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  <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">2164-5337</issn>
      <issn pub-type="ppub">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.2026.161003</article-id>
      <article-id pub-id-type="publisher-id">wjcd-148929</article-id>
      <article-categories>
        <subj-group>
          <subject>Article</subject>
        </subj-group>
        <subj-group>
          <subject>Medicine</subject>
          <subject>Healthcare</subject>
        </subj-group>
      </article-categories>
      <title-group>
        <article-title>Epidemiology, Clinical and Paraclinical Profiles of Heart Failure in Elderly Patients: A Cross-Sectional Study in Cameroon</article-title>
      </title-group>
      <contrib-group>
        <contrib contrib-type="author" corresp="yes">
          <name name-style="western">
            <surname>Owona</surname>
            <given-names>Amalia</given-names>
          </name>
          <xref ref-type="aff" rid="aff1">1</xref>
          <xref ref-type="aff" rid="aff2">2</xref>
        </contrib>
        <contrib contrib-type="author">
          <name name-style="western">
            <surname>Ebode</surname>
            <given-names>Marie Josiane</given-names>
          </name>
          <xref ref-type="aff" rid="aff2">2</xref>
          <xref ref-type="aff" rid="aff3">3</xref>
        </contrib>
        <contrib contrib-type="author">
          <name name-style="western">
            <surname>Mintom</surname>
            <given-names>Pierre</given-names>
          </name>
          <xref ref-type="aff" rid="aff1">1</xref>
          <xref ref-type="aff" rid="aff2">2</xref>
        </contrib>
        <contrib contrib-type="author">
          <name name-style="western">
            <surname>Ondobo</surname>
            <given-names>Emmanuel Germain Ngah</given-names>
          </name>
          <xref ref-type="aff" rid="aff2">2</xref>
        </contrib>
        <contrib contrib-type="author">
          <name name-style="western">
            <surname>Lom</surname>
            <given-names>Bill</given-names>
          </name>
          <xref ref-type="aff" rid="aff2">2</xref>
        </contrib>
        <contrib contrib-type="author">
          <name name-style="western">
            <surname>Ebene</surname>
            <given-names>Manon</given-names>
          </name>
          <xref ref-type="aff" rid="aff2">2</xref>
          <xref ref-type="aff" rid="aff3">3</xref>
        </contrib>
        <contrib contrib-type="author">
          <name name-style="western">
            <surname>Ndobo</surname>
            <given-names>Valérie</given-names>
          </name>
          <xref ref-type="aff" rid="aff2">2</xref>
          <xref ref-type="aff" rid="aff3">3</xref>
        </contrib>
        <contrib contrib-type="author">
          <name name-style="western">
            <surname>Boombhi</surname>
            <given-names>Jerôme</given-names>
          </name>
          <xref ref-type="aff" rid="aff1">1</xref>
          <xref ref-type="aff" rid="aff2">2</xref>
        </contrib>
        <contrib contrib-type="author">
          <name name-style="western">
            <surname>Kuate-Mfeukeu</surname>
            <given-names>Liliane</given-names>
          </name>
          <xref ref-type="aff" rid="aff2">2</xref>
          <xref ref-type="aff" rid="aff3">3</xref>
        </contrib>
        <contrib contrib-type="author">
          <name name-style="western">
            <surname>Menanga</surname>
            <given-names>Alain Patrick</given-names>
          </name>
          <xref ref-type="aff" rid="aff1">1</xref>
          <xref ref-type="aff" rid="aff2">2</xref>
        </contrib>
      </contrib-group>
      <aff id="aff1"><label>1</label> Yaounde General Hospital, Yaounde, Cameroon </aff>
      <aff id="aff2"><label>2</label> Faculty of Medicine and Biomedical Sciences, The University of Yaounde I, Yaounde, Cameroon </aff>
      <aff id="aff3"><label>3</label> Yaounde Central Hospital, Yaounde, Cameroon </aff>
      <author-notes>
        <fn fn-type="conflict" id="fn-conflict">
          <p>The authors declare no conflicts of interest regarding the publication of this paper.</p>
        </fn>
      </author-notes>
      <pub-date pub-type="epub">
        <day>13</day>
        <month>01</month>
        <year>2026</year>
      </pub-date>
      <pub-date pub-type="collection">
        <month>01</month>
        <year>2026</year>
      </pub-date>
      <volume>16</volume>
      <issue>01</issue>
      <fpage>24</fpage>
      <lpage>35</lpage>
      <history>
        <date date-type="received">
          <day>25</day>
          <month>11</month>
          <year>2025</year>
        </date>
        <date date-type="accepted">
          <day>16</day>
          <month>01</month>
          <year>2026</year>
        </date>
        <date date-type="published">
          <day>19</day>
          <month>01</month>
          <year>2026</year>
        </date>
      </history>
      <permissions>
        <copyright-statement>© 2026 by the authors and Scientific Research Publishing Inc.</copyright-statement>
        <copyright-year>2026</copyright-year>
        <license license-type="open-access">
          <license-p> This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license ( <ext-link ext-link-type="uri" xlink:href="https://creativecommons.org/licenses/by/4.0/">https://creativecommons.org/licenses/by/4.0/</ext-link> ). </license-p>
        </license>
      </permissions>
      <self-uri content-type="doi" xlink:href="https://doi.org/10.4236/wjcd.2026.161003">https://doi.org/10.4236/wjcd.2026.161003</self-uri>
      <abstract>
