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  <front>
    <journal-meta>
      <journal-id journal-id-type="publisher-id">ijohns</journal-id>
      <journal-title-group>
        <journal-title>International Journal of Otolaryngology and Head &amp;amp; Neck Surgery</journal-title>
      </journal-title-group>
      <issn pub-type="epub">2168-5460</issn>
      <issn pub-type="ppub">2168-5452</issn>
      <publisher>
        <publisher-name>Scientific Research Publishing</publisher-name>
      </publisher>
    </journal-meta>
    <article-meta>
      <article-id pub-id-type="doi">10.4236/ijohns.2026.152013</article-id>
      <article-id pub-id-type="publisher-id">ijohns-149824</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>Rapid Antigen Testing for Acute Pharyngitis in a Tertiary Hospital in Chad: A Prospective Cross-Sectional Study</article-title>
      </title-group>
      <contrib-group>
        <contrib contrib-type="author">
          <contrib-id contrib-id-type="orcid">0000-0003-1122-1856</contrib-id>
          <name name-style="western">
            <surname>Taoussi</surname>
            <given-names>Aboubakar Assidick</given-names>
          </name>
          <xref ref-type="aff" rid="aff1">1</xref>
        </contrib>
        <contrib contrib-type="author">
          <name name-style="western">
            <surname>Attimer</surname>
            <given-names>Khadidja Adoum</given-names>
          </name>
          <xref ref-type="aff" rid="aff2">2</xref>
        </contrib>
        <contrib contrib-type="author">
          <name name-style="western">
            <surname>Ousmane</surname>
            <given-names>Naïm Mahamout</given-names>
          </name>
          <xref ref-type="aff" rid="aff3">3</xref>
        </contrib>
      </contrib-group>
      <aff id="aff1"><label>1</label> Department of Otorhinolaryngology-Head and Neck Surgery, Renaissance University Hospital Center, N’Djamena, Chad </aff>
      <aff id="aff2"><label>2</label> Department of Pediatrics, University Hospital Center of Mother and Child, N’Djamena, Chad </aff>
      <aff id="aff3"><label>3</label> Faculty of Health Sciences, University of Abeché, Abeché, Chad </aff>
      <author-notes>
        <fn fn-type="conflict" id="fn-conflict">
          <p>The authors declare that they have no conflicts of interest related to this study.</p>
        </fn>
      </author-notes>
      <pub-date pub-type="epub">
        <day>15</day>
        <month>03</month>
        <year>2026</year>
      </pub-date>
      <pub-date pub-type="collection">
        <month>03</month>
        <year>2026</year>
      </pub-date>
      <volume>15</volume>
      <issue>02</issue>
      <fpage>142</fpage>
      <lpage>152</lpage>
      <history>
        <date date-type="received">
          <day>27</day>
          <month>01</month>
          <year>2026</year>
        </date>
        <date date-type="accepted">
          <day>25</day>
          <month>02</month>
          <year>2026</year>
        </date>
        <date date-type="published">
          <day>28</day>
          <month>02</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/ijohns.2026.152013">https://doi.org/10.4236/ijohns.2026.152013</self-uri>
      <abstract>
        <p><bold>Background:</bold> Acute pharyngitis is a common reason for consultation in otorhinolaryngology. Distinguishing viral from bacterial etiologies, particularly group A streptococcal (GAS) infection, is essential to reduce inappropriate antibiotic prescribing, especially in low-resource settings where rapid antigen detection testing (RADT) is not widely implemented. <bold>Objective:</bold> To assess the value of RADT in the management of acute pharyngitis at the Renaissance University Hospital Center in N’Djamena, Chad. <bold>Methods:</bold> We conducted a descriptive cross-sectional study with prospective data collection over 18 months. Patients aged ≥3 years presenting with acute pharyngitis were included. All underwent clinical examination with McIsaac score calculation. RADT was performed systematically in children aged 3 - 15 years and in adolescents/adults (≥16 years) when the McIsaac score was ≥3. Data were analyzed using SPSS version 26.0. <bold>Results:</bold> A total of 136 patients were included (mean age 19.8 ± 13.2 years; male-to-female ratio 0.92). RADT was performed in 