<?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.2022.124020</article-id><article-id pub-id-type="publisher-id">WJCD-116821</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>
 
 
  Venous Thromboembolic Disease and Thrombolysis at the Yaound&#233; Emergency Center during the Past Five Years, Cameroon
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Chris</surname><given-names>Nadège Nganou-Gnindjio</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>Bâ</surname><given-names>Hamadou</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>Ludovic</surname><given-names>Kadji</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>Jules</surname><given-names>Thierry Elong</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>Daryl</surname><given-names>Tcheutchoua Nzokou</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>Honoré</surname><given-names>Kemnang Yemele</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>Alain</surname><given-names>Patrick Menanga</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>Samuel</surname><given-names>Kingue</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>Jacqueline</surname><given-names>Ze Minkande</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib></contrib-group><aff id="aff1"><addr-line>Faculty of Medicine and Biomedical Sciences, University of Yaoundé I, Yaoundé, Cameroon</addr-line></aff><pub-date pub-type="epub"><day>14</day><month>04</month><year>2022</year></pub-date><volume>12</volume><issue>04</issue><fpage>199</fpage><lpage>208</lpage><history><date date-type="received"><day>9,</day>	<month>March</month>	<year>2022</year></date><date date-type="rev-recd"><day>24,</day>	<month>April</month>	<year>2022</year>	</date><date date-type="accepted"><day>27,</day>	<month>April</month>	<year>2022</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: 
  Venous thromboembolic disease (VTE) is a clinical entity whose two clinical manifestations are deep vein thrombosis (DVT) and pulmonary embolism (PE). It is a frequent and severe disease in Cameroon, thus constituting a significant public health problem.
   
  We aimed to describe VTE management in the Yaound&#233; Emergency Center, in particular the use of thrombolysis. <b>Methods:</b> This was a retrospective study on patients hospitali
  z
  ed at the Yaound&#233; Emergency Center for DVT and/or PE from January 1, 2015, to December 31, 2020. We collected clinical signs, paraclinical signs, risk factors of VTE, and management methods from each patient. <b>Results:</b> We recruited 106 participants. Dyspnea
   
  was the most frequent symptom; PE was the most common form of VTE 
  i
  n eight patients on 10. Obesity and high blood pressure were the main cardiovascular risk factors. The main clinical signs were 
  o
  edema and pain in the limb for DVT, dyspnea
  ,
   and tachycardia for PE. Heparinotherapy was the most commonly used management modality. Thrombolysis was performed in 7.5% of participants, especially in the case of hypotension or massive PE. <b>Conclusion: </b>In VTE management, thrombolysis remains the least used therapeutic modality in our context. Heparinotherapy remains the basis of the therapy.
 
</p></abstract><kwd-group><kwd>Venous Thromboembolic Disease</kwd><kwd> Thrombolysis</kwd><kwd> Yaound&#233;-Cameroon</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Introduction</title><p>Cardiovascular diseases are the leading cause of death worldwide [<xref ref-type="bibr" rid="scirp.116821-ref1">1</xref>]. They are responsible for approximately 17.5 million deaths, i.e. overall mortality estimated at 31%, of which more than 75% concerns middle- or low-income countries [<xref ref-type="bibr" rid="scirp.116821-ref2">2</xref>]. Venous thromboembolic disease (VTE) is the third leading cause of cardiovascular disease and is associated with mortality and high social cost, especially in resource-limited countries [<xref ref-type="bibr" rid="scirp.116821-ref3">3</xref>] [<xref ref-type="bibr" rid="scirp.116821-ref4">4</xref>]. VTE is a clinical entity that includes deep vein thrombosis (DVT) and pulmonary embolism (PE). It is a common condition, and its incidence increases with age [<xref ref-type="bibr" rid="scirp.116821-ref5">5</xref>]. Hospital studies carried out in 2015 in Mali and Cameroon reported 4.02% and 1.6%, respectively [<xref ref-type="bibr" rid="scirp.116821-ref6">6</xref>] [<xref ref-type="bibr" rid="scirp.116821-ref7">7</xref>].