<?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.2019.98053</article-id><article-id pub-id-type="publisher-id">WJCD-94618</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>
 
 
  100 Cases of Clinical and Etiological Aspects of Cardiac Insufficiency in N’Djamena, Chad
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Natingar</surname><given-names>Madjirangar</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>Adam</surname><given-names>Ahamat Ali</given-names></name><xref ref-type="aff" rid="aff2"><sup>2</sup></xref><xref ref-type="corresp" rid="cor1"><sup>*</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Bekoutou</surname><given-names>Amngar</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>Jean</surname><given-names>Philippe Lesbre</given-names></name><xref ref-type="aff" rid="aff3"><sup>3</sup></xref></contrib></contrib-group><aff id="aff3"><addr-line>The Good Samaritan Hospital of N’Djamena, N’Djamena, Chad</addr-line></aff><aff id="aff2"><addr-line>Faculty of Human Health Sciences of N’Djamena, N’Djamena, Chad</addr-line></aff><aff id="aff1"><addr-line>National General Reference Hospital of N’Djamena, N’Djamena, Chad</addr-line></aff><pub-date pub-type="epub"><day>08</day><month>08</month><year>2019</year></pub-date><volume>09</volume><issue>08</issue><fpage>612</fpage><lpage>619</lpage><history><date date-type="received"><day>13,</day>	<month>June</month>	<year>2019</year></date><date date-type="rev-recd"><day>24,</day>	<month>August</month>	<year>2019</year>	</date><date date-type="accepted"><day>27,</day>	<month>August</month>	<year>2019</year></date></history><permissions><copyright-statement>&#169; Copyright  2014 by authors and Scientific Research Publishing Inc. </copyright-statement><copyright-year>2014</copyright-year><license><license-p>This work is licensed under the Creative Commons Attribution International License (CC BY). http://creativecommons.org/licenses/by/4.0/</license-p></license></permissions><abstract><p>
 
 
   
    Introduction:
    Cardiac Insufficiency
    
   is progressively taking over as the leading cause of morbidity and mortality in the world and a major public health problem in Chad. Our study was to contribute and provide a deeper understanding of the clinical and etiological aspects concerning the etiology and management of Cardiac Insufficiency in N’Djamena, Chad.
    
   Due to having no published data to distinctly understand this pathology in this part of the world, we represent here a summary of available data which could be used to describe the clinical and etiological aspects of Cardiac Insufficiency and to help in changing practices for an optimal management as a baseline for comparison in future studies.
    
   <b style="line-height:1.5;">Patients and Methods:</b>
    This was a prospective, descriptive study conducted 
   from
    November 30th 2011 to May 30th 2013 at the Good Samaritan Hospital of N’Djamena.
    
   <b style="line-height:1.5;">Results:</b>
    100 hospitalized patients were included consecutively. The sex ratio was 1.08 with an average age of 40.21 &#177; 21.30 years. The main cardiovascular risk factors were high blood pressure (15%), obesity (12%) and diabetes (11%). Clinically, exertional dyspnea was found in 95% of cases, and signs of congestive heart failure in 61% of cases. The etiologies were 50% of Rheumatic valvulopathy, 22% of Dilated cardiomyopathy, 13% of Hypertensive cardiomyopathy and 12% of Congenital heart disease.
    
   <b style="line-height:1.5;">Conclusion:</b>
    The most common etiologies were Rheu
   matic valvulopathy, Congenital heart disease, Dilated cardiomyopathy and Hypertensive cardiomyopathy. 
  