91/136 patients (66.9%), including all children and only adolescents/adults with a McIsaac score ≥ 3. Among this selected subgroup, RADT was positive in 65/91 cases (71.4%). RADT positivity was significantly associated with the McIsaac score (p &lt; 0.05). All RADT-positive patients received antibiotics, whereas most RADT-negative patients did not; RADT result was strongly associated with antibiotic prescribing (Fisher’s exact test, p &lt; 0.001). <bold>Conclusion:</bold> Rapid antigen testing appears to be a useful tool for guiding antibiotic prescription in acute pharyngitis, particularly in resource-limited settings, by reducing unnecessary antibiotic use.</p>
      </abstract>
      <kwd-group kwd-group-type="author-generated" xml:lang="en">
        <kwd>Acute Pharyngitis</kwd>
        <kwd>Rapid Antigen Detection Test</kwd>
        <kwd>Group A Streptococcus</kwd>
        <kwd>Antibiotic Prescribing</kwd>
      </kwd-group>
    </article-meta>
  </front>
  <body>
    <sec id="sec1">
      <title>1. Introduction</title>
      <p>Acute pharyngitis is one of the most common reasons for consultation in general practice and otorhinolaryngology, particularly among children and young adults [<xref ref-type="bibr" rid="B1">1</xref>][<xref ref-type="bibr" rid="B2">2</xref>]. Although most cases are of viral origin, a substantial proportion of acute pharyngitis is caused by <italic>Streptococcus pyogenes</italic> (group A streptococcus), for which antibiotic therapy is indicated in order to prevent potentially serious complications such as acute rheumatic fever and post-streptococcal renal disease [<xref ref-type="bibr" rid="B3">3</xref>][<xref ref-type="bibr" rid="B4">4</xref>]. </p>
      <p>In daily clinical practice, the diagnosis of acute pharyngitis still relies largely on clinical assessment. Several clinical scoring systems, including the McIsaac score, have been developed to estimate the likelihood of streptococcal infection [<xref ref-type="bibr" rid="B5">5</xref>]. However, these tools have limited predictive value and do not always allow reliable differentiation between bacterial and viral pharyngitis [<xref ref-type="bibr" rid="B6">6</xref>]. This diagnostic uncertainty often leads to excessive and sometimes inappropriate antibiotic prescribing, contributing to the emergence of antimicrobial resistance, which is now recognized as a major global public health concern [<xref ref-type="bibr" rid="B7">7</xref>]. </p>
      <p>Rapid antigen detection testing (RADT) for group A streptococcal pharyngitis represents a simple, rapid, and recommended approach to improve diagnostic accuracy and guide therapeutic decision-making [<xref ref-type="bibr" rid="B8">8</xref>][<xref ref-type="bibr" rid="B9">9</xref>]. Its benefit has been well established in high-income countries, where its use has been shown to significantly reduce unnecessary antibiotic prescriptions [<xref ref-type="bibr" rid="B8">8</xref>]. In contrast, in low-resource settings, the integration of RADT into routine clinical practice remains insufficiently documented, particularly in hospital settings, due to constraints related to accessibility, healthcare worker training, and health system organization [<xref ref-type="bibr" rid="B10">10</xref>][<xref ref-type="bibr" rid="B11">11</xref>]. </p>
      <p>In Chad, the hospital-based management of acute pharyngitis still relies predominantly on clinical evaluation, as RADT for group A streptococcal pharyngitis is not routinely used in everyday practice. This situation occurs in a context characterized by a high patient burden, limited access to conventional microbiological investigations, and frequent reliance on empirical antibiotic therapy, making the evaluation of RADT under real-world clinical conditions particularly relevant. </p>
      <p>This study therefore provides original data from a tertiary university hospital, contributing to the documentation of the role of RADT in the diagnostic and therapeutic management of acute pharyngitis in a low-resource setting. </p>
      <p>The objective of this study was to assess the value of rapid antigen detection testing in the diagnosis and management of acute pharyngitis at the Renaissance University Hospital Center in N’Djamena, Chad. </p>
    </sec>
    <sec id="sec2">
      <title>2. Materials and Methods</title>