</p><p>Although their clinical presentations are described in the literature, the particularities of the sub-Saharan context are rarely specified. Indeed, VTE is a multifactorial entity resulting from an interaction between genetic predisposition and acquired factors [<xref ref-type="bibr" rid="scirp.116821-ref8">8</xref>] [<xref ref-type="bibr" rid="scirp.116821-ref9">9</xref>]. In addition, factors such as late consultation are specific to the context of developing countries and can lead to unclassical clinical presentations. The rapid identification of these presentations is essential for good management [<xref ref-type="bibr" rid="scirp.116821-ref10">10</xref>].</p><p>This study aimed to describe the management of VTE disease in the Yaound&#233; Emergency Center (CURY), mainly the frequency of the use of thrombolysis.</p></sec><sec id="s2"><title>2. Methods</title><sec id="s2_1"><title>2.1. Study Design and Setting</title><p>We carried out a retrospective study on hospitalized patient records from January 2015 to December 2020 at the Yaound&#233; Emergency Center (CURY), Yaound&#233;, Cameroon. CURY is a hospital specializing in emergency management in Yaound&#233;, Cameroon.</p></sec><sec id="s2_2"><title>2.2. Participants</title><p>All records of patients admitted for VTE and whose diagnosis was confirmed by venous Doppler ultrasound of the limbs and/or chest CT angiography were included. Incomplete forms were not included.</p></sec><sec id="s2_3"><title>2.3. Data Collection</title><p>Using a questionnaire pretested and validated, data were collected including: sociodemographic, clinical, paraclinical data, and the management modalities. Paraclinical data included D-dimers, Doppler ultrasound and thoracic CT angiography results. Therapeutic data contained the treatment received, particularly the administration of low molecular weight heparin and thrombolytics.</p></sec><sec id="s2_4"><title>2.4. Statistical Analysis</title><p>Data recording and analysis were performed using SPSS version 23.0 software. Quantitative data were presented as mean and standard deviation and qualitative data as proportions. The association between qualitative variables was assessed using The Chi-square test. The threshold of significance was 0.05.</p></sec></sec><sec id="s3"><title>3. Results</title><sec id="s3_1"><title>3.1. General Characteristics of the Population Study</title><p>We included 106 patients aged 22 to 96 years, with an average of 58.03 &#177; 14.92 years. About 46% of our study population was between 61 and 80 years old, with a male/female sex ratio of 0.56.</p><p>In consultation, dyspnea was the main symptom, found in 48.1% of patients, followed by chest pain (22.6%). The VTE risk factors identified were high blood pressure (38.7%), overweight (26.4%), type 2 diabetes and sedentary lifestyle (see <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> General characteristics of the study population</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Variables</th><th align="center" valign="middle" >Effective (n = 106)</th><th align="center" valign="middle" >Percentage (%)</th></tr></thead><tr><td align="center" valign="middle" >Sex</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Male</td><td align="center" valign="middle" >38</td><td align="center" valign="middle" >35.8</td></tr><tr><td align="center" valign="middle" >Female</td><td align="center" valign="middle" >68</td><td align="center" valign="middle" >64.2</td></tr><tr><td align="center" valign="middle" >Age (years)</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >&lt;40</td><td align="center" valign="middle" >16</td><td align="center" valign="middle" >15.1</td></tr><tr><td align="center" valign="middle" >41 - 60</td><td align="center" valign="middle" >37</td><td align="center" valign="middle" >34.9</td></tr><tr><td align="center" valign="middle" >61 - 80</td><td align="center" valign="middle" >49</td><td align="center" valign="middle" >46.2</td></tr><tr><td align="center" valign="middle" >&gt;80</td><td align="center" valign="middle" >4</td><td align="center" valign="middle" >3.8</td></tr><tr><td align="center" valign="middle" >Cardiovascular and/or VTE risk factors</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >History of VTE</td><td align="center" valign="middle" >4</td><td align="center" valign="middle" >3.8</td></tr><tr><td align="center" valign="middle" >Obese or overweight</td><td align="center" valign="middle" >28</td><td align="center" valign="middle" >26.4</td></tr><tr><td align="center" valign="middle" >Tobacco</td><td align="center" valign="middle" >1</td><td align="center" valign="middle" >0.9</td></tr><tr><td align="center" valign="middle" >Prolonged bed rest</td><td align="center" valign="middle" >16</td><td align="center" valign="middle" >15.1</td></tr><tr><td align="center" valign="middle" >cast immobilization</td><td align="center" valign="middle" >8</td><td align="center" valign="middle" >7.5</td></tr><tr><td align="center" valign="middle" >Neoplasia</td><td align="center" valign="middle" >7</td><td align="center" valign="middle" >6.6</td></tr><tr><td align="center" valign="middle" >Heart failure</td><td align="center" valign="middle" >10</td><td align="center" valign="middle" >9.4</td></tr><tr><td align="center" valign="middle" >Diabetes</td><td align="center" valign="middle" >16</td><td align="center" valign="middle" >15.1</td></tr><tr><td align="center" valign="middle" >Hypertension</td><td align="center" valign="middle" >41</td><td align="center" valign="middle" >38.7</td></tr><tr><td align="center" valign="middle" >HIV infection</td><td align="center" valign="middle" >2</td><td align="center" valign="middle" >1.9</td></tr><tr><td align="center" valign="middle" >Recent trauma</td><td align="center" valign="middle" >18</td><td align="center" valign="middle" >17</td></tr><tr><td align="center" valign="middle" >Recent surgery</td><td align="center" valign="middle" >13</td><td align="center" valign="middle" >12.3</td></tr><tr><td align="center" valign="middle" >Recent delivery (&lt;45 days)</td><td align="center" valign="middle" >2</td><td align="center" valign="middle" >1.9</td></tr><tr><td align="center" valign="middle" >Recent trip</td><td align="center" valign="middle" >17</td><td align="center" valign="middle" >16</td></tr><tr><td align="center" valign="middle" >COVID-19</td><td align="center" valign="middle" >2</td><td align="center" valign="middle" >1.9</td></tr></tbody></table></table-wrap></sec><sec id="s3_2"><title>3.2. Clinical Characteristics of the Study Population</title><p>Clinically, the signs of DVT found were mainly edema and pain in the lower limbs in 96.4% and 85.7% of patients, respectively. <xref ref-type="table" rid="table2">Table 2</xref> shows that dyspnea and tachycardia were the main signs of PE, found in 97.7% and 79.5% of patients.</p></sec><sec id="s3_3"><title>3.3. Paraclinical Characteristics of the Study Population</title><p>D-dimer levels were &gt; 500 ng/mL at the biology level in all patients. An electrocardiogram was performed in 54 patients, and the S1Q3 aspect was the majority electrical anomaly in 22.2% of patients, followed by the right bundle branch block (11.1%). A transthoracic Doppler ultrasound was performed in 35 patients and found pulmonary arterial hypertension (77.1%), the right cavities dilatation (60%) and dilatation of the trunk of the pulmonary artery (54.3%) as the major abnormalities. Venous Doppler ultrasound of the limbs found a thrombus in 28 of the 106 patients. The lower limbs were the most affected by DVT (92.9%). The most common location was popliteal in 46.4%, followed by the femoral site (25%). Chest CT angiography was performed in 88 patients. PE was bilateral in 65.9% and massive in 13.6% of patients. The main location was segmental and</p><table-wrap id="table2" ><label><xref ref-type="table" rid="table2">Table 2</xref></label><caption><title> Clinical characteristics of the study population</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Variables</th><th align="center" valign="middle" >Effective</th><th align="center" valign="middle" >Percentage (%)</th></tr></thead><tr><td align="center" valign="middle" >Chief complaint (n = 106)</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Limb pain</td><td align="center" valign="middle" >14</td><td align="center" valign="middle" >13.2</td></tr><tr><td align="center" valign="middle" >Oedema or swelling of a limb</td><td align="center" valign="middle" >14</td><td align="center" valign="middle" >13.2</td></tr><tr><td align="center" valign="middle" >Chest pain</td><td align="center" valign="middle" >24</td><td align="center" valign="middle" >22.6</td></tr><tr><td align="center" valign="middle" >Dyspnea</td><td