<?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">WJCD</journal-id><journal-title-group><journal-title>World Journal of Cardiovascular Diseases</journal-title></journal-title-group><issn pub-type="epub">2164-5329</issn><publisher><publisher-name>Scientific Research Publishing</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.4236/wjcd.2018.88039</article-id><article-id pub-id-type="publisher-id">WJCD-86666</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>
 
 
  Ventricular Septal Defects at the Souro Sanou University Hospital Center (CHUSS): Ultrasound, Therapeutic and Evolutionary Aspects of 88 Cases
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Somnoma</surname><given-names>Jean-Baptiste Tougouma</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>Oumarou</surname><given-names>Sombie</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>Makoura</surname><given-names>Barro</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>Aimé</surname><given-names>Bama</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>Georges</surname><given-names>Kinda</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>Samba</surname><given-names>Sidibé</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>Boubacar</surname><given-names>Nacro</given-names></name><xref ref-type="aff" rid="aff2"><sup>2</sup></xref></contrib></contrib-group><aff id="aff3"><addr-line>Charles de Gaulle Pediatrics University Hospital Center, Ouagadougou, Burkina Faso</addr-line></aff><aff id="aff4"><addr-line>Cardiology Department, Point G University Hospital Center, Bamako, Mali</addr-line></aff><aff id="aff1"><addr-line>Higher Institute of Health Sciences (INSSA), Nazi Boni University, Bobo-Dioulasso, Burkina Faso</addr-line></aff><aff id="aff2"><addr-line>Pediatrics Department, Sour&amp;amp;ocirc; Sanou University Hospital Center, Bobo-Dioulasso, Burkina Faso</addr-line></aff><author-notes><corresp id="cor1">* E-mail:<email>tougjb@yahoo.fr(SJT)</email>;</corresp></author-notes><pub-date pub-type="epub"><day>14</day><month>08</month><year>2018</year></pub-date><volume>08</volume><issue>08</issue><fpage>403</fpage><lpage>410</lpage><history><date date-type="received"><day>7,</day>	<month>June</month>	<year>2018</year></date><date date-type="rev-recd"><day>12,</day>	<month>August</month>	<year>2018</year>	</date><date date-type="accepted"><day>15,</day>	<month>August</month>	<year>2018</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: 
  There is a need for data on epidemiological, clinical and therapeutic aspects of ventricular septal defect among children in Sub-Saharan Africa.
   
  <b>Objective: </b>
  The aim of
   
  this study
   
  was to determine the prevalence, epidemioclinical, echocardiographic, therapeutic and evolutionary aspects of ventricular septal defects (VSD) in the pediatric department of the University Hospital Center (CHUSS) of Bobo-Dioulasso. <b>Methods:</b> This study was a descriptive cross-sectional study, conducted from Novem
  ber 2013 to December 2016. All children aged 1 to 179 months seen at the pediatric consultation in CHUSS
   
  were included. CIV was confirmed with Doppler echocardiography. <b>Results:</b>
   
  Out of 36,240 children who received consultation in the pediatric ward of CHUSS during the study period, one hundred (100) cases of them had congenital heart disease representing a hospital prevalence of 2.76%. This was
   
  diagnosed with Doppler echocardiography. Of these, 88% were VSD isolated or associated with other cardiac malformations. Isolated form was reported in 54.3% of cases.
   
  The average age at diagnosis was 39.6 months. The sex ratio was 1.05. Perimembranous topography and hemodynamic type 
  2
   were the highest, representing 56.8% and 35.2% respectively. The indication for surgical repair was recommended for 81.8% of the cases, but only 9.7% of these cases benefited from cardiac surgery. The rest were for medicalcare with a high proportion of lost to follow-up (48.9%). <b>Conclusion:</b>
  <b> </b>
  VSD is the most common congenital heart disease. Its care is mainly surgical. This cardiac surgery is non-existent in Burkina Faso. The design of multidisciplinary
   
  strategies associated with an optimization of the means of the countries of Sub-Saharan Africa could improve the management of this cardiopathy.