      <sec id="sec2dot1">
        <title>2.1. Study Design</title>
        <p>This was a prospective cross-sectional descriptive study including both descriptive and analytical components. </p>
      </sec>
      <sec id="sec2dot2">
        <title>2.2. Study Setting and Period</title>
        <p>The study was conducted at the Renaissance University Hospital Center in N’Djamena, Chad, a tertiary referral hospital with a dedicated otorhinolaryngology department. Data collection was carried out over an 18-month period, from July 1, 2022 to December 31, 2023. </p>
      </sec>
      <sec id="sec2dot3">
        <title>2.3. Study Population</title>
        <p>The study population consisted of patients aged 3 years and older who presented with acute pharyngitis to the otorhinolaryngology department of the Renaissance University Hospital Center during the study period. </p>
      </sec>
      <sec id="sec2dot4">
        <title>2.4. Inclusion and Non-Inclusion Criteria</title>
        <p>Patients aged 3 years and older presenting with acute pharyngitis were included after receiving information about the study and providing consent. </p>
        <p>Patients with complicated pharyngitis, those who had received prior antibiotic therapy, and patients or legal guardians who declined participation were not included. </p>
      </sec>
      <sec id="sec2dot5">
        <title>2.5. Clinical Assessment and McIsaac Score</title>
        <p>All included patients underwent a systematic clinical examination performed by the consulting clinician. The McIsaac score, validated for patients aged 3 years and older, was calculated during the consultation. The score is based on five clinical criteria (fever &gt;38˚C, absence of cough, tender anterior cervical lymphadenopathy, tonsillar hypertrophy or exudate, and age) and ranges from −1 to 5, with higher scores indicating a greater probability of group A streptococcal infection. </p>
      </sec>
      <sec id="sec2dot6">
        <title>2.6. Rapid Antigen Detection Test: Characteristics and Indications</title>
        <p>The rapid antigen detection test (RADT) for group A streptococcal pharyngitis was continuously available throughout the study period. It was an immunochromatographic qualitative test detecting group A streptococcal antigen from a pharyngeal swab. </p>
        <p>RADT was performed systematically in children aged 3 to 15 years. In adolescents and adults (≥16 years), RADT was recommended when the McIsaac score was ≥3; however, due to a high clinical workload and organizational constraints related to patient flow, the test could not be performed systematically in all eligible patients. RADT was not performed in patients with a McIsaac score &lt;3. Each test included an internal control band and was used in accordance with the manufacturer’s recommendations. </p>
        <p>During the study period, rapid antigen detection tests were provided free of charge to patients as part of routine hospital care, ensuring that economic barriers did not influence test utilization. </p>
      </sec>
      <sec id="sec2dot7">
        <title>2.7. Sampling Procedure and Interpretation of RADT</title>
        <p>Pharyngeal sampling was performed using a sterile swab rubbed over both tonsils and the posterior pharyngeal wall, avoiding contact with adjacent oral structures. Results were obtained after an approximate reading time of 5 minutes and interpreted by the clinician based on the presence of test and control bands. </p>
        <p>RADT sampling and interpretation were performed by the attending physicians of the otorhinolaryngology department, all of whom received standardized training on RADT procedures prior to the start of the study. </p>
      </sec>
      <sec id="sec2dot8">
        <title>2.8. Data Collection</title>
        <p>Data were collected prospectively using a standardized data collection form completed by the consulting clinician. Collected variables included sociodemographic characteristics, clinical findings, McIsaac score, performance and result of RADT, and antibiotic prescription. </p>
      </sec>
      <sec id="sec2dot9">
        <title>2.9. Statistical Analysis</title>