 
</p></abstract><kwd-group><kwd>Cardiac Insufficiency</kwd><kwd> Etiology</kwd><kwd> Echocardiography</kwd><kwd> N’Djamena</kwd><kwd> Chad</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Introduction</title><p>Cardiac Insufficiency (CI) is a common pathology worldwide. It is a clinical syndrome characterized by chronic symptoms (e.g. dyspnea, fatigue) that may be accompanied by physical signs (e.g. crepitations, peripheral edema) caused by a structural and/or functional cardiac abnormality, which causes a decrease in cardiac output [<xref ref-type="bibr" rid="scirp.94618-ref1">1</xref>] . CI is a major global public health problem affecting 40 million people worldwide in 2015 [<xref ref-type="bibr" rid="scirp.94618-ref2">2</xref>] . CI represents one of the leading causes of hospitalization, morbidity and mortality, especially among the elderly [<xref ref-type="bibr" rid="scirp.94618-ref3">3</xref>] . In western countries, the incidence and prevalence of CI are increasing due to the aging of the population [<xref ref-type="bibr" rid="scirp.94618-ref1">1</xref>] . The prevalence was estimated at 1% - 2% of the adult population [<xref ref-type="bibr" rid="scirp.94618-ref1">1</xref>] [<xref ref-type="bibr" rid="scirp.94618-ref4">4</xref>] , while the incidence rate is generally estimated at 2 to 5 per 1000 people annually [<xref ref-type="bibr" rid="scirp.94618-ref5">5</xref>] [<xref ref-type="bibr" rid="scirp.94618-ref6">6</xref>] . In Africa, CI is one of the main circumstances in the discovery of cardiovascular disease with an incidence of 1 to 3 per 1000 people annually and a prevalence of 3 to 20 per 1000 people annually, often at an advanced stage [<xref ref-type="bibr" rid="scirp.94618-ref7">7</xref>] . According to World Health Organization estimates, cardiovascular disease is the second leading cause of death in Africa. In 2015, nearly 1.2 million people died of heart disease in Africa, which is more than Malaria and Tuberculosis combined [<xref ref-type="bibr" rid="scirp.94618-ref8">8</xref>] . Despite improvements observed in the survival of patients with CI in recent years, overall prognosis remains poor [<xref ref-type="bibr" rid="scirp.94618-ref3">3</xref>] [<xref ref-type="bibr" rid="scirp.94618-ref9">9</xref>] with 50% survival estimates at 5 years after initial CI diagnosis [<xref ref-type="bibr" rid="scirp.94618-ref10">10</xref>] [<xref ref-type="bibr" rid="scirp.94618-ref11">11</xref>] . However, in Chad, we do not have data on this pathology. The objective of this work was to identify the etiology of CI in Chad.</p></sec><sec id="s2"><title>2. Patients and Methods</title><p>This was a study conducted from November 30th 2011 to May 30th 2013 at the Good Samaritan Hospital of N’Djamena. We consecutively included all the patients that were hospitalized for CI during this study period. Patients who refused to give their consent were excluded. There were no specific selection criteria. The variable studies were clinical (history, cardiovascular risk factors, functional signs, physical signs), biological (HIV serology, blood count, thyroid hormone, serum creatinine, blood urea, electrolyte panel, blood glucose) and echocardiographic (dilation, hypertrophy and left ventricular ejection fraction, valvular abnormalities, pulmonary arterial pressures, and pericardial abnormalities).</p><p>The system used was the HP 1000 ET 5500 model. The following parameters were specified:</p><p>&#183; Dilation of the Left Ventricle</p><p>&#183; Left Ventricular Hypertrophy</p><p>&#183; Systolic Dysfunction</p><p>&#183; Valvulopathy</p><p>&#183; Congenital Heart Disease</p><p>Statistical analysis</p><p>In this study, a descriptive statistical analysis was applied using Microsoft Excel, quantitative variables were presented by their mean and standard deviation and qualitative variables were by percentages.