        <p><bold>Background:</bold> Heart failure (HF) is a major cause of morbidity and mortality worldwide, with a growing burden in sub-Saharan Africa. Data remain limited in Cameroon, particularly among older adults. This study aimed to describe the epidemiologic, clinical, and paraclinical profile of geriatric patients admitted for HF in two hospitals in Yaoundé. <bold>Methods:</bold> We conducted a cross-sectional study with a retrospective and prospective phase of data collection over six months (November 2021-April 2022) in the cardiology units of the Yaoundé Central Hospital and the Yaoundé General Hospital which are on our pyramid of our national health care facilities on the top. We aimed then to carry out this study in those highest level of care facilities. Patients aged ≥65 years with a diagnosis of HF based on clinical and echocardiographic criteria were included. Sociodemographic, clinical, geriatric, and paraclinical data were collected after informed patient consent. Analyses were performed using SPSS 23.0, with results expressed as means and proportions. The hospital prevalence was calculated by the ratio of patients above 65 years old admitted for heart failure over all the patients above 65 years old admitted in the selected hospitals during our period of study. We did not include in the study patients aged less than 65 years old, incomplete records and medical files without a clear diagnosis of deep veinous thrombosis (DVT) and or pulmonary embolism (PE). <bold>Results:</bold> 267 elderly patients have been admitted in those two hospitals among which 92 presented with heart failure. We included 63 elderly patients with HF, giving a hospital prevalence of 34.5% (95% CI: 28.9 - 40.2). The mean age was 75.0 ± 6.4 years. Hypertension (81.0%) and sedentary lifestyle (74.6%) were the most frequent risk factors. Acute decompensated HF was the commonest presentation (38.1%), and therapeutic non-compliance the leading precipitating factor (83.3%) for decompensation. Dyspnea (95.2%) and peripheral edema (82.5%) predominated as symptoms at presentation. On examination, jugular venous distension, hepatomegaly, ascites, basal crackles, and pulmonary congestion were frequently found. Frailty was the most common geriatric syndrome (42.9%). The majority of patients (58.7%) had HF with a preserved LVEF. <bold>Conclusion:</bold> In our context, studies on heart failure are common but to the best of our knowledge, this is the first study focusing on elderly patients. We have then found out that, the hospital prevalence of heart failure in elderly patients was 34.5% with a confidence interval of 28.9% - 40.2% which was high in our milieu due the high prevalence of uncontrolled hypertension among those group of patients. Dyspnea (95.2%) and peripheral edema (82.5%) was the predominated symptoms at presentation. Frailty was the most common geriatric syndrome (42.9%). The majority of patients (58.7%) had Left Hypertrophy associated with a preserved LVEF.</p>
      </abstract>
      <kwd-group kwd-group-type="author-generated" xml:lang="en">
        <kwd>Heart Failure</kwd>
        <kwd>Elderly</kwd>
        <kwd>Cameroon</kwd>
      </kwd-group>
    </article-meta>
  </front>
  <body>
    <sec id="sec1">
      <title>1. Introduction</title>
      <p>Heart failure (HF) represents the final common pathway of many cardiovascular diseases and is associated with high morbidity and mortality [<xref ref-type="bibr" rid="B1">1</xref>]. Globally, more than 64 million people are affected, with prevalence rising sharply in those over 65 years [<xref ref-type="bibr" rid="B2">2</xref>]. In sub-Saharan Africa, HF accounts for up to 30% of cardiovascular hospital admissions and contributes substantially to mortality [<xref ref-type="bibr" rid="B3">3</xref>].</p>
      <p>In Cameroon, HF is increasingly encountered, yet published data on its epidemiologic, clinical, and paraclinical characteristics in older adults is sparse. Understanding the local profile is crucial for prevention, timely diagnosis, and appropriate management. This study therefore aimed to describe the epidemiologic, clinical, and paraclinical profile of HF in elderly patients admitted in two tertiary hospitals in Yaoundé.</p>
    </sec>
    <sec id="sec2">
      <title>2. Methods</title>
      <p><bold>Study design and setting:</bold>We carried out a retrospective cross-sectional study supplemented by prospective data collection from November 2021 to April 2022 in the cardiology units of the Yaoundé Central Hospital and the Yaoundé General Hospital; Cameroon.</p>
      <p><bold>Study population:</bold>Patients aged ≥65 years with HF were included. Patients aged ≥65 years with a diagnosis of HF based on clinical and echocardiographic criteria were included. Sociodemographic, clinical, geriatric, and paraclinical data were collected after informed patient consent. Analyses were performed using SPSS 23.0, with results expressed as means and proportions. The hospital prevalence was calculated by the ratio of patients above 65 years old admitted for heart failure over all the patients above 65 years old admitted in the selected hospitals during our period of study. We did not include in the study patients aged less than 65 years old, incomplete records and medical files without a clear diagnosis of deep veinous thrombosis (DVT) and or pulmonary embolism (PE). The diagnosis of HF was based on symptoms and signs supported by echocardiographic findings. The ICOPE question via the application dedicated was used by the geriatrician to assess the geriatric syndrome.</p>
      <p><bold>Data collection:</bold>Data was extracted from medical records and supplemented with prospective interviews. Variables included: sociodemographic characteristics, cardiovascular risk factors, comorbidities, presenting symptoms and signs, decompensating factors, geriatric syndromes (according to the ICOPE, MNA-SF and Rockwood questionnaires), and paraclinical investigations.</p>
      <p><bold>Statistical analysis:</bold>Data was entered and analysed using SPSS version 23.0. Continuous variables were expressed as mean ± standard deviation and categorical variables as frequencies and percentages. Statistical significance was set at p &lt; 0.05.</p>
      <p><bold>Ethical considerations:</bold>Ethical clearance No. 173/UY1/FMSB/VDRC/CSD was obtained from the Institutional Ethics Committee of the Faculty of Medicine and Biomedical Sciences; University of Yaoundé I. Administrative authorization was granted by the two hospitals. Confidentiality was maintained.</p>
    </sec>
    <sec id="sec3">
      <title>3. Results</title>
      <sec id="sec3dot1">
        <title>3.1. Sociodemographic Characteristics and Comorbidities</title>
        <p>A total of 63 patients were included, corresponding to a hospital prevalence of 34.5% (CI: 28.9 - 40.2). The mean age was 75.0 ± 6.4 years. The age group 70 - 79 years was most represented. There was a female predominance, with a sex ratio (M/F) of 0.5 (<bold>Table 1</bold>).</p>
        <p><bold>Table 1.</bold> Sociodemographic characteristics of study Population.</p>
