Hepatic encephalopathy in non-cirrhotic portal hypertension
- PMID: 39821852
- DOI: 10.1007/s11011-024-01522-5
Hepatic encephalopathy in non-cirrhotic portal hypertension
Abstract
Hepatic encephalopathy (HE) is traditionally associated with hepatic parenchymal diseases, such as acute liver failure and cirrhosis. Its prevalence in non-cirrhotic portal hypertension (NCPH) patients, extrahepatic portal vein obstruction (EHPVO), and non-cirrhotic portal fibrosis (NCPF) is less well described. HE in NCPH allows one to study the effect of portosystemic shunting and ammonia without significant hepatic parenchymal injury. The current review narrates the spectrum and management of hepatic encephalopathy in NCPH patients. We synthesized data from various studies on the occurrence and management of HE in NCPH, mainly EHPVO, idiopathic non-cirrhotic portal hypertension (INCPH), and porto-sinusoidal vascular disease (PSVD). The prevalence of minimal hepatic encephalopathy (MHE) in NCPH is reported from 12 to 60%, depending on the condition and diagnostic criteria. MHE was reported in nearly a third of EHPVO patients. Studies show that venous ammonia levels are significantly elevated in patients with MHE and spontaneous shunts (82.4 ± 20.3 vs. 47.1 ± 16.7 µmol/L, P = 0.001). Large portosystemic shunts substantially increase the risk of HE, with 46-71% of patients with persistent or recurrent HE having identifiable shunts. Management of HE in NCPH primarily focuses on reducing ammonia levels through lactulose, which has shown improvement in 53% of patients with MHE after three months (P = 0.001). Shunt occlusion in patients with large portosystemic shunts is helpful in selected cases. HE in NCPH, particularly in EHPVO, is associated with elevated ammonia levels and spontaneous shunts. Despite the high prevalence of HE in NCPH, this is still a neglected aspect in the care of NCPH. A high index of suspicion and the application of appropriate screening tools are crucial for timely diagnosis and management. HE screening tools that are well-studied in cirrhosis, are also valid in NCPH. Effective management strategies include lactulose, rifaximin, dietary modifications, and shunt embolisation in some cases. Future research should focus on the long-term natural history and efficacy of treatment strategies in this population.
Keywords: Hepatic encephalopathy; Lactulose; NCPH; PARTO; PSVD; Rifaximin.
© 2025. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.
Conflict of interest statement
Declarations. Competing interests: The authors declare no competing interests.
Similar articles
-
Prevalence of hepatic encephalopathy in patients with non-cirrhotic portal hypertension: A systematic review and meta-analysis.Indian J Gastroenterol. 2023 Oct;42(5):642-650. doi: 10.1007/s12664-023-01412-1. Epub 2023 Aug 17. Indian J Gastroenterol. 2023. PMID: 37589913
-
Non-cirrhotic portal hypertension - diagnosis and management.J Hepatol. 2014 Feb;60(2):421-41. doi: 10.1016/j.jhep.2013.08.013. Epub 2013 Aug 23. J Hepatol. 2014. PMID: 23978714 Review.
-
Hepatic encephalopathy in patients with non-cirrhotic portal hypertension: Description, prevalence and risk factors.Dig Liver Dis. 2016 Sep;48(9):1072-7. doi: 10.1016/j.dld.2016.06.014. Epub 2016 Jun 30. Dig Liver Dis. 2016. PMID: 27448844
-
[Analysis of influencing factors on hepatic encephalopathy in patients with non-cirrhotic portal hypertension].Zhonghua Gan Zang Bing Za Zhi. 2019 Sep 20;27(9):673-676. doi: 10.3760/cma.j.issn.1007-3418.2019.09.003. Zhonghua Gan Zang Bing Za Zhi. 2019. PMID: 31594090 Chinese.
-
Noncirrhotic portal hypertension: current trends and future directions.Curr Opin Gastroenterol. 2025 Jul 1;41(4):271-280. doi: 10.1097/MOG.0000000000001106. Epub 2025 May 2. Curr Opin Gastroenterol. 2025. PMID: 40396916 Review.
Cited by
-
Brain Functional Connectivity Significantly Improves After Surgical Eradication of Porto-Systemic Shunting in Pediatric Patients.Life (Basel). 2025 Feb 13;15(2):290. doi: 10.3390/life15020290. Life (Basel). 2025. PMID: 40003699 Free PMC article.
References
-
- Ahuja H, Sharma BC, Sachdeva S et al (2023) A double blind randomized controlled trial to assess efficacy of nutritional therapy for prevention of recurrence of hepatic encephalopathy in patients with cirrhosis. J Gastroenterol Hepatol 38:433–440. https://doi.org/10.1111/jgh.16096 - DOI - PubMed
-
- An J, Kim KW, Han S et al (2014) Improvement in survival associated with embolisation of spontaneous portosystemic shunt in patients with recurrent hepatic encephalopathy. Aliment Pharmacol Ther 39:1418–1426. https://doi.org/10.1111/apt.12771 - DOI - PubMed
-
- Bischoff SC, Bernal W, Dasarathy S et al (2020) ESPEN Guideline ESPEN practical guideline: Clinical nutrition in liver disease. https://doi.org/10.1016/j.clnu.2020.09.001
-
- Butterworth RF (1996) The neurobiology of hepatic encephalopathy. Semin Liver Dis 16:235–244. https://doi.org/10.1055/s-2007-1007236 - DOI - PubMed
-
- Butterworth RF (2003) Pathogenesis of hepatic encephalopathy: new insights from neuroimaging and molecular studies. J Hepatol 39:278–285. https://doi.org/10.1016/s0168-8278(03)00267-8 - DOI - PubMed
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources