<?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.2015.57017</article-id><article-id pub-id-type="publisher-id">OJGas-58223</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>
 
 
  Prognostic Factors for Cirrhosis Hospital in Abidjan (C&#244;te d’Ivoire)
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>amert</surname><given-names>Fulgence Yao Bathaix</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>Akelesso</surname><given-names>Bagny</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Kouamé</surname><given-names>Alassane Mahassadi</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Anassé</surname><given-names>Jean-Baptiste Okon</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Ya</surname><given-names>Henriette Kissi-Anzouan</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Stanislas</surname><given-names>Doffou</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Aboubacar</surname><given-names>Demba Bangoura</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Hatrydt</surname><given-names>Dimitri Kouamé</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Kadiatou</surname><given-names>Diallo</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Antonin</surname><given-names>N’Dam</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Aoudi</surname><given-names>Ousman De</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Koffi</surname><given-names>Alain Attia</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Aya</surname><given-names>Thérèse N’dri Yoman</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib></contrib-group><aff id="aff1"><addr-line>Department of Hepatology and Gastroenterology of the Centre Hospitalier Universitaire de Yopougon (CHU-Y), 
Abidjan, Cote d’Ivoire</addr-line></aff><author-notes><corresp id="cor1">* E-mail:<email>bathaixful@yahoo.fr(AFYB)</email>;</corresp></author-notes><pub-date pub-type="epub"><day>15</day><month>07</month><year>2015</year></pub-date><volume>05</volume><issue>07</issue><fpage>103</fpage><lpage>109</lpage><history><date date-type="received"><day>17</day>	<month>June</month>	<year>2015</year></date><date date-type="rev-recd"><day>accepted</day>	<month>20</month>	<year>July</year>	</date><date date-type="accepted"><day>23</day>	<month>July</month>	<year>2015</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>
 
 
  Cirrhosis is the cause of a high rate of death in hospitals. The aim of this research was to estimate the incidence of mortality and identify the risk factors associated with cirrhosis patients in hospital in Cote d’Ivoire. Methodology: It is a retrospective study covering from January 1st, 2002 to December 31st, 2011 at Centre Hospitalier et Universitaire de Yopougon in Abidjan. We concerned the cirrhosis patients that have been followed at the hepatology and gastroenterology department. Survival was estimated by the Kaplan-Meier curve and comparison of survival curves by the log-rank test. The multi-varied analysis of the survivals has been achieved with the Cox proportional Hazard regression. A p value &lt; 0.05 was taken as significant. Results: We recruited, 221 patients (135 men) of whom the medium age was 59 &#177; 15.12 years. Among those patients, 34.5% were classified as Child Pugh C and 52.94% Child Pugh B, 19.45% suffered from digestive hemorrhage, 26.5% suffered from renal deficiency, 47% suffered from hepatic encephalopathy and 10.7% from hyponatremia. The median overall survival of patients was 0.50 person-months. The variables that were significantly associated to a reduction of survival were hepatic encephalopathy (p = 0.0029), spontaneous ascitesfluid infection (p = 0.0208), hyponatremia (p = 0.0434) and stage Cof Child- Pugh score (p = 0.046). Conclusion: The incidence of mortality in cirrhotic patients hospitalized in Abidjan is high. Pejorative prognostic factors were essentially hepatic encephalopathy, spontaneous ascites fluid infection, hyponatremia and stage C of Child-Pugh score.