        <table-wrap id="tbl1">
          <label>Table 1</label>
          <table>
            <tbody>
              <tr>
                <td>
                  <bold>Sociodemographic Characteristics</bold>
                </td>
                <td>
                  <bold>Total</bold>
                </td>
                <td>
                  <bold>Percentages (%)</bold>
                </td>
              </tr>
              <tr>
                <td>
                  <bold>Age Ranges</bold>
                </td>
                <td>
                </td>
                <td>
                </td>
              </tr>
              <tr>
                <td>[65 - 75[</td>
                <td>32</td>
                <td>50.8</td>
              </tr>
              <tr>
                <td>[75 - 85[</td>
                <td>24</td>
                <td>38.1</td>
              </tr>
              <tr>
                <td>≥85</td>
                <td>7</td>
                <td>11.1</td>
              </tr>
              <tr>
                <td>
                  <bold>Sex</bold>
                </td>
                <td>
                </td>
                <td>
                </td>
              </tr>
              <tr>
                <td>Male</td>
                <td>21</td>
                <td>33.3</td>
              </tr>
              <tr>
                <td>Female</td>
                <td>42</td>
                <td>66.7</td>
              </tr>
              <tr>
                <td>
                  <bold>Educational Level</bold>
                </td>
                <td>
                </td>
                <td>
                </td>
              </tr>
              <tr>
                <td>No formal education</td>
                <td>19</td>
                <td>30.2</td>
              </tr>
              <tr>
                <td>Primary</td>
                <td>26</td>
                <td>41.3</td>
              </tr>
              <tr>
                <td>Secondary</td>
                <td>13</td>
                <td>20.6</td>
              </tr>
              <tr>
                <td>Higher</td>
                <td>5</td>
                <td>7.9</td>
              </tr>
              <tr>
                <td>
                  <bold>Employment status</bold>
                </td>
                <td>
                </td>
                <td>
                </td>
              </tr>
              <tr>
                <td>Active service</td>
                <td>18</td>
                <td>28.6</td>
              </tr>
              <tr>
                <td>Retired</td>
                <td>45</td>
                <td>71.4</td>
              </tr>
              <tr>
                <td>
                  <bold>Marital Status</bold>
                </td>
                <td>
                </td>
                <td>
                </td>
              </tr>
              <tr>
                <td>Single</td>
                <td>11</td>
                <td>17.5</td>
              </tr>
              <tr>
                <td>Married</td>
                <td>28</td>
                <td>44.4</td>
              </tr>
              <tr>
                <td>Divorced</td>
                <td>18</td>
                <td>28.6</td>
              </tr>
              <tr>
                <td>Widow/widower</td>
                <td>6</td>
                <td>9.5</td>
              </tr>
            </tbody>
          </table>
        </table-wrap>
        <p>Hypertension was present in 81.0% of patients being the most common comorbidity followed by a sedentary lifestyle in 74.6% (<xref ref-type="fig" rid="fig1">Figure 1</xref>). </p>
        <fig id="fig1">
          <label>Figure 1</label>
          <graphic xlink:href="https://html.scirp.org/file/1911720-rId13.jpeg?20260119040441" />
        </fig>
        <p>HBP: High Blood Pressure; HF: Heart Failure; CKD: Chronic Kidney Disease.</p>
        <p><bold>Figure 1</bold><bold>.</bold> Comorbidities and Cardiovascular risk factors.</p>
      </sec>
      <sec id="sec3dot2">
        <title>3.2. Clinical Profile</title>
        <p>Overall, 52 (82.5%) had global heart-failure symptoms. The most frequent symptom was dyspnea on exertion (n = 53; 84.1%). Six patients (9.5%) were asymptomatic at baseline. </p>
        <p>The most frequent NYHA class of dyspnea was stage III (n = 21; 33.3%) followed by stage II (n = 20; 31.7%).</p>
        <p>At admission 33 (52.4%) had an elevated blood pressure and 42 (66.7%) were polypneic (&gt;20 cycles/min); altered consciousness (GCS &lt; 15) occurred in 6 patients (9.5%). Concerning the signs of HF, right heart failure signs were present in majority of patients: lower-limb edema 41 (65.1%), jugular venous distension 38 (60.3%). Left heart failure signs were dominated by crackles 29 (46.0%) followed by displaced apex beat 25 (39.7). (See <bold>Table 2</bold>). 41 patients (65.1%) of our study population were admitted with 24 patients being admitted for Acute Heart Failure. Of the 24 patients admitted for acute HF, 21 (87.5%) had congestive HF and 3 (12.5%) had acute pulmonary edema. The dominant decompensating factor recorded was non-adherence to treatment. (See <xref ref-type="fig" rid="fig2">Figure 2</xref> and <bold>Table 3</bold>).</p>
        <p><bold>Table 2.</bold> Clinical profile of patients with HF in our study population.</p>
        <table-wrap id="tbl2">
          <label>Table 2</label>
          <table>
            <tbody>
              <tr>
                <td rowspan="2">
                  <bold>Variables</bold>
                </td>
                <td rowspan="2">
                  <bold>Study Population</bold>
                  <italic>
                    <bold>N</bold>
                  </italic>
                  <bold>=</bold>
                  <bold>63 (%)</bold>
                </td>
                <td colspan="3">
                  <bold>Age range</bold>
                </td>
              </tr>
              <tr>
                <td>
                  [65 - 75[
                  <italic>n</italic>
                  = 32 (%)
                </td>
                <td>
                  [75 - 85[
                  <italic>n</italic>
                  = 24 (%)
                </td>
                <td>
                  ≥85
                  <italic>n</italic>
                  = 7 (%)
                </td>
              </tr>
