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<front>
<journal-meta>
<journal-id journal-id-type="publisher-id">J. Abdom. Wall Surg.</journal-id>
<journal-title-group>
<journal-title>Journal of Abdominal Wall Surgery</journal-title>
<abbrev-journal-title abbrev-type="pubmed">J. Abdom. Wall Surg.</abbrev-journal-title>
</journal-title-group>
<issn pub-type="epub">2813-2092</issn>
<publisher>
<publisher-name>Frontiers Media S.A.</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id pub-id-type="publisher-id">14476</article-id>
<article-id pub-id-type="doi">10.3389/jaws.2025.14476</article-id>
<article-version article-version-type="Version of Record" vocab="NISO-RP-8-2008"/>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Case Report</subject>
</subj-group>
</article-categories>
<title-group>
<article-title>Preoperative Botulinum Toxin for Complex Diaphragmatic Paralysis: A Case Series</article-title>
<alt-title alt-title-type="left-running-head">S&#xe1;nchez Moreno et al.</alt-title>
<alt-title alt-title-type="right-running-head">Boyulinum Toxin in Diaphragmatic Eventrations</alt-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname>S&#xe1;nchez Moreno</surname>
<given-names>L.</given-names>
</name>
<xref ref-type="aff" rid="aff1"/>
<uri xlink:href="https://loop.frontiersin.org/people/2986177"/>
</contrib>
<contrib contrib-type="author" corresp="yes">
<name>
<surname>Valera S&#xe1;nchez</surname>
<given-names>Z.</given-names>
</name>
<xref ref-type="aff" rid="aff1"/>
<xref ref-type="corresp" rid="c001">&#x2a;</xref>
<uri xlink:href="https://loop.frontiersin.org/people/2923637"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Naranjo Fern&#xe1;ndez</surname>
<given-names>J. R.</given-names>
</name>
<xref ref-type="aff" rid="aff1"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Morales-Conde</surname>
<given-names>S.</given-names>
</name>
<xref ref-type="aff" rid="aff1"/>
<uri xlink:href="https://loop.frontiersin.org/people/129082"/>
</contrib>
</contrib-group>
<aff id="aff1">
<institution>Department of General and Digestive Surgery, University Hospital Virgen Macarena</institution>, <city>Seville</city>, <country country="ES">Spain</country>
</aff>
<author-notes>
<corresp id="c001">
<label>&#x2a;</label>Correspondence: Z. Valera S&#xe1;nchez, <email xlink:href="mailto:zoraidavalera@hotmail.com">zoraidavalera@hotmail.com</email>
</corresp>
</author-notes>
<pub-date publication-format="electronic" date-type="pub" iso-8601-date="2026-01-07">
<day>07</day>
<month>01</month>
<year>2026</year>
</pub-date>
<pub-date publication-format="electronic" date-type="collection">
<year>2025</year>
</pub-date>
<volume>4</volume>
<elocation-id>14476</elocation-id>
<history>
<date date-type="received">
<day>10</day>
<month>02</month>
<year>2025</year>
</date>
<date date-type="rev-recd">
<day>30</day>
<month>09</month>
<year>2025</year>
</date>
<date date-type="accepted">
<day>19</day>
<month>12</month>
<year>2025</year>
</date>
</history>
<permissions>
<copyright-statement>Copyright &#xa9; 2026 S&#xe1;nchez Moreno, Valera S&#xe1;nchez, Naranjo Fern&#xe1;ndez and Morales-Conde.</copyright-statement>
<copyright-year>2026</copyright-year>
<copyright-holder>S&#xe1;nchez Moreno, Valera S&#xe1;nchez, Naranjo Fern&#xe1;ndez and Morales-Conde</copyright-holder>
<license>
<ali:license_ref start_date="2026-01-07">https://creativecommons.org/licenses/by/4.0/</ali:license_ref>
<license-p>This is an open-access article distributed under the terms of the <ext-link ext-link-type="uri" xlink:href="https://creativecommons.org/licenses/by/4.0/">Creative Commons Attribution License (CC BY)</ext-link>. The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.</license-p>
</license>
</permissions>
<abstract>
<sec>
<title>Introduction</title>
<p>The management of giant diaphragmatic paralysis remains a significant surgical challenge, frequently associated with high rates of recurrence and the risk of developing abdominal compartment syndrome. While the use of Botulinum Toxin Type A (BTX- A) as an adjuvant therapy has been established in complex ventral hernia repair, its application in diaphragmatic paralysis is novel and sparsely documented. This study aims to present our institutional experience with BTX-A as a prehabilitation strategy in patients with complex diaphragmatic paralysis and to evaluate short- and long-term outcomes.</p>
</sec>
<sec>
<title>Materials and Methods</title>
