<?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.2020.1012080</article-id><article-id pub-id-type="publisher-id">WJCD-106266</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>
 
 
  Congenital Heart Disease: Epidemiological and Echocardiography Aspects in the Cardiology Department of Tombouctou Hospital, Mali
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Souleymane</surname><given-names>Mariko</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>Samba</surname><given-names>Sidibé</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>Massama</surname><given-names>Konaté</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>Karamoko</surname><given-names>Kantako</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>Charles</surname><given-names>Dara</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>Djibril</surname><given-names>Kassogué</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>Zoumana</surname><given-names>Diallo</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>Konimba</surname><given-names>Sanogo</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>Nouhoum</surname><given-names>Diallo</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>Aniessa</surname><given-names>Kodio</given-names></name><xref ref-type="aff" rid="aff5"><sup>5</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Mariam</surname><given-names>Sako</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>Abdoul</surname><given-names>Karim Sacko</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>Coumba</surname><given-names>A. Thiam</given-names></name><xref ref-type="aff" rid="aff6"><sup>6</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Mamadou</surname><given-names>Diakité</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>Souleymane</surname><given-names>Coulibaly</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>Ichaka</surname><given-names>Menta</given-names></name><xref ref-type="aff" rid="aff7"><sup>7</sup></xref></contrib></contrib-group><aff id="aff6"><addr-line>Cardiology Department of the University Hospital Center, Kati, Mali</addr-line></aff><aff id="aff5"><addr-line>Cardiology Department, Ségou Hospital, Ségou, Mali</addr-line></aff><aff id="aff7"><addr-line>Cardiology Department of University Hospital Center, Bamako, Mali</addr-line></aff><aff id="aff4"><addr-line>Médical Department, Tombouctou Hospital, Tombouctou, Mali</addr-line></aff><aff id="aff2"><addr-line>Cardiology Department of the University Hospital Center Point G, Bamako, Mali</addr-line></aff><aff id="aff1"><addr-line>Cardiology Department, Tombouctou Hospital, Tombouctou, Mali</addr-line></aff><aff id="aff3"><addr-line>Cardiology Department, Mali Hospital, Bamako, Mali</addr-line></aff><pub-date pub-type="epub"><day>09</day><month>12</month><year>2020</year></pub-date><volume>10</volume><issue>12</issue><fpage>839</fpage><lpage>846</lpage><history><date date-type="received"><day>5,</day>	<month>November</month>	<year>2020</year></date><date date-type="rev-recd"><day>28,</day>	<month>December</month>	<year>2020</year>	</date><date date-type="accepted"><day>31,</day>	<month>December</month>	<year>2020</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>
 
 
  Congenital heart diseases are abnormalities of heart that occur during intrauterine life. Our work aimed to study the epidemiological and echocardiographic aspects of congenital heart disease with Cardiology Department of the Tombouctou hospital. This was a descriptive cross-sectional study from November 2018 to December 31, 2019 on Doppler echocardiography reports from patients admitted to the Cardiology department. The probes used were 3.5 and 5 MHz on an Esaote Mylab40 device. The inclusion criteria concerned patients of both sexes under the age of 16, hospitalized or followed in the cardiology department for cardiac symptoms and having benefited from a cardiac Doppler ultrasound. Results
  :
   During the study period, 370 echocardiographic examinations were performed and revealed 20 cases of congenital heart disease with a prevalence of 5.45%. The female sex was the majority 13/7 cases which makes a sex ratio of 0.54. Heart murmurs were the main reason for requesting cardiac Doppler ultrasound with the 13 out of 20 cases of congenital heart disease (65%). Interventricular communication was represented by 15 cases (75%). Congenital heart disease is a reality in Africa
  .
   Its frequenc
  y
   and reported series are underestimated due to the inaccessibility of Doppler echocardiography.
