A #tweetorial about the outcomes of hepatic coma, how far we have come, and how wild things got along the way #livertwitter
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Up first: the lingo
Hepatic encephalopathy (HE) presents as a spectrum with subtle cognitive/motor deficits at one end (AKA "Covert HE") and coma at the other
HE/Coma can be caused by #cirrhosis (Type C, more common) and acute liver failure (Type A)
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What used to (1950s/60s) happen to patients with coma due to hepatic encephalopathy ("HE coma")?
1⃣Gabuzda said everyone died
2⃣Sherlock said it was 68% mortality, Stormont 63%
3⃣Prytz said it was 80% mortality at 6-months
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HE coma was hopeless
And then, 1952-54, the big bang moment
We discovered ammonia as a trigger
While ammonia was n̳e̳v̳e̳r̳ thought to be the whole story, it was directly linked to HE and was a modifiable target
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Ammonia comes from the gut.
You know what reduces ammonia?
Antibiotics!
Maybe by changing bacterial or gut metabolism, maybe by changing the bacteria themselves
In 1955, Silen showed that neomycin ⬇️⬇️ammonia levels.
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So do antibiotics help in hepatic coma?
Many tried
Sadly, Not. good. enough.
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We also learned that the liver efficiently clears ammonia from the blood but not so much in #cirrhosis
Check out the "Ammonium Tolerance Test"
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💡Can we treat HE by cleaning the blood with healthy liver?
Step One:
In 1958, Otto created "Eck fistulas" (connect the SMV-IVC) in dogs.
He then hooked another dog liver up to a circuit with the femoral artery and vein.
It cleared the ammonia.
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Step two:
In 1961, Eiseman showed you could run blood through a liver removed from a recently deceased person. "Ex vivo" perfusion
It cleared the ammonia
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Step 3: Use it to treat hepatic coma
In 1965, an upstart surgeon named Starzl sewed a liver to the groin of comatose kids
In 1966, Sen reported 'ex vivo' perfusion of human livers hooked up to people in coma from acute liver failure or #cirrhosis
It rarely worked
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💡Do we really need to take the donor liver out of the body??
In 1965, Burnell teamed up with Scribner to do “dialysis” by cross-circulating the blood of a woman in hepatic coma into a man dying of cancer.
She woke up! (though she later died from GI bleeding)
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Despite poor outcomes, people were excited
But it was just not feasible to:
1⃣find people willing to be human dialysis machines
2⃣find suitable donors for ex-vivo liver perfusion
Two alternatives were considered
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First, people like Charlie Trey tried exchange transfusions.
Basically, replacing the blood with donor blood products.
It was mainly tried for acute viral hepatitis or halothane hepatitis.
Seemed promising.
But controlled trials failed.
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Second, many thought it would be easier to use animal livers
In 1965, Eiseman hooked up a pig liver to 8 patients with #cirrhosis in coma.
All patients died within 8 days.
But many woke up, including one man who requested a cigarette while still in the OR
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The concept of cross-circulation - liver dialysis using a living being - again took hold
In 1968, Christian Barnard published twin papers in @TheLancet describing how to do it with a baboon and the outcome in one young woman with #cirrhosis
She left the hospital
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Which brings me to Hume's 1969 description:
He brought an awake baboon to the bedside, immobilized him in a cast, flushed his blood out and replaced it with human blood, and then hooked him up to a patient in hepatic coma who would awake to find a baboon in the room.
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By the mid 1970's, animal-man cross-circulation was on the out
1⃣It was HARD
2⃣often ineffective
3⃣...complicated
4⃣👇And Starzl started getting good at liver transplantation
⭐️HE is a biomarker of badness
⭐️People with HE died of sepsis, bleeding, not HE!
⭐️We learned to treat the badness
Bam! our patients started surviving
Game changers
1⃣Endoscopy/banding
2⃣Good antibiotics
3⃣ICU care
4⃣Lactulose!
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Proof of progress: Remember how basically everyone in HE coma due to #cirrhosis used to die in the hospital?
1⃣By the 1970's, 49% died
2⃣By the 2000's, 30% died by 1-year
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Liver support (eg MARS) have been trialed, rarely improving HE in #cirrhosis
They havent ⬆️survival
But HE in acute liver failure is different
Patients still die waiting for transplant, keeping the liver support dream alive
See: pig perfusion redux, auxiliary tx
/Summary
☑️People with HE coma die because of the triggers: bleeding, infection.
☑️⬆️survival for coma due to HE is mostly a triumph for supportive care
☑️Patients in coma inspired us to try wild things, and ultimately led us to learn how to transplant
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This concludes a #tweetorial on the history of outcomes and management of hepatic encephalopathy coma. Thank you for reading. I hope you enjoyed.
Thank you to @BloomPringle for reviewing and @HPB_Txp_Surg for the story (with @PeterAttiaMD) that inspired this
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WHAT is the deal with Milk Thistle?
WHY is it used to treat liver disease?
HOW does it work?
DOES it work?
ARE you ready for a #tweetorial?
🧵 #medtwitter#livertwitter
Milk Thistle, a history:
1⃣Use to treat snake bites (Dioscorides)
2⃣To carry off bile (Pliny the Elder)
3⃣Great for liver disease (1500's: Otto Brunfels)
4⃣In 19th Century 🇺🇸, the 'Eclectics' popularized herbology, especially milk thistle, for the liver
Fast forward to today:
1⃣Herbal supplements are a multibillion dollarindustry
2⃣A quarter of the population takes an herbal supplement
3⃣~5% of the US population is using Milk Thistle, including 12% of people with liver disease
We found that broad testing didn’t add much costs but increased false positives, especially when pretest probability of NAFLD was high
Then, In this RCT, John Dillon comparing usual care to broad evaluation of elevated liver enzymes, the cost per incremental diagnosis was 284💷 but was def cost-effective
This is a powerful method. But poorly understood, often maligned. My goal is to improve critical appraisal and help good analyses get the appreciation they deserve
All CEA begins with a clinical decision where we are uncertain about the best path forward. Nevertheless, when we face patients we must do something, even if that something is nothing. CEA brings our dilemma to life. Helping us quantify trade offs
Usually we compare a fair description of usual care to an alternative - make sure you agree the choice is fair, realistic, and represents an actual clinical dilemma
There's lots of tests you can order.
But most diagnoses are made in the H+P
Like this one
In fact, in this case, my attending said the diagnosis was obvious from the beginning
Just not to me
When I meet someone with ALT>1000, I think:
1⃣Ischemic hepatitis. Right 🫀failure? 🫀-genic shock? Cool legs?
2⃣Biliary 🪨. Pain? imaging!
3⃣Drug induced liver injury. Tylenol? Run every med through livertox.gov
4⃣Viral hep. Hep A/B/C
First, the lactate is up. Take this patient seriously
Second, the obvious clues are lower hemoglobin, platelet consumption.
Third, the ammonia is crazy high. This seals the deal for variceal bleeding.
The answer is hemoglobin and albumin are isoleucine-poor. This means that when our blood enters the gut, it is not a nutritious source of protein. It gets broken down for waste. That waste, my friends, is ammonia