              <tr>
                <td>
                  <bold>Symptoms of RHF</bold>
                </td>
                <td>
                </td>
                <td>
                </td>
                <td>
                </td>
                <td>
                </td>
              </tr>
              <tr>
                <td>Anorexia</td>
                <td>22 (34.9)</td>
                <td>5 (15.6)</td>
                <td>11(45.8)</td>
                <td>6 (85.7)</td>
              </tr>
              <tr>
                <td>Hepatalgia</td>
                <td>4 (6.3)</td>
                <td>1 (3.1)</td>
                <td>2 (8.3)</td>
                <td>1 (14.1)</td>
              </tr>
              <tr>
                <td colspan="5">
                  <bold>Symptoms of LHF</bold>
                </td>
              </tr>
              <tr>
                <td>Dyspnea on exertion</td>
                <td>53 (84.1)</td>
                <td>28 (87.5)</td>
                <td>19 (79.2)</td>
                <td>6 (85.7)</td>
              </tr>
              <tr>
                <td>Orthopnea</td>
                <td>19 (30.2)</td>
                <td>9 (28.1)</td>
                <td>9 (37.5)</td>
                <td>1 (14.3)</td>
              </tr>
              <tr>
                <td>Cough on effort or decubitus</td>
                <td>15 (23.8)</td>
                <td>7 (21.9)</td>
                <td>7 (29.2)</td>
                <td>1 (14.3)</td>
              </tr>
              <tr>
                <td>Paroxysmal Nocturnal Dyspnea</td>
                <td>1 (1.6)</td>
                <td>1 (3.1)</td>
                <td>0 (0)</td>
                <td>0 (0)</td>
              </tr>
              <tr>
                <td>Hemoptysis</td>
                <td>1 (1.6)</td>
                <td>0 (0)</td>
                <td>1 (4.2)</td>
                <td>0 (0)</td>
              </tr>
              <tr>
                <td colspan="5">NYHA stage</td>
              </tr>
              <tr>
                <td>Stage I</td>
                <td>13 (20.6)</td>
                <td>6 (18.8)</td>
                <td>6 (25)</td>
                <td>1(14.1)</td>
              </tr>
              <tr>
                <td>Stage II</td>
                <td>20 (31.7)</td>
                <td>12 (37.5)</td>
                <td>7 (29.2)</td>
                <td>1 (14.1)</td>
              </tr>
              <tr>
                <td>Stage III</td>
                <td>21 (33.3)</td>
                <td>10 (31.3)</td>
                <td>8 (33.3)</td>
                <td>3 (42.9)</td>
              </tr>
              <tr>
                <td>Stage IV</td>
                <td>9 (14.3)</td>
                <td>4 (12.5)</td>
                <td>3(12.5)</td>
                <td>2 (28.7)</td>
              </tr>
              <tr>
                <td colspan="5">
                  <bold>Vital Parameters</bold>
                </td>
              </tr>
              <tr>
                <td>Hypotension</td>
                <td>2 (3.2)</td>
                <td>2 (6.3)</td>
                <td>0 (0)</td>
                <td>0 (0)</td>
              </tr>
              <tr>
                <td>Hypertension</td>
                <td>33 (52.4)</td>
                <td>15 (46.9)</td>
                <td>15 (62.5)</td>
                <td>3 (42.8)</td>
              </tr>
              <tr>
                <td>Bradycardia (HR &lt; 60)</td>
                <td>8 (12.7)</td>
                <td>4 (12.5)</td>
                <td>3 (12.5)</td>
                <td>1 (14.1)</td>
              </tr>
              <tr>
                <td>Tachycardia (HR &gt; 100)</td>
                <td>16 (25.4)</td>
                <td>10 (31.2)</td>
                <td>4 (16.7)</td>
                <td>2 (28.6)</td>
              </tr>
              <tr>
                <td>Polypnea (RR &gt; 20)</td>
                <td>42 (66.7)</td>
                <td>23 (71.9)</td>
                <td>15 (62.5)</td>
                <td>4 (57.1)</td>
              </tr>
              <tr>
                <td>Hypoxia (SO2 &lt; 95%)</td>
                <td>17 (26.9)</td>
                <td>7 (21.9)</td>
                <td>7 (29.2)</td>
                <td>3 (42.9)</td>
              </tr>
              <tr>
                <td colspan="5">
                  <bold>Signs of RHF</bold>
                </td>
              </tr>
              <tr>
                <td>Oedema</td>
                <td>41(65.1)</td>
                <td>16 (50)</td>
                <td>19 (79.2)</td>
                <td>6 (85.7)</td>
              </tr>
              <tr>
                <td>Jugular Veinous Distension</td>
                <td>38 (60.3)</td>
                <td>17 (53.1)</td>
                <td>16 (66.7)</td>
                <td>5 (71.4)</td>
              </tr>
              <tr>
                <td>Hepatojugular Reflux</td>
                <td>25 (39.7)</td>
                <td>12 (37.5)</td>
                <td>10 (41.7)</td>
                <td>3 (42.9)</td>
              </tr>
              <tr>
                <td>Harzer’s sign</td>
                <td>15 (23.8)</td>
                <td>4 (12.5)</td>
                <td>8 (33.3)</td>
                <td>3 (42.9)</td>
              </tr>
              <tr>
                <td>Functional Systolic Mumur</td>
                <td>15 (23.8)</td>
                <td>8 (25)</td>
                <td>6 (25)</td>
                <td>1 (14.3)</td>
              </tr>
              <tr>
                <td>Hepatomegaly</td>
                <td>9 (14.3)</td>
                <td>0 (0)</td>
                <td>7(29.2)</td>
                <td>2 (28.6)</td>
              </tr>
              <tr>
                <td>Ascitis</td>
                <td>5 (7.9)</td>
                <td>0 (0)</td>
                <td>5 (20.8)</td>
                <td>0 (0)</td>
              </tr>
              <tr>
                <td colspan="5">
                  <bold>Signs of LHF</bold>
                </td>
              </tr>
              <tr>
                <td>Crackles</td>
                <td>29 (46)</td>
                <td>12 (37.5)</td>
                <td>13 (54.2)</td>
                <td>4 (57.1)</td>
              </tr>
              <tr>
                <td>Deviated Apex Beat</td>
                <td>25 (39.7)</td>
