<?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">OJRD</journal-id><journal-title-group><journal-title>Open Journal of Respiratory Diseases</journal-title></journal-title-group><issn pub-type="epub">2163-940X</issn><publisher><publisher-name>Scientific Research Publishing</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.4236/ojrd.2019.93008</article-id><article-id pub-id-type="publisher-id">OJRD-93944</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>
 
 
  Epidemiology, Clinical and Paraclinical Presentations of Pulmonary Embolism: A Cross-Sectional Study in a Sub-Saharan Africa Setting
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Bertrand</surname><given-names>Hugo Mbatchou Ngahane</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>Félicité</surname><given-names>Kamdem</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>Silvain</surname><given-names>Raoul Simeni Njonnou</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>Nina</surname><given-names>Chebou</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>Anastase</surname><given-names>Dzudie</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>Serge</surname><given-names>Arnold Ebongue</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>Bruno</surname><given-names>Tengang</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>Fernando</surname><given-names>Kemta Lekpa</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>Yacouba</surname><given-names>Mapoure Njankouo</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>Sidick</surname><given-names>Mouliom</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>Henri</surname><given-names>Roger Ngote</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>Henry</surname><given-names>Luma Namme</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib></contrib-group><aff id="aff1"><addr-line>Douala General Hospital, Douala, Cameroon</addr-line></aff><aff id="aff4"><addr-line>Military Hospital, Douala, Cameroon</addr-line></aff><aff id="aff3"><addr-line>Faculty of Medicine and Biomedical Sciences, University of Yaounde 1, Yaounde, Cameroon</addr-line></aff><aff id="aff2"><addr-line>Faculty of Medicine and Pharmaceutical Sciences, University of Douala, Douala, Cameroon</addr-line></aff><aff id="aff5"><addr-line>Centre des Maladies Respiratoires, Douala, Cameroon</addr-line></aff><pub-date pub-type="epub"><day>09</day><month>07</month><year>2019</year></pub-date><volume>09</volume><issue>03</issue><fpage>89</fpage><lpage>99</lpage><history><date date-type="received"><day>26,</day>	<month>April</month>	<year>2019</year></date><date date-type="rev-recd"><day>26,</day>	<month>July</month>	<year>2019</year>	</date><date date-type="accepted"><day>29,</day>	<month>July</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>
 
 
  Background: Venous thromboembolic (VTE) disease burden is increasing worldwide, representing a major cause of cardiovascular death and public health problem. Pulmonary embolism (PE) is the most serious clinical presentation of VTE. Epidemiological and clinical data on PE are still lacking in Africa, particularly in Cameroon. This study aimed at determining the clinical features as well as imaging presentation and outcome of pulmonary embolism. Methods: A cross-sectional study was carried out in three hospitals in Douala. We retrospectively reviewed patient records admitted for PE from January 2009 to May 2017. We collected data on epidemiology, clinical presentation, venous Doppler/pulmonary computed tomographic angiography (CTA), and outcome. Results: We included 103 patients (56 males) with PE. Their median age was 52 years. The main risk factors were obesity (49.5%), hypertension (35.0%), long trip (24.3%) and cancer (18.4%). The most frequent clinical presentations were dyspnoea (83.4%), chest pain (78.6%), and cough (40.8%). Additionally, pleural effusion (32.8%), atelectasis (25.7%) and pulmonary hyperlucency (20.0%) were the most frequent findings on chest X-ray. The main abnormalities found in electrocardiogram were sinus tachycardia (63.4%), S1Q3T3 aspect (37.6%) and right axial deviation (28.7%). Moreover, right cavities dilatation (26.0%), pulmonary artery hypertension (35.0%) and pulmonary artery dilatation (21.0%) were the main echocardiographic findings. Low-molecular-weight heparin (LMWH) was the initial anticoagulant in all cases. There were 19 (18.4%) in-hospital deaths, and the mean hospital stay was 8.5 &#177; 5 days. Conclusion: PE is not rare in our setting. Obesity, long trip and cancer are the main risk factors, while dyspnoea, chest pain and respiratory distress are the main clinical presentation for PE. LMWH remains the therapeutic agent of choice. Lastly, in-hospital mortality is very high.
