From Citizendium - Reading time: 2 min
In gastroenterology, alcoholic hepatitis is "inflammation of the liver due to alcohol abuse. It is characterized by necrosis of hepatocytes, infiltration by neutrophils, and deposit of mallory hyaline bodies. depending on its severity, the inflammatory lesion may be reversible or progress to liver cirrhosis."[1]A practice guideline is available from the American College of Gastroenterology.[2]
Corticosteroids may help in severe cases, but not all cases according to a meta-analysis. [3] In this study, the relative risk ratio of glucocorticosteroids for patients with severe hepatitis for mortality at various times was 0.4 and the relative risk reduction was 63%. In populations similar to those in this study which had a rate of risk as measured by the mortality at various times of 38% without treatment, the number needed to treat is 4. [3]
The role of pentoxifylline is uncertain. "The current available data may indicate a possible positive intervention effect of pentoxifylline on all-cause mortality and mortality due to hepatorenal syndrome, and conversely, an increase in serious and non-serious adverse events" according to a meta-analysis by the Cochrane Collaboration. [4] In this study, the relative risk ratio of pentoxifylline for mortality at various times was 0.6 and the relative risk reduction was 36.8%. In populations similar to those in this study which had a rate of risk as measured by the mortality at various times of 38% without treatment, the number needed to treat is 7. [4] the mortality during hospitalization of 46% without treatment, the number needed to treat is 5.
"Although combination therapy with prednisolone plus N-acetylcysteine increased 1-month survival among patients with severe acute alcoholic hepatitis, 6-month survival, the primary outcome, was not improved" according to a randomized controlled trial. [5] In this trial, the relative risk ratio of N-acetylcysteine for mortality at one month was 0.3 and the relative risk reduction was 66.7%. In populations similar to those in this study which had a rate of risk as measured by the mortality at one month of 24% without treatment, the number needed to treat is 6. [5]
| Trial | Patients | Intervention | Comparison | Outcome | Results | Comment | |
|---|---|---|---|---|---|---|---|
| Intervention | Control | ||||||
| Cochrane[3] 2008 Meta-analysis |
Six trials • 249 patients |
Glucocorticosteroids | Placebo | Mortality at various times | 14% | 38% | RRR = 63% (subgroup with severe hepatitis) |
| Nguyen-Khac[5] 2011 Randomized controlled trial |
One trial • 174 patients • All patients receiving steroids |
N-Acetylcysteine | Placebo | Mortality at one month | 8% | 24% | RRR = 67% • No benefit after 3 months |
| Cochrane 2009 Meta-analysis |
Five trials • 336 patients • Unclear if all patients receiving steroids |
Pentoxifylline | Placebo | Mortality at various times | 24% | 38% | RRR = 35% • May cause epigastric discomfort |