<p>Three patients with complex diaphragmatic paralysis underwent preoperative administration as part of a prehabilitation protocol prior to surgical repair. Loss of domain (LD) was calculated using the Sabbagh formula. According to Sabbagh, LD is defined as the ratio of herniated volume to total peritoneal volume (LD &#x3d; HV/TPV), with a loss &#x3e;20% being considered significant. All patients received a standardized BTX-A administration protocol consisting of ultrasound-guided injection of 500 units of botulinum toxin type A, administered at six sites following the technique described by Smoot, with three injection points on each side targeting the internal oblique muscle 4 weeks before surgery.</p>
</sec>
<sec>
<title>Results</title>
<p>Preoperative administration of Botulinum Toxin Type A (BTX-A) was safe in all three patients, with no postoperative complications or development of abdominal compartment syndrome, which was monitored through continuous intra-abdominal pressure measurements during the hospital stay (short-term outcomes). Six months postoperatively, all patients demonstrated significant improvement in respiratory function, assessed by standard pulmonary function tests, and reported improved quality of life, including relief from dyspnoea and enhanced daily functioning. At twelve months, two patients remained asymptomatic, with no clinical or radiological evidence of recurrence (long-term outcomes). Overall, preoperative BTX-A was associated with both short-term safety and sustained long-term functional benefits in this series.</p>
</sec>
<sec>
<title>Conclusion</title>
<p>Preoperative BTX-A appears to be safe and well-tolerated in complex diaphragmatic paralysis. The results suggest that BTX-A may reduce complications, improve functional outcomes, enhance respiratory function, and increase quality of life, with effects maintained for at least 1&#xa0;year in most patients.</p>
</sec>
</abstract>
<kwd-group>
<kwd>botulinum toxin type A</kwd>
<kwd>compartment syndrome</kwd>
<kwd>diaphragmatic paralysis</kwd>
<kwd>prehabilitation</kwd>
<kwd>surgical treatment</kwd>
</kwd-group>
<funding-group>
<funding-statement>The author(s) declared that financial support was not received for this work and/or its publication.</funding-statement>
</funding-group>
<counts>
<fig-count count="4"/>
<table-count count="0"/>
<equation-count count="0"/>
<ref-count count="18"/>
<page-count count="6"/>
</counts>
</article-meta>
</front>
<body>
<sec sec-type="intro" id="s1">
<title>Introduction</title>
<p>Diaphragmatic eventration is a congenital or acquired condition characterized by abnormal elevation of the diaphragm due to muscular or phrenic nerve dysfunction while maintaining its continuity and attachment to the costal margins [<xref ref-type="bibr" rid="B1">1</xref>]. Phrenic paralysis, often secondary to nerve injury, thoracic or cervical surgery, trauma, or neurological disease, represents the most frequent functional disorder of the diaphragm [<xref ref-type="bibr" rid="B2">2</xref>, <xref ref-type="bibr" rid="B3">3</xref>]. Symptomatic patients may present with dyspnoea, orthopnoea, hypoxemia, and nonspecific gastrointestinal complaints.</p>
<p>Surgical treatment, particularly diaphragmatic plication, remains the mainstay of therapy for symptomatic patients, aiming to improve respiratory function and relieve dyspnoea [<xref ref-type="bibr" rid="B1">1</xref>, <xref ref-type="bibr" rid="B2">2</xref>]. However, giant or complex diaphragmatic paralysis poses significant challenges, with high recurrence rates and risk of abdominal compartment syndrome [<xref ref-type="bibr" rid="B4">4</xref>].</p>
<p>Botulinum Toxin Type A (BTX-A) has been increasingly used in complex ventral hernia repair. By inducing temporary flaccid paralysis of abdominal wall muscles, BTX-A facilitates fascial closure and reduces tension [<xref ref-type="bibr" rid="B5">5</xref>&#x2013;<xref ref-type="bibr" rid="B12">12</xref>]. Its application in diaphragmatic paralysis remains scarcely documented. This study presents our experience using BTX-A as a prehabilitation strategy prior to diaphragmatic plication.</p>
</sec>
<sec id="s2">
<title>Case Report</title>
<sec id="s2-1">
<title>Case 1</title>
