Role of ammonia in predicting the outcome of patients with acute-on-chronic liver failure

被引:12
作者
Chiriac, Stefan [1 ,2 ]
Stanciu, Carol [2 ]
Cojocariu, Camelia [1 ,2 ]
Singeap, Ana-Maria [1 ,2 ]
Sfarti, Catalin [1 ,2 ]
Cuciureanu, Tudor [1 ]
Girleanu, Irina [1 ,2 ]
Igna, Razvan Alexandru [3 ]
Trifan, Anca [1 ,2 ]
机构
[1] Grigore T Popa Univ Med & Pharm, Dept Gastroenterol, 16 Univ St, Iasi 700115, Romania
[2] St Spiridon Emergency Hosp, Inst Gastroenterol & Hepatol, Iasi 700111, Romania
[3] Grigore T Popa Univ Med Pharm, Intens Care, Iasi 700115, Romania
关键词
Venous ammonia; Hepatic encephalopathy; Acute-on-chronic liver failure; Asian Pacific Association for the Study of the Liver Acute-on-chronic Liver Failure Research Consortium score; Cirrhosis; Mortality; HEPATIC-ENCEPHALOPATHY; CEREBRAL EDEMA; SERUM AMMONIA; INFLAMMATION;
D O I
10.12998/wjcc.v9.i3.552
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND High venous ammonia (VA) values have been proven to be a part of the mechanism of hepatic encephalopathy in patients with liver cirrhosis (LC) as well as acute hepatitis. Moreover, VA has been associated with poor prognosis and high mortality in these clinical settings. However, the role of ammonia in acute-on-chronic liver failure (ACLF) has not yet been clearly established. AIM To assess the role of VA in predicting the outcome of cirrhotic patients with ACLF in a tertiary care center. METHODS We performed a retrospective observational study including consecutive patients with LC hospitalized for acute non-elective indications such as ascites, hepatic encephalopathy (HE), upper gastrointestinal bleeding, or bacterial infections that fulfilled the Asian Pacific Association for the Study of the Liver (APASL) criteria for ACLF. The study was conducted in "St. Spiridon" University Hospital, Iasi, Romania, a tertiary care center, between January 2017 and January 2019. The APASL ACLF Research Consortium (AARC) score was calculated and ACLF grade was established accordingly. West-haven classification was used for HE. Statistical analysis was performed using IBM SPSS version 22.0. RESULTS Four hundred and forty-six patients were included, aged 59 (50-65) years, 57.4% men. Child-Pugh, model for end-stage liver disease (MELD) and AARC scores were 11 (10-12), 19.13 +/- 6.79, and 7 (6-8), respectively. 66.4% had ACLF grade I, 31.2% ACLF grade II, and 2.5% ACLF grade III. HE was diagnosed in 83.9%, 34% grade I, 37.2% grade II, 23.5% grade III, and 5.3% grade IV. Overall mortality was 7.8%. VA was 103 (78-148) mu mol/L. Receiver operating characteristic analysis showed good accuracy for the prediction of in-hospital mortality for the AARC score [Area under the curve (AUC) = 0.886], MELD score (AUC = 0.816), VA (AUC = 0.812) and a fair accuracy for the Child-Pugh score (AUC = 0.799). Subsequently, a cut-off value for the prediction of mortality was identified for VA (152.5 mu mol/L, sensitivity = 0.706, 1-specificity = 0.190). Univariate analysis found acute kidney injury, severe HE (grade III or IV), VA >= 152.5 mu mol/L, MELD score >= 22.5, Child-Pugh score >= 12.5, and AARC score >= 8.5 to be associated with in-hospital mortality. Multivariate analysis identified AARC score >= 8.5 and venous ammonia >= 152 mu mol/L to be independent predictors of in-hospital mortality. CONCLUSION VA could be used as an inexpensive predictor of in-hospital mortality in patients with ACLF. Patients with both ACLF and VA > 152.5 mu mol/L have a high risk for a poor outcome.
