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<front>
<journal-meta>
<journal-id journal-id-type="publisher-id">Front. Pediatr.</journal-id>
<journal-title>Frontiers in Pediatrics</journal-title>
<abbrev-journal-title abbrev-type="pubmed">Front. Pediatr.</abbrev-journal-title>
<issn pub-type="epub">2296-2360</issn>
<publisher>
<publisher-name>Frontiers Media S.A.</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id pub-id-type="doi">10.3389/fped.2025.1630918</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Pediatrics</subject>
<subj-group>
<subject>Mini Review</subject>
</subj-group>
</subj-group>
</article-categories>
<title-group>
<article-title>Lung ultrasound in the management of mechanical ventilation in pediatric critical care: a narrative review</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author"><name><surname>Lopes</surname><given-names>Nailu Lealina Garrido</given-names></name>
<xref ref-type="aff" rid="aff1"><sup>1</sup></xref>
<xref ref-type="aff" rid="aff2"><sup>2</sup></xref><role content-type="https://credit.niso.org/contributor-roles/writing-original-draft/"/><role content-type="https://credit.niso.org/contributor-roles/writing-review-editing/"/><role content-type="https://credit.niso.org/contributor-roles/methodology/"/><role content-type="https://credit.niso.org/contributor-roles/conceptualization/"/></contrib>
<contrib contrib-type="author" corresp="yes"><name><surname>Amaral</surname><given-names>Vivian Henriques do</given-names></name>
<xref ref-type="aff" rid="aff1"><sup>1</sup></xref>
<xref ref-type="aff" rid="aff3"><sup>3</sup></xref>
<xref ref-type="aff" rid="aff4"><sup>4</sup></xref>
<xref ref-type="corresp" rid="cor1">&#x002A;</xref><uri xlink:href="https://loop.frontiersin.org/people/1330393/overview"/><role content-type="https://credit.niso.org/contributor-roles/writing-original-draft/"/><role content-type="https://credit.niso.org/contributor-roles/methodology/"/><role content-type="https://credit.niso.org/contributor-roles/conceptualization/"/></contrib>
<contrib contrib-type="author"><name><surname>Minozzi</surname><given-names>Marina Sim&#x00F5;es</given-names></name>
<xref ref-type="aff" rid="aff1"><sup>1</sup></xref>
<xref ref-type="aff" rid="aff5"><sup>5</sup></xref><role content-type="https://credit.niso.org/contributor-roles/conceptualization/"/><role content-type="https://credit.niso.org/contributor-roles/writing-original-draft/"/><role content-type="https://credit.niso.org/contributor-roles/methodology/"/></contrib>
<contrib contrib-type="author"><name><surname>Guazzelli Pitta Madureira</surname><given-names>Paola</given-names></name>
<xref ref-type="aff" rid="aff1"><sup>1</sup></xref>
<xref ref-type="aff" rid="aff3"><sup>3</sup></xref>
<xref ref-type="aff" rid="aff6"><sup>6</sup></xref><role content-type="https://credit.niso.org/contributor-roles/conceptualization/"/><role content-type="https://credit.niso.org/contributor-roles/writing-original-draft/"/></contrib>
<contrib contrib-type="author"><name><surname>Zagne Braz</surname><given-names>Luisa</given-names></name>
<xref ref-type="aff" rid="aff1"><sup>1</sup></xref>
<xref ref-type="aff" rid="aff7"><sup>7</sup></xref><role content-type="https://credit.niso.org/contributor-roles/conceptualization/"/><role content-type="https://credit.niso.org/contributor-roles/validation/"/><role content-type="https://credit.niso.org/contributor-roles/supervision/"/><role content-type="https://credit.niso.org/contributor-roles/writing-review-editing/"/></contrib>
<contrib contrib-type="author"><name><surname>da Hora Passos</surname><given-names>Rogerio</given-names></name>
<xref ref-type="aff" rid="aff8"><sup>8</sup></xref>
<xref ref-type="aff" rid="aff9"><sup>9</sup></xref><uri xlink:href="https://loop.frontiersin.org/people/3112603/overview" /><role content-type="https://credit.niso.org/contributor-roles/supervision/"/><role content-type="https://credit.niso.org/contributor-roles/conceptualization/"/><role content-type="https://credit.niso.org/contributor-roles/investigation/"/><role content-type="https://credit.niso.org/contributor-roles/writing-review-editing/"/><role content-type="https://credit.niso.org/contributor-roles/validation/"/></contrib>
</contrib-group>