<p>A 44-year-old man (body mass index 39&#xa0;kg/m<sup>2</sup>) was evaluated for chest pain and dyspnoea with a two-year history. After assessment by the pulmonology, cardiology, and neurology departments, a diagnosis of idiopathic left diaphragmatic relaxation was made, and the patient was referred for thoracic surgery. His medical history was notable for suspected obstructive sleep apnoea syndrome (OSAS), managed with non-invasive mechanical ventilation (NIV). Physical examination was unremarkable.</p>
<p>A neurophysiological study and thoracic computed tomography scan (<xref ref-type="fig" rid="F1">Figure 1</xref>) revealed a serious elevation of the left hemidiaphragm and herniation of abdominal contents into the thorax, including stomach, spleen, and colon splenic flexure, occupying approximately 50% of the left hemithorax and causing right mediastinal shift, with 20% of abdominal viscera displaced into the thorax according to Sabagg&#x2019;s formula [<xref ref-type="bibr" rid="B13">13</xref>]. Preoperative preparation focused on prehabilitation with respiratory physiotherapy.</p>
<fig id="F1" position="float">
<label>FIGURE 1</label>
<caption>
<p>Computed tomography scan (coronal and transverse section). Significant elevation of the left hemidiaphragm and infradiaphragmatic abdominal contents, including the stomach, spleen, and splenic flexure of the colon and deviation of the mediastinum to the right.</p>
</caption>
<graphic xlink:href="jaws-04-14476-g001.tif">
<alt-text content-type="machine-generated">Two CT scan images of the thorax. The left coronal section shows upward displacement of organs into the thorax, including the stomach, spleen, and splenic flexure of the colon, along with the spine. The right transverse view shows measurements in green highlighting herniated abdominal contents into the thoracic cavity.</alt-text>
</graphic>
</fig>
<p>Given the size of the defect, adjuvant therapy was performed with botulinum toxin injection following the Smoot technique [<xref ref-type="bibr" rid="B14">14</xref>], without complications.</p>
<p>Four weeks later, a left diaphragmatic plication was performed via posterolateral thoracotomy, using non-absorbable monofilament barbed sutures and reinforced with a Gore- Tex&#xae; mesh. Intraoperative findings confirmed significant diaphragmatic laxity, with the dome of the diaphragm reaching the level of the bronchial carina. A pleural drain and an epidural catheter were placed for postoperative management.</p>
<p>The patient was extubated in the operating room and transferred to the postoperative recovery unit, where he remained for 4&#xa0;days, hemodynamically stable, eupnoeic, and without need for supplemental oxygen. Intra-abdominal pressure was monitored, with values of 10&#xa0;mmHg preoperatively, 11&#xa0;mmHg at the end of surgery, and less than 15&#xa0;mmHg over the subsequent days. The epidural catheter was removed at 72&#xa0;h, the pleural drain removed on postoperative day 5, and the patient was discharged on day 6.</p>
<p>At the six-month follow-up, the patient reported significant improvement in quality of life, including the ability to tolerate the supine position, which had previously been intolerable. He demonstrated good respiratory function, and a follow-up chest radiograph (<xref ref-type="fig" rid="F2">Figure 2</xref>) showed no elevation of the left hemidiaphragm. At twelve months, the patient remained asymptomatic and recurrence-free.</p>
<fig id="F2" position="float">
<label>FIGURE 2</label>
<caption>
<p>Postoperative Chest X-ray showed no elevation of the left hemidiaphragm.</p>
</caption>
<graphic xlink:href="jaws-04-14476-g002.tif">
<alt-text content-type="machine-generated">Chest X-ray showing the rib cage, spine, and clavicles. The lungs appear as dark areas on both sides of the centrally located heart. No elevation of the left hemidiaphragm is observed. Bones are visible as white structures.</alt-text>
</graphic>
</fig>
</sec>
<sec id="s2-2">
<title>Case 2</title>
<p>A 63-year-old woman (body mass index 35&#xa0;kg/m<sup>2</sup>) was evaluated for dyspnoea and digestive symptoms of 2&#xa0;years&#x2019; duration. After being evaluated by the pulmonology department, idiopathic left diaphragmatic relaxation was diagnosed, and the patient was referred for thoracic surgery. Her medical history included being a former smoker for 20 years, and she was diagnosed with severe OSAHS (obstructive sleep apnoea-hypopnea syndrome). The physical examination was normal.</p>
