<?xml version="1.0" encoding="UTF-8"?><!DOCTYPE article  PUBLIC "-//NLM//DTD Journal Publishing DTD v3.0 20080202//EN" "http://dtd.nlm.nih.gov/publishing/3.0/journalpublishing3.dtd"><article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" dtd-version="3.0" xml:lang="en" article-type="research article"><front><journal-meta><journal-id journal-id-type="publisher-id">OJGas</journal-id><journal-title-group><journal-title>Open Journal of Gastroenterology</journal-title></journal-title-group><issn pub-type="epub">2163-9450</issn><publisher><publisher-name>Scientific Research Publishing</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.4236/ojgas.2019.911026</article-id><article-id pub-id-type="publisher-id">OJGas-96657</article-id><article-categories><subj-group subj-group-type="heading"><subject>Articles</subject></subj-group><subj-group subj-group-type="Discipline-v2"><subject>Medicine&amp;Healthcare</subject></subj-group></article-categories><title-group><article-title>
 
 
  Clinical Aspects and Precipitating Factors of Hepatic Encephalopathy Associated with Cirrhosis in a Cameroonian Population
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Mathurin</surname><given-names>Pierre Kowo</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref><xref ref-type="corresp" rid="cor1"><sup>*</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Edgar</surname><given-names>Kenne Yimagou</given-names></name><xref ref-type="aff" rid="aff2"><sup>2</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Firmin</surname><given-names>Ankouane Andoulo</given-names></name><xref ref-type="aff" rid="aff3"><sup>3</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Antonin</surname><given-names>Wilson Ndjitoyap Ndam</given-names></name><xref ref-type="aff" rid="aff2"><sup>2</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Bonaventure</surname><given-names>Jemea</given-names></name><xref ref-type="aff" rid="aff2"><sup>2</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Servais</surname><given-names>Albert Fiacre Eloumou Bagnaka</given-names></name><xref ref-type="aff" rid="aff4"><sup>4</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Patricia</surname><given-names>Ouamba Guekam</given-names></name><xref ref-type="aff" rid="aff5"><sup>5</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Larissa</surname><given-names>Pessidjo</given-names></name><xref ref-type="aff" rid="aff2"><sup>2</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Eric</surname><given-names>Tchoumi Leuwat</given-names></name><xref ref-type="aff" rid="aff3"><sup>3</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Dominique</surname><given-names>Noah Noah</given-names></name><xref ref-type="aff" rid="aff4"><sup>4</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Oudou</surname><given-names>Njoya</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib></contrib-group><aff id="aff4"><addr-line>Faculty of Medicine and Pharmaceutical Sciences, The University of Douala, Douala, Cameroon</addr-line></aff><aff id="aff2"><addr-line>Faculty of Medicine and Biomedical Sciences, The University of Yaoundé I, Yaoundé, Cameroon</addr-line></aff><aff id="aff3"><addr-line>Gastroenterology Unit, Central Hospital, Yaoundé, Cameroon</addr-line></aff><aff id="aff5"><addr-line>Internal Medicine Unit Yaounde University Teaching Hospital, Yaoundé, Cameroon</addr-line></aff><aff id="aff1"><addr-line>Research Laboratory on Viral Hepatitis and Health Communication, Yaoundé, Cameroon</addr-line></aff><pub-date pub-type="epub"><day>15</day><month>11</month><year>2019</year></pub-date><volume>09</volume><issue>11</issue><fpage>228</fpage><lpage>238</lpage><history><date date-type="received"><day>17,</day>	<month>September</month>	<year>2019</year></date><date date-type="rev-recd"><day>25,</day>	<month>November</month>	<year>2019</year>	</date><date date-type="accepted"><day>28,</day>	<month>November</month>	<year>2019</year></date></history><permissions><copyright-statement>&#169; Copyright  2014 by authors and Scientific Research Publishing Inc. </copyright-statement><copyright-year>2014</copyright-year><license><license-p>This work is licensed under the Creative Commons Attribution International License (CC BY). http://creativecommons.org/licenses/by/4.0/</license-p></license></permissions><abstract><p>
 
 
  Background: Hepatic Encephalopathy (HE), a common complication of cirrhosis, is associated with a pejorative prognosis. This study aims to describe the clinical presentation, precipitating factors and outcome of HE. 