<aff id="aff1"><label><sup>1</sup></label><institution>Departamento Materno Infantil, Einstein Hospital Israelita</institution>, <addr-line>Sao Paulo</addr-line>, <country>Brazil</country></aff>
<aff id="aff2"><label><sup>2</sup></label><institution>Nucleo de Dados e Informa&#x00E7;&#x00F5;es Gerenciais, Einstein Hospital Israelita</institution>, <addr-line>Sao Paulo</addr-line>, <country>Brazil</country></aff>
<aff id="aff3"><label><sup>3</sup></label><institution>Hospital Municipal Gilson de Cassia Marques de Carvalho, Einstein Hospital Israelita</institution>, <addr-line>Sao Paulo</addr-line>, <country>Brazil</country></aff>
<aff id="aff4"><label><sup>4</sup></label><institution>Instituto do Cancer do Estado de S&#x00E3;o Paulo, Universidade de S&#x00E3;o Paulo</institution>, <addr-line>Sao Paulo</addr-line>, <country>Brazil</country></aff>
<aff id="aff5"><label><sup>5</sup></label><institution>Departamento de Pr&#x00E1;tica M&#x00E9;dica, Hospital Municipal Gilson de Cassia Marques de Carvalho, Einstein Hospital Israelita</institution>, <addr-line>S&#x00E3;o Paulo</addr-line>, <country>Brazil</country></aff>
<aff id="aff6"><label><sup>6</sup></label><institution>UTI Pedi&#x00E1;trica, AC Camargo Cancer Center</institution>, <addr-line>Sao Paulo</addr-line>, <country>Brazil</country></aff>
<aff id="aff7"><label><sup>7</sup></label><institution>Diretoria de Qualidade, Seguran&#x00E7;a e SCIH, Einstein Hospital Israelita</institution>, <addr-line>Sao Paulo</addr-line>, <country>Brazil</country></aff>
<aff id="aff8"><label><sup>8</sup></label><institution>Departamento de Pacientes Graves, Einstein Hospital Israelita</institution>, <addr-line>Sao Paulo</addr-line>, <country>Brazil</country></aff>
<aff id="aff9"><label><sup>9</sup></label><institution>DaVita Tratamento Renal</institution>, <addr-line>Sao Paulo</addr-line>, <country>Brazil</country></aff>
<author-notes>
<fn fn-type="edited-by"><p><bold>Edited by:</bold> <ext-link ext-link-type="uri" xlink:href="https://loop.frontiersin.org/people/69785/overview">Oguz Dursun</ext-link>, Akdeniz University, T&#x00FC;rkiye</p></fn>
<fn fn-type="edited-by"><p><bold>Reviewed by:</bold> <ext-link ext-link-type="uri" xlink:href="https://loop.frontiersin.org/people/1216305/overview">Marcin Miko&#x015B;</ext-link>, Paediatric pulmonology private practice, Poland</p></fn>
<corresp id="cor1"><label>&#x002A;</label><bold>Correspondence:</bold> Vivian Henriques Do Amaral <email>vivian.hamaral@hc.fm.usp.br</email></corresp>
</author-notes>
<pub-date pub-type="epub"><day>05</day><month>09</month><year>2025</year></pub-date>
<pub-date pub-type="collection"><year>2025</year></pub-date>
<volume>13</volume><elocation-id>1630918</elocation-id>
<history>
<date date-type="received"><day>18</day><month>05</month><year>2025</year></date>
<date date-type="accepted"><day>11</day><month>08</month><year>2025</year></date>
</history>
<permissions>
<copyright-statement>&#x00A9; 2025 Lopes, Amaral, Minozzi, Guazzelli Pitta Madureira, Zagne Braz and da Hora Passos.</copyright-statement>
<copyright-year>2025</copyright-year><copyright-holder>Lopes, Amaral, Minozzi, Guazzelli Pitta Madureira, Zagne Braz and da Hora Passos</copyright-holder><license license-type="open-access" xlink:href="http://creativecommons.org/licenses/by/4.0/">
<p>This is an open-access article distributed under the terms of the <ext-link ext-link-type="uri" xlink:href="http://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.</p></license>
</permissions>
<abstract>
<p>Lung ultrasound (LUS) has become an increasingly valuable tool in the management of critically ill pediatric patients, offering dynamic, radiation-free bedside evaluation of pulmonary function. This narrative review synthesizes current evidence on the application of LUS in the context of ventilation in children and neonates. Key domains include its role in determining the indication for ventilation, guiding ventilatory adjustments, assessing positive end-expiratory pressure (PEEP) response, supporting lung recruitment maneuvers, and aiding in weaning and extubation decisions. The use of LUS in diagnosing ventilator-associated pneumonia (VAP) is also addressed, highlighting characteristic sonographic findings and their limitations. The I-VENT mnemonic is proposed as a practical framework for clinicians to integrate LUS into ventilatory management. While further research is needed to standardize protocols and validate scoring systems, current evidence supports the routine use of LUS in pediatric intensive care as a safe, accessible, and informative tool for optimizing respiratory support.</p>
