WHY are steroids used for alcoholic hepatitis?
SHOULD we?
WHAT is the deal with prednisolone vs prednisone?
WHERE did the discriminant function come from?
ARE you ready for a #tweetorial
Alcoholic hepatitis is a life-threatening acute liver injury featuring a liver full of necrotic cells, "Mallory bodies" of cellular junk, & severe inflammation (neutrophils)
Fig1: Mallory's original description
Fig2: Alc hep Mortality in 1966 according to bilirubin
3/
Where did we get the idea for steroids in alc hep?
Everyone in 1950's France was using steroids to treat #cirrhosis. As in the examples below, Prednisone/prednisolone were said to resolve ascites, edema, jaundice, and fevers. They made patients hungry and happy too
4/
The 1st RCT
Based on the French experience, Wells published in @TheLancet an RCT of Prednisolone+Corticotrophin, Testosterone, or control for all-comers with #cirrhosis at one hospital
Corticosteroids did not⬇️ascites but they did⬇️mortality.
Steroids for all?
5/
Were Wells' results legit?
1⃣Helman gave prednisolone or control for #cirrhosis stratified by hepatic encephalopathy (HE). For the 14 with high bili & HE, prednisolone⬇️mortality
2⃣Porter enrolled 20 patients with biopsy-proven alc hep with a 'trend' favoring prednisolone
6/
These underpowered studies got people excited about improving outcomes for alcoholic hepatitis. This field was about to take off after Willis Maddrey published his RCTs of prednisolone
But! Before we get to Maddrey, we have to ask:
why prednisolone and not prednisone?
7/
Prednisone is a prodrug converted to prednisolone by 11β-HSD1 enzyme, which is mainly in liver. Given the new interest in steroids for alc hep, Powell looked at metabolism and found conversion of prednisone to prednisolone was⬇️in liver injury
Case closed...or is it?
8/
Turns out: pred=pred
1⃣Powell's findings were irreproducible
2⃣Prednisone is just converted more slowly in liver disease. Also 11β-HSD1 is in muscle, fat
3⃣Prednisone/prednisolone have equal bioavailability
4⃣Treatment failure is unrelated to pred metabolism
9/
Enter Maddrey
Although we learned prednisone=prednisolone, Maddrey enrolled 55 pts in a prednisolone RCT after the Powell's 1971 study
😢No survival benefit from steroids
🧐But wait, when you adjust for disease severity, prednisolone came out on top. How? Next slide pls
10/
Introducing the Discriminant Function (DF)
Using stepwise regression, Maddrey found all ppl who died had 96+ using: 4.6 x prothrombin time x bilirubin
For a multicenter trial, he updated the DF (subtracting normal PT) & only included people with DF>32 (or HE)
11/
In a multicenter RCT with 66 patients who had DF>32 (or HE), prednisolone was associated with a major reduction in mortality. These results were confirmed in a trial of 61 patients from France
Both prednisolone and the DF were looking like they were here to stay
12/
Since those landmarks, many trials have been undertaken
1⃣Prednisolone has been mostly used; out of convention, not b/c it's >prednisone
2⃣we tried many other treatments, eg pentoxifylline, thought to⬇️tnf
3⃣All results have been conflicting
Then came STOPAH
13/
STOPAH was:
1⃣The largest Alc hep RCT
2⃣2x2 factorial: pred, pentox, placebo
STOPAH found:
3⃣🚫improved survival at 90, 365 days
4⃣Possible⬆️survival at 28d for pred
Conclusion
🪦pentoxifylline
🤔use steroids carefully, if at all
(Confirmed by meta-analysis)
14/
What else did STOPAH show?
28d mortality was 17% in the placebo group (13-14% in the pred groups). We have far to go but we have come a LONG way!
Why? Better supportive care, eg:
1⃣nutritional support
2⃣Screen/treat for infection
3⃣Endoscopy for bleeding
15/
Where are we at with DF these days?
1⃣If we choose pred using DF, we only want 2 use in ppl who r benefitting by ~ day 7 (i.e. Lille score)
2⃣MELD score may be better than DF for prognosis at baseline; MELD + Lille for pred users
3⃣If pred has benefit, it's in MELD 25-39
16/
SUMMARY
1⃣Pred was used to treat #cirrhosis but trials showed only ppl with alc hep may benefit
2⃣Prednisone➡️prednisolone. Bioavailability is the same
3⃣The DF was associated w/death & then used 2 select pts 4 trials
4⃣Pred may⬆️28-day but not longterm survival
/end
This concludes a #tweetorial on the use of steroids for patients with alcohol-associated hepatitis. I hope you enjoyed. I would like to thank @BloomPringle for peer-review and thank those whose work benefits patients with AH like J `Mellinger, @MarkThursz, and Maddrey
• • •
Missing some Tweet in this thread? You can try to
force a refresh
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