 
</p></abstract><kwd-group><kwd>Epidemiology</kwd><kwd> Africa</kwd><kwd> Venous Thromboembolism</kwd><kwd> Symptoms</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Introduction</title><p>Venous thromboembolic (VTE) disease is a public health problem worldwide. Pulmonary embolism (PE), which is the most serious presentation of VTE, is the third most common cause of death from cardiovascular disease after heart attack and stroke [<xref ref-type="bibr" rid="scirp.93944-ref1">1</xref>] [<xref ref-type="bibr" rid="scirp.93944-ref2">2</xref>]. It is still undiagnosed, due to the lack of suspicion and availability of appropriate diagnostic testing such as multi-detector computed tomographic angiography (CTA), especially in low resource setting [<xref ref-type="bibr" rid="scirp.93944-ref3">3</xref>] [<xref ref-type="bibr" rid="scirp.93944-ref4">4</xref>] [<xref ref-type="bibr" rid="scirp.93944-ref5">5</xref>]. Moreover, it has a 30-day mortality rate between 9% and 11% [<xref ref-type="bibr" rid="scirp.93944-ref2">2</xref>]. Incidence of PE is growing worldwide, particularly in high income countries [<xref ref-type="bibr" rid="scirp.93944-ref6">6</xref>] [<xref ref-type="bibr" rid="scirp.93944-ref7">7</xref>] [<xref ref-type="bibr" rid="scirp.93944-ref8">8</xref>] [<xref ref-type="bibr" rid="scirp.93944-ref9">9</xref>]. The clinical presentation of pulmonary embolism is non-specific. Symptoms may vary from mild chest pain to shock due to right ventricular failure in patients with massive PE. However, patients with PE sometimes present without any symptoms, the diagnosis being coincidently when investigating for other conditions [<xref ref-type="bibr" rid="scirp.93944-ref10">10</xref>]. Major risk factors for PE include recent surgery or trauma, lower limb fractures and joint replacements, and spinal cord injury, immobilization, malignancy. However 30% of patients with PE have no detectable provoking factors [<xref ref-type="bibr" rid="scirp.93944-ref11">11</xref>]</p><p>In Sub-Saharan Africa, preliminary studies have shown that PE was scarce [<xref ref-type="bibr" rid="scirp.93944-ref5">5</xref>] [<xref ref-type="bibr" rid="scirp.93944-ref12">12</xref>] [<xref ref-type="bibr" rid="scirp.93944-ref13">13</xref>] [<xref ref-type="bibr" rid="scirp.93944-ref14">14</xref>] [<xref ref-type="bibr" rid="scirp.93944-ref15">15</xref>]. Recent studies on the continent have reported more cases, but the limited resources, especially the access to CTA, still contribute to the reduced number of PE cases reported [<xref ref-type="bibr" rid="scirp.93944-ref16">16</xref>] [<xref ref-type="bibr" rid="scirp.93944-ref17">17</xref>] [<xref ref-type="bibr" rid="scirp.93944-ref18">18</xref>] [<xref ref-type="bibr" rid="scirp.93944-ref19">19</xref>] [<xref ref-type="bibr" rid="scirp.93944-ref20">20</xref>]. Despite this situation, the increase in the prevalence of risk factors of VTE suggests that pulmonary embolism will be more frequent in Sub-Saharan Africa. The present study aimed at determining the clinical features as well as imaging presentation and outcome of pulmonary embolism.</p></sec><sec id="s2"><title>2. Methods</title><sec id="s2_1"><title>2.1. Study Design and Setting</title><p>This is a descriptive study which was carried out in the intensive care unit and medical services of three hospitals in Douala. Douala is a city of 3 million inhabitants and the economic capital of Cameroon. The three hospitals were selected for the study: 1) Douala General Hospital (DGH), a tertiary care level and teaching hospital; 2) Douala Military Hospital (DMH), a second level hospital; and 3) the Centre des Maladies Respiratoires (CMR), a private clinic in charge of patients who present respiratory problems. These three medical centres easily have access to chest X-ray and computed tomographic angiography, as well as to intensive care unit.</p></sec><sec id="s2_2"><title>2.2. Study Participants</title><p>Patients admitted for a pulmonary embolism between January 2009 and May 2017 were included in the study. Patients aged less than 18 years were excluded as well as patients whose medical records were lacking data on the finding of thoracic CTA. Ethics approval was obtained from the ethical Review Board of the University of Douala.</p></sec><sec id="s2_3"><title>2.3. Data Collection</title><p>Patients were identified using the registers of the services. The medical files were retrieved from the archives and the following data were extracted: sociodemographic factors (age and sex), clinical presentation (chest pain, dyspnoea, haemoptysis, cough, syncope, pulse rate and blood pressure), comorbidities and risk factors of VTE, as well as the results of chest X-ray, electrocardiogram, echocardiography and CTA. The diagnosis of PE was defined by the identification of a thrombus in the pulmonary artery or any of its branches. The following risk factors were investigated: obesity (body mass index of 30 kg/m<sup>2</sup>), cancer, previous VTE, HIV infection, pulmonary tuberculosis, myocardiopathy, vascular trauma, chronic kidney disease, recent long trip (duration &gt; 4 hours within the last 4 weeks), pregnancy/early post-partum or post-abortum (&lt;6 weeks) and recent surgery (&lt;4 weeks). Immobilisation was defined as bed rest for more than three consecutive days in preceding month, irrespective of the cause. Additionally, the medication used for the initial anticoagulant treatment and the hospitalisation outcome were recorded. The possible outcomes were death, discharge and complications (lung infection, bleeding and bed sores).</p></sec><sec id="s2_4"><title>2.4. Statistical Analysis</title><p>Data were entered and analysed using IBM SPSS Statistics 20 software. Continuous variables were expressed as mean &#177; standard deviation. Dichotomous variables were expressed as counts and percentages.