align="center" valign="middle" >51</td><td align="center" valign="middle" >48.1</td></tr><tr><td align="center" valign="middle" >Hemoptysis</td><td align="center" valign="middle" >1</td><td align="center" valign="middle" >0.9</td></tr><tr><td align="center" valign="middle" >Syncope or malaise</td><td align="center" valign="middle" >6</td><td align="center" valign="middle" >5.7</td></tr><tr><td align="center" valign="middle" >Clinical signs of DVT (n = 28)</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Fever</td><td align="center" valign="middle" >17</td><td align="center" valign="middle" >60.7</td></tr><tr><td align="center" valign="middle" >Oedema and swelling of a limb</td><td align="center" valign="middle" >27</td><td align="center" valign="middle" >96.4</td></tr><tr><td align="center" valign="middle" >Erythema or local heat</td><td align="center" valign="middle" >21</td><td align="center" valign="middle" >75</td></tr><tr><td align="center" valign="middle" >Decreased calf sway</td><td align="center" valign="middle" >17</td><td align="center" valign="middle" >60.7</td></tr><tr><td align="center" valign="middle" >Limb pain</td><td align="center" valign="middle" >24</td><td align="center" valign="middle" >85.7</td></tr><tr><td align="center" valign="middle" >Homans sign</td><td align="center" valign="middle" >12</td><td align="center" valign="middle" >42.9</td></tr><tr><td align="center" valign="middle" >Signs of pulmonary embolism (n = 88)</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Acute dyspnea</td><td align="center" valign="middle" >86</td><td align="center" valign="middle" >97.7</td></tr><tr><td align="center" valign="middle" >Chest pain</td><td align="center" valign="middle" >42</td><td align="center" valign="middle" >47.7</td></tr><tr><td align="center" valign="middle" >Hemoptysis</td><td align="center" valign="middle" >3</td><td align="center" valign="middle" >3.4</td></tr><tr><td align="center" valign="middle" >Tachycardia</td><td align="center" valign="middle" >70</td><td align="center" valign="middle" >79.5</td></tr></tbody></table></table-wrap><p>sub-segmental (53.4%). PE was the most form (73.60%) regarding the type of lesion, followed by DVT (17%) and VTE (both PE and DVT) on 9.4% (see <xref ref-type="table" rid="table3">Table 3</xref>).</p></sec><sec id="s3_4"><title>3.4. Management of VTE in Our Population Study</title><p>Concerning therapy, the various management methods used are presented in <xref ref-type="table" rid="table4">Table 4</xref>. Low molecular weight heparin (LMWH) was used in 97.2% and</p><table-wrap id="table3" ><label><xref ref-type="table" rid="table3">Table 3</xref></label><caption><title> Paraclinical characteristics of the study population</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Variables</th><th align="center" valign="middle" >Effective</th><th align="center" valign="middle" >Percentages (%)</th></tr></thead><tr><td align="center" valign="middle" >Electrocardiogram (n = 54)</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Right bundle branch block</td><td align="center" valign="middle" >6</td><td align="center" valign="middle" >11.1</td></tr><tr><td align="center" valign="middle" >Appearance S1Q3</td><td align="center" valign="middle" >12</td><td align="center" valign="middle" >22.2</td></tr><tr><td align="center" valign="middle" >Transthoracic echocardiography (n = 35)</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Dilation of the trunk of the pulmonary artery</td><td align="center" valign="middle" >19</td><td align="center" valign="middle" >54.3</td></tr><tr><td align="center" valign="middle" >Right cavity dilation</td><td align="center" valign="middle" >21</td><td align="center" valign="middle" >60</td></tr><tr><td align="center" valign="middle" >Pulmonary arterial hypertension</td><td align="center" valign="middle" >27</td><td align="center" valign="middle" >77.1</td></tr><tr><td align="center" valign="middle" >Thrombus in the right ventricle</td><td align="center" valign="middle" >0</td><td align="center" valign="middle" >0</td></tr><tr><td align="center" valign="middle" >Venous ultrasound of the limbs (n = 28)</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Site</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Lower limb</td><td align="center" valign="middle" >26</td><td align="center" valign="middle" >92.9</td></tr><tr><td