 
</p></abstract><kwd-group><kwd>Ventricular Septal Defect</kwd><kwd> Congenital Heart Disease</kwd><kwd> Echocardiography</kwd><kwd>  Burkina Faso</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Introduction</title><p>Congenital heart disease is a real public health problem. Indeed their frequency is estimated globally at 5% - 8‰ of live births [<xref ref-type="bibr" rid="scirp.86666-ref1">1</xref>] ; which corresponds to 40% of all fetal malformations. They cause 50% of deaths related to all malformations [<xref ref-type="bibr" rid="scirp.86666-ref2">2</xref>] . Ventricular septal defects (VSD) accounts for 30% of these malformations and is particularly serious because of its anatomical and hemodynamic polymorphism [<xref ref-type="bibr" rid="scirp.86666-ref3">3</xref>] . VSD has been reported to be the most common congenital heart disease in many countries with a frequency of 32.3% and 27.2% in the United States of America and Burkina Faso respectively [<xref ref-type="bibr" rid="scirp.86666-ref4">4</xref>] [<xref ref-type="bibr" rid="scirp.86666-ref5">5</xref>] . This work has been done to better define the anatomical and hemodynamic profile as well as the therapeutic and evolutionary modalities of VSD in the context of our country with limited resources; to optimize its support.</p></sec><sec id="s2"><title>2. Methods</title><p>This study was a cross-sectional descriptive study that ran from November 2013 to December 2016 in the pediatric department of the Souro Sanou University Hospital Center (CHUSS) in Bobo-Dioulasso. This period coincided with the installation of Doppler echocardiography in the CHUSS. The study population consisted of all children from 1 to 179 months who were received at the Pediatrics Department of the hospital. Those with suspected congenital heart disease had Doppler echocardiography performed for them by a cardio pediatrician. The examinations were standardized and the reports were written and archived in real time. A 5 MHz cardiac probe on an Aloka Prosound 4000 Plus device with pulsed, continuous and color Doppler was used.</p><p>All cases of VSD isolated or in combination with other malformations that have been identified. Isolated VSDs were classified according to the classification of Nadas based on the size of the shunt and on the pulmonary blood flow [<xref ref-type="bibr" rid="scirp.86666-ref6">6</xref>] . Aspects associated with other malformations, as well as sociodemographic, clinical, therapeutic and evolutionary data were extracted from clinical records. The socioeconomic level of the child’s family was defined according to the parents’ occupation which is an indicator of their monthly incomes. These socioeconomic level are: High (upper-level management and liberal professions), Middle (middle managers) and Low (farm workers, housewife etc.) [<xref ref-type="bibr" rid="scirp.86666-ref7">7</xref>] . The Epi data 3.4.1 software was used for the statistical analysis of the data.</p></sec><sec id="s3"><title>3. Results</title><sec id="s3_1"><title>3.1. Prevalence of VSD</title><p>Out of 36,240 children seen at the pediatric ward of CHUSS during the study period, one hundred (100) cases of congenital heart disease were diagnosed with a hospital prevalence of 2.76‰. Of these cases, 88% of the congenital heart defects were VSD isolated or associated with other cardiac malformations.</p></sec><sec id="s3_2"><title>3.2. Sociodemographic Characteristics of Children with VSD</title><p>The mean age was 39.6 months. The age group of 1 - 12 months was the highest, representing 44.3% of the cases. The sex ratio m/f was 1.05. The majority of children lived in urban areas (64.7%) and the low socio-economic level of parents was predominant (<xref ref-type="table" rid="table1">Table 1</xref>).