</abstract>
<kwd-group>
<kwd>ultrasonography</kwd>
<kwd>lung</kwd>
<kwd>respiration</kwd>
<kwd>artificial</kwd>
<kwd>intensive care units</kwd>
<kwd>pediatric</kwd>
<kwd>child</kwd>
<kwd>weaning</kwd>
</kwd-group><counts>
<fig-count count="0"/>
<table-count count="2"/><equation-count count="0"/><ref-count count="38"/><page-count count="6"/><word-count count="0"/></counts><custom-meta-wrap><custom-meta><meta-name>section-at-acceptance</meta-name><meta-value>Pediatric Pulmonology</meta-value></custom-meta></custom-meta-wrap>
</article-meta>
</front>
<body><sec id="s1" sec-type="intro"><label>1</label><title>Introduction</title>
<p>Lung ultrasound (LUS) has become an essential bedside tool in pediatric and neonatal care due to its portability, speed, absence of ionizing radiation, and diagnostic accuracy (<xref ref-type="bibr" rid="B1">1</xref>). In children, the partially ossified chest and reduced subcutaneous tissue provide excellent acoustic windows for pulmonary imaging (<xref ref-type="bibr" rid="B1">1</xref>).</p>
<p>Historically, the lung parenchyma was considered inaccessible to ultrasound due to the presence of air and the bony thoracic framework, which hinders sound wave propagation. However, a better understanding of ultrasound artifacts and their correlation with lung pathology has led to the growing use of LUS in respiratory assessment (<xref ref-type="bibr" rid="B2">2</xref>).</p>
<p>LUS has demonstrated high performance in diagnosing pneumonia, ARDS, bronchiolitis, atelectasis, pleural effusion, and pneumothorax in the pediatric population (<xref ref-type="bibr" rid="B4">4</xref>). Probe selection varies by age and region of interest, with high-frequency linear transducers preferred in neonates and convex or microconvex probes used for deeper lesions in older children (<xref ref-type="bibr" rid="B1">1</xref>, <xref ref-type="bibr" rid="B5">5</xref>, <xref ref-type="bibr" rid="B6">6</xref>). A systematic scanning approach&#x2014;covering anterior, lateral, and posterior zones&#x2014;is essential for comprehensive evaluation (<xref ref-type="bibr" rid="B1">1</xref>, <xref ref-type="bibr" rid="B3">3</xref>, <xref ref-type="bibr" rid="B6">6</xref>).</p>
<p>Despite the growing body of literature on point-of-care lung ultrasound, there is still limited synthesis of its targeted applications in the context of invasive mechanical ventilation in children. This narrative review aims to consolidate current evidence on the use of LUS to guide ventilatory management in pediatric intensive care units (PICUs), including lung recruitment maneuvers, diagnosis of ventilator-associated complications, and optimization of ventilation parameters. By exploring the specific sonographic patterns and their clinical implications, we aim to provide practical insights for integrating LUS into routine respiratory management of critically ill pediatric patients.</p>
</sec>
<sec id="s2"><label>2</label><title>Lung ultrasound in mechanical ventilation</title>
<sec id="s2a"><label>2.1</label><title>Mechanical ventilation indication and LUS score</title>
<p>Lung ultrasound (LUS) scores have been proposed to quantify lung aeration and guide clinical decisions in both adults and children. In adults, a common scoring method evaluates 12 thoracic regions (six per lung), with scores from 0 (normal aeration) to 3 (consolidation). In neonates, six regions are typically assessed, yielding a total score from 0 to 18 (<xref ref-type="table" rid="T1">Table&#x00A0;1</xref>) (<xref ref-type="bibr" rid="B7">7</xref>&#x2013;<xref ref-type="bibr" rid="B9">9</xref>).</p>
<table-wrap id="T1" position="float"><label>Table 1</label>
<caption><p>Comparison of adult and neonatal lung ultrasound scoring systems.</p></caption>
<table frame="hsides" rules="groups">
<colgroup>
<col align="left"/>
<col align="left"/>