                <td>17 (53.1)</td>
                <td>7 (29.2)</td>
                <td>1 (14.3)</td>
              </tr>
              <tr>
                <td>Gallop Rythm (S3)</td>
                <td>5 (7.9)</td>
                <td>2 (6.3)</td>
                <td>3 (12.5)</td>
                <td>0 (0)</td>
              </tr>
            </tbody>
          </table>
        </table-wrap>
        <p><bold>RHF:</bold>Right Heart failure<bold>, LHF:</bold>Left heart failure<bold>, HR:</bold>Heart rate<bold>, RR:</bold>Respiratory rate<bold>.</bold></p>
        <p><bold>Table 3.</bold> Decompensating factors for HF and mode of decompensation of HF.</p>
        <table-wrap id="tbl3">
          <label>Table 3</label>
          <table>
            <tbody>
              <tr>
                <td rowspan="2">
                  <bold>Variables</bold>
                </td>
                <td rowspan="2">
                  <bold>Acute HF</bold>
                  <italic>n</italic>
                  = 24 (%)
                </td>
                <td colspan="3">
                  <bold>Age Range</bold>
                </td>
              </tr>
              <tr>
                <td>
                  [65 - 75[
                  <italic>n</italic>
                  = 32
                </td>
                <td>
                  [75 - 85[
                  <italic>n</italic>
                  = 24
                </td>
                <td>
                  ≥85
                  <italic>n</italic>
                  = 7
                </td>
              </tr>
              <tr>
                <td colspan="5">
                  <bold>Decompensating Factors</bold>
                </td>
              </tr>
              <tr>
                <td>Non-adherence to Treatment</td>
                <td>20 (83.3)</td>
                <td>9 (28.1)</td>
                <td>9 (37.5)</td>
                <td>7 (28.6)</td>
              </tr>
              <tr>
                <td>Arrythmias</td>
                <td>17 (70.8)</td>
                <td>6 (18.7)</td>
                <td>9 (37.5)</td>
                <td>7 (28.6)</td>
              </tr>
              <tr>
                <td>Infections</td>
                <td>14 (58.3)</td>
                <td>5 (15.6)</td>
                <td>6 (25)</td>
                <td>3 (42.8)</td>
              </tr>
              <tr>
                <td>Anemia</td>
                <td>13 (54.2)</td>
                <td>6 (18.7)</td>
                <td>4 (16.7)</td>
                <td>3 (42.8)</td>
              </tr>
              <tr>
                <td>Cardiac Conduction Blocks</td>
                <td>5 (20.8)</td>
                <td>1 (3.1)</td>
                <td>4 (16.7)</td>
                <td>0 (0)</td>
              </tr>
              <tr>
                <td>Pulmonary Embolism</td>
                <td>3 (12.5)</td>
                <td>0 (0)</td>
                <td>3 (12.5)</td>
                <td>0 (0)</td>
              </tr>
              <tr>
                <td>Myocardial Infaction</td>
                <td>2 (8.3)</td>
                <td>0 (0)</td>
                <td>2 (8.3)</td>
                <td>0 (0)</td>
              </tr>
              <tr>
                <td colspan="5">Mode of Decompensation of HF</td>
              </tr>
              <tr>
                <td>Congestive HF</td>
                <td>21 (87.5)</td>
                <td>8 (25)</td>
                <td>11 (45.8)</td>
                <td>3 (42.8)</td>
              </tr>
              <tr>
                <td>Pulmonary Edema</td>
                <td>3 (12.5)</td>
                <td>1(3.1)</td>
                <td>2 (8.3)</td>
                <td>0 (0)</td>
              </tr>
            </tbody>
          </table>
        </table-wrap>
        <p>HF: Heart Failure.</p>
        <fig id="fig2">
          <label>Figure 2</label>
          <graphic xlink:href="https://html.scirp.org/file/1911720-rId14.jpeg?20260119040442" />
        </fig>
        <p>HF: Heart Failure.</p>
        <p><bold>Figure 2</bold><bold>.</bold> Distribution of admissions in study population.</p>
      </sec>
      <sec id="sec3dot3">
        <title>3.3. Geriatric Syndromes</title>
        <p>A geriatric evaluation carried out by a geriatrician with the ICOPE application was based on evaluating the intrinsic capacity by assessing the physical and mental capacities and frailty assessing the vulnerability to health issues. Thus, the decline in intrinsic capacity was the most common finding on comprehensive geriatric evaluation with 41 patients (65.1%) recorded as having a decreased intrinsic capacity. Frailty was present in 27 patients (42.9%). Both decrease intrinsic capacity and frailty were present in 100% of patients aged 85 years and above. Cognitive impairment was identified in 14 (22.2%), depressive symptoms in 23 (36.5%), malnutrition in 9 (14.3%), and social dependence in 19 (30.2%) (<bold>Table 4</bold>). </p>
        <p><bold>Table 4.</bold> Distribution of geriatric syndromes in study population.</p>
        <table-wrap id="tbl4">
          <label>Table 4</label>
          <table>
            <tbody>
              <tr>
                <td rowspan="2">
                  <bold>Geriatric Syndrome</bold>
                </td>
                <td rowspan="2">
                  <bold>Study</bold>
                  <bold>Population</bold>
                  <bold>N</bold>
                  <bold>=</bold>
                  <bold>63</bold>
                </td>
                <td colspan="3">
                  <bold>Age Range</bold>
                </td>
              </tr>
              <tr>
                <td>
                  [65 - 75[
                  <italic>n</italic>
                  = 32
                </td>
                <td>
                  [75 - 85[
                  <italic>n</italic>
                  = 24
                </td>
                <td>
                  ≥85
                  <italic>n</italic>
                  = 7
                </td>
              </tr>
              <tr>
                <td>Decline in Intrinsic capacity</td>
                <td>41 (65.1)</td>
                <td>14 (43.7)</td>
                <td>20 (83.3)</td>
                <td>7 (100)</td>
              </tr>
              <tr>
                <td>Frailty</td>
                <td>27 (42.9)</td>
                <td>13 (40.6)</td>