 
</p></abstract><kwd-group><kwd>Cirrhosis</kwd><kwd> Portal Hypertension</kwd><kwd> Child-Pugh</kwd><kwd> Encephalopathy</kwd><kwd> Prognostic</kwd><kwd> C&#244;te d’Ivoire</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Introduction</title><p>Cirrhosis is the final stage of development of liver fibrosis induced more by chronic liver disease. It is defined by the existence of an architectural modification diffuse hepatic parenchyma characterized by the existence of extensive fibrosis, dissecting and delimiting annular hepatocyte nodules so-called regeneration [<xref ref-type="bibr" rid="scirp.58223-ref1">1</xref>] . The complications of cirrhosis are frequent and potentially serious: portal hypertension, the cause of bleeding from ruptured gastroesophageal varices, hepatic encephalopathy, infection of ascites fluid, hepatorenal syndrome and hepatocellular carcinoma [<xref ref-type="bibr" rid="scirp.58223-ref2">2</xref>] .</p><p>Cirrhosis is an important hepatobiliary disorder under our tropics [<xref ref-type="bibr" rid="scirp.58223-ref3">3</xref>] and is the leading cause of hospitalize- tion for chronic liver disease in gastro enterology hospital in C&#244;te d’Ivoire [<xref ref-type="bibr" rid="scirp.58223-ref4">4</xref>] .</p><p>The management of portal hypertension with cirrhotic patients is a major concern for hospital practitioners. It is the cause of a high rate of mortality [<xref ref-type="bibr" rid="scirp.58223-ref5">5</xref>] [<xref ref-type="bibr" rid="scirp.58223-ref6">6</xref>] . In fact, many factors predispose cirrhosis patient to the risk of unexpected arrival of a multi deep-rooted default likely to imperil the vital prognostic: immune dysregulation that will promote the risk of infection, pulmonary involvement by the hepatopulmonary syndrome, a decrease of coagulation factors and renal hypoperfusion caused by the hepatorenal syndrome [<xref ref-type="bibr" rid="scirp.58223-ref7">7</xref>] . The evaluation of the prognosis of cirrhotic patients followed in hospitalization would improve their care. We conducted this study in cirrhotic patients in order to estimate the death incidence and to identify risk factors to which cirrhotic patients in Ivorian hospitals are exposed.</p></sec><sec id="s2"><title>2. Methodology</title><sec id="s2_1"><title>2.1. Study Oversight</title><p>From January 2002 through December 2011, we consecutively enrolled patients with cirrhosis and portal hypertension who were admitted to Centre Hospitalier et Universitaire de Yopougon in Abidjan. No commercial support was involved in the study. All the authors vouch for the integrity and the accuracy of the analysis and for the fidelity of the study. No one who is not an author contributed to the manuscript.</p></sec><sec id="s2_2"><title>2.2. Selection of Patients</title><p>Patients who had cirrhosis and portal hypertension were considered for the inclusion. The diagnosis of cirrhosis was based on the combination of clinical, biological, echographical and/or endoscopical criteria. Exclusion criteria were a lost sight below12-months-follow-up and hepatocellular carcinoma (HCC) at the inclusion, whose diagnosis was based on the Barcelona criteria.</p></sec><sec id="s2_3"><title>2.3. Studied Variables</title><p>The sociodemo graphic variables were the age, the gender and the socioeconomic status. The clinic variables studied were ascites, limbs edema, gastrointestinal bleeding, hepatic encephalopathy. The endoscopic variables were the esophageal varices, the gastric varices and the portal hypertensive gastropathy. The biological variables were the prothrombin rate, the bilirubin, the albuminemia, the natremia, the creatinine and the platelets. The etiology of cirrhosis has also been studied.</p><p>These data were collected from the files of hospitalized patients on pre-established survey forms.