<col align="left"/>
</colgroup>
<thead>
<tr>
<th valign="top" align="left">Criteria</th>
<th valign="top" align="center">Adult LUS score (<xref ref-type="bibr" rid="B7">7</xref>, <xref ref-type="bibr" rid="B8">8</xref>)</th>
<th valign="top" align="center">Neonatal LUS score (<xref ref-type="bibr" rid="B9">9</xref>)</th>
</tr>
</thead>
<tbody>
<tr>
<td valign="top" align="left">Regions</td>
<td valign="top" align="left">6 for each lung (upper and lower parts of the anterior, lateral, and posterior regions)</td>
<td valign="top" align="left">3 for each lung (upper anterior, lower anterior, and lateral)</td>
</tr>
<tr>
<td valign="top" align="left" rowspan="4">Scores</td>
<td valign="top" align="left" colspan="2">0: normal aeration/A-line pattern (presence of lung sliding with A-lines and, occasionally, an isolated B-line)</td>
</tr>
<tr>
<td valign="top" align="left" colspan="2">1: B-pattern (three or more well-spaced B-lines)</td>
</tr>
<tr>
<td valign="top" align="left" colspan="2">2: coalescent B-lines (with possible subpleural consolidations)</td>
</tr>
<tr>
<td valign="top" align="left" colspan="2">3: tissue-like pattern (complete loss of aeration/ extended consolidations)</td>
</tr>
<tr>
<td valign="top" align="left"><bold>Total Score</bold></td>
<td valign="top" align="left"><bold>0&#x2013;36</bold></td>
<td valign="top" align="left"><bold>0&#x2013;18</bold></td>
</tr>
</tbody>
</table>
</table-wrap>
<p>In neonates with acute respiratory distress syndrome (ARDS), a LUS score &#x2265;8 is associated with the need for invasive mechanical ventilation (MV), while lower scores may support a trial of non-invasive ventilation (NIV) (<xref ref-type="bibr" rid="B10">10</xref>). Additionally, bilateral &#x201C;white lung&#x201D; patterns on nasal CPAP have been predictive of NIV failure (<xref ref-type="bibr" rid="B11">11</xref>).</p>
<p>LUS also assists in confirming tracheal intubation by detecting bilateral pleural sliding and identifying misplacement (<xref ref-type="bibr" rid="B12">12</xref>). In pediatric ARDS, findings include diffuse B-lines, consolidations, pleural line abnormalities, and effusion. Given disease heterogeneity, semiquantitative scoring systems offer more accuracy than isolated B-line counts (<xref ref-type="bibr" rid="B13">13</xref>).</p>
<p>It&#x0027;s important to interpret LUS with age-related differences in mind. Infants under 6 months may display B-lines due to incomplete alveolarization, which typically normalize over time. In these cases, the diagnosis may require other complementary tests and ultrasound changes monitored over time (<xref ref-type="bibr" rid="B14">14</xref>).</p>
</sec>
<sec id="s2b"><label>2.2</label><title>Ventilation mode and diaphragm monitoring</title>
<p>LUS and diaphragmatic ultrasound can assist in choosing ventilator modes and optimizing support. LUS scores inversely correlate with lung compliance, suggesting that higher scores may signal reduced aeration or atelectasis (<xref ref-type="bibr" rid="B9">9</xref>).</p>
<p>Diaphragm thickening fraction (TF), calculated as the percentage change in diaphragm thickness during inspiration, serves as a marker of respiratory effort. TF between 15&#x0025;&#x2013;30&#x0025; has been associated with shorter ventilation duration and preserved muscle mass in adults (<xref ref-type="bibr" rid="B10">10</xref>, <xref ref-type="bibr" rid="B11">11</xref>). In preterm infants, modes such as NIV-NAVA may enhance diaphragm function through improved synchrony, with higher diaphragmatic excursion than other NIV modalities (<xref ref-type="bibr" rid="B12">12</xref>, <xref ref-type="bibr" rid="B13">13</xref>).</p>
<p>Anatomical differences in neonates&#x2014;such as a flatter diaphragm with steeper costal angles&#x2014;necessitate careful interpretation (<xref ref-type="bibr" rid="B14">14</xref>). Diaphragm dysfunction (DD), marked by reduced thickening or excursion, is influenced by ventilation duration and mode. TF &#x003C;20&#x0025; is often used to identify dysfunction, and diaphragm thickness may decline by &#x223C;2&#x0025; per day during MV in children (<xref ref-type="bibr" rid="B15">15</xref>&#x2013;<xref ref-type="bibr" rid="B17">17</xref>).</p>
</sec>
