<?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.2015.512030</article-id><article-id pub-id-type="publisher-id">OJGas-62120</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>
 
 
  The &lt;i&gt;Helicobacter pylori&lt;/i&gt; Eradication Rate in a High Prevalence Area (West Africa): Three Triple Therapy Comparative Study
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>djéka</surname><given-names>Stanislas 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>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>Mamert</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>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>Ya</surname><given-names>Henriette Kissy-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>Hartrydt</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>Kouamé</surname><given-names>Alassan 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>Kouamé</surname><given-names>Justin N’Da</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>Mohamed</surname><given-names>Kouyaté</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>Constant</surname><given-names>Assi</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>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="aff2"><addr-line>Anatomopathology Laboratory of the Centre Hospitalier Universitaire de Cocody (CHU-C), Abidjan, Cote d’Ivoire</addr-line></aff><aff id="aff1"><addr-line>Department of Hepatology and Gastroenterology, Centre Hospitalier Universitaire de Yopougon (CHU-Y), Abidjan, Cote d’Ivoire</addr-line></aff><aff id="aff3"><addr-line>Department of Hepatology and Gastroenterology, Centre Hospitalier Universitaire de Cocody (CHU-C), 
Abidjan, Cote d’Ivoire</addr-line></aff><author-notes><corresp id="cor1">* E-mail:<email>bathaixful@yahoo.fr(MFYB)</email>;</corresp></author-notes><pub-date pub-type="epub"><day>16</day><month>12</month><year>2015</year></pub-date><volume>05</volume><issue>12</issue><fpage>200</fpage><lpage>206</lpage><history><date date-type="received"><day>30</day>	<month>October</month>	<year>2015</year></date><date date-type="rev-recd"><day>accepted</day>	<month>20</month>	<year>December</year>	</date><date date-type="accepted"><day>23</day>	<month>December</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>
 
 
  In Western countries, the current trend is to use sequential quadruple therapy or bismuth-based instead of triple therapy for the eradication of 
  Helicobacter pylori (
  H. pylori). In sub-Saharan Africa, high prevalence area of the 
  H. pylori infection, the effectiveness of these triple therapies widely used in routine has been little evaluated. The purpose of this study was to evaluate and compare the effectiveness of three patterns of first-line triple therapy based on combining a proton pump inhibitors (PPI), and 3 types of antibiotics: omeprazole (O), amoxicillin (A), clarythromycin (C) and metronidazole (M). Patients and Methods: This is a randomized clinical trial opened on 3 parallel arms: OAM (group 1 or G1), OAC (group 2 or G2) or OCM (group 3 or G3). The primary endpoint was 
  H. pylori eradication rate after seven days triple therapy. 
  H. pylori diagnosis infection was based on bacterium detection on the histological examination of the gastric biopsies. Histological control was performed 4 weeks after the end of treatment to assess 
  H. pylori eradication rate. Results: The average age of our 153 patients included in the study (86 men) was 44.33 &#177; 11.72 years. The main reason of the endoscopy was the dyspeptic syndrome (75.16%). The gastroscopy was normal in 28.76%. A Gastric or duodenal peptic ulcer was found in 17% of cases and gastropathy in 45.75%. Histologically, the GC was active in 90.9% of cases, follicular in 35.3% of cases, atrophic in 22.5% of cases and was associated with intestinal metaplasia (IM) in 5.2% of cases. Patients of these three groups (n = 64 for G1, n = 56 for G2 and n = 33 for G3) were comparable for age, gender, endoscopy indications, alcohol consumption history or smoking, and anti-inflammatory drugs taking. Approximately 23% of patients experienced adverse reactions. The overall 
  H. pylori eradication rate was 22.3%. There was no significant difference 
  H. pylori eradication rate depending on the treatment used (28.1%, 21.4% and 15.1% for G1, G2 and G3, p = 0.34). Conclusion: The 
  H. pylori eradication rate was poor regardless of the triple therapy used. It is desirable in the absence of bacteriological data on the primary and secondary resistance levels to optimize the eradication rate advocating the use of quadruple therapy at outset in first-line.