</p></sec><sec id="s2_4"><title>2.4. Statistical Analysis</title><p>The results are expressed as frequency, percentage, or mean &#177; standard deviation and median. The survival is estimated by the Kaplan-Meier Curve and the comparison of survival curbs by the Log-rank test. The multivariable analysis was conducted with Cox proportional Hazard regression. A p value &lt; 0.05 was taken as significant.</p></sec></sec><sec id="s3"><title>3. Results</title><p>Over the period of our study we recruited 221 patients (135 men) with an average of 59 &#177; 15.12 years. The middle socio-economic status was the most represented with 56.15% of the patients. The main etiology of cirrhosis was HVB (76.04%) followed by alcohol. The edema and ascites syndrome was present in almost all patients. Also 19.45% of patients had gastrointestinal bleeding and hepatic encephalopathy (47.05%). On average, patients had a high rate of creatinine (16.18 mg/L &#177; 19.58) and a decreasing of platelet (131.27 &#215; 10<sup>9</sup> L<sup>−</sup><sup>1</sup> &#177; 96.82). Patients were classified as Child-Pugh B and C in the respective proportions of 52.92% and 32.76%. The epidemiological, clinical, biological and endoscopic characteristics of the patients during their hospitalization are shown in <xref ref-type="table" rid="table1">Table 1</xref>.</p><p>The overall survival of patients was between 0.03 and 16.66 person-months, with a median of 0.50 person-months (<xref ref-type="fig" rid="fig1">Figure 1</xref>).In univariate analysis, hepatic encephalopathy, Child-Pugh C, renal failure, spontaneous ascites fluid infection (SAI) and hyponatremia were associated with a significant survival decrease. However, the diuretic outlet would significantly improve the survival (<xref ref-type="table" rid="table2">Table 2</xref>).</p><p>Stage C of the Child-Pugh score was associated with a significant increase (p = 0.046) of 3.351 times of death</p><table-wrap id="table1" ><label><xref ref-type="table" rid="table1">Table 1</xref></label><caption><title> Demographics, clinical, biological and endoscopic characteristics of patients</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Number of patients</th><th align="center" valign="middle" >221</th></tr></thead><tr><td align="center" valign="middle" >Socio-demography</td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >-Age</td><td align="center" valign="middle" >14 years - 86 years (59 &#177; 15.12 years)</td></tr><tr><td align="center" valign="middle" >-Sex ratio (M/F)</td><td align="center" valign="middle" >2.06</td></tr><tr><td align="center" valign="middle" >-Socioeconomic status</td><td align="center" valign="middle" >high (8), middle (117), low (80), unspecified (16)</td></tr><tr><td align="center" valign="middle" >Etiology</td><td align="center" valign="middle" >HBV<sup>*</sup> (76.04%), alcohol (11.06%) not identified (9%), HCV<sup>**</sup> (3%)</td></tr><tr><td align="center" valign="middle" >Clinic</td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >-Ascites &#177; edema in the lowerextremities</td><td align="center" valign="middle" >ascite (136), ascite + ankle edema (91)</td></tr><tr><td align="center" valign="middle" >-gastrointestinal bleeding</td><td align="center" valign="middle" >43</td></tr><tr><td align="center" valign="middle" >- hepatic encephalopathy</td><td align="center" valign="middle" >104</td></tr><tr><td align="center" valign="middle" >Portal hypertension endoscopicsigns (113 patients)</td><td align="center" valign="middle" >OVs<sup>***</sup> stage I (20), OVs Stage II (58), OVs stage III (35), bleeding gastric varices (04) Gastropathy http (71)</td></tr><tr><td align="center" valign="middle" >Biologicalparameters</td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >-Prothrombinrate (N ≥ 70%)</td><td align="center" valign="middle" >16% - 100% (mean 57.27 &#177; 23.21; median 55)</td></tr><tr><td align="center" valign="middle" >- Bilirubin (N ˂ 10 mg/l)</td><td align="center" valign="middle" >0.28 - 6.2 mg/l (mean30.66 &#177; 