<sec id="s2c"><label>2.3</label><title>PEEP titration and alveolar recruitment assessment</title>
<p>LUS is valuable for titrating positive end-expiratory pressure (PEEP) and evaluating recruitment responses. Patients with diffuse aeration loss on LUS typically respond better to PEEP, while focal findings increase the risk of overdistension. Trials comparing LUS-guided PEEP to ARDSnet tables show better oxygenation and compliance in the LUS groups, though caution is needed in interpretation (<xref ref-type="bibr" rid="B15">15</xref>&#x2013;<xref ref-type="bibr" rid="B18">18</xref>).</p>
<p>Bouhemad et al. proposed a reaeration score based on ultrasound pattern changes across 12 lung zones, correlating with pressure&#x2013;volume curve analysis. Most reaeration is seen in anterior/lateral zones, while posterior consolidations are less responsive due to gravity and dependent atelectasis (<xref ref-type="table" rid="T2">Table&#x00A0;2</xref>) (<xref ref-type="bibr" rid="B15">15</xref>, <xref ref-type="bibr" rid="B19">19</xref>).</p>
<table-wrap id="T2" position="float"><label>Table 2</label>
<caption><p>Lung ultrasound reaeration score.</p></caption>
<table frame="hsides" rules="groups">
<colgroup>
<col align="left"/>
<col align="left"/>
<col align="left"/>
<col align="left"/>
</colgroup>
<tbody>
<tr>
<td valign="top" align="left" colspan="4">
<list list-type="simple">
<list-item><label>1.</label>
<p>Ultrasound lung aeration is assessed in each of the 12 lung regions before the intervention.</p></list-item>
</list></td>
</tr>
<tr>
<td valign="top" align="left"><italic>N: 5 normal pattern (normal lung aeration)</italic></td>
<td valign="top" align="left"><italic>B1: 5 multiple well-defined either regularly spaced 7-mm apart or irregularly spaced B lines (moderate loss of lung aeration)</italic></td>
<td valign="top" align="left"><italic>B2: 5 multiple coalescent B lines (severe loss of lung aeration)</italic></td>
<td valign="top" align="left"><italic>C: 5 lung consolidation</italic></td>
</tr>
<tr>
<td valign="top" align="left" colspan="4">
<list list-type="simple">
<list-item><label>2.</label>
<p>Ultrasound lung aeration is assessed in each of the 12 lung regions after the intervention.</p></list-item>
</list></td>
</tr>
<tr>
<td valign="top" align="left" colspan="4">
<list list-type="simple">
<list-item><label>3.</label>
<p>Ultrasound lung reaeration score is calculated as the sum of each score (for each lung region examined) according to the scale below:</p></list-item>
</list></td>
</tr>
<tr>
<td valign="top" align="left" rowspan="4">Quantification of reaeration:</td>
<td valign="top" align="center"><bold>1 point</bold></td>
<td valign="top" align="center"><bold>3 points</bold></td>
<td valign="top" align="center"><bold>5 points</bold></td>
</tr>
<tr>
<td valign="top" align="center">B1&#x2009;&#x2192;&#x2009;N</td>
<td valign="top" align="center">B2&#x2009;&#x2192;&#x2009;N</td>
<td valign="top" align="center">C&#x2009;&#x2192;&#x2009;N</td>
</tr>
<tr>
<td valign="top" align="center">B2&#x2009;&#x2192;&#x2009;B1</td>
<td valign="top" align="center">C&#x2009;&#x2192;&#x2009;B1</td>
<td valign="top" align="left"/>
</tr>
<tr>
<td valign="top" align="center">C&#x2009;&#x2192;&#x2009;B2</td>
<td valign="top" align="left"/>
<td valign="top" align="left"/>
</tr>
<tr>
<td valign="top" align="left" rowspan="4">Quantification of loss of aeration:</td>
<td valign="top" align="center"><bold>5 point</bold></td>
<td valign="top" align="center"><bold>3 points</bold></td>
<td valign="top" align="center"><bold>1 points</bold></td>
</tr>
<tr>
<td valign="top" align="center">N&#x2009;&#x2192;&#x2009;C</td>
<td valign="top" align="center">N&#x2009;&#x2192;&#x2009;B2</td>
<td valign="top" align="center">N&#x2009;&#x2192;&#x2009;B1</td>
</tr>
<tr>
<td valign="top" align="left"/>
<td valign="top" align="center">B1&#x2009;&#x2192;&#x2009;C</td>
<td valign="top" align="center">B1&#x2009;&#x2192;&#x2009;2</td>
</tr>
<tr>
<td valign="top" align="left"/>
<td valign="top" align="left"/>
<td valign="top" align="center">B2&#x2009;&#x2192;&#x2009;C</td>
</tr>
</tbody>
</table>
</table-wrap>