align="center" valign="middle" >Upper limb</td><td align="center" valign="middle" >2</td><td align="center" valign="middle" >7.1</td></tr><tr><td align="center" valign="middle" >Degree of extension</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Proximal thrombosis</td><td align="center" valign="middle" >8</td><td align="center" valign="middle" >28.6</td></tr><tr><td align="center" valign="middle" >Distal thrombosis</td><td align="center" valign="middle" >6</td><td align="center" valign="middle" >21.4</td></tr><tr><td align="center" valign="middle" >Extensive thrombosis</td><td align="center" valign="middle" >14</td><td align="center" valign="middle" >50</td></tr><tr><td align="center" valign="middle" >Location</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Tibial</td><td align="center" valign="middle" >5</td><td align="center" valign="middle" >17.9</td></tr><tr><td align="center" valign="middle" >Popliteus</td><td align="center" valign="middle" >13</td><td align="center" valign="middle" >46.4</td></tr><tr><td align="center" valign="middle" >Femoral</td><td align="center" valign="middle" >7</td><td align="center" valign="middle" >25</td></tr><tr><td align="center" valign="middle" >Iliac</td><td align="center" valign="middle" >1</td><td align="center" valign="middle" >3.6</td></tr><tr><td align="center" valign="middle" >Other</td><td align="center" valign="middle" >2</td><td align="center" valign="middle" >7.1</td></tr><tr><td align="center" valign="middle" >CT Pulmonary angiography (n = 88)</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Site</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Left EP</td><td align="center" valign="middle" >7</td><td align="center" valign="middle" >8</td></tr><tr><td align="center" valign="middle" >Right EP</td><td align="center" valign="middle" >23</td><td align="center" valign="middle" >26.1</td></tr><tr><td align="center" valign="middle" >Bilateral PE</td><td align="center" valign="middle" >58</td><td align="center" valign="middle" >65.9</td></tr><tr><td align="center" valign="middle" >Location</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Truncular</td><td align="center" valign="middle" >14</td><td align="center" valign="middle" >15.9</td></tr><tr><td align="center" valign="middle" >Segmental</td><td align="center" valign="middle" >18</td><td align="center" valign="middle" >20.5</td></tr><tr><td align="center" valign="middle" >Subsegmental</td><td align="center" valign="middle" >9</td><td align="center" valign="middle" >10.2</td></tr><tr><td align="center" valign="middle" >Segmental and sub-segmental</td><td align="center" valign="middle" >47</td><td align="center" valign="middle" >53.4</td></tr><tr><td align="center" valign="middle" >Massive pulmonary embolism</td><td align="center" valign="middle" >12</td><td align="center" valign="middle" >13.6</td></tr></tbody></table></table-wrap><table-wrap id="table4" ><label><xref ref-type="table" rid="table4">Table 4</xref></label><caption><title> Treatment of venous thromboembolic disease</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Variables</th><th align="center" valign="middle" >Effective (n = 106)</th><th align="center" valign="middle" >Percentage (%)</th></tr></thead><tr><td align="center" valign="middle" >Compression stockings</td><td align="center" valign="middle" >65</td><td align="center" valign="middle" >61.3</td></tr><tr><td align="center" valign="middle" >Enoxaparin</td><td align="center" valign="middle" >103</td><td align="center" valign="middle" >97.2</td></tr><tr><td align="center" valign="middle" >Rivaroxaban</td><td align="center" valign="middle" >81</td><td align="center" valign="middle" >76.4</td></tr><tr><td align="center" valign="middle" >Acenocoumarol</td><td align="center" valign="middle" >7</td><td align="center" valign="middle" >6.6</td></tr><tr><td align="center" valign="middle" >Fluindione</td><td align="center" valign="middle" >2</td><td align="center" valign="middle" >1.9</td></tr><tr><td align="center" valign="middle" >Streptokinase</td><td align="center" valign="middle" >8</td><td align="center" valign="middle" >7.5</td></tr></tbody></table></table-wrap><p>thrombolytics in 7.5% of patients. Anticoagulation switched heparin therapy with direct oral anticoagulants, Rivaroxaban in 76.4% of patients or vitamin K antagonists, such as Acenocoumarol and Fluindione, in 8.5% of patients.