The Portal Hypertension Decompensation Score: A Validated Predictive Model of Liver Decompensation Related to Portal

Angus W Jeffrey1,2, Avik Majumdar3,4, Gary Jeffrey1,2

  • 1Medical School, The University of Western Australia, Perth.

Insights

A new Portal Hypertension Decompensation Score (PDS) accurately predicts decompensation in compensated advanced chronic liver disease (cACLD) patients. This non-invasive score helps identify high-risk individuals needing further evaluation without liver stiffness measurement.

Area of Science:

  • Hepatology
  • Clinical Prediction Models
  • Non-invasive Diagnostics

Background:

  • Compensated advanced chronic liver disease (cACLD) requires non-invasive risk stratification for prognostication and management.
  • Current methods may involve invasive procedures like liver stiffness measurement (LSM).

Purpose of the Study:

  • To develop and validate a novel, non-invasive score to predict decompensation in cACLD patients.
  • To create a tool that avoids the need for LSM in risk assessment.

Main Methods:

  • Development of a predictive score using serum markers in a large training cohort (n=967) with competing risk analysis.
  • Internal validation (n=417) and external validation (n=315) of the score.
  • Comparison with existing scores in external validation cohorts.

Main Results:

  • The Portal Hypertension Decompensation Score (PDS) was developed using bilirubin, ALT, ALP, albumin, and platelets.
  • The PDS demonstrated good calibration and discrimination, with high accuracy (AUC 0.74-0.83) for predicting decompensation at 2 and 5 years.
  • Low PDS scores showed high sensitivity (74-84%) for predicting no decompensation (NPV 91-95%), while high scores were specific (87-93%) for future decompensation (PPV 33-58%).

Conclusions:

  • The PDS is an accurate and validated predictor of decompensation in cACLD.
  • It effectively differentiates low-risk from high-risk patients, guiding further management decisions.
  • The PDS offers a non-invasive alternative to LSM for risk stratification in cACLD.
Abstract