<?xml version="1.0" encoding="UTF-8"?><!DOCTYPE article PUBLIC "-//NLM//DTD Journal Publishing DTD v2.0 20040830//EN" "journalpublishing.dtd"><article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" dtd-version="2.0" xml:lang="en" article-type="review-article"><front><journal-meta><journal-id journal-id-type="nlm-ta">J Med Internet Res</journal-id><journal-id journal-id-type="publisher-id">jmir</journal-id><journal-id journal-id-type="index">1</journal-id><journal-title>Journal of Medical Internet Research</journal-title><abbrev-journal-title>J Med Internet Res</abbrev-journal-title><issn pub-type="epub">1438-8871</issn><publisher><publisher-name>JMIR Publications</publisher-name><publisher-loc>Toronto, Canada</publisher-loc></publisher></journal-meta><article-meta><article-id pub-id-type="publisher-id">v28i1e85416</article-id><article-id pub-id-type="doi">10.2196/85416</article-id><article-categories><subj-group subj-group-type="heading"><subject>Review</subject></subj-group></article-categories><title-group><article-title>Telehealth Approaches for Pediatric Otitis Media and Clinical Outcomes: Scoping Review</article-title></title-group><contrib-group><contrib contrib-type="author" corresp="yes" equal-contrib="yes"><name name-style="western"><surname>Noda</surname><given-names>Masao</given-names></name><degrees>MD, PhD, MBA</degrees><xref ref-type="aff" rid="aff1">1</xref><xref ref-type="fn" rid="equal-contrib1">*</xref></contrib><contrib contrib-type="author" equal-contrib="yes"><name name-style="western"><surname>Akiyoshi</surname><given-names>Ryohei</given-names></name><degrees>MD, PhD</degrees><xref ref-type="aff" rid="aff2">2</xref><xref ref-type="fn" rid="equal-contrib1">*</xref></contrib><contrib contrib-type="author"><name name-style="western"><surname>Hosoya</surname><given-names>Makoto</given-names></name><degrees>MD, PhD</degrees><xref ref-type="aff" rid="aff3">3</xref></contrib><contrib contrib-type="author"><name name-style="western"><surname>Shinkawa</surname><given-names>Chikako</given-names></name><degrees>MD, PhD</degrees><xref ref-type="aff" rid="aff4">4</xref></contrib><contrib contrib-type="author"><name name-style="western"><surname>Koshu</surname><given-names>Ryota</given-names></name><degrees>MD</degrees><xref ref-type="aff" rid="aff1">1</xref></contrib><contrib contrib-type="author"><name name-style="western"><surname>Yoshimura</surname><given-names>Hidekane</given-names></name><degrees>MD, PhD</degrees><xref ref-type="aff" rid="aff5">5</xref></contrib><contrib contrib-type="author"><name name-style="western"><surname>Monden</surname><given-names>Yukifumi</given-names></name><degrees>MD, PhD</degrees><xref ref-type="aff" rid="aff6">6</xref></contrib><contrib contrib-type="author"><name name-style="western"><surname>Fushiki</surname><given-names>Hiroaki</given-names></name><degrees>MD, PhD</degrees><xref ref-type="aff" rid="aff7">7</xref></contrib><contrib contrib-type="author"><name name-style="western"><surname>Tanaka</surname><given-names>Yasuhiro</given-names></name><degrees>MD, PhD</degrees><xref ref-type="aff" rid="aff2">2</xref></contrib><contrib contrib-type="author"><name name-style="western"><surname>Ito</surname><given-names>Makoto</given-names></name><degrees>MD, PhD</degrees><xref ref-type="aff" rid="aff1">1</xref></contrib></contrib-group><aff id="aff1"><institution>Department of Otolaryngology and Head and Neck Surgery, Jichi Medical University</institution><addr-line>3311-1, Yakushiji</addr-line><addr-line>Shimotsuke</addr-line><country>Japan</country></aff><aff id="aff2"><institution>Department of Otolaryngology and Head and Neck Surgery, Dokkyo Medical University Saitama Medical Center</institution><addr-line>Saitama</addr-line><country>Japan</country></aff><aff id="aff3"><institution>Department of Otolaryngology and Head and Neck Surgery, Keio University</institution><addr-line>Tokyo</addr-line><country>Japan</country></aff><aff id="aff4"><institution>Department of Otolaryngology and Head and Neck Surgery, Yamagata University</institution><addr-line>Yamagata</addr-line><country>Japan</country></aff><aff id="aff5"><institution>Department of Otolaryngology &#x2013; Head and Neck Surgery, Shinshu University School of Medicine</institution><addr-line>Matsumoto</addr-line><country>Japan</country></aff><aff id="aff6"><institution>Department of Pediatrics, Jichi Medical University Hospital</institution><addr-line>Shimotsuke</addr-line><country>Japan</country></aff><aff id="aff7"><institution>Department of Otolaryngology, Mejiro University Ear Institute Clinic</institution><addr-line>Saitama</addr-line><country>Japan</country></aff><contrib-group><contrib contrib-type="editor"><name name-style="western"><surname>Brini</surname><given-names>Stefano</given-names></name></contrib></contrib-group><contrib-group><contrib contrib-type="reviewer"><name name-style="western"><surname>Singh</surname><given-names>Deepak</given-names></name></contrib><contrib contrib-type="reviewer"><name name-style="western"><surname>Mansoor</surname><given-names>Masab</given-names></name></contrib></contrib-group><author-notes><corresp>Correspondence to Masao Noda, MD, PhD, MBA, Department of Otolaryngology and Head and Neck Surgery, Jichi Medical University, 3311-1, Yakushiji, Shimotsuke, 3290498, Japan, 81 0285442111; <email>doforanabdosuc@gmail.com</email></corresp><fn fn-type="equal" id="equal-contrib1"><label>*</label><p>these authors contributed equally</p></fn></author-notes><pub-date pub-type="collection"><year>2026</year></pub-date><pub-date pub-type="epub"><day>18</day><month>3</month><year>2026</year></pub-date><volume>28</volume><elocation-id>e85416</elocation-id><history><date date-type="received"><day>07</day><month>10</month><year>2025</year></date><date date-type="rev-recd"><day>14</day><month>02</month><year>2026</year></date><date date-type="accepted"><day>23</day><month>02</month><year>2026</year></date></history><copyright-statement>&#x00A9; Masao Noda, Ryohei Akiyoshi, Makoto Hosoya, Chikako Shinkawa, Ryota Koshu, Hidekane Yoshimura, Yukifumi Monden, Hiroaki Fushiki, Yasuhiro Tanaka, Makoto Ito. Originally published in the Journal of Medical Internet Research (<ext-link ext-link-type="uri" xlink:href="https://www.jmir.org">https://www.jmir.org</ext-link>), 18.3.2026. </copyright-statement><copyright-year>2026</copyright-year><license license-type="open-access" xlink:href="https://creativecommons.org/licenses/by/4.0/"><p>This is an open-access article distributed under the terms of the Creative Commons Attribution 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>), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work, first published in the Journal of Medical Internet Research (ISSN 1438-8871), is properly cited. The complete bibliographic information, a link to the original publication on <ext-link ext-link-type="uri" xlink:href="https://www.jmir.org/">https://www.jmir.org/</ext-link>, as well as this copyright and license information must be included.</p></license><self-uri xlink:type="simple" xlink:href="https://www.jmir.org/2026/1/e85416"/><abstract><sec><title>Background</title><p>Otitis media (OM) is a common pediatric infection worldwide. Conventionally, accurate diagnosis depends on in-person pneumatic otoscopy, which is not always accessible, contributing to delayed care and inappropriate prescribing, especially in underserved settings. Rapid advances in telemedicine and digital tools have accelerated the development of remote approaches for assessing pediatric ear diseases, while diagnostic quality maintenance, care models, and real-world outcomes have not been comprehensively mapped in children.