Medical and Dental Consultants’ Association of Nigeria
Home - About us - Editorial board - Search - Ahead of print - Current issue - Archives - Submit article - Instructions - Subscribe - Advertise - Contacts - Login 
  Users Online: 17   Home Print this page Email this page Small font sizeDefault font sizeIncrease font size
 

  Table of Contents 
ORIGINAL ARTICLE
Year : 2011  |  Volume : 14  |  Issue : 2  |  Page : 181-185

Chronic liver disease and hepatic encephalopathy: Clinical profile and outcomes


1 Department of Medicine, Lagos State University Teaching Hospital, Ikeja, Nigeria
2 Department of Medicine, Lagos State University Teaching Hospital, Ikeja; Department of Medicine, ­General Hospital Gbagada, Lagos, Nigeria

Date of Acceptance08-Mar-2011
Date of Web Publication19-Aug-2011

Correspondence Address:
C A Onyekwere
Department of Medicine, Lagos State University Teaching Hospital, Ikeja, Lagos
Nigeria
Login to access the Email id


DOI: 10.4103/1119-3077.84011

PMID: 21860136

Get Permissions

   Abstract 

Background: Hepatic encephalopathy (HE) is an important neuropsychiatry complication of liver disease causing significant morbidity and mortality worldwide. Efforts at improving the outcome have resulted in development of new strategies in the management given the background of new insights in the pathogenesis of this disease entity. Understanding the disease profile including precipitants as well as prognostic factors will contribute in this regard as new strategies are yet to be widely applied. The aim of this report is to document the profile of patients with HE, the precipitants, prognostic factors as well as the scope of the burden associated with it.
Materials and Methods: In this prospective study, all patients managed for HE from January to December 2008 were recruited. A questionnaire was used to extract their basic demographics, clinical features noting any possible precipitants, complications, management protocol as well as outcome.
Results:
A total of 21 subjects (11 females and 10 males) within the age range of 16-83 years were seen during the period under review. (mean age 57.9 ΁ 13). There was no significant difference in the mean ages of males and females. Two patients had acute encephalopathy, while others had acute-on chronic encephalopathy. The risk factors for liver disease included significant alcohol ingestion, hepatitis B virus infection, and previous jaundice, while other complications of liver disease noted were deepening jaundice, ascites, bleeding tendencies, and renal failure. The identified precipitants for HE were sepsis 6 (29%), electrolyte inbalance 3 (14%), gastrointestinal bleed 5 (24%), drugs (5%), and possible malignant transformation 6 (29%). Focus of sepsis was bacterial peritonitis in two cases. Majority of our patients (61%) came during advanced stage of liver disease (Child-Pugh class C). Length of hospital stay ranged from 1 to 7 weeks and a mortality of 48% was observed. Predictors of mortality were a history of significant alcohol ingestion, previous blood transfusion, Hepatitis B and C infections, and severe liver dysfunction on presentation (Child-Pugh class C).
Conclusions: HE is associated with a high mortality rate and this scenario is associated with a history of previous blood transfusion, Hepatitis B and C infections, and severe liver dysfunction on presentation. Measures to reduce the burden of viral Hepatitis B and C, safe blood transfusion, and responsible use of alcohol should be promoted. Screening of those at risk of encephalopathy (liver disease patients) with a psychometric test of good predictability should be part of their routine evaluation in daily practice so as to detect cases of latent encephalopathy. Intensive care facilities and necessary personnel should be provided.