<p>Serial LUS can also guide recruitment maneuvers and prevent unnecessary interventions. However, LUS does not detect hyperinflation or deep parenchymal overdistension. Thus, findings should be interpreted in conjunction with compliance, gas exchange, and clinical data (<xref ref-type="bibr" rid="B2">2</xref>, <xref ref-type="bibr" rid="B18">18</xref>).</p>
<p>Despite the lack of standardized protocols in pediatrics, LUS-guided recruitment is feasible&#x2014;especially in neonates&#x2014;and helps minimize radiation exposure. Further research is needed to refine scoring and clinical application.</p>
<p>Prone positioning (PP) represents an additional strategy to improve oxygenation and regional aeration through postural recruitment. Performing LUS in the prone position is feasible and can be used to monitor its effects. Although oxygenation improvement after PP does not correlate with a specific sonographic pattern, studies show increased LUS scores in dependent regions after approximately 3&#x2005;h of PP, with associated rises in the PaO<sub>2</sub>/FiO<sub>2</sub> ratio. However, this effect may diminish after prolonged sessions (&#x003E;6&#x2005;h) (<xref ref-type="bibr" rid="B20">20</xref>&#x2013;<xref ref-type="bibr" rid="B23">23</xref>).</p>
</sec>
<sec id="s2d"><label>2.4</label><title>Patient-ventilator asynchrony</title>
<p>Patient&#x2013;ventilator asynchrony (PVA) is a mismatch between patient effort and ventilator response. Diaphragm ultrasound can help identify PVA by correlating muscle movement with airway pressure, often more feasibly than invasive monitoring or waveform analysis (<xref ref-type="bibr" rid="B11">11</xref>, <xref ref-type="bibr" rid="B24">24</xref>, <xref ref-type="bibr" rid="B25">25</xref>).</p>
</sec>
<sec id="s2e"><label>2.5</label><title>Weaning and extubation prediction</title>
<p>LUS and diaphragm ultrasound are increasingly used to assess readiness for weaning. In adults, a LUS score &#x003C;13 after spontaneous breathing trial (SBT) predicts extubation success, while &#x003E;17 indicates failure (<xref ref-type="bibr" rid="B9">9</xref>, <xref ref-type="bibr" rid="B26">26</xref>). A rise in B-lines during SBT may also signal fluid overload and weaning risk.</p>
<p>In neonates, LUS score &#x2264;6 before and &#x2264;7 after nCPAP removal predicted successful weaning (<xref ref-type="bibr" rid="B25">25</xref>, <xref ref-type="bibr" rid="B26">26</xref>). TF &#x003C;23.2&#x0025; and diaphragmatic excursion &#x003C;6.2&#x2005;mm have been associated with weaning failure in children, though thresholds vary by age and condition (<xref ref-type="bibr" rid="B27">27</xref>&#x2013;<xref ref-type="bibr" rid="B31">31</xref>).</p>
<p>Several factors influence LUS predictive value, including timing relative to SBT, ventilatory support settings, and zone count (6&#x2013;14) used during assessment.</p>
</sec>
</sec>
<sec id="s3"><label>3</label><title>Diagnosis of ventilator-associated pneumonia</title>
<p>Ventilator-associated pneumonia (VAP) is the most common hospital-acquired infection in pediatric intensive care, contributing to significant morbidity, mortality, and prolonged mechanical ventilation. Its reported incidence varies from 3&#x0025; to 32&#x0025; in children and up to 20&#x0025; in neonates, depending on definitions and diagnostic methods used (<xref ref-type="bibr" rid="B32">32</xref>, <xref ref-type="bibr" rid="B33">33</xref>). While adult criteria integrate clinical, radiologic, and microbiological findings, pediatric and neonatal populations lack standardized diagnostic frameworks. In neonates, particularly, radiographic and clinical signs are often nonspecific and overlap with other conditions such as RDS or sepsis, making the diagnosis especially challenging (<xref ref-type="bibr" rid="B34">34</xref>&#x2013;<xref ref-type="bibr" rid="B37">37</xref>).</p>
<p>This diagnostic uncertainty may result in delayed treatment, increased antibiotic use, and prolonged ventilation. In this context, lung ultrasound (LUS) has emerged as a valuable tool for early, radiation-free, and bedside diagnosis of VAP. Studies report sensitivity and specificity above 90&#x0025; for pneumonia detection using LUS in children, often exceeding the performance of chest radiography (<xref ref-type="bibr" rid="B35">35</xref>&#x2013;<xref ref-type="bibr" rid="B37">37</xref>).</p>