23.64; median 22.5)</td></tr><tr><td align="center" valign="middle" >-Albumin (N = 35 - 50 g/l)</td><td align="center" valign="middle" >6.1 - 63.7 g/l (mean 25.35 &#177; 9.98; median 25)</td></tr><tr><td align="center" valign="middle" >-Natremia (N = 135 - 145 meq/l)</td><td align="center" valign="middle" >96 - 172 meq/l (mean 135.08 &#177; 9.52; median 135)</td></tr><tr><td align="center" valign="middle" >-Creatinine (N ˂ 15)</td><td align="center" valign="middle" >3 - 176 mg/l (mean 16.18 &#177; 19.58; median 10.25)</td></tr><tr><td align="center" valign="middle" >-platelets (N = 150 - 450 GIGA/L)</td><td align="center" valign="middle" >14 - 670 GIGA/L (mean 131.27 &#177; 96.82; median 108)</td></tr><tr><td align="center" valign="middle" >Child Pugh score</td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Stage A/Stage B/Stage C</td><td align="center" valign="middle" >28/117/76</td></tr></tbody></table></table-wrap><p>HBV<sup>*</sup>: hepatitis B; HCV<sup>**</sup>: Hepatitis C; OVs<sup>***</sup>: Bleeding esophageal varices.</p><table-wrap id="table2" ><label><xref ref-type="table" rid="table2">Table 2</xref></label><caption><title> Prognostic factors in univariate analysis</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Variables</th><th align="center" valign="middle" >n</th><th align="center" valign="middle" >p</th></tr></thead><tr><td align="center" valign="middle" >Male</td><td align="center" valign="middle" >149</td><td align="center" valign="middle" >0.3029</td></tr><tr><td align="center" valign="middle" >Ascite decompensation</td><td align="center" valign="middle" >163</td><td align="center" valign="middle" >0.4457</td></tr><tr><td align="center" valign="middle" >hepatic encephalopathy</td><td align="center" valign="middle" >104</td><td align="center" valign="middle" >0.0029<sup>*</sup></td></tr><tr><td align="center" valign="middle" >Infection of ascites</td><td align="center" valign="middle" >50</td><td align="center" valign="middle" >0.0208<sup>*</sup></td></tr><tr><td align="center" valign="middle" >Child Pugh C</td><td align="center" valign="middle" >76</td><td align="center" valign="middle" >0.0460<sup>*</sup></td></tr><tr><td align="center" valign="middle" >gastrointestinal bleeding</td><td align="center" valign="middle" >43</td><td align="center" valign="middle" >0.0992</td></tr><tr><td align="center" valign="middle" >Thrombocytopenia</td><td align="center" valign="middle" >124</td><td align="center" valign="middle" >0.5693</td></tr><tr><td align="center" valign="middle" >Renal failure</td><td align="center" valign="middle" >38</td><td align="center" valign="middle" >0.0858</td></tr><tr><td align="center" valign="middle" >Diuretics</td><td align="center" valign="middle" >60</td><td align="center" valign="middle" >0.0458<sup>*</sup></td></tr><tr><td align="center" valign="middle" >Administration of beta blockers</td><td align="center" valign="middle" >84</td><td align="center" valign="middle" >0.3010</td></tr><tr><td align="center" valign="middle" >Hyponatremia</td><td align="center" valign="middle" >35</td><td align="center" valign="middle" >0.0434<sup>*</sup></td></tr></tbody></table></table-wrap><p><sup>*</sup>p ˂ 0.05.</p><p>Hazard Ratio [CI: 1.023 to 10.977] as compared with stage A (<xref ref-type="fig" rid="fig2">Figure 2</xref>). In multivariate analysis, hepatic encephalopathy and gastrointestinal bleeding were associated with the survival decrease and the use of diuretic would improve the prognostic (<xref ref-type="table" rid="table3">Table 3</xref>).</p></sec><sec id="s4"><title>4. Discussion</title><p>This study confirms the high frequency of viral B cirrhosis in our country in the light of our literary review [<xref ref-type="bibr" rid="scirp.58223-ref4">4</xref>] .