Keywords: Hepatic encephalopathy, Liver failure, Nigeria


How to cite this article:
Onyekwere C A, Ogbera A O, Hameed L. Chronic liver disease and hepatic encephalopathy: Clinical profile and outcomes. Niger J Clin Pract 2011;14:181-5

How to cite this URL:
Onyekwere C A, Ogbera A O, Hameed L. Chronic liver disease and hepatic encephalopathy: Clinical profile and outcomes. Niger J Clin Pract [serial online] 2011 [cited 2014 Oct 25];14:181-5. Available from: http://www.njcponline.com/text.asp?2011/14/2/181/84011


   Introduction Top


Hepatic encephalopathy (HE) is a common neuropsychiatric syndrome seen in patients with significant hepatic dysfunction in the absence of neurological disorders. [1] It is seen in upto 30-45% of patients with cirrhosis and its latent or sub clinical form (minimal hepatic encephalopathy can affect upto 60% of patients with liver disease. [2] Although controversy about the exact pathogenetic mechanism exists, certain factors like hyper ammonia and increased blood-brain permeability to ammonia, increased brain concentration of manganese and inhibitory neurosteroids (allopregnanolone) have been documented. [3] Based on the underlying hepatic abnormality, encephalopathy is subdivided into three types; [1] type A (associated with acute liver disease), type B (associated with portosystemic bypass and no intrinsic hepatocellular disease), and type C (associated with chronic liver disease).

Current recommendation [1] of the working party on its definition suggest guidelines that would allow even the diagnosis of the sub clinical form (latent encephalopathy) and the use of the newer neuroimaging techniques. However, this is yet to be widely applied in clinical practice as some report indicates. [4] Available reports [4],[5],[6] have identified factors such as sepsis, gastrointestinal bleeding, constipation, and diuretic use as common precipitating factors of encephalopathy in patients with liver disease. Identification of these precipitants and other prognostic indices would enable institution of more rationale measures in the management of this condition, which has been associated with poor outcome. [7] This is even worse in resource poor countries that often lack necessary manpower, newer imaging techniques, and dedicated specialized care unit. The cornerstone of therapy is still the nonabsorbable disaccharides, since the new therapeutic agents with broad-spectrum activity against urease producing bacteria are yet to be available. Also, dietary manipulation is still protein restriction and not protein maintenance with glutein and casein-free diet (GCFD), which has recently been recommended in view of its role in lowering opioid peptides that have been implicated in the pathogenesis.

An earlier report [6] from this locality in children had shown a very poor outcome (95% mortality), although these were mostly fulminant cases (type A encephalopathy). There is a need to document the pattern of hepatic encephalopathy in adult population in our setting as only reports from resource-endowed countries abound in the literature. This will no doubt allow a more appropriate management guideline-taking cognizance of resource availability. We therefore set out to redress this issue in our study. The aim of this report is documenting the profile of patients admitted with features of HE from January to December 2008 and note possible precipitants, complications, and management outcome.


   Materials and Methods Top


This was a prospective and observational study and was conducted in line with the principle of the Declaration of Helsinki as amended in Tokyo (1975), Venice (1983), and Hong Kong (1989). All patients with HE admitted into the Medical Wards of the Lagos State University Teaching Hospital, Ikeja from January to December 2008 were recruited. A patient was included if he had impaired consciousness with a background liver disease (acute or chronic on basis of clinical findings, liver biochemistry, and sonographic findings) in the absence of any neurological disorder or other cause of impaired consciousness. A questionnaire was used to extract the following: Bio data, clinical features including laboratory findings, any identified precipitants, complications as well as management and outcome. Brain imaging with computerized tomographic scan was done where possible to exclude primary neurological cause. Diagnosis of spontaneous bacterial peritonitis was based on demonstration of more than 250 WBC/cm 3 in ascitic fluid. The presence of elevated serum creatinine (>1.5 mg/dl) in the absence of shock, hematuria, or proteinuria with a normal renal sonogram was taken to be indicative of hepatorenal syndrome. The Child-Pugh scoring system [7] was used for assessing the severity of liver disease on patient presentation. The scoring system takes into account the serum albumin, serum prothrombin time, and bilirubin as well as presence of fluid retention and encephalopathy; each of which is given a numerical score. There are 3 grades: A, B, and C depending on the total scores. The West Haven criteria [8] was used in grading the encephalopathy. It is a semi-quantitative grading of mental state from trivial lack of awareness (grade 1) to coma (unresponsive to verbal or noxious stimuli (grade 4).