</p></sec></sec><sec id="s3"><title>3. Results</title><p>During the study period, 130 patients were identified with a diagnosis of pulmonary embolism. Twenty-seven of them were excluded because of missing or incomplete medical records. Finally, a total of 103 cases of PE were included in the study. Among them, 56 (54.4%) were males, and the median age was 52 years (interquartile range: 41 - 63). Participants aged 50 to 59 years were the most represented (26.2%). <xref ref-type="table" rid="table1">Table 1</xref> shows the baseline characteristics of the study population.</p><p>Obesity (49.5), hypertension (35.0%) and cancer (18.4%) were the most common underlying comorbidities. The risk factors of venous thromboembolism found in this study are shown in <xref ref-type="table" rid="table2">Table 2</xref>. Obesity (49.5%), hypertension (35.0%), recent long travel (24.3%), cancer (18.4%), immobilisation (16.5%) and recent surgery (15.5%) were the most common risk factors. Moreover, <xref ref-type="table" rid="table3">Table 3</xref> shows that the most frequent symptom in patients with PE was dyspnoea (83.4%). Eight patients (7.8%) presented signs of cardiogenic shock, while syncope was seen in 6 patients (5.8%). Signs of deep venous thrombosis were found in 27 patients (24.3%).</p><p>At presentation, electrocardiography was performed for 101 patients. Among them, 16 patients (15.5%) had a normal electrocardiogram. Sinus tachycardia (63.4%) was the most common finding. The S1Q3T3 pattern was seen in 38 patients (37.6%) and the right bundle branch block in 11 patients (10.9%). Among the 68 patients whose oxygen saturation (SpO<sub>2</sub>) was noted upon arrival at the hospital, 23.5% (16 patients) had SpO<sub>2</sub> less than 90%. The median SpO<sub>2 </sub>was 96% (interquartile range: 91 - 98).</p><table-wrap id="table1" ><label><xref ref-type="table" rid="table1">Table 1</xref></label><caption><title> General characteristics of study population (N = 103)</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Variables</th><th align="center" valign="middle" >Frequency (%)</th></tr></thead><tr><td align="center" valign="middle" >Gender</td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Male</td><td align="center" valign="middle" >56 (54.4)</td></tr><tr><td align="center" valign="middle" >Female</td><td align="center" valign="middle" >47 (45.6)</td></tr><tr><td align="center" valign="middle" >Age (years)</td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Median age (IQR*)</td><td align="center" valign="middle" >52 (41 - 63)</td></tr><tr><td align="center" valign="middle" >&lt;30</td><td align="center" valign="middle" >8 (7.8)</td></tr><tr><td align="center" valign="middle" >30 - 39</td><td align="center" valign="middle" >12 (11.7)</td></tr><tr><td align="center" valign="middle" >40 - 49</td><td align="center" valign="middle" >23 (22.3)</td></tr><tr><td align="center" valign="middle" >50 - 59</td><td align="center" valign="middle" >27 (26.2)</td></tr><tr><td align="center" valign="middle" >60 - 69</td><td align="center" valign="middle" >21 (20.4)</td></tr><tr><td align="center" valign="middle" >≥70</td><td align="center" valign="middle" >12 (11.7)</td></tr><tr><td align="center" valign="middle" >Admission service</td><td align="center" valign="middle" >21 (22.6)</td></tr><tr><td align="center" valign="middle" >Internal Medicine</td><td align="center" valign="middle" >83 (80.6)</td></tr><tr><td align="center" valign="middle" >Intensive care unit</td><td align="center" valign="middle" >20 (19.4)</td></tr><tr><td align="center" valign="middle" >Origin</td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Home</td><td align="center" valign="middle" >53 (52.4 )</td></tr><tr><td align="center" valign="middle" >Referred from other hospitals</td><td align="center" valign="middle" >41 (39.9)</td></tr><tr><td align="center" valign="middle" >Transfered from other wards</td><td align="center" valign="middle" >9 (8.7)</td></tr></tbody></table></table-wrap><p>(*) interquartile range.</p><table-wrap id="table2" ><label><xref ref-type="table" rid="table2">Table 2</xref></label><caption><title> Venous thromboembolism risk factors in the study population (N = 103)</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Risks factors</th><th align="center" valign="middle" >Frequency (%)</th></tr></thead><tr><td align="center" valign="middle" >Medical risk factors</td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Hypertension</td><td align="center" valign="middle" >36 (35)</td></tr><tr><td align="center" valign="middle" >Cancer</td><td align="center" valign="middle" >19 (18.4)</td></tr><tr><td align="center" valign="middle" >Past history of deep venous thrombosis</td><td align="center" valign="middle" >15 (14.6)</td></tr><tr><td align="center" valign="middle" >Myocardiopathy</td><td align="center" valign="middle" >10 (9.7)</td></tr><tr><td align="center" valign="middle" >Diabetes</td><td align="center" valign="middle" >9 (8.7)</td></tr><tr><td align="center" valign="middle" >HIV infection</td><td align="center" valign="middle" >8 (7.8)</td></tr><tr><td align="center" valign="middle" >Arrhythmia</td><td align="center" valign="middle" >7 (6.8)</td></tr><tr><td align="center" valign="middle" >Chronic Kidney disease</td><td align="center" valign="middle" >5 (4.9)</td></tr><tr><td align="center" valign="middle" >Autoimmune disease</td><td align="center" valign="middle" >3 (2.9)</td></tr><tr><td align="center" valign="middle" >Recent infection</td><td align="center" valign="middle" >3 (2.9)</td></tr><tr><td align="center" valign="middle" >Sickle cell disease</td><td align="center" valign="middle" >2 (1.9)</td></tr><tr><td align="center" valign="middle" >Stroke</td><td align="center" valign="middle" >1 (1)</td></tr><tr><td align="center" valign="middle" >Pulmonary tuberculosis</td><td align="center" valign="middle" >1 (1)</td></tr><tr><td align="center" valign="middle" >Varicose veins</td><td