</p><p>Declaration of ethics</p><p>The study was conducted after an agreement of the Ethics Committee of the Faculty of Medicine of N’Djamena and with the consent of patients.</p></sec><sec id="s3"><title>3. Results</title><p>100 patients were included. <xref ref-type="table" rid="table1">Table 1</xref> summarizes the characteristics of this population. The sex ratio was 1.08 (52 men) with an average age of 40.21 &#177; 21.30 years with a predominance of patients aged 20 to 29 years and those with an age greater than or equal to 50 years of age. The main cardiovascular risk factors were high blood pressure (15%), obesity (12%) and diabetes (11%). Other risk factors identified were dyslipidemia (02%), alcohol (10%), smoking (04%), and renal dysfunction (09%).</p><p>Clinically (<xref ref-type="table" rid="table2">Table 2</xref>), exertional dyspnea was observed in 95% of cases, and the signs of global CI were 61% of cases.</p><table-wrap id="table1" ><label><xref ref-type="table" rid="table1">Table 1</xref></label><caption><title> Characteristics of the population</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Settings</th><th align="center" valign="middle" >Number (N)</th><th align="center" valign="middle" >Percentage (%)</th></tr></thead><tr><td align="center" valign="middle" >Sex: Women Man</td><td align="center" valign="middle" >48 52</td><td align="center" valign="middle" >48 52</td></tr><tr><td align="center" valign="middle" >Age (year): Means &lt;20 20 - 29 30 - 39 40 - 49 ≥50</td><td align="center" valign="middle" >40.21 &#177; 21.30 24 27 10 12 27</td><td align="center" valign="middle" >24 27 10 12 27</td></tr><tr><td align="center" valign="middle" >Risk factors: Obesity Diabetes Dyslipidemia Alcohol Smoking Hypertension Renal Dysfunction</td><td align="center" valign="middle" >12 11 02 10 04 15 09</td><td align="center" valign="middle" >12 11 02 10 04 15 09</td></tr></tbody></table></table-wrap><table-wrap id="table2" ><label><xref ref-type="table" rid="table2">Table 2</xref></label><caption><title> Clinical manifestations</title></caption><table><tbody><thead><tr><th align="center" valign="middle" ></th><th align="center" valign="middle" >Number (N)</th><th align="center" valign="middle" >Percentage (%)</th></tr></thead><tr><td align="center" valign="middle" >Functional signs: Dyspnea Orthopnea Hemoptysis Palpitations Hepatalgia</td><td align="center" valign="middle" >95 15 18 53 15</td><td align="center" valign="middle" >95 15 18 53 15</td></tr><tr><td align="center" valign="middle" >Physical signs: Left CI signs Right CI signs Signs of global CI</td><td align="center" valign="middle" >29 10 61</td><td align="center" valign="middle" >29 10 61</td></tr></tbody></table></table-wrap><p>Regarding the etiologies of CI (<xref ref-type="table" rid="table3">Table 3</xref>), Rheumatic heart valve disease was found in 48% of cases including (11%) Mitral stenosis, (13%) Mitral insufficiency, (06%) Mitral diseases, (3%) Aortic stenosis, (2%) Aortic insufficiency, (4%) Aortic disease, and (9%) Polyvalvulopathy. The dysfunctions of the prosthetic valves were found in (2%) of cases all in the mitral position, which were mechanical and bioprosthetic. 22% of Dilated cardiomyopathies (DCM) including (8%) primary DCM, (4%) Ischemic DCM, (5%) Peripartum DCM, (3%) Ethyl DCM, (1%) Cardiothorosis DCM and (1%) Rhythmic DCM. Hypertensive cardiomyopathies were found in 13% of cases, 12% congenital heart disease, 2% pericardial disease, and 1% idiopathic pulmonary arterial hypertension (IPAH). <xref ref-type="table" rid="table3">Table 3</xref> presents the etiologies of CI by age group (<xref ref-type="fig" rid="fig1">Figure 1</xref>).