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Pentoxifylline for alcoholic hepatitis
Kate Whitfield1, Andrea Rambaldi, Jørn Wetterslev
1Copenhagen Trial Unit, Centre for Clinical Intervention Research, Department 3344, Rigshospitalet, Copenhagen University Hospital, Blegdamsvej 9, Copenhagen, Denmark, DK-2100.
Insights
Pentoxifylline may reduce mortality in alcoholic hepatitis, but evidence is limited. The drug might also increase adverse events, and firm conclusions cannot be drawn due to study limitations.
Area of Science:
- Hepatology
- Gastroenterology
- Clinical Pharmacology
Background:
- Alcoholic hepatitis is a severe liver disease with high mortality and no established effective treatments.
- Pentoxifylline is a medication used for alcoholic hepatitis, but its efficacy requires systematic evaluation.
Purpose of the Study:
- To systematically review and assess the benefits and harms of pentoxifylline in patients with alcoholic hepatitis.
Main Methods:
- A comprehensive search of multiple databases (Cochrane, MEDLINE, EMBASE, etc.) was conducted up to August 2009.
- Included were all randomized clinical trials comparing pentoxifylline to control in alcoholic hepatitis patients.
- Data extraction, risk of bias assessment, and statistical analysis (including Trial Sequential Analysis) were performed.
Main Results:
- Five trials with 336 participants were included; 31% died. Four trials had a high risk of bias.
- Meta-analysis suggested pentoxifylline reduced all-cause mortality (RR 0.64) and hepatorenal syndrome mortality (RR 0.40), but Trial Sequential Analysis did not support these findings.
- One trial indicated pentoxifylline may increase adverse events.
Conclusions:
- Available data suggest a potential benefit of pentoxifylline on mortality, but the evidence is not robust.
- The risk of increased serious and non-serious adverse events with pentoxifylline warrants consideration.
- No definitive conclusions can be made regarding the overall effect of pentoxifylline in alcoholic hepatitis due to the low quality and limited quantity of evidence.
Background:
Alcoholic hepatitis is a life-threatening disease, with an average mortality of approximately 40%. There is no widely accepted, effective treatment for alcoholic hepatitis. Pentoxifylline is used to treat alcoholic hepatitis, but there has been no systematic review to assess its effects.
Objectives:
To assess the benefits and harms of pentoxifylline in alcoholic hepatitis.
Search Strategy:
The Cochrane Hepato-Biliary Group Controlled Trials Register, The Cochrane Central Register of Controlled Trials (CENTRAL) in The Cochrane Library, MEDLINE, EMBASE, Science Citation Index Expanded, LILACS, clinicaltrials.gov, and full text searches were conducted until August 2009. Manufacturers and authors were contacted.
Selection Criteria:
All randomised clinical trials of pentoxifylline in participants with alcoholic hepatitis compared to control were selected for inclusion.
Data Collection And Analysis:
Two authors extracted data and evaluated the risk of bias. RevMan Analysis was used for statistical analysis of dichotomous data with risk ratio (RR) and of continuous data with mean difference (MD), both with 95% confidence intervals (CI). Trial sequential analysis (TSA) was also used for statistical analysis of dichotomous and continuous data in order to control for random error. Where data were only available from one trial, we used Fisher's exact test or Student's t-test.
Main Results:
Five trials, with a total of 336 randomised participants, were included. A total of 105 participants (31%) died. Of the five included trials, four (80%) had a high risk of bias. Meta-analysis using all five trials showed that pentoxifylline reduced mortality compared with control (RR 0.64; 95% CI 0.46 to 0.89). However, this result was not supported by trial sequential analysis, which adjusts for multiple testing on accumulating data. Furthermore, four of the five trials were judged to have a high risk of bias, thus risking an overestimated intervention effect. Meta-analysis showed that pentoxifylline reduced the hepatic-related mortality due to hepatorenal syndrome (RR 0.40; 95% CI 0.22 to 0.71), but trial sequential analysis did not support this result. Data from one trial suggests that pentoxifylline may increase the occurrence of serious and non-serious adverse events compared to control.
Authors' Conclusions:
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. However, the evidence is not firm; no conclusions can be drawn regarding whether pentoxifylline has a positive, negative, or neutral effect on participants with alcoholic hepatitis.
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