align="center" valign="middle" >1 (1)</td></tr><tr><td align="center" valign="middle" >Surgical and gynecological risk factors</td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Recent surgery</td><td align="center" valign="middle" >16 (15.5)</td></tr><tr><td align="center" valign="middle" >Post partum</td><td align="center" valign="middle" >2 (1.9)</td></tr><tr><td align="center" valign="middle" >Pregnancy</td><td align="center" valign="middle" >1 (1)</td></tr><tr><td align="center" valign="middle" >Abortion</td><td align="center" valign="middle" >1 (1)</td></tr><tr><td align="center" valign="middle" >Other risk factors</td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Obesity</td><td align="center" valign="middle" >51 (49.5)</td></tr><tr><td align="center" valign="middle" >Long trip</td><td align="center" valign="middle" >25 (24.3)</td></tr><tr><td align="center" valign="middle" >Smoking</td><td align="center" valign="middle" >18 (17.5)</td></tr><tr><td align="center" valign="middle" >Immobility</td><td align="center" valign="middle" >17 (16.5)</td></tr><tr><td align="center" valign="middle" >Hormone therapy replacement</td><td align="center" valign="middle" >6 (5.8)</td></tr></tbody></table></table-wrap><table-wrap-group id="3"><label><xref ref-type="table" rid="table3">Table 3</xref></label><caption><title> Clinical and para-clinical presentation of pulmonary embolism</title></caption><table-wrap id="3_1"><table><tbody><thead><tr><th align="center" valign="middle" >Variables</th><th align="center" valign="middle" >Frequency (%)</th></tr></thead><tr><td align="center" valign="middle" >Signs and symptoms (n = 103)</td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Dyspnea</td><td align="center" valign="middle" >86 (83.4)</td></tr><tr><td align="center" valign="middle" >Chest pain</td><td align="center" valign="middle" >81 (78.6%)</td></tr><tr><td align="center" valign="middle" >Cough</td><td align="center" valign="middle" >42 (40.8)</td></tr><tr><td align="center" valign="middle" >Hemoptysis</td><td align="center" valign="middle" >11 (10.7)</td></tr><tr><td align="center" valign="middle" >Right heart failure</td><td align="center" valign="middle" >24 (23.3)</td></tr><tr><td align="center" valign="middle" >Cardiogenic shock</td><td align="center" valign="middle" >8 (7.8)</td></tr></tbody></table></table-wrap><table-wrap id="3_2"><table><tbody><thead><tr><th align="center" valign="middle" >Syncope</th><th align="center" valign="middle" >6 (5.8)</th></tr></thead><tr><td align="center" valign="middle" >Signs of deep venous thrombosis</td><td align="center" valign="middle" >27 (24.3)</td></tr><tr><td align="center" valign="middle" >Chest X-ray finding (n = 70)</td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Pleural effusion</td><td align="center" valign="middle" >23 (32.8)</td></tr><tr><td align="center" valign="middle" >Atelectasis</td><td align="center" valign="middle" >18 (25.7)</td></tr><tr><td align="center" valign="middle" >Pulmonary hyperlucency</td><td align="center" valign="middle" >14 (20)</td></tr><tr><td align="center" valign="middle" >Pulmonary artery enlargement</td><td align="center" valign="middle" >12 (17.1)</td></tr><tr><td align="center" valign="middle" >ECG (n = 101)</td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Sinus Tachycardia</td><td align="center" valign="middle" >64 (63.4)</td></tr><tr><td align="center" valign="middle" >S1Q3T3 pattern</td><td align="center" valign="middle" >38 (37.6)</td></tr><tr><td align="center" valign="middle" >Right axis deviation</td><td align="center" valign="middle" >29 (28.7)</td></tr><tr><td align="center" valign="middle" >T-wave inversion in leads V1-V4</td><td align="center" valign="middle" >26 (25.7)</td></tr><tr><td align="center" valign="middle" >Right bundle branch block</td><td align="center" valign="middle" >11 (10.9)</td></tr><tr><td align="center" valign="middle" >Cardiac echography (n = 100)</td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Right ventricle dilatation</td><td align="center" valign="middle" >26 (26)</td></tr><tr><td align="center" valign="middle" >Elevated pulmonary systolic pressure</td><td align="center" valign="middle" >35 (35)</td></tr><tr><td align="center" valign="middle" >Pulmonary artery enlargement</td><td align="center" valign="middle" >21 (21)</td></tr><tr><td align="center" valign="middle" >Right ventricle hypokinesis</td><td align="center" valign="middle" >13 (13)</td></tr><tr><td align="center" valign="middle" >Mobile right heart thrombi</td><td align="center" valign="middle" >9 (9)</td></tr></tbody></table></table-wrap></table-wrap-group><p>Chest X-ray was available in 70 patients, and the main findings were pleural effusion (32.3%) and atelectasis (25.7%). Transthoracic echocardiography was performed in 101 patients. Right ventricle dilatation (26.0%) and elevated pulmonary systolic pressure (35.0%) were the most frequent echocardiographic findings. The pulmonary CTA showed a bilateral pulmonary embolism in 40 patients (38.8%) and a proximal location of pulmonary embolism in 75 participants (72.8%).</p><p>Anticoagulant therapy was commenced in all cases with Low-molecular-weight heparin (LMWH) and followed with vitamin K antagonists (VKA) in 92 (89.3%) and a new oral anticoagulant (rivaroxaban) in 11 (10.7%) cases. Complications were mostly represented by pulmonary infection in 31 (30.1%) patients and cardiogenic shock in 14 (13.6%). Median duration of the hospital stay was 7 days (interquartile range: 5 - 11), while the in-hospital mortality rate was 18.4%.