</p></sec><sec><title>Objective</title><p>This study aimed to map existing telehealth technologies and operational models used for pediatric OM and report their diagnostic and implementation outcomes to guide practice and further research.</p></sec><sec sec-type="methods"><title>Methods</title><p>PRISMA-ScR (Preferred Reporting Items for Systematic Reviews and Meta-Analyses extension for Scoping Reviews) guided this scoping review (protocol not registered). MEDLINE (via PubMed), Scopus, Web of Science, and the Cochrane Central Register of Controlled Trials were searched for original English-language studies (published between January 1, 2010, and February 9, 2026) reporting the clinical implementation of telemedicine or digital health in children (&#x003C;18 years) with suspected or confirmed OM. We excluded reviews, editorials, and protocols; conference abstracts; adult-only studies; and purely technical evaluations. Two reviewers independently extracted and charted the study characteristics: telemedicine model, technology, users, comparators, outcomes, and limitations. Findings were synthesized using practice-oriented mapping that aligned technologies with care models and implementation conditions.</p></sec><sec sec-type="results"><title>Results</title><p>Fifty-two studies across 18 countries and various settings met the inclusion criteria. Sample sizes ranged from 6 to 3950, with heterogeneous reporting units (children, ears, episodes, or screening assessments). Asynchronous store-and-forward tele-otoscopy was the most common approach. The rest used synchronous or hybrid models. Image capture by trained personnel and review by experienced clinicians yielded substantial diagnostic consistency with in-person microscopy (&#x03BA; 0.68&#x2010;0.89, sensitivity 72%&#x2010;94%, specificity 93%&#x2010;98%, where available). However, the diagnostic yield was highly dependent on the training level: structured instruction improved video capture by parents and nonspecialists, whereas brief or written-only guidance resulted in low rates of diagnostically useful videos. Telemedicine approaches improved access, supported perioperative follow-up, and, in some contexts, reduced reexaminations and promoted more judicious antibiotic use. Televisits without otoscopy were associated with lower confirmation rates of middle ear effusion during tympanostomy tube placement. Evidence was heterogeneous, with predominantly small single-site studies, variable reference standards and operator training, and rapidly evolving device ecosystems.</p></sec><sec sec-type="conclusions"><title>Conclusions</title><p>This review provides a practice-oriented map of telehealth approaches for pediatric OM. Tele-otoscopy and adjunct digital tools are feasible, achieving diagnostic accuracy comparable to in-person assessments while enhancing access and service efficiency. However, important evidence gaps remain, including the need for large multisite trials, evaluation of long-term child outcomes, economic evaluations, and robust external validation of artificial intelligence&#x2013;based diagnostic tools. Standardization of image capture protocols and integration into hybrid care models should be prioritized for scaling up.</p></sec></abstract><kwd-group><kwd>pediatrics</kwd><kwd>acute otitis media</kwd><kwd>otitis media with effusion</kwd><kwd>telemedicine</kwd><kwd>telehealth</kwd><kwd>smartphone otoscopy</kwd><kwd>digital otoscopy</kwd><kwd>artificial intelligence</kwd><kwd>tympanostomy</kwd></kwd-group></article-meta></front><body><sec id="s1" sec-type="intro"><title>Introduction</title><p>Telemedicine has expanded rapidly across pediatrics over the past decade, further accelerated by the COVID-19 pandemic. Telehealth performance is disease specific, determined by whether robust remote proxies for the examination exist and are embedded in workflows [<xref ref-type="bibr" rid="ref1">1</xref>,<xref ref-type="bibr" rid="ref2">2</xref>]. In practice, the feasibility and safety of remote pediatric care depend on whether key physical findings can be reliably captured and shared. Equity concerns related to devices, connectivity, and digital literacy also underscore the need to track and address the digital divide [<xref ref-type="bibr" rid="ref3">3</xref>]. For ear disease, this principally entails dependable tympanic membrane visualization and measures of middle ear status [<xref ref-type="bibr" rid="ref4">4</xref>,<xref ref-type="bibr" rid="ref5">5</xref>].</p><p>Within this context, otitis media (OM) is among the most common pediatric infections worldwide and a leading cause of health care visits, antibiotic prescriptions, and tympanostomy tube placement [<xref ref-type="bibr" rid="ref6">6</xref>,<xref ref-type="bibr" rid="ref7">7</xref>]. In 2021, the estimated global incident cases of OM in children were 297 million, highlighting the substantial population burden [<xref ref-type="bibr" rid="ref6">6</xref>]. OM also contributes substantially to pediatric antibiotic exposure; a previous study reports that in a large outpatient cohort, antibiotics were prescribed in 44.8% of OM encounters [<xref ref-type="bibr" rid="ref8">8</xref>]. Recent evidence from large outpatient datasets suggests that antibiotic prescribing patterns can differ between telemedicine and in-person visits for acute respiratory infections, raising concerns that diagnostic uncertainty&#x2014;particularly when objective otoscopic findings are unavailable&#x2014;may influence management [<xref ref-type="bibr" rid="ref9">9</xref>]. Acute OM (AOM) and OM with effusion (OME) impose substantial morbidity, reduced quality of life, and increased health care costs across diverse settings [<xref ref-type="bibr" rid="ref7">7</xref>,<xref ref-type="bibr" rid="ref10">10</xref>], with a global review reporting annual costs as high as US $5 billion in the United States [<xref ref-type="bibr" rid="ref10">10</xref>]. Accurate diagnosis hinges on direct visualization of the tympanic membrane and assessment of middle ear status&#x2014;ideally by pneumatic otoscopy&#x2014;which requires specific training and equipment [<xref ref-type="bibr" rid="ref7">7</xref>,<xref ref-type="bibr" rid="ref11">11</xref>]. Limited access to clinicians trained in pediatric otoscopy, particularly in rural and underserved regions, can contribute to delayed assessment and potentially inappropriate treatment [<xref ref-type="bibr" rid="ref7">7</xref>].</p><p>Concurrently, digital health technologies relevant to ear disease have proliferated [<xref ref-type="bibr" rid="ref12">12</xref>-<xref ref-type="bibr" rid="ref14">14</xref>], including smartphone-connected and USB video-otoscopes, non-smartphone digital otoscopes, remote monitoring platforms, and early artificial intelligence&#x2013;assisted decision support [<xref ref-type="bibr" rid="ref15">15</xref>,<xref ref-type="bibr" rid="ref16">16</xref>]. Beyond clinician-facilitated workflows, newer models increasingly rely on caregiver- or patient-captured otoscopic media for asynchronous review; however, interpretability can vary markedly depending on who captures the recordings, indicating that real-world deployment requires systems that standardize capture quality through clear thresholds, training, and feedback loops [<xref ref-type="bibr" rid="ref17">17</xref>]. When paired with appropriate workflows, these tools enable asynchronous review by experts or real-time supervision and can be complemented by adjunct tests such as tympanometry or acoustic methods [<xref ref-type="bibr" rid="ref18">18</xref>-<xref ref-type="bibr" rid="ref23">23</xref>]. Emerging studies suggest that telemedicine can approximate in-person diagnostic performance for pediatric OM when image capture is standardized and operators are trained while also reducing barriers to care and supporting antibiotic stewardship [<xref ref-type="bibr" rid="ref20">20</xref>,<xref ref-type="bibr" rid="ref21">21</xref>,<xref ref-type="bibr" rid="ref24">24</xref>]. However, important uncertainties remain regarding feasibility, usability, and sustainable integration into clinical practice.