy
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or their weight, 7 cents, seven out
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of 77 would be 9% of the total.
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So the same photons going into the photon counting detector,
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they have greater weight to those low energy photons.
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So there's greater iodine contrast to noise.
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In addition, every scan is a multier energy scan,
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it's detector based spectral imaging.
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Finally, you can electronically remove the photons whose
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energy is too low to have possibly penetrated
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the body as noise.
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Here's a schematic of another uh,
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photon gowning counting detector.
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This one uses silicon, which due to its uh,
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low atomic number, it has an edge on geometry
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and it has to be between three and six centimeters thick.
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In order to achieve a stopping power in the diagnostic x-ray
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range, it has eight energy bins, three of which are
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below 33 KEV to capture scatter,
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and then five of increasing energy
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and height in order to ensure a relatively consistent
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energy distribution.
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So something that I think is really exciting about photon
5:17
counting CT is the CT number accuracy and reliability.
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So I'll share with you two studies from the Wisconsin
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group where they were looking at.
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The first one was looking at patient size
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and with varying patient size, they found
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that the CT number was closer
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to ideal at foton counting than dual energy
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and single energy at various sizes with less variability.
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And looking at size and positioning, well first they found
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that size contributes more than positioning
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to CT number fluctuations
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and they found again, smaller changes in hounds field units
5:49
with greater accuracy with photon counting than
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with dual energy and conventional ct.
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So in general you're seeing increased CT number reliability.
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So here's a table from a nice review article
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that was published earlier this year in radiology
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where they were uh, this, this table summarizes the
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photon county detector scanners that are in development
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with all the vendors and you could see
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that many vendors are working on it.
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We're not gonna go through this whole table,
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but I do wanna just highlight a few things
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in this general area.
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So first you can see most of the vendors are using some sort
6:21
of cadmium telluride combination.
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There's one vendor that's working with silicon.
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Something else. If you look at the implants,
6:27
spatial resolution, nearly all
6:29
of them are less than 0.2 millimeters.
6:31
That's because of the absence of the opaque septa.
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And the last thing I wanted
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to highlight is the number of energy bins.
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So conventional dual energy CT dual is two, right?
6:41
But here most
6:42
of these vendors have more than two available VIN bins,
6:45
which brings up the potential
6:47
for multier energy imaging in the future.
6:50
Okay, so now let's talk about the clinical applications.
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We'll discuss them in order of these clinical, UH,
6:55
or physics related scanner related,
6:57
uh, benefits that we talked about.
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So there's higher spatial resolution
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because you don't have those opaque septa.
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There's higher iodine contrast to noise
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because there's greater weight given to low energy photons.
7:07
Also noise removal at the detector
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we just discussed the noise reduction
7:11
and then spectral imaging is always available.
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So let's start with spatial resolution.
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So we'll do this more or less head to toe.
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So we'll start in the temporal bones, which is a huge area
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of opportunity for this improved spatial resolution.
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Here's two images in the temporal bone in the same patient.
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The left is photon counting. The right is conventional ct.
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This patient has a cholesteatoma, which I've annotated.
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But looking at these images, you can see there's really
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better image quality
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and less visible noise on the photon counting than the
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conventional ct.
7:40
This study reported superior spatial resolution
7:43
and better critical structure visibility
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with significant radiation exposure reduction at photon
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counting compared with conventional ct.
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Another temporal bone example,
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these are two images in the same patient.
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The left is photon counting the right's conventional ct.
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You can see this cochlear implant
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to better advantage on the photon counting than you can on
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the conventional CT with less artifact.
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And as expected, it's been reported
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that photon counting CT does have a more precise
8:07
postoperative cochlear implant.
8:09
Uh, electro contact determination
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with the reported substantial advantages compared
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with conventional ct.
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So a real practice changing area
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of the spatial resolution
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and iodine contrast to noise at photon counting CT are the
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detection of CSF venous fistulas.
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So here's a study where patients had an MRI with some degree
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of probability of CSF venous fistula
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but it wasn't detected on the MRI
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and then they underwent a photon counting CT myelogram.
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And in those patients you can see there's a drastic number
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of these patients that had definitive CSF venous fistulas
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identified on the photon counting CT myelogram
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and it increased with degree of suspicion on MRI.
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So this really is a practice changing area, excuse me,
8:51
of uh, photon counting ct.
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There's some centers that are really uh,
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really doing a tremendous job with this for their patients.
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So now moving down to the lungs,
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interstitial lung disease is another disease process
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that really benefits from the spatial resolution.
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So here we have two high resolution images
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from the lungs in the same patient.
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The left is photon counting CT high pitch pitch
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of 3.2 millimeter slice thickness,
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whereas the image on the right it's 0.6 millimeters.
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So the highest we can get on that conventional CT scanner,
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which it happens to be a very excellent scanner.
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If you look at these images, you can see improved visibility
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of the architecture of this honeycombing, uh,
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or these cysts at least uh,
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on the photon counting than you can in the conventional ct.
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You can see the architecture more clearly
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and as expected, it's been reported in the literature
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that ultra high resolution photon counting CT does have a
9:38
more precise depiction of interstitial lung disease.
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CT features with significant radiation exposure reduction
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compared with conventional CT In terms of detect detection
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of nodules and airways.
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Uh, this group did a study looking at the barely detectable
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nodule and barely detectable airway for both photon counting
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and conventional ct.
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And as expected you can see statistically significant uh,
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smaller nodules
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and airways are detected at photon counting ct.
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And I realized this isn't a micro nodule,
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I just thought it would be a little bit dry
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to put a micro nodule on a slide.
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So moving on to the abdomen, these are two axial images
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through the kidney and the same patient both on
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photon counting ct.
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These are from the same exam and localized to the same slice
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and the image on your left is four millimeter slice thick
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and you can see that there's a smudge
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of a non obstructing stone which would be very easy
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to overlook and you really wouldn't be so confident
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that's there compared with other areas of image noise.
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But if you look at the very thinner,
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the very thin slice 0.2 millimeter,
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you can clearly see the stone.
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You're confident it's there. Uh, really no debate here.