</p></sec><sec id="s4"><title>4. Discussion</title><p>This study is part of the rare studies on pulmonary embolism in Sub-Saharan Africa. It presents the key findings with regard to clinical characteristics and outcome of patients with PE. We found that PE mostly affects a younger population, with a median age of 52 years. In the northwest region of Cameroon, Abah et al. found a mean age of 56 years among patients with a diagnosed venous thromboembolism [<xref ref-type="bibr" rid="scirp.93944-ref21">21</xref>]. Similar results were noted in previous studies in other Sub-Saharan African countries [<xref ref-type="bibr" rid="scirp.93944-ref12">12</xref>] [<xref ref-type="bibr" rid="scirp.93944-ref16">16</xref>] [<xref ref-type="bibr" rid="scirp.93944-ref22">22</xref>] and in Asia [<xref ref-type="bibr" rid="scirp.93944-ref23">23</xref>] [<xref ref-type="bibr" rid="scirp.93944-ref24">24</xref>]. On the contrary, PE population consists of middle age to elderly people in western countries [<xref ref-type="bibr" rid="scirp.93944-ref2">2</xref>] [<xref ref-type="bibr" rid="scirp.93944-ref25">25</xref>]. Knowing that the risk of pulmonary embolism increases with age, the higher prevalence in developed countries is probably due to the increase of the life expectancy in these countries [<xref ref-type="bibr" rid="scirp.93944-ref26">26</xref>] [<xref ref-type="bibr" rid="scirp.93944-ref27">27</xref>].</p><p>The main risk factors in this study were obesity, hypertension, recent long trip, cancer, immobilisation and recent surgery. These results were similar to those found in previous reports in Sub-Saharan Africa [<xref ref-type="bibr" rid="scirp.93944-ref12">12</xref>] [<xref ref-type="bibr" rid="scirp.93944-ref15">15</xref>] [<xref ref-type="bibr" rid="scirp.93944-ref17">17</xref>] [<xref ref-type="bibr" rid="scirp.93944-ref18">18</xref>] , Europe and Asia [<xref ref-type="bibr" rid="scirp.93944-ref25">25</xref>] [<xref ref-type="bibr" rid="scirp.93944-ref26">26</xref>]. The main symptoms at presentation in this study were dyspnoea, followed by chest pain and cough. These findings are similar to those found in other African countries [<xref ref-type="bibr" rid="scirp.93944-ref12">12</xref>] [<xref ref-type="bibr" rid="scirp.93944-ref16">16</xref>] [<xref ref-type="bibr" rid="scirp.93944-ref22">22</xref>] and in other parts of the world [<xref ref-type="bibr" rid="scirp.93944-ref2">2</xref>] [<xref ref-type="bibr" rid="scirp.93944-ref28">28</xref>] [<xref ref-type="bibr" rid="scirp.93944-ref29">29</xref>]. Syncope was the reason of admission in 5.8%. A similar result was noted by Bakebe et al. in Democratic Republic of Congo [<xref ref-type="bibr" rid="scirp.93944-ref16">16</xref>]. A systematic review on PE in Europe showed a variation of syncope frequency from 6% to 39% [<xref ref-type="bibr" rid="scirp.93944-ref28">28</xref>]. This heterogeneity is probably due to the fact that syncope is usually present in severe PE, which had various frequencies in different reports. The proposed mechanisms of syncope in PE includes 1) reduction of cerebral blood flow due to the decrease in cardiac output, 2) the vasovagal reflex and 3) cardiac arrhythmia and conduction disturbances due to right ventricle overload [<xref ref-type="bibr" rid="scirp.93944-ref30">30</xref>].</p><p>Signs of deep venous thrombosis were noted in 24.3%, which is also found in previous reports [<xref ref-type="bibr" rid="scirp.93944-ref10">10</xref>] [<xref ref-type="bibr" rid="scirp.93944-ref31">31</xref>]. On the chest X-ray, pleural effusion, atelectasis and pulmonary hyperlucency were the most common findings, as reported in the literature [<xref ref-type="bibr" rid="scirp.93944-ref12">12</xref>] [<xref ref-type="bibr" rid="scirp.93944-ref16">16</xref>] [<xref ref-type="bibr" rid="scirp.93944-ref28">28</xref>]. It is established that chest X-ray is not a sensitive and specific tool for the diagnosis of PE [<xref ref-type="bibr" rid="scirp.93944-ref32">32</xref>] , which was normal in 24.3% in our study. Moreover, chest X-ray is a non-invasive diagnostic assessment that can be used for the differential diagnosis of pulmonary embolism. Unsurprisingly, sinus tachycardia was the most observed on electrocardiography.</p><p>Pulmonary CTA was the diagnostic tool for PE. Its advent has been a major progress in the diagnosis of pulmonary embolism, especially in developing countries where the ventilation/perfusion scan is not available. Pulmonary CTA is known to have a good sensitivity and specificity for proximal PE, but less sensitive for distal location [<xref ref-type="bibr" rid="scirp.93944-ref33">33</xref>]. We found a proximal location of PE in 72.8% of participants. Similar result was found by Calwin Davidsingh et al. in India [<xref ref-type="bibr" rid="scirp.93944-ref32">32</xref>].</p><p>The most frequent abnormality on electrocardiogram (ECG) was sinus tachycardia, as found also in previous reports [<xref ref-type="bibr" rid="scirp.93944-ref12">12</xref>] [<xref ref-type="bibr" rid="scirp.93944-ref25">25</xref>] [<xref ref-type="bibr" rid="scirp.93944-ref32">32</xref>]. Although ECG can be normal in PE, other findings in PE include SIQ3T3 pattern, ST and T wave changes in anterior leads, RBBB, axis changes, transition zone shift to the right, P-pulmonale and atrial arrhythmia in severe PE. Cardiac echography findings were similar to the reports by Houenassi et al. and Bakebe et al., where right cavities dilatation and pulmonary arterial hypertension were the most frequent anomalies (13, 16). On the other hand, paradoxical septum, right ventricular dysfunction and right ventricular hypokinesis were noted by other previous reports. This discrepancy is probably due to the fact that in the latter reports, the proportion of severe PE was more important [<xref ref-type="bibr" rid="scirp.93944-ref2">2</xref>] [<xref ref-type="bibr" rid="scirp.93944-ref12">12</xref>] [<xref ref-type="bibr" rid="scirp.93944-ref32">32</xref>].