</p><p>The short-term complications of thrombolysis reported were bleeding in 25% of patients and shock and death in 12.5% of patients. The factors associated with the administration of thrombolysis were arterial hypotension (p &lt; 0.001) and massive PE (p &lt; 0.001). They were no significant association between electrocardiographic and echocardiographic parameters and thrombolysis.</p></sec></sec><sec id="s4"><title>4. Discussion</title><p>To describe the therapeutic modalities of VTE in an emergency center in Yaound&#233;, Cameroon, we conducted a cross-sectional study at the Yaound&#233; Emergency Center.</p><p>Swelling and pain in the lower limb were the main signs of DVT, while dyspnea and tachycardia were the most common signs of PE. Walbane et al. in Mali in 2015 found similar results for PE with tachycardia and dyspnea found respectively in 100% and 95.24% of patients [<xref ref-type="bibr" rid="scirp.116821-ref6">6</xref>].</p><p>The main cardiovascular risk factors identified were arterial hypertension, overweight, and type 2 diabetes. Prolonged bed rest was the most found risk factor for VTE. A study conducted in the intensive care unit of the Yaound&#233; Central Hospital by Etoundi et al. in 2015 found that cardiovascular risk factors, particularly hypertension, were the most frequent and found in 54.43% of patients [<xref ref-type="bibr" rid="scirp.116821-ref7">7</xref>]. These factors lead to vascular fragility and/or stasis, which promote thrombosis formation [<xref ref-type="bibr" rid="scirp.116821-ref11">11</xref>].</p><p>The prominent electrical abnormalities found were the S1Q3 aspect and the right bundle branch block. Coulibaly and al. found comparable results in Mali, with the S1Q3 appearance and right bundle branch block found in 18.91% and 14.8% of patients, respectively [<xref ref-type="bibr" rid="scirp.116821-ref12">12</xref>]. These results show the interest of the ECG, a simple and accessible means of diagnosis, in the diagnostic approach of pulmonary embolism. On transthoracic ultrasound, right cavitary dilatation and pulmonary arterial hypertension were the preeminent abnormalities, present in 60% and 77.1%, respectively, of patients with PE. Soumaoro and al., in a study conducted in Mali in 2006, found right cavitary dilatation in 40.8% of cases [<xref ref-type="bibr" rid="scirp.116821-ref7">7</xref>]. Indeed, the presence of a clot in the pulmonary arterial territory leads to an increase in pulmonary arterial pressure and, therefore, in the afterload in the right cavities, resulting in the dilation of these cavities [<xref ref-type="bibr" rid="scirp.116821-ref13">13</xref>].</p><p>In our study, isolated PE (73.6%) was the dominant type of VTE, followed by DVT (17%), the two being associated in 9.4% of patients. These results agreed with those found by Coulibaly et al., i.e. 60.9% isolated PE, 37.9% isolated DVT and in disagreement with the results of Etoundi et al., where isolated DVT was predominant [<xref ref-type="bibr" rid="scirp.116821-ref7">7</xref>] [<xref ref-type="bibr" rid="scirp.116821-ref12">12</xref>] [<xref ref-type="bibr" rid="scirp.116821-ref14">14</xref>]. The place of our study can explain this difference, and it is a reference hospital center for the management of emergencies in Yaound&#233;. It, therefore, mainly receives patients with serious pathologies, with life-threatening consequences such as PE.</p><p>PE was bilateral in the majority of our patients, as in the work of Walbane and al., who found 61.9% of bilateral PE [<xref ref-type="bibr" rid="scirp.116821-ref6">6</xref>]. In agreement with the literature, the lower limb was the prominent localization of DVT, i.e. 92.9% against 7.1% for the upper limb. Involvement of the upper limb is rarer in DVT, representing approximately 10% of cases [<xref ref-type="bibr" rid="scirp.116821-ref15">15</xref>] [<xref ref-type="bibr" rid="scirp.116821-ref16">16</xref>].