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  <front>
    <journal-meta>
      <journal-id journal-id-type="publisher-id">jct</journal-id>
      <journal-title-group>
        <journal-title>Journal of Cancer Therapy</journal-title>
      </journal-title-group>
      <issn pub-type="epub">2151-1942</issn>
      <issn pub-type="ppub">2151-1934</issn>
      <publisher>
        <publisher-name>Scientific Research Publishing</publisher-name>
      </publisher>
    </journal-meta>
    <article-meta>
      <article-id pub-id-type="doi">10.4236/jct.2026.179038</article-id>
      <article-id pub-id-type="publisher-id">jct-153907</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>Palliative Radiotherapy for Painful Bone Metastases: Experience from Bogodogo University Teaching Hospital, Burkina Faso</article-title>
      </title-group>
      <contrib-group>
        <contrib contrib-type="author" corresp="yes">
          <name name-style="western">
            <surname>Kietga</surname>
            <given-names>Gael</given-names>
          </name>
          <xref ref-type="aff" rid="aff1">1</xref>
        </contrib>
        <contrib contrib-type="author">
          <name name-style="western">
            <surname>Compaore</surname>
            <given-names>Bertrand</given-names>
          </name>
          <xref ref-type="aff" rid="aff1">1</xref>
        </contrib>
        <contrib contrib-type="author">
          <name name-style="western">
            <surname>Zoungrana</surname>
            <given-names>Landry</given-names>
          </name>
          <xref ref-type="aff" rid="aff1">1</xref>
        </contrib>
        <contrib contrib-type="author">
          <name name-style="western">
            <surname>Ouedraogo</surname>
            <given-names>Noufou</given-names>
          </name>
          <xref ref-type="aff" rid="aff1">1</xref>
        </contrib>
        <contrib contrib-type="author">
          <name name-style="western">
            <surname>Zongo</surname>
            <given-names>Esdras</given-names>
          </name>
          <xref ref-type="aff" rid="aff1">1</xref>
        </contrib>
      </contrib-group>
      <aff id="aff1"><label>1</label> Department of Radiotherapy, CHU Bogodogo University Teaching, Training and Research Unit in Health Sciences (UFR/SDS), Joseph Ki-Zerbo University, Ouagadougou, Burkina Faso </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>17</day>
        <month>09</month>
        <year>2026</year>
      </pub-date>
      <pub-date pub-type="collection">
        <month>09</month>
        <year>2026</year>
      </pub-date>
      <volume>17</volume>
      <issue>09</issue>
      <fpage>449</fpage>
      <lpage>459</lpage>
      <history>
        <date date-type="received">
          <day>05</day>
          <month>08</month>
          <year>2026</year>
        </date>
        <date date-type="accepted">
          <day>14</day>
          <month>09</month>
          <year>2026</year>
        </date>
        <date date-type="published">
          <day>17</day>
          <month>09</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/jct.2026.179038">https://doi.org/10.4236/jct.2026.179038</self-uri>
      <abstract>
        <p><bold>Introduction:</bold> Cancer remains a leading cause of global mortality, and bone metastases are among the most frequent complications of solid tumors, with incidence rising as survival after primary cancer treatment improves. Since bone metastases usually signal incurable disease, palliative radiotherapy accounting for over half of radiation oncology workloads worldwide is the mainstay of symptom management. While practice patterns have been well documented in North America, Europe, and Oceania, data from Africa remain limited. This study reports the experience of Bogodogo University Teaching Hospital (Burkina Faso) in managing patients receiving radiotherapy for painful bone metastases. <bold>Methods:</bold> A retrospective observational study included all patients treated with palliative radiotherapy for symptomatic bone metastases. Pain response was assessed against pre-treatment scores using internationally recognized criteria. Collected variables included age, sex, primary tumor site, metastatic site, lesion number, analgesic use, radiation dose/fractionation, and clinical evolution. Asymptomatic bone metastases, symptomatic non-bone metastases, and primary bone cancers were excluded. Follow-up