AH2023: Prothrombin Time Predicts Steroid Response in Severe Alcoholic Hepatitis.

Sponsor
Fondazione Policlinico Universitario Agostino Gemelli IRCCS (Other)
Overall Status
Completed
CT.gov ID
NCT05883891
Collaborator
(none)
52
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66
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Study Details

Study Description

Brief Summary

Alcoholic hepatitis (AH) is the most severe form of acute alcohol-related liver disease. Maddrey's discriminant function (mDF) >32 defines the severe form of AH, which is associated with a high mortality. Corticosteroid therapy (CS) represents the main medical treatment that may reduce short-term mortality. Lille score at day 7 assesses the therapeutic response to steroid therapy. At present, no parameters able to predict the response to steroid therapy have been highlighted. The mDF depends mainly on prothrombin time (PT). Aim of the present study was to evaluate if the PT value could predict the response to CS in severe AH (sAH).

Condition or Disease Intervention/Treatment Phase
  • Diagnostic Test: prothrombin time

Study Design

Study Type:
Observational
Actual Enrollment :
52 participants
Observational Model:
Case-Only
Time Perspective:
Retrospective
Official Title:
Prothrombin Time Predicts Steroid Response in Severe Alcoholic Hepatitis.
Actual Study Start Date :
Jun 1, 2017
Actual Primary Completion Date :
Sep 30, 2022
Actual Study Completion Date :
Nov 30, 2022

Arms and Interventions

Arm Intervention/Treatment
severe alcoholic hepatitis

Patients admitted with a clinical diagnosis of severe alcoholic hepatitis eligible to corticosteroid treatment. Prothrombin time at diagnosis was registered to evaluate wether it correlated with Lille score at day 7 and therefore response to standard medical treatment.

Diagnostic Test: prothrombin time
Prothrombin time at value at diagnosis was used to assess the presence of a correlation with Lille score at day 7 and therefore wether it could predict response to medical treatment.

Outcome Measures

Primary Outcome Measures

  1. response to steroid treatment [seven days]

    response to standard medical treatment assessed with Lille scoremat day 7

Secondary Outcome Measures

  1. death [28 days]

    death occurring during hospitalization from any cause

  2. early liver transplantation [7 days]

    early transplantation in case of failure of medical treatment

  3. infection [28 days]

    occurrence of opportunistic infections following steroid treatment

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 70 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • clinical diagnosis of first episode of severe alcoholic hepatitis with Maddrey's function score of 32 or higher, and the absence of contraindication to CS therapy (non-controlled infections/sepsis, hepatic encephalopathy, recent acute gastrointestinal bleeding, severe kidney dysfunction). The diagnosis of AH was based on the criteria of the National Institute on Alcohol Abuse and Alcoholism (NIAAA)-funded Alcoholic Hepatitis Consortia (Crabb DW, 2016). In particular, were enrolled in the study patients with: heavy alcohol use for >6 months, with an average consumption of more than 3 drinks (∼40 g) per day for women and 4 drinks (∼50-60 g) per day for men and with <30 days of abstinence before the onset of jaundice; AST/ALT ratio > 1.5 with an AST level > 45 IU/L (1.5 times upper limit of normal) and < 400 IU/L; serum bilirubin >3 mg/dL.
Exclusion Criteria:
  • acute or chronic viral hepatitis,

  • nonalcoholic steatohepatitis,

  • cocaine use,

  • drug-induced liver injury,

  • fulminant Wilsons disease,

  • hepatocellular carcinoma,

  • portal vein thrombosis,

  • biliary obstruction,

  • severe autoimmune liver disease,

  • neoplasms,

  • severe comorbidities.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Agostino Gemelli Polyclinic Rome Roma (provincia) Italy 00168

Sponsors and Collaborators

  • Fondazione Policlinico Universitario Agostino Gemelli IRCCS

Investigators

  • Principal Investigator: Giovanni Addolorato, Internal Medicine and Alcohol Related Disease Unit, Department of Medical and Surgical Sciences, Columbus-Gemelli Hospital, Fondazione Policlinico Universitario A. Gemelli IRCCS, Catholic University of Rome, Rome, Italy

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Fondazione Policlinico Universitario Agostino Gemelli IRCCS
ClinicalTrials.gov Identifier:
NCT05883891
Other Study ID Numbers:
  • 5840
First Posted:
Jun 1, 2023
Last Update Posted:
Jun 1, 2023
Last Verified:
May 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Fondazione Policlinico Universitario Agostino Gemelli IRCCS
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jun 1, 2023