</p><p>Regarding VTE management, LMWH was used in almost all cases, mainly relay oral anticoagulants. Similarly, for Coulibaly and al., heparin therapy was the most used therapeutic means found in 98.8% of patients [<xref ref-type="bibr" rid="scirp.116821-ref12">12</xref>]. These results are explained by the availability of heparin and the difficulties of access to other modalities such as thrombolysis in low-income countries such as sub-Saharan African countries [<xref ref-type="bibr" rid="scirp.116821-ref17">17</xref>] [<xref ref-type="bibr" rid="scirp.116821-ref18">18</xref>]. A retrospective study from 2006 to 2016 on VTE at the Abidjan Cardiology Institute found that VKAs (89%) were the most prescribed therapeutic class to patients after VTE [<xref ref-type="bibr" rid="scirp.116821-ref19">19</xref>]. This difference observed in our study is explained by the fact that oral anticoagulants are recent molecules increasingly prescribed in our countries. Indeed, unlike vitamin K antagonists, the latter does not require regular monitoring of the INR. Thus, their prescription has increased for several years [<xref ref-type="bibr" rid="scirp.116821-ref20">20</xref>].</p><p>Thrombolysis was administered in 7.5% of patients. The only molecule used was Streptokinase. This rate is lower than that found by Pessinaba and al. in 2018 in a cardiology department in Togo, which had shown a rate of administration of thrombolysis of 21.6%, all based on Streptokinase [<xref ref-type="bibr" rid="scirp.116821-ref21">21</xref>]. This difference could be explained by the recent commissioning of the Yaound&#233; emergency center, which dates from 2015, and the cost (38.000FCFA ≈ 57.93USD for one dose) and relative availability of Streptokinase. The factors associated with the performance of thrombolysis were arterial hypotension and the presence of a massive PE, following the recommendations on the indications for thrombolysis [<xref ref-type="bibr" rid="scirp.116821-ref22">22</xref>]. The evolution after thrombolysis was favorable, returning home in 87.5% of patients. The mortality rate was 12.5%, similar to that found by Pessinaba and al. and caused mainly by the persistence of the state of shock after thrombolysis [<xref ref-type="bibr" rid="scirp.116821-ref21">21</xref>].</p></sec><sec id="s5"><title>5. Limitations to Study</title><p>This study has some limitations. The main weakness of this study is its small sample size. Nevertheless, our study has the advantage of being one of the pioneers aiming to evaluate the management of VTE in our context, especially the use of thrombolysis.</p></sec><sec id="s6"><title>6. Conclusion</title><p>Management of venous thromboembolic disease in the Yaound&#233; Emergency Center is mainly based on low molecular weight heparin administration. Thrombolysis is achieved in only 7.5% of cases, particularly in patients with hypotension or massive pulmonary embolism.</p></sec><sec id="s7"><title>Acknowledgements</title><p>The authors would like to thank Dr Louis Bitang, Dr Sandrine Edie, and the staffs of Yaound&#233; Emergency Center.</p></sec><sec id="s8"><title>Authors’ Contribution</title><p>Conception and design: Chris Nad&#232;ge Nganou-Gnindjio, Jacqueline Ze Minkande.</p><p>Data collection: Chris Nad&#232;ge Nganou-Gnindjio, Ludovic Kadji.</p><p>Data analysis and interpretation: Ludovic Kadji, Daryl Tcheutchoua Nzokou.</p><p>Manuscript drafting: Chris Nad&#232;ge Nganou-Gnindjio, Daryl Tcheutchoua Nzokou.</p><p>Manuscript revision: Honor&#233; Kemnang Yemele, Chris Nad&#232;ge Nganou-Gnindjio.</p><p>Approval of the final manuscript: All the authors.</p></sec><sec id="s9"><title>Availability of Data and Materials</title><p>The datasets used for this study are available from the corresponding author on request.</p></sec><sec id="s10"><title>Ethical Approval and Consent to Participate</title><p>The study was approved by the Institutional Ethical Review Board of the University Yaound&#233; I (Cameroon). All the participants read and signed informed consent before their inclusion in the study.</p></sec><sec id="s11"><title>Competing Interest</title><p>The authors declare that they have no competing interests.</p></sec><sec id="s12"><title>Cite this paper</title><p>Nganou-Gnindjio, C.N., Hamadou, B., Kadji, L., Elong, J.T., Nzokou, D.T., Yemele, H.K., Menanga, A.P., Kingue, S. and Minkande, J.Z. (2022) Venous Thromboembolic Disease and Thrombolysis at the Yaound&#233; Emergency Center during the Past Five Years, Cameroon. World Journal of Cardiovascular Diseases, 12, 199-208. https://doi.org/10.4236/wjcd.2022.124020</p></sec></body><back><ref-list><title>References</title><ref id="scirp.116821-ref1"><label>1</label><mixed-citation publication-type="other" xlink:type="simple">OMS. à propos des maladies cardiovasculaires. WHO.  
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