</p><p>Given the rapidly expanding yet fragmented evidence base, we conducted a scoping review to (1) map the technologies and care models used in telehealth for pediatric OM, (2) summarize diagnostic and implementation outcomes, and (3) identify evidence gaps to guide future research and clinical implementation. This review further aims to identify the key barriers and enablers of feasibility and to provide actionable guidance for implementing pediatric OM telehealth&#x2014;across technologies, care models, and settings.</p></sec><sec id="s2" sec-type="methods"><title>Methods</title><sec id="s2-1"><title>Overall Study Design</title><p>A scoping review was performed according to the PRISMA-ScR (Preferred Reporting Items for Systematic Reviews and Meta-Analyses extension for Scoping Reviews) checklist [<xref ref-type="bibr" rid="ref25">25</xref>]. The review process progressed through the stages outlined in the framework of Arksey and O&#x2019;Malley [<xref ref-type="bibr" rid="ref26">26</xref>], which included formulating the research question; identifying relevant studies; selecting studies; extracting and organizing the data; and synthesizing, summarizing, and presenting the findings. The protocol for this scoping review was neither registered nor published. Core decisions were defined a priori (research questions, eligibility criteria, databases, and data items). Minor refinements to the screening guidance, including operational definitions of clinical implementation and tele-otoscopy, were made iteratively during pilot screening to improve consistency and were applied uniformly thereafter. In addition, reporting of the literature search was guided by the PRISMA-S statement (an extension to the PRISMA Statement for Reporting Literature Searches in Systematic Reviews) to enhance transparency and reproducibility of the search methods [<xref ref-type="bibr" rid="ref27">27</xref>].</p></sec><sec id="s2-2"><title>Information Sources and Search Strategy</title><p>MEDLINE (via PubMed), Scopus, Web of Science Core Collection, and the Cochrane Central Register of Controlled Trials (CENTRAL) were searched for studies published between January 1, 2010, to February 9, 2026 (publication cutoff date), using a predefined strategy developed by 3 authors (MN, RA, and MH). Searches were last run on February 9, 2026, as the final rerun during the revision process; no publication date restrictions were applied beyond the search date, and no automated alerts were used. Each database was searched separately on its native platform rather than via a single multidatabase interface.</p><p>The strategy combined controlled vocabulary and free-text terms for three concepts: (1) otitis media, (2) pediatrics, and (3) telehealth or digital health. The start date (January 2010) was selected because smartphone-enabled imaging and telehealth implementations relevant to pediatric otoscopy began to emerge and diffuse in clinical practice around that period. Full strategies for each database are provided exactly as run in <xref ref-type="supplementary-material" rid="app1">Multimedia Appendix 1</xref>. The strategy was developed de novo and was not adapted from prior reviews, and no published search filters were used.</p><p>In addition, forward citation searching was performed in Web of Science (using &#x201C;Times Cited&#x201D; and &#x201C;Cited Reference Search&#x201D;) for key included articles, and reference lists of included studies were manually screened. Study registries were not searched, and study authors, experts, or manufacturers were not contacted for additional or missing information. The search strategy was not formally peer-reviewed using a dedicated tool but was iteratively reviewed within the author team. Duplicates were removed by automated matching of title, author, and publication year, followed by manual verification.</p></sec><sec id="s2-3"><title>Eligibility Criteria</title><p>We defined the eligibility criteria using the population, concept, and context (PCC) framework developed by the Joanna Briggs Institute (JBI):</p><list list-type="bullet"><list-item><p>Population: children and adolescents aged &#x003C;18 years with suspected or confirmed OM (AOM/OME/recurrent acute OM [RAOM]), including mixed-age studies if pediatric data were separable</p></list-item><list-item><p>Concept: telehealth or digital health approaches for middle ear evaluation and/or OM management, including tele-otoscopy (image/video capture with remote review), tele-otoscopy plus adjunct testing (tympanometry, acoustic methods), and other clinically implemented digital tools relevant to OM assessment or follow-up</p></list-item><list-item><p>Context: any clinical or community setting (primary care, ED, specialty clinics, schools, outreach programs, home)</p></list-item><list-item><p>Types of sources: original research reporting clinical implementation outcomes (diagnostic, clinical, implementation, or economic outcomes)</p></list-item></list><p>We excluded conference abstracts, protocols, reviews or editorials, adult-only studies, and purely technical evaluations without clinical implementation.</p></sec><sec id="s2-4"><title>Data Items and Operational Definitions</title><p>We used &#x201C;tele-otoscopy&#x201D; to describe capture of otoscopic media (images/videos) for remote interpretation (store and forward or real time). We distinguished this from &#x201C;video visits without otoscopy,&#x201D; in which no ear imaging was obtained. &#x201C;Adjunct digital diagnostics&#x201D; referred to nonimaging tools to assess middle ear status (eg, tympanometry and smartphone acoustics).</p></sec><sec id="s2-5"><title>Study Inclusion Criteria and Exclusion Criteria</title><p>Studies were considered eligible if they were published in English between January 1, 2010, and February 9, 2026, and focused on telemedicine, telehealth, or other digital health interventions for pediatric OM. Eligible designs included qualitative, quantitative, or mixed-method approaches, provided that they reported outcomes of implementation in clinical practice. Studies that enrolled children and adolescents aged &#x003C;18 years with suspected or confirmed OM&#x2014;in which patients were assessed, monitored, or treated using telemedicine-supported interventions&#x2014;were included.</p><p>Conference abstracts, reviews, editorials, and study protocols were excluded. Studies were also excluded if they focused exclusively on adult populations or conditions other than OM or those that did not involve the clinical application of telemedicine. Purely technical studies&#x2014;including device prototype development and retrospective artificial intelligence model performance evaluations without prospective or clinical validation&#x2014;and conference-only publications were excluded. Studies centered solely on audiology or hearing assessment without otoscopic or middle ear evaluation were also excluded.