10:42
So as expected, it's been reported that there's greater odds
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of detecting stones at photon counting compared
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with thin section conventional ct
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and there's significantly higher sensitivity
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for renal stones at the thin section 0.4 millimeter compared
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with one millimeter, especially the
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detection of small stones.
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So really important for people with stone disease,
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we can give a more accurate
11:00
assessment of their stone burden.
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Now in terms of pancreatic cyst,
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there's also improved visibility of pancreatic cysts,
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which I think is due to a combination
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of the improved implant spatial resolution
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and also the iodine contrast to noise.
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So here's two contrast enhanced images
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through the abdomen in the same patient.
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The left is photon counting. The right is conventional ct.
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Looking at the photon counting ct,
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you see there's a six millimeter pancreatic tail cyst.
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You see it, you know it's cyst.
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It's frankly not that interesting
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and maybe you wish you didn't see it,
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but if you look at the conventional CT on your right,
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this is the optimally selected image from that scan
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and you really frankly can't see it as well.
11:36
So this ability to see these cysts more clearly on on photon
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counting has been reported in the literature
11:40
that there's greater pancreatic cyst visibility,
11:42
particularly for CT angiography which also leverages
11:45
that iodine contrast to noise improvement in terms of bones.
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Here's two axial images through the ankle.
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These are in the same patient at the same window with level
11:55
and kernel, but you can see the improved trabecular
11:58
visibility on photon counting and conventional ct.
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And this is supported in the literature.
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So if I were to think of an area where spatial
12:06
and temporal resolution are really married,
12:08
it's coronary CT angiography
12:10
and as expected photon counting ct coronary CT angiography
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has been reported to have improved objective
12:16
and subjective image quality compared with conventional ct.
12:19
But we need better than just excellent image quality.
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We need diagnostic performance.
12:23
So a study of one type
12:24
of photon counting CT reported 100% sensitivity
12:27
and 90% specificity compared with conventional ct.
12:31
So it was better, it was 75 and 50%
12:33
and this was using invasive coronary angiography
12:35
as the reference standard in a very high risk population.
12:38
Another study looking at a high risk population of patients
12:41
with severe coronary calcium and prior stents.
12:44
So really patients that are very difficult
12:45
to do an excellent coronary CT angiography on.
12:49
They reported that ultra high resolution photon counting CT
12:52
had 95% accuracy per segment in this population.
12:57
There's also another study
12:58
that reported strong inter reader agreement at photon
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counting where it was moderate at conventional ct.
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So not only only only are we accurate
13:04
but we're also reliable in our interpretation.
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Finally, another study looked at instant stenosis assessment
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and compared ultra high resolution photon counting CT
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with invasive coronary angiography
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and found 100% sensitivity specificity and accuracy.
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So this is huge. This is practice changing
13:24
because there's some centers
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that are foregoing invasive coronary angiography
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and instead undergoing ultra high resolution
13:30
photon counting ct.
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Uh, so it's avoiding an invasive procedure.
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So keeping all of this in mind, there's a group
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that was looking at patients
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who underwent ultra high resolution photon counting, uh,
13:41
coronary CT angiography patients who had stable chest pain,
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they assumed 15,000 patients
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and reported a 19% reduction in functional follow-up
13:49
and a 6% reduction in invasive coronary angiography.
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And assuming a 10 year life expectancy per patient,
13:56
this resulted in SI $790 per patient saved,
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which over the 10 year period was about $11 million.
14:03
So overall the ability
14:04
to reduce follow up saves uh, quite a bit of money.
14:09
Okay, so next higher iodine contrasted noise.
14:12
So this again was
14:13
because there's greater weight
14:14
to the low energy photons at the detector
14:17
and noise removal at the detector.
14:19
So whatever iodine is there you can see better.
14:21
So if you can see better, you can give less.
14:24
You also have improved visibility
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of small vessels in small people
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and there's improved lesion conspicuity particularly in
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low contrast visibility areas.
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So I'll show you examples of each of these now.
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So here's two CT angiograms in the same patient.
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The left is photon counting. The right is conventional ct.
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You can see that we gave 70 ccs
14:43
of intravenous contrast on photon counting ct.
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So 30 ccs less than the conventional CT
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and the iodine conspicuity is quite similar
14:50
between the two studies.
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Here's an example of a 50 cc uh, TAVR study.
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It was a CTA chest, abdomen, pelvis and coronaries.
14:59
We only gave 50 ccs um, for CT angiography of the aorta.
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There's a study that reported that a 25% intravenous
15:06
contrast reduction at photon counting CT had non-inferior
15:08
image quality compared with conventional ct.
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So this phenomenon of reduced contrast has been pretty
15:14
well documented so far.
15:15
So for CT pulmonary angiography,
15:17
one study reported no reduction in image quality using only
15:20
35 ccs of intravenous contrast.
15:22
Another study, again,
15:23
no reduction in image quality at coronary CT angiography
15:26
using a 40% intravenous contrast reduction.
15:31
So all of these examples are CTAs.
15:33
So you're leveraging more dense contrast,
15:34
higher concentration contrast,
15:36
maybe leveraging low KEV reconstructions.
15:38
So what about venous imaging? Right?
15:40
This is the workhorse of what we do in abdominal imaging.
15:43
So here we have two axial portal venous
15:45
phase images in the same patient.
15:46
The left is photon counting ct,
15:47
the right is a conventional ct.
15:49
In the conventional CT we gave 95 ccs
15:52
of intravenous contrast, which is based on weight-based
15:54
dosing of 1.5 milliliters, uh, kilograms per milliliter.
15:57
But if milliliters per kilogram, sorry,
15:59
but if you look at the photon counting ct,
16:02
I'm showing you a 70 KV image.
16:04
So this has a similar appearance to
16:05
that conventional one 20 KVP scan.
16:08
So you're not leveraging low KEV reconstructions here.
16:11
Here we subtracted nearly 30 ccs off of that
16:14
and the iodine conspicuity is quite similar.
16:17
One other thing to highlight is the radiation exposure is
16:19
half and the image quality is still adequate.
16:22
So we did a study where we looked at these 70 KEV
16:25
reconstructions at photon counting CT
16:27
and showed that with a 20 uh cc reduction off
16:30
of weight-based dosing photon counting CT still had similar
16:33
attenuation and image quality as conventional ct.
