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GlobalCast MD, along with Cincinnati Children's Hospital, sharing knowledge to improve child

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health around the globe.

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Hello pediatric surgery family.

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I'm Cecilia Gigena, a research fellow from Cincinnati Children's Hospital Medical Center.

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Our 11th annual update course in pediatric surgery was held this past August.

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In this video, we are going to talk about management of recurrent pancreatitis.

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And for that, we have Dr. Juan Gurria, a pediatric surgeon from Cincinnati Children's Hospital.

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So first, we started with a case.

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Seven-year-old with acute recurrent pancreatitis, abdominal pain, has a diagnosis of ARP, referred

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to you with an ERCP showing a stricture in the head of the pancreas and a dilated duct

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distal, we've seen this multiple times.

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Has had seven ERCPs and a stent in the past.

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So this is an ERCP.

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So we have a clear stricture in the area of the head of the pancreas and a dilated duct

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distal and you see clearly the branches.

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So what is your plan?

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MRCP to evaluate for chronic changes, repeat ERCP balloon dilation and stent placement,

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MRCP and obtain genetics, or admin implant for FRIE procedure.

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The FRIE procedure is a partial head pancreatectomy with duodenal preservation and a pancreatic

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jejunostomy.

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And it's interesting to see this very divided.

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So the main is repeat ERCP.

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So keep doing it.

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We're seven ERCPs in.

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The question is, when do you stop, right?

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Every time you get an ERCP, you have a risk of getting post ERCP pancreatitis.

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It's slow, right?

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But still a risk and you lose eyelid cells with every attack.

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So we're losing cells down the road.

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And as he said, genetic is key.

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So it is really important to get a genetic panel.

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PRS1 is the most common one, which is a trypsinogen activator.

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It activates trypsin inside the pancreas.

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There's CTRC, CFTR, you know, CPA1.

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There's a whole bunch of mutations that we now know.

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Our gene panel in Cincinnati runs 10 different genetic markers.

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So that's how we're changing the approach to pediatric pancreatitis, chronic pancreatitis

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treatment because of the genetic factors.

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Awesome.

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So if a patient has more than one episode of acute pancreatitis or a first really bad

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episode of it, we should perform an MRCP and a genetic panel to rule out genetic anomalies.

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Now, you have that patient that has the mutation that they're there, trypsin activated.

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How do you mediate that?

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Is there medication or is there another path that you can do to?

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Wonderful question.

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No, no, there's no, unfortunately, we don't have that just yet.

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That's why I still have a job.

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But I hope some one day we have, you know, I would do a PUSTO on this kid.

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What's the downside of that?

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So excellent question.

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If there's a generic mutation, say there's a PRS1 mutation, right?

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For a PUSTO, you have to like get the top of the top half of the pancreas out to open

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the duct, right?

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You throw some eyelid cells to the trash.

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This patient most likely is going to keep getting pancreatitis despite you draining

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the duct.

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The parenchyma is going to keep getting attacked by the mutation.

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So you're temporizing the attack by draining the duct, but you're not fixing the problem.

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Great.

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So genetics are very important before any resection procedure to avoid losing pancreatic

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cells in pathologies that will not benefit from a resection and drainage, but instead

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from an eyelid cells transplant.

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So I know the scenario pretty much points towards, okay, maybe recurrent or chronic

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pancreatitis, but after how many do you feel like, okay, this is what we're dealing with?

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Two, ERCPs, three, when do you start thinking considering that this might be a problem?

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That's a great question.

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We don't have a set number of ERCPs.

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So there's no set limit on that, the sooner the referral, the better for an evaluation.

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We don't offer to take out the pancreas unless you've maximized medical and endoscopic management.

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If there's no other options and your endoscopic guy tells you, you know what, there's nothing

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for me to balloon dilate, open drain or anything.

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There's been a stent, even with the stent, the patient keeps getting pancreatitis.

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There's no reason to keep going with ERCPs.

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So do endoscopic treatment at first, but if it fails, transfer to a specialized center

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that does TPIAT or total pancreatectomy with eyelid auto transplantation.

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Now what about imaging for this patient?

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So we use endoscopic ultrasound and ultrasound CT scan is imaging of choice once they come.

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MRCP is the best non-invasive study for pancreas by far with different T2 sequences.

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They're great and ERCP of course is more therapeutic than diagnostic.

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Awesome.

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Start with ultrasound, then CT and for better see the pancreatic anatomy, MRCP with T2 sequences.

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Now what about fluid collections?

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Once the wall is mature in four to six weeks, if there's symptoms, drain it.

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If there's no symptoms, don't drain it.

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If the patient is not having gastric alveolar obstruction or pain, there's no need to drain

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this.

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They will self-resolve and of course there's no need for antibiotics.

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Awesome.

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Time to summarize.

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Recurrent pancreatitis is a rare pathology that can lead to chronic pancreatitis and it

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is associated with genetic mutations.

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If genetic mutations are confirmed, we should avoid partially resecting pancreatic tissue

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as in a fry procedure to avoid losing pancreatic cells.

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The treatment should start with endoscopic approach, keeping in mind that if it fails,

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a TPIAT should be considered sooner rather than later.

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For liquid collection, surgical treatment should be only done if the patient is symptomatic.

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I hope you enjoyed the video and thank you for watching.

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Follow our social media channels and download the Stay Current MD app for tons of content

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in pediatric surgery.

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Global Cast MD along with Cincinnati Children's Hospital, sharing knowledge to improve child

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health around the globe.