                <td>19 (79.2)</td>
                <td>7 (100)</td>
              </tr>
              <tr>
                <td>Depression</td>
                <td>23 (36.5)</td>
                <td>8 (25)</td>
                <td>13(54.2)</td>
                <td>2 (28.6)</td>
              </tr>
              <tr>
                <td>Dependence</td>
                <td>19 (30.2)</td>
                <td>5 (15.6)</td>
                <td>9 (37.5)</td>
                <td>5 (71.4)</td>
              </tr>
              <tr>
                <td>Cognitive Impairment</td>
                <td>14 (22.2)</td>
                <td>1 (3.2)</td>
                <td>7 (29.2)</td>
                <td>5 (71.4)</td>
              </tr>
              <tr>
                <td>Malnutrition</td>
                <td>9 (14.3)</td>
                <td>3 (9.4)</td>
                <td>2 (8.3)</td>
                <td>4 (57.1)</td>
              </tr>
            </tbody>
          </table>
        </table-wrap>
      </sec>
      <sec id="sec3dot4">
        <title>3.4. Paraclinical Profile</title>
        <p>Arrythmia was the most frequent ECG abnormality in the study population seen in 66.7% of patients with atrial fibrillation being the most common arrythmia; 39.7% of patients. Only 9 patients (14.3%) had signs of previous myocardial ischemia (<bold>Table 5</bold>). On cardiac echography, Left ventricular hypertrophy (LVH) was the predominant abnormality marked by eccentric LVH in 27 patients (42.8%), concentric LVH in 23 patients (36.5%) and concentric remodeling in 13 patients (20.6%). The majority of patients (58.7%) had a preserved LVEF while mildly reduced LVEF and reduced LVEF represented 17.5% and 23.8% respectively. Patients aged ≥ 85 years had the highest prevalence of reduced LVEF. </p>
        <p><bold>Table 5.</bold> Electrocardiographic abnormalities in our study population.</p>
        <table-wrap id="tbl5">
          <label>Table 5</label>
          <table>
            <tbody>
              <tr>
                <td>
                  <bold>ECG Abnormality</bold>
                </td>
                <td>
                  <bold>Total</bold>
                </td>
                <td>
                  <bold>Percentage (%)</bold>
                </td>
              </tr>
              <tr>
                <td>Arrythmia</td>
                <td>42</td>
                <td>66.7</td>
              </tr>
              <tr>
                <td>Atrial Fibrillation</td>
                <td>25</td>
                <td>39.7</td>
              </tr>
              <tr>
                <td>Ventricular Extrasystoles</td>
                <td>13</td>
                <td>20.6</td>
              </tr>
              <tr>
                <td>Sinus Tachycardia</td>
                <td>13</td>
                <td>20.6</td>
              </tr>
              <tr>
                <td>ECG Left Ventricular Hypertrophy</td>
                <td>40</td>
                <td>63.5</td>
              </tr>
              <tr>
                <td>Conduction Abnormalities</td>
                <td>19</td>
                <td>30.2</td>
              </tr>
              <tr>
                <td>First degree Atrioventricular block</td>
                <td>5</td>
                <td>7.9</td>
              </tr>
              <tr>
                <td>Complete Right Bundle Branch Block</td>
                <td>4</td>
                <td>6.3</td>
              </tr>
              <tr>
                <td>Repolarization Abnormalities</td>
                <td>13</td>
                <td>20.6</td>
              </tr>
              <tr>
                <td>Pathologic Q waves</td>
                <td>9</td>
                <td>14.3</td>
              </tr>
              <tr>
                <td>Left atrial Hypertrophy</td>
                <td>9</td>
                <td>14.3</td>
              </tr>
            </tbody>
          </table>
        </table-wrap>
        <p>Chest radiography showed cardiomegaly in 61.9% being the most common radiographic abnormality in the study population followed by pulmonary congestion in 23 patients (43.4%). Laboratory results found hypokalemia in 28.6%, anemia in 22.2%, and renal dysfunction in 15.9% of the patients (<bold>Table 6</bold>).</p>
        <p><bold>Table 6.</bold> Paraclinical profile of study population.</p>
        <table-wrap id="tbl6">
          <label>Table 6</label>
          <table>
            <tbody>
              <tr>
                <td rowspan="2">
                  <bold>Paraclinical Characteristics</bold>
                </td>
                <td rowspan="2">
                  <bold>Study</bold>
                  <bold>Population</bold>
                  <italic>
                    <bold>n</bold>
                  </italic>
                  <bold>=</bold>
                  <bold>63 (%)</bold>
                </td>
                <td colspan="3">
                  <bold>Age Range</bold>
                </td>
              </tr>
              <tr>
                <td>
                  [65 - 75[
                  <italic>n</italic>
                  <italic>=</italic>
                  32 (%)
                </td>
                <td>
                  [75 - 85[
                  <italic>n</italic>
                  = 24 (%)
                </td>
                <td>
                  ≥85
                  <italic>n</italic>
                  = 7 (%)
                </td>
              </tr>
              <tr>
                <td colspan="5">Echography Characteristics</td>
              </tr>
              <tr>
                <td>Left Ventricular Ejection Fraction (%)</td>
                <td>
                </td>
                <td>
                </td>
                <td>
                </td>
                <td>
                </td>
              </tr>
              <tr>
                <td>≤40</td>
                <td>15 (23.8)</td>
                <td>7 (21.9)</td>
                <td>5 (20.8)</td>
                <td>3 (42.9)</td>
              </tr>
              <tr>
                <td>41 - 49</td>
                <td>11 (17.5)</td>
                <td>8 (25)</td>
                <td>3 (12.5)</td>
                <td>0 (0)</td>
              </tr>
              <tr>
                <td>≥50</td>
                <td>37 (58.7)</td>
                <td>17(53.1)</td>
                <td>16 (66.7)</td>