16:36
Another group reported 27% intravenous contrast reduction
16:39
had maintained image quality compared
16:41
with second generation dual source dual energy ct.
16:44
And a third group looked at thorac abdominal CT
16:46
and again reported a 17% contrast reduction had superior
16:49
image quality than conventional ct.
16:53
So now small people and small vessels.
16:55
Uh, here's a patient who had a nine cc angiogram.
16:59
So really putting that into perspective,
17:00
it's about a test bolus
17:01
and you can, you can see it's an excellent study.
17:04
There was a study that was done
17:05
of 113 children all younger than three years old,
17:08
median 66 days
17:09
and they reported better image quality at the same
17:11
dose, which is quite low.
17:12
And they directly measured signal to noise
17:14
and contrast to noise and said it was statistically higher
17:16
than a dual source dual energy ct.
17:19
Here's a nice clinical example of
17:21
where this iodine contrast to noise is important.
17:24
So here's a six month old who had a prenatal lesion that was
17:26
concerning for sequestration.
17:28
This was a non sedated scan.
17:29
So really leveraging that high pitch imaging.
17:32
You can see on this sagittal image this is the celiac
17:34
artery, this is the left gastric artery
17:36
and you can see it's supplying this extra low bar upper
17:38
abdominal broncho pulmonary sequestration.
17:40
Bonus is its normal coronary origins,
17:43
again this is non sedated patient only received nine ccs
17:46
of intravenous contrast and the CTDI is 1.2.
17:49
So low radiation, very little uh, contrasting.
17:53
We can make an excellent diagnosis really due to
17:55
that improved iodine contrast to noise.
17:59
Another area that benefits from this is lower
18:01
extremity CT angiography.
18:03
So here's two axial images from below the knee
18:05
and these are the same patient one month apart.
18:09
You can see on the photon counting CT we gave 30 ccs less
18:12
contrast but there's improved visibility
18:14
of these small structures
18:15
and again, bonus lower radiation exposure.
18:18
There was a nice study outta the Mayo group
18:19
where they did same day photon counting CTA
18:22
and conventional CTA
18:23
and even with greater than 50% intravenous contrast
18:26
reduction at photon counting ct.
18:28
They still reported
18:29
that more fibular perforator arteries were identified
18:31
with improved arterial sharpness at photon counting compared
18:34
with conventional ct.
18:37
In terms of diagnostic performance,
18:38
this group was looking at patients
18:40
with peripheral arterial disease
18:41
and they reported 91% sensitivity, 95% specificity
18:45
and 93% accuracy for the detection
18:48
and diagnosis of peripheral arterial disease compared
18:51
with digital subtraction an geography.
18:52
So again, we're particularly accurate in our diagnoses.
18:58
So now moving on to the last category in this section
19:01
lesion conspicuity.
19:02
So I think this is most evident in the low contrast
19:05
visibility areas such as the liver
19:07
and the pancreas, which is what I'll show you now.
19:09
So here we have two axial portal venous phase
19:11
images in the same patient.
19:12
The left is photon counting ct,
19:14
the right is conventional ct.
19:16
I'm showing you a 70 K EV image at photon counting ct.
19:18
So not leveraging low K EV reconstructions
19:21
but I think we'd all agree we could see this metastasis more
19:23
clearly at photon counting than we can a conventional ct.
19:27
So it's not quite fair. These are abdomen window,
19:29
these are the same uh, window width and level.
19:32
So I'll put this into liver window
19:34
and now you can still see on this locate UV
19:36
image not even on liver window.
19:38
You can see still improved visibility
19:40
of this metastasis at photon counting.
19:41
Then conventional CT as expected, it's been reported
19:46
that at photon counting CT there's improved visibility
19:48
of these hypovascular liver metastases
19:50
and improved contrasted noise compared with conventional ct.
19:53
This is for low K EV reconstructions but also 70 DK ev.
19:57
So you don't have to use the locate EV
19:59
reconstructions to get that benefit.
20:01
So something that I think is challenging
20:04
with cancer studies is if you're comparing an old
20:07
to a new study, you never know if anything is new.
20:10
But something that I love about this study which is from the
20:12
Duke group which was published in radiology is they used
20:15
anthropomorphic phantoms and had 183 generated lesions
20:19
and then they scanned it with both photon counting
20:20
and conventional ct.
20:22
So now these are exactly the same lesions in both
20:25
of the scans they looked at the 70 KEV reconstruction
20:28
so you don't have to leverage low KEV
20:30
and they reported higher sensitivity with photon counting CT
20:34
and at low doses they had increased
20:36
sensitivity for small lesions.
20:37
So you really do see lesions better at photon counting ct,
20:40
which I think is due to that improved iodine contrast
20:42
to noise and also the in plain spatial resolution.
20:47
So the other low contrast visibility area
20:49
that I think is valuable is the pancreas.
20:52
So here's two axial pancreatic parenchymal phase
20:54
images in the same patient.
20:55
The left is photon counting. The right is conventional ct.
20:58
Looking at the conventional ct,
21:00
you can see there's an ill-defined uncinate mass
21:02
and I think the borders of it are difficult to discern.
21:05
If you look at the photon counting ct, again 70 KEV,
21:08
we're not leveraging low KEV reconstructions.
21:10
You can see the tumor more clearly than you
21:12
count in conventional ct.
21:14
We do have the ability to use low KEV reconstructions.
21:17
I did tell you at the very beginning
21:18
that spectral imaging is always available.
21:20
So here's a low KEV
21:21
where you can see a drastic improvement in the borders
21:23
of this tumor at photon counting compared
21:25
with conventional ct.
21:28
As expected there's improved pancreatic ductal adeno
21:30
carcinoma tumor conspicuity at photon counting compared
21:32
with conventional CT for low KV reconstructions
21:35
but again also at 70 KV.
21:39
So with the ability to see these tumors more clearly,
21:41
you'd imagine it would make us more reliable.
21:43
In our assessment we did a study
21:46
of four fellowship trained abdominal radiologists
21:48
and they had substantial interrater agreement
21:51
for celiac artery S-M-A-S-M-V
21:53
and common hepatic artery involvement.