</p><p>The in-hospital mortality rate of patients diagnosed with pulmonary embolism varies, depending on the setting of the studies. The 18.4% mortality rate found in our study is consistent with data reported by Kingue et al. [<xref ref-type="bibr" rid="scirp.93944-ref15">15</xref>] and Houenassi et al. [<xref ref-type="bibr" rid="scirp.93944-ref13">13</xref>]. However, Bakebe et al. found a mortality rate of 7.0% in Kinshasa [<xref ref-type="bibr" rid="scirp.93944-ref16">16</xref>]. The difference in severity of PE and the relatively low sample sizes of studies in Sub-Saharan Africa could explain the variability of the mortality rate. A remarkably low mortality rate of 3.4% was noted in a large study conducted in emergency department setting in the United States of America [<xref ref-type="bibr" rid="scirp.93944-ref2">2</xref>]. This difference in mortality rate could be explained by the fact that the length of stay in emergency department is usually lower than in conventional medical ward.</p><p>Although the present study is among the first multicentre report on PE in Sub-Saharan Africa, some limitations could be noted. First, the retrospective design used could be a source of recall bias. Herein, data were extracted from the medical records, and the findings could be underestimated, depending on the documentation of the records by physicians. However, a standardised data collection sheet was used in this study. Second, the reduced sample size in our study, compared to other studies in western countries, could be another limitation.</p></sec><sec id="s5"><title>5. Conclusion</title><p>Obesity, long trip and cancer are the main risk factors for PE in Cameroon. Symptoms and imaging are similar to those of previous reports. In our setting, in-hospital mortality remains very high. Further studies with larger sample size are thus needed for a detailed description in Sub-Saharan Africa with a focus on the outcome.</p></sec><sec id="s6"><title>Funding</title><p>The present study received no external funding.</p></sec><sec id="s7"><title>Authors’ Contribution</title><p>Conception and Design: MNBH, KF; Data collection: CN; Data analysis and Interpretation: MNBH; Drafting of the manuscript: NSRS. Reviewing the manuscript: DA, ESA, TB, KLF, MNY, MS, NHR, LNH. All authors read and approved the final draft for publication.</p></sec><sec id="s8"><title>Acknowledgements</title><p>We thank the International Multidisciplinary Programme to Adress Lung Health in Africa (IMPALA) for its support.</p></sec><sec id="s9"><title>Conflicts of Interest</title><p>The authors declare no conflicts of interest regarding the publication of this paper.</p></sec><sec id="s10"><title>Cite this paper</title><p>Mbatchou Ngahane, B.H., Kamdem, F., Njonnou, S.R.S., Chebou, N., Dzudie, A., Ebongue, S.A., Tengang, B., Lekpa, F.K., Njankouo, Y.M., Mouliom, S., Ngote, H.R. and Namme, H.L. (2019) Epidemiology, Clinical and Paraclinical Presentations of Pulmonary Embolism: A Cross-Sectional Study in a Sub-Saharan Africa Setting. Open Journal of Respiratory Diseases, 9, 89-99. https://doi.org/10.4236/ojrd.2019.93008</p></sec></body><back><ref-list><title>References</title><ref id="scirp.93944-ref1"><label>1</label><mixed-citation publication-type="other" xlink:type="simple">Goldhaber, S.Z. and Bounameaux, H. (2012) Pulmonary Embolism and Deep Vein Thrombosis. The Lancet, 379, 1835-1846.  
https://doi.org/10.1016/S0140-6736(11)61904-1</mixed-citation></ref><ref id="scirp.93944-ref2"><label>2</label><mixed-citation publication-type="other" xlink:type="simple">Pollack, C.V., Schreiber, D., Goldhaber, S.Z., Slattery, D., Fanikos, J., O’Neil, B.J., et al. (2011) Clinical Characteristics, Management, and Outcomes of Patients Diagnosed with Acute Pulmonary Embolism in the Emergency Department: Initial Report of EMPEROR (Multicenter Emergency Medicine Pulmonary Embolism in the Real World Registry). Journal of the American College of Cardiology, 57, 700-706.  
https://doi.org/10.1016/j.jacc.2010.05.071</mixed-citation></ref><ref id="scirp.93944-ref3"><label>3</label><mixed-citation publication-type="other" xlink:type="simple">Goldhaber, S.Z., Hennekens, C.H., Evans, D.A., Newton, E.C. and Godleski, J.J. (1982) Factors Associated with Correct Antemortem Diagnosis of Major Pulmonary Embolism. The American Journal of Medicine, 73, 822-826.  
https://doi.org/10.1016/0002-9343(82)90764-1</mixed-citation></ref><ref id="scirp.93944-ref4"><label>4</label><mixed-citation publication-type="other" xlink:type="simple">Tambe, J., Moifo, B., Fongang, E., Guegang, E. and Juimo, A.G. (2012) Acute Pulmonary Embolism in the Era of Multi-Detector CT: A Reality in Sub-Saharan Africa. BMC Medical Imaging, 12, 31. https://doi.org/10.1186/1471-2342-12-31</mixed-citation></ref><ref id="scirp.93944-ref5"><label>5</label><mixed-citation publication-type="other" xlink:type="simple">Saleh, J.A. and Alasia, D.D. (2007) Acute Pulmonary Embolism: A Review. Nigerian Journal of Medicine, 6, 11-17. https://doi.org/10.4314/njm.v16i1.37274</mixed-citation></ref><ref id="scirp.93944-ref6"><label>6</label><mixed-citation publication-type="other" xlink:type="simple">DeMonaco, N.A., Dang, Q., Kapoor, W.N. and Ragni, M.V. (2008) Pulmonary Embolism Incidence Is Increasing with Use of Spiral Computed Tomography. The American Journal of Medicine, 121, 611-617.  
https://doi.org/10.1016/j.amjmed.2008.02.035</mixed-citation></ref><ref id="scirp.93944-ref7"><label>7</label><mixed-citation publication-type="other" xlink:type="simple">Minges, K.E., Bikdeli, B., Wang, Y., Kim, N., Curtis, J.P., Desai, M.M., et al. (2015) National Trends in Pulmonary Embolism Hospitalization Rates and Outcomes for Adults Aged ≥65 Years in the United States (1999 to 2010). American Journal of Cardiology, 116, 1436-1442. https://doi.org/10.1016/j.amjcard.2015.07.068</mixed-citation></ref><ref id="scirp.93944-ref8"><label>8</label><mixed-citation publication-type="other" xlink:type="simple">Bouée, S., Emery, C., Samson, A., Gourmelen, J., Bailly, C. and Cotté, F.-E. (2016) Incidence of Venous Thromboembolism in France: A Retrospective Analysis of a National Insurance Claims Database. Thrombosis Journal, 14, 2-9.  