        <p>Data were analyzed using the Statistical Package for the Social Sciences (SPSS), version 26.0. Descriptive and analytical analyses were performed to assess the association between the McIsaac score and RADT results, as well as between RADT results and antibiotic prescription. Pearson’s chi-square test or Fisher’s exact test was used as appropriate, with statistical significance set at p &lt; 0.05. </p>
      </sec>
      <sec id="sec2dot10">
        <title>2.10. Ethical Considerations</title>
        <p>The study was conducted in accordance with ethical principles for health research. Participation was voluntary after appropriate information. For patients under 18 years of age, parental or guardian consent was required. Anonymity and confidentiality of data were strictly ensured. </p>
      </sec>
    </sec>
    <sec id="sec3">
      <title>3. Results</title>
      <sec id="sec3dot1">
        <title>3.1. Sociodemographic Characteristics of Patients</title>
        <p>A total of 136 patients aged between 3 and 67 years were included in the study. The mean age was 19.8 ± 13.2 years. The 3 - 15-year age group was the most represented, with 69 patients (50.7%), followed by the 16 - 28-year group (33 patients; 24.3%) and the 29 - 41-year group (24 patients; 17.6%). </p>
        <p>There were 71 females (52.2%) and 65 males (47.8%), yielding a male-to-female ratio of 0.92. </p>
        <p>The distribution of patients according to age and sex is presented in <bold>Table 1</bold>. </p>
        <p><bold>Table 1.</bold> Distribution of patients by age group and sex (n = 136). </p>
        <table-wrap id="tbl1">
          <label>Table 1</label>
          <table>
            <tbody>
              <tr>
                <td>Age group (years)</td>
                <td>Total n (%)</td>
                <td>Male n (%)</td>
                <td>Female n (%)</td>
              </tr>
              <tr>
                <td>3 - 15</td>
                <td>69 (50.7)</td>
                <td>36 (52.2)</td>
                <td>33 (47.8)</td>
              </tr>
              <tr>
                <td>16 - 28</td>
                <td>33 (24.3)</td>
                <td>13 (39.4)</td>
                <td>20 (60.6)</td>
              </tr>
              <tr>
                <td>29 - 41</td>
                <td>24 (17.6)</td>
                <td>11 (45.8)</td>
                <td>13 (54.2)</td>
              </tr>
              <tr>
                <td>42 - 54</td>
                <td>8 (5.9)</td>
                <td>4 (50.0)</td>
                <td>4 (50.0)</td>
              </tr>
              <tr>
                <td>55 - 67</td>
                <td>2 (1.5)</td>
                <td>1 (50.0)</td>
                <td>1 (50.0)</td>
              </tr>
              <tr>
                <td>Total</td>
                <td>136 (100)</td>
                <td>65 (47.8)</td>
                <td>71 (52.2)</td>
              </tr>
            </tbody>
          </table>
        </table-wrap>
        <p>Percentages by sex were calculated within each age group. </p>
      </sec>
      <sec id="sec3dot2">
        <title>3.2. Distribution of Patients According to McIsaac Score</title>
        <p>The McIsaac score ranged from 1 to 5. Score 4 was the most frequently observed, recorded in 52 patients (38.2%), followed by score 3 in 28 patients (20.6%). The detailed distribution of McIsaac scores is shown in <bold>Table 2</bold>. </p>
        <p><bold>Table 2.</bold> Distribution of patients according to McIsaac score (n = 136). </p>
        <table-wrap id="tbl2">
          <label>Table 2</label>
          <table>
            <tbody>
              <tr>
                <td>McIsaac score</td>
                <td>n</td>
                <td>%</td>
              </tr>
              <tr>
                <td>1</td>
                <td>10</td>
                <td>7.4</td>
              </tr>
              <tr>
                <td>2</td>
                <td>19</td>
                <td>14.0</td>
              </tr>
              <tr>
                <td>3</td>
                <td>28</td>
                <td>20.6</td>
              </tr>
              <tr>
                <td>4</td>
                <td>52</td>
                <td>38.2</td>
              </tr>
              <tr>
                <td>5</td>
                <td>27</td>
                <td>19.9</td>
              </tr>
              <tr>
                <td>Total</td>
                <td>136</td>
                <td>100</td>
              </tr>
