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The Portal Hypertension Decompensation Score: A Validated Predictive Model of Liver Decompensation Related to Portal Hypertension
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INTRODUCTION:
There is a need for noninvasive risk stratification in people with compensated advanced chronic liver disease (cACLD) to prognosticate and guide management. We aimed to develop a score that predicts decompensation in people with cACLD without the need for a liver stiffness measurement.
METHODS:
A multicenter state-wide cohort of patients with cACLD between 2004 and 2015 were followed until decompensation. A predictive score using serum markers was developed in a training cohort (n = 967) using competing risk analysis and internally validated (n = 417). Further external validation and comparison with other scores was undertaken in 315 patients between 2017 and 2024.
RESULTS:
Decompensation occurred in 172 (17.8%), 64 (15.3%), and 51 patients (16.2%) in the training and 2 validation cohorts (P = 0.60) after median follow-up of 3.2, 3.4, and 1.9 years, respectively. Bilirubin, alanine aminotransferase, alkaline phosphatase, albumin, and platelets predicted decompensation and combined into a final model—the Portal Hypertension Decompensation Score (PDS). The PDS was well calibrated with good discrimination for predicting decompensation. In the 2 validation cohorts, accuracy (time-dependent area under the curve) of the PDS for predicting decompensation was high at 2 years (0.75 and 0.82) and 5 years (0.74 and 0.83). A low score (< −3.348) had a sensitivity of 74%–84% in prediction of no decompensation with a negative predictive value of 91%–95%, whereas a high score (> −2.828) was 87%–93% specific for future decompensation with a positive predictive value of 33%–58%.
DISCUSSION:
The PDS is an accurate predictor of decompensation in cACLD. It discriminates patients who are low risk from those who are high risk and who may benefit from further evaluation or treatment, without requiring the use of liver stiffness measurement.
Ovid Technologies (Wolters Kluwer Health)
Title: The Portal Hypertension Decompensation Score: A Validated Predictive Model of Liver Decompensation Related to Portal Hypertension
Description:
INTRODUCTION:
There is a need for noninvasive risk stratification in people with compensated advanced chronic liver disease (cACLD) to prognosticate and guide management.
We aimed to develop a score that predicts decompensation in people with cACLD without the need for a liver stiffness measurement.
METHODS:
A multicenter state-wide cohort of patients with cACLD between 2004 and 2015 were followed until decompensation.
A predictive score using serum markers was developed in a training cohort (n = 967) using competing risk analysis and internally validated (n = 417).
Further external validation and comparison with other scores was undertaken in 315 patients between 2017 and 2024.
RESULTS:
Decompensation occurred in 172 (17.
8%), 64 (15.
3%), and 51 patients (16.
2%) in the training and 2 validation cohorts (P = 0.
60) after median follow-up of 3.
2, 3.
4, and 1.
9 years, respectively.
Bilirubin, alanine aminotransferase, alkaline phosphatase, albumin, and platelets predicted decompensation and combined into a final model—the Portal Hypertension Decompensation Score (PDS).
The PDS was well calibrated with good discrimination for predicting decompensation.
In the 2 validation cohorts, accuracy (time-dependent area under the curve) of the PDS for predicting decompensation was high at 2 years (0.
75 and 0.
82) and 5 years (0.
74 and 0.
83).
A low score (< −3.
348) had a sensitivity of 74%–84% in prediction of no decompensation with a negative predictive value of 91%–95%, whereas a high score (> −2.
828) was 87%–93% specific for future decompensation with a positive predictive value of 33%–58%.
DISCUSSION:
The PDS is an accurate predictor of decompensation in cACLD.
It discriminates patients who are low risk from those who are high risk and who may benefit from further evaluation or treatment, without requiring the use of liver stiffness measurement.
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