</p></sec><sec id="s2-6"><title>Selection of Sources of Evidence</title><p>Titles and abstracts were independently screened by 2 reviewers (MN and RA). Full-text articles were retrieved for studies deemed potentially eligible and assessed against the predefined inclusion and exclusion criteria. Studies were excluded at the full-text stage for reasons including lack of clinical implementation, exclusive focus on retrospective algorithm performance, conference-only publications, absence of pediatric populations, or absence of OM-specific outcomes. Any disagreements were resolved through discussion and consensus. As part of the revision process, the rerun search results were screened using the same procedures and criteria as the original search.</p></sec><sec id="s2-7"><title>Data Charting Process and Items</title><p>Data extraction was independently performed by 2 reviewers (MN and RA) using a standardized charting form. Extracted items included bibliographic details (author and year) and study design; country and setting (clinic, community, school, or home; level of care); population characteristics (age range, sample size, and OM phenotype when specified); care model (asynchronous, synchronous, or hybrid) and workflow description; operator roles (who captured and who interpreted) and training protocols (duration and content and any quality thresholds); technology and device or system characteristics (type, smartphone requirement, platform, and manufacturer when available); comparator and reference standard (otomicroscopy, pneumatic otoscopy, or surgical findings); outcomes (diagnostic performance, clinical outcomes, implementation outcomes, economic outcomes, and equity-relevant outcomes when reported); and study limitations, potential biases, and funding or conflict of interest statements when reported. Any discrepancies between reviewers were resolved through discussion and consensus. Some included studies reported diagnostic accuracy outcomes; thus, we conducted a targeted assessment for the subset of diagnostic accuracy studies using the revised Quality Assessment of Diagnostic Accuracy Studies (QUADAS-2) tool. Two reviewers independently assessed the risk of bias and applicability, with disagreements being resolved by consensus; detailed judgments are provided in <xref ref-type="supplementary-material" rid="app2">Multimedia Appendix 2</xref>.</p></sec><sec id="s2-8"><title>Synthesis of Results</title><p>We summarized the extracted data descriptively (counts/percentages) and synthesized the findings narratively. We created evidence maps (technology category &#x00D7; care model; operator capture vs interpretation) and an outcome-domain frequency figure to visualize evidence distribution and gaps. To apply an implementation science lens, we mapped the reported implementation outcomes and determinants across included studies to the reach, effectiveness, adoption, implementation, and maintenance (RE-AIM) framework. A summary of the RE-AIM framework analysis of each study included in this review is provided in <xref ref-type="supplementary-material" rid="app3">Multimedia Appendix 3</xref>.</p></sec></sec><sec id="s3" sec-type="results"><title>Results</title><sec id="s3-1"><title>Selection of Sources of Evidence</title><p>The database search retrieved 8356 articles from MEDLINE via PubMed (n=1687), Scopus (n=4810), Web of Science Core Collection (n=1775), and CENTRAL (n=84). In addition, 1911 records were identified through forward citation searching in Web of Science (and backward reference checking). Following the removal of duplicates, 5537 articles remained for the screening of titles and abstracts; of these, 5402 irrelevant articles were excluded, and 135 articles remained. The full texts of 135 articles were subsequently evaluated for eligibility; of these, 83 articles were excluded for the following reasons: nonpediatric population (n=9), absence of telemedicine interventions (n=17), review or commentary articles (n=13), unrelated to OM (n=13), not implemented in clinical practice (n=23), not in English (n=1), and unavailability of full text (n=7). Ultimately, 52 studies were included in this scoping review (<xref ref-type="fig" rid="figure1">Figure 1</xref>, PRISMA flow diagram).</p><fig position="float" id="figure1"><label>Figure 1.</label><caption><p>Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) flow diagram.</p></caption><graphic alt-version="no" mimetype="image" position="float" xlink:type="simple" xlink:href="jmir_v28i1e85416_fig01.png"/></fig></sec><sec id="s3-2"><title>Characteristics of Sources of Evidence</title><p>The 52 included studies were published between 2012 and 2026, representing a geographically diverse evidence base encompassing high-, low-, and middle-income settings (summarized in <xref ref-type="supplementary-material" rid="app2">Multimedia Appendix 2</xref>) [<xref ref-type="bibr" rid="ref12">12</xref>-<xref ref-type="bibr" rid="ref16">16</xref>,<xref ref-type="bibr" rid="ref22">22</xref>-<xref ref-type="bibr" rid="ref24">24</xref>,<xref ref-type="bibr" rid="ref28">28</xref>-<xref ref-type="bibr" rid="ref71">71</xref>]. QUADAS-2 judgements for diagnostic accuracy studies are summarized in <xref ref-type="supplementary-material" rid="app4">Multimedia Appendix 4</xref>. The largest number of included studies (n=15) were conducted in the United States [<xref ref-type="bibr" rid="ref39">39</xref>,<xref ref-type="bibr" rid="ref41">41</xref>,<xref ref-type="bibr" rid="ref42">42</xref>,<xref ref-type="bibr" rid="ref44">44</xref>,<xref ref-type="bibr" rid="ref49">49</xref>,<xref ref-type="bibr" rid="ref52">52</xref>-<xref ref-type="bibr" rid="ref55">55</xref>,<xref ref-type="bibr" rid="ref58">58</xref>-<xref ref-type="bibr" rid="ref60">60</xref>,<xref ref-type="bibr" rid="ref66">66</xref>,<xref ref-type="bibr" rid="ref67">67</xref>,<xref ref-type="bibr" rid="ref71">71</xref>], followed by Australia (n=10) [<xref ref-type="bibr" rid="ref14">14</xref>,<xref ref-type="bibr" rid="ref22">22</xref>,<xref ref-type="bibr" rid="ref23">23</xref>,<xref ref-type="bibr" rid="ref28">28</xref>,<xref ref-type="bibr" rid="ref31">31</xref>,<xref ref-type="bibr" rid="ref32">32</xref>,<xref ref-type="bibr" rid="ref61">61</xref>,<xref ref-type="bibr" rid="ref64">64</xref>,<xref ref-type="bibr" rid="ref65">65</xref>,<xref ref-type="bibr" rid="ref70">70</xref>], the United Kingdom (n=5) [<xref ref-type="bibr" rid="ref45">45</xref>,<xref ref-type="bibr" rid="ref50">50</xref>,<xref ref-type="bibr" rid="ref51">51</xref>,<xref ref-type="bibr" rid="ref62">62</xref>,<xref ref-type="bibr" rid="ref68">68</xref>], India (n=4) [<xref ref-type="bibr" rid="ref35">35</xref>,<xref ref-type="bibr" rid="ref40">40</xref>,<xref ref-type="bibr" rid="ref46">46</xref>,<xref ref-type="bibr" rid="ref57">57</xref>], and China (n=2) [<xref ref-type="bibr" rid="ref16">16</xref>,<xref ref-type="bibr" rid="ref56">56</xref>], with additional studies from other countries, including developing countries (<xref ref-type="table" rid="table1">Table 1</xref>).</p><table-wrap id="t1" position="float"><label>Table 1.</label><caption><p>Geographic distribution of included pediatric otitis media telemedicine studies by country (N=52).