 
</p></abstract><kwd-group><kwd>&lt;i&gt; Helicobacter pylori&lt;/i&gt;</kwd><kwd> Triple Therapy</kwd><kwd> Eradication</kwd><kwd> West Africa</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Introduction</title><p>The Helicobacter pylori (H. pylori) infection is a public health problem not insignificant [<xref ref-type="bibr" rid="scirp.62120-ref1">1</xref>] , which affects 20% - 50% of the population in industrialized nations and more than 80% in less developed countries [<xref ref-type="bibr" rid="scirp.62120-ref2">2</xref>] [<xref ref-type="bibr" rid="scirp.62120-ref3">3</xref>] . This bacterium is associated with many gastric or duodenal pathologies and extra-digestive [<xref ref-type="bibr" rid="scirp.62120-ref2">2</xref>] -[<xref ref-type="bibr" rid="scirp.62120-ref4">4</xref>] . In high incidence of gastric carcinoma areas, the H. pylori eradication is recommended to prevent the development of this disease [<xref ref-type="bibr" rid="scirp.62120-ref5">5</xref>] - [<xref ref-type="bibr" rid="scirp.62120-ref7">7</xref>] .</p><p>The European treatment guidelines revised in 2005 [<xref ref-type="bibr" rid="scirp.62120-ref4">4</xref>] and amended again after the “Maastricht IV” meeting of November 2010 are almost gone because of the need to adapt to the resistances’ appearance more and more to the antibiotics of classic triple therapy. In Western countries, the current trend is to use sequential quadruple therapy or bismuth-based instead of triple therapy for the H. pylori eradication due to a decline in efficiency related to resistance problems for antibiotics [<xref ref-type="bibr" rid="scirp.62120-ref8">8</xref>] [<xref ref-type="bibr" rid="scirp.62120-ref9">9</xref>] .</p><p>In sub-Saharan Africa, high prevalence area of the H. pylori infection, the effectiveness of these triple therapies widely used in routine has been little evaluated [<xref ref-type="bibr" rid="scirp.62120-ref10">10</xref>] . This widespread use of triple therapies could be explained by the low level of knowledge of general practitioners and the high cost of quadruple therapy.</p><p>The purpose of this study was to evaluate and compare the effectiveness of three patterns of first-line triple therapy based on combining a proton pump inhibitors (PPI): omeprazole (O) and 3 types of antibiotics: amoxicillin (A), clarythromycin (C) and metronidazole (M).</p></sec><sec id="s2"><title>2. Patients and Methods</title><sec id="s2_1"><title>2.1. Study Oversight</title><p>Our study was conducted in the centre hopitalier et universitaire de Yopougon’s endoscopy unit from June 2010 through November 2011. This was a prospective, comparative study of 3 combinations of classic triple therapy for H. pylori eradication. During the period of the study, all patients that had to undergo a gastroscopy and had no indication against the realization of gastric biopsies were routinely included.</p></sec><sec id="s2_2"><title>2.2. Exclusion Criterea</title><p>Pregnant women/or nursing mothers, patients with liver cirrhosis, renal failure, patients with a history of gastro- intestinal surgery, gastroesophageal reflux disease, and those who had taken proton pump inhibitor, bismuth salts, H2 blockers and/or antibiotic treatment in the previous 2 months were excluded from the study.</p></sec><sec id="s2_3"><title>2.3. Study Conduct</title><p>For each patient, we routinely practiced five gastric biopsies: two biopsy specimens (one each from the antrum and corpus) and one to angular stomach. Biopsy specimens were fixed in formalin at 10% and sent to Cocody (Abidjan) teaching hospital’s anatomy pathology laboratory. The histological assessment of H. pylori status was performed using a further four biopsy (stained with Giemsa), for histological examination to characterize chronic gastritis thanks to hematein eosin staining according to the Sydney system.</p><p>We included patients whose gastric biopsies were positive for H. pylori histology. To each patient it has been assigned by drawing lots one of three protocols of triple therapy for 7 days: G1 (n = 64): Omeprazole 20 mg + Amoxicillin 1 g + Metronidazole 500 mg (OAM); G2 (n = 56): Omeprazole 20 mg + Amoxicillin 1 g + clarithromycin 500 mg (OAC); G3 (n = 33): Omeprazole 20 mg + clarithromycin 500 mg + metronidazole 500 mg (CMO). During the seven days, the capsules of Omeprazole, Amoxicillin, clarithromycin and metronidazole were taken twice daily (morning and evening before meals). Four weeks after the end of treatment, the effectiveness of each triple therapy was evaluated by performing a gastroscopy with five new gastric biopsies for histological analysis in search of a negativity or persistence of Helicobacter pylori infection in the same laboratory and using the same techniques mentioned above.</p></sec><sec id="s2_4"><title>2.4. Studied Variables</title><p>The parameters studied were the age, the gender, the lifestyle (alcohol, tobacco), the reason for gastroscopy, the endoscopic and histological parameters, and the medication side effects.</p><p>All these data were collected on individual survey forms, entered and processed by Excel.</p></sec><sec id="s2_5"><title>2.5. Ethics</title><p>Before the study began, the patients signed an informed consent form which included, age, gender, chief com- plaint, drug history and past medical history.</p></sec><sec id="s2_6"><title>2.6. Statistical Analysis</title><p>Statistical analysis of the factors studied was made by a correct Chi<sup>2</sup> Pearson test to compare the different groups in terms of the general data, the eradication rate and side effects with a significance coefficient p &lt; 0.05. Comparing the quantitative variables (average and median) was made by an analysis of variance (Anova).