occurred at day 3 and month 1. <bold>Results:</bold> Among 300 patients treated over one year, 24 (8%) had symptomatic bone metastases (58% male; median age 57.5, range 36 - 87). Prostate (41.67%), lung (33.33%), and breast (25%) cancers were the leading primary sites. The lumbar spine (58%) was the most common metastatic location. CT scan was the predominant imaging modality (66.6%). Most patients received 30 Gy (58%) or 20 Gy (42%). Overall pain response was 66.66% at 72 hours and 83.33% at one month. <bold>Discussion/Conclusion:</bold> Despite retrospective, single-center limitations and the difficulty of isolating radiotherapy’s effect from adjustments in oral analgesics, our results demonstrate an improvement in pain following radiotherapy of palliative radiotherapy in resource-limited settings. Expanding this research through larger multicenter cohorts will be essential to optimize palliative care delivery regionally.</p>
      </abstract>
      <kwd-group kwd-group-type="author-generated" xml:lang="en">
        <kwd>Bone Metastases</kwd>
        <kwd>Palliative Radiotherapy</kwd>
        <kwd>Pain Relief</kwd>
        <kwd>Sub-Saharan Africa</kwd>
      </kwd-group>
    </article-meta>
  </front>
  <body>
    <sec id="sec1">
      <title>1. Introduction</title>
      <p>Cancer is a major and growing global public health challenge, making it one of the top causes of mortality after Cardiovascular diseases, with nearly one in six deaths globally attributing to cancer each year [<xref ref-type="bibr" rid="B1">1</xref>].</p>
      <p>Bones are one of the most common sites of metastases for many types of solid cancers [<xref ref-type="bibr" rid="B2">2</xref>]-[<xref ref-type="bibr" rid="B4">4</xref>].</p>
      <p>The number of patients with this metastasis is likely to increase due to improved treatment options for primary tumors and subsequent longer survival [<xref ref-type="bibr" rid="B5">5</xref>].</p>
      <p>As the diagnosis of bone metastases often represents incurable disease, the main treatment goal is palliation of symptoms [<xref ref-type="bibr" rid="B6">6</xref>][<xref ref-type="bibr" rid="B7">7</xref>].</p>
      <p>Palliative radiotherapy (RT) constitutes more than 50% of the workload in radiation oncology departments worldwide: [<xref ref-type="bibr" rid="B8">8</xref>]. </p>
      <p>Surveys of patterns of practice in North America, Europe, Australia, and New Zealand [<xref ref-type="bibr" rid="B9">9</xref>]-[<xref ref-type="bibr" rid="B15">15</xref>] have been published, mainly regarding management of bone metastases.</p>
      <p>Few studies have evaluated the management of bone metastases using radiotherapy in Africa. </p>
      <p>The aim of this study was to report the experience of the Bogodogo University Teaching Hospital in the care pathway of patients treated with radiotherapy for bone metastases in Burkina Faso.</p>
    </sec>
    <sec id="sec2">
      <title>2. Methods</title>
      <p>This retrospective observational study included all consecutive patients who received palliative radiotherapy for painful bone metastases at the Radiotherapy Department of CHU Bogodogo between 02/09/2024 and 08/09/2025. Data were extracted from <italic>patient medical records</italic>and all eligible patients meeting the inclusion criteria during this period were included, with no additional sampling.</p>
      <p>Baseline demographic information was collected from all patients including age, gender, primary cancer site, site of bone metastases, number of bone metastases, Analgesy, Radiation: dose, number of fractions, evolution. Non-inclusion criteria: All patients with asymptomatic bone metastasis; Symptomatic non-bone metastasis; Primary Bone cancers.</p>
      <p>Follow up was after Day 3 and Month 1.</p>
      <table-wrap id="tbl1">
        <label>Table 1</label>
        <table>
          <tbody>
            <tr>
              <td>
              </td>
              <td>Definition of response criteria</td>
            </tr>
            <tr>
              <td>Complete response</td>
              <td>Pain score = 0 at the treated site Without concomitant increase in analgesic consumption, which remained stable or decreased</td>
            </tr>
            <tr>
              <td>Partial response</td>
              <td>Reduction in pain score ≥2 at the treated site without increase in analgesic consumption or decrease in analgesic consumption ≥25% without increase in pain</td>