            </tbody>
          </table>
        </table-wrap>
      </sec>
      <sec id="sec3dot3">
        <title>3.3. Performance of the Rapid Antigen Detection Test</title>
        <p>The rapid antigen detection test (RADT) was performed in 91 patients, representing 66.9% of the total study population (91/136). </p>
        <p>All patients aged 3 - 15 years underwent RADT (69/69). Among patients aged 16 years and older (n = 67), RADT was performed in 22 patients (32.4%), while 45 patients (67.6%) were not tested. This included 16 adults with a McIsaac score of 3 who were eligible for testing but did not undergo RADT due to logistical and organizational constraints. </p>
        <p>The distribution of RADT performance according to age group is presented in <bold>Table 3</bold>. </p>
        <p><bold>Table 3.</bold> Performance of RADT according to age group (n = 136). </p>
        <table-wrap id="tbl3">
          <label>Table 3</label>
          <table>
            <tbody>
              <tr>
                <td>Age group (years)</td>
                <td>Total n (%)</td>
                <td>RADT performed n (%)</td>
                <td>RADT not performed n (%)</td>
              </tr>
              <tr>
                <td>3 - 15</td>
                <td>69 (50.7)</td>
                <td>69 (100)</td>
                <td>0 (0)</td>
              </tr>
              <tr>
                <td>≥16</td>
                <td>67 (49.3)</td>
                <td>22 (32.4)</td>
                <td>45 (67.6)</td>
              </tr>
              <tr>
                <td>Total</td>
                <td>136 (100)</td>
                <td>91 (66.9)</td>
                <td>45 (33.1)</td>
              </tr>
            </tbody>
          </table>
        </table-wrap>
        <p>Percentages were calculated by row. </p>
      </sec>
      <sec id="sec3dot4">
        <title>3.4. Results of the Rapid Antigen Detection Test</title>
        <p>Among the 91 patients who underwent RADT, the test was positive in 65 patients (71.4%) and negative in 26 patients (28.6%). </p>
        <p>Most RADT-positive results were observed in children aged 3 - 15 years, accounting for 56 cases. </p>
        <p>The distribution of RADT results by age group is presented in <bold>Table 4</bold>. </p>
        <p>RADT positivity was significantly more frequent in patients aged 3 - 15 years compared with those aged 16 years and older (Fisher’s exact test, p &lt; 0.01) (<bold>Table 5</bold>). </p>
        <p><bold>Table 4.</bold> RADT results according to age group (n = 91). </p>
        <table-wrap id="tbl4">
          <label>Table 4</label>
          <table>
            <tbody>
              <tr>
                <td>Age group (years)</td>
                <td>RADT performed n (%) of 136</td>
                <td>RADT positive n (%) within tested group</td>
                <td>RADT negative n (%) within tested group</td>
              </tr>
              <tr>
                <td>3 - 15</td>
                <td>69 (50.7)</td>
                <td>56 (81.2)</td>
                <td>13 (18.8)</td>
              </tr>
              <tr>
                <td>16 - 28</td>
                <td>13 (9.6)</td>
                <td>5 (38.5)</td>
                <td>8 (61.5)</td>
              </tr>
              <tr>
                <td>29 - 41</td>
                <td>8 (5.9)</td>
                <td>3 (37.5)</td>
                <td>5 (62.5)</td>
              </tr>
              <tr>
                <td>42 - 54</td>
                <td>1 (0.7)</td>
                <td>1 (100)</td>
                <td>0 (0)</td>
              </tr>
              <tr>
                <td>55 - 67</td>
                <td>0 (0.0)</td>
                <td>—</td>
                <td>—</td>
              </tr>
              <tr>
                <td>Total</td>
                <td>91 (66.9)</td>
                <td>65 (71.4)</td>
                <td>26 (28.6)</td>
              </tr>
            </tbody>
          </table>
        </table-wrap>
        <p><bold>Table 5.</bold> Association between age group and RADT result (n = 91). </p>
        <table-wrap id="tbl5">
          <label>Table 5</label>
          <table>
            <tbody>
              <tr>
                <td>Age group (years)</td>
                <td>RADT positive n (%)</td>
                <td>RADT negative n (%)</td>