</p></sec></sec><sec id="s3"><title>3. Results</title><p>Over the period of our study we recruited 153 patients (86 men) with an average of 44.33 &#177; 11.72 years. All patients included were positive to H. pylori. The demographic and clinical characteristics of these patients are reported in <xref ref-type="table" rid="table1">Table 1</xref>. Fifty-four point twenty five percent (54.25%) patients complained of chronic epigastric pain. Five patients were taking NSAIDs before treatment (<xref ref-type="table" rid="table1">Table 1</xref>). The main reason for endoscopy was the dyspeptic syndrome (75.16%). Gastroscopy found a gastric or duodenal peptic ulcer in 17% of cases and could not find mucosal lesion in 28.76%. The most important histological aspect associated with H. Pylori infection was gastritis’ activity (90.9%), while atrophy and intestinal metaplasia were found respectively in 22.9% and 5.23% cases (<xref ref-type="table" rid="table2">Table 2</xref>). Thirty-five of the 153 patients, 22.9% had side effects including 30 patients who had nausea (19.6%), three had vomit (1.96%), one felt faint (0.65%) and one had nausea and vomit the same time (0.65%). The overall eradication rate in our study was low in the order of 22.9%. In univariate analysis, we noted no significant difference in H. pylori eradication rate among the three groups which were respectively 28.1%, 21.4% and 15.1% for G1, G2 and G3 (<xref ref-type="table" rid="table3">Table 3</xref>).</p></sec><sec id="s4"><title>4. Discussion</title><p>Ivory Coast like most African countries is regarded as an area of high prevalence of the H. pylori infection</p><table-wrap id="table1" ><label><xref ref-type="table" rid="table1">Table 1</xref></label><caption><title> Demographic and clinical characteristics of the patients at baseline</title></caption><table><tbody><thead><tr><th align="center" valign="middle" ></th><th align="center" valign="middle" >G1 (n = 64)</th><th align="center" valign="middle" >G2 (n = 56)</th><th align="center" valign="middle"  colspan="2"  >G3 (n = 33)</th><th align="center" valign="middle" >p value</th></tr></thead><tr><td align="center" valign="middle" >Mean age &#177; SD ( year)</td><td align="center" valign="middle" >45 &#177; 10.63</td><td align="center" valign="middle"  colspan="2"  >44 &#177; 13.3</td><td align="center" valign="middle" >42.9 &#177; 11.60</td><td align="center" valign="middle" >0.56</td></tr><tr><td align="center" valign="middle" >Median age ( years)</td><td align="center" valign="middle" >45.5 (36.5 - 52)</td><td align="center" valign="middle"  colspan="2"  >44 (36.5 - 52)</td><td align="center" valign="middle" >43 (37 - 49)</td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Male</td><td align="center" valign="middle" >36 (60.9%)</td><td align="center" valign="middle"  colspan="2"  >29 (51.8%)</td><td align="center" valign="middle" >18 (54.6%)</td><td align="center" valign="middle" >0.59</td></tr><tr><td align="center" valign="middle" >Alcohol consumption</td><td align="center" valign="middle" >1 (1.56%)</td><td align="center" valign="middle"  colspan="2"  >00 (0%)</td><td align="center" valign="middle" >00 (0%)</td><td align="center" valign="middle" >0.50</td></tr><tr><td align="center" valign="middle" >Tobacco consumption</td><td align="center" valign="middle" >0</td><td align="center" valign="middle"  colspan="2"  >0</td><td align="center" valign="middle" >0</td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >NSAIDs<sup>*</sup> taking</td><td align="center" valign="middle" >2 (3.1%)</td><td align="center" valign="middle"  colspan="2"  >3 (3.6%)</td><td align="center" valign="middle" >1 (3%)</td><td align="center" valign="middle" >0.98</td></tr><tr><td align="center" valign="middle" ></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><td align="center" valign="middle" ></td></tr></tbody></table></table-wrap><p>NSAIDs<sup>*</sup>: non-steroidal anti-inflammatory drug-related stomach.</p><table-wrap id="table2" ><label><xref ref-type="table" rid="table2">Table 2</xref></label><caption><title> Histology results of patients included in the study</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Histology results</th><th align="center" valign="middle" >Frequency (%)</th></tr></thead><tr><td align="center" valign="middle" >Chronic gastritis</td><td align="center" valign="middle" >153 (100%)</td></tr><tr><td align="center" valign="middle" >Active gastritis</td><td align="center" valign="middle" >149 (90.9%)</td></tr><tr><td align="center" valign="middle" >Follicular gastritis</td><td align="center" valign="middle" >54 (35.3%)</td></tr><tr><td align="center" valign="middle" >Atrophic gastritis</td><td align="center" valign="middle" >35 (22,9%)</td></tr><tr><td align="center" valign="middle" >Intestinal metaplasia</td><td align="center" valign="middle" >8 (5.2%)</td></tr></tbody></table></table-wrap><table-wrap id="table3" ><label><xref ref-type="table" rid="table3">Table 3</xref></label><caption><title> H. pylori eradication rate according treatment</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Treatment</th><th align="center" valign="middle" >Frequency (%)</th><th align="center" valign="middle" >p</th></tr></thead><tr><td align="center" valign="middle" >OAM</td><td align="center" valign="middle" >18/64 (22.1%)</td><td align="center" valign="middle"  rowspan="3"  >0.336</td></tr><tr><td align="center" valign="middle" >OAC</td><td align="center" valign="middle" >12/56 (21.6%)</td></tr><tr><td align="center" valign="middle" >OCM</td><td align="center" valign="middle" >5/33 (15.2%)</td></tr></tbody></table></table-wrap><p>omeprazole (O), amoxicillin (A), clarythromycin (C), metronidazole (M).