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Chinese Journal of Critical Care Medicine(Electronic Edition) ›› 2016, Vol. 09 ›› Issue (01): 20-27. doi: 10.3877/cma.j.issn.1674-6880.2016.01.004

Special Issue:

• Original Article • Previous Articles     Next Articles

Prognostic value of hepatitis B-related liver failure patients treated with non-biotype artificial liver by model for end-stage liver disease and Child-Turcotte-Pugh score systems

Wenlong Yang1, Shuilin Sun1,(), Xijing Zhou2, Mingfa Chen1, Wenna Xi1, Zhen Gao1, Lingling Yang3, Jie Luo1, Jinqiu He3   

  1. 1. Department of Infectious Diseases, The Second Affiliated Hospital of Nanchang University, Nanchang 330006, China
    2. Department of Gastroenterology, The First Affiliated Hospital of Nanchang University, Nanchang 330006, China
    3. Artificial Liver Treatment Center, Infectious Diseases Hospital Affiliated of Nanchang University, Nanchang, 330002, China
  • Received:2015-06-16 Online:2016-02-01 Published:2016-02-01
  • Contact: Shuilin Sun
  • About author:
    Corresponding author: Sun Shuilin, Email:

Abstract:

Objective

To assess and predict the effect and the clinical prognostic value of non-biotype artificial liver support system (NB-ALSS) in hepatitis B-related liver failure patients by model for end-stage liver disease (MELD) and Child-Turcotte-Pugh (CTP) score systems.

Methods

The randomly selected 210 cases of hepatitis B-related liver failure patients were divided into the artificial liver group(n = 115) and control group(n = 95), based on MELD and CTP scores. Each group were further divided into four subgroups: MELD< 20, 20 ≤ MELD< 30, 30 ≤ MELD< 40, and MELD> 40. The changes of MELD score between these two groups and of the laboratory parameters in the artificial liver group before and after the treatment were observed, and actual short-term mortality rate with expected mortality according to CTP score system were compared.

Results

After the artificial liver treatment, prothrombin time international normalized ratio (INR) decreased significantly in four artificial liver subgroups [(1.3 ± 0.3) vs. (1.4 ± 0.3); (2.2 ± 0.8) vs. (2.6 ± 0.8); (4.1 ± 1.5) vs. (5.2 ± 1.7); (9.6 ± 2.8) vs. (12.2 ± 4.8); t = 4.303, 3.152, 3.545, 3.130; all P< 0.05], total bilirubin (TBIL) also showed significant improvement in these artificial liver groups after the treatment [(152 ± 74) μmol/L vs. (287 ± 118) μmol/L; (266 ± 160) μmol/L vs. (422 ± 114) μmol/L; (370 ± 144) μmol/L vs. (517 ± 126) μmol/L; (564 ± 180) μmol/L vs.(628 ± 121) μmol/L; t = 4.960, 5.951, 4.915, 2.577; all P< 0.05]. Except the MELD ≥ 40 subgroup, MELD scores in the other three artificial liver subgroups were markedly dropped after the treatment [(10.2 ± 3.4) vs. (16.6 ± 2.5); (18.2 ± 4.2) vs. (24.7 ± 2.6); (30.1 ± 7.5) vs. (36.2 ± 2.3); t = 7.036, 9.094, 5.476; all P< 0.05], MELD score decreased (△MELD) between the artificial liver groups and control groups were statistically significant in these three subgroups (t = 2.286, 2.906, 2.021; all P < 0.05). In the 20 ≤ MELD< 30 and 30 ≤ MELD< 40 subgroups, the mortality rates of the artificial liver groups were lower than expected mortality rates (40.8% vs. 76.0%, 51.4% vs. 83.0%; χ2 = 12.119, 8.880; all P < 0.05), and also lower than that of the control groups (40.8% vs. 61.9%, 51.4% vs. 82.4%; χ2 = 4.03, 4.71; all P < 0.05). Comparing the mortality rates between the artificial liver groups and control groups in the CTP C level: in the 20 ≤ MELD< 30 and 30 ≤ MELD< 40 subgroups, the mortality rates of two sets were significantly different(38.8% vs. 59.6%, 51.4% vs. 76.5%; χ2 = 3.90, 4.40; all P < 0.05). Kaplan-Meier survival curves showed that in the 20 ≤ MELD< 30 and 30 ≤ MELD< 40 subgroups, the short-term survival rates in the artificial liver groups was higher than that in the control groups (χ2 = 3.89, 5.70; all P < 0.05).

Conclusion

Combined MELD score and CTP classification system can assess the prognosis of NB-ALSS in treatment of hepatitis B-related liver failure patients.

Key words: Hepatitis B virus, Liver failure, Artificial liver support system, Model for end-stage liver disease, Child-Turcotte-Pugh score

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