<p>A chest CT (<xref ref-type="fig" rid="F3">Figure 3</xref>) scan revealed a severe elevation of the left hemidiaphragm and herniation of abdominal contents into the thorax, including stomach, spleen, and colon splenic flexure, with a percentage of herniated viscera of 23% according to Sabagg&#x2019;s formula [<xref ref-type="bibr" rid="B13">13</xref>], which occupied more than half of the left hemithorax. It is associated with compressive atelectasis and a moderate contralateral mediastinal shift. No image of a diaphragmatic defect was observed. Preoperative preparation focused on prehabilitation with chest physiotherapy. Given the size of the defect, adjuvant therapy was performed with botulinum toxin injection following the Smoot technique [<xref ref-type="bibr" rid="B14">14</xref>], without complications.</p>
<fig id="F3" position="float">
<label>FIGURE 3</label>
<caption>
<p>Computed tomography (coronal and transverse section) marked elevation of the left hemidiaphragm and herniation of abdominal contents into the thoracic cavity, including the stomach, spleen, and splenic flexure of the colon with a moderate contralateral mediastinal shift.</p>
</caption>
<graphic xlink:href="jaws-04-14476-g003.tif">
<alt-text content-type="machine-generated">CT scan (coronal and transverse sections) showing marked elevation of the left hemidiaphragm and herniation of abdominal contents into the thoracic cavity, including the stomach, spleen, and splenic flexure of the colon, with a moderate contralateral mediastinal shift.</alt-text>
</graphic>
</fig>
<p>Four weeks later, a left diaphragmatic plication was performed via posterolateral thoracotomy, using nonabsorbable monofilament barbed sutures reinforced with Gore- Tex&#xae; mesh. Intraoperative findings confirmed significant diaphragmatic laxity, with the dome of the diaphragm reaching the main carina. A pleural drain and an epidural catheter were placed for postoperative management.</p>
<p>The patient was extubated in the operating room and transferred to the Postoperative Recovery Unit, where she remained hemodynamically stable, eupnoeic, and without the need for supplemental oxygen for 2&#xa0;days. Intra-abdominal pressure was monitored, with values of 12&#xa0;mmHg preoperatively, 12&#xa0;mmHg at the end of surgery, and less than 15&#xa0;mmHg in the following days. The epidural catheter was removed 72&#xa0;h later, the pleural drain was removed on the fourth postoperative day, and the patient was discharged on the fifth day.</p>
<p>At a six-month follow-up, the patient reported a significant improvement in her quality of life, with improved respiratory function and digestive symptoms. At 12&#xa0;months, the patient remained asymptomatic and without recurrence. The follow-up postoperative X-ray showing decreased&#x2014;but not complete resolution of&#x2014;left hemidiaphragm elevation compared to the preoperative state, which did not show an elevated diaphragm (<xref ref-type="fig" rid="F4">Figure 4</xref>).</p>
<fig id="F4" position="float">
<label>FIGURE 4</label>
<caption>
<p>Postoperative image showing decreased&#x2014;but not complete resolution of&#x2014;left hemidiaphragm elevation compared to the preoperative state.</p>
</caption>
<graphic xlink:href="jaws-04-14476-g004.tif">
<alt-text content-type="machine-generated">Side-by-side postoperative chest X-ray images. The left lateral view shows the profile of the chest and spine. The right frontal view shows the rib cage and lungs, with decreased&#x2014;but not complete resolution of&#x2014;left hemidiaphragm elevation compared to the preoperative state.</alt-text>
</graphic>
</fig>
</sec>
<sec id="s2-3">
<title>Case 3</title>
<p>A 45-year-old man (body mass index 30&#xa0;kg/m<sup>2</sup>) was evaluated for mild haemoptysis, moderate exertional dyspnoea, episodes of central chest tightness, and exercise intolerance. After being evaluated by the pulmonology department, he was diagnosed with idiopathic left diaphragmatic relaxation and referred for thoracic surgery. His medical history included being a former smoker for 2&#xa0;months, asthmatic bronchitis in childhood, and admission to the emergency department in November 2022 for extensive deep vein thrombosis in the right lower extremity and acute pulmonary thromboembolism in the inferior lobar pulmonary artery and left basal segmental pulmonary arteries. Physical examination was normal.</p>
