Clin Mol Hepatol.  2023 Jan;29(1):135-145. 10.3350/cmh.2022.0181.

Baveno-VII criteria to predict decompensation and initiate non-selective beta-blocker in compensated advanced chronic liver disease patients

Affiliations
  • 1Department of Gastroenterology & Hepatology, Changi General Hospital, Singapore
  • 2Duke-NUS Academic Clinical Program, SingHealth, Singapore
  • 3Biostatistics Unit, Yong Loo Lin School of Medicine, National University of Singapore, Singapore
  • 4Division of Gastroenterology and Hepatology, Foundation IRCCS Ca’ Granda Ospedale Maggiore Policlinico, Milan, Italy
  • 5Department of Gastroenterology and Human Nutrition Unit, All India Institute of Medical Science, New Dehli, India
  • 6CHESS Center, Institute of Portal Hypertension, the First Hospital of Lanzhou University, Lanzhou, China
  • 7Department of Gastroenterology & Hepatology, Tianjin Second People’s Hospital, Tianjin, China

Abstract

Background/Aims
The utility of Baveno-VII criteria of clinically significant portal hypertension (CSPH) to predict decompensation in compensated advanced chronic liver disease (cACLD) patient needs validation. We aim to validate the performance of CSPH criteria to predict the risk of decompensation in an international real-world cohort of cACLD patients.
Methods
cACLD patients were stratified into three categories (CSPH excluded, grey zone, and CSPH). The risks of decompensation across different CSPH categories were estimated using competing risk regression for clustered data, with death and hepatocellular carcinoma as competing events. The performance of “treating definite CSPH” strategy to prevent decompensation using non-selective beta-blocker (NSBB) was compared against other strategies in decision curve analysis.
Results
One thousand one hundred fifty-nine cACLD patients (36.8% had CSPH) were included; 7.2% experienced decompensation over a median follow-up of 40 months. Non-invasive assessment of CSPH predicts a 5-fold higher risk of liver decompensation in cACLD patients (subdistribution hazard ratio, 5.5; 95% confidence interval, 4.0–7.4). “Probable CSPH” is suboptimal to predict decompensation risk in cACLD patients. CSPH exclusion criteria reliably exclude cACLD patients at risk of decompensation, regardless of etiology. Among the grey zone, the decompensation risk was negligible among viral-related cACLD, but was substantially higher among the non-viral cACLD group. Decision curve analysis showed that “treating definite CSPH” strategy is superior to “treating all varices” or “treating probable CSPH” strategy to prevent decompensation using NSBB.
Conclusions
Non-invasive assessment of CSPH may stratify decompensation risk and the need for NSBB in cACLD patients.

Keyword

Portal hypertension; Hypertension, portal; Liver cirrhosis
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