21:55
Whereas three of these had moderate involvement at
21:57
conventional ct.
21:59
In terms of metastasis identification,
22:00
again we had substantial interrater agreement at photon
22:03
counting where it was moderate at conventional CT
22:05
and this is with about a 40% radiation exposure reduction.
22:11
Okay, so now let's move on to noise reduction.
22:14
So really noise reduction at the detector translates
22:17
to better image quality and lower radiation exposure.
22:20
So here's two axial portal venous
22:22
phase images in the same patient.
22:23
The left is spoke on counting. The right is conventional ct.
22:26
I think the image quality looks the same on these two
22:28
studies but you'll note that this is
22:29
with 50% radiation exposure reduction on photon counting ct.
22:34
This is well documented
22:35
for pretty much every exam type to date in the literature.
22:37
So I just picked a couple of highlights
22:39
in an oncologic cohort.
22:40
One study reported that a 32% size specific dose estimate
22:44
reduction at photon counting again had the same image
22:46
quality and noise as dual source dual energy ct.
22:50
Another group looking at TAVR studies which are pretty high
22:52
radiation in general reported statistically significant
22:55
reductions in radiation with better image quality at photon
22:57
counting compared with conventional CT
23:00
for CT pulmonary angiography.
23:02
This group reported nearly 50% reductions in radiation at
23:05
photon counting compared with conventional ct.
23:08
But a nice perk that they noted was
23:10
that spectral imaging was available in all patients in their
23:13
study at photon counting, whereas a conventional ct,
23:16
this was dual source, dual energy ct,
23:17
it was only available in 66% of the patients
23:20
because of the need for high pitch imaging in others.
23:24
Back to pediatrics.
23:25
So here was a 16 month old who had concern
23:28
for childhood interstitial lung disease.
23:29
Again another non sedated scan.
23:31
So you're leveraging high pitch imaging.
23:33
Here we only gave five ccs
23:34
of intravenous contrast CTDI less than one.
23:36
We see the lungs are normal.
23:38
So in terms of radiation, uh Marilyn Siegel's group,
23:42
they found statistically significant reductions in radiation
23:45
at photon counting compared with conventional ct
23:47
but no difference in image quality signal to noise,
23:49
lung attenuation or noise.
23:51
Clearly just documentation
23:53
of this noise reduction which benefits
23:55
our pediatric patients.
23:58
So now moving on. So uh, another group was looking at
24:01
low dose kidney stones.
24:03
So most institutions have some sort
24:04
of low dose kidney stone protocol
24:06
and even off of already low dose they showed 44%
24:10
radiation exposure reduction.
24:12
They've marry, uh, measured the signal
24:14
to noise ratio at various portions along the collecting
24:17
system such as in the kidneys at the level of the
24:19
so acid at the level of the operators
24:20
and showed higher signal
24:21
to noise at photon counting than conventional CT
24:24
and no difference in radiologist confidence.
24:26
So really with the noise reduction we can reduce radiation,
24:29
we get better image quality, better signal to noise,
24:31
better contrast to noise
24:32
and no change in our confidence for diagnoses.
24:36
So a group of patients that particularly
24:38
benefits from this noise reduction or obese patients.
24:41
Here we have two axial CT angiograms in the same patient.
24:44
The left is photon counting.
24:45
The right is conventional ct other than decreased size
24:48
of this pancreatic tail collection on the subsequent photon
24:52
counting ct, I think the image quality is quite similar
24:54
between these but again this is
24:55
with a 40% radiation exposure reduction on photon counting
24:58
CT in obese patients,
25:01
one study reported 25% CTDI reduction again had similar
25:04
to improved image quality at photon counting compared
25:07
with dual energy ct.
25:10
So something else that I like about photon counting CT is
25:14
that spectral information is available
25:15
for the entire scan field of view.
25:17
So here's two completely uncropped images
25:19
and on photon counting CT you can see this iodine
25:22
information available everywhere whereas in the same patient
25:24
the patient is slightly off ISO center,
25:26
you only have the spectral information in the
25:29
smaller B tiled field of use.
25:30
So you're missing quite a bit of this patient's anatomy.
25:34
So now to show you a clinical application
25:36
of this noise reduction, here's three thin images uh,
25:39
in the same patient all on photon counting ct.
25:42
The left two images are the same exam in the
25:44
right as a prior study.
25:45
So with the noise reduction we really can use sharper
25:48
kernels than we've been able to
25:50
for clinical purposes At conventional CT
25:54
here these are localized to the same exam.
25:55
You can see this right lumbar artery
25:57
and actually you can see it's supplying this tiny type two
26:00
endoleak and it's literally blurred out
26:02
by the blooming on the softer kernel from the same exam.
26:06
These sharp kernels have been shown
26:07
to improve stent lumen visibility and sharpness
26:10
and compared with digital subtraction angiography,
26:12
radiologists have had greater confidence.
26:14
They reported improved vessel definition,
26:17
rep reduced calcium blooming and still acceptable noise.
26:23
So now let's talk about spectral imaging.
26:25
So spectral imaging is always available.
26:27
You have the gamut of what you're used to.
26:28
It's really detector based spectral imaging.
26:30
So here's a nice clinical example of how you can use it.
26:33
These are three images in a uh,
26:35
from the same exam localized to the same slice.
26:37
This patient had a colon cancer metastasis
26:39
in their liver ablated.
26:40
Looking at the 70 K UV image,
26:42
I can clearly see there's no recurrence here,
26:44
but I really love these iodine maps
26:46
because it's really like a black hole.
26:48
You can see there's no recurrence here,
26:50
there's no debate in the decision.
26:53
So in this section I'll talk about the virtual non-contrast
26:55
images and iodine.
26:56
We've already sort of talked about the
26:58
virtual monogenic images.
27:00
So the virtual non-contrast images do
27:02
have excellent image quality.
27:04
Here's two portal venous phase derived virtual non-contrast
27:07
images in the same patient.
27:08
The left is photon counting. The right is conventional ct.