                <td>4 (57.1)</td>
              </tr>
              <tr>
                <td>Left atrial dilatation</td>
                <td>48 (76.2)</td>
                <td>22 (68.7)</td>
                <td>19 (79.2)</td>
                <td>7 (100)</td>
              </tr>
              <tr>
                <td>Diastolic Dysfunction</td>
                <td>46 (73)</td>
                <td>21 (65.6)</td>
                <td>20 (83.3)</td>
                <td>5 (71.4)</td>
              </tr>
              <tr>
                <td>Left Ventricular Dilatation</td>
                <td>37 (58.7)</td>
                <td>16 (50)</td>
                <td>17 (70.8)</td>
                <td>4 (57.1)</td>
              </tr>
              <tr>
                <td>Right Atrial Dilatation</td>
                <td>37 (58.7)</td>
                <td>14 (43.7)</td>
                <td>18 (75)</td>
                <td>5 (71.4)</td>
              </tr>
              <tr>
                <td>Post Capillary Pulmonary hypertension</td>
                <td>37 (58.7)</td>
                <td>16 (50)</td>
                <td>16 (66.7)</td>
                <td>5 (71.4)</td>
              </tr>
              <tr>
                <td>Valvulopathy</td>
                <td>33 (52.4)</td>
                <td>15 (46.8)</td>
                <td>6 (25)</td>
                <td>3 (42.8)</td>
              </tr>
              <tr>
                <td>Eccentric Left Ventricular Hypertrophy</td>
                <td>27(42.8)</td>
                <td>16 (50)</td>
                <td>10 (41.7)</td>
                <td>1 (14.3)</td>
              </tr>
              <tr>
                <td>Concentric Left Ventricular Hypertrophy</td>
                <td>23(36.5)</td>
                <td>13 (40.6)</td>
                <td>6 (25)</td>
                <td>4 (57.1)</td>
              </tr>
              <tr>
                <td colspan="5">Chest X ray Characteristics</td>
              </tr>
              <tr>
                <td>Cardiomegaly</td>
                <td>39 (73.6)</td>
                <td>15(46.9)</td>
                <td>17 (62.9)</td>
                <td>7 (100)</td>
              </tr>
              <tr>
                <td>Interstitial Edema</td>
                <td>23 (4.4)</td>
                <td>7 (21.9)</td>
                <td>13 (54.2)</td>
                <td>3 (42.8)</td>
              </tr>
              <tr>
                <td>Alveolar edema</td>
                <td>21 (39.6)</td>
                <td>7 (21.9)</td>
                <td>11 (45.8)</td>
                <td>3 (42.8)</td>
              </tr>
              <tr>
                <td>Vascular redistribution to the summits</td>
                <td>12 (22.4)</td>
                <td>5 (15.6)</td>
                <td>6 (25)</td>
                <td>1 (14.3)</td>
              </tr>
              <tr>
                <td>Pleural Effusion</td>
                <td>6 (11.3)</td>
                <td>1 (3.1)</td>
                <td>3 (12.5)</td>
                <td>2 (28.6)</td>
              </tr>
              <tr>
                <td colspan="5">Biologic Paraclinicals</td>
              </tr>
              <tr>
                <td>Anemia</td>
                <td>32 (50.8)</td>
                <td>16 (50)</td>
                <td>13 (54.2)</td>
                <td>3 (42.8)</td>
              </tr>
              <tr>
                <td>Creatinine clearance &lt;60 ml/min</td>
                <td>32 (50.8)</td>
                <td>10 (31.2)</td>
                <td>15 (62.5)</td>
                <td>7 (100)</td>
              </tr>
              <tr>
                <td>Hypokalemia (&lt;3.5 mmol/l)</td>
                <td>18 (28.6)</td>
                <td>8 (25)</td>
                <td>9 (37.5)</td>
                <td>1 (14.3)</td>
              </tr>
              <tr>
                <td>Hyperkalemia (&gt;5.5 mmol/l)</td>
                <td>1 (1.6)</td>
                <td>1(3.1)</td>
                <td>0 (0)</td>
                <td>0 (0)</td>
              </tr>
              <tr>
                <td>Hyponatremia (&lt;135 mmol/l)</td>
                <td>15 (23.8)</td>
                <td>8 (25)</td>
                <td>5 (20.8)</td>
                <td>2 (28.6)</td>
              </tr>
            </tbody>
          </table>
        </table-wrap>
      </sec>
    </sec>
    <sec id="sec4">
      <title>4. Discussion</title>
      <p>This study aimed to describe the epidemiologic, clinical, and paraclinical profile of HF in elderly patients admitted in two tertiary hospitals in Yaoundé.</p>
      <sec id="sec4dot1">
        <title>4.1. Sociodemographic Characteristics and Comorbidities</title>
        <p>In our study, the hospital prevalence of HF was 34.5% (CI: 28.9 - 40.2). This is similar to the 40.8% reported by Mfeukeu <italic>et al.</italic> in 2021 in the same hospitals [<xref ref-type="bibr" rid="B1">1</xref>], and to the 49.7% found by Bivigou <italic>et al.</italic> in Gabon in 2018 [<xref ref-type="bibr" rid="B4">4</xref>]. The mean age of our patients was 75.0 ± 6.4 years, with the 70 - 79 year group most represented. This is close to the 66 ± 15 years reported by Mfeukeu <italic>et al.</italic> and the 57.4 ± 17 years reported by Bivigou <italic>et al.</italic> [<xref ref-type="bibr" rid="B1">1</xref>][<xref ref-type="bibr" rid="B4">4</xref>]. Our average age is also consistent with data from developed countries where Saudubray <italic>et al.</italic> in France and Obata <italic>et al.</italic> in Japan reported averages of 79 and 84.7 years, respectively [<xref ref-type="bibr" rid="B5">5</xref>][<xref ref-type="bibr" rid="B6">6</xref>]. The female predominance observed (sex ratio 0.5) has also been reported in other African and international series [<xref ref-type="bibr" rid="B1">1</xref>][<xref ref-type="bibr" rid="B4">4</xref>].</p>
        <p>Hypertension was the leading comorbidity (81.0%), followed by sedentary lifestyle (74.6%) and diabetes (28.6%). The frequency of hypertension in our series is higher than that reported in other African and Asian studies where prevalence usually ranges around 60% [<xref ref-type="bibr" rid="B4">4</xref>][<xref ref-type="bibr" rid="B7">7</xref>]. This may be explained by the older age of our population, as vascular aging is an established contributor to hypertension.</p>
      </sec>
      <sec id="sec4dot2">