</p></sec><sec id="s3_3"><title>3.3. Anatomical and Hemodynamic Aspects of VSDs</title><p>Isolated VSD was the highest number of cases, representing (54.3%). Of these, type 2 hemodynamic form was the most common, representing 64.5% of cases; and that of type 3 was found in 4 children (4.5% of cases). The VSD was predominantly single (97.7%), perimembranous localization (56.8%). Ten cases of VSD 2a (10.4%) were complicated by aortic insufficiency resulting in Laubry’s and Pezzi’s syndrome. <xref ref-type="table" rid="table2">Table 2</xref>(a) and <xref ref-type="table" rid="table2">Table 2</xref>(b) give us the distribution of VSD according to the anatomical forms.</p><p>The form associated with other cardiac malformations was dominated by T4F (26.1% of cases). The other associated malformations are summarized in <xref ref-type="table" rid="table3">Table 3</xref>.</p></sec><sec id="s3_4"><title>3.4. Therapeutic and Evolutionary Aspects of VSDs</title><p>The indication of surgical repair was asked in 72 patients, 81.8% of the cases. Those who had cardiac surgery were 7 (9.7% of cases). Thirteen (13) children were hospitalized during the study period with a maximum of 3 hospitalizations per child, representing a hospitalization rate of 1.5%. The most common reasons for hospitalization were cardiac decompensation (45.7%) and infectious endocarditis (14.3%). The mean duration of hospitalization was 6.7 days &#177; 5.2. Four (4) patients died of respiratory complications, 43 (48.8%) were lost to follow-up and 7 (7%, 9%) were waiting for cardiac surgery (<xref ref-type="table" rid="table4">Table 4</xref>).</p></sec></sec><sec id="s4"><title>4. Discussion</title><p>Only children with suspected congenital heart disease had benefited from</p><table-wrap id="table1" ><label><xref ref-type="table" rid="table1">Table 1</xref></label><caption><title> Distribution according to socio-demographic and economic characteristics of the 88 children having VSD; CHUSS, Bobo-Dioulasso, November 2013 to December 2016</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Variables</th><th align="center" valign="middle" >Characteristics</th><th align="center" valign="middle" >Number of children</th><th align="center" valign="middle" >Percentage (%)</th></tr></thead><tr><td align="center" valign="middle"  rowspan="3"  >Sex</td><td align="center" valign="middle" >M</td><td align="center" valign="middle" >45</td><td align="center" valign="middle" >51.1</td></tr><tr><td align="center" valign="middle" >F</td><td align="center" valign="middle" >43</td><td align="center" valign="middle" >48.9</td></tr><tr><td align="center" valign="middle" >Total</td><td align="center" valign="middle" >88</td><td align="center" valign="middle" >100.0</td></tr><tr><td align="center" valign="middle"  rowspan="6"  >Age at echocardiographic diagnosis (in months)</td><td align="center" valign="middle" >&lt;1</td><td align="center" valign="middle" >2</td><td align="center" valign="middle" >2.2</td></tr><tr><td align="center" valign="middle" >1 - 12</td><td align="center" valign="middle" >39</td><td align="center" valign="middle" >44.3</td></tr><tr><td align="center" valign="middle" >13 - 59</td><td align="center" valign="middle" >26</td><td align="center" valign="middle" >29.6</td></tr><tr><td align="center" valign="middle" >60 - 120</td><td align="center" valign="middle" >14</td><td align="center" valign="middle" >15.9</td></tr><tr><td align="center" valign="middle" >&gt;120</td><td align="center" valign="middle" >7</td><td align="center" valign="middle" >8.0</td></tr><tr><td align="center" valign="middle" >Total</td><td align="center" valign="middle" >88</td><td align="center" valign="middle" >100.0</td></tr><tr><td align="center" valign="middle"  rowspan="6"  >Level of schooling</td><td align="center" valign="middle" >Preschool</td><td align="center" valign="middle" >39</td><td align="center" valign="middle" >44.3</td></tr><tr><td align="center" valign="middle" >Primary</td><td align="center" valign="middle" >3</td><td align="center" valign="middle" >3.4</td></tr><tr><td align="center" valign="middle" >Secondary</td><td align="center" valign="middle" >1</td><td align="center" valign="middle" >1.1</td></tr><tr><td