 
</p></abstract><kwd-group><kwd>Congenital Heart Disease</kwd><kwd> Cardiology</kwd><kwd> Tombouctou</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Introduction</title><p>Congenital heart diseases are abnormalities of the heart that occur during heart formation during intrauterine life [<xref ref-type="bibr" rid="scirp.106266-ref1">1</xref>]. They constitute a major public health problem in Mali and are increasingly described in Africa where the incidence is estimated at 8 per 1.000 births [<xref ref-type="bibr" rid="scirp.106266-ref2">2</xref>]. Hospital prevalence varies from country to country with 4.9% in Mali [<xref ref-type="bibr" rid="scirp.106266-ref3">3</xref>], 0.98% in Burkina Faso [<xref ref-type="bibr" rid="scirp.106266-ref4">4</xref>], 5.09% in Congo [<xref ref-type="bibr" rid="scirp.106266-ref5">5</xref>] and 4.18% in Senegal [<xref ref-type="bibr" rid="scirp.106266-ref6">6</xref>]. The Doppler echocardiography is nowadays the essential examination in the diagnosis of congenital heart disease.</p><p>The absence of epidemiological data on congenital heart disease at the Tombouctou hospital and the opening of a cardiac surgery Department of University Hospital center Luxembourg “M&#232;re-enfant” Bamako-Mali justify the present study aimed at describing the epidemiological aspects and echocardiography of congenital heart disease in the Cardiology Department, Tombouctou Hospital, Mali.</p><p>Material and Methods: This was a descriptive cross-sectional study from November 2018 to December 31, 2019 on Doppler echocardiography reports from patients admitted to the Cardiology department. The inclusion criteria concerned patients of both sexes under 16 years of age presenting symptoms suggesting cardiac involvement and having undergone a cardiac Doppler ultrasound and were not included patients over 16 years of age and those under 16 years old who did not have a cardiac Doppler echo.</p><p>The outcome measures were: Patients with symptoms of cardiac involvement. Cardiac Doppler ultrasound was the confirmatory diagnostic examination by revealing structural abnormalities.</p><p>The treatment was medical due to the lack of technical platform.</p><p>Definitions of terms:</p><p>Interventricular communication is a dehiscence of the interventricular septum. They are accompanied by an abnormal diversion of arterial blood into venous blood. It is a predominant left-right shunt between the left ventricle and the right ventricle through a septal defect.</p><p>Persistence of the ductus arteriosus is the persistence after birth of a fetal physiological communication between the pulmonary artery and the trunk of the descending aorta just downstream of the left subclavian artery responsible for a congenital non-cyanogenic heart disease with shunt left - right arterial.</p><p>Atrioventricular canal is a complex malformation caused by partial or complete absence of the atrioventricular floor resulting in abnormal communication between the atrial and ventricular stages. It is caused by a developmental disorder of the endocardial bulges which normally divide the common ostium into the mitral orifice and the tricuspid orifice.</p><p>Inter atrial communication corresponds to abnormal communication between at them atria (right and left).</p><p>Ethics: Informed consent was obtained with strict respect for confidentiality.</p><p>The data collection: Patients were recruited from an anonymity survey sheet with the cardiac Doppler ultrasound report. The parameters studied were socio-demographic data, clinical circumstances of discovery, CBC results, fasting blood glucose, serum creatinine, frontal chest X-ray and cardiac Doppler echo.</p><p>Word and Excel 2013 software were used for data entry and SPSS 11 and Epi Info 3.3.2 software for their analysis. The static test used was the ki2 with a significance level of 5%.