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The natural history of compensated HCV-related cirrhosis: a prospective long-term study
Eduardo Vilar Gomez1, Yoan Sanchez Rodriguez, Luis Calzadilla Bertot
1Department of Researches, National Institute of Gastroenterology, Havana, Cuba. vilar@infomed.sld.cu
Insights
Compensated cirrhosis from Hepatitis C virus (HCV) in Latin America shows high risks. Patients with esophageal varices face significantly greater mortality, liver transplantation, and complication rates over six years.
Area of Science:
- Hepatology
- Gastroenterology
- Viral Hepatitis Research
Background:
- The natural history of Hepatitis C virus (HCV)-related compensated cirrhosis is understudied in Latin America.
- Limited data exists on long-term outcomes for this patient population.
Purpose of the Study:
- To evaluate mortality and clinical outcomes in patients with compensated HCV-related cirrhosis.
- To assess the impact of esophageal varices on patient prognosis over a 6-year follow-up period.
Main Methods:
- Prospective recruitment of 402 patients with compensated HCV-related cirrhosis.
- Stratification into stage 1 (no varices) and stage 2 (presence of varices) based on D'Amico criteria.
- Follow-up for overall mortality, liver transplantation, and clinical complication rates.
Main Results:
- Over 6 years, cumulative mortality or liver transplantation was 15% for stage 1 and 45% for stage 2 (p<0.001).
- Hepatocellular carcinoma (HCC) incidence was 9% in patients without varices versus 29% with varices (p<0.001).
- Clinical liver-related complications occurred in 26% of stage 1 patients compared to 66% of stage 2 patients (p<0.001).
Conclusions:
- Compensated cirrhotic patients with esophageal varices (stage 2) experience significantly higher morbidity and mortality.
- Early identification and management of varices are crucial for improving outcomes in HCV-related cirrhosis.
Background & Aims:
The natural history of HCV-related compensated cirrhosis has been poorly investigated in Latin-American countries. Our study evaluated mortality and clinical outcomes in compensated cirrhotic patients followed for 6 years.
Methods:
Four hundred and two patients with compensated HCV-related cirrhosis were prospectively recruited in a tertiary care academic center. At the time of admission, patients were stratified as compensated (absence [stage 1] or presence [stage 2] of esophageal varices) as defined by D'Amico et al. Subjects were followed to identify overall mortality or liver transplantation and clinical complication rates.
Results:
Among 402 subjects, 294 were categorized as stage 1 and 108 as stage 2. Over a median of 176 weeks, 42 deaths occurred (10%), of which 30 were considered liver-related (7%) and 12 non-liver-related (3%); eight individuals (2%) underwent liver transplantation; 30 patients (7%) developed HCC, 67 individuals in stage 1 (22%) developed varices and any event of clinical decompensation occurred in 80 patients (20%). The 6-year cumulative overall mortality or liver transplantation was 15% and 45%, for stages 1 and 2, respectively (p<0.001). The cumulative 6-year HCC incidence was significantly higher among patients with varices (29%) than those without varices (9%), p<0.001. Similarly, the cumulative 6-year incidence of any clinical liver-related complication was higher in patients with stage 2 (66%) as compared to 26% in those with stage 1, respectively (p<0.001).
Conclusions:
Our results indicate significant morbidity and mortality and clinical outcome rates in compensated cirrhotic patients with varices (stage 2).
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