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收藏
页码:552 / 564
页数:14
相关论文
共 27 条
[1]   Hepatic Encephalopathy Is Associated With Mortality in Patients With Cirrhosis Independent of Other Extrahepatic Organ Failures [J].
Bajaj, Jasmohan S. ;
O'Leary, Jacqueline G. ;
Tandon, Puneeta ;
Wong, Florence ;
Garcia-Tsao, Guadalupe ;
Kamath, Patrick S. ;
Maliakkal, Benedict ;
Biggins, Scott W. ;
Thuluvath, Paul J. ;
Fallon, Michael B. ;
Subramanian, Ram M. ;
Vargas, Hugo E. ;
Lai, Jennifer ;
Thacker, Leroy R. ;
Reddy, K. Rajender .
CLINICAL GASTROENTEROLOGY AND HEPATOLOGY, 2017, 15 (04) :565-+
[2]   Comparing Eight Prognostic Scores in Predicting Mortality of Patients with Acute-On-Chronic Liver Failure Who Were Admitted to an ICU: A Single-Center Experience [J].
Chen, Bo-Huan ;
Tseng, Hsiao-Jung ;
Chen, Wei-Ting ;
Chen, Pin-Cheng ;
Ho, Yu-Pin ;
Huang, Chien-Hao ;
Lin, Chun-Yen .
JOURNAL OF CLINICAL MEDICINE, 2020, 9 (05)
[3]   Definition and Nomenclature of Hepatic Encephalopathy [J].
Dharel, Narayan ;
Bajaj, Jasmohan S. .
JOURNAL OF CLINICAL AND EXPERIMENTAL HEPATOLOGY, 2015, 5 :S37-S41
[4]   Low grade cerebral edema and the pathogenesis of hepatic encephalopathy in cirrhosis [J].
Haeussinger, Dieter .
HEPATOLOGY, 2006, 43 (06) :1187-1190
[5]   Ammonia Levels Do Not Guide Clinical Management of Patients With Hepatic Encephalopathy Caused by Cirrhosis [J].
Haj, Mona ;
Rockey, Don C. .
AMERICAN JOURNAL OF GASTROENTEROLOGY, 2020, 115 (05) :723-728
[6]   Serum ammonia is a strong prognostic factor for patients with acute-on-chronic liver failure [J].
Hu, Chenxia ;
Huang, Kaizhou ;
Zhao, Lingfei ;
Zhang, Fen ;
Wu, Zhongwen ;
Li, Lanjuan .
SCIENTIFIC REPORTS, 2020, 10 (01)
[7]   Characteristics and outcomes of critically ill patients with severe hyperammonemia [J].
Jacoby, Katherine J. ;
Singh, Parvati ;
Prekker, Matthew E. ;
Leatherman, James W. .
JOURNAL OF CRITICAL CARE, 2020, 56 :177-181
[8]   The Direct Contribution of Astrocytes and Microglia to the Pathogenesis of Hepatic Encephalopathy [J].
Jaeger, Victoria ;
DeMorrow, Sharon ;
McMillin, Matthew .
JOURNAL OF CLINICAL AND TRANSLATIONAL HEPATOLOGY, 2019, 7 (04) :352-361
[9]   Cerebral oedema is rare in acute-on-chronic liver failure patients presenting with high-grade hepatic encephalopathy [J].
Joshi, Deepak ;
O'Grady, John ;
Patel, Amit ;
Shawcross, Debbie ;
Connor, Steven ;
Deasy, Neil ;
Willars, Chris ;
Bernal, William ;
Wendon, Julia ;
Auzinger, Georg .
LIVER INTERNATIONAL, 2014, 34 (03) :362-366
[10]   Demonstration of interstitial cerebral edema with diffusion tensor MR imaging in type C hepatic encephalopathy [J].
Kale, RA ;
Gupta, RK ;
Saraswat, VA ;
Hasan, KM ;
Trivedi, R ;
Mishra, AM ;
Ranjan, P ;
Pandey, CM ;
Narayana, PA .
HEPATOLOGY, 2006, 43 (04) :698-706