Steroids or pentoxifylline for alcoholic hepatitis (STOPAH): study protocol for a randomised controlled trial

被引:69
作者
Forrest, Ewan [1 ]
Mellor, Jane [2 ]
Stanton, Louise [2 ]
Bowers, Megan [2 ]
Ryder, Priscilla [1 ]
Austin, Andrew [3 ]
Day, Christopher [4 ]
Gleeson, Dermot [5 ]
O'Grady, John [6 ]
Masson, Steven [7 ]
McCune, Anne [8 ]
Patch, David [9 ]
Richardson, Paul [10 ]
Roderick, Paul [11 ]
Ryder, Stephen [12 ]
Wright, Mark [13 ]
Thursz, Mark [14 ]
机构
[1] Glasgow Royal Infirm, Dept Gastroenterol, Glasgow G4 0SF, Lanark, Scotland
[2] Univ Southampton, Clin Trials Unit, Southampton Gen Hosp, MP 131, Southampton SO16 6YD, Hants, England
[3] Royal Derby Hosp, Fac Med Sci, Derby DE22 3NE, England
[4] Univ Newcastle, Sch Med, Newcastle Upon Tyne NE2 4HH, Tyne & Wear, England
[5] Royal Hallamshire Hosp, Liver Unit, Sheffield S10 2JF, S Yorkshire, England
[6] Kings Coll Hosp London, Inst Liver Studies, London SE5 9RS, England
[7] Freeman Rd Hosp, Liver Unit, Newcastle Upon Tyne, Tyne & Wear, England
[8] Bristol Royal Infirm & Gen Hosp, Dept Hepatol, Bristol BS2 8HW, Avon, England
[9] Royal Free Hosp, Royal Free Sheila Sherlock Liver Ctr, London NW3 2QG, England
[10] Royal Liverpool Univ Hosp, Liverpool L7 8XP, Merseyside, England
[11] Univ Southampton, Southampton Gen Hosp, Southampton SO16 6YD, Hants, England
[12] Univ Nottingham, Hosp NHS Trust, Dept Gastroenterol, Nottingham NG7 2UH, England
[13] Southampton Gen Hosp, Southampton SO16 6YD, Hants, England
[14] Imperial Coll, Hepatol Sect, London W2 1NY, Paddington, England
关键词
Factorial design; Alcoholic hepatitis; Prednisolone; Pentoxifylline; Maddrey's discriminant function (DF); Glasgow alcoholic hepatitis score (GAHS); SHORT-TERM SURVIVAL; LIVER-DISEASE; DOUBLE-BLIND; CORTICOSTEROIDS; PREDNISOLONE; THERAPY; METAANALYSIS; MORTALITY; CIRRHOSIS; FEATURES;
D O I
10.1186/1745-6215-14-262
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
100103 [病原生物学]; 100218 [急诊医学];
摘要
Background: Alcoholic hepatitis is the most florid presentation of alcohol-related liver disease. In its severe form, defined by a Maddrey's discriminant function (DF) >= 32, the 28-day mortality rate is approximately 35%. A number of potential treatments have been subjected to clinical trials, of which two, corticosteroids and pentoxifylline, may have therapeutic benefit. The role of corticosteroids is controversial as trial results have been inconsistent, whereas the role of pentoxifylline requires confirmation as only one previous placebo-controlled trial has been published. Methods/design: STOPAH is a multicentre, double-blind, factorial (2 x 2) trial in which patients are randomised to one of four groups: 1. Group A: placebo / placebo 2. Group B: placebo / prednisolone 3. Group C: pentoxifylline / placebo 4. Group D: pentoxifylline / prednisolone The trial aims to randomise 1,200 patients with severe alcoholic hepatitis, in order to provide sufficient power to determine whether either of the two interventions is effective. The primary endpoint of the study is mortality at 28 days, with secondary endpoints being mortality at 90 days and 1 year. Discussion: STOPAH aims to be a definitive study to resolve controversy around the existing treatments for alcoholic hepatitis. Eligibility criteria are based on clinical parameters rather than liver biopsy, which are aligned with standard clinical practice in most hospitals. The use of a factorial design will allow two treatments to be evaluated in parallel, with efficient use of patient numbers to achieve high statistical power.
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