  Methods: This was a cross-sectional multicenter inpatient study in cirrhotic patients admitted for HE in four tertiary hospitals in Yaound&#233; (Cameroon) from December 2016 to May 2017. The diagnosis of HE was based on West Haven clinical criteria. The diagnosis of cirrhosis was made using clinical and/or biological, endoscopic and/or ultrasonography signs. 
  Results: A total of 53 patients with HE (mean age: 49.9 &#177; 18.9 years, 35 Males) were included. The frequency of hospital admission for HE was 4.9%. HE grade III was the most common (37.7%), followed by grades I and II (26.4% and 26.4%, respectively). Grade IV was present in 9.4% of cases. According to the Child-Pugh score, 72.1% of the patients were at stage C and 27.9% at stage B. The main precipitating factors found were: constipation (38.5%), hyponatremia (35.9%), hepatocellular carcinoma (HCC) (31.7%), herbal medicine (28.3%), hypokalemia (25.6%), gastrointestinal bleeding (22.6%) and ascitic fluid infection (spontaneous bacterial peritonitis) (13.8%). In 5.7% of cases, no factor was identified. Mortality rate during hospitalization was 45.3% and was significantly associated with stage III (RR = 11.1; 95% CI: 1.9 - 64.5; 
  <em>p</em> = 0.003) and IV (RR = 24; 95% CI: 1.6 - 40.9; 
  <em>p</em> = 0.01) of HE; Child-Pugh C score (RR = 15.2; 95% CI: 1.7 - 30.1; 
  <em>p</em> = 0.003) and hypokalemia (RR = 12.2; 95% CI: 1.3 - 19; 
  <em>p</em> = 0.01). 
  Conclusion: HE is a common complication during cirrhosis with a poor prognosis. In the majority of cases, a precipitating factor could be determined.
 
</p></abstract><kwd-group><kwd>Hepatic Encephalopathy</kwd><kwd> Liver Cirrhosis</kwd><kwd> West Haven Criteria</kwd><kwd> Child-Pugh</kwd><kwd> Cameroon</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Introduction</title><p>Hepatic encephalopathy (HE) associated with cirrhosis is a spectrum of neurological or neuropsychiatric manifestations occurring in patients with hepatic cirrhosis [<xref ref-type="bibr" rid="scirp.96657-ref1">1</xref>]. The symptoms of HE can range from simple neurological disorders detectable only by psychometric tests to coma [<xref ref-type="bibr" rid="scirp.96657-ref2">2</xref>]. The prevalence of overt HE at the time of diagnosis of cirrhosis varies from 10% to 50% depending on whether cirrhosis is compensated or decompensated and/or the presence of transjugular intrahepatic porto-systemic shunt (TIPS) [<xref ref-type="bibr" rid="scirp.96657-ref2">2</xref>]. The positive diagnosis of HE is based on a bundle of arguments in association with a particular clinical context. There are no specific clinical signs associated with HE. This disorder is classified into 4 stages according to the classification of the West Haven Criteria (WHC), ranging from simple neurological disorders detectable by psychometric tests to coma [<xref ref-type="bibr" rid="scirp.96657-ref3">3</xref>]. The onset of HE must be investigated for a precipitating factor, especially an infectious episode, gastrointestinal bleeding, electrolyte imbalance, constipation, diuretic use [<xref ref-type="bibr" rid="scirp.96657-ref4">4</xref>] [<xref ref-type="bibr" rid="scirp.96657-ref5">5</xref>]. HE in liver cirrhosis is disabling and associated with poor prognosis and high mortality without liver transplantation [<xref ref-type="bibr" rid="scirp.96657-ref6">6</xref>] [<xref ref-type="bibr" rid="scirp.96657-ref7">7</xref>] [<xref ref-type="bibr" rid="scirp.96657-ref8">8</xref>]. In Cameroon, due to the high prevalence of chronic viral hepatitis B and C both in general population and in high-risk group population [<xref ref-type="bibr" rid="scirp.96657-ref9">9</xref>] [<xref ref-type="bibr" rid="scirp.96657-ref10">10</xref>], there is a high incidence of cirrhosis and its complications, including HE. Data on HE during cirrhosis is scarce. We therefore, sought to describe the clinical presentation, precipitating factors and outcome of HE among cirrhotic patients.</p></sec><sec id="s2"><title>2. Methods</title><sec id="s2_1"><title>2.1. Study Population</title><p>This was a cross-sectional multicenter inpatient study on cirrhotic admitted for HE in the internal medicine departments of the Yaounde Teaching Hospital, the Yaounde General Hospital, the Yaounde Military Hospital and the gastroenterology department of Yaounde Central Hospital. This study was conducted over a period of 6 months, from December 2016 to May 2017.