align="center" valign="middle" >No schooling</td><td align="center" valign="middle" >2</td><td align="center" valign="middle" >2.3</td></tr><tr><td align="center" valign="middle" >Not specified</td><td align="center" valign="middle" >43</td><td align="center" valign="middle" >48.9</td></tr><tr><td align="center" valign="middle" >Total</td><td align="center" valign="middle" >88</td><td align="center" valign="middle" >100.0</td></tr><tr><td align="center" valign="middle"  rowspan="5"  >Residence</td><td align="center" valign="middle" >Urban</td><td align="center" valign="middle" >57</td><td align="center" valign="middle" >64.7</td></tr><tr><td align="center" valign="middle" >Rural</td><td align="center" valign="middle" >11</td><td align="center" valign="middle" >12.5</td></tr><tr><td align="center" valign="middle" >Semi-urban</td><td align="center" valign="middle" >10</td><td align="center" valign="middle" >11.4</td></tr><tr><td align="center" valign="middle" >Not specified</td><td align="center" valign="middle" >10</td><td align="center" valign="middle" >11.4</td></tr><tr><td align="center" valign="middle" >Total</td><td align="center" valign="middle" >88</td><td align="center" valign="middle" >100.0</td></tr><tr><td align="center" valign="middle"  rowspan="5"  >Socio-economic level</td><td align="center" valign="middle" >Low</td><td align="center" valign="middle" >48</td><td align="center" valign="middle" >54.5</td></tr><tr><td align="center" valign="middle" >Middle</td><td align="center" valign="middle" >27</td><td align="center" valign="middle" >30.7</td></tr><tr><td align="center" valign="middle" >High</td><td align="center" valign="middle" >3</td><td align="center" valign="middle" >3.4</td></tr><tr><td align="center" valign="middle" >Unspecified</td><td align="center" valign="middle" >10</td><td align="center" valign="middle" >11.4</td></tr><tr><td align="center" valign="middle" >Total</td><td align="center" valign="middle" >88</td><td align="center" valign="middle" >100.0</td></tr></tbody></table></table-wrap><table-wrap-group id="2"><label><xref ref-type="table" rid="table2">Table 2</xref></label><caption><title> (a) Distribution of VSDs according to the anatomical forms (number of VSD) of the 88 children carrying VICs; CHUSS, Bobo-Dioulasso, November 2013 to December 2016; (b) Distribution of VSDs according to the anatomical forms (VSD size) of the 88 children carrying VICs; CHUSS, Bobo-Dioulasso, November 2013 to December 2016</title></caption><table-wrap id="2_1"><caption><title> (b)</title></caption><table><tbody><thead><tr><th align="center" valign="middle"  rowspan="2"  >Number of VSD</th><th align="center" valign="middle"  colspan="4"  >Location</th><th align="center" valign="middle"  colspan="2"  ></th></tr></thead><tr><td align="center" valign="middle" >Perimembranous</td><td align="center" valign="middle" >Infundibular</td><td align="center" valign="middle" >Admission</td><td align="center" valign="middle" >Trabecular</td><td align="center" valign="middle"  colspan="2"  >Total (%)</td></tr><tr><td align="center" valign="middle" >Unique</td><td align="center" valign="middle" >50</td><td align="center" valign="middle" >30</td><td align="center" valign="middle" >6</td><td align="center" valign="middle" >0</td><td align="center" valign="middle" >97.7</td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Multiple</td><td align="center" valign="middle" >0</td><td align="center" valign="middle" >0</td><td align="center" valign="middle" >0</td><td align="center" valign="middle" >2</td><td align="center" valign="middle" >2.3</td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Total (%)</td><td align="center" valign="middle" >56.8</td><td align="center" valign="middle" >34.1</td><td align="center" valign="middle" >6.8</td><td align="center" valign="middle" >2.3</td><td align="center" valign="middle" >100</td><td align="center" valign="middle" ></td></tr></tbody></table></table-wrap><table-wrap