</p></sec><sec id="s4"><title>4. Discussion</title><p>CI is a global public health problem. In Chad, we do not have epidemiological data on this pathology. In this study the mean age was 40.21 &#177; 21.30 years and more than half of our patients were under 50 years of age. Several authors in Sub-Saharan Africa have found similar results [<xref ref-type="bibr" rid="scirp.94618-ref12">12</xref>] [<xref ref-type="bibr" rid="scirp.94618-ref13">13</xref>] [<xref ref-type="bibr" rid="scirp.94618-ref14">14</xref>] . In the West, according to the Framingham Cohort study, the average age was 70 [<xref ref-type="bibr" rid="scirp.94618-ref15">15</xref>] . This difference in the average age with the West, is related to the lack of medical coverage and the reduced life expectancy at home. The leading cardiovascular risk</p><table-wrap id="table3" ><label><xref ref-type="table" rid="table3">Table 3</xref></label><caption><title> Etiologies of CI</title></caption><table><tbody><thead><tr><th align="center" valign="middle"  colspan="2"  >Etiology</th><th align="center" valign="middle" >Number (N)</th><th align="center" valign="middle" >Percentage (%)</th></tr></thead><tr><td align="center" valign="middle"  rowspan="3"  >Rheumatic Valvulopathy</td><td align="center" valign="middle" >Mitral stenosis Mitral insufficiency Mitral disease</td><td align="center" valign="middle" >11 13 06</td><td align="center" valign="middle" >11 13 06</td></tr><tr><td align="center" valign="middle" >Aortic stenosis Aortic insufficiency Aortic disease</td><td align="center" valign="middle" >03 02 04</td><td align="center" valign="middle" >03 02 04</td></tr><tr><td align="center" valign="middle" >Polyvalvulopathy</td><td align="center" valign="middle" >09</td><td align="center" valign="middle" >09</td></tr><tr><td align="center" valign="middle"  colspan="2"  >Prosthesis Dysfunction</td><td align="center" valign="middle" >02</td><td align="center" valign="middle" >02</td></tr><tr><td align="center" valign="middle" >Congenital Heart Disease</td><td align="center" valign="middle" >Inter auricular communication Inter ventricular communication Atrio-ventricular canal Complex heart disease</td><td align="center" valign="middle" >01 04 02 05</td><td align="center" valign="middle" >01 04 02 05</td></tr><tr><td align="center" valign="middle" >Dilated Cardiomyopathy</td><td align="center" valign="middle" >Ischemic Peripartum Ethyl Cardiothyreosis Rhythmic Primitive</td><td align="center" valign="middle" >04 05 03 01 01 08</td><td align="center" valign="middle" >04 05 03 01 01 08</td></tr><tr><td align="center" valign="middle"  colspan="2"  >Hypertensive Cardiomyopathy</td><td align="center" valign="middle" >13</td><td align="center" valign="middle" >13</td></tr><tr><td align="center" valign="middle"  colspan="2"  >IPAH</td><td align="center" valign="middle" >01</td><td align="center" valign="middle" >01</td></tr><tr><td align="center" valign="middle"  colspan="2"  >Pericardial Disease</td><td align="center" valign="middle" >02</td><td align="center" valign="middle" >02</td></tr></tbody></table></table-wrap><p>factors in our study were high blood pressure, obesity, diabetes, alcohol and renal dysfunction. The same risk factors have been found in most studies in both developed and Sub-Saharan Africa [<xref ref-type="bibr" rid="scirp.94618-ref16">16</xref>] [<xref ref-type="bibr" rid="scirp.94618-ref17">17</xref>] . Our patients often presented with a global CI chart (61%) because of the delayed diagnosis related to difficulties in access to health care and the lack of specialists. This clinical presentation was noted by several authors in Sub-Saharan Africa [<xref ref-type="bibr" rid="scirp.94618-ref14">14</xref>] [<xref ref-type="bibr" rid="scirp.94618-ref18">18</xref>] [<xref ref-type="bibr" rid="scirp.94618-ref19">19</xref>] . The etiologies of CI in this study were dominated by non-ischemic causes. Rheumatic