</p><p>where it affects over 80% of the population [<xref ref-type="bibr" rid="scirp.62120-ref11">11</xref>] - [<xref ref-type="bibr" rid="scirp.62120-ref14">14</xref>] . The role of the bacteria in the dyspeptic syndrome, peptic ulcers, and precancerous lesions of the stomach has been established [<xref ref-type="bibr" rid="scirp.62120-ref15">15</xref>] . Indications for research and treatment of H. pylori infection are the subject of an international consensus that has been taken up in various expert conferences, European or [<xref ref-type="bibr" rid="scirp.62120-ref4">4</xref>] [<xref ref-type="bibr" rid="scirp.62120-ref16">16</xref>] , North American [<xref ref-type="bibr" rid="scirp.62120-ref6">6</xref>] , Asian [<xref ref-type="bibr" rid="scirp.62120-ref7">7</xref>] .</p><p>In many studies, the breath test with urea labeled with carbon-13 is still the most used examination for checking the efficiency of H. pylori eradicating treatments as noninvasive with excellent sensitivity and available in Western countries and Asia [<xref ref-type="bibr" rid="scirp.62120-ref15">15</xref>] [<xref ref-type="bibr" rid="scirp.62120-ref17">17</xref>] - [<xref ref-type="bibr" rid="scirp.62120-ref19">19</xref>] .</p><p>In Ivory Coast, histological examination is the most used method for the H. pylori detection and the only way to control the eradication of bacteria because breath test is not available.</p><p>The 7-day triple therapy from PPI, clarithromycin and amoxicillin or metronidazole is the first-line eradica- tion treatment of the H. pylori still prescribed by most general practitioners as European Consensus’ recom- mandations [<xref ref-type="bibr" rid="scirp.62120-ref4">4</xref>] [<xref ref-type="bibr" rid="scirp.62120-ref20">20</xref>] [<xref ref-type="bibr" rid="scirp.62120-ref21">21</xref>] in C&#244;te d’Ivoire.</p><p>This treatment’s effectiveness was established in 1996, with an eradication rate of over 80% by intention-to- treat (ITT) [<xref ref-type="bibr" rid="scirp.62120-ref22">22</xref>] . Clinical trials that have been accumulated over the last decade show throughout the world a decrease of the effectiveness of this triple combination therapy with eradication rates below 70% [<xref ref-type="bibr" rid="scirp.62120-ref23">23</xref>] - [<xref ref-type="bibr" rid="scirp.62120-ref26">26</xref>] so that the current trend in the developed countries is the sequential therapy or bismuth-based quadruple therapy as first-line [<xref ref-type="bibr" rid="scirp.62120-ref15">15</xref>] .</p><p>No published study has been made to our knowledge to assess and compare different classic triple therapy eradication of H. pylori in sub-Saharan Africa. We conducted this study in order to evaluate H. pylori eradication rate in C&#244;te d’Ivoire by three triple therapy. We included in our study 153 patients divided into three groups according to the possible combinations of standard triple therapy (G1 = OAM, G2 = OAC and G3 = CMO). All patients were comparable with respect to gender, age, alcohol intake, tobacco or NSAIDs, as well as gastroscopy pattern.</p><p>We consider that both sexes are equally affected by the H. pylori infection [<xref ref-type="bibr" rid="scirp.62120-ref27">27</xref>] , but some studies have noted a male predominance [<xref ref-type="bibr" rid="scirp.62120-ref13">13</xref>] [<xref ref-type="bibr" rid="scirp.62120-ref28">28</xref>] as in our studied sample with a rate of 56.21%. Unlike developed countries, H. pylori infection predominates with young adults in developing countries [<xref ref-type="bibr" rid="scirp.62120-ref11">11</xref>] [<xref ref-type="bibr" rid="scirp.62120-ref13">13</xref>] [<xref ref-type="bibr" rid="scirp.62120-ref19">19</xref>] . This is verified in our study with an average age of subjects infected with H. pylori whish was 44.3 years. No case of normal gastric mucosa was found in our study. All had chronic gastritis confirming the H. pylori pathogenesis in its occurrence [<xref ref-type="bibr" rid="scirp.62120-ref29">29</xref>] . Precancerous lesions such as atrophy and intestinal metaplasia were found in respective proportions of 22.9% and 5.2%. These data are comparable with those found by other authors in the Ivory Coast [<xref ref-type="bibr" rid="scirp.62120-ref11">11</xref>] [<xref ref-type="bibr" rid="scirp.62120-ref30">30</xref>] . Despite these relatively low proportions of these precancerous lesions, the H. pylori infection treatment is still required.</p><p>Our results show that seven days of classic triple therapy used enable to obtain global eradication rates below 25% (22.9%). Although it is described a progressively high failure rate with standard triple therapy, our results show very high failure rate (over 75%) in contrast to more work done in the West and Asia that show rates increasing gradually to reach 40% failure since the 2000s [<xref ref-type="bibr" rid="scirp.62120-ref8">8</xref>] [<xref ref-type="bibr" rid="scirp.62120-ref17">17</xref>] [<xref ref-type="bibr" rid="scirp.62120-ref25">25</xref>] . In these studies predictors of failure were mainly of antibiotic resistance strains especially to clarithromycin and poor medical compliance; other factors seem to have no significant effect (alcohol, tobacco, food) [<xref ref-type="bibr" rid="scirp.62120-ref31">31</xref>] [<xref ref-type="bibr" rid="scirp.62120-ref32">32</xref>] .