https://doi.org/10.1186/s12959-016-0078-0</mixed-citation></ref><ref id="scirp.93944-ref9"><label>9</label><mixed-citation publication-type="other" xlink:type="simple">Yang, Y., Liang, L., Zhai, Z., He, H., Xie, W., Peng, X., et al. (2011) Pulmonary Embolism Incidence and Fatality Trends in Chinese Hospitals from 1997 to 2008: A Multicenter Registration Study. PLoS ONE, 6, e26861.  
https://doi.org/10.1371/journal.pone.0026861</mixed-citation></ref><ref id="scirp.93944-ref10"><label>10</label><mixed-citation publication-type="other" xlink:type="simple">Bajaj, N., Bozarth, A.L., Guillot, J., Kojokittah, J., Appalaneni, S.R., Cestero, C., et al. (2014) Clinical Features in Patients with Pulmonary Embolism at a Community Hospital: Analysis of 4 Years of Data. Journal of Thrombosis and Thrombolysis, 37, 287-292. https://doi.org/10.1007/s11239-013-0942-8</mixed-citation></ref><ref id="scirp.93944-ref11"><label>11</label><mixed-citation publication-type="other" xlink:type="simple">European Society of Cardiology (ESC) (2014) 2014 ESC Guidelines on the Diagnosis and Management of Acute Pulmonary Embolism. Endorsed by the European Respiratory Society. European Heart Journal, 35, 3033-3080.  
https://doi.org/10.1093/eurheartj/ehu283</mixed-citation></ref><ref id="scirp.93944-ref12"><label>12</label><mixed-citation publication-type="other" xlink:type="simple">Diall, I.B., Coulibaly, S., Minta, I., Ho, B., Diakite, M., Sidibe, N., et al. (2011) Causes, Signs and Outcome of 30 Patients with Pulmonary Embolus. Le Mali Médical, 26, 3-6.</mixed-citation></ref><ref id="scirp.93944-ref13"><label>13</label><mixed-citation publication-type="other" xlink:type="simple">Houenassi, M., Sacca-Vehounkkpe, J. and Tchabi, Y. (2013) Evaluation de la prise en charge de l’embolie pulmonaire dans un pays à faible niveau socio-économique: Cas du Benin. Cardiologie Tropicale, 136, 1-8.</mixed-citation></ref><ref id="scirp.93944-ref14"><label>14</label><mixed-citation publication-type="other" xlink:type="simple">Elegbeleye, O.O. and Femi-Pearse, D. (1975) Pulmonary Embolism in Africans. Tropical and Geographical Medicine, 27, 31-33.</mixed-citation></ref><ref id="scirp.93944-ref15"><label>15</label><mixed-citation publication-type="other" xlink:type="simple">Kingue, S., Tagny-Zukam, D., Binam, F., Nouedoui, C., Teyang, A. and Muna, W.F. (2002) Venous Thromboembolism in Cameroon (Report of 18 Cases). Medecine Tropicale: Revue du Corps de Sante Colonial, 62, 47-50.</mixed-citation></ref><ref id="scirp.93944-ref16"><label>16</label><mixed-citation publication-type="other" xlink:type="simple">Bakebe, A., Kashongwe, I., Mulenga, C., Tshiasuma, M., Kabengele, B., Bisuta, S.F., et al. (2017) Pulmonary Embolism: Epidemiological Data and Diagnosis in Kinshasa Hospitals. International Journal of Tuberculosis and Lung Disease, 21, 875-879.  
https://doi.org/10.5588/ijtld.16.0418</mixed-citation></ref><ref id="scirp.93944-ref17"><label>17</label><mixed-citation publication-type="other" xlink:type="simple">Kamdem, F., Ngahane, B.H.M., Hamadou, B., Mongyui, A., Doualla, M.S., Jingi, A.M., et al. (2018) Epidemiology, Clinical Presentations and In-Hospital Mortality of Venous Thromboembolism at the Douala General Hospital: A Cross-Sectional Study in Cameroon, Sub-Saharan Africa. World Journal of Cardiovascular Diseases, 8, 123-132. https://doi.org/10.4236/wjcd.2018.82012</mixed-citation></ref><ref id="scirp.93944-ref18"><label>18</label><mixed-citation publication-type="other" xlink:type="simple">Manuel, A., Aufico, A., Africano, R., Peralta, T., Salas, A., Silva, A., et al. (2017) Clinical Profile, Management and Outcomes of Patients with Pulmonary Embolism: A Retrospective Tertiary Centre Study in Angola. Cardiovascular Journal of Africa, 28, 356-361. https://doi.org/10.5830/CVJA-2017-017</mixed-citation></ref><ref id="scirp.93944-ref19"><label>19</label><mixed-citation publication-type="other" xlink:type="simple">Nganou-Gnindjio, C.N., Njonnou, S.R.S., Hamadou, B., Jemea, B., Mbede, M., Jingi, A.M., et al. (2018) Characteristics of Venous Thrombo-Embolic Disease in People with and without HIV Infection in Yaounde: A Cross-Sectional Study. Health Sciences and Diseases, 19, 21-26.</mixed-citation></ref><ref id="scirp.93944-ref20"><label>20</label><mixed-citation publication-type="other" xlink:type="simple">Pessinaba, S., Atti, Y.D.M., Baragou, S., Pio, M., Afassinou, Y., Kpélafia, M., et al. (2017) Pulmonary Embolism at the University Hospital Campus of Lome (Togo): A Retrospective Study about 51 Cases. Pan African Medical Journal, 27, 129.  
https://doi.org/10.11604/pamj.2017.27.129.6855</mixed-citation></ref><ref id="scirp.93944-ref21"><label>21</label><mixed-citation publication-type="other" xlink:type="simple">Abah, J.P., Menanga, A., Ngahane, B.H.M., Minkande, J.Z., Akono, M.N. and Kingue, S. (2016) Pattern of Venous Thromboembolic Diseases in a Resources-Limited Setting in Cameroon. Pan African Medical Journal, 23, 236.  