valvulopathy were the main causes (48%), followed by DCM (22%) and hypertensive cardiomyopathy (13%). Ischemic cardiomyopathy was found only in 4% of cases. These results are consistent with most of the study series in Sub-Saharan Africa, where these 3 etiologies account for more than 65% of the causes of CI [<xref ref-type="bibr" rid="scirp.94618-ref13">13</xref>] [<xref ref-type="bibr" rid="scirp.94618-ref14">14</xref>] [<xref ref-type="bibr" rid="scirp.94618-ref19">19</xref>] [<xref ref-type="bibr" rid="scirp.94618-ref20">20</xref>] [<xref ref-type="bibr" rid="scirp.94618-ref21">21</xref>] . In the West, Ischemic heart disease is the most common etiology of CI. However, in Africa, Hypertensive cardiomyopathy is predominant [<xref ref-type="bibr" rid="scirp.94618-ref16">16</xref>] [<xref ref-type="bibr" rid="scirp.94618-ref22">22</xref>] . In a recent systematic review and meta-analysis of 22 African studies (1999-2017) 10098 patients; Hypertensive heart disease was the most common cause of CI (39.2%), followed by Cardiomyopathy (21.4%) and Rheumatic heart disease (14.1%) [<xref ref-type="bibr" rid="scirp.94618-ref23">23</xref>] . Ischemic heart disease was rare (7.2%) [<xref ref-type="bibr" rid="scirp.94618-ref23">23</xref>] . The size of our sample was not representative to assert the rarity of ischemic heart disease in Ndjamena, Chad. Further studies will be needed to provide an answer to this trend. However, according to age groups, our study revealed a clear predominance of Rheumatic heart disease and Congenital heart disease in children and young adults (&lt;30 years of age). The dilated cardiomyopathies and the hypertensive heart diseases mainly affected adults beyond 30 years of age.</p></sec><sec id="s5"><title>5. Limitations of Our Study</title><p>The sample size of our study is not significant enough to reach formal conclusions. In this study, we did not include the therapeutic and evolutionary aspect of the patients which could have given us an idea about the overall care of the patients. Therefore, further studies are needed in the future with larger samples to better describe this pathology.</p></sec><sec id="s6"><title>6. Conclusion</title><p>Cardiac Insufficiency is the main reason for hospitalization in the Cardiology Department at the Good Samaritan Hospital of N’Djamena in Chad. In this study, the four leading causes of CI were Rheumatic valvulopathy, congenital heart disease, dilated cardiomyopathy, and hypertensive cardiomyopathy. However, Ischemic heart disease was rare. In young people, the main etiology was rheumatic valvulopathy, whereas, in the elderly it was DCM.</p></sec><sec id="s7"><title>Conflicts of Interest</title><p>The authors do not declare any conflict of interest.</p></sec><sec id="s8"><title>Cite this paper</title><p>Madjirangar, N., Ali, A.A., Amngar, B. and Lesbre, J.P. (2019) 100 Cases of Clinical and Etiological Aspects of Cardiac Insufficiency in N’Djamena, Chad. World Journal of Cardiovascular Diseases, 9, 612-619. https://doi.org/10.4236/wjcd.2019.98053</p></sec><sec id="s9"><title>Abbreviation</title><p>CI: Cardiac Insufficiency; DCM: Dilated Cardiomyopathie; IPAH: Idiopathic Pulmonary Arterial Hypertension.</p></sec></body><back><ref-list><title>References</title><ref id="scirp.94618-ref1"><label>1</label><mixed-citation publication-type="other" xlink:type="simple">Ponikowski, P., Voors, A.A., Anker, S.D., et al. (2016) ESC Guidelines for the Diagnosis and Treatment of Acute and Chronic Heart Failure: The Task Force for the Diagnosis and Treatment of Acute and Chronic Heart Failure of the European Society of Cardiology (ESC). Developed with the Special Contribution of the Heart Failure Association (HFA) of the ESC. European Heart Journal, 18, 891-975.  
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