</p><p>All patients with hepatic cirrhosis complicated by HE and hospitalized in the study sites were included. Patients with chronic liver disease other than cirrhosis, acute liver disease and neurological impairment other than HE associated to cirrhosis were excluded.</p></sec><sec id="s2_2"><title>2.2. Diagnosis of Cirrhosis and of HE</title><p>The diagnosis of cirrhosis was based on clinical and/or biological (including signs of liver failure and portal hypertension) and/or ultrasonographic signs of cirrhosis (irregular aspect of the liver surface, liver parenchymal texture heterogenous, dilatation of the portal venous system vessels) and/or endoscopic signs of portal hypertension. HE was diagnosed based on clinical signs and they were classified using the WHC classification [<xref ref-type="bibr" rid="scirp.96657-ref3">3</xref>].</p></sec><sec id="s2_3"><title>2.3. Data Collection</title><p>Participants in the study were conveniently recruited. Data collected included age, gender, symptoms of HE, signs and symptoms of cirrhosis, signs and symptoms of infection. Laboratory investigations requested included: serum electrolytes, random blood glucose, renal function tests, hepatitis B surface antigen, and hepatitis C antibodies. Ascitic tap was done and sent for analysis in order to diagnose spontaneous bacterial peritonitis (SBP). The diagnosis of SBP was made in presence of more than 250 of polymorphonuclear cells per ml. Any identified HE precipitating factor was recorded and during hospitalization, clinical outcome was also recorded.</p></sec><sec id="s2_4"><title>2.4. Statistical Analysis</title><p>Data was registered using CsPro 6.3 software and analyzed using SPSS 23.0 software (SPSS Inc., Chicago, IL). Relative risk (RR) and the 95% confidence interval (95% CI) were calculated to assess associations between mortality and stage of HE, severity of cirrhosis and precipitating factors of HE in univariate analysis. A p value of &lt;0.05 was considered significant.</p></sec></sec><sec id="s3"><title>3. Ethical Considerations</title><p>Ethical clearance was obtained from the Institutional Research Ethical Committee of the Faculty of Medicine and Biomedical Sciences of the University of Yaound&#233; I. The administrative authorizations were received from directors of the various hospitals involved in the study and written consent were obtained from all patients included or from their guardians.</p></sec><sec id="s4"><title>4. Results</title><p>Characteristics of the study population</p><p>During the study period, 53 (4.9%) patients with cirrhosis associated HE were enrolled out of 1081 hospitalized patients. The mean age was 49.9 &#177; 18.9 years (minimum: 17 and maximum: 85 years). The sex ratio was 2.3.</p><p>Etiologies of cirrhosis</p><p>The most frequent cause of cirrhosis was chronic hepatitis B virus alone (60%), followed by chronic hepatitis C virus alone (22.6%), hepatitis B virus associated to hepatitis D virus (7.5%) and alcohol consumption alone (3.8%). In 5.7% of cases the etiology of cirrhosis was unknown. The characteristics of patients are summarized in <xref ref-type="table" rid="table1">Table 1</xref>.</p><p>Description of the different clinical aspects of HE</p><p>According to the WHC, stage III of HE was the most represented (37.7%), followed by grades I and II, respectively in 26.4% and 26.4% of cases. Grade IV</p><table-wrap id="table1" ><label><xref ref-type="table" rid="table1">Table 1</xref></label><caption><title> Baseline characteristics of the study population</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Variables</th><th align="center" valign="middle" >Number</th><th align="center" valign="middle" >Percentage (%)</th></tr></thead><tr><td align="center" valign="middle" >Gender Male Female</td><td align="center" valign="middle" >37 16</td><td align="center" valign="middle" >69.8 30.2</td></tr><tr><td align="center" valign="middle" >Age groups Mean &#177; SD (49.9 &#177; 18.9) &lt;20 20 - 40 41 - 60 &gt;60</td><td align="center" valign="middle" >1 