</p><p>In our study, we certainly did not assess treatment adherence, but all patients took all their H. pylori eradication treatment, despite the gastrointestinal occurrence side effects about 30% of patients. Therefore, we cannot attribute this therapeutic failure to poor compliance therapy neither in the tobacco nor the alcoholic because no patient took snuff and only one patient was alcohol consumer. Antibiotic resistance is the main factor contributing to the failure of PPI-based triple therapies for the H. pylori eradication adequately. Amoxicillin currently seems untouched by the resistance problem. Indeed, the highest rate of resistance is now described below 1% [<xref ref-type="bibr" rid="scirp.62120-ref8">8</xref>] . However, various studies show a high rate of strains resistant to clarithromycin, which rose from 15% to over 20% [<xref ref-type="bibr" rid="scirp.62120-ref8">8</xref>] [<xref ref-type="bibr" rid="scirp.62120-ref33">33</xref>] - [<xref ref-type="bibr" rid="scirp.62120-ref35">35</xref>] .</p><p>This rate is 13% in African countries where the molecule has been tested [<xref ref-type="bibr" rid="scirp.62120-ref36">36</xref>] . The metronidazole resistance would cover up to 59% of strains [<xref ref-type="bibr" rid="scirp.62120-ref33">33</xref>] in the West. In Africa, this H. Pylori eradication rate is variable. In Senegal, it is estimated at 90% in Seck’s study [<xref ref-type="bibr" rid="scirp.62120-ref37">37</xref>] . While this rate is 55% in Nigeria [<xref ref-type="bibr" rid="scirp.62120-ref36">36</xref>] .</p><p>The prevalence of resistance in 2009 in France evaluated on 530 strains showed that 13% were resistant to both clarithromycin and metronidazole [<xref ref-type="bibr" rid="scirp.62120-ref33">33</xref>] . The primary resistance appearance to clarithromycin is the major cause of the inefficiency of clarithromycin-based triple therapy [<xref ref-type="bibr" rid="scirp.62120-ref38">38</xref>] . This resistance is associated to different mutations in the V domain of the 23S ribosomal RNA gene [<xref ref-type="bibr" rid="scirp.62120-ref39">39</xref>] . The clinical impact of resistance to metronidazole is lower [<xref ref-type="bibr" rid="scirp.62120-ref32">32</xref>] .</p><p>The triple therapy having lost its effectiveness in the past decade, several quadruple therapies combining a PPI with amoxicillin, clarithromycin and a nitro-imidazole (metronidazole or tinidazole) or bismuth have been studied. A meta-analysis incorporating 10 controlled trials in 3006 patients shows that the sequential therapy permitted to obtain a significantly higher eradication rates (91.0% eradication; 95% CI: 89.6 to 92.1) than the triple therapy containing clarithromycin or metronidazole (75.7% eradication; 95% CI: 73.6 to 77.7) [<xref ref-type="bibr" rid="scirp.62120-ref40">40</xref>] .</p><p>This result was associated with better efficacy of sequential therapy on strains resistant to clarithromycin. In the same study, with 45 patients with resistant strain, H. pylori eradication rate was 83.3% (95% CI: 60.8 to 94.2) with the sequential therapy and 25.9% (95% CI: 13.2 to 44.7) with triple therapy. The compliance and safety of the sequential therapy seemed as good as that of the clarithromycin triple therapy based. Finally, concurrent and sequential quadruple therapy tolerances seemed equivalent [<xref ref-type="bibr" rid="scirp.62120-ref41">41</xref>] .</p><p>Furthermore, an European multi-centre randomized study showed more eradication rates with bismuth -based quadruple therapy than with clarithromycin-based triple therapy: 93% (95% CI: 89% - 97%) in per-protocole (PP) and 80% (95% CI: 74% - 85%) ITT versus 70% (CI 72% - 77%) in PP and 55% (CI 49% - 62%) in ITT (p &lt; 0.0001) [<xref ref-type="bibr" rid="scirp.62120-ref42">42</xref>] .</p><p>Two other studies previously had found comparable eradication rates [<xref ref-type="bibr" rid="scirp.62120-ref43">43</xref>] . The frequency of adverse effects of bismuth-based quadruple therapy is comparable to those of the clarithromycin-based triple therapy [<xref ref-type="bibr" rid="scirp.62120-ref44">44</xref>] . In countries where it is permitted, the bismuth-based quadruple therapy is an alternative to sequential processing and can be used with patients allergic to beta-lactams or macrolides receiving whatever the indication.</p><p>The study limitations are small number of patients and absence compliance therapy evaluation.</p></sec><sec id="s5"><title>5. Conclusion</title><p>Seven days of anti H. pylori triple therapy in a high prevalence context with poor overall results. It is desirable in the absence of bacteriological data on the primary and secondary resistance levels to optimize the eradication rate advocating the immediately use of quadruple therapy in first intention.</p></sec><sec id="s6"><title>Conflict of Interest</title><p>Authors declare having not got conflict of interest.