</p><table-wrap id="table3" ><label><xref ref-type="table" rid="table3">Table 3</xref></label><caption><title> Prognostic factors of survival in multi varied analysis</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Variables</th><th align="center" valign="middle" >Hazard Ratio</th><th align="center" valign="middle" >p</th><th align="center" valign="middle" >Interval of confidence</th></tr></thead><tr><td align="center" valign="middle" >Child-Pugh score C</td><td align="center" valign="middle" >1.281</td><td align="center" valign="middle" >0.497</td><td align="center" valign="middle" >0.627 - 2.618</td></tr><tr><td align="center" valign="middle" >Added bacterial infection</td><td align="center" valign="middle" >1.794</td><td align="center" valign="middle" >0.169</td><td align="center" valign="middle" >0.779 - 4.131</td></tr><tr><td align="center" valign="middle" >Diuretics</td><td align="center" valign="middle" >0.387</td><td align="center" valign="middle" >0.002<sup>*</sup></td><td align="center" valign="middle" >0.209 - 0.714</td></tr><tr><td align="center" valign="middle" >Hyponatremia</td><td align="center" valign="middle" >1.093</td><td align="center" valign="middle" >0.788</td><td align="center" valign="middle" >0.571 - 2.094</td></tr><tr><td align="center" valign="middle" >Gastrointestinal bleeding</td><td align="center" valign="middle" >0.402</td><td align="center" valign="middle" >0.030<sup>*</sup></td><td align="center" valign="middle" >0.177 - 0.917</td></tr><tr><td align="center" valign="middle" >Encephalopathy</td><td align="center" valign="middle" >2.223</td><td align="center" valign="middle" >0.035<sup>*</sup></td><td align="center" valign="middle" >1.056 - 4.699</td></tr></tbody></table></table-wrap><p><sup>*</sup>p ˂ 0.05.</p><fig id="fig1"  position="float"><label><xref ref-type="fig" rid="fig1">Figure 1</xref></label><caption><title> Distribution of patients according to survival time</title></caption><graphic mimetype="image"   position="float"  xlink:type="simple"  xlink:href="http://html.scirp.org/file/5-1900285x6.png"/></fig><fig id="fig2"  position="float"><label><xref ref-type="fig" rid="fig2">Figure 2</xref></label><caption><title> Survival in patients with cirhhosis according to the child-pugh score</title></caption><graphic mimetype="image"   position="float"  xlink:type="simple"  xlink:href="http://html.scirp.org/file/5-1900285x7.png"/></fig><p>Besides, we have also established a weak proportion of alcoholic cirrhosis which is quite probably under estimated because of the consumption of alcohol that was not confessed. On the contrary, the etiology of the cirrhosis has not been established within 10% of the cases. This considerable proportion is due to many factors: insufficiency of investigations because of lack of means, undeclared consumption of alcohol.</p><p>The duration of the overall survival of the patients has run from 0.03 to 16.66 per month with a median of 0.50 patient-month. This means that we have registered 0.5 deaths out of 221 patients-months. Also, this is a proof that the patients were at an advanced stage of cirrhosis before their hospitalization with a reserved prognostic. In fact, in our study 34.39% of the cirrhosis patients were classified at stage C where as 52.94% of them were classified in stage B. It is not easy to establish the direct causes of cirrhosis patient’s death [<xref ref-type="bibr" rid="scirp.58223-ref7">7</xref>] . In univariate analysis, 5 parameters (encephalopathy, spontaneous ascetic fluid infection, hyponatremia, renal failure and the score Child-Pugh C) were significantly associated with bad prognosis and the taking of diuretic was significantly associated with improved survival.</p><p>The occurrence of hepatic encephalopathy significantly has decreased the survival of our patients (p = 0.0029). This is consistent with several studies that have shown that hepatic encephalopathy was responsible for a high rate of death with cirrhotic patients [<xref ref-type="bibr" rid="scirp.58223-ref8">8</xref>] .