id="2_2"><caption><title></title></caption><table><tbody><thead><tr><th align="center" valign="middle"  rowspan="2"  >VSD Size</th><th align="center" valign="middle"  colspan="4"  >Location</th><th align="center" valign="middle"  colspan="2"  ></th></tr></thead><tr><td align="center" valign="middle" >Perimembranous</td><td align="center" valign="middle" >Infundibular</td><td align="center" valign="middle" >Admission</td><td align="center" valign="middle" >Trabecular</td><td align="center" valign="middle"  colspan="2"  >Total (%)</td></tr><tr><td align="center" valign="middle" >Small</td><td align="center" valign="middle" >14</td><td align="center" valign="middle" >00</td><td align="center" valign="middle" >00</td><td align="center" valign="middle" >02</td><td align="center" valign="middle" >18.2</td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Large</td><td align="center" valign="middle" >36</td><td align="center" valign="middle" >30</td><td align="center" valign="middle" >06</td><td align="center" valign="middle" >00</td><td align="center" valign="middle" >81.8</td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Total (%)</td><td align="center" valign="middle" >56.8</td><td align="center" valign="middle" >34.1</td><td align="center" valign="middle" >6.8</td><td align="center" valign="middle" >2.3</td><td align="center" valign="middle" >100</td><td align="center" valign="middle" ></td></tr></tbody></table></table-wrap></table-wrap-group><table-wrap id="table3" ><label><xref ref-type="table" rid="table3">Table 3</xref></label><caption><title> Distribution according to hemodynamic forms of isolated VSD and forms associated with other cardiac malformations of 88 children with VSD; CHUSS, Bobo-Dioulasso, November 2013 to December 2016</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Form</th><th align="center" valign="middle" >Type</th><th align="center" valign="middle" >Frequency</th><th align="center" valign="middle" >Percentage (%)</th><th align="center" valign="middle" >Total (%)</th></tr></thead><tr><td align="center" valign="middle"  rowspan="5"  >Isolated</td><td align="center" valign="middle" >1</td><td align="center" valign="middle" >10</td><td align="center" valign="middle" >11.4</td><td align="center" valign="middle"  rowspan="5"  >54.3</td></tr><tr><td align="center" valign="middle" >2<sub>a </sub></td><td align="center" valign="middle" >16</td><td align="center" valign="middle" >18.2</td></tr><tr><td align="center" valign="middle" >2<sub>b </sub></td><td align="center" valign="middle" >15</td><td align="center" valign="middle" >17.0</td></tr><tr><td align="center" valign="middle" >3</td><td align="center" valign="middle" >04</td><td align="center" valign="middle" >4.5</td></tr><tr><td align="center" valign="middle" >4</td><td align="center" valign="middle" >03</td><td align="center" valign="middle" >3.4</td></tr><tr><td align="center" valign="middle"  rowspan="5"  >Associated</td><td align="center" valign="middle" >T4F</td><td align="center" valign="middle" >23</td><td align="center" valign="middle" >26.1</td><td align="center" valign="middle"  rowspan="5"  >45.7</td></tr><tr><td align="center" valign="middle" >CAV</td><td align="center" valign="middle" >11</td><td align="center" valign="middle" >12.5</td></tr><tr><td align="center" valign="middle" >TAC</td><td align="center" valign="middle" >04</td><td align="center" valign="middle" >4.5</td></tr><tr><td align="center" valign="middle" >SP open septum</td><td align="center" valign="middle" >1</td><td align="center" valign="middle" >1.1</td></tr><tr><td align="center" valign="middle" >TGV</td><td align="center" valign="middle" >1</td><td align="center" valign="middle" >1.1</td></tr><tr><td align="center" valign="middle" >Total</td><td align="center" valign="middle" ></td><td align="center" valign="middle" >88</td><td align="center" valign="middle" >100</td><td align="center" valign="middle" ></td></tr></tbody></table></table-wrap><p>T4F = Tetralogy of Fallot; CAV = Atrioventricular canal; TAC = Common arterial trunk; SP = Pulmonary stenosis; TGV = Transposition of the great vessels.