   Results Top


There were 21 subjects (11 females and 10 males) with HE seen within the period of study. Age ranged from 16 to 83 years with a median age of 61 years. The mean age of the study subjects was 57.9 ± 13 years, and the mean age of the males and females were comparable [(57.7 (±18) years vs. 58 (±8) years; P = 0.7]. Total emergency admission for the gastroenterology/liver unit during this period was 362, thus, HE accounted for 6% of this.

Two patients had acute encephalopathy (type A), while 19 had acute on chronic liver disease (type C). The two acute encephalopathy were drug induced, one of whom survived.

Risk factors for chronic liver disease

Significant alcohol and previous blood transfusion histories were documented in 10 (48%) and 2 (10%), respectively, of the study subjects. Also, a history of previous jaundice and use of herbal medications was documented in 9 (43%) and 2 (10%), respectively, of the subjects under study.

These and other risk factors are shown in [Table 1].
Table 1: Clinical characteristics of the study subjects


Click here to view


Clinical presentation

Of the stigmata of chronic liver disease, 4 (40%) of the males had testicular atrophy. The distribution of stigmata of chronic liver disease (CLI) is shown in [Figure 1].
Figure 1 : Prevalence of stigmata of CLD

Click here to view


Some of the patients presented with complications of CLD and the distribution of these are shown in [Figure 2].
Figure 2 : Distribution of complications of CLD

Click here to view


Severity of liver disease on presentation as assessed using the Child-Pugh's classification is shown in [Figure 3].
Figure 3 : Child-Pugh's classification in study subjects

Click here to view


Grading of HE

[Table 2] shows the distribution of the grade of encephalopathy and outcome of management among study participants.
Table 2: Grade of hepatic encephalopathy using West Haven criteria and outcome


Click here to view


Precipitating factors

Identified precipitants of encephalopathy in the patients were sepsis 6 (29%), electrolyte inbalance 3 (14%), gastrointestinal bleed 5 (24%), drug induced (5%), and possible malignant transformation 6 (29%). Focus of sepsis was bacterial peritonitis in two cases.

Treatment and duration of hospitalization

Treatment type varied and included the use of mannitol, especially in acute encephalopathy. Various treatment types are shown in [Table 3]. The duration of hospitalization is shown in [Table 4].
Table 3: Treatment modalities for hepatic encephalopathy


Click here to view
Table 4: Duration of hospitalization and survival


Click here to view


Outcome of management

In all, 10 (48%) of the subjects expired. The number of females who passed away was more than males, with the female: Male ratio being 7:3. Possible determinants of mortality are shown in [Table 5]. A history of significant alcohol ingestion, previous blood transfusion, Hepatitis B and C infections, and severe liver dysfunction on presentation (Child-Pugh class C) are highly predictive of mortality from encephalopathy.
Table 5: Predictive factors of mortality from hepatic encephalopathy


Click here to view



   Discussion Top


HE remains an important complication of liver disease associated with high mortality even in developed nations. Newer insight into its pathogenesis [4] has led to newer approaches [9],[10] in its management, though these are yet to be widely applied particularly in the resource poor nations. [3] Documentation of its profile including precipitating factors will go a long way in formulating rational strategies in its management including prophylaxis in view of the reported poor outcome. [11]

Majority of the patients in our study had encephalopathy complicating underlying chronic liver disease with only two having fulminant failure, one of whom survived. About half of study subjects had Hepatitis B-related liver disease, while significant alcohol consumption was noted in majority, which may have contributed to the progression of liver disease. This is in keeping with earlier reports [12] about the role of hepatitis B in causation of liver disease in our setting. Efforts at improving the coverage of current immunization campaign [13] against Hepatitis B certainly will help reduce the burden of Hepatitis B virus infection, whilst promotion of sensible use of alcohol should be encouraged.