</p></caption><table id="table1" frame="hsides" rules="groups"><thead><tr><td align="left" valign="bottom">Country</td><td align="left" valign="bottom">Included studies, n (%)<sup><xref ref-type="table-fn" rid="table1fn1">a</xref></sup></td><td align="left" valign="bottom">Author (year)</td></tr></thead><tbody><tr><td align="left" valign="top">United States</td><td align="char" char="." valign="top">15 (28.8%)</td><td align="left" valign="top">Rappaport et al (2016) [<xref ref-type="bibr" rid="ref66">66</xref>], Richards et al (2015) [<xref ref-type="bibr" rid="ref71">71</xref>], Shah et al (2018) [<xref ref-type="bibr" rid="ref39">39</xref>], Chan et al (2019) [<xref ref-type="bibr" rid="ref41">41</xref>], Chan et al (2019) [<xref ref-type="bibr" rid="ref42">42</xref>], Hakimi et al (2019) [<xref ref-type="bibr" rid="ref44">44</xref>], Jayawardena et al (2020) [<xref ref-type="bibr" rid="ref49">49</xref>], Kolb et al (2021) [<xref ref-type="bibr" rid="ref52">52</xref>], Kleinman et al (2021) [<xref ref-type="bibr" rid="ref53">53</xref>], Don et al (2021) [<xref ref-type="bibr" rid="ref54">54</xref>], Ni et al (2021) [<xref ref-type="bibr" rid="ref67">67</xref>], Manayan et al (2022) [<xref ref-type="bibr" rid="ref55">55</xref>], Schafer et al (2022) [<xref ref-type="bibr" rid="ref58">58</xref>], Smola et al (2022) [<xref ref-type="bibr" rid="ref59">59</xref>], Chan et al (2022) [<xref ref-type="bibr" rid="ref60">60</xref>]</td></tr><tr><td align="left" valign="top">Australia</td><td align="char" char="." valign="top">10 (19.2%)</td><td align="left" valign="top">Smith et al (2012) [<xref ref-type="bibr" rid="ref28">28</xref>], Phillips et al (2014) [<xref ref-type="bibr" rid="ref70">70</xref>], Smith et al (2015) [<xref ref-type="bibr" rid="ref31">31</xref>], Jacups et al (2017) [<xref ref-type="bibr" rid="ref32">32</xref>], Habib et al (2023) [<xref ref-type="bibr" rid="ref61">61</xref>], Alenezi et al (2024) [<xref ref-type="bibr" rid="ref14">14</xref>], Quick et al (2024) [<xref ref-type="bibr" rid="ref22">22</xref>], Habib et al (2024) [<xref ref-type="bibr" rid="ref23">23</xref>], Bowers et al (2025) [<xref ref-type="bibr" rid="ref64">64</xref>], Altamimi et al (2025) [<xref ref-type="bibr" rid="ref65">65</xref>]</td></tr><tr><td align="left" valign="top">United Kingdom</td><td align="char" char="." valign="top">5 (9.6%)</td><td align="left" valign="top">Fordington and Holland Brown (2020) [<xref ref-type="bibr" rid="ref45">45</xref>], Cottrell et al (2020) [<xref ref-type="bibr" rid="ref50">50</xref>], Schuster-Bruce et al (2021) [<xref ref-type="bibr" rid="ref51">51</xref>], Patel et al (2024) [<xref ref-type="bibr" rid="ref62">62</xref>], Stancel-Lewis et al (2025) [<xref ref-type="bibr" rid="ref68">68</xref>]</td></tr><tr><td align="left" valign="top">India</td><td align="char" char="." valign="top">4 (7.7%)</td><td align="left" valign="top">Ramkumar et al (2018) [<xref ref-type="bibr" rid="ref35">35</xref>], Bhavana et al (2018) [<xref ref-type="bibr" rid="ref40">40</xref>], Gupta et al (2020) [<xref ref-type="bibr" rid="ref46">46</xref>], Deshmukh et al (2022) [<xref ref-type="bibr" rid="ref57">57</xref>]</td></tr><tr><td align="left" valign="top">China</td><td align="char" char="." valign="top">2 (3.8%)</td><td align="left" valign="top">Meng et al (2022) [<xref ref-type="bibr" rid="ref56">56</xref>], Jin and Fan (2024) [<xref ref-type="bibr" rid="ref16">16</xref>]</td></tr><tr><td align="left" valign="top">France</td><td align="char" char="." valign="top">2 (3.8%)</td><td align="left" valign="top">Venail et al (2018) [<xref ref-type="bibr" rid="ref38">38</xref>], Dubois et al (2024) [<xref ref-type="bibr" rid="ref15">15</xref>]</td></tr><tr><td align="left" valign="top">Nepal</td><td align="char" char="." valign="top">2 (3.8%)</td><td align="left" valign="top">Mandavia et al (2018) [<xref ref-type="bibr" rid="ref36">36</xref>], Gyawali et al (2024) [<xref ref-type="bibr" rid="ref63">63</xref>]</td></tr><tr><td align="left" valign="top">South Africa</td><td align="char" char="." valign="top">2 (3.8%)</td><td align="left" valign="top">Biagio et al (2014) [<xref ref-type="bibr" rid="ref29">29</xref>], Lundberg et al (2017) [<xref ref-type="bibr" rid="ref34">34</xref>]</td></tr><tr><td align="left" valign="top">Netherlands</td><td align="char" char="." valign="top">1 (1.9%)</td><td align="left" valign="top">Prins-van Ginkel et al (2017) [<xref ref-type="bibr" rid="ref33">33</xref>]</td></tr><tr><td align="left" valign="top">Brazil</td><td align="char" char="." valign="top">1 (1.9%)</td><td align="left" valign="top">Wagner et al (2023) [<xref ref-type="bibr" rid="ref13">13</xref>]</td></tr><tr><td align="left" valign="top">Canada</td><td align="char" char="." valign="top">1 (1.9%)</td><td align="left" valign="top">Mousseau et al (2018) [<xref ref-type="bibr" rid="ref37">37</xref>]</td></tr><tr><td align="left" valign="top">Finland</td><td align="char" char="." valign="top">1 (1.9%)</td><td align="left" valign="top">Erkkola-Anttinen et al (2019) [<xref ref-type="bibr" rid="ref12">12</xref>]</td></tr><tr><td align="left" valign="top">Greenland</td><td align="char" char="." valign="top">1 (1.9%)</td><td align="left" valign="top">Demant et al (2019) [<xref ref-type="bibr" rid="ref43">43</xref>]</td></tr><tr><td align="left" valign="top">Hungary</td><td align="char" char="." valign="top">1 (1.9%)</td><td align="left" valign="top">Pannonhalmi et al (2025) [<xref ref-type="bibr" rid="ref24">24</xref>]</td></tr><tr><td align="left" valign="top">Taiwan</td><td align="char" char="." valign="top">1 (1.9%)</td><td align="left" valign="top">Wu et al (2014) [<xref ref-type="bibr" rid="ref30">30</xref>]</td></tr><tr><td align="left" valign="top">Turkey</td><td align="char" char="." valign="top">1 (1.9%)</td><td align="left" valign="top">Durgut et al (2020) [<xref ref-type="bibr" rid="ref48">48</xref>]</td></tr><tr><td align="left" valign="top">Republic of Korea</td><td align="char" char="." valign="top">1 (1.9%)</td><td align="left" valign="top">Cha et al (2020) [<xref ref-type="bibr" rid="ref47">47</xref>]</td></tr><tr><td align="left" valign="top">Kenya</td><td align="char" char="." valign="top">1 (1.9%)</td><td align="left" valign="top">Yancey et al (2019) [<xref ref-type="bibr" rid="ref69">69</xref>]</td></tr></tbody></table><table-wrap-foot><fn id="table1fn1"><p><sup>a</sup>Percentages may not sum to 100% due to rounding.</p></fn></table-wrap-foot></table-wrap><p>Designs encompassed diagnostic accuracy comparisons, pragmatic service evaluations, prospective and retrospective cohorts, case series, and education and simulation trials; most studies either enrolled children exclusively or included defined pediatric subsets. Across studies, sample sizes ranged from small pilot cohorts to large-scale community and school-based screening programs.</p></sec><sec id="s3-3"><title>Results of Individual Sources of Evidence</title><sec id="s3-3-1"><title>Telemedicine Models, Users, and Settings</title><p>Across the included studies, asynchronous store-and-forward approach was the most commonly used approach, accounting for 35 studies (67.3%; <xref ref-type="table" rid="table2">Table 2</xref>).</p><table-wrap id="t2" position="float"><label>Table 2.</label><caption><p>Telemedicine care model classification across included studies on pediatric otitis media (N=52).