27:11
I think we would agree that there's better image quality on
27:13
the photon counting CT with visibly less noise
27:15
and you could see improved uh, visibility
27:17
of these small structures such
27:19
as these gastro hepatic ligament vessels.
27:21
And this is with a quite substantial
27:22
radiation exposure reduction.
27:24
And we did document this in the literature
27:27
so we do need more than excellent image quality.
27:28
We need hounsfield unit reliability.
27:30
So here's a true non-contrast
27:32
and a virtual non-contrast in the same
27:34
patient and then I copied it.
27:35
They were quite similar frankly I copied
27:37
and pasted ROIs here so they'd be the same location and size
27:40
and you see that the household units are
27:41
effectively the same.
27:44
These are older studies
27:45
but one study reported
27:46
that the virtual non-contract household unit errors were
27:49
less than five household units in 76% of patients.
27:51
So really within calibration are
27:53
and less than 10 household units in 95% of patients.
27:56
In terms of diagnoses for hepatic steatosis,
27:58
there was an a UC of 0.97 for virtual compared
28:01
with true non-contrast.
28:02
So really it does quite well.
28:04
And if you were to use a liver
28:05
to spleen hansfield unit ratio less than 0.96,
28:08
it had 95% sensitivity
28:09
and nearly 100% specificity for the diagnosis.
28:14
So still, uh, speaking about steatosis here was a study
28:17
of over 500 patients, over 100 of whom had macd
28:20
and they compared the folks on counting fat fraction
28:23
with M-R-I-P-D-F-F.
28:25
Ultimately their conclusions were
28:27
that the CT fat fraction was both reliable
28:29
and precise compared with M-R-I-P-D-F-F
28:31
and that it was reliable across various radiation exposures
28:35
and tube voltages.
28:38
So we've had spec imaging for quite some time.
28:40
That's not really new
28:41
but something that is exciting is that we can leverage it
28:44
with high pitch imaging.
28:45
So here's images from a TAVR study.
28:48
So high pitch, you can see this is the contrast enhanced
28:50
image 70 KV
28:51
and you see an 83 hounds field unit left renal lesion
28:54
on a single phase study.
28:55
This would be in determinate, right?
28:57
We would say this is a hyperdense or a mass.
28:59
It would need some sort of follow up imaging.
29:01
I don't know if your institution recommends
29:02
ultrasound or MRI.
29:04
Mine usually recommends MRI but we can do better than that.
29:07
Here's the virtual non-contrast derived from the same image
29:10
where you can see it's 82 hence reel units.
29:12
So we know this is a hyperdense, the thought
29:14
of tumor never reaches the report,
29:16
neither does the recommendation for follow-up imaging.
29:19
The virtual non-contrast images when derived from both the
29:22
arterial and venous space have been shown to be accurate
29:24
and reliable for renal cyst characterization.
29:27
So another common scenario, this is a patient
29:29
who has lung cancer and adrenal nodule.
29:31
It's 31 hounds field units on this contrast enhanced image.
29:35
So as we know, lung cancer does have a propensity
29:37
to metastasize to the adrenals.
29:39
So on a single study, single phase study with no priors,
29:42
you're unfortunately left with could be an adenoma
29:45
or a metastasis and it would most definitely be recommended
29:47
for a follow-up study whether MRI
29:49
or pet, uh, whatever your institution does.
29:51
Mine usually does MRI.
29:54
But here's the virtual non-contrast from the same image
29:56
showing it to be 10 hansfield units.
29:58
So we know this is an adrenal adenoma, the thought
30:00
of metastasis never reaches the report, neither does
30:02
that recommendation for follow-up imaging.
30:07
Uh, here's a study that was looking at the difference in
30:09
virtual non-contrast attenuation
30:10
between adenomas and metastases.
30:12
And they showed statistically a significantly lower
30:15
attenuation in the adenomas and metastases
30:18
and they reported a 26 handhold unit threshold had 87%
30:21
sensitivity and 76% specificity for this differentiation.
30:27
So a big question is can the virtual non-contrast uh,
30:30
reconstruction replace a true non-contrast?
30:32
Well here's a single phase CTA
30:34
and a patient has an endograft and you can see
30:35
that there's a small hyperdense focus anterior
30:37
to the endograft which is not present on the arterial drive
30:41
virtual non-contrast.
30:42
So even though this is a single phase study,
30:43
I'm quite confident that this is an endoleak
30:46
and it has been reported
30:47
that there's comparable endoleak detection on image quality
30:49
comparing virtual versus true non-contrast images.
30:52
So something else that I wanna highlight is
30:54
that there's actually excellent iodine removal here on the
30:56
virtual non-contrast image even though it's from a dense
30:58
phase of contrast, which I think is something
31:00
that the dual energy CT systems have really
31:02
had difficulty with.
31:05
So keeping that in mind, something that we uh, experimented
31:07
with at RX institution was a graphic derived virtual
31:10
non-contrast image in our young patients to avoid radiation.
31:14
So here's an example of the urogram
31:15
and here's the graphic derived virtual non-contrast image
31:18
where you can see there's excellent iodine removal
31:20
and we could still see that bladder stone.
31:23
So we did study this before doing it of course,
31:25
and we found that at one 40 kv, which is
31:27
what we do these at the median collecting system
31:29
attenuation was 0.9.
31:31
So really close to zero.
31:32
And we had three fellowship trained abdominal radiologists.
31:35
82% of their scores were five outta five
31:37
for calculi detection.
31:40
So something else that's new is the ability
31:43
to leverage spectral imaging for coronary CT angiography.
31:46
So on your left is a true non-contrast
31:48
and the right is a virtual non-contract intended
31:51
for a calcium score from the coronary ct.
31:53
I think the calcium deposits look quite similar on these
31:56
images, but obviously we need more than that.
31:57
We need diagnostics.
31:58
So here's a study in radiology of 170 patients
32:01
where they reported no difference in a Augustine scores
32:03
and strong correlation between the true
32:05
and the virtual non-contrast.
32:06
So perhaps in the future maybe we'll see
32:09
that true non-contrast, uh, replaced
32:11
by the virtual non-contrast,
32:12
but I think uh, more studies will be performed.
32:15
Here's another example.
32:16
These are spectral images from coronary CTA.