</p></sec><sec id="s7"><title>Cite this paper</title><p>Adj&#233;ka StanislasDoffou,Koffi AlainAttia,Mamert Fulgence YaoBathaix,Aboubacar DembaBangoura,Ya HenrietteKissy-Anzouan,Hartrydt DimitriKouam&#233;,Kouam&#233; AlassanMahassadi,Kouam&#233; JustinN’Da,MohamedKouyat&#233;,ConstantAssi,Aya Th&#233;r&#232;seN’dri-Yoman, (2015) The Helicobacter pylori Eradication Rate in a High Prevalence Area (West Africa): Three Triple Therapy Comparative Study. Open Journal of Gastroenterology,05,200-206. doi: 10.4236/ojgas.2015.512030</p></sec></body><back><ref-list><title>References</title><ref id="scirp.62120-ref1"><label>1</label><mixed-citation publication-type="other" xlink:type="simple">Moayyedi, P. and Hunt, R.H. (2004) Helicobacter pylori Public Health Implications. Helicobacter, 9, 67-72. http://dx.doi.org/10.1111/j.1083-4389.2004.00250.x</mixed-citation></ref><ref id="scirp.62120-ref2"><label>2</label><mixed-citation publication-type="other" xlink:type="simple">Suerbaum, S. and Michetti, P. (2002) Helicobacter pylori Infection. New England Journal of Medicine, 347, 1175- 1186.</mixed-citation></ref><ref id="scirp.62120-ref3"><label>3</label><mixed-citation publication-type="other" xlink:type="simple">Malferthiner, P., Chan, F.K. and Mc Coll, K.E. (2009) Peptic Ulcer Disease. Lancet, 374, 1449-1461. http://dx.doi.org/10.1016/S0140-6736(09)60938-7</mixed-citation></ref><ref id="scirp.62120-ref4"><label>4</label><mixed-citation publication-type="other" xlink:type="simple">Malfertheiner, P., Mégraud, F., O’Morain, C., et al. (2007) Current Concepts in the Management of Helicobacter pylori Infection—The Maastricht III Consensus Report. Gut, 56, 772-781. http://dx.doi.org/10.1136/gut.2006.101634</mixed-citation></ref><ref id="scirp.62120-ref5"><label>5</label><mixed-citation publication-type="journal" xlink:type="simple"><name name-style="western"><surname>Asaka</surname><given-names> M.</given-names></name>,<name name-style="western"><surname> Kato</surname><given-names> M.</given-names></name>,<name name-style="western"><surname> Takahashi</surname><given-names> S.</given-names></name>,<name name-style="western"><surname> et al.</surname><given-names> The Japanese Society for Helicobacter Rechearch </given-names></name>,<etal>et al</etal>. (<year>2010</year>)<article-title>Guidelines for the Management of Helicobacter pylori Infection in Japan: 2009 Revised Edition</article-title><source> Helicobacrer</source><volume> 15</volume>,<fpage> 1</fpage>-<lpage>20</lpage>.<pub-id pub-id-type="doi"></pub-id></mixed-citation></ref><ref id="scirp.62120-ref6"><label>6</label><mixed-citation publication-type="other" xlink:type="simple">Chey, W.D. and Wong, B.C.Y. (2007) American College of Gastroenterology Guideline on the Management of Helicobacter pylori Infection. American Journal of Gastroenterology, 102, 1808-1825. http://dx.doi.org/10.1111/j.1572-0241.2007.01393.x</mixed-citation></ref><ref id="scirp.62120-ref7"><label>7</label><mixed-citation publication-type="other" xlink:type="simple">Fock, K.M., Katelaris, P., Sugano, K., et al. (2009) Second Asia-Pacific Consensus Guidelines for Helicobacter pylori Infection. Journal of Gastroenterology and Hepatology, 24, 1587-1600. http://dx.doi.org/10.1111/j.1440-1746.2009.05982.x</mixed-citation></ref><ref id="scirp.62120-ref8"><label>8</label><mixed-citation publication-type="other" xlink:type="simple">Mégraud, F. (2004) H. pylori Antibiotic Resistance: Prevalence, Importance and Advances in Testing. Gut, 53, 1374- 1384. http://dx.doi.org/10.1136/gut.2003.022111</mixed-citation></ref><ref id="scirp.62120-ref9"><label>9</label><mixed-citation publication-type="other" xlink:type="simple">Fischbach, L. and Evans, E.L. (2007) Meta-Analysis: The Effect of Antibiotic Resistance Status on the Efficacy of Triple and Quadruple First-Line Therapies for Helicobacter pylori. Alimentary Pharmacology &amp; Therapeutics, 26, 343-357. http://dx.doi.org/10.1111/j.1365-2036.2007.03386.x</mixed-citation></ref><ref id="scirp.62120-ref10"><label>10</label><mixed-citation publication-type="other" xlink:type="simple">Fall, F., Diagne, A., Ndiaye, B., et al. (2011) Trithérapie par oméprazole, amoxicilline et clarithromycine dans la maladie ulcéreuse duodénale associée à Helicobacter pylori au Sénégal. Journal African d’Hépato-Gastroentérologie, 5, 28-32.</mixed-citation></ref><ref id="scirp.62120-ref11"><label>11</label><mixed-citation publication-type="other" xlink:type="simple">Assi, C., Ndah, K.J., Allah-Kouadio, E., et al. (2010) Prévalence de l’infection à Helicobacter pylori et lésions pré-cancéreuses du cancer gastrique chez les patients souffrant d’épigastralgies chroniques. Revue Africaine de Pathologie, 9, 25-31.</mixed-citation></ref><ref id="scirp.62120-ref12"><label>12</label><mixed-citation publication-type="other" xlink:type="simple">Werme, K., Bisseye, C., Ouedraogo, I., et al. (2015) Diagnostic moléculaire d’helicobacter pylori par PCR chez les patients en consultation gastroentérologique au Centre Médical Saint Camille de Ouagadougou. The Pan African Medical Journal, 21, 123. http://dx.doi.org/10.11604/pamj.2015.21.123.6001</mixed-citation></ref><ref id="scirp.62120-ref13"><label>13</label><mixed-citation publication-type="other" xlink:type="simple">Ramanampamonjy, R.M., Randria, M.J.D., Razafimahefa, S.H., et al. (2007) Séroprévalence de l’infection due à Helicobacter pylori dans un échantillon de population malgache. Bulletin de la Société de pathologie exotique, 100, 57-60.</mixed-citation></ref><ref id="scirp.62120-ref14"><label>14</label><mixed-citation publication-type="other" xlink:type="simple">Konate, A., Diarra, M., Soucko-Diarra, A., et al. (2007) Gastrites chroniques à l’ère d’Helicobacter pylori au Mali. Acta Endoscopica, 37, 315-320. http://dx.doi.org/10.1007/BF02961921</mixed-citation></ref><ref id="scirp.62120-ref15"><label>15</label><mixed-citation publication-type="other" xlink:type="simple">Lamarque, D., Burucoa, C., Courillon-Mallet, A., et al. (2012) Révision des recommandations francaises sur la prise en charge de l’infection par Helicobacter pylori. Hépato-Gastro, 19, 475-502.