The observed precipitants in this study, sepsis (29%), electrolyte inbalance (14%), gastrointestinal bleed (24%), drug induced (5%), and possible malignant transformation (29%), do not differ from those in previous reports. [3],[5] No other precipitants were found in 5 (29%) with sonographic features of PLCC as well as elevated alpha fetoprotein and were considered as having PLCC. [14] Majority of our patients came in fairly advanced stage of liver dysfunction (Child-pugh class B and C), which may have contributed to observed mortality [Odds ratio (OR) 2.7 (95% CI) 0.56-13.28). Higher fatality rate were recorded with increasing severity of encephalopathy (OR 5.1, 95% CI).

It is noteworthy that our management protocol (nonabsorbable disaccharides, antibiotics, and protein restriction) did not involve any of the newer therapeutic regime (antibiotics with broad spectrum activity against urease producing bacteria as well as GCFD). The patients in this study were nursed in the open ward and this was largely due to financial constraints. In our setting, usually healthcare costs are borne by the patients and payment often has to be made before some facilities are made available for use. Management in an intensive care unit as well as employment of the newer therapeutic measures may have improved the outcome.

Apart from advanced stage presentation, other predictors of fatal outcome are; severe grade of encephalopathy, a history of significant alcohol ingestion, previous blood transfusion, Hepatitis B and C infections. Identification of early encephalopathy by screening of those at risk (patients with pre-existing liver disease) using the psychometric tests [15],[16] will go a long way in reducing the fatal outcome since advanced stage presentation as was documented in this study is associated with less favourable outcome.

Due to the high cost of imaging patients in this study, we did not have brain computerized tomographic scan (CT scan) to exclude primary neurological disease. However, most of these patients already had pre-existing liver disease.

The limitations of this report include a small sample size.


   Conclusions Top


The disease burden of HE is high and the contributory factors of this scenario are potentially remediable. Possible measures that may ameliorate the dismal statistics associated with HE include routine vaccination against viral Hepatitis B and C, ensuring safe blood transfusion as well as responsible use of alcohol. Screening of those at risk of encephalopathy (liver disease patients) with a psychometric test of good predictability should be part of their routine evaluation in daily practice so as to detect cases of latent encephalopathy. Intensive care facilities and necessary personnel should be provided for the care of these patients in health institution.


   Acknowledgment Top


We acknowledge the Nursing staff for their support in data collation.

 
   References Top

1.Ferenci P, Lockwood A, Mullen K, Tarter R. Hepatic encephalopathy-definition, nomenclature, diagnosis, and quantification: Final report of the working party at the 11 th World Congresses of Gastroenterology, Vienna, 1998. Hepatology 2002;35:716-21.  Back to cited text no. 1
    
2.Poordad F. The burden of hepatic encephalopathy. Aliment Pharmacol Ther 2007;25:3-9.  Back to cited text no. 2
    
3.Yergara-Gomez M, Flavia-Olivella M, Gil-Prades M, Dalmau-Obrador B. Diagnosis and treatment of hepatic encephalopathy in Spain: Results of a survey of hepatologist. Gastroenterology 2006;29:1-6.  Back to cited text no. 3
    
4.Butterworth RF. Pathophysiology of hepatic encephalopathy a new look at ammonia. Metab Brain Dis 2004;17:221-7.  Back to cited text no. 4
    
5.Maqsood S, Saleem A, Iqbal A, Butt JA. Precipitating factors of hepatic encephalopathy: Experience at Pakistan Institute of medical sciences Islamabad. J Ayub Med coll Abottabad 2006;18:58-62.  Back to cited text no. 5
    