            </tr>
            <tr>
              <td>Progression</td>
              <td>Increase in pain score ≥2 at the irradiated site with stable pain medication consumption Or Increase ≥25% in pain medication consumption with stable pain score ±1 point</td>
            </tr>
            <tr>
              <td>Undetermined response</td>
              <td>Any response that does not meet the definition of a complete, partial or progressive response</td>
            </tr>
          </tbody>
        </table>
      </table-wrap>
      <sec id="sec2dot1">
        <title>2.1. Ethical Considerations</title>
        <p>This study was conducted in strict accordance with the ethical principles for medical research involving human subjects outlined in the Declaration of Helsinki. Administrative and institutional authorization to access and analyze the medical records was granted by the management of the Centre Hospitalier Universitaire de Bogodogo (Ouagadougou, Burkina Faso). Owing to the retrospective, non-interventional design of the study utilizing secondary routine clinical data, the requirement for individual written informed consent was waived. Patient confidentiality was strictly preserved; all data were fully anonymized and de-identified using numerical codes prior to statistical analysis traduction.</p>
      </sec>
      <sec id="sec2dot2">
        <title>2.2. Radiotherapy Technique and Fractionation Selection</title>
        <p>Fractionation schedule (20 Gy in 5 fractions or 30 Gy in 10 fractions) was selected by the treating radiation oncologist based on <italic>performance status</italic>. All patients were treated using 3<italic>D-conformal radiotherapy and IMRT</italic>. Target volume delineation was performed in accordance with the French Society for Radiation Oncology (SFRO) RecoRad™ 2022 guidelines. For standard spinal bone metastases, the clinical target volume (CTV) encompassed the involved vertebra along with the adjacent upper and lower vertebral levels (<italic>N</italic> ± 1). In the presence of epidural extension (epiduritis), target delineation was modified to extend the CTV longitudinally further above and below the affected segment to ensure full coverage of intraspinal tumor spread. An isotropic expansion margin of 5 to 10 mm was applied to the CTV to construct the planning target volume (PTV) to account for patient positioning and setup uncertainties.</p>
      </sec>
      <sec id="sec2dot3">
        <title>2.3. Assessment of Pain Response</title>
        <p>Pain intensity was assessed using the <italic>Visual Analogue Scale</italic>(<italic>VAS</italic>), 0<italic>-</italic>10, recorded at baseline and at each follow-up visit by the <italic>treating radiation oncologist</italic>. Analgesic consumption was quantified by converting all analgesics to oral morphine equivalent daily dose (OMEDD) using standard equianalgesic conversion tables, recorded by <italic>the same evaluator</italic> at baseline, day 3, and month 1.</p>
        <p>Treatment response was classified according to the International Consensus Endpoints for palliative bone metastases radiotherapy trials (Chow <italic>et al</italic>., 2012, International Journal of Radiation Oncology, Biology, Physics). Complete response was defined as a pain score of 0 at the treated site with no increase in analgesic intake; partial response as a pain score reduction of ≥2 points without an increase in analgesic intake, or a reduction in OMEDD of ≥25% without an increase in pain score; progression as an increase in pain score of ≥2 points with a stable or increased OMEDD, or a ≥25% increase in OMEDD with a stable or increased pain score; and indeterminate response as any case not meeting the above criteria, including missing data. Analgesic doses were converted to oral morphine equivalents (OMEDD) prior to applying these criteria.</p>
      </sec>
    </sec>
    <sec id="sec3">
      <title>3. Results</title>
      <p>Over a 1-year period, our radiotherapy department treated 300 patients across all cancer stages. Among them, 24 consecutive patients with symptomatic bone metastases were included in this study, comprising 14 males (58.3%) and 10 females (41.7%).</p>
      <p>At Day 3 (72 hours), pain evaluation was performed for all 24 patients (100.0%). Based on international consensus criteria, 18 patients (75.0%) had a classified clinical response 4 (16.7%) complete responses, 12 (50.0%) partial responses, and 2 (8.3%) progressions while 6 patients (25.0%) were categorized as undetermined response due to incomplete analgesic or pain score documentation.</p>