</p><p>In our study, ascites was the most common complication of cirrhosis [<xref ref-type="bibr" rid="scirp.58223-ref9">9</xref>] and is associated with a bad prognosis with a considerable reduction of survival-rate of patients [<xref ref-type="bibr" rid="scirp.58223-ref10">10</xref>] [<xref ref-type="bibr" rid="scirp.58223-ref11">11</xref>] .</p><p>Moreover, with regard to our test sample, the spontaneous ascites fluid infection with our patients significantly reduced their chances of survival (p = 0.0208). This massive mortality can be likely associated with the development of a systematic inflammatory reaction [<xref ref-type="bibr" rid="scirp.58223-ref12">12</xref>] . The spontaneous ascites fluid infection is a frequent factor of complication with cirrhotic patients [<xref ref-type="bibr" rid="scirp.58223-ref13">13</xref>] .</p><p>The survival of patients who have recovered from a prior episode of spontaneous ascites fluid infection is 30% over a period of 1 year with a prognostic that depends on the gravity of cirrhosis [<xref ref-type="bibr" rid="scirp.58223-ref14">14</xref>] .</p><p>The risk factors of the spontaneous ascites fluid infection are manifold: antecedents of ascites fluid infection in the absence of antibiotic prophylaxis [<xref ref-type="bibr" rid="scirp.58223-ref15">15</xref>] , gastrointestinal bleeding [<xref ref-type="bibr" rid="scirp.58223-ref16">16</xref>] , albuminemiea ˂ 28 gr/l, alcoholic etiology and Child-Pugh C [<xref ref-type="bibr" rid="scirp.58223-ref17">17</xref>] . In Ivory Coast, the ascites fluid infection is the first cause of death with cirrhotic patients [<xref ref-type="bibr" rid="scirp.58223-ref18">18</xref>] . The prognosis has improved considerably in recent years with the early use of antibiotic, a support of renal failure when it exists and a primary or secondary antibiotic prophylaxis [<xref ref-type="bibr" rid="scirp.58223-ref14">14</xref>] .</p><p>The use of diuretic has improved significantly the survival of patients (p = 0.0458). Research studies should be urged on in order to better assess the added value of diuretics in the survival of cirrhosis patients with edema and ascites syndrome. However, their side effects and unfitness with cirrhosis patients minimize their use [<xref ref-type="bibr" rid="scirp.58223-ref19">19</xref>] .</p><p>The presence of an hyponatremiea was forcibly associated with a decrease of a survival among the study sample (p = 0.0434). Many studies [<xref ref-type="bibr" rid="scirp.58223-ref20">20</xref>] [<xref ref-type="bibr" rid="scirp.58223-ref21">21</xref>] have revealed that a natremia ≤ 130 m・mol/l was a negative prognostic factor to which an elevated rate of death is associated with cirrhotic patients.</p><p>Renal failure has decreased survival without statistical significance with our patients (p = 0.0858) in contrast to the literature [<xref ref-type="bibr" rid="scirp.58223-ref21">21</xref>] where they are significantly associated. This lack of significance of our results can be explained by the fact that the inclusion criteria of hepato-renal syndrome were not clearly established during our inquiry, which means that it was under estimated and that the retrospective character of our study did not allow us to reach that stage. Renal function is frequently impaired in cirrhosis [<xref ref-type="bibr" rid="scirp.58223-ref7">7</xref>] [<xref ref-type="bibr" rid="scirp.58223-ref21">21</xref>] [<xref ref-type="bibr" rid="scirp.58223-ref22">22</xref>] . Hospital mortality due to renal failure despite adequate support is around 30% [<xref ref-type="bibr" rid="scirp.58223-ref23">23</xref>] .</p><p>Stage C of Child-Pugh score was associated with an important increase (p = 0.046) by 3.351 time of death hazard-ratio in our sample.</p><p>Stage C of the Child-Pugh score is an independent factor that predisposes the patient to death [<xref ref-type="bibr" rid="scirp.58223-ref24">24</xref>] [<xref ref-type="bibr" rid="scirp.58223-ref25">25</xref>] .