                <td>Total tested n (%)</td>
              </tr>
              <tr>
                <td>3 - 15</td>
                <td>56 (81.2)</td>
                <td>13 (18.8)</td>
                <td>69 (75.8)</td>
              </tr>
              <tr>
                <td>≥16</td>
                <td>9 (40.9)</td>
                <td>13 (59.1)</td>
                <td>22 (24.2)</td>
              </tr>
              <tr>
                <td>Total</td>
                <td>65 (71.4)</td>
                <td>26 (28.6)</td>
                <td>91 (100)</td>
              </tr>
            </tbody>
          </table>
        </table-wrap>
        <p>Statistical test: Fisher’s exact test; p &lt; 0.01. Percentages were calculated by row. </p>
      </sec>
      <sec id="sec3dot5">
        <title>3.5. Association between McIsaac Score and RADT Result</title>
        <p>Among the 91 tested patients, RADT positivity increased with higher McIsaac scores. RADT was positive in 25.0% of patients with a score of 3, 75.0% with a score of 4, and 85.2% with a score of 5. </p>
        <p><bold>Table 6.</bold> Association between McIsaac score and RADT result among tested patients (n = 91). </p>
        <table-wrap id="tbl6">
          <label>Table 6</label>
          <table>
            <tbody>
              <tr>
                <td>McIsaac score</td>
                <td>RADT positive n (%)</td>
                <td>RADT negative n (%)</td>
                <td>Total n (%)</td>
              </tr>
              <tr>
                <td>3</td>
                <td>3 (25.0)</td>
                <td>9 (75.0)</td>
                <td>12 (13.2)</td>
              </tr>
              <tr>
                <td>4</td>
                <td>39 (75.0)</td>
                <td>13 (25.0)</td>
                <td>52 (57.1)</td>
              </tr>
              <tr>
                <td>5</td>
                <td>23 (85.2)</td>
                <td>4 (14.8)</td>
                <td>27 (29.7)</td>
              </tr>
              <tr>
                <td>Total</td>
                <td>65 (71.4)</td>
                <td>26 (28.6)</td>
                <td>91 (100)</td>
              </tr>
            </tbody>
          </table>
        </table-wrap>
        <p>Statistical test: Fisher’s exact test; p &lt; 0.05. RADT positive and negative percentages were calculated by row. Percentages in the “Total” column were calculated based on tested patients (n = 91). </p>
        <p>Statistical analysis showed a significant association between McIsaac score and RADT result (Fisher’s exact test, p &lt; 0.05). Detailed results are shown in <bold>Table 6</bold>. </p>
      </sec>
      <sec id="sec3dot6">
        <title>3.6. Antibiotic Prescription</title>
        <p>Among the 91 patients who underwent RADT, antibiotic therapy was prescribed in 69 patients (75.8%). </p>
        <p>All patients with a positive RADT result (65/65) received antibiotic treatment. Among patients with a negative RADT result, antibiotics were prescribed in 4 cases (15.4%), while 22 patients (84.6%) did not receive antibiotic therapy. Among the RADT-negative patients who received antibiotics, severe clinical signs were observed, including persistent high fever, marked tonsillar inflammation, or significant cervical lymphadenopathy. </p>
        <p>Statistical analysis using Fisher’s exact test demonstrated a highly significant association between RADT result and antibiotic prescription (p &lt; 0.001). The relationship between RADT result and antibiotic prescription is presented in <bold>Table 7</bold>. </p>
        <p><bold>Table 7.</bold> Association between RADT result and antibiotic prescription (n = 91). </p>
        <table-wrap id="tbl7">
          <label>Table 7</label>
          <table>
            <tbody>
              <tr>
                <td>RADT result</td>
                <td>Antibiotics prescribed n (%)</td>
                <td>Antibiotics not prescribed n (%)</td>
                <td>Total n (%)</td>
              </tr>
              <tr>
                <td>Positive</td>
                <td>65 (100)</td>
                <td>0 (0)</td>
                <td>65 (71.4)</td>
              </tr>
              <tr>
                <td>Negative</td>
                <td>4 (15.4)</td>
                <td>22 (84.6)</td>
