The clinical characteristics and prognosis of liver cirrhotic patients with acute decompensation
Xu Danqing, Mu Huan, Zhang Yingyuan, Mou Chunyan, Sa Caifen, Liu Li, Li Weikun
2026, 31(8):
1084-1090.
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Objective To analyze the clinical characteristics of cirrhotic patients with acute decompensation events and to investigate the factors influencing their prognosis. Methods Patients diagnosed with decompensated cirrhosis due to HBV, HCV, alcoholic hepatitis, and autoimmune hepatitis who visited the Third People's Hospital of Kunming from January 1, 2016 to December 31, 2022 were collected. Relevant clinical data of all patients were collected and they were divided into an acute de-compensation group and a non-acute de-compensation group. The clinical characteristics of the two groups were analyzed. At the end of the study, patients who developed hepatocellular carcinoma (HCC) or died were classified as the poor prognosis group, while those who did not were classified as the control group. Univariate and multivariate logistic regression analyses were conducted to identify the factors that might affect the poor prognosis of patients with decompensated cirrhosis. Kaplan-Meier method was used to estimate survival rates and draw survival curves for patients with different compensation status. Log-rank test was used to compare their survival curves. Results A total of 863 patients with decompensated cirrhosis were included, with 624 in the acute decompensation group and 239 in the non-acute decompensation group. The incidence of acute decompensation was 72.3%. Among them, 116 patients died (97 in the acute decompensation group and 19 in the non-acute decompensation group), 109 patients developed HCC (83 in the acute decompensation group and 26 in the non-acute decompensation group), and 558 achieved recompensation (428 in the acute decompensation group and 130 in the non-acute decompensation group). The result of log-rank test showed that there were statistically significant differences between the two groups in recompensation rate (χ2=15.509, P<0.001) and liver disease-related mortality (χ2=7.359, P=0.007), with Kaplan-Meier curves clearly separated. However, there was no statistically significant difference in the incidence of HCC (χ2=0.757, P=0.384). Univariate Logistic regression analysis showed that in the poor prognosis group, there were 159 cases of acute decompensation (79.5%), Child classification [A grade 23 cases (11.5%), B grade 88 cases (44.0%), C grade 89 cases (44.5%)], age 53.0 (46.0, 60.0) years, TBil 40.05 (24.95,80.25) μmol/L, GGT 81.50 (40.55,149.00) U/L, ALP 143.80 (108.00,210.00) U/L, Alb 28.65 (24.40,32.80) g/L, IL-6 20.11 (10.28,41.35) pg/mL, PT 17.50 (15.70,19.75) s, compared with the control group with 468 cases of acute decompensation (70.1%), Child-Pugh classification [A grade 106 cases (16.0%), B grade 338 cases (46.5%), C grade 219 cases (33.0%)], age 50.0 (44.0, 57.0) years, TBil 31.80 (21.10,57.75) μmol/L, GGT 40.55 (28.00,68.00) U/L, ALP 108.00 (80.00,148.00) U/L, Alb 29.00 (25.00, 32.00) g/L, IL-6 10.28 (5.28, 19.35) pg/mL, PT 15.70 (14.00,17.40) s. The differences in 63.00 (35.00,134.50) U/L, ALP 132.00 (98.50,179.00) U/L, Alb 30.00 (26.15,34.80) g/L, IL-6 15.27 (9.00,28.51) pg/mL, and PT 17.00 (15.40,18.83) S were statistically significant (χ2=6.728, χ2=9.249, Z=-2.652, -0.331, -2.057, -2.140, -3.229, -3.465, -2.240, all P<0.05). The results of the multivariate analysis showed that age [OR 95% CI:1.024 (1.008~1.041), P=0.003], TBil [OR 95% CI:1.003 (1.001~1.005), P=0.010], and Alb [OR 95% CI:0.962 (0.929~0.996), P=0.030] were independent influencing factors for poor prognosis in decompensated patients. Conclusion Elevated total bilirubin, decreased albumin, and increasing age are key risk factors for poor prognosis in patients with decompensated liver cirrhosis. Acute decompensated cirrhosis events are significantly associated with increased liver disease-related mortality and decreased re-compensation rate.