</p></sec><sec id="s2"><title>2. Results</title><p>During the study period, 370 echocardiographic examinations were carried out and made it possible to highlight 20 cases of congenital heart disease with a hospital prevalence of 5.45%, achieving four (4) different nosological entities (<xref ref-type="table" rid="table1">Table 1</xref>).</p><p>We have not objectified any case of association of congenital heart disease. The interventricular Communication were prominent in congenital heart disease 15 cases (75%), followed by atrioventricular duct and ductus arteriosus with the same percentage of 10 (<xref ref-type="table" rid="table2">Table 2</xref>).</p><p>The majority of congenital heart disease was diagnosed between 5 and 30 months with 45%.</p><p>The mean age at the time of the Doppler echocardiogram was 96.95 months with ranges of 5 months and 53 years. The 5 - 30 month age group was the most represented with 9 cases (45%), followed by those over 60 months with 7 cases (35%) (<xref ref-type="fig" rid="fig1">Figure 1</xref> &amp; <xref ref-type="table" rid="table3">Table 3</xref>).</p><p>The female gender was predominantly represented with 13 cases, which makes a sex ratio of 0.54.</p><p>Clinically, cardiac murmur and respiratory distress were the major functional signs (<xref ref-type="table" rid="table4">Table 4</xref>). The result of the cardiac Doppler echo made it possible to retain four (4) nosological entities (<xref ref-type="table" rid="table1">Table 1</xref>).</p><table-wrap id="table1" ><label><xref ref-type="table" rid="table1">Table 1</xref></label><caption><title> Distribution of cases of congenital heart disease according to echocardiographic data</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Type of congenital heart disease</th><th align="center" valign="middle" >Frequency</th><th align="center" valign="middle" >Percent%</th></tr></thead><tr><td align="center" valign="middle" >Interventricular Communication Inter-Atrial Communication Atrio-Ventricular Canal Persistent ductus arteriosus</td><td align="center" valign="middle" >15 1 2 2</td><td align="center" valign="middle" >75 5 10 10</td></tr></tbody></table></table-wrap><table-wrap id="table2" ><label><xref ref-type="table" rid="table2">Table 2</xref></label><caption><title> Distribution of the different types of heart disease according to age</title></caption><table><tbody><thead><tr><th align="center" valign="middle"  rowspan="2"  >Heart disease type</th><th align="center" valign="middle"  colspan="4"  >Age group (months)</th></tr></thead><tr><td align="center" valign="middle" >[5 - 30]</td><td align="center" valign="middle" >]30 - 60]</td><td align="center" valign="middle" >&gt;60</td><td align="center" valign="middle" >TOTAL</td></tr><tr><td align="center" valign="middle" >Ventricular communication</td><td align="center" valign="middle" >8</td><td align="center" valign="middle" >4</td><td align="center" valign="middle" >3</td><td align="center" valign="middle" >15</td></tr><tr><td align="center" valign="middle" >Persistent ductus arteriosus</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</td></tr><tr><td align="center" valign="middle" >Atrioventricular channel</td><td align="center" valign="middle" >1</td><td align="center" valign="middle" >0</td><td align="center" valign="middle" >1</td><td align="center" valign="middle" >2</td></tr><tr><td align="center" valign="middle" >Inter atrial communication</td><td align="center" valign="middle" >0</td><td align="center" valign="middle" >0</td><td align="center" valign="middle" >1</td><td align="center" valign="middle" >1</td></tr><tr><td align="center" valign="middle" >TOTAL</td><td align="center" valign="middle" >9</td><td align="center" valign="middle" >4</td><td align="center" valign="middle" >7</td><td align="center" valign="middle" >20</td></tr></tbody></table></table-wrap><table-wrap id="table3" ><label><xref ref-type="table" rid="table3">Table 3</xref></label><caption><title> The nosological distribution of the 20 cases of