21 12 19</td><td align="center" valign="middle" >1.9 39.6 22.6 35.8</td></tr><tr><td align="center" valign="middle" >Comorbidities Diabetes HIV Hypertension Alcohol HCC</td><td align="center" valign="middle" >8 5 8 11 7</td><td align="center" valign="middle" >15.1 10 15.1 20.8 13.2</td></tr><tr><td align="center" valign="middle" >Etiologies of cirrhosis HBV HCV Alcohol Not identified</td><td align="center" valign="middle" >32 12 2 3</td><td align="center" valign="middle" >60 22.6 3.8 5.7</td></tr><tr><td align="center" valign="middle" >Child Pugh score Child B Child C</td><td align="center" valign="middle" >12 31</td><td align="center" valign="middle" >27.9 72.1</td></tr><tr><td align="center" valign="middle" >Outcome Alive Dead</td><td align="center" valign="middle" >29 24</td><td align="center" valign="middle" >54.7 45.3</td></tr><tr><td align="center" valign="middle" >Biological parameters (Mean &#177; SD) Bilirubin (mg/l) Albumin (g/l) TP (%) Glycemia (g/l) Creatinemia (mg/l) Natremia (mEq/l) Kalemia (mEq/l)</td><td align="center" valign="middle"  colspan="2"  >57.2 &#177; 80 20.3 &#177; 14.4 46.9 &#177; 27.4 0.8 &#177; 0.6 13.6 &#177; 16.5 103.5 &#177; 59.9 3.02 &#177; 1.9</td></tr><tr><td align="center" valign="middle" >Duration of hospitalization (days)</td><td align="center" valign="middle"  colspan="2"  >8.7 &#177; 6</td></tr></tbody></table></table-wrap><p>was present in 9.4% of cases. Distribution of the grade of HE is show in <xref ref-type="table" rid="table2">Table 2</xref>.</p><p>Child-Pugh classification could be performed in 43 patients. According to this score, 31 patients (72.1%) and 12 patients (27.9%) were classified Child C and Child B respectively.</p><p>Precipitating factors</p><p>The main precipitating factors found were: constipation (37.7%), herbal medicine (28.3%), hyponatremia (26.4%), HCC (24.5%), gastrointestinal bleeding (22.6%), hypokalemia (15%), and ascitic fluid infection (7.5%). No factor was identified in 5.7% of participants. The precipitating factors are detailed in <xref ref-type="table" rid="table3">Table 3</xref>.</p><p>Outcome:</p><p>The mortality rate during hospitalization was 45.3%. The average admission duration was 8.7 &#177; 6 days. Mortality was significantly associated with stages III [RR = 11.1; 95% CI: 1.9 - 64.5; p = 0.003] and IV [RR = 24; 95% CI: 1.6 - 40.9; p = 0.01] of HE, Child C score of cirrhosis [RR = 15.2; 95% CI: 1.7 - 30.1; p = 0.003] and Hypokaliemia [RR = 12.2; 95% CI: 1.3 - 19; p = 0.01] (<xref ref-type="table" rid="table4">Table 4</xref>).</p><table-wrap id="table2" ><label><xref ref-type="table" rid="table2">Table 2</xref></label><caption><title> Grades of HE according to the WHC classification</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Stages</th><th align="center" valign="middle" >Number</th><th align="center" valign="middle" >Percentage (%)</th></tr></thead><tr><td align="center" valign="middle" >Stage I</td><td align="center" valign="middle" >14</td><td align="center" valign="middle" >26.4</td></tr><tr><td align="center" valign="middle" >Stage II</td><td align="center" valign="middle" >14</td><td align="center" valign="middle" >26.4</td></tr><tr><td align="center" valign="middle" >Stage III</td><td align="center" valign="middle" >20</td><td align="center" valign="middle" >37.7</td></tr><tr><td align="center" valign="middle" >Stage IV</td><td align="center" valign="middle" >5</td><td align="center" valign="middle" >9.4</td></tr><tr><td align="center" valign="middle" >Total</td><td align="center" valign="middle" >53</td><td align="center" valign="middle" >100</td></tr></tbody></table></table-wrap><table-wrap id="table3" ><label><xref ref-type="table" rid="table3">Table 3</xref></label><caption><title> The precipitating factors of HE</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Variables</th><th align="center" valign="middle" >Number</th><th align="center" valign="middle" >Percentage (%)</th></tr></thead><tr><td align="center" valign="middle" >SBP</td><td align="center" valign="middle" >4</td><td align="center" valign="middle" >7.5</td></tr><tr><td align="center" valign="middle" >Gastrointestinal bleeding</td><td align="center" valign="middle" >12</td><td align="center" valign="middle" >22.6</td></tr><tr><td