</mixed-citation></ref><ref id="scirp.62120-ref16"><label>16</label><mixed-citation publication-type="other" xlink:type="simple">Malfertheiner, P., Megraud, F., O’Morain, C.A., et al. (2012) Management of Helicobacter pylori Infection—The Maastricht IV/Florence Consensus Report. Gut, 61, 646-664. http://dx.doi.org/10.1136/gutjnl-2012-302084</mixed-citation></ref><ref id="scirp.62120-ref17"><label>17</label><mixed-citation publication-type="other" xlink:type="simple">Ma, H.-J. and Wang, J.-L. (2013) Quadruple Therapy for Eradication of Helicobacter pylori. World Journal of Gastroenterology, 19, 931-935. http://dx.doi.org/10.3748/wjg.v19.i6.931</mixed-citation></ref><ref id="scirp.62120-ref18"><label>18</label><mixed-citation publication-type="other" xlink:type="simple">Pan, K.F., Zhang, L., Gerhard, M., et al. (2016) A Large Randomised Controlled Intervention Trial to Prevent Gastric Cancer by Eradication of Helicobacter pylori in Linqu County, China: Baseline Results and Factors Affecting the Eradication. Gut, 65, 9-18.</mixed-citation></ref><ref id="scirp.62120-ref19"><label>19</label><mixed-citation publication-type="other" xlink:type="simple">Seyedmajidi, S., Mirsattari, D., Zojaji, H., et al. (2013) Penbactam for Helicobacter pylori Eradication: A Randomised Comparison of Quadruple and Triple Treatment Schedules in an Iranian Population. Arab Journal of Gastroenterology, 14, 1-5. http://dx.doi.org/10.1016/j.ajg.2012.12.004</mixed-citation></ref><ref id="scirp.62120-ref20"><label>20</label><mixed-citation publication-type="other" xlink:type="simple">(1999) Conférence de consensus sur Helicobacter pylori. Revision des conclusions et recommandations du groupe de travail. Gastroenterologie Clinique et Biologique, 23, C95-C104.</mixed-citation></ref><ref id="scirp.62120-ref21"><label>21</label><mixed-citation publication-type="other" xlink:type="simple">Lamouliatte, H., Megraud, F., Delchier, J.C., et al. (2003) Second Line Treatment for Failure to Eradicate Helicobacter pylori: A Randomized Trial Comparing Four Treatment Strategies. Alimentary Pharmacology &amp; Therapeutics, 18, 791-797. http://dx.doi.org/10.1046/j.1365-2036.2003.01759.x</mixed-citation></ref><ref id="scirp.62120-ref22"><label>22</label><mixed-citation publication-type="other" xlink:type="simple">Lind, T., van Zanten, S.V., Unge, P., et al. (1996) Eradication of Helicobacter pylori Using One-Week Triple Therapies Combining Omeprazole with Two Antimicrobials: The MACH I Study. Helicobacter, 1, 138-144.http://dx.doi.org/10.1111/j.1523-5378.1996.tb00027.x</mixed-citation></ref><ref id="scirp.62120-ref23"><label>23</label><mixed-citation publication-type="other" xlink:type="simple">Graham, D.Y. and Fischbach, L. (2010) Helicobacter pylori Treatment in the Era of Increasing Antibiotic Resistance. Gut, 59, 1143-1153. http://dx.doi.org/10.1136/gut.2009.192757</mixed-citation></ref><ref id="scirp.62120-ref24"><label>24</label><mixed-citation publication-type="other" xlink:type="simple">Kuo, C.H., Hu, H.M., Kuo, F.C., et al. (2009) Efficacy of Levofloxacin-Based Rescue Therapy for Helicobacter pylori Infection after Standard Triple Therapy: A Randomized Controlled Trial. Journal of Antimicrobial Chemotherapy, 63, 1017-1024. http://dx.doi.org/10.1093/jac/dkp034</mixed-citation></ref><ref id="scirp.62120-ref25"><label>25</label><mixed-citation publication-type="other" xlink:type="simple">Tzathas, C., Triantafyllou, K., Mallas, E., et al. (2008) Effect of Helicobacter pylori Eradication and Antisecretory Maintenance Therapy on Peptic Ulcer Recurrence in Cirrhotic Patients: A Prospective, Cohort 2-Year Follow-Up Study. Journal of Clinical Gastroenterology, 42, 744-749. http://dx.doi.org/10.1097/MCG.0b013e3180381571</mixed-citation></ref><ref id="scirp.62120-ref26"><label>26</label><mixed-citation publication-type="other" xlink:type="simple">Fuccio, L., Minardi, M.E., Zagari, R.M., et al. (2007) Meta-Analysis: Duration of First-Line Proton-Pump Inhibitor Based Triple Therapy for Helicobacter pylori Eradication. Annals of Internal Medicine, 147, 553-562.http://dx.doi.org/10.7326/0003-4819-147-8-200710160-00008</mixed-citation></ref><ref id="scirp.62120-ref27"><label>27</label><mixed-citation publication-type="other" xlink:type="simple">Graham, D.Y., Malaty, H.M., Evans, D.G., et al. (1991) Epidemiology of Helicobacter pylori in an Asymptomatic Population in the United States. Gastroenterology, 100, 1495-1501.</mixed-citation></ref><ref id="scirp.62120-ref28"><label>28</label><mixed-citation publication-type="other" xlink:type="simple">Replogle, M.L., Glasser, S.L., Hiatt, R.A. and Parsonnet, J. (1995) Biologic Sex as a Risk Factor for Helicobacter pylori Infection in Healthy Young Adults. American Journal of Epidemiology, 142, 856-863.</mixed-citation></ref><ref id="scirp.62120-ref29"><label>29</label><mixed-citation publication-type="other" xlink:type="simple">Stolte, M. and Meining, A. (2001) The Updated Sydney System: Classification and Grading of Gastritis as the Basis of Diagnosis and Treatment. Canadian Journal of Gastroenterology, 5, 591-598.</mixed-citation></ref><ref id="scirp.62120-ref30"><label>30</label><mixed-citation publication-type="other" xlink:type="simple">Attia, K.A., N’Dri Yoman, T., Diomandé, M.I., et al. (2001) Aspects cliniques, endoscopiques et histologiques des gastrites chroniques à Helicobacter pylori en Cote d’Ivoire: Etude de 102 patients. Bulletin de la Société de pathologie exotique, 94, 5-8.