6.Ekanem EE, Etuk IS, Uniga AJ. Features of childhood hepatic failure in Calabar, Nigeria. Niger Postgrad Med J 2001;8:86-9.  Back to cited text no. 6
[PUBMED]    
7.Pugh RN, Murray-Lyon IM, Dawson JL, Pietroni MC, Williams R. Transection of the Oesophagus for bleeding varices. British J Surg 1973;60:649-9.  Back to cited text no. 7
    
8.Atterbury CE, Maddrey WC, Conn HO. Neomycin-sorbitol and lactulose in the treatment of acute portal-systemic encephalopathy. A controlled, double-blind clinical trial. Am J Dig Dis 1978;23:398-406.  Back to cited text no. 8
[PUBMED]    
9.Neff GW, Kemmer N, Zacharias VC. Analysis of hospitalisations comparing rifaximin versus lactulose in management of hepatic encephalopathy. Transplant Proct 2006;38:3552-5.  Back to cited text no. 9
    
10.Millward C, Ferriter M, Calver S0, Connell-Jones G. Gluten-and casein- free diets for autistic spectrum disorder. Cochrane database Syst Rev 2008;16: CDOO3498.  Back to cited text no. 10
    
11.Bustamante J, Rimola A, Ventura PJ, Navasa M, Cirera I, Reggiardo V, et al. Prognostic significance of hepatic encephalopathy in patients with cirrhosis. J Hepatol 1999:30:890-5.  Back to cited text no. 11
    
12.Bojuwoye BJ. The burden of viral hepatitis in Africa. West Afr J Med 1997;16:198-203.  Back to cited text no. 12
[PUBMED]    
13.Lavanchy D. Hepatitis B virus epidemiology, disease burden, treatment and current and emerging prevention and control measures. J Viral Hepat 2004;2:97-107.  Back to cited text no. 13
    
14.Ryder SD. Guidelines for the diagnosis and treatment of HCC in adults. Gut 2003;52:1-8.  Back to cited text no. 14
    
15.Bajaj JS, Saeian K, Verber MD, Hischke D, Hoffmann RG. Inhibitory control test is simple method to diagnose minimal hepatic encephalopathy and predict development of overt hepatic encephalopathy. Am J Gastroent 2007;102:754-60.  Back to cited text no. 15
    
16.Iduru S, Hisamuddin K, Mullen KD. Minimal hepatic encephalopathy: Simplifying its diagnosis. Am J Gastroent 2007;102:1537-8.  Back to cited text no. 16
[PUBMED]  [FULLTEXT]  


    Figures

  [Figure 1], [Figure 2], [Figure 3]
 
 
    Tables

  [Table 1], [Table 2], [Table 3], [Table 4], [Table 5]


This article has been cited by
1 Efficacy of rifaximin in prevention of recurrence of hepatic encephalopathy in patients with cirrhosis of liver
Ali B, Zaidi YA, Alam A, Anjum HS
Journal of the College of Physicians and Surgeons Pakistan. 2014; 24(4): 269-273
[Pubmed]
2 Hyperammonaemia induces hepatic injury with alteration of gene expression profiles
Bin Jia,Zu-Jiang Yu,Zhen-Feng Duan,Xin-Quan Lü,Jing-Jing Li,Xiao-Rui Liu,Ran Sun,Xiao-Juan Gao,Yan-Fang Wang,Jing-Ya Yan,Quan-Cheng Kan
Liver International. 2014; 34(5): 748-758
[Pubmed]



 

Top
  
 
  Search
 
    Similar in PUBMED
   Search Pubmed for
   Search in Google Scholar for
 Related articles
    Access Statistics
    Email Alert *
    Add to My List *
* Registration required (free)  

 
  In this article
    Abstract
   Introduction
    Materials and Me...
   Results
   Discussion
   Conclusions
   Acknowledgment
    References
    Article Figures
    Article Tables

 Article Access Statistics
    Viewed3489    
    Printed178    
    Emailed2    
    PDF Downloaded912    
    Comments [Add]    
    Cited by others 2    

Recommend this journal