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<ArticleSet>
<Article>
<Journal>
<PublisherName>Science and Education Publishing</PublisherName>
<JournalTitle>American Journal of Clinical Medicine Research</JournalTitle>
<Issn>2328-403X</Issn>
<Volume>4</Volume>
<Issue>1</Issue>
<PubDate PubStatus="epublish">
<Year>2016</Year>
<Month>2</Month>
<Day>25</Day>
</PubDate>
</Journal>
<ArticleTitle>Budesonide in Severe Alcoholic Hepatitis: Results of the Original Research</ArticleTitle>
<FirstPage>7</FirstPage>
<LastPage>10</LastPage>
<Language>EN</Language>
<AuthorList>
<Author>
<FirstName>Komkova</FirstName>
<LastName>I.I.</LastName>
</Author>
<Author>
<FirstName>Tkachenko</FirstName>
<LastName>P.E.</LastName>
<Affiliation>Hepatology department, I.M.Sechenov First State Medical University, Moscow, Russia</Affiliation>
</Author>
<Author>
<FirstName>Maevskaya</FirstName>
<LastName>M.V.</LastName>
</Author>
<Author>
<FirstName>Ivashkin</FirstName>
<LastName>V.T.</LastName>
</Author>

</AuthorList>
<ArticleIdList>
<ArticleId IdType="pii">AJCMR2016412</ArticleId>
<ArticleId IdType="doi">10.12691/ajcmr-4-1-2</ArticleId>
</ArticleIdList>
<History>
<PubDate PubStatus="received">
<Year>2015</Year>
<Month>9</Month>
<Day>25</Day>
</PubDate>
<PubDate PubStatus="revised">
<Year>2015</Year>
<Month>12</Month>
<Day>14</Day>
</PubDate>
<PubDate PubStatus="accepted">
<Year>2016</Year>
<Month>2</Month>
<Day>23</Day>
</PubDate>
</History>
<Abstract>Background and aim: Severe alcoholic hepatitis (AH) is a life-threatening alcoholic liver disease with a potential of 30-40% mortality at 1 month. While steroids remain to be a first line therapy, there is a need in alternative treatment. The aim of the study is to compare efficacy and safety of budesonide and prednisolone in treatment of severe AH and to determine predictors of none-response, predictors of short-term mortality. Methods: 37 patients with severe AH were randomized in 2 groups and enrolled in the prospective trial. Group 1 (n=17) patients received budesonide 9 mg/daily per os, group 2 (n=20) patients were managed with prednisolone 40 mg/daily per os. Treatment duration was 28 days. Response criteria - Lille model. Results: There were no significant differences in short-term survival (р = 0,857). In group 2 adverse events were statistically more frequently than in group 1 (70% vs. 26,7%, р = 0,011). Hepatorenal syndrome occurred more frequently in group 2 (р = 0,033). Predictors of non-response were MELD score (р = 0,009), ABIC score (р = 0,011), hepatic encephalopathy (p=0,035), total bilirubin (p=0,016). Predictors of mortality were Lille score (p=0,018), serum glucose (p=0,017), total bilirubin level at the 7th day of the therapy (p=0,030). Conclusions: Budesonide therapy for patients with severe alcoholic hepatitis showed same efficacy as prednisolone treatment with significantly less adverse events. Budesonide appears to be effective in prevention of hepatorenal syndrome.</Abstract>
</Article>
</ArticleSet>