</p><table-wrap id="table4" ><label><xref ref-type="table" rid="table4">Table 4</xref></label><caption><title> Distribution of 88 children with VSD according to evolutionary aspects; CHUSS, Bobo-Dioulasso, November 2013 to December 2016</title></caption><table><tbody><thead><tr><th align="center" valign="middle"  colspan="2"  >Evolution</th><th align="center" valign="middle" >Frequency</th><th align="center" valign="middle" >Percentage (%)</th></tr></thead><tr><td align="center" valign="middle"  colspan="2"  >Stabilised</td><td align="center" valign="middle" >26</td><td align="center" valign="middle" >29.6</td></tr><tr><td align="center" valign="middle"  rowspan="2"  >Evacuated</td><td align="center" valign="middle" >Surgical repair</td><td align="center" valign="middle" >7</td><td align="center" valign="middle" >7.9</td></tr><tr><td align="center" valign="middle" >No surgical repair</td><td align="center" valign="middle" >1</td><td align="center" valign="middle" >1.1</td></tr><tr><td align="center" valign="middle"  colspan="2"  >Deceased</td><td align="center" valign="middle" >4</td><td align="center" valign="middle" >4.5</td></tr><tr><td align="center" valign="middle"  colspan="2"  >Waiting for evacuation</td><td align="center" valign="middle" >7</td><td align="center" valign="middle" >7.9</td></tr><tr><td align="center" valign="middle"  colspan="2"  >Lost to follow-up</td><td align="center" valign="middle" >43</td><td align="center" valign="middle" >48.9</td></tr><tr><td align="center" valign="middle"  colspan="2"  >Total</td><td align="center" valign="middle" >88</td><td align="center" valign="middle" >100.0</td></tr></tbody></table></table-wrap><p>Doppler echocardiography for confirmation of the VSD. There is a risk of underestimation of VSD prevalence due to this information bias. The study was a cross sectional hospital-based study. The sample of children included may not accurately reflect the general population of children. This selection bias reduces the generalizability of our results. Despite these limitations, our study is the first to report on hospital prevalence and the echocardiographic, therapeutic and evolutionary aspects of VSDs in a resource-poor country such as Burkina Faso.</p><p>Our study reports a low prevalence of 2.76‰ of congenital heart disease in children 1 to 176 months in a hospital. This prevalence is significantly lower than that reported by most of the African authors which varies from 4.8‰ to 9.8‰ [<xref ref-type="bibr" rid="scirp.86666-ref8">8</xref>] [<xref ref-type="bibr" rid="scirp.86666-ref9">9</xref>] [<xref ref-type="bibr" rid="scirp.86666-ref10">10</xref>] [<xref ref-type="bibr" rid="scirp.86666-ref11">11</xref>] . It could be explained by an underestimation of the cases because only those who had a suspicion of heart disease and who had echocardiographic confirmation were taken into account in our study. There is still no data on the overall prevalence of congenital heart disease in hospitals in Burkina Faso. It is therefore necessary to conduct new studies in the general population to better understand the weight of these pathologies in our contexts.</p><p>VSD accounted for 88% of congenital heart defects in our series, confirming its high frequency as documented in the literature [<xref ref-type="bibr" rid="scirp.86666-ref1">1</xref>] [<xref ref-type="bibr" rid="scirp.86666-ref12">12</xref>] [<xref ref-type="bibr" rid="scirp.86666-ref13">13</xref>] [<xref ref-type="bibr" rid="scirp.86666-ref14">14</xref>] . Our proportion, higher than the averages of other countries, could be explained by the clinical characteristics of the CIV. Indeed the presence of a heart murmur as the main clinical sign of the VSD motivates more the demand for echo cardiac by pediatricians and or general practitioners for VSD compared to other congenital heart diseases that are clinically less obvious. This result indicates the need for better training of doctors and the institution in our countries of prenatal echocardiographic screening, which is currently non-existent.