      <p>At Month 1, an overall pain response (complete or partial) was observed in 20 patients (83.3%). A total of 4 patients (16.7%) were classified as undetermined response: 3 due to missing follow-up data comprising intercurrent death (n = 2) and loss to follow-up/unavailable records (n = 1) and 1 due to incomplete pain assessment documentation.</p>
      <p>Males predominate with 14 (58%) out of 10 (42%) female.</p>
      <p>The characteristics of the patients are summarised in <bold>Table 1</bold>.</p>
      <p><bold>Table 1.</bold> Demographics.</p>
      <table-wrap id="tbl2">
        <label>Table 2</label>
        <table>
          <tbody>
            <tr>
              <td>Characteristics</td>
              <td>n (%)</td>
            </tr>
            <tr>
              <td>Total Number of patients</td>
              <td>24 (100)</td>
            </tr>
            <tr>
              <td>Male</td>
              <td>14 (58%)</td>
            </tr>
            <tr>
              <td>Female</td>
              <td>10 (42%)</td>
            </tr>
            <tr>
              <td>Mean age (range)</td>
              <td>57.5 years (36 - 87 years)</td>
            </tr>
          </tbody>
        </table>
      </table-wrap>
      <p>The median ages were 57.5 with extremes 36 and 87. Primary sites were balanced with Prostate 10 (41.67%) Lung 8 (33.33%) Breast 6 (25%) <bold>Table 2</bold>. </p>
      <p><bold>Table 2.</bold>Primary sites.</p>
      <table-wrap id="tbl3">
        <label>Table 3</label>
        <table>
          <tbody>
            <tr>
              <td>Location</td>
              <td>Number of Patients</td>
            </tr>
            <tr>
              <td>Prostate</td>
              <td>10 (41.67%)</td>
            </tr>
            <tr>
              <td>Lung</td>
              <td>8 (33.33%)</td>
            </tr>
            <tr>
              <td>Breast</td>
              <td>6 (25%)</td>
            </tr>
          </tbody>
        </table>
      </table-wrap>
      <p>Lumbar location was the most frequent with 14 cases (58%), Follow by sacrum 4 (16.66%) <bold>Table 3</bold>.</p>
      <p><bold>Table 3.</bold>Sites of secondary location.</p>
      <table-wrap id="tbl4">
        <label>Table 4</label>
        <table>
          <tbody>
            <tr>
              <td>Location</td>
              <td>Number of patients</td>
            </tr>
            <tr>
              <td>Lumbar bone</td>
              <td>14 (58.33%)</td>
            </tr>
            <tr>
              <td>Sacrum</td>
              <td>4 (16.68%)</td>
            </tr>
            <tr>
              <td>Shoulder</td>
              <td>2 (8.33%)</td>
            </tr>
            <tr>
              <td>Cervical bone</td>
              <td>2 (8.33%)</td>
            </tr>
            <tr>
              <td>Thoracic bone</td>
              <td>2 (8.33%)</td>
            </tr>
          </tbody>
        </table>
      </table-wrap>
      <p>CT scan was the most frequently used imaging modality for the detection of bone metastases, representing 16 cases (66.6%), followed by MRI in 6 cases (25%) and bone scintigraphy in 2 case (8.3%) <bold>Table 4</bold>. </p>
      <p><bold>Table 4.</bold>Imaging modalities used for diagnostic of metastatic sites.</p>
      <table-wrap id="tbl5">
        <label>Table 5</label>
        <table>
          <tbody>
            <tr>
              <td>Type of imaging modalities</td>
              <td>Number of patients (%)</td>
            </tr>
            <tr>
              <td>CTAP</td>
              <td>16 (66.67%)</td>
            </tr>
            <tr>
              <td>MRI</td>
              <td>6 (25%)</td>
            </tr>
            <tr>
              <td>BONE SCINTIGRAPHY</td>
              <td>2 (8.33%)</td>
            </tr>
          </tbody>
        </table>
      </table-wrap>
      <p>Patients were seen in consultation, simulated, started on treatment within the same week. 14 patients (58%) received a dose of 30 Gy of antalgic radiation therapy 10 Patients (42%) dose of 20 Gy <bold>Table 5</bold>.</p>
      <p><bold>Table 5.</bold>Radiation therapy dose.</p>
      <table-wrap id="tbl6">
        <label>Table 6</label>
        <table>
          <tbody>
            <tr>