</p></caption><table id="table2" frame="hsides" rules="groups"><thead><tr><td align="left" valign="bottom">Telemedicine model</td><td align="left" valign="bottom">Included studies, n (%)<sup><xref ref-type="table-fn" rid="table2fn1">a</xref></sup></td><td align="left" valign="bottom">Author (year)</td></tr></thead><tbody><tr><td align="left" valign="top">Asynchronous<sup><xref ref-type="table-fn" rid="table2fn2">b</xref></sup></td><td align="char" char="." valign="top">35 (67.3%)</td><td align="left" valign="top">Smith et al (2012) [<xref ref-type="bibr" rid="ref28">28</xref>], Biagio et al (2014) [<xref ref-type="bibr" rid="ref29">29</xref>], Phillips et al (2014) [<xref ref-type="bibr" rid="ref70">70</xref>], Smith et al (2015) [<xref ref-type="bibr" rid="ref31">31</xref>], Rappaport et al (2016) [<xref ref-type="bibr" rid="ref66">66</xref>], Prins-van Ginkel et al (2017) [<xref ref-type="bibr" rid="ref33">33</xref>], Lundberg et al (2017) [<xref ref-type="bibr" rid="ref34">34</xref>], Mandavia et al (2018) [<xref ref-type="bibr" rid="ref36">36</xref>], Shah et al (2018) [<xref ref-type="bibr" rid="ref39">39</xref>], Bhavana et al (2018) [<xref ref-type="bibr" rid="ref40">40</xref>], Chan et al (2019) [<xref ref-type="bibr" rid="ref42">42</xref>], Demant et al (2019) [<xref ref-type="bibr" rid="ref43">43</xref>], Erkkola-Anttinen et al (2019) [<xref ref-type="bibr" rid="ref12">12</xref>], Yancey et al (2019) [<xref ref-type="bibr" rid="ref69">69</xref>], Fordington and Holland Brown (2020) [<xref ref-type="bibr" rid="ref45">45</xref>], Gupta et al (2020) [<xref ref-type="bibr" rid="ref46">46</xref>], Cha et al (2020) [<xref ref-type="bibr" rid="ref47">47</xref>], Durgut et al (2020) [<xref ref-type="bibr" rid="ref48">48</xref>], Cottrell et al (2020) [<xref ref-type="bibr" rid="ref50">50</xref>], Don et al (2021) [<xref ref-type="bibr" rid="ref54">54</xref>], Ni et al (2021) [<xref ref-type="bibr" rid="ref67">67</xref>], Manayan et al (2022) [<xref ref-type="bibr" rid="ref55">55</xref>], Meng et al (2022) [<xref ref-type="bibr" rid="ref56">56</xref>], Deshmukh et al (2022) [<xref ref-type="bibr" rid="ref57">57</xref>], Smola et al (2022) [<xref ref-type="bibr" rid="ref59">59</xref>], Chan et al (2022) [<xref ref-type="bibr" rid="ref60">60</xref>], Habib et al (2023) [<xref ref-type="bibr" rid="ref61">61</xref>], Alenezi et al (2024) [<xref ref-type="bibr" rid="ref14">14</xref>], Patel et al (2024) [<xref ref-type="bibr" rid="ref62">62</xref>], Dubois et al (2024) [<xref ref-type="bibr" rid="ref15">15</xref>], Jin and Fan (2024) [<xref ref-type="bibr" rid="ref16">16</xref>], Habib et al (2024) [<xref ref-type="bibr" rid="ref23">23</xref>], Gyawali et al (2024) [<xref ref-type="bibr" rid="ref63">63</xref>], Altamimi et al (2025) [<xref ref-type="bibr" rid="ref65">65</xref>], Pannonhalmi et al (2025) [<xref ref-type="bibr" rid="ref24">24</xref>]</td></tr><tr><td align="left" valign="top">Hybrid<sup><xref ref-type="table-fn" rid="table2fn3">c</xref></sup></td><td align="char" char="." valign="top">6 (11.5%)</td><td align="left" valign="top">Ramkumar et al (2018) [<xref ref-type="bibr" rid="ref35">35</xref>], Jayawardena et al (2020) [<xref ref-type="bibr" rid="ref49">49</xref>], Wagner et al (2023) [<xref ref-type="bibr" rid="ref13">13</xref>],Quick et al (2024) [<xref ref-type="bibr" rid="ref22">22</xref>], Bowers et al (2025) [<xref ref-type="bibr" rid="ref64">64</xref>], Stancel-Lewis et al (2025) [<xref ref-type="bibr" rid="ref68">68</xref>]</td></tr><tr><td align="left" valign="top">Synchronous<sup><xref ref-type="table-fn" rid="table2fn4">d</xref></sup></td><td align="char" char="." valign="top">11 (21.2%)</td><td align="left" valign="top">Wu et al (2014) [<xref ref-type="bibr" rid="ref30">30</xref>], Richards et al (2015) [<xref ref-type="bibr" rid="ref71">71</xref>], Jacups et al (2017) [<xref ref-type="bibr" rid="ref32">32</xref>], Mousseau, et al (2018) [<xref ref-type="bibr" rid="ref37">37</xref>], Venail et al (2018) [<xref ref-type="bibr" rid="ref38">38</xref>], Chan et al (2019) [<xref ref-type="bibr" rid="ref41">41</xref>], Hakimi et al (2019) [<xref ref-type="bibr" rid="ref44">44</xref>], Schuster-Bruce et al (2021) [<xref ref-type="bibr" rid="ref51">51</xref>], Kolb et al (2021) [<xref ref-type="bibr" rid="ref52">52</xref>], Kleinman et al (2021) [<xref ref-type="bibr" rid="ref53">53</xref>], Schafer et al (2022) [<xref ref-type="bibr" rid="ref58">58</xref>]</td></tr></tbody></table><table-wrap-foot><fn id="table2fn1"><p><sup>a</sup>Percentages may not total 100% because of rounding.</p></fn><fn id="table2fn2"><p><sup>b</sup>Asynchronous: capture of images or videos or data with later remote interpretation.</p></fn><fn id="table2fn3"><p><sup>c</sup>Hybrid: combination of stored media and real-time guidance or interconsultation within the care process.</p></fn><fn id="table2fn4"><p><sup>d</sup>Synchronous: real-time assessment or interaction (typically video visit or live otoscopy visualization).</p></fn></table-wrap-foot></table-wrap><p>In this approach, images or videos were captured by nonphysicians or caregivers and interpreted remotely by otolaryngologists. This includes laptop-tethered video-otoscopy in primary care [<xref ref-type="bibr" rid="ref29">29</xref>], smartphone otoscopy with consultant review in rural clinics [<xref ref-type="bibr" rid="ref36">36</xref>], parent-submitted videos in specialty care [<xref ref-type="bibr" rid="ref39">39</xref>], nurse or technician capture with specialist interpretation in community programs [<xref ref-type="bibr" rid="ref61">61</xref>], and a multidisciplinary pathway using scheduled remote reviews [<xref ref-type="bibr" rid="ref14">14</xref>].</p><p>Synchronous models accounted for 11 of 52 studies (21.2%) and included real-time postoperative reviews and acute assessments [<xref ref-type="bibr" rid="ref32">32</xref>,<xref ref-type="bibr" rid="ref37">37</xref>,<xref ref-type="bibr" rid="ref52">52</xref>,<xref ref-type="bibr" rid="ref53">53</xref>,<xref ref-type="bibr" rid="ref58">58</xref>], whereas blended stored media with live guidance or interconsultation accounted for 6 of 52 studies (11.5%) [<xref ref-type="bibr" rid="ref13">13</xref>,<xref ref-type="bibr" rid="ref22">22</xref>,<xref ref-type="bibr" rid="ref35">35</xref>,<xref ref-type="bibr" rid="ref49">49</xref>,<xref ref-type="bibr" rid="ref64">64</xref>,<xref ref-type="bibr" rid="ref68">68</xref>]. Telemedicine-supported otologic care was implemented across a variety of settings, including primary care clinics, emergency departments, specialty outpatient services, schools, community screening programs, and home environments.</p></sec><sec id="s3-3-2"><title>Technologies and Devices</title><p>A diverse range of hardware and software solutions were reported across the included studies (<xref ref-type="table" rid="table3">Table 3</xref>).</p><table-wrap id="t3" position="float"><label>Table 3.</label><caption><p>Summary of technologies and key outcomes across included pediatric otitis media telemedicine studies (N=52).</p></caption><table id="table3" frame="hsides" rules="groups"><thead><tr><td align="left" valign="bottom">References</td><td align="left" valign="bottom">Implementation/clinical outcome</td><td align="left" valign="bottom">Diagnostic performance</td><td align="left" valign="bottom">Typical setting</td><td align="left" valign="bottom">Representative device/system</td><td align="left" valign="bottom">Technology category</td></tr></thead><tbody><tr><td align="char" char="." valign="top">[<xref ref-type="bibr" rid="ref12">12</xref>,<xref ref-type="bibr" rid="ref36">36</xref>,<xref ref-type="bibr" rid="ref37">37</xref>,<xref ref-type="bibr" rid="ref41">41</xref>,<xref ref-type="bibr" rid="ref44">44</xref>,<xref ref-type="bibr" rid="ref49">49</xref>-<xref ref-type="bibr" rid="ref51">51</xref>,<xref ref-type="bibr" rid="ref53">53</xref>,<xref ref-type="bibr" rid="ref54">54</xref>,<xref ref-type="bibr" rid="ref71">71</xref>]</td><td align="left" valign="top">Repeat confirmatory examinations decreased from 97.9% to 27.2% when digital otoscopy was used in training clinics [<xref ref-type="bibr" rid="ref53">53</xref>]. Image acquisition required a median of ~6 minutes per case in rural outpatient workflows [<xref ref-type="bibr" rid="ref36">36</xref>]. For home tympanostomy tube surveillance, clinicians completed remote reviews in 1&#x2010;3 minutes, families reported mean savings of ~US $127 per episode, and satisfaction was high [<xref ref-type="bibr" rid="ref54">54</xref>].