congenital heart disease according to sex</title></caption><table><tbody><thead><tr><th align="center" valign="middle"  rowspan="2"  >Heart disease type</th><th align="center" valign="middle"  colspan="2"  >sex</th><th align="center" valign="middle"  rowspan="2"  >Total</th></tr></thead><tr><td align="center" valign="middle" >M</td><td align="center" valign="middle" >F</td></tr><tr><td align="center" valign="middle" >Ventricular communication</td><td align="center" valign="middle" >5</td><td align="center" valign="middle" >10</td><td align="center" valign="middle" >15</td></tr><tr><td align="center" valign="middle" >Persistent ductus arteriosus</td><td align="center" valign="middle" >0</td><td align="center" valign="middle" >1</td><td align="center" valign="middle" >1</td></tr><tr><td align="center" valign="middle" >Atrioventricular channel</td><td align="center" valign="middle" >0</td><td align="center" valign="middle" >2</td><td align="center" valign="middle" >2</td></tr><tr><td align="center" valign="middle" >Inter atrial communication</td><td align="center" valign="middle" >2</td><td align="center" valign="middle" >0</td><td align="center" valign="middle" >2</td></tr><tr><td align="center" valign="middle" >TOTAL</td><td align="center" valign="middle" >7</td><td align="center" valign="middle" >13</td><td align="center" valign="middle" >20</td></tr></tbody></table></table-wrap><table-wrap id="table4" ><label><xref ref-type="table" rid="table4">Table 4</xref></label><caption><title> Distribution of reasons for requesting echocardiography</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Reasons for request</th><th align="center" valign="middle" >Frequency</th><th align="center" valign="middle" >Percent%</th></tr></thead><tr><td align="center" valign="middle" >Heart murmur</td><td align="center" valign="middle" >13</td><td align="center" valign="middle" >65</td></tr><tr><td align="center" valign="middle" >Respiratory distress</td><td align="center" valign="middle" >4</td><td align="center" valign="middle" >20</td></tr><tr><td align="center" valign="middle" >Growth retardation and heart murmur</td><td align="center" valign="middle" >2</td><td align="center" valign="middle" >10</td></tr><tr><td align="center" valign="middle" >Heart failure</td><td align="center" valign="middle" >1</td><td align="center" valign="middle" >5</td></tr><tr><td align="center" valign="middle" >TOTAL</td><td align="center" valign="middle" >20</td><td align="center" valign="middle" >100</td></tr></tbody></table></table-wrap></sec><sec id="s3"><title>3. Discussion</title><p>Overall results</p><p>Frequency: our study, out of 370 echo cardiac Doppler ultrasound examinations carried out, we objectified 20 cases of congenital heart disease with a prevalence of 5.40%. Several studies reported by different authors show variable frequencies. However, these series all concordantly underscore the worrisome nature of congenital heart disease in Africa. <xref ref-type="table" rid="table5">Table 5</xref> gives the comparative results of the prevalence of congenital heart disease from different African series. These differences in prevalence could be linked to the following factors: difference in the selection criteria for pediatric series in certain studies [<xref ref-type="bibr" rid="scirp.106266-ref5">5</xref>] - [<xref ref-type="bibr" rid="scirp.106266-ref12">12</xref>] and finally ultrasound series [<xref ref-type="bibr" rid="scirp.106266-ref4">4</xref>].</p><p>Distribution of patients by sex</p><p>The female sex predominated in our study with a sex ratio of 0.54. This disagrees with the results of Kinda, Kokou, Ould Zein, Tour&#233;, Diop, M'pemba-Loufoua, Acrachi [<xref ref-type="bibr" rid="scirp.106266-ref4">4</xref>] [<xref ref-type="bibr" rid="scirp.106266-ref7">7</xref>] [<xref ref-type="bibr" rid="scirp.106266-ref9">9</xref>] [<xref ref-type="bibr" rid="scirp.106266-ref10">10</xref>] [<xref ref-type="bibr" rid="scirp.106266-ref11">11</xref>] [<xref ref-type="bibr" rid="scirp.106266-ref12">12</xref>] [<xref ref-type="bibr" rid="scirp.106266-ref13">13</xref>] which noted a preponderance of the male sex. This difference can be explained by the nature of our study which looked at patients under the age of 16.