              <td>DOSE</td>
              <td>Number of patients (%)</td>
            </tr>
            <tr>
              <td>30 Gy</td>
              <td>14 (58.33%)</td>
            </tr>
            <tr>
              <td>20Gy</td>
              <td>10 (41.67%)</td>
            </tr>
          </tbody>
        </table>
      </table-wrap>
      <p>Seventy-two hours after treatment 16 (66.66%) patients have overall response <bold>Table 6</bold><bold>.</bold></p>
      <p><bold>Table 6.</bold>Evaluation after 72 h.</p>
      <table-wrap id="tbl7">
        <label>Table 7</label>
        <table>
          <tbody>
            <tr>
              <td>EVALUATION</td>
              <td>Number of Patients (%)</td>
            </tr>
            <tr>
              <td>COMPLETE RESPONSE</td>
              <td>4 (16.66%)</td>
            </tr>
            <tr>
              <td>PARTIAL RESPONSE</td>
              <td>12 (50%)</td>
            </tr>
            <tr>
              <td>PROGRESSION</td>
              <td>2 (8.33%)</td>
            </tr>
            <tr>
              <td>UNDETERMINED</td>
              <td>6 (25%)</td>
            </tr>
          </tbody>
        </table>
      </table-wrap>
      <p>After 1 month 20 (83.33%) have an overall response <bold>Table 7</bold>.</p>
      <p><bold>Table 7.</bold>Evaluation after 1 month.</p>
      <table-wrap id="tbl8">
        <label>Table 8</label>
        <table>
          <tbody>
            <tr>
              <td>EVALUATION</td>
              <td>Number of Patients (%)</td>
            </tr>
            <tr>
              <td>COMPLETE RESPONSE</td>
              <td>8 (33.33%)</td>
            </tr>
            <tr>
              <td>PARTIAL RESPONSE</td>
              <td>12 (50%)</td>
            </tr>
            <tr>
              <td>PROGRESSION</td>
              <td>0</td>
            </tr>
            <tr>
              <td>UNDETERMINED</td>
              <td>4 (16.66%)</td>
            </tr>
          </tbody>
        </table>
      </table-wrap>
    </sec>
    <sec id="sec4">
      <title>4. Discussion</title>
      <sec id="sec4dot1">
        <title>4.1. Median Age</title>
        <p>The median age at diagnosis of cancer in our study is globally lower 57.5 years. It’s globally the same like a others study in Africa in Ibadan Nigeria 45 years and Dakar 53 years Senegal [<xref ref-type="bibr" rid="B16">16</xref>][<xref ref-type="bibr" rid="B17">17</xref>] but remains lower than that reported in European populations [<xref ref-type="bibr" rid="B5">5</xref>]. This difference reflects the younger age structure of the Africa population and delayed diagnosis may contribute to earlier presentation with advanced disease.</p>
      </sec>
      <sec id="sec4dot2">
        <title>4.2. Sex Ratio</title>
        <p>The sex ratio observed in metastatic cancer cohorts is closely related to the distribution of primary tumor types. Male predominance is commonly reported in series with a high prevalence of prostate cancer, while female predominance is more frequently observed in cohorts where breast and gynecological malignancies are major contributors to metastatic disease. </p>
        <p>Our study showed no more differences between male and female. In high income countries the sex ratio tends to be balanced due to significant contribution of breast cancer in women and lung cancer in both sexes [<xref ref-type="bibr" rid="B18">18</xref>]-[<xref ref-type="bibr" rid="B21">21</xref>].</p>
      </sec>
      <sec id="sec4dot3">
        <title>4.3. Primary Site</title>
        <p>In Our study, the three main primary tumors leading to bone metastases were Prostate 10 (41.67%) Lung 8 (33.33%) Breast 6 (25%). Similar distributions have been reported in African series [<xref ref-type="bibr" rid="B22">22</xref>]-[<xref ref-type="bibr" rid="B24">24</xref>]. In a large retrospective analysis of the National Cancer Database (NCDB), encompassing 50,929 patients received palliative radiotherapy for osseous metastases. The most frequently represented primary tumor was non-small cell lung cancer (NSCLC), accounting for 45.2% of cases, followed by breast cancer (15.1%) and prostate cancer (10.8%) among patients treated with palliative bone radiotherapy [<xref ref-type="bibr" rid="B25">25</xref>]. </p>
        <p>The difference in ranking between African studies, where prostate cancer predominates, and the American NCDB study, where lung cancer is leading, may be explained by the late stage of presentation and underdiagnosis of lung cancer in African settings.</p>