align="center" valign="middle" >Constipation</td><td align="center" valign="middle" >20</td><td align="center" valign="middle" >37.7</td></tr><tr><td align="center" valign="middle" >Hypokaliemia</td><td align="center" valign="middle" >8</td><td align="center" valign="middle" >15</td></tr><tr><td align="center" valign="middle" >Hyponatremia</td><td align="center" valign="middle" >14</td><td align="center" valign="middle" >26.4</td></tr><tr><td align="center" valign="middle" >Herbal medicine</td><td align="center" valign="middle" >15</td><td align="center" valign="middle" >28.3</td></tr><tr><td align="center" valign="middle" >Diuretics overdose</td><td align="center" valign="middle" >6</td><td align="center" valign="middle" >11.3</td></tr><tr><td align="center" valign="middle" >Paracentesis</td><td align="center" valign="middle" >2</td><td align="center" valign="middle" >3,8</td></tr><tr><td align="center" valign="middle" >Diarrhoea</td><td align="center" valign="middle" >8</td><td align="center" valign="middle" >15</td></tr><tr><td align="center" valign="middle" >HCC</td><td align="center" valign="middle" >13</td><td align="center" valign="middle" >24.5</td></tr><tr><td align="center" valign="middle" >Sedative drugs intake</td><td align="center" valign="middle" >1</td><td align="center" valign="middle" >1.9</td></tr><tr><td align="center" valign="middle" >Unidentified</td><td align="center" valign="middle" >3</td><td align="center" valign="middle" >5.7</td></tr><tr><td align="center" valign="middle" >Cutaneous infection</td><td align="center" valign="middle" >3</td><td align="center" valign="middle" >5.7</td></tr><tr><td align="center" valign="middle" >Lower respiratory tract infection</td><td align="center" valign="middle" >3</td><td align="center" valign="middle" >5.7</td></tr><tr><td align="center" valign="middle" >Urinary tract infection</td><td align="center" valign="middle" >2</td><td align="center" valign="middle" >3.8</td></tr><tr><td align="center" valign="middle" >Malaria</td><td align="center" valign="middle" >1</td><td align="center" valign="middle" >1.9</td></tr><tr><td align="center" valign="middle" >Vomiting</td><td align="center" valign="middle" >1</td><td align="center" valign="middle" >1.9</td></tr></tbody></table></table-wrap><table-wrap id="table4" ><label><xref ref-type="table" rid="table4">Table 4</xref></label><caption><title> Factors associated to mortality of HE</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Factors</th><th align="center" valign="middle" >Mortality n (%)</th><th align="center" valign="middle" >RR</th><th align="center" valign="middle" >IC &#224; 95%</th><th align="center" valign="middle" >P</th></tr></thead><tr><td align="center" valign="middle" >Precipitating factors</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Gastrointestinal bleeding<sup> </sup></td><td align="center" valign="middle" >6 (25.0)</td><td align="center" valign="middle" >1.2</td><td align="center" valign="middle" >0.3 - 4.6</td><td align="center" valign="middle" >0.7</td></tr><tr><td align="center" valign="middle" >Constipation</td><td align="center" valign="middle" >8 (34.8)</td><td align="center" valign="middle" >0.7</td><td align="center" valign="middle" >0.2 - 2.3</td><td align="center" valign="middle" >0.6</td></tr><tr><td align="center" valign="middle" >Hyponatremia</td><td align="center" valign="middle" >6 (35.3)</td><td align="center" valign="middle" >0.9</td><td align="center" valign="middle" >0.25 - 3.5</td><td align="center" valign="middle" >0.9</td></tr><tr><td align="center" valign="middle" >Hypokaliemia</td><td align="center" valign="middle" >7 (36.8)</td><td align="center" valign="middle" >12.2</td><td align="center" valign="middle" >1.3 - 19</td><td align="center" valign="middle" >0.01</td></tr><tr><td align="center" valign="middle" >Diuretics overdose</td><td align="center" valign="middle" >4 (18.2)</td><td align="center" valign="middle" >3.0</td><td align="center" valign="middle" >0.4 - 18.1</td><td align="center" valign="middle" >0.3</td></tr><tr><td align="center" valign="middle" >Diarrhoea</td><td align="center" valign="middle" >6 (25.0)</td><td align="center" valign="middle" >4.5</td><td align="center" valign="middle" >0.8 - 24.8</td><td align="center" valign="middle" >0.1</td></tr><tr><td align="center" valign="middle" >Paracentesis</td><td align="center" valign="middle" >1 (4.2)</td><td align="center" valign="middle" >1.2</td><td align="center" valign="middle" >0.07 - 20.5</td><td align="center" valign="middle" >1.0</td></tr><tr><td align="center" valign="middle" >HCC</td><td align="center" valign="middle" >7 (41.2)</td><td align="center" valign="middle" >2.1</td><td align="center" valign="middle" >0.5 - 7.9</td><td align="center" valign="middle" >0.2</td></tr><tr><td align="center" valign="middle" >Herbal medicine</td><td align="center" valign="middle" >5 (20.8)</td><td align="center" valign="middle" >0.5</td><td align="center" valign="middle" >0.1 - 1.7</td><td align="center" valign="middle" >0.2</td></tr><tr><td align="center" valign="middle" >Urinary tract infection</td><td align="center" valign="middle" >2 (8.3)</td><td align="center" valign="middle" >1.2</td><td align="center" valign="middle" >0.1 - 9.4</td><td align="center" valign="middle" >1.0</td></tr><tr><td align="center" valign="middle" >Cutaneous infection</td><td align="center" valign="middle" >2 (8.3)</td><td align="center" valign="middle" >2.5</td><td align="center" valign="middle" >0.2 - 29.9</td><td align="center" valign="middle" >0.5</td></tr><tr><td align="center" valign="middle" >Lower respiratory tract infection</td><td align="center" valign="middle" >3 (12.5)</td><td align="center" valign="middle" >2.3</td><td align="center" valign="middle" >1.7 - 3.2</td><td align="center" valign="middle" >0.08</td></tr><tr><td align="center" valign="middle" >Vomiting</td><td align="center" valign="middle" >1 (4.2)</td><td align="center" valign="middle" >2,2</td><td align="center" valign="middle" >1.7- 3.1</td><td align="center" valign="middle" >0.4</td></tr><tr><td align="center" valign="middle" >Grades of HE</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Grade I</td><td align="center" valign="middle" >2 (8.3)</td><td align="center" valign="middle" >1</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td></tr><tr><td align="center" valign="middle" >Grade II</td><td align="center" valign="middle" >5 (20.8)</td><td align="center" valign="middle" >3.3</td><td align="center" valign="middle" >0.5 - 21.7</td><td align="center" valign="middle" >0.3</td></tr><tr><td align="center" valign="middle" >Grade III</td><td align="center" valign="middle" >13 (54.2)</td><td align="center" valign="middle" >11.1</td><td align="center" valign="middle" >1.9 - 64.5</td><td align="center" valign="middle" >0.003</td></tr><tr><td align="center" valign="middle" >Garde IV</td><td align="center" valign="middle" >4 (16.7)</td><td align="center" valign="middle" >24</td><td align="center" valign="middle" >1.6 - 40.9</td><td align="center" valign="middle" >0.01</td></tr><tr><td align="center" valign="middle" >Severity of cirrhosis</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Child B</td><td align="center" valign="middle" >1 (2.3</td><td align="center" valign="middle" >1</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td></tr><tr><td align="center" valign="middle" >Child C</td><td align="center" valign="middle" >18 (41.9)</td><td align="center" valign="middle" >15.2</td><td align="center" valign="middle" >1.7 - 30.1</td><td align="center" valign="middle" >0.003</td></tr></tbody></table></table-wrap><p>RR: Relative Risk; CI: Confidence Interval; HCC: Hepatocellular Carcinoma.</p></sec><sec id="s5"><title>5. Discussion</title><p>This study aimed to describe the clinical profile of cirrhosis associated HE, specifically to describe the clinical aspects of HE, determine precipitating factors, and the outcome of cirrhotic related HE in Cameroon.</p><sec id="s5_1"><title>5.1. Age and Sex</title><p>The mean age of patients with HE was 49.9 &#177; 18.9 years old. The relatively young age of these patients could be explained by the etiology of cirrhosis. Indeed, the most common cause of cirrhosis in Cameroon is chronic HBV infection, which affects mostly young people [<xref ref-type="bibr" rid="scirp.96657-ref9">9</xref>]. In this area of high endemicity for HBV infection, high prevalence of the HBV infection has mainly been attributed to HBV transmission occurring predominantly early in the life either through mother to child transmission or horizontal transmission [<xref ref-type="bibr" rid="scirp.96657-ref11">11</xref>] [<xref ref-type="bibr" rid="scirp.96657-ref12">12</xref>].