</p><p>The age of discovery of VSD was relatively high in our study with greater than 5 years for 23.8% of patients. This could be explained by the delay in the consultation of multifactorial causes (ignorance, poverty, use of traditional therapy) (<xref ref-type="fig" rid="fig1">Figure 1</xref>). These late discoveries are of a formidable prognosis when one knows the evolutionary potential of the VSD towards pulmonary obstructive vascular disease. Since March 2016, with a view to reducing maternal and infant mortality in Burkina Faso, the Ministry of Health has set up health insurance to provide free health care for children under 5 years and pregnant women. This measure should eventually improve access to child care to enable early diagnosis of VSDs.</p><p>In terms of hemodynamics, type 2a and 2b CIVs were the most recovered with 64.5% as in other African studies [<xref ref-type="bibr" rid="scirp.86666-ref5">5</xref>] [<xref ref-type="bibr" rid="scirp.86666-ref14">14</xref>] . This high frequency could be explained by the noisy symptomatology of VSD at these stages motivating consultation at baseline levels.</p><p>The surgical indication was asked in 81.8 of the cases, but only seven (9.7%) received corrective surgery outside the country thanks to the support of sponsoring organizations. This finding of powerlessness is reported by all African studies, which report a proportion of operated cases varying between 0% and 21% [<xref ref-type="bibr" rid="scirp.86666-ref5">5</xref>] [<xref ref-type="bibr" rid="scirp.86666-ref14">14</xref>] [<xref ref-type="bibr" rid="scirp.86666-ref15">15</xref>] [<xref ref-type="bibr" rid="scirp.86666-ref16">16</xref>] . This situation could be explained by the lack of a cardiac surgery center in Burkina Faso and the impossibility for the country to carry out this surgery outside the country at an excessively high cost. This highlights the urgency of setting up pediatric cardiac surgery services in our sub-region to make this vital service more accessible.</p><p>We reported a high proportion of lost to follow-up (48.9%) in our study. This situation, with dramatic consequences, could be explained by lack of adequate</p><p>care, the high cost of medical care, and the ignorance of our populations. The lack of a conventional medical response to parents’ requests leads them to turn to traditional medicine in our setting (<xref ref-type="fig" rid="fig1">Figure 1</xref>). Rapid access to cardiac surgery and universal health insurance could reverse this trend.</p></sec><sec id="s5"><title>5. Conclusion</title><p>VSD is the most frequently diagnosed cardiac malformation at CHUSS in Bobo-Dioulasso. It is characterized by a late discovery and insufficiency of surgical management rendering uncertainty and the vital prognosis of children having this congenital heart disease. The design of multidisciplinary strategies associated with pooling resources of Sub-Saharan African countries could improve the management of this heart disease.</p></sec><sec id="s6"><title>Conflicts of Interest</title><p>The authors declare no conflicts of interest regarding the publication of this paper.</p></sec><sec id="s7"><title>Cite this paper</title><p>Tougouma, S.J.-B., Sombie, O., Barro, M., Bama, A., Kinda, G., Sidib&#233;, S. and Nacro, B. (2018) Ventricular Septal Defects at the Souro Sanou University Hospital Center (CHUSS): Ultrasound, Therapeutic and Evolutionary Aspects of 88 Cases. World Journal of Cardiovascular Diseases, 8, 403-410. https://doi.org/10.4236/wjcd.2018.88039</p></sec></body><back><ref-list><title>References</title><ref id="scirp.86666-ref1"><label>1</label><mixed-citation publication-type="other" xlink:type="simple">OMS. Aide-Mémoire N°370: Anomalies congénitales. 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