</td><td align="left" valign="top">Diagnostic concordance with in-person otoscopy was 95%, with &#x03BA;=0.89, sensitivity 0.94, and specificity 0.96 [<xref ref-type="bibr" rid="ref36">36</xref>]. In a randomized comparison, trainee diagnostic accuracy improved by 11.2% using digital otoscopy, and interrater agreement rose to Fleiss &#x03BA;<sup><xref ref-type="table-fn" rid="table3fn1">a</xref></sup>=0.69 versus Fleiss &#x03BA;=0.40 with a conventional otoscope [<xref ref-type="bibr" rid="ref53">53</xref>]. Parent-captured videos yielded 40% diagnostic-quality submissions, allowed 87% detection or exclusion of AOM<sup><xref ref-type="table-fn" rid="table3fn2">b</xref></sup> during acute episodes, and achieved &#x03BA;=0.69 between raters [<xref ref-type="bibr" rid="ref12">12</xref>].</td><td align="left" valign="top">Emergency, outpatient, school, home; clinicians, trainees, parents</td><td align="left" valign="top">CellScope Oto, Cupris TYM, TYMPA system, endoscope-i</td><td align="left" valign="top">Smartphone-connected digital otoscopes or otoendoscopes</td></tr><tr><td align="char" char="." valign="top">[<xref ref-type="bibr" rid="ref29">29</xref>,<xref ref-type="bibr" rid="ref32">32</xref>,<xref ref-type="bibr" rid="ref34">34</xref>]</td><td align="left" valign="top">Short, focused training improved diagnostic agreement and enabled reliable store-and-forward workflows in primary care [<xref ref-type="bibr" rid="ref29">29</xref>,<xref ref-type="bibr" rid="ref34">34</xref>].</td><td align="left" valign="top">Agreement with otomicroscopy was Cohen &#x03BA;=0.68&#x2010;0.75, with 72.4%&#x2010;79.3% sensitivity and 93.2%&#x2010;98% specificity [<xref ref-type="bibr" rid="ref29">29</xref>]. In facilitator-collected video-otoscopy reviewed by a general practitioner, repeat video review improved weighted &#x03BA; from 0.69 to 0.82 (OMgrade), and specificity reached 0.98 [<xref ref-type="bibr" rid="ref34">34</xref>].</td><td align="left" valign="top">Primary care; CHWs<sup><xref ref-type="table-fn" rid="table3fn3">c</xref></sup> or GPs<sup><xref ref-type="table-fn" rid="table3fn4">d</xref></sup></td><td align="left" valign="top">Dino-Lite Pro Earscope</td><td align="left" valign="top">USB video-otoscopes</td></tr><tr><td align="char" char="." valign="top">[<xref ref-type="bibr" rid="ref42">42</xref>]</td><td align="left" valign="top">Users constructed the funnel in a mean (SD) time of 2.8 (0.9) minutes and rated usability as 8.9/10; performance was consistent across phone models following calibration.</td><td align="left" valign="top">Discrimination of middle ear effusion achieved an AUC<sup><xref ref-type="table-fn" rid="table3fn5">e</xref></sup> 0.898, with 84.6% sensitivity and 81.9% specificity, outperforming commercial acoustic reflectometry (AUC 0.776). Caregivers&#x2019; classifications closely matched that of clinicians in 24/25 ears [<xref ref-type="bibr" rid="ref42">42</xref>].</td><td align="left" valign="top">Home; caregivers</td><td align="left" valign="top">Paper funnel + smartphone microphone</td><td align="left" valign="top">Smartphone-based acoustic system</td></tr><tr><td align="char" char="." valign="top">[<xref ref-type="bibr" rid="ref60">60</xref>]</td><td align="left" valign="top">Materials cost was &#x003C;US $30 while maintaining functional parity with a commercial device; the clinical cohort excluded infants younger than 9 months, defining the initial applicability window.</td><td align="left" valign="top">Classification by 5 audiologists, 86% (2%) agreement; all Type B correctly identified. Bland-Altman in 45 intact ears: peak admittance bias=&#x2013;0.02 (0.14) mL, peak pressure bias=&#x2013;1 (17) daPa, and ear canal volume bias=&#x2013;0.09 (0.25) mL [<xref ref-type="bibr" rid="ref60">60</xref>].</td><td align="left" valign="top">Outpatient; audiologists</td><td align="left" valign="top">Open-source prototype vs GSI TympStar</td><td align="left" valign="top">Low-cost smartphone tympanometer</td></tr><tr><td align="char" char="." valign="top">[<xref ref-type="bibr" rid="ref33">33</xref>,<xref ref-type="bibr" rid="ref45">45</xref>,<xref ref-type="bibr" rid="ref70">70</xref>]</td><td align="left" valign="top">Adoption was high, with 87% of families downloading the app and 74% using it between visits, and clinicians reported improved information exchange during care [<xref ref-type="bibr" rid="ref45">45</xref>].</td><td align="left" valign="top">A clinic-based app hearing test correlated with pure-tone audiometry (r=&#x2013;0.656) [<xref ref-type="bibr" rid="ref45">45</xref>]. In a cohort comparison, the app arm recorded a higher proportion of symptom days (44%) than the paper diary arm (32.5%) and achieved near-complete questionnaire return [<xref ref-type="bibr" rid="ref33">33</xref>].</td><td align="left" valign="top">Home; parents/patients</td><td align="left" valign="top">Diary tracking, Hear Glue Ear, Mimi</td><td align="left" valign="top">mHealth applications</td></tr><tr><td align="char" char="." valign="top">[<xref ref-type="bibr" rid="ref15">15</xref>,<xref ref-type="bibr" rid="ref16">16</xref>,<xref ref-type="bibr" rid="ref47">47</xref>]</td><td align="left" valign="top">Systems supported self-examination and automated triage, yet generalizability across sites, devices, and pediatric populations remains limited pending broader external validation.</td><td align="left" valign="top">Internal validation of a CNN<sup><xref ref-type="table-fn" rid="table3fn6">f</xref></sup> model reported sensitivity and specificity &#x003E;98% with AUROC<sup><xref ref-type="table-fn" rid="table3fn7">g</xref></sup> 1.00 across classes; external testing showed reduced sensitivity for AOM (58.3%) and OME (58.3%) with high specificity (100% and 98.1%) [<xref ref-type="bibr" rid="ref15">15</xref>]. A low-cost USB device with DenseNet<sup><xref ref-type="table-fn" rid="table3fn8">h</xref></sup> achieved 95.7% overall accuracy; for OME<sup><xref ref-type="table-fn" rid="table3fn9">i</xref></sup>, sensitivity 0.77 and specificity 0.99; for cholesteatoma, sensitivity 0.79 [<xref ref-type="bibr" rid="ref16">16</xref>]. A rule-based model reached Top-1 accuracy of 69.5% versus 83% by human telemedicine reviewers [<xref ref-type="bibr" rid="ref47">47</xref>].</td><td align="left" valign="top">Mixed otology; clinicians and self-examination users</td><td align="left" valign="top">Karl Storz Smart Scope + i-Nside (Inception-v2), DenseNet USB endoscope, rule-based Android</td><td align="left" valign="top">Artificial intelligence&#x2013;assisted digital otoscopy</td></tr><tr><td align="char" char="." valign="top">[<xref ref-type="bibr" rid="ref13">13</xref>,<xref ref-type="bibr" rid="ref22">22</xref>,<xref ref-type="bibr" rid="ref64">64</xref>]</td><td align="left" valign="top">Image capture success reached 96.3% during remote sessions [<xref ref-type="bibr" rid="ref22">22</xref>]. School programs achieved &#x003E;85% coverage and reduced costs relative to standard pathways and were rated highly by families, supporting feasibility for integrated tele-audiology [<xref ref-type="bibr" rid="ref13">13</xref>,<xref ref-type="bibr" rid="ref64">64</xref>].</td><td align="left" valign="top">In school-entry children, remote testing matched face-to-face within &#x00B1;10 dB for air conduction at 1 kHz (98%) and 4 kHz (97.8%), bone conduction matched in 100%/95.7%, otoscopy agreement was &#x03BA;=0.60, and tympanometry agreement was &#x03BA;=0.90 [<xref ref-type="bibr" rid="ref64">64</xref>]. Live video-otoscopy showed substantial agreement (&#x03BA;=0.68 for videos; &#x03BA;=0.83 for still images) and identified more landmarks (2.79 vs 1.68) [<xref ref-type="bibr" rid="ref22">22</xref>]. Using a multisensor kit in pediatrics, ear-specific sensitivity was 64.4% (tympanic membrane) and 66.1% (ear canal), with specificity consistently above 70% [<xref ref-type="bibr" rid="ref13">13</xref>].