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Relationship between updated MELD and prognosis in alcohol-associated hepatitis: Opportunities for more efficient trial design.
Al-Karaghouli, Mustafa; Ventura-Cots, Meritxell; Wong, Yu Jun; Genesca, Joan; Bosques, Francisco; Brown, Robert S; Mathurin, Philippe; Louvet, Alexandre; Shawcross, Debbie; Vargas, Victor; Verna, Elizabeth C; Schnabl, Bernd; Caballeria, Joan; Shah, Vijay J; Kamath, Patrick S; Lucey, Michael R; Garcia-Tsao, Guadalupe; Bataller, Ramon; Abraldes, Juan G.
Afiliação
  • Al-Karaghouli M; Division of Gastroenterology (Liver Unit). University of Alberta, Edmonton, Alberta, Canada.
  • Ventura-Cots M; Liver Unit, Hospital Universitari Vall d'Hebron, Vall d'Hebron Research Institute (VHIR), Vall d'Hebron Barcelona Hospital Campus, Universitat Autònoma de Barcelona, Barcelona, Spain.
  • Wong YJ; Centro de Investigación Biomédica en Red Enfermedades Hepáticas y Digestivas (CIBEREHD), Instituto de Salud Carlos III, Madrid, Spain.
  • Genesca J; Division of Gastroenterology (Liver Unit). University of Alberta, Edmonton, Alberta, Canada.
  • Bosques F; Liver Unit, Hospital Universitari Vall d'Hebron, Vall d'Hebron Research Institute (VHIR), Vall d'Hebron Barcelona Hospital Campus, Universitat Autònoma de Barcelona, Barcelona, Spain.
  • Brown RS; Centro de Investigación Biomédica en Red Enfermedades Hepáticas y Digestivas (CIBEREHD), Instituto de Salud Carlos III, Madrid, Spain.
  • Mathurin P; Hospital Universitario Dr Jose E. Gonzalez, Servicio de Gastroenterologia, Universidad Autonoma de Nuevo Leon Monterrey, Mexico.
  • Louvet A; Division of Gastroenterology and Hepatology, Weill Cornell Medical College, New York, New York, USA.
  • Shawcross D; University of Lille, Inserm, CHU Lille, U1286-INFINITI-Institute for Translational Research in Inflammation, Lille, France.
  • Vargas V; University of Lille, Inserm, CHU Lille, U1286-INFINITI-Institute for Translational Research in Inflammation, Lille, France.
  • Verna EC; Department of Inflammation Biology, Institute of Liver Studies, School of Immunology and Microbial Sciences, Faculty of Life Sciences and Medicine, King's College, London, UK.
  • Schnabl B; Liver Unit, Hospital Universitari Vall d'Hebron, Vall d'Hebron Research Institute (VHIR), Vall d'Hebron Barcelona Hospital Campus, Universitat Autònoma de Barcelona, Barcelona, Spain.
  • Caballeria J; Centro de Investigación Biomédica en Red Enfermedades Hepáticas y Digestivas (CIBEREHD), Instituto de Salud Carlos III, Madrid, Spain.
  • Shah VJ; Division of Digestive and Liver Diseases, Department of Medicine, Columbia College of Physicians and Surgeons, Columbia University Medical Center, New York, New York, USA.
  • Kamath PS; Medicine, University of California San Diego, La Jolla, California, USA.
  • Lucey MR; Centro de Investigación Biomédica en Red Enfermedades Hepáticas y Digestivas (CIBEREHD), Instituto de Salud Carlos III, Madrid, Spain.
  • Garcia-Tsao G; Mayo Clinic and Mayo Medical School, Rochester, Minnesota, USA.
  • Bataller R; Mayo Clinic and Mayo Medical School, Rochester, Minnesota, USA.
  • Abraldes JG; Division of Gastroenterology and Hepatology, Department of Medicine, University of Wisconsin School of Medicine and Public Health, Madison, Wisconsin, USA.
Hepatol Commun ; 8(8)2024 Aug 01.
Article em En | MEDLINE | ID: mdl-39082963
ABSTRACT

BACKGROUND:

Alcohol-associated hepatitis (AH) is associated with significant mortality. Model for End-Stage Liver Disease (MELD) score is used to predict short-term mortality and aid in treatment decisions. MELD is frequently updated in the course of AH. However, once the most updated MELD is known, it is uncertain if previous ones still have prognostic value, which might be relevant for transplant allocation and trial design. We aimed to investigate the predictive performance of updated MELDs in a prospectively collected cohort of patients with AH by the InTeam consortium.

METHODS:

Three hundred seven patients (with 859 MELD values within 60 d of admission) fulfilled the inclusion criteria. The main endpoint was time to death or transplant up to 90 days. We used a joint model approach to assess the predictive value of updated MELDs.

RESULTS:

Updated MELD measurements had a strong prognostic value for death/transplant (HR 1.20, 95% CI 1.14-1.27) (p < 0.0001). Previous MELD values did not add predictive value to the most current MELD. We also showed that MELD at day 28 (MELD28) had a significant predictive value for subsequent mortality/transplant in a landmark analysis (HR 1.18, 95% CI 1.12-1.23). We show that the use of an ordinal scale including death, transplant, and MELD28 as a trial outcome could substantially reduce the sample size required to demonstrate short-term benefit of an intervention.

CONCLUSION:

We show that updated MELDs during the trajectory of AH predict subsequent mortality or the need for transplant. MELD28 inclusion in an ordinal outcome (together with death or transplant) could increase the efficiency of randomized controlled trials.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Índice de Gravidade de Doença / Transplante de Fígado / Hepatite Alcoólica Limite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: Hepatol Commun Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Canadá País de publicação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Índice de Gravidade de Doença / Transplante de Fígado / Hepatite Alcoólica Limite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: Hepatol Commun Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Canadá País de publicação: Estados Unidos