                <td>26 (28.6)</td>
              </tr>
              <tr>
                <td>Total</td>
                <td>69 (75.8)</td>
                <td>22 (24.2)</td>
                <td>91 (100)</td>
              </tr>
            </tbody>
          </table>
        </table-wrap>
        <p>Statistical test: Fisher’s exact test; p &lt; 0.001. Percentages were calculated by row. </p>
      </sec>
    </sec>
    <sec id="sec4">
      <title>4. Discussion</title>
      <p>The present study provides original data on the diagnostic and therapeutic management of acute pharyngitis in a tertiary hospital in sub-Saharan Africa. It highlights the value of the rapid antigen detection test (RADT) as a clinical decision-support tool, both for diagnostic orientation and for the rationalization of antibiotic prescribing, in a resource-limited setting. </p>
      <sec id="sec4dot1">
        <title>4.1. Patient Profile and Distribution of Acute Pharyngitis</title>
        <p>The study population was predominantly young, with a majority of patients aged 3 - 15 years, accounting for more than half of the included cases. This age distribution is consistent with international data showing that acute pharyngitis, particularly streptococcal pharyngitis, primarily affects school-aged children and adolescents [<xref ref-type="bibr" rid="B4">4</xref>][<xref ref-type="bibr" rid="B12">12</xref>]. </p>
        <p>The near-equal sex ratio observed in our series is also comparable to that reported in other clinical and epidemiological studies, suggesting no marked sex-related difference in the occurrence of acute pharyngitis [<xref ref-type="bibr" rid="B1">1</xref>][<xref ref-type="bibr" rid="B8">8</xref>]. </p>
      </sec>
      <sec id="sec4dot2">
        <title>4.2. Contribution of the McIsaac Score to Diagnostic Orientation</title>
        <p>The McIsaac score is a validated clinical tool used to estimate the probability of streptococcal pharyngitis and to guide diagnostic strategies [<xref ref-type="bibr" rid="B5">5</xref>][<xref ref-type="bibr" rid="B6">6</xref>]. In our study, high scores (4 and 5) were frequently observed, reflecting a strong initial clinical suspicion of bacterial infection. </p>
        <p>However, the association between the McIsaac score and RADT results showed that, despite a statistically significant correlation, some patients with high clinical scores had negative RADT results. This finding is consistent with previous studies indicating that clinical scores, while useful for triage, are insufficient on their own to reliably confirm group A streptococcal infection [<xref ref-type="bibr" rid="B2">2</xref>][<xref ref-type="bibr" rid="B6">6</xref>][<xref ref-type="bibr" rid="B13">13</xref>]. The McIsaac score should therefore be regarded as a tool for clinical orientation rather than a definitive diagnostic test. </p>
      </sec>
      <sec id="sec4dot3">
        <title>4.3. Utility of RADT in Our Setting</title>
        <p>In our series, RADT was positive in 71.4% of tested patients. This relatively high positivity rate should be interpreted with caution. It is largely explained by the targeted testing strategy adopted, based on strict clinical criteria, particularly among adolescents and adults, in whom RADT was performed only when the McIsaac score was ≥3. </p>
        <p>This approach introduces a selection bias, as RADT was not performed in all patients presenting with acute pharyngitis, especially among those aged 16 years and older with low clinical scores. Consequently, the proportion of RADT-positive results among tested patients does not reflect the true prevalence of streptococcal pharyngitis in the overall study population. </p>
        <p>Moreover, in the absence of microbiological culture as a reference standard, our study does not allow assessment of the sensitivity or specificity of RADT. Rather, it primarily evaluates the practical usefulness of RADT in clinical decision-making, rather than its intrinsic diagnostic performance, as emphasized in previous methodological studies [<xref ref-type="bibr" rid="B9">9</xref>][<xref ref-type="bibr" rid="B14">14</xref>][<xref ref-type="bibr" rid="B15">15</xref>]. </p>
      </sec>
      <sec id="sec4dot4">
        <title>4.4. Impact of RADT on Antibiotic Prescribing</title>