32:18
This is the iodine map
32:19
and this is the virtual non-contrast image.
32:21
You can see there's no atrial linage clot
32:22
here quite confidently.
32:26
So moving on, this is something near and dear to my heart.
32:29
So iodine density. So why iodine density?
32:32
So iodine density, it's a parameter that's only attainable
32:35
for multier GCT
32:37
and it only reflects the iodine content within a voxel which
32:40
is from contrast.
32:41
Whereas hounds field units
32:42
or CT numbers, they vary based on intrinsic tissue
32:46
attenuation which will be incorporated
32:47
and they may vary with other exam related characteristics.
32:51
So we've been looking at iodine density as a marker
32:53
of con's disease activity.
32:54
So if you look at this image, you see the terminal ium,
32:56
it's thick walled, it's stratified, it looks bright, uh,
32:59
compared with the rest of the bowel.
33:00
So you already think this is active inflammation,
33:02
but if you like numbers we can draw do a mural region
33:05
of interest and you can see
33:06
that it's 3.6 milligram per milliliter.
33:09
What we did a study compared with endoscopic histopathology
33:11
where we found that 2.7 milligram per milliliter was a
33:14
threshold between active and no active inflammation
33:17
with 97% sensitivity and 100% specificity.
33:20
And we even found that we could differentiate
33:22
inflammation severity.
33:23
So an iodine density of 3.4 milligram per milliliter could
33:26
differentiate mild from moderate to severe inflammation,
33:28
again with excellent diagnostic performance.
33:31
So this patient's iodine density is 3.6, which is
33:34
above our 3.4 milligram per milliliter threshold.
33:36
So it correlates with moderate to severe active inflammation
33:39
and that's concordant with endoscopic
33:40
histopathology from two weeks prior.
33:44
Another group was looking at iodine concentration
33:46
as a marker of neoadjuvant therapy response
33:48
and here they drew free hand region
33:50
of interest measurements bound
33:51
around rectal tumors on the iodine map
33:53
and they had an A UCF 0.85.
33:55
So I think this is exciting for the possibility
33:57
of iodine concentration as a biomarker of disease processes.
34:02
So finally the last thing in spectral imaging
34:04
that I'm excited about for the future.
34:06
So this is an animal model
34:08
and the animal was injected with a, uh,
34:10
it was a dual injection with iodine
34:12
and then gadolinium at different time points,
34:15
but a single imaging acquisition.
34:17
They then imaged the animal once and generated iodine maps
34:20
and gadolinium maps.
34:22
The iodine was time to be for the hepatic artery
34:24
and you can nicely see the branches
34:25
of the hepatic artery here, whereas the gadolinium was time
34:28
to be for the portal veins
34:29
and you can nicely see these branches
34:30
of the portal of means.
34:32
So I think this is something that's exciting for the future,
34:34
the possibility of eliminating uh, imaging acquisitions
34:38
by using multiple contrast agent imaging.
34:41
So is it ready for prime time?
34:43
So here's a phantom study recently published in A JR
34:45
where they looked at uh, gadolinium based contrast
34:48
and they showed that there was appreciable hepatic
34:51
enhancement at 200 micromoles per kilogram,
34:53
which is much lower than previously seen
34:55
with conventional ct,
34:57
but no enhancement
34:58
of observed at the clinically approved 25 micromoles per
35:01
kilogram uh, concentration.
35:03
So not quite ready, uh, for real life yet.
35:05
So now let's talk about some PAX considerations.
35:09
So here's four images of different kvs,
35:11
the same window within level 4,400.
35:14
So I showed you a few examples
35:15
of why we like low KEV reconstructions.
35:17
They increase lesion conspicuity in low contrast visibility
35:21
areas, but they also are noisier
35:23
and everything gets brighter.
35:24
So if I were to look at this reconstruction at this window
35:27
within level, it really is isn't that appealing to my eye?
35:30
Whereas this reconstruction on your right is,
35:33
and you know, it brings up the concept
35:34
of default window width levels.
35:36
So you probably have fewer photon counting cts than
35:39
conventional cts in your practice.
35:41
And you know you have two choices.
35:43
Do you want to integrate your scanner
35:45
in with the rest of your scanners?
35:46
Use your default window within level level settings,
35:48
then maybe use something like 70 K EV
35:50
or go all in on low K EV reconstructions
35:53
and have optimized window width
35:55
and level settings for photon counting ct.
35:58
Most people in the country have selected this 70 KEV sort
36:01
of same window width and level approach,
36:03
but that's an institutional sort of decision.
36:06
One other concept when looking at low KEV reconstructions is
36:09
the concept of pseudo enhancement.
36:11
So everything gets brighter on low KEV reconstructions.
36:14
So here we have a 70 K ev.
36:16
So similar to that one 20 KVP scan.
36:18
We have a low KEV at 55 KEV, these are the same window width
36:21
and level and then a virtual non-contrast.
36:24
So looking at this renal lesion on the virtual non-contrast,
36:26
it's five hounds field units.
36:27
So I know it's a cyst.
36:28
I copied and pasted the ROI onto each of these images.
36:30
So they're the same place
36:31
and size on the 70 KEV, it's 18 household units.
36:35
So this 13 household unit change
36:36
I would never say is enhancement.
36:37
I would be perfectly happy saying this is a
36:39
cyst, simple cyst.
36:41
But if I look at this low KEV reconstruction,
36:43
you see there's a 19 household unit attenuation change.
36:46
So for people that are sticklers to
36:47
that 20 household unit attenuation change rule
36:49
for enhancement, this would make you bat twice for sure.
36:52
So there definitely would need to be a larger threshold
36:54
for low KEV reconstructions.
36:57
So here's the axial single shot fast pin echo
36:59
and the post con T one post contrast subtraction image
37:01
showing that this is clearly just cyst the 70 KEV
37:03
and the virtual non-contrast didn't lie.
37:06
So there was a study looking at this concept
37:08
of pseudo enhancement in renal cyst
37:10
and they actually showed no pseudo enhancement for CIS
37:13
between 70 and 190 KEV,
37:15
but increasing degrees of pseudo enhancement
37:17
with decreasing KEV.