<p>A chest CT scan showed left lung volume loss due to a large diaphragmatic elevation with intra-abdominal visceral contents in the chest and a right-sided mediastinal shift (<xref ref-type="sec" rid="s10">Supplementary Figure 1</xref>). Preoperative preparation focused on prehabilitation with respiratory physiotherapy. Given the size of the defect, adjuvant therapy was performed with botulinum toxin injection following the Smoot technique [<xref ref-type="bibr" rid="B14">14</xref>], without complications.</p>
<p>Four weeks later, diaphragmatic plication was performed with a non-absorbable barbed suture without the need for reinforcing mesh using video-assisted thoracoscopy. A pleural drain and an epidural catheter were placed for pain control. The patient was extubated in the operating room and transferred to the postoperative recovery unit, where he remained for 24&#xa0;h, hemodynamically stable, eupnoeic, and without the need for supplemental oxygen. Intra-abdominal pressure was monitored, with values of 13&#xa0;mmHg at the end of surgery. The epidural catheter and pleural drain were removed 48&#xa0;h later, and the patient was discharged on the third day.</p>
<p>At a six-month follow-up, respiratory function improved without dyspnoea or recurrence (<xref ref-type="sec" rid="s10">Supplementary Figure 2</xref>).</p>
</sec>
</sec>
<sec sec-type="discussion" id="s3">
<title>Discussion</title>
<p>Diaphragmatic paralysis and eventration represent a complex surgical challenge, and several studies have evaluated diaphragmatic plication as a standard intervention.</p>
<p>Reviews and series in adults and children have consistently shown improvements in respiratory function, including increased forced vital capacity and reduced dyspnoea, as well as relief of symptoms such as orthopnoea and exercise intolerance following plication [<xref ref-type="bibr" rid="B1">1</xref>&#x2013;<xref ref-type="bibr" rid="B3">3</xref>], [<xref ref-type="bibr" rid="B15">15</xref>]. However, complications such as abdominal compartment syndrome, although rare, have been reported in cases of diaphragmatic paralysis or large diaphragmatic eventrations [<xref ref-type="bibr" rid="B4">4</xref>], highlighting the need for careful perioperative planning. In parallel, the use of botulinum toxin type A as a preoperative adjunct has been extensively studied in the context of large ventral hernias and abdominal wall reconstruction. Multiple studies and systematic reviews have demonstrated that preoperative botulinum toxin A increases abdominal wall compliance, reduces tension during closure, facilitates the reduction of herniated contents, and, in some series, decreases postoperative complications such as seroma, infection, or hernia recurrence [<xref ref-type="bibr" rid="B5">5</xref>&#x2013;<xref ref-type="bibr" rid="B12">12</xref>]. Specifically, volumetric analyses and clinical measurements have shown improved abdominal cavity accommodation and decreased intra-abdominal pressure after toxin administration [<xref ref-type="bibr" rid="B6">6</xref>, <xref ref-type="bibr" rid="B9">9</xref>].</p>
<p>Evidence specifically addressing the use of botulinum toxin A prior to diaphragmatic plication is extremely limited. In isolated reports, such as the use in Morgagni hernias [<xref ref-type="bibr" rid="B16">16</xref>], botulinum toxin A facilitated abdominal wall relaxation, allowing for tension-free closure and reducing the risk of postoperative complications. Similarly, in giant hiatal hernias with loss of domain [<xref ref-type="bibr" rid="B17">17</xref>, <xref ref-type="bibr" rid="B18">18</xref>], preoperative toxin injection improved diaphragmatic mobility and abdominal cavity accommodation, contributing to successful surgical reduction and repair without major adverse events. These findings suggest potential benefits, but the evidence is limited to case reports and small series, leaving a significant gap in systematic data for complex diaphragmatic eventrations.</p>
<p>To our knowledge, no previous study has systematically described the use of botulinum toxin type A as a prehabilitation strategy prior to diaphragmatic plication. Our series of three patients provides new evidence supporting the safety and feasibility of this approach in complex diaphragmatic paralysis with large eventrations. In all cases, preoperative botulinum toxin administration facilitated abdominal wall relaxation, allowed for tension-free plication, and was associated with favourable postoperative outcomes, including the absence of abdominal compartment syndrome and sustained clinical and radiological stability at 12&#xa0;months in two patients. These findings suggest that the benefits previously observed in abdominal wall reconstruction may be extended to thoracic surgery, offering a novel strategy to optimize surgical conditions and patient outcomes in this underexplored field.</p>