<p>Typical sonographic findings in VAP include subpleural consolidations, often with dynamic air bronchograms, pleural effusions, and B-lines. Although these signs support the diagnosis of pneumonia, their interpretation must consider the clinical context, as similar patterns may be seen in atelectasis, ARDS, or bronchiolitis (<xref ref-type="bibr" rid="B37">37</xref>, <xref ref-type="bibr" rid="B38">38</xref>).</p>
<p>To enhance diagnostic consistency, structured scoring systems have been proposed. One of the most studied is the VPLUS score, which assigns 1 point for the presence of two or more subpleural consolidations, 2 points for at least one dynamic air bronchogram, and 1 point for purulent tracheal secretions. A total score of 2 or more indicates a high probability of VAP. Two expanded versions&#x2014;VPLUS-EAgram and VPLUS-EAquant&#x2014;add microbiological data such as Gram stain or quantitative cultures, increasing diagnostic specificity to above 95&#x0025; when scores reach 3 (<xref ref-type="bibr" rid="B38">38</xref>). For neonates, a Multiparametric Score was developed to integrate clinical, ultrasound, and microbiological criteria. On day 1, the score includes clinical signs such as temperature instability, changes in secretions, and respiratory deterioration (1 point each), along with ultrasound findings: subpleural consolidations over 0.5&#x2005;cm, dynamic air bronchograms, and pleural effusion (2 points each). On day 3, a positive bacterial culture from tracheal aspirate adds 1 additional point. A total score above 4 on day 1 or above 5 on day 3 has shown excellent diagnostic performance (AUC &#x003E;0.9) (<xref ref-type="bibr" rid="B37">37</xref>).</p>
<p>Despite its advantages, LUS is not without limitations. Findings such as consolidations and B-lines are not exclusive to pneumonia and may occur in atelectasis, ARDS, and bronchiolitis (<xref ref-type="bibr" rid="B37">37</xref>). Additionally, subcutaneous emphysema&#x2014;a recurrent condition in Pediatric Intensive Care Units&#x2014;may also compromise the quality of the ultrasound window in critically ill patients.</p>
<p>Moreover, LUS only detects lesions that reach the pleural surface and lie within intercostal windows, limiting its ability to evaluate apical, central, or subdiaphragmatic consolidations. In adults, this may result in up to 8&#x0025; of lesions being missed (<xref ref-type="bibr" rid="B38">38</xref>); in children, this limitation is less pronounced but still relevant (<xref ref-type="bibr" rid="B37">37</xref>). Operator experience also influences diagnostic performance, especially when distinguishing subtle findings.</p>
<p>Nevertheless, compared with chest radiography, LUS demonstrates superior sensitivity and specificity for detecting consolidations and effusions, and allows serial monitoring of disease progression and complications (<xref ref-type="bibr" rid="B37">37</xref>, <xref ref-type="bibr" rid="B38">38</xref>). It also enables dynamic evaluation of treatment response, guiding drainage of effusions, and identifying complications such as empyema. The integration of color Doppler can help differentiate inflammatory consolidations, which typically show preserved perfusion, from atelectasis, where vascular flow is often reduced or absent (<xref ref-type="bibr" rid="B37">37</xref>).</p>
<p>In summary, LUS is a powerful diagnostic tool for ventilator-associated pneumonia in pediatric and neonatal intensive care. Through the recognition of key findings and use of structured diagnostic scores, it enhances bedside clinical decision-making and reduces dependence on radiation-based imaging in this vulnerable population.</p>
</sec>
<sec id="s4"><label>4</label><title>Practical summary: the I-VENT mnemonic</title>
<p>To facilitate the structured application of lung ultrasound in the management of mechanically ventilated pediatric patients, we propose the I-VENT mnemonic, which encompasses the key domains covered in this review:
<list list-type="simple">
<list-item>
<p>I&#x2014;Indication for ventilation: LUS scores can aid in identifying the need for mechanical ventilation, particularly in neonates with ARDS or those at risk of NIV failure.</p></list-item>
<list-item>