37:19
So really something to keep in mind when routinely viewing
37:22
low KEV reconstructions.
37:25
Finally, something that's really important is the concept
37:27
of image overload and you really have
37:28
to be thoughtful in building your protocols.
37:31
So something exciting for me as a spectral enthusiast is
37:33
that most people are routinely viewing low KEV
37:36
reconstruction, such as, I mean, sorry, uh,
37:37
virtual mono energetic reconstruction such as stone here.
37:39
So this is a complete sub in sub out,
37:42
but um, you know, you also could add a virtual non-contrast
37:44
and an iodine map in my center.
37:46
P people really like them and if they're not there,
37:48
you know, that would, that would be a complaint.
37:50
So I'm thrilled with that. And we, we do
37:52
that on our conventional dual energy scanners too.
37:54
So that's really not a difference for us compared
37:55
with conventional dual energy ct.
37:58
But I mentioned in the very beginning that you can go down
38:00
to 0.2 millimeter slice thickness.
38:02
So if you're routinely reading off of three millimeters,
38:04
for example, and then you start sending 0.2 millimeters,
38:06
that's a huge change for your practice.
38:09
For us, we routinely send thin images to PAX for all
38:12
of our scans for a variety of reasons.
38:13
They're usually at 0.6 to 0.8 on all of our scanners.
38:16
So if I were to go from 0.6 to 0.4 for example,
38:18
that's really not that big a change,
38:20
but you have to keep in mind, you can go down to 0.2,
38:23
but if you want spectral reconstructions
38:25
with the clinically available model, you have
38:27
to use 0.4 millimeter.
38:29
So would you send 0.2 millimeter and 0.4 millimeter to pax?
38:32
Clearly the answer is no, you wouldn't.
38:34
You have to be thoughtful in your protocols.
38:36
Do you really need the 0.2?
38:38
If you do like temporal bone
38:39
or interstitial lung disease, then use it
38:41
in abdominal imaging.
38:42
We use 0.4 because, uh, you know,
38:44
i i I value spectral imaging.
38:47
So that's it for our talk on FO count counting ct.
38:49
We started by talking about the detector basics, really how
38:52
that difference in the detector, uh,
38:54
really brought out the clinical applications.
38:56
So we talked about the higher spatial resolution
38:58
because there's no opaque SEPTA particularly valuable
39:01
for looking at temporal bones and interstitial lung disease.
39:03
For example, the higher iodine contrast to noise is
39:07
because there's greater weight through the low energy
39:08
photons, also noise removal at the detector
39:10
so you can see your contrast better.
39:12
So that's helpful for reducing contrast,
39:14
seeing small vessels and lesion conspicuity.
39:18
The noise reduction at the detector translates
39:20
to improved image quality, uh,
39:22
with lower radiation exposure.
39:23
Also really helpful in obese patients.
39:25
And finally, spectral imaging is always available.
39:27
You have the gamut of what you're used to.
39:28
We talked a lot about virtual non-contrast
39:30
images and iodine.
39:32
And finally for pax, when you're building your protocol,
39:34
please be thoughtful about what you need.
39:36
There's lots of choices and you, uh,
39:38
don't wanna overwhelm your radiologists.
39:40
So that's it for photon counting ct,
39:42
thank you for your time and attention.
39:44
Thank you so much Dr. Dane. That was wonderful.
39:46
We are now going to open up the floor to questions.
39:50
At the moment there is nothing in that q
39:52
and A feature, so we'll pause for a couple seconds.
39:55
Sometimes it takes a bit for folks to ask.
39:59
If you've got questions, go ahead and place them in that q
40:02
and A feature in the zoom
40:05
and we'll try to get to as many as we can.
40:08
The first question is,
40:09
are there any applications for neuroimaging?
40:12
Yes, there's a number of applications for neuroimaging.
40:15
So we talked about uh, temporal bones, we talked about uh,
40:19
CSF venous fistulas.
40:20
Those are, you know, big impact applications.
40:23
Um, I think vascular imaging in general is a huge
40:25
application because
40:26
of the improved iodine contrast to noise.
40:28
Uh, so many groups are looking at that as well.
40:30
And then finally, um, if there's any vascular stents, um,
40:33
I think you can see those more crisp and sharp as well.
40:38
Um, okay, our next question,
40:45
uh, sorry it's scrolling.
40:48
Uh, is about ways to offload MRI volumes.
40:52
Do I have insights to specific use cases
40:53
where photon counting can offer similar diagnostic
40:55
information as MRI, such as liver fat quantification?
40:59
So, um, liver fat's a really good one
41:01
because there's data that shows that it's comparable.
41:03
So I think one of the things that's interesting is photon
41:05
counting CT is very new.
41:06
So you know, the clinical comparisons with conventional CT
41:09
and MRI are still coming out.
41:11
There's, you know, yeah there's specific disease entities
41:14
that have been reported in, you know, in terms of uh,
41:18
diagnostics compared with MRI, um, it's not
41:22
as widespread yet as we'd like.
41:23
Um, but you know, I, I think yeah,
41:25
liver fat is a really good one right now.
41:28
Also, I mean there's plenty of patients
41:29
that can't undergo MRI, um, like pancreatic cysts.
41:32
I think we can do a great job with CT as well.
41:36
Um, what are some pitfalls or weaknesses of photon counting?
41:40
I think um, I think when you get a new
41:45
uh, scanner, I think
41:46
whenever you get any new scanner, it's sort of like a plug
41:49
and play, not photon counting ct.
41:50
You can in general take your protocols,
41:52
you put them on the scanner, you know,
41:54
you look at the images and you know, you check them
41:56
and it's really not that much interaction,
41:58
but foton counting CT is completely different
42:00
than all of your other scanners.
42:01
So it really does require, um, a lot more work
42:04
to develop your protocols, uh,
42:06
because there's a lot more choices.
42:08
And I think some of those things are institution specific.
42:11
Like for example, I got
42:13
to the point I I I mentioned the
42:14
radiation exposure and image quality.
42:16
It's not like there's one size fits all.
42:18
There's, you know, some institutions may choose
42:21
to have better image quality, uh,
42:23
and the same radiation,
42:24
whereas others may choose some sort of combination.
