MELD score to predict outcome in adult patients with non-acetaminophen-induced acute liver failure

被引:96
作者
Katoonizadeh, Aezam
Decaestecker, Jochen
Wilmer, Alexander
Aerts, Raymond
Verslype, Chris
Vansteenbergen, Werner
Yap, Paul
Fevery, Johan
Roskams, Tania
Pirenne, Jacques
Nevens, Frederik
机构
[1] Katholieke Univ Leuven, Univ Hosp Gasthuisberg, Dept Hepatol, B-3000 Louvain, Belgium
[2] Katholieke Univ Leuven, Univ Hosp Gasthuisberg, Med Intens Care Unit, B-3000 Louvain, Belgium
关键词
acute liver failure; Clichy criteria; hepatic encephalopathy; King's College Hospital criteria; liver transplantation; MELD score;
D O I
10.1111/j.1478-3231.2006.01429.x
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
A model for end stage liver disease (MELD) score > 30 was proposed as an excellent predictor of mortality in patients with non-acetaminophen-induced acute liver failure (ALF). We analyzed the prognostic value of MELD score in our patients with ALF who were prospectively registered in our database since 1990. Overall, 106 patients met the criteria of ALF. Excluding seven patients with acetaminophen etiology, 99 patients (42 +/- 15 years, 40M/59F) were studied. Causes were cryptogenic (n=38), viral (n=29), drugs (n=20) and miscellaneous (n=12). Of these, 37% (n=37) survived with medical management alone (group I), 16% (n=16) died (group II) and 46% (n=46) underwent liver transplantation (group III). The strongest predictors of poor outcome were advanced encephalopathy, cryptogenic/drug-induced/hepatitis B etiology and a high MELD score. At the time of diagnosis, King's College Hospital criteria and MELD score > 30 had similar high negative predictive value (92% and 91%, respectively) and low positive predictive value (52% and 56%, respectively). The predictive values improved only slightly during follow-up. The best cut-off point for MELD score to discriminate between survivors and nonsurvivors was > 35, with a sensitivity and specificity of 86% and 75%, respectively. MELD score, which mostly takes into consideration the degree of liver impairment, has a similar prognostic value as King's College Hospital criteria to predict outcome in adult patients with nonacetaminophen-induced ALF. Overall, all current scores miss accuracy and therefore there is a clear need for factors that can better predict the regeneration of the liver in this setting.
引用
收藏
页码:329 / 334
页数:6
相关论文
共 35 条
  • [1] Early indicators of prognosis in fulminant hepatic failure: An assessment of the King's criteria
    Anand, AC
    Nightingale, P
    Neuberger, JM
    [J]. JOURNAL OF HEPATOLOGY, 1997, 26 (01) : 62 - 68
  • [2] Liver transplantation in adults with acute liver failure
    Bernal, W
    Wendon, J
    [J]. JOURNAL OF HEPATOLOGY, 2004, 40 (02) : 192 - 197
  • [3] More on serum phosphate and prognosis of acute liver failure
    Bernal, W
    Wendon, J
    [J]. HEPATOLOGY, 2003, 38 (02) : 533 - 534
  • [4] Blood lactate as an early predictor of outcome in paracetamol-induced acute liver failure: a cohort study
    Bernal, W
    Donaldson, N
    Wyncoll, D
    Wendon, J
    [J]. LANCET, 2002, 359 (9306) : 558 - 563
  • [5] MULTIVARIATE-ANALYSIS OF PROGNOSTIC FACTORS IN FULMINANT HEPATITIS-B
    BERNUAU, J
    GOUDEAU, A
    POYNARD, T
    DUBOIS, F
    LESAGE, G
    YVONNET, B
    DEGOTT, C
    BEZEAUD, A
    RUEFF, B
    BENHAMOU, JP
    [J]. HEPATOLOGY, 1986, 6 (04) : 648 - 651
  • [6] Serum phosphorus levels predict clinical outcome in fulminant hepatic failure
    Chung, PY
    Sitrin, MD
    Te, HS
    [J]. LIVER TRANSPLANTATION, 2003, 9 (03) : 248 - 253
  • [7] Biochemical prognostic markers of outcome in non-paracetamol-induced fulminant hepatic failure
    Dabos, KJ
    Newsome, PN
    Parkinson, JA
    Mohammed, HH
    Sadler, IH
    Plevris, JN
    Hayes, PC
    [J]. TRANSPLANTATION, 2004, 77 (02) : 200 - 205
  • [8] Prognostic evaluation of early indicators in fulminant hepatic failure by multivariate analysis
    Dhiman, RK
    Seth, AK
    Jain, S
    Chawla, YK
    Dilawari, JB
    [J]. DIGESTIVE DISEASES AND SCIENCES, 1998, 43 (06) : 1311 - 1316
  • [9] DONALDSON BW, 1993, HEPATOLOGY, V18, P1370, DOI 10.1016/0270-9139(93)90226-D
  • [10] Hadem J, 2005, J HEPATOL, V42, P52