        <title>4.2. Clinical Profile</title>
        <p>Dyspnea on exertion was the most common symptom (84.1%), and the majority of patients were in NYHA class III (33.3%) or II (31.7%). These findings are consistent with reports from the literature that indicate advanced dyspnea is the predominant mode of presentation in African HF patients [<xref ref-type="bibr" rid="B8">8</xref>]-[<xref ref-type="bibr" rid="B10">10</xref>]. Altered consciousness was present in 9.5% of patients, reflecting the severity of decompensation and mechanisms as cerebral hypoxia and severe hyponatremia.</p>
        <p>Acute HF was the most frequent mode of admission, observed in 38.1% of patients. This is higher than the 33.3% reported by Boombhi <italic>et al.</italic> in 2017 [<xref ref-type="bibr" rid="B11">11</xref>]. The main decompensating factor was non-adherence to treatment (83.3%), a finding similar to that of Bivigou <italic>et al.</italic> in Libreville who reported 88.6% [<xref ref-type="bibr" rid="B4">4</xref>]. This result is also in line with Kuate <italic>et al.</italic>, who found a prevalence of 35.3% in 2021 [<xref ref-type="bibr" rid="B1">1</xref>]. Poor treatment adherence has been widely described among African HF patients, explained in part by low therapeutic education and socioeconomic constraints [<xref ref-type="bibr" rid="B1">1</xref>][<xref ref-type="bibr" rid="B12">12</xref>]. In deed, in our milieu, there is no national medical support in terms of social insurance. Therefore each patient has to afford his management which limits the adherence and when it comes ton therapeutic education, if consider all the previous cross sectional studies carried out, the majority of patients were not aware of the long term aspect of their treatment. Besides in our milieu, its very difficult for the families to invest a lot of finances in elderly patients for according to them their prognosis most of the time are unfavorable. </p>
        <p>Signs of right heart failure were predominant, particularly lower-limb edema (65.1%) and jugular venous distension (60.3%), while left-sided signs were dominated by crackles (46.0%). These findings are comparable to those from earlier Cameroonian series [<xref ref-type="bibr" rid="B9">9</xref>].</p>
      </sec>
      <sec id="sec4dot3">
        <title>4.3. Geriatric Profile</title>
        <p>Decline in intrinsic capacity was the most common finding on comprehensive geriatric evaluation. Frailty was documented in 42.9% consistent with the range of 15% - 74% reported internationally [<xref ref-type="bibr" rid="B13">13</xref>]. Our results differ from those of Essomba <italic>et al.</italic>, who found dependence as the most frequent geriatric syndrome (70.5%) [<xref ref-type="bibr" rid="B14">14</xref>], while in our study dependence was noted in only 30.2% of patients. This discrepancy may be related to differences in assessment tools, since Essomba <italic>et al.</italic> used the ADL scale while we applied the ICOPE questionnaire.</p>
        <p>Malnutrition was present in 14.3%, with prevalence rising in patients ≥85 years. Obata <italic>et al.</italic> in Japan reported 44.1% malnutrition assessed by GNRI [<xref ref-type="bibr" rid="B6">6</xref>]. Our prevalence is closer to that found by Essomba <italic>et al.</italic> in Cameroon (17%) [<xref ref-type="bibr" rid="B15">15</xref>], likely reflecting the use of the same MNA-SF tool.</p>
      </sec>
      <sec id="sec4dot4">
        <title>4.4. Paraclinical Profile</title>
        <p>Arrhythmia was the most common ECG abnormality, present in 66.7% of patients, with atrial fibrillation being the most frequent rhythm disorder (39.7%). These findings are in line with Sung <italic>et al.</italic> in China (33.8%) [<xref ref-type="bibr" rid="B7">7</xref>] and Obata <italic>et al.</italic> in Japan (53.8%). Signs of previous myocardial ischemia were present in 14.3%, reflecting the contribution of ischemic heart disease to HF in the elderly.</p>
        <p>On echocardiography, preserved LVEF was the predominant phenotype (58.7%), while 17.5% had mildly reduced LVEF and 23.8% reduced LVEF. Boombhi <italic>et al.</italic> reported preserved EF in 49% [<xref ref-type="bibr" rid="B11">11</xref>], which is close to our result. As in other studies, patients ≥85 years in our series had a higher frequency of HF with reduced LVEF, suggesting age-related decline in systolic function.</p>
      </sec>
      <sec id="sec4dot5">
        <title>4.5. Limitations</title>
        <p>Our study has some limitations. First, the sample size was relatively small and limited to two hospitals, which may restrict the generalizability of our findings. Second, the cross-sectional design does not allow inference of causal relationships between comorbidities, precipitating factors, and outcomes. Third, some investigations such as BNP were rarely performed, reflecting local practice constraints, and this limited our ability to analyze their role in the clinical profile of HF. Finally, the use of retrospective medical records for part of the data collection may have introduced information bias.</p>
      </sec>
    </sec>
    <sec id="sec5">
      <title>5. Conclusion</title>
      <p>Heart failure is frequent among elderly patients in the studied services, with a higher prevalence in women. Acute decompensated heart failure with preserved ejection fraction was the most common clinical presentation. Electrocardiographic and echocardiographic abnormalities, including atrial fibrillation and left ventricular hypertrophy, were frequent. Functional decline and frailty were common in this population.</p>
    </sec>
  </body>
  <back>
    <ref-list>
      <title>References</title>
      <ref id="B1">
        <label>1.</label>
        <citation-alternatives>
          <mixed-citation publication-type="other">Kuate, L.M., Boombhi, J., Danwe, D., Tankmi, W., Amougou, S.N., Ouankou, C.N., <italic>et al.</italic> (2021) Prevalence and Factors Associated with In-Hospital Mortality of Patients with Heart Failure in Two Referral Hospitals in Yaoundé. <italic>Health Sciences and Disease</italic>, 22, 44-49.</mixed-citation>
          <element-citation publication-type="other">
            <person-group person-group-type="author">
              <string-name>Kuate, L.M.</string-name>
              <string-name>Boombhi, J.</string-name>
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