42:27
Um, so I think the adjustment
42:28
to the new technology was definitely, um,
42:31
was definitely uh, something to adjust to.
42:35
How long does it take to reconstruct photon counting ct?
42:38
Um, so today it keeps up with our practice.
42:41
So we have um,
42:42
our photon counting CT is in a busy clinical uh, practice.
42:47
We scan it's open for about 10 hours.
42:49
We scan 55 patients in that time.
42:51
Many of those are chest, abdomen, and pelvis.
42:53
Um, and it keeps up with the images on pax so um, you know,
42:56
keeps up at the moment.
43:00
Um, how long have I been using Photon County ct?
43:02
We got ours in 2022.
43:04
We were uh, among the first in the country to get it.
43:07
What QIR setting
43:12
are you using in your institution?
43:15
Um, R docs like QIR one
43:18
but that limits how much we can optimize radiation.
43:20
Yeah, so we usually do um, we do QIR of three or two.
43:25
So in abdomen we're using QIR three
43:27
and chest three using QIR two.
43:29
So one of those
43:33
mm well it's scrolling.
43:37
I'm sorry, what abdomen kernel are you using?
43:40
We're using 60 KEV bbr 40.
43:43
We've tried increasing to 70 but it looks a bit uh, soft.
43:47
Um, we like br uh, 44 actually we recently did a uh,
43:52
consensus in abdominal, uh, A JR from the um, SAR
43:57
of photon counting ETC,
43:59
and uh, we actually came to consensus on that BBR 44.
44:01
For what it's worth, do I prefer certain exams on
44:05
the photon counting ct?
44:07
Um, well as an abdominal radiologist I wish all
44:09
of my abdominal imaging could be there,
44:11
but that's obviously not uh, how life works.
44:13
So, uh, in general, cardiac is really a winner.
44:16
So patients that have stents or calcium
44:19
or high BMI for cardiac would go there, TAVRs must go there.
44:23
Um, our pediatric patients, we really try to get them there.
44:26
Um, you know,
44:27
and then the other applications that we've shown, like if,
44:30
you know, our scanner is at a site
44:32
where we also have a single energy conventional CT
44:35
and you know, like if a temporal bone comes, we would try
44:37
to put it there and you
44:39
know, okay.
44:43
I think there are three photon
44:44
counting scanners available now.
44:45
What are the differences? Can all do spectral imaging?
44:47
So yeah, so all can do spectral imaging.
44:49
So uh, the top model, uh, you know,
44:53
has a bigger detector, it's dual source.
44:55
The second model it's uh, four centimeters smaller.
44:58
The detector is still dual source.
45:00
The third model is single source.
45:02
So, um, all can do spectral imaging.
45:04
I think the only difference would really be cardiac.
45:05
Um, 'cause with the dual source scanners you'll get
45:07
higher, uh, pitch imaging.
45:12
Uh, do I think the applications in liver fat quantification
45:15
steatosis evaluation are useful?
45:17
Given how common MRI
45:18
and ultrasound are for that purpose, are there instances
45:20
where the immediacy of CT is worth the radiation
45:22
dose compared to those modalities?
45:24
You know, so that's a good question.
45:26
Um, not everywhere does, um,
45:31
not everywhere does ultrasound for example, for,
45:34
you know, quantification.
45:35
Um, many places do mr but not every patient can tolerate mr.
45:40
Um, you know, MR takes a long time. Mr.
45:43
Elastography is not always available.
45:44
Some patients have, you know, pacemakers
45:46
or things that make it really difficult.
45:48
So I do think it's worthwhile to look at ct especially
45:51
because we can get such low doses radiation exposures.
45:56
Um,
45:59
I think you got 'em all.
46:00
Got 'em All the questions we finished.
46:04
Thank you so much for this lecture
46:05
and thank you so much for hanging out
46:06
and answering all those questions.
46:08
There's one more that just came in,
46:09
I don't know if it's okay.
46:12
Um, what was your method
46:13
for optimizing the window level on low energy?
46:16
That's a great question. So, um,
46:18
with our pacs there's an auto window, um, auto window,
46:22
auto window tool where you literally just draw a circle
46:26
around whatever you want and it'll optimize it for you.
46:28
So that's what I personally use in practice.
46:30
Um, there's another site that is using optimized window
46:34
with her levels for low KEV
46:35
and they just send it routinely from the scanner at
46:39
that low KEV.
46:40
Um, I think, you know, one of the challenges of that is,
46:43
so I'm an abdominal radiologist, the scan starts at,
46:46
you know, at the lung basis.
46:47
So the first thing I would do would change it
46:48
to lung windows so I could look at the lung and,
46:50
and then I'd have to go back to abdomen.
46:52
So, um, it may be helpful to have, uh, you know,
46:56
some presets a hot key for it if
46:58
that's what you choose to do.
47:00
Um, that's not the path that we've chosen.
47:01
Um, there is a center that's that, that has done that
47:03
and they actually published a paper this week, um,
47:06
in European Journal of Radiology
47:07
with suggested optimized defaults.
47:11
Could all that liver fat quantification be done on routine
47:14
liver surveillance ct?
47:15
Uh, yeah, theoretically it can.
47:17
Um, which pax my using visage.
47:24
All right. Shall we call it?
47:29
Thank you so much. Thank no for your
47:30
attention and for your questions.
47:31
Uh, I really appreciate the, you know,
47:33
the engagement and participation.
47:36
Yeah, for sure. And thank you so much for this lecture.
47:38
It's been a big request.
47:39
So appreciate you filling a huge
47:41
educational need for our audience.
47:43
Glad to, glad to be here. Thanks for having me. Awesome.
47:45
Yeah, and thank you so much for everyone else
47:47
for participating in today's conference
47:49
and all our previous new conferences.
47:51
Um, be sure to look out for that email later today
47:54
with a link to the replay so you can watch us again.
47:58
Please join us next week, Wednesday,
48:00
November 26th at 11:00 AM Eastern.
48:02
Dr. Csh McCury is going
48:04
to deliver a lecture entitled Anatomy
48:06
and Pathology of the Lateral and Posterior Skull Base.
48:09
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48:11
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48:14
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