</td><td align="left" valign="top">School and pediatric tele-audiology</td><td align="left" valign="top">TytoPro; Otometrics A450 + Aurical Otocam 300 + Interacoustics MT10</td><td align="left" valign="top">Multisensor or hybrid diagnostic kits</td></tr><tr><td align="char" char="." valign="top">[<xref ref-type="bibr" rid="ref14">14</xref>,<xref ref-type="bibr" rid="ref65">65</xref>]</td><td align="left" valign="top">Median time to diagnosis and care plan fell to 28 days compared with 450 days in standard care (<italic>P</italic>&#x003C;.001) [<xref ref-type="bibr" rid="ref14">14</xref>]. A hospital cost analysis estimated ~US $67 per initial visit (vs US $155) with a break-even point at 223 appointments and about 3-fold greater specialist throughput [<xref ref-type="bibr" rid="ref65">65</xref>].</td><td align="left" valign="top">Performance was driven by the integrated, multitest pathway rather than a single diagnostic metric [<xref ref-type="bibr" rid="ref14">14</xref>,<xref ref-type="bibr" rid="ref65">65</xref>].</td><td align="left" valign="top">Multidisciplinary teleclinic</td><td align="left" valign="top">&#x201C;Ear Portal&#x201D;: HearScope + HearScreen + Titan (WBT<sup><xref ref-type="table-fn" rid="table3fn10">j</xref></sup>) + DPOAE<sup><xref ref-type="table-fn" rid="table3fn11">k</xref></sup></td><td align="left" valign="top">Integrated multidisciplinary pathway</td></tr><tr><td align="char" char="." valign="top">[<xref ref-type="bibr" rid="ref28">28</xref>,<xref ref-type="bibr" rid="ref31">31</xref>,<xref ref-type="bibr" rid="ref43">43</xref>,<xref ref-type="bibr" rid="ref46">46</xref>,<xref ref-type="bibr" rid="ref57">57</xref>,<xref ref-type="bibr" rid="ref69">69</xref>]</td><td align="left" valign="top">In a 45-camp program, 3000 individuals were screened; 54% were referred, 13% presented to hospital, and roughly half of presenters required surgery; procedures were delivered at about 40% of usual cost [<xref ref-type="bibr" rid="ref46">46</xref>]. Longitudinal regional programs achieved ~85% coverage and reduced referrals and waits [<xref ref-type="bibr" rid="ref28">28</xref>,<xref ref-type="bibr" rid="ref31">31</xref>].</td><td align="left" valign="top">In CHW-led screening, overall sensitivity was 96.9% with condition-specific concordance of CSOM<sup><xref ref-type="table-fn" rid="table3fn12">l</xref></sup> 96.2%, wax 98%, ASOM<sup><xref ref-type="table-fn" rid="table3fn13">m</xref></sup> 93.9%, foreign body 100%, and OME 100% [<xref ref-type="bibr" rid="ref57">57</xref>]. When operators received only written instructions, diagnostically useful video yield was 18.1% with substantial interrater agreement (Fleiss &#x03BA;=0.67) and higher usefulness in older children [<xref ref-type="bibr" rid="ref43">43</xref>].</td><td align="left" valign="top">Community/schools; CHWs, teachers</td><td align="left" valign="top">ENTraview + ClickMedix; Mebird T5 video-otoscopy + EMRs<sup><xref ref-type="table-fn" rid="table3fn14">n</xref></sup> support follow-up</td><td align="left" valign="top">Community and school screening programs</td></tr><tr><td align="char" char="." valign="top">[<xref ref-type="bibr" rid="ref48">48</xref>,<xref ref-type="bibr" rid="ref55">55</xref>]</td><td align="left" valign="top">High false-positive rates led to a 66% referral rate in a cohort with 27% hearing loss prevalence; performance was limited by ambient noise and lack of standardized calibration [<xref ref-type="bibr" rid="ref55">55</xref>].</td><td align="left" valign="top">The Hearing Test app showed &#x03BA;=0.059, indicating poor agreement with conventional audiometry [<xref ref-type="bibr" rid="ref48">48</xref>]. The hearScreen app achieved 85% sensitivity and 41% specificity, with ambient noise at 500 Hz significantly increasing false positives (<italic>P</italic>=.01) [<xref ref-type="bibr" rid="ref55">55</xref>].</td><td align="left" valign="top">Clinics/non-soundproof rooms</td><td align="left" valign="top">Hearing Test, hearScreen</td><td align="left" valign="top">App-based hearing screening</td></tr></tbody></table><table-wrap-foot><fn id="table3fn1"><p><sup>a</sup>&#x03BA;: Cohen kappa.</p></fn><fn id="table3fn2"><p><sup>b</sup>AOM: acute otitis media.</p></fn><fn id="table3fn3"><p><sup>c</sup>CHW: community health worker.</p></fn><fn id="table3fn4"><p><sup>d</sup>GP: general practitioner.</p></fn><fn id="table3fn5"><p><sup>e</sup>AUC: area under the receiver operating characteristic curve.</p></fn><fn id="table3fn6"><p><sup>f</sup>CNN: convolutional neural network.</p></fn><fn id="table3fn7"><p><sup>g</sup>AUROC: area under the receiver operating characteristic curve.</p></fn><fn id="table3fn8"><p><sup>h</sup>DenseNet: Dense Convolutional Network.</p></fn><fn id="table3fn9"><p><sup>i</sup>OME: otitis media with effusion.</p></fn><fn id="table3fn10"><p><sup>j</sup>WBT: wideband tympanometry.</p></fn><fn id="table3fn11"><p><sup>k</sup>DPOAE: distortion product otoacoustic emissions.</p></fn><fn id="table3fn12"><p><sup>l</sup>CSOM: chronic suppurative otitis media.</p></fn><fn id="table3fn13"><p><sup>m</sup>ASOM: acute suppurative otitis media.</p></fn><fn id="table3fn14"><p><sup>n</sup>EMR: electronic medical record.</p></fn></table-wrap-foot></table-wrap><p>The most frequently used solution was smartphone-connected digital otoscopes and otoendoscopes, such as CellScope Oto, Cupris TYM, TYMPA system (TympaHealth), and endoscope-i, which were applied in emergency, outpatient, school, and home settings [<xref ref-type="bibr" rid="ref11">11</xref>,<xref ref-type="bibr" rid="ref36">36</xref>,<xref ref-type="bibr" rid="ref37">37</xref>,<xref ref-type="bibr" rid="ref41">41</xref>,<xref ref-type="bibr" rid="ref44">44</xref>,<xref ref-type="bibr" rid="ref49">49</xref>-<xref ref-type="bibr" rid="ref51">51</xref>,<xref ref-type="bibr" rid="ref53">53</xref>,<xref ref-type="bibr" rid="ref54">54</xref>,<xref ref-type="bibr" rid="ref71">71</xref>]. Earlier clinical evaluation of smartphone-enabled otoscopy for OM diagnosis and management were reported, supporting feasibility in routine care [<xref ref-type="bibr" rid="ref66">66</xref>]. USB video-otoscopes, including the Dino-Lite Pro Earscope, were used to support store-and-forward apps in clinics [<xref ref-type="bibr" rid="ref29">29</xref>,<xref ref-type="bibr" rid="ref34">34</xref>]. Non-smartphone digital otoscopes, such as Welch Allyn Digital MacroView Otoscope, TeleHealth Flexican Otoscope, and Welch Allyn USB Otoscope, were used for real-time follow-up and teleconsultations [<xref ref-type="bibr" rid="ref22">22</xref>,<xref ref-type="bibr" rid="ref32">32</xref>].</p><p>Apart from imaging, several digital tools were used. A smartphone-only acoustic system, using a paper funnel and the phone&#x2019;s microphone, enabled the detection of middle ear effusion (MEE) [<xref ref-type="bibr" rid="ref42">42</xref>]. Mobile health (mHealth) apps facilitated diary-based episode detection and home management [<xref ref-type="bibr" rid="ref33">33</xref>,<xref ref-type="bibr" rid="ref45">45</xref>]. By contrast, although acceptability was high, a culturally tailored multimedia or text messaging intervention for Aboriginal children with tympanic membrane perforation did not improve clinic attendance or short-term ear health outcomes [<xref ref-type="bibr" rid="ref70">70</xref>]. A low-cost, open-source smartphone tympanometer was evaluated against the GSI TympStar systems (Grason-Stadler) [<xref ref-type="bibr" rid="ref60">60</xref>]. Decision support innovations included the Karl Storz Smart Scope with the i-Nside app