</p><p>By a multivariate analysis, the survival of a hepatic encephalopathy in the course of cirrhosis was an independent parameter that has significantly reduced the patients chances of survival. In fact, the hepatic encephalopathy was associated with a significant increase in mortality (p = 0.035). Despite a better understanding of hepatic encephalopathy, of its symptomatic factors and its care taking, its mortality both in hospitalization as well as in the reanimation units remains high [<xref ref-type="bibr" rid="scirp.58223-ref26">26</xref>] . The development of hepatic encephalopathy with cirrhosis patients is associated with high lethality: 41% to 80% at one (1) year and 77% to 85% at three (3) years [<xref ref-type="bibr" rid="scirp.58223-ref26">26</xref>] [<xref ref-type="bibr" rid="scirp.58223-ref27">27</xref>] .</p><p>The use of diuretics was associated with a significant decrease (p = 0.002) of 0.386 time (more than half) of the death Hazard Ratio. The gastrointestinal bleeding was associated with a significant decrease of mortality (p = 0.030). Indeed, the death cases that are caused by the first episodes of gastrointestinal bleeding of portal hypertension on cirrhosis is high but is also dependent on the area where bleeding occurs [<xref ref-type="bibr" rid="scirp.58223-ref28">28</xref>] . Our results could be explained by a proper application of resuscitation measures especially with patients having crossed the transfusion threshold although the specific charge made is not optimal [<xref ref-type="bibr" rid="scirp.58223-ref29">29</xref>] and the high rate of primary and secondary prophylaxis with beta blockers [<xref ref-type="bibr" rid="scirp.58223-ref22">22</xref>] [<xref ref-type="bibr" rid="scirp.58223-ref25">25</xref>] .</p><p>The score of Child-Pugh is not independently associated to morality (p = 0.497) as the literary review seems to indicate [<xref ref-type="bibr" rid="scirp.58223-ref7">7</xref>] . Indeed, it does not take into account some factors that may have a significant impact on prognosis as renal function. This has led to the creation of other scores such as the MELD score (model for end-stage liver disease) [<xref ref-type="bibr" rid="scirp.58223-ref30">30</xref>] which is used in the assessment of medium prognostic of cirrhotic patients and the indication of hepatic transplantation. However, the prognostic value of the Child-Pugh score at one (1) or two (2) years is clearly known [<xref ref-type="bibr" rid="scirp.58223-ref6">6</xref>] [<xref ref-type="bibr" rid="scirp.58223-ref24">24</xref>] .</p><p>The limitations to our study are the relatively small number of patients, due to the retrospective nature of the study with several missing data. Indeed, some hospitalized patients have not been able to do their para clinical examinations. Therefore, the survival time associated with the various parameter studied could be less than the duration of survival in subjects with cirrhosis and portal hypertension in the general population. Insufficient etiological research because of the cost of viral markers and the lack of quantitative and qualitative assessment of the consumption of alcohol is prior to the study.</p></sec><sec id="s5"><title>5. Conclusion</title><p>Cirrhotic patients with portal hypertension mortality are high in Abidjan. Pejorative prognostic factors are hyponatremia, ascites fluid infection and hepatic encephalopathy. The use of diuretics and beta blockers were indicated when associated with improved survival.</p></sec><sec id="s6"><title>Cite this paper</title><p>Mamert Fulgence YaoBathaix,AkelessoBagny,Kouam&#233; AlassaneMahassadi,Anass&#233; Jean-BaptisteOkon,Ya HenrietteKissi-Anzouan,StanislasDoffou,Aboubacar DembaBangoura,Hatrydt DimitriKouam&#233;,KadiatouDiallo,AntoninN’Dam,Aoudi OusmanDe,Koffi AlainAttia,Aya Th&#233;r&#232;se N’driYoman, (2015) Prognostic Factors for Cirrhosis Hospital in Abidjan (C&#244;te d’Ivoire). 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