</p><p>HE was most common in men (69.8%). The reason for this finding is not clear but similar results have been reported by some other studies. In the study on precipitating factors and treatment outcomes of hepatic encephalopathy in Liver Cirrhosis in Nepal by Poudyal et al., 78% of patients included were male [<xref ref-type="bibr" rid="scirp.96657-ref5">5</xref>]. In another study by Gad et al. in Egypt 63.3% of patients with HE in liver cirrhosis were male [<xref ref-type="bibr" rid="scirp.96657-ref13">13</xref>]. This could be as the result of men being more exposed to various risk factors of cirrhosis.</p></sec><sec id="s5_2"><title>5.2. Etiologies of Cirrhosis</title><p>Chronic HBV was found to be the main etiology of cirrhosis in our study. HBV infection is frequent in Cameroon which is considered as one of most affected countries in the world with an overall pooled prevalence of 11.2% [<xref ref-type="bibr" rid="scirp.96657-ref9">9</xref>]. The predominance of hepatitis B as the etiology of cirrhosis could be explained by the high prevalence of HBV in Cameroonian population. Chronic HCV was found in 22.6% of patients. The high prevalence of HCV reported by several studies in the Cameroonian population [<xref ref-type="bibr" rid="scirp.96657-ref14">14</xref>] [<xref ref-type="bibr" rid="scirp.96657-ref15">15</xref>] might explained this finding.</p></sec><sec id="s5_3"><title>5.3. Description of the Different Clinical Aspects of HE</title><p>Grade III of HE was the most represented type in this study. Gad Y et al. in Egypt [<xref ref-type="bibr" rid="scirp.96657-ref13">13</xref>] and Devrajani et al. in Pakistan [<xref ref-type="bibr" rid="scirp.96657-ref16">16</xref>] respectively reported a 54.0% (128/237) and 80% (70/87) prevalence of grade III and grade IV HE among admitted patients presenting with signs and symptoms of HE. Most patients in resource limited settings usually present with advanced disease due to late consultations and this might explain the above finding.</p></sec><sec id="s5_4"><title>5.4. Precipitating Factors</title><p>Constipation, herbal medicine, hyponatremia, HCC and gastrointestinal bleeding were the most frequent precipitating factors of HE in our study population. These findings are consistent with those reported by several authors in Pakistan, Egypt and United States of America [<xref ref-type="bibr" rid="scirp.96657-ref4">4</xref>] [<xref ref-type="bibr" rid="scirp.96657-ref13">13</xref>] [<xref ref-type="bibr" rid="scirp.96657-ref17">17</xref>]. In our study, constipation appears to be the most frequent precipitating factor of HE (37.7%). In fact, gastrointestinal symptoms are common in cirrhotics and constipation has been reported in 8% of cases [<xref ref-type="bibr" rid="scirp.96657-ref18">18</xref>]. The underlying mechanisms are complex and involve abnormalities in gut motility such as delayed gastric emptying, altered intestinal permeability [<xref ref-type="bibr" rid="scirp.96657-ref19">19</xref>]. Patients with advance cirrhosis are more at risk of developing gut dysfunctions symptoms [<xref ref-type="bibr" rid="scirp.96657-ref19">19</xref>]. In this study 72% of patients were stage C of Child-Pugh classification and hence justifying constipation as the most common precipitating factor of HE.</p><p>The frequency of electrolytes imbalance was high (hyponatremia: 26.4%; Hypokaliemia: 15%) and could be partly explained by the effect of diuretics on one hand and secondary hyperaldosteronism on the other hand. Diarrhea found in 15% of cases could also contribute to electrolytes abnormalities in this study. Spontaneous bacterial peritonitis was found in 4 patients (7.4%). Increase intestinal permeability, bacterial translocation and decrease in host immunity have been associated with SBP in advanced liver cirrhosis [<xref ref-type="bibr" rid="scirp.96657-ref20">20</xref>]. Therapeutic ascitic tap done in dubious conditions in some cases could also explain some cases of ascitic fluid infections. In some patients (5.7%), no precipitating factor was identified.