FU Haiyan, ZHAO Ruiqin, BAI Gelan, YIN Chunlan, JIA Xiaoyun, LI Guigui, LI Xiaolei. Etiology and prognostic indicators of pediatric acute liver failure[J]. Journal of Clinical Medicine in Practice, 2021, 25(8): 79-83. DOI: 10.7619/jcmp.20201505
Citation: FU Haiyan, ZHAO Ruiqin, BAI Gelan, YIN Chunlan, JIA Xiaoyun, LI Guigui, LI Xiaolei. Etiology and prognostic indicators of pediatric acute liver failure[J]. Journal of Clinical Medicine in Practice, 2021, 25(8): 79-83. DOI: 10.7619/jcmp.20201505

Etiology and prognostic indicators of pediatric acute liver failure

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  • Received Date: November 21, 2020
  • Available Online: March 24, 2021
  • Published Date: April 27, 2021
  •   Objective  To analyze the etiology and the prognostic indicators of pediatric acute liver failure (PALF).
      Methods  A retrospective study was performed on the data of 64 patients with PALF. The patients were then divided into survival group and death group based on their prognosis. Age, gender, biochemical indicators and pediatric of end-stage liver disease (PELD) were compared between the two groups.
      Results  The common causes of PALF were identified as genetic and metabolic diseases (18 cases), followed by infectious diseases (13 cases), drug adverse reations and toxicity(8 cases), hematopathy (4 cases), immunologic liver diseases (2 cases), ischemic liver disease (1 case), and unclear causes (18 cases). The levels of total bilirubin (TB), international standardized ratio (INR) and PELD score in the death group were higher than those in the survival group, and the level of γ-glutamyl transpeptidase (GGT) in the death group was lower than that in the survival group (P < 0.05 or P < 0.01). Receiver operating characteristic (ROC) curve analysis showed that the combined area under the curve of GGT, TB and INR in combination was 0.793 (95%CI, 0.684 to 0.903), and the prognostic sensitivity and specificity of PALF diagnosis were 0.828 and 0.626, respectively.
      Conclusion  Inherited metabolic disorders are the most common known cause of PALF. For patients with PALF, higher levels of TB, INR and lower level of GGT may indicate a poor prognosis.
  • [1]
    LEE W M, SQUIRES R H, NYBERG S L, et al. Acute liver failure: Summary of a workshop[J]. Hepatology, 2008, 47(4): 1401-1415.
    [2]
    CIOCCA M, RAMONET M, CUARTEROLO M, et al. Prognostic factors in paediatric acute liver failure[J]. Arch Dis Child, 2008, 93(1): 48-51. doi: 10.1136/adc.2006.115113
    [3]
    DHAWAN A. Acute liver failure in children and adolescents[J]. Clin Res Hepatol Gastroenterol, 2012, 36(3): 278-283. doi: 10.1016/j.clinre.2012.03.022
    [4]
    KAMATH P S, WIESNER R H, MALINCHOC M, et al. A model to predict survival in patients with end-stage liver disease[J]. Hepatology, 2001, 33(2): 464-470. doi: 10.1053/jhep.2001.22172
    [5]
    NEWLAND C D. Acute Liver Failure[J]. Pediatr Ann, 2016, 45(12): e433-e438.
    [6]
    HEGARTY R, HADZIC N, GISSEN P, et al. Inherited metabolic disorders presenting as acute liver failure in newborns and young children: King's College Hospital experience[J]. Eur J Pediatr, 2015, 174(10): 1387-1392. doi: 10.1007/s00431-015-2540-6
    [7]
    DIAS C F, MOINHO R, FERREIRA S, et al. Acute liver failure related to inherited metabolic diseases in young children[J]. An Pediatr (Barc), 2018, 88(2): 69-74. doi: 10.1016/j.anpedi.2017.02.012
    [8]
    WANG J S, TAN N, DHAWAN A. Significance of low or normal serum gamma glutamyl transferase level in infants with idiopathic neonatal hepatitis[J]. Eur J Pediatr, 2006, 165(11): 795-801. doi: 10.1007/s00431-006-0175-3
    [9]
    徐惠敏, 兰小勤, 纪雅丽. 肝功能衰竭合并肝硬化患者血清γ-谷氨酰转肽酶与前白蛋白水平的相关性[J]. 中国肝脏病杂志: 电子版, 2018, 10(3): 90-93. https://www.cnki.com.cn/Article/CJFDTOTAL-GZBZ201803023.htm
    [10]
    LU F T, WU J F, HSU H Y, et al. gamma-Glutamyl transpeptidase level as a screening marker among diverse etiologies of infantile intrahepatic cholestasis[J]. J Pediatr Gastroenterol Nutr, 2014, 59(6): 695-701. doi: 10.1097/MPG.0000000000000538
    [11]
    ABUDUXIKUER K, CHEN R, WANG Z L, et al. Risk factors associated with mortality in neonatal intrahepatic cholestasis caused by citrin deficiency (NICCD) and clinical implications[J]. BMC Pediatr, 2019, 19(1): 18-25. doi: 10.1186/s12887-018-1383-5
    [12]
    OSWARI H, WIDJAJA R K, ROHSISWATMO R, et al. Prognostic value of biochemical liver parameters in neonatal sepsis-associated cholestasis[J]. J Paediatr Child Health, 2013, 49(1): E6-E11. doi: 10.1111/jpc.12053
    [13]
    CHEN H L, WU S H, HSU S H, et al. Jaundice revisited: recent advances in the diagnosis and treatment of inherited cholestatic liver diseases[J]. J Biomed Sci, 2018, 25(1): 75-87. doi: 10.1186/s12929-018-0475-8
    [14]
    ZHANG J, YANG Y, GONG J Y, et al. Low-GGT intrahepatic cholestasis associated with biallelic USP53 variants: Clinical, histological and ultrastructural characterization[J]. Liver Int, 2020, 40(5): 1142-1150. doi: 10.1111/liv.14422
    [15]
    姜涛, 欧阳文献, 谭艳芳, 等. 儿童急性肝衰竭120例病因和预后分析[J]. 中华实用儿科临床杂志, 2020, 35(6): 422-425.
    [16]
    苗敏, 钱素云. 儿童急性肝衰竭流行病学研究进展及预后因素分析[J]. 中华急诊医学杂志, 2018, 27(11): 1302-1307.
    [17]
    LÓPEZ-VELÁZQUEZ J A, CHÁVEZ-TAPIA N C, PONCIANO-RODRÍGUEZ G, et al. Bilirubin alone as a biomarker for short-term mortality in acute-on-chronic liver failure: an important prognostic indicator[J]. Ann Hepatol, 2013, 13(1): 98-104. http://europepmc.org/abstract/med/24378272
    [18]
    苗敏, 钱素云. 儿童急性肝衰竭病因及转归相关因素分析[J]. 中华实用儿科临床杂志, 2019, 34(19): 1462-1466.
    [19]
    罗兰, 刘萍萍, 隆彩霞, 等. 重症儿童急性肝衰竭预后的相关因素[J]. 中华实用儿科临床杂志, 2019, 34(18): 1390-1393.

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