<p>When comparing these findings with the present series, there is consistency in the effectiveness of botulinum toxin type A in improving preoperative abdominal and thoracic dynamics, reducing postoperative risks, and enhancing patient quality of life. However, it is important to note that most existing studies consist of case reports or small series, which limits the generalizability of their findings. Additionally, it would be of interest to assess the quantitative impact of botulinum toxin type A on intra-abdominal pressure, postoperative respiratory function, and objective markers of quality of life, which would enable the establishment of stronger and standardized recommendations for its use in thoracic surgery.</p>
<p>The present study has some limitations, such as its retrospective nature, the small number of patients included, short follow-up, and lack of a comparison group. However, this series contributes to the growth of evidence supporting the use of botulinum toxin type A as an adjunctive tool in prehabilitation before complex diaphragmatic eventrations repair.</p>
<p>In conclusion, although this is a novel and still underexplored indication, the preoperative administration of botulinum toxin type A as part of a prehabilitation protocol in patients with complex diaphragmatic paralysis appears to be a safe and effective strategy and may represent a significant advancement in the management of these conditions. Larger prospective studies are needed to establish standardized protocols and to validate these findings in broader populations with long-term follow-up in order to draw definitive conclusions.</p>
</sec>
</body>
<back>
<sec sec-type="data-availability" id="s4">
<title>Data Availability Statement</title>
<p>The raw data supporting the conclusions of this article will be made available by the authors, without undue reservation.</p>
</sec>
<sec sec-type="ethics-statement" id="s5">
<title>Ethics Statement</title>
<p>For the purpose if this study and for the study design (case report) ethical approval was not required. The studies were conducted in accordance with the local legislation and institutional requirements. The participants provided their written informed consent to participate in this study. Written informed consent was obtained from the individual(s) for the publication of any potentially identifiable images or data included in this article.</p>
</sec>
<sec sec-type="author-contributions" id="s6">
<title>Author Contributions</title>
<p>All authors participated in the design, interpretation of the studies and analysis of the data and review of the manuscript: ZV, JN, LS, and SM-C. All authors contributed to the article and approved the submitted version.</p>
</sec>
<sec sec-type="COI-statement" id="s9">
<title>Conflict of Interest</title>
<p>The author(s) declared that this work was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.</p>
</sec>
<sec sec-type="ai-statement" id="s10">
<title>Generative AI Statement</title>
<p>The author(s) declared that generative AI was not used in the creation of this manuscript.</p>
<p>Any alternative text (alt text) provided alongside figures in this article has been generated by Frontiers with the support of artificial intelligence and reasonable efforts have been made to ensure accuracy, including review by the authors wherever possible. If you identify any issues, please contact us.</p>
</sec>
<sec sec-type="disclaimer" id="s8">
<title>Publisher&#x2019;s Note</title>
<p>All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.</p>
</sec>
<sec sec-type="supplementary-material" id="s11">
<title>Supplementary Material</title>
<p>The Supplementary Material for this article can be found online at: <ext-link ext-link-type="uri" xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="https://www.frontierspartnerships.org/articles/10.3389/jaws.2025.14476/full#supplementary-material">https://www.frontierspartnerships.org/articles/10.3389/jaws.2025.14476/full#supplementary-material</ext-link>
</p>
<supplementary-material xlink:href="Supplementaryfile1.docx" id="SM1" mimetype="application/docx" xmlns:xlink="http://www.w3.org/1999/xlink"/>
</sec>
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