</p><p>For most authors, gender was not implicated in the genesis of congenital heart disease and there was no clear predominance.</p><p>Distribution of patients by age</p><p>The mean age of our patients in our series was 96.95 months with extremes of 5 months and less than 16 years. The 5 to 30 month age group was the most represented with 9 cases (45%); followed by more than 60 months with 7 cases (35%). This is in agreement with Ab&#233;na [<xref ref-type="bibr" rid="scirp.106266-ref9">9</xref>] and Cloarec [<xref ref-type="bibr" rid="scirp.106266-ref14">14</xref>] who noted that most congenital heart disease was diagnosed from an early age between 0 and 2 years old respectively 70% and 61%. This high rate of congenital heart disease is explained by the lack of technical facilities in many African countries and the high cost of evacuation to an appropriate center. However, the intake was symptomatic and purely medical.</p><p>Certain congenital heart diseases such as Interventricular Communications, Inter-atrial Communications and Persistence of the Ductile Arterial, which represented 90% of cases in our study, progress spontaneously towards closure [<xref ref-type="bibr" rid="scirp.106266-ref15">15</xref>] [<xref ref-type="bibr" rid="scirp.106266-ref16">16</xref>] [<xref ref-type="bibr" rid="scirp.106266-ref17">17</xref>]; late onset congenital heart disease is most often benign and compatible with an almost normal life.</p><p>Indications for echocardiography</p><p>Murmurs were the predominant reason for performing a cardiac Doppler echo with 65% followed by respiratory distress in 20% of cases. These results could be explained by the intense character and irradiation in radius of a wheel of the murmur in the interventricular communication an almost constant sign [<xref ref-type="bibr" rid="scirp.106266-ref18">18</xref>]. With regard to respiratory distress, it is most often recurrent bronchopneumopathies as a revelation of congenital heart disease favored on the one hand by precarious hygienic conditions, immunodeficiency in newborns or children and on the other hand by flooding and pulmonary hypersecretion.</p><p>The different heart diseases encountered</p><p>The heart disease most frequently found in our study and in most studies in Africa [<xref ref-type="bibr" rid="scirp.106266-ref4">4</xref>] [<xref ref-type="bibr" rid="scirp.106266-ref9">9</xref>] [<xref ref-type="bibr" rid="scirp.106266-ref10">10</xref>] and in the world [<xref ref-type="bibr" rid="scirp.106266-ref16">16</xref>] [<xref ref-type="bibr" rid="scirp.106266-ref19">19</xref>] was Interventricular communication with a preponderance of the peri-membranous form: 98, 4%) or associated with other heart disease (<xref ref-type="table" rid="table6">Table 6</xref>).</p><table-wrap id="table5" ><label><xref ref-type="table" rid="table5">Table 5</xref></label><caption><title> Comparative table of the prevalence of congenital heart disease from different African series</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Studies</th><th align="center" valign="middle" >Prevalence</th><th align="center" valign="middle" >Place of study</th></tr></thead><tr><td align="center" valign="middle" >Kinda, Burkina [<xref ref-type="bibr" rid="scirp.106266-ref4">4</xref>] Mayanda, Congo-Brazzaville [<xref ref-type="bibr" rid="scirp.106266-ref5">5</xref>] Niakara, Burkina-Faso [<xref ref-type="bibr" rid="scirp.106266-ref6">6</xref>] Georges Kinda, Burkina-Faso [<xref ref-type="bibr" rid="scirp.106266-ref7">7</xref>] Samandoulougou, Burkina-Faso [<xref ref-type="bibr" rid="scirp.106266-ref8">8</xref>] Our study Tombouctou-Mali Abena-Obama, Cameroun [<xref ref-type="bibr" rid="scirp.106266-ref9">9</xref>] M’pembaLoufoua Lemay, Congo-Brazza [<xref ref-type="bibr" rid="scirp.106266-ref10">10</xref>] Amon-Tanoh-Dick, C&#244;te d’Ivoire [<xref ref-type="bibr" rid="scirp.106266-ref11">11</xref>] KokouOutcha, Togo [<xref ref-type="bibr" rid="scirp.106266-ref13">13</xref>]</td><td align="center" valign="middle" >0.98% 5.09% 6% 0.98% 0.78% 5.40% 0.64% 0.5% 0.1% 0.48%</td><td align="center" valign="middle" >Studies carried out in a cardiological environment Studies carried out in pediatric settings</td></tr></tbody></table></table-wrap><table-wrap id="table6" ><label><xref ref-type="table" rid="table6">Table 6</xref></label><caption><title> Comparative table of the frequency of VICs in the world</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Country</th><th align="center" valign="middle" >Authors</th><th align="center" valign="middle"  colspan="2"  >VIC frequency (%)</th></tr></thead><tr><td align="center" valign="middle" >Togo</td><td align="center" valign="middle" >KokouOutcha [<xref ref-type="bibr" rid="scirp.106266-ref10">10</xref>]</td><td align="center" valign="middle"  colspan="2"  >24.4</td></tr><tr><td align="center" valign="middle" >S&#233;n&#233;gal</td><td align="center" valign="middle" >Acrachi [<xref ref-type="bibr" rid="scirp.106266-ref9">9</xref>]</td><td align="center" valign="middle"  colspan="2"  >38</td></tr><tr><td align="center" valign="middle" >Burkina-Faso</td><td align="center" valign="middle" >Kinda [<xref ref-type="bibr" rid="scirp.106266-ref4">4</xref>]</td><td align="center" valign="middle"  colspan="2"  >23.33</td></tr><tr><td align="center" valign="middle" >France</td><td align="center" valign="middle" >Joly et al. [<xref ref-type="bibr" rid="scirp.106266-ref16">16</xref>]</td><td align="center" valign="middle"  colspan="2"  >30 &#224; 40</td></tr><tr><td align="center" valign="middle" >Etats-Unis</td><td align="center" valign="middle" >Sables [<xref ref-type="bibr" rid="scirp.106266-ref19">19</xref>]</td><td align="center" valign="middle"  colspan="2"  >30</td></tr><tr><td align="center" valign="middle" >Mali notre &#233;tude</td><td align="center" valign="middle" >Mariko S</td><td align="center" valign="middle" >75</td><td align="center" valign="middle" ></td></tr></tbody></table></table-wrap></sec><sec id="s4"><title>4. Conclusions</title><p>Congenital heart disease is a reality in Africa. It is described in Africa where interventricular communication is frequent. Its frequency is probably underestimated due to the unavailability of echocardiography in certain regions, the lack of financial means and the growing insecurity in Africa.</p><p>Its management requires:</p><p>- equipping our cardiology and radiology departments with efficient diagnostic means;</p><p>- opening of cardiovascular surgery units.</p></sec><sec id="s5"><title>Acknowledgements</title><p>We thank the management of the Tombouctou hospital for completing the administrative and regulatory formalities for this work, as well as the parents of the patients for their trust.</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>Mariko, S., Sidib&#233;, S., Konat&#233;, M., Kantako, K., Dara, C., Kassogu&#233;, D., Diallo, Z., Sanogo, K., Diallo, N., Kodio, A., Sako, M., Sacko, A.K., Thiam, C.A., Diakit&#233;, M., Coulibaly, S. and Menta, I. (2020) Congenital Heart Disease: Epidemiological and Echocardiography Aspects in the Cardiology Department of Tombouctou Hospital, Mali. World Journal of Cardiovascular Diseases, 10, 839-846. https://doi.org/10.4236/wjcd.2020.1012080</p></sec></body><back><ref-list><title>References</title><ref id="scirp.106266-ref1"><label>1</label><mixed-citation publication-type="other" xlink:type="simple">Sable, C.A. (2004) Ultrasound of Congenital Heart Disease: A Review of Prenatal and Postnatal Echocardiography. Seminars in Roentgenology, 39, 215-233.  
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