</p></sec></sec><sec id="s6"><title>6. Outcome</title><p>The mortality rate associated with HE was 45.3% and significantly associated with stages III (p = 0.003) and IV (p = 0.01) of HE, Child C score of cirrhosis (p = 0.003) and Hypokaliemia (p = 0.01). Similar high mortality rates have been reported by studies in Africa. In 2016, Ntagirabiri et al. found a 56% HE mortality rate among cirrhotic patients [<xref ref-type="bibr" rid="scirp.96657-ref7">7</xref>]. In Nigeria, Onyek were reported a mortality rate of 48% [<xref ref-type="bibr" rid="scirp.96657-ref21">21</xref>]. This high mortality rate could be explained firstly by the severity of cirrhosis because the majority of patients usually consult in advanced stage of the disease and secondly by the various complications associated with cirrhosis. More so the absence of optimal treatment for certain complications and of liver transplantation in our setting could also explain this high mortality rate. Electrolyte imbalance is common in cirrhotic patients with hyponatremia being most frequently associated with hepatic encephalopathy [<xref ref-type="bibr" rid="scirp.96657-ref22">22</xref>]. In our study, only hypokalemia was found to be significantly associated with mortality among Cameroonian patients with cirrhosis related hepatic encephalopathy. Hypokalemia has been shown to induce hepatic encephalopathy and this is modulated by the kidneys. As less potassium enters the collecting tubules, more hydrogen ions are moved into the cells leading to increase intracellular acidosis. This triggers the conversion of glutamine to ammonia and bicarbonate. The ammonia is selectively either excreted in urine or returned to venous circulation. Ammonia that subsequently enters portal circulation is not metabolized by the cirrhotic patient likely therefore to precipitate hepatic encephalopathy [<xref ref-type="bibr" rid="scirp.96657-ref23">23</xref>].</p>Limitations of the Study<p>One of the limitations of this study is that electroencephalography and brain scan were not done in certain cases to exclude central nervous system involvement. The retrospective nature of the study reduced the number of included files because of their incomplete nature.</p></sec><sec id="s7"><title>7. Conclusion</title><p>HE is a frequent complication during cirrhosis with a high mortality. The main precipitating factors were constipation, herbal medicine, electrolyte imbalance, gastrointestinal bleeding and HCC.</p></sec><sec id="s8"><title>Data Availability</title><p>All the data used to support the findings of this study are available from the corresponding author upon request.</p></sec><sec id="s9"><title>Authors Contributions</title><p>This work was jointly carried out by all the authors.</p><p>Author MK contributed in collection of data, analysis and editing the article; Author FA contributed in study conception and editing the article. Author EKY wrote the protocol and the first draft of the manuscript. Authors AWNN, BJ, SFEB, POG, ETL, DNN contributed in collection of data and follow-up of the patients. Author ON supervised all the activities and approved the final version to be submitted for publication. All authors read and approved the final manuscript.</p></sec><sec id="s10"><title>Acknowledgements</title><p>None.</p></sec><sec id="s11"><title>Funding</title><p>No funding was available for this study.</p></sec><sec id="s12"><title>Conflicts of Interest</title><p>The authors declare no conflicts of interest regarding the publication of this paper.</p></sec><sec id="s13"><title>Cite this paper</title><p>Kowo, M.P., Yimagou, E.K., Andoulo, F.A., Ndam, A.W.N., Jemea, B., Bagnaka, S.A.F.E., Guekam, P.O., Pessidjo, L., Leuwat, E.T., Noah, D.N. and Njoya, O. (2019) Clinical Aspects and Precipitating Factors of Hepatic Encephalopathy Associated with Cirrhosis in a Cameroonian Population. Open Journal of Gastroenterology, 9, 228-238. https://doi.org/10.4236/ojgas.2019.911026</p></sec></body><back><ref-list><title>References</title><ref id="scirp.96657-ref1"><label>1</label><mixed-citation publication-type="other" xlink:type="simple">Weissenborn, K. 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