<p>V&#x2014;Ventilation adjustment: LUS supports titration of ventilatory parameters, including detection of overdistension and atelectasis, as well as optimization of modes such as SIMV or NIV-NAVA.</p></list-item>
<list-item>
<p>E&#x2014;Effusion and edema detection: LUS enables bedside detection of pleural effusions and interstitial syndromes, guiding fluid management and differential diagnoses.</p></list-item>
<list-item>
<p>N&#x2014;Non-aerated areas: Consolidations, atelectatic regions, and regional heterogeneity can be identified, supporting decisions on positioning, recruitment, and antibiotic therapy.</p></list-item>
<list-item>
<p>T&#x2014;Thoracic sliding and tube position: Visualization of pleural sliding confirms correct tracheal intubation, rules out selective intubation, and helps exclude pneumothorax.</p></list-item>
</list>This framework may serve as a practical bedside checklist and an educational tool to reinforce the comprehensive use of LUS throughout the continuum of ventilatory support.</p>
</sec>
<sec id="s5" sec-type="discussion"><label>5</label><title>Discussion</title>
<p>This narrative review highlights the growing and multifaceted role of lung ultrasound (LUS) in the management of mechanically ventilated pediatric patients. From guiding the indication for ventilation to optimizing PEEP, assessing recruitment, predicting weaning success, and diagnosing complications such as ventilator-associated pneumonia, LUS offers a dynamic, radiation-free, bedside tool that enhances clinical decision-making.</p>
<p>The pediatric and neonatal populations, with their unique anatomical characteristics and vulnerability to radiation, particularly benefit from the incorporation of LUS into routine care. Despite the promising results, certain limitations must be acknowledged, including reduced sensitivity for consolidations not adjacent to the pleura and challenges in standardizing protocols across age groups and clinical scenarios. Moreover, the absence of universally accepted pediatric-specific diagnostic criteria for conditions such as VAP underscores the importance of combining LUS findings with clinical judgment.</p>
<p>Future research should aim to validate existing scoring systems, establish evidence-based protocols, and integrate LUS training into pediatric critical care curricula. With ongoing advancements in portable ultrasound technology and increasing clinician familiarity, LUS is poised to become a cornerstone of respiratory management in pediatric intensive care units worldwide.</p>
</sec>
</body>
<back>
<sec id="s6" sec-type="author-contributions"><title>Author contributions</title>
<p>NL: Writing &#x2013; original draft, Writing &#x2013; review &#x0026; editing, Methodology, Conceptualization. VA: Writing &#x2013; original draft, Methodology, Conceptualization. MM: Conceptualization, Writing &#x2013; original draft, Methodology. PGPM: Conceptualization, Writing &#x2013; original draft. LZB: Conceptualization, Validation, Supervision, Writing &#x2013; review &#x0026; editing. RdHP: Supervision, Conceptualization, Investigation, Writing &#x2013; review &#x0026; editing, Validation.</p>
</sec>
<sec id="s7" sec-type="funding-information"><title>Funding</title>
<p>The author(s) declare that no financial support was received for the research and/or publication of this article.</p>
</sec>
<sec id="s8" sec-type="COI-statement"><title>Conflict of interest</title>
<p>The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.</p>
</sec>
<sec id="s9" sec-type="ai-statement"><title>Generative AI statement</title>
<p>The author(s) declare that no Generative AI was 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 id="s10" sec-type="disclaimer"><title>Publisher&#x0027;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 id="s18" sec-type="supplementary-material"><title>Supplementary material</title>
<p>The Supplementary Material for this article can be found online at: <ext-link ext-link-type="uri" xlink:href="https://www.frontiersin.org/articles/10.3389/fped.2025.1630918/full#supplementary-material">https://www.frontiersin.org/articles/10.3389/fped.2025.1630918/full#supplementary-material</ext-link></p>
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