Transient elastography can stratify patients with Child-Pugh A cirrhosis according to risk of early decompensation
Audrey Dillon1, Zita Galvin1, Alyshah A Sultan2
1Centre for Liver Disease, Mater Misericordiae University Hospital, Dublin, Ireland.
Insights
Transient elastography liver stiffness measurement (LSM) can predict decompensation in compensated cirrhosis. A low LSM (<21 kPa) indicates no risk, while higher LSMs correlate with increased decompensation risk.
Area of Science:
- Hepatology
- Gastroenterology
- Medical Diagnostics
Background:
- Compensated cirrhosis prognosis varies, lacking robust tools for predicting decompensation in Child-Pugh A stage.
- Transient elastography (TE) is explored as a potential tool to assess decompensation risk across diverse liver disease causes.
Purpose of the Study:
- To evaluate the utility of transient elastography (TE) in predicting liver decompensation in patients with compensated cirrhosis.
- To determine if liver stiffness measurement (LSM) can stratify risk for decompensation events in a mixed-etiology cohort.
Main Methods:
- 259 participants with compensated cirrhosis were enrolled across two sites and followed for at least 2 years.
- Liver stiffness measurement (LSM) via TE and routine blood tests were performed at baseline and follow-up visits.
- Liver decompensation (hepatic encephalopathy, ascites, variceal bleeding) was the primary outcome.
Main Results:
- The overall rate of liver-related outcomes was 31 per 1000 person-years.
- No decompensation events occurred in patients with LSM < 21 kPa.
- LSM > 35 kPa was linked to a 39% decompensation risk at 4 years; each 1 kPa increase above 20 kPa raised risk by 6% (HR=1.06).
Conclusions:
- Increasing LSM in compensated cirrhosis correlates with a higher risk of liver decompensation.
- LSM can effectively risk-stratify patients with compensated cirrhosis.
- Low LSM scores may reassure patients, while high scores can identify candidates for clinical trials.
Background:
Compensated cirrhosis has a variable prognosis depending on stage. There are currently no straightforward and robust tools in clinical practice to predict decompensation in Child-Pugh A cirrhosis. We set out to determine whether transient elastography (TE) could be used across liver disease aetiologies to determine risk of decompensation.
Patients And Methods:
Participants were enrolled at two sites (Dublin and Nottingham) and followed up for a minimum of 2 years. The primary outcome of the study was liver decompensation, defined as the development of overt hepatic encephalopathy or ascites or presentation with bleeding varices. All patients received a TE examination to measure liver stiffness measurement (LSM) and had routine blood measurements taken at the baseline visit and on each subsequent visit.
Results:
In 259 participants, the overall rate of liver-related outcome was 31 per 1000 person-years (95% confidence interval: 19-47 per 1000 person-years). Of the total population, 6 and 11% developed a liver-related outcome within 2 and 4 years of follow-up, respectively. There were no events in the population with a LSM less than 21 kPa. A LSM of more than 35 kPa was associated with a decompensation risk of 39% at 4 years. For each unit increase in the LSM above 20 kPa, the risk of liver-related outcome increased by 6% (hazard ratio=1.06; 95% confidence interval: 1.04-1.82) after adjusting for age, sex Mayo End Liver Disease Score, cohort source and aetiology.
Conclusion:
The risk of liver decompensation increased with increasing LSM in mixed aetiology compensated cirrhosis. LSM may be used to risk stratify patients, potentially reassure patients with low scores, and select patients with higher scores for experimental therapeutic studies with acceptable timelines.
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