Indeterminate etiology of acute liver failure in North America: Less common, still grave prognosis.

acute liver failure indeterminate acute liver failure transplant free survival

Journal

Clinical transplantation
ISSN: 1399-0012
Titre abrégé: Clin Transplant
Pays: Denmark
ID NLM: 8710240

Informations de publication

Date de publication:
Dec 2023
Historique:
revised: 22 08 2023
received: 04 07 2023
accepted: 03 09 2023
pubmed: 14 9 2023
medline: 14 9 2023
entrez: 14 9 2023
Statut: ppublish

Résumé

The etiology of acute liver failure (ALF) remains one of the most important factors in determining prognosis and predicting outcomes. In a significant proportion of ALF cases, however, the etiology remains unknown and is categorized as indeterminate ALF (IND-ALF). In this study, we summarize findings from patients with IND-ALF from 32 transplant centers across the United States, and we compare laboratory, prognostic, and outcome data for patients with IND-ALF. Between 1998 and 2019, 3364 adult patients with ALF or acute liver injury (ALI) from 32 liver transplant centers were enrolled in the ALFSG registry. The primary clinical outcome of interest was 21-day transplant-free survival (TFS). Of the 3364 patients enrolled in the ALFSG registry, 3.4 % (n = 114) were adjudicated as true indeterminate. On multivariate analysis, patients with a lower bilirubin, lower INR, lack of use of mechanical ventilation and no clinical features of coma at baseline had a higher odds ratio of transplant free survival. The number of deaths were similar between patients with true-IND ALF versus patients with indeterminable ALF (29.8% vs. 27.2%), with almost half of the patients requiring liver transplant (42.1% vs. 45.7%). We illustrate the poor prognoses that true-IND-ALF and indeterminable ALF carry and the need for emergency liver transplantation in most cases.

Sections du résumé

BACKGROUND BACKGROUND
The etiology of acute liver failure (ALF) remains one of the most important factors in determining prognosis and predicting outcomes. In a significant proportion of ALF cases, however, the etiology remains unknown and is categorized as indeterminate ALF (IND-ALF). In this study, we summarize findings from patients with IND-ALF from 32 transplant centers across the United States, and we compare laboratory, prognostic, and outcome data for patients with IND-ALF.
METHODS METHODS
Between 1998 and 2019, 3364 adult patients with ALF or acute liver injury (ALI) from 32 liver transplant centers were enrolled in the ALFSG registry. The primary clinical outcome of interest was 21-day transplant-free survival (TFS).
RESULTS RESULTS
Of the 3364 patients enrolled in the ALFSG registry, 3.4 % (n = 114) were adjudicated as true indeterminate. On multivariate analysis, patients with a lower bilirubin, lower INR, lack of use of mechanical ventilation and no clinical features of coma at baseline had a higher odds ratio of transplant free survival. The number of deaths were similar between patients with true-IND ALF versus patients with indeterminable ALF (29.8% vs. 27.2%), with almost half of the patients requiring liver transplant (42.1% vs. 45.7%).
CONCLUSION CONCLUSIONS
We illustrate the poor prognoses that true-IND-ALF and indeterminable ALF carry and the need for emergency liver transplantation in most cases.

Identifiants

pubmed: 37705387
doi: 10.1111/ctr.15128
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e15128

Subventions

Organisme : NIDDK NIH HHS
ID : R01 DK058369
Pays : United States
Organisme : NIDDK NIH HHS
ID : U01 DK058369
Pays : United States

Informations de copyright

© 2023 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.

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Auteurs

Parita V Patel (PV)

Department of Medicine, Northwestern University, Chicago, Illinois, USA.

Sherry Livingston (S)

Department of Medicine, Medical University of South Carolina, Charleston, South Carolina, USA.

Jorge L Rakela (JL)

Department of Medicine, Mayo Clinic Arizona, Scottsdale, Arizona, USA.

R Todd Stravitz (RT)

Department of Medicine, Virginia Commonwealth University, Richmond, Virginia, USA.

Adrian Reuben (A)

Department of Medicine, Medical University of South Carolina, Charleston, South Carolina, USA.

Nathan M Bass (NM)

Department of Medicine, University of California, San Francisco, California, USA.

Shannan R Tujios (SR)

Department of Medicine, University of Texas Southwestern Medical Center, Dallas, Texas, USA.

Anne M Larson (AM)

Department of Medicine, University of Washington, Seattle, Washington, USA.

Norman L Sussman (NL)

Department of Medicine, Baylor College of Medicine, Houston, Texas, USA.

Jody A Rule (JA)

Department of Medicine, University of Texas Southwestern Medical Center, Dallas, Texas, USA.

Valerie L Durkalski-Mauldin (VL)

Department of Medicine, Medical University of South Carolina, Charleston, South Carolina, USA.

William M Lee (WM)

Department of Medicine, University of Texas Southwestern Medical Center, Dallas, Texas, USA.

Daniel R Ganger (DR)

Department of Medicine, Northwestern University, Chicago, Illinois, USA.

Classifications MeSH