</mixed-citation></ref><ref id="scirp.62120-ref31"><label>31</label><mixed-citation publication-type="other" xlink:type="simple">Graham, D.Y. (1998) Antibiotic Resistance in Helicobacter pylori: Implications for Therapy. Gastroenterology, 115, 1272-1277. http://dx.doi.org/10.1016/S0016-5085(98)70100-3</mixed-citation></ref><ref id="scirp.62120-ref32"><label>32</label><mixed-citation publication-type="other" xlink:type="simple">Megraud, F. and Lamouliatte, H. (2003) Review Article: The Treatment of Refractory Helicobacter pylori Infection. Alimentary Pharmacology &amp; Therapeutics, 17, 1333-1343. http://dx.doi.org/10.1046/j.1365-2036.2003.01592.x</mixed-citation></ref><ref id="scirp.62120-ref33"><label>33</label><mixed-citation publication-type="other" xlink:type="simple">Raymond, J., Lamarque, D., Kalach, N., et al. (2010) High Level of Antimicrobial Resistance in French Helicobacter pylori Isolates. Helicobacter, 15, 21-27. http://dx.doi.org/10.1111/j.1523-5378.2009.00737.x</mixed-citation></ref><ref id="scirp.62120-ref34"><label>34</label><mixed-citation publication-type="other" xlink:type="simple">Romano, M., Iovene, M.R., Russo, M.I., et al. (2008) Failure of First-Line Eradication Treatment Significantly Increases Prevalence of Antimicrobial-Resistant Helicobacter pylori Clinical Isolates. Journal of Clinical Pathology, 61, 1112-1115. http://dx.doi.org/10.1136/jcp.2008.060392</mixed-citation></ref><ref id="scirp.62120-ref35"><label>35</label><mixed-citation publication-type="other" xlink:type="simple">Horiki, N., Omata, F., Uemura, M., et al. (2009) Annual Change of Primary Resistance to Clarithromycin among Helicobacter pylori Isolates from1996 through 2008 in Japan. Helicobacter, 14, 86-90.</mixed-citation></ref><ref id="scirp.62120-ref36"><label>36</label><mixed-citation publication-type="other" xlink:type="simple">Hunt, R.H., Xiao, S.D., Megraud, F., et al. (2011) Helicobacter pylori in Developing Countries. World Gastroenterology Organisation Global Guideline. Journal of Gastrointestinal and Liver Diseases, 20, 299-304.</mixed-citation></ref><ref id="scirp.62120-ref37"><label>37</label><mixed-citation publication-type="other" xlink:type="simple">Seck, A., Mbengue, M., Gassama-Sow, A., et al. (2009) Antibiotic Susceptibility of Helicobacter pylori Isolates in Dakar, Senegal. The Journal of Infection in Developing Countries, 3, 137-140. http://dx.doi.org/10.3855/jidc.512</mixed-citation></ref><ref id="scirp.62120-ref38"><label>38</label><mixed-citation publication-type="other" xlink:type="simple">Lee, J.H., Shin, J.H., Roe, I.H., et al. (2005) Impact of Clarithromycin Resistance on Eradication of Helicobacter pylori in Infected Adults. Antimicrobial Agents and Chemotherapy, 49, 1600-1603.http://dx.doi.org/10.1128/AAC.49.4.1600-1603.2005</mixed-citation></ref><ref id="scirp.62120-ref39"><label>39</label><mixed-citation publication-type="other" xlink:type="simple">De Francesco, V., Margiotta, M., Zullo, A., et al. (2006) Clarithromycin-Resistant Genotypes and Eradication of Helicobacter pylori. Annals of Internal Medicine, 144, 94-100. http://dx.doi.org/10.7326/0003-4819-144-2-200601170-00006</mixed-citation></ref><ref id="scirp.62120-ref40"><label>40</label><mixed-citation publication-type="other" xlink:type="simple">Vaira, D., Zullo, A., Vakil, N., et al. (2007) Sequential Therapy versus Standard Triple-Drug Therapy for Helicobacter pylori Eradication: A Randomized Trial. Annals of Internal Medicine, 146, 556-563.http://dx.doi.org/10.7326/0003-4819-146-8-200704170-00006</mixed-citation></ref><ref id="scirp.62120-ref41"><label>41</label><mixed-citation publication-type="other" xlink:type="simple">Wu, D.C., Hsu, P.I., Wu, J.Y., et al. (2010) Sequential and Concomitant Therapy with Four Drugs Is Equally Effective for Eradication of H pylori Infection. Clinical Gastroenterology and Hepatology, 8, 36-41.http://dx.doi.org/10.1016/j.cgh.2009.09.030</mixed-citation></ref><ref id="scirp.62120-ref42"><label>42</label><mixed-citation publication-type="other" xlink:type="simple">Malfertheiner, P., Bazzoli, F., Delchier, J.C., et al. (2011) Helicobacter pylori Eradication with a Capsule Containing Bismuth Subcitrate Potassium, Metronidazole, and Tetracycline Given with Omeprazole versus Clarithromycin-Based Triple Therapy: A Randomised, Open-Label, Non-Inferiority, Phase 3 Trial. The Lancet, 377, 905-913.http://dx.doi.org/10.1016/S0140-6736(11)60020-2</mixed-citation></ref><ref id="scirp.62120-ref43"><label>43</label><mixed-citation publication-type="other" xlink:type="simple">Laine, L., Hunt, R., El-Zimaity, H., et al. (2003) Bismuth-Based Quadruple Therapy Using a Single Capsule of Bismuth Biskalcitrate, Metronidazole, and Tetracycline Given with Omeprazole versus Omeprazole, Amoxicillin, and Clarithromycin for Eradication of Helicobacter pylori in Duodenal Ulcer Patients: A Prospective, Randomized, Multicenter, North American Trial. American Journal of Gastroenterology, 98, 562-567.http://dx.doi.org/10.1111/j.1572-0241.2003.t01-1-07288.x</mixed-citation></ref><ref id="scirp.62120-ref44"><label>44</label><mixed-citation publication-type="other" xlink:type="simple">Luther, J., Higgins, P.D., Schoenfeld, P.S., et al. (2010) Empiric Quadruple vs. Triple Therapy for Primary Treatment of Helicobacter pylori Infection: Systematic Review and Meta-Analysis of Efficacy and Tolerability. American Journal of Gastroenterology, 105, 65-73. http://dx.doi.org/10.1038/ajg.2009.508</mixed-citation></ref></ref-list></back></article>