https://doi.org/10.11604/pamj.2016.23.236.7034</mixed-citation></ref><ref id="scirp.93944-ref22"><label>22</label><mixed-citation publication-type="other" xlink:type="simple">Ogeng’o, J.A., Obimbo, M.M., Olabu, B.O., Gatonga, P.M. and Ong’era, D. (2011) Pulmonary Thromboembolism in an East African Tertiary Referral Hospital. Journal of Thrombosis and Thrombolysis, 32, 386-391.  
https://doi.org/10.1007/s11239-011-0607-4</mixed-citation></ref><ref id="scirp.93944-ref23"><label>23</label><mixed-citation publication-type="other" xlink:type="simple">Husain, S.J., Zubairi, A.B.S., Fatima, K., Irfan, M., Atif, M. and Saeed, M.A. (2009) Clinical Characteristics, Management and Outcome of Major Pulmonary Embolism: An Experience from a Tertiary Care Center in Pakistan. Journal of Pakistan Medical Association, 59, 372-375.</mixed-citation></ref><ref id="scirp.93944-ref24"><label>24</label><mixed-citation publication-type="other" xlink:type="simple">Algahtani, F.H., Bayoumi, N., Abdelgadir, A., Al-Nakshabandi, N., Al Aseri, Z., Al Ghamdi, M., et al. (2013) Clinical Characteristics and Risk Factors of Pulmonary Embolism: Data from a Saudi Tertiary-Care Center. Journal of Thrombosis and Haemostasis, 11, 388-390. https://doi.org/10.1111/jth.12083</mixed-citation></ref><ref id="scirp.93944-ref25"><label>25</label><mixed-citation publication-type="other" xlink:type="simple">Casazza, F., Becattini, C., Bongarzoni, A., Cuccia, C., Roncon, L., Favretto, G., et al. (2012) Clinical Features and Short Term Outcomes of Patients with Acute Pulmonary Embolism. The Italian Pulmonary Embolism Registry (IPER). Thrombosis Research, 130, 847-852. https://doi.org/10.1016/j.thromres.2012.08.292</mixed-citation></ref><ref id="scirp.93944-ref26"><label>26</label><mixed-citation publication-type="other" xlink:type="simple">Alikhan, R., Cohen, A.T., Combe, S., Samama, M.M., Desjardins, L., Eldor, A., et al. (2004) Risk Factors for Venous Thromboembolism in Hospitalized Patients with Acute Medical Illness: Analysis of the MEDENOX Study. Archives of Internal Medicine, 164, 963-968. https://doi.org/10.1001/archinte.164.9.963</mixed-citation></ref><ref id="scirp.93944-ref27"><label>27</label><mixed-citation publication-type="other" xlink:type="simple">Anderson, F.A., Wheeler, H.B., Goldberg, R.J., Hosmer, D.W., Patwardhan, N.A., Jovanovic, B., et al. (1991) A Population-Based Perspective of the Hospital Incidence and Case-Fatality Rates of Deep Vein Thrombosis and Pulmonary Embolism. The Worcester DVT Study. Archives of Internal Medicine, 151, 933-938.  
https://doi.org/10.1001/archinte.151.5.933</mixed-citation></ref><ref id="scirp.93944-ref28"><label>28</label><mixed-citation publication-type="other" xlink:type="simple">Morrone, D. and Morrone, V. (2018) Acute Pulmonary Embolism: Focus on the Clinical Picture. Korean Circulation Journal, 48, 365-3681.  
https://doi.org/10.4070/kcj.2017.0314</mixed-citation></ref><ref id="scirp.93944-ref29"><label>29</label><mixed-citation publication-type="other" xlink:type="simple">NATSPUTE (2006) The Clinical Features of 516 Patients with Acute Pulmonary Thromboembolism. Chinese Medical Journal, 86, 2161-2165.</mixed-citation></ref><ref id="scirp.93944-ref30"><label>30</label><mixed-citation publication-type="other" xlink:type="simple">Alt&amp;#305;nsoy, B., Erboy, F., Tanr&amp;#305;verdi, H., Uygur, F., &amp;#214;rnek, T., Atalay, F., et al. (2016) Syncope as a Presentation of Acute Pulmonary Embolism. Therapeutics and Clinical Risk Management, 12, 1023-1028. https://doi.org/10.2147/TCRM.S105722</mixed-citation></ref><ref id="scirp.93944-ref31"><label>31</label><mixed-citation publication-type="other" xlink:type="simple">Stein, P.D., Matta, F., Musani, M.H. and Diaczok, B. (2010) Silent Pulmonary Embolism in Patients with Deep Venous Thrombosis: A Systematic Review. The American Journal of Medicine, 123, 426-431.  
https://doi.org/10.1016/j.amjmed.2009.09.037</mixed-citation></ref><ref id="scirp.93944-ref32"><label>32</label><mixed-citation publication-type="other" xlink:type="simple">Calwin Davidsingh, S., Srinivasan, N., Balaji, P., Kalaichelvan, U. and Mullasari, A.S. (2014) Study of Clinical Profile and Management of Patients with Pulmonary Embolism—Single Center Study. Indian Heart Journal, 66, 197-202.  
https://doi.org/10.1016/j.ihj.2013.12.037</mixed-citation></ref><ref id="scirp.93944-ref33"><label>33</label><mixed-citation publication-type="other" xlink:type="simple">Padley, S.P.G. (2002) Lung Scintigraphy vs. Spiral CT in the Assessment of Pulmonary Emboli. The British Journal of Radiology, 75, 5-8.  
https://doi.org/10.1259/bjr.75.889.750005</mixed-citation></ref></ref-list></back></article>