        <p>One of the major findings of this study is the highly significant association between RADT results and antibiotic prescription. All patients with a positive RADT received antibiotic therapy, whereas most patients with a negative RADT did not. </p>
        <p>These results indicate that RADT contributed to better alignment between therapeutic decisions and objective diagnostic evidence, thereby limiting unnecessary antibiotic prescriptions. This observation is consistent with numerous studies demonstrating that integrating RADT into the management of acute pharyngitis significantly reduces inappropriate antibiotic use [<xref ref-type="bibr" rid="B3">3</xref>][<xref ref-type="bibr" rid="B8">8</xref>][<xref ref-type="bibr" rid="B14">14</xref>]. </p>
        <p>In a context marked by the growing burden of antimicrobial resistance, particularly in sub-Saharan Africa, this impact represents an important public health benefit [<xref ref-type="bibr" rid="B7">7</xref>][<xref ref-type="bibr" rid="B16">16</xref>]. </p>
      </sec>
      <sec id="sec4dot5">
        <title>4.5. Relevance of RADT in African and Resource-Limited Settings</title>
        <p>In sub-Saharan Africa, the management of acute pharyngitis often relies solely on clinical assessment, due to limited access to microbiological investigations and organizational constraints within health systems [<xref ref-type="bibr" rid="B10">10</xref>][<xref ref-type="bibr" rid="B11">11</xref>]. Several African studies have reported a tendency toward antibiotic overprescription for upper respiratory tract infections, contributing to the emergence of bacterial resistance [<xref ref-type="bibr" rid="B16">16</xref>]-[<xref ref-type="bibr" rid="B18">18</xref>]. </p>
        <p>Our study demonstrates that the rational use of RADT is feasible in an African tertiary hospital and may contribute to improving the quality of care for patients with acute pharyngitis. These local data support international recommendations advocating for simple, accessible diagnostic strategies to combat antimicrobial resistance [<xref ref-type="bibr" rid="B7">7</xref>][<xref ref-type="bibr" rid="B9">9</xref>][<xref ref-type="bibr" rid="B19">19</xref>]. </p>
      </sec>
      <sec id="sec4dot6">
        <title>4.6. Study Limitations</title>
        <p>This study has several limitations. Its single-center design may limit the generalizability of the findings to other healthcare settings. In addition, the lack of microbiological confirmation by culture prevents assessment of the diagnostic accuracy of RADT in our context. </p>
        <p>Furthermore, in children, asymptomatic carriage of group A streptococcus—well documented in the literature—may lead to a positive RADT result in the absence of active infection, representing a recognized limitation of rapid antigen tests [<xref ref-type="bibr" rid="B12">12</xref>][<xref ref-type="bibr" rid="B20">20</xref>]. Nevertheless, the prospective nature of data collection, the use of standardized clinical criteria, and appropriate statistical analyses strengthen the validity of the observed results. </p>
      </sec>
    </sec>
    <sec id="sec5">
      <title>5. Conclusions</title>
      <p>This study highlights the value of rapid antigen detection testing in the management of acute pharyngitis at the Renaissance University Hospital Center in N’Djamena. The significant association between the McIsaac score and RADT positivity confirms the usefulness of the clinical score as a tool for diagnostic orientation, while RADT appears to be a relevant aid for confirming group A streptococcal pharyngitis. </p>
      <p>The use of RADT contributed to better alignment between therapeutic decision-making and the probability of streptococcal infection, in line with principles of appropriate antibiotic use. In an African context characterized by a high infectious disease burden and a concerning rise in antimicrobial resistance, the rational and expanded integration of RADT into the management of acute pharyngitis represents a promising strategy to improve quality of care and support antimicrobial stewardship policies. </p>
    </sec>
    <sec id="sec6">
      <title>Acknowledgements</title>
      <p>The authors would like to thank the patients and their families for their voluntary participation in this study. </p>
    </sec>
  </body>
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