      </sec>
      <sec id="sec4dot4">
        <title>4.4. Imaging</title>
        <p>In our study, CT scan was the most frequently used imaging modality for the detection of bone metastases, followed by MRI and bone scintigraphy. His finding is consistent with several international reports showing that CT remains one of the most commonly used imaging techniques in routine oncologic practice because it is widely available, fast, and frequently performed as part of staging or restaging examinations [<xref ref-type="bibr" rid="B26">26</xref>]-[<xref ref-type="bibr" rid="B28">28</xref>] although MRI and PET imaging have higher sensitivity for early marrow involvement [<xref ref-type="bibr" rid="B29">29</xref>]-[<xref ref-type="bibr" rid="B31">31</xref>].</p>
        <p>In the African setting, the predominance of CT may also be explained by the limited availability of advanced imaging modalities such as MRI and PET, due to high costs, shortage of equipment, and unequal distribution of radiologic resources in Sub-Saharan Africa [<xref ref-type="bibr" rid="B32">32</xref>][<xref ref-type="bibr" rid="B33">33</xref>]<bold>.</bold></p>
      </sec>
      <sec id="sec4dot5">
        <title>4.5. Evaluation</title>
        <p>In our study, overall response was observed in 66.66% of patients at 72 hours and increased to 83.33% at one month after radiotherapy.</p>
        <p>In this large prospective realworld cohort study of patients with painful bone metastases treated with external beam radiotherapy (EBRT), approximately 70 % (n = 1442/2067) of patients experienced a partial or complete pain response between 2 and 12 weeks after treatment, according to internationally accepted response criteria. The median time to pain response was 4 weeks [<xref ref-type="bibr" rid="B34">34</xref>].</p>
        <p>A recent Ethiopian prospective study reported overall response rates of 65%, 67%, and 78% at 2, 4, and 8 weeks respectively [<xref ref-type="bibr" rid="B35">35</xref>]. The higher responses rate observed in our study may be related to the small size. </p>
        <p>Interestingly, the proportion of undetermined responses decreased from 25.0% at Day 3 to 16.7% at Month 1. This difference reflects the acute post-treatment phase, where rapid analgesic titrations and the lack of structured outpatient visits at 72 hours generated missing data, whereas the 1-month evaluation benefited from formal clinical consultation.</p>
        <p>Our study is primarily limited by its retrospective, single-center design and small sample size, which naturally come with risks of selection bias and incomplete medical records. Additionally, separating the precise effect of radiotherapy from adjustments in oral pain medication was difficult. Nevertheless, these limitations reflect the true landscape of everyday palliative care, where radiation therapy is never an isolated intervention but part of a collaborative, urgent effort to ease patient suffering.</p>
      </sec>
    </sec>
    <sec id="sec5">
      <title>5. Conclusion</title>
      <p>This study describes the experience of Bogodogo University Teaching Hospital in the management of patients with bone metastases treated with palliative radiotherapy in Burkina Faso. Although the retrospective design and concurrent changes in analgesic treatment limit the interpretation of our findings, an improvement in pain was observed following radiotherapy. However, in the absence of a comparison group, this improvement cannot be attributed only to radiotherapy. Nevertheless, these findings provide real-world insight into the use of palliative radiotherapy for bone metastases in a low-income setting where access to advanced cancer treatments remains limited. Larger prospective and multicenter studies are needed to further evaluate pain outcomes and help develop treatment strategies suited to resource-limited settings.</p>
    </sec>
    <sec id="sec6">
      <title>Author Contributions</title>
      <p>Gaël Kietga: Conceptualization, Methodology, Formal analysis, Writing—original draft; Bertrand Compaore, Zoungrana Landry, Ouedraogo Noufou, Zongo Esdras—Data curation, Investigation, Resources.</p>
    </sec>
  </body>
  <back>
    <ref-list>
      <title>References</title>
      <ref id="B1">
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