Interactive Transcript
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In this section we're gonna go over how to display
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and read a pet study.
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In this section we'll discuss some points
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that have been also covered in other sections,
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but this section is meant
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to be more practical, less theoretical.
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So let's dive in. This is going to be the content.
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We are going to discuss basic information from
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the PET CT study.
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Uh, we're gonna see a report example, this is the one I use.
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We're gonna discuss basic components of the PET CT
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and specifically discuss the non attenuation corrected
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images and attenuation corrected images.
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We are going to go over a study together
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and I'm gonna, uh, show you my systematic approach
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and then we'll briefly mention the most common protocols.
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So where to start. This listed information
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is the most basic
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and should be available to you in different ways.
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Uh, each uh, institution works a little bit different,
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but you should be given indication
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what the tracer is that you've administered in case
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of an FDG pet.
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You also want to know the blood glucose level.
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If the patient is diabetic,
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was the patient on any medication such
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as insulin or metformin?
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Did the patient follow the instructions of fasting?
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Other things that are important to know are the site
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of injection because sometimes when there's a little bit of
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extravasation and infiltration of the tracer, this may lead
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to uptake in axillary lymph nodes
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as we commonly inject in the anti cubital fossa.
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And that would help you troubleshoot the interpretation
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of these lymph nodes.
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Also very important is the uptake phase can also be called
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delta phase uptake phase or delta time.
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And this is the time between the injection
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of the tracer and the imaging.
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Each tracer will require a different range of time,
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and it is important to mention that in your report
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and, uh, notice if this is,
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if the time is longer than expected.
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For each tracer in the section of imaging acquisition
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and quantification of activity, we mentioned
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that there are certain factors
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that may affect the SUV calculation
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and that's why this item is important
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as this is one of them.
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It would also good to have access
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to relevant clinical information such as prior history of
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surgeries or, uh, recent vaccination.
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I noticed this particular item in
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Orange because particularly
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after COVID-19 pandemic
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and the vaccination
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and booster, we saw an increase in number of cases
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that had, we saw reactive lymph nodes that made
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sometimes cases more challenging to interpret
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as differentiating malignancy from reactive lymph
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nodes was difficult.
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Other things that, uh, would be important to have is access
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to recent or remote imaging,
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particularly if those studies are from outside
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specific medications.
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Some physicians add the last menstrual cycle date
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because, um, this may
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help you interpret the variable activity in the endometrium
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and ovaries in female patients as well as, uh,
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other prior treatments.
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So here I'm showing you what we have, uh,
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at my institution, this Willy Fair,
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you know, center to center.
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But I'm showing you the example of
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how all these information is available to us.
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On top we have the patient date and date of birth
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and we have the indication,
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we have the code for the study
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and important information also
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for the study is the height and weight.
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Then we have, uh, category of data that is related
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to the injection, what the tracer was, the site
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of the injection, and the time as well as the dose
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in the prescreening data.
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We ask if the patient has been fasting, the glucose level,
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and uh, other relevant information specific to the patient.
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We have under the medical history.
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We have added, for instance, surgical history
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and patient can list their surgeries.
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Sometimes you will find that these are relevant,
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some are not, but it's always good to have that available
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if there's recent imaging.
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And, uh, we started adding in additional notes the
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history of vaccination.
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As I mentioned earlier, for a specific brain studies,
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we have additional questions for other type of studies
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that are non oncologic like cardiac pits.
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We also have more questions as well in orange and marking.
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The one that is more relevant for FDG,
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probably FDG is the one
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that you're gonna be reading the most.
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So always remember to make sure that the preparation
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of the patient is appropriate
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and that you have glucose levels that are within the range,
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uh, where you can inject the tracer. So before
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I read a pity, I try to find out the following questions.
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Number one is, what is the indication
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or what is the specific question to answer
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because I want to address this in my report,
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but particularly in my impression.
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Number two, is there a diagnosis already?
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And then this would be for staging
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or do we need to guide
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the clinician for tissue sampling?
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Number three is, do we know where the primary lesion was
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or the extent of disease on priors?
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And in this case, I actually more often than not go back
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to even the baseline PET
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or baseline imaging to understand where was the disease
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and how extensive and how it has changed over time.
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It becomes very relevant to understand the treatment
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timeline, particularly when certain therapies were started
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and if there has been an interval change.
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Also, it's important to know if this is a baseline
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or is this a new baseline after, uh, treatment.
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And also as a fourth uh, question,
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have there been any changes in other imaging or new symptoms
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or something that has triggered
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the acquisition of this PET ct?
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So for every PET C, you will
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commonly find three type of series.
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The first one will be the city,
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the second one will be the non attenuation corrected
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PET series.
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And then the third one will be the attenuation
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corrected PET series.
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Names may differ depending on vendors,
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but you should always be
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provided with these three series
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have listed the three most common protocols.
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And I add this in the technique section of the reports,
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obviously for billing purposes,
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but most importantly to make the clinician
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that is reading the report aware of what areas were included
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and what areas were not.
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So the most commonly used protocol is gonna be from the
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skull base to mid thigh.
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Then we can include the, from the vertex of the skull
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to mid thigh in cases of head and neck cancer.
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Or in cases
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where we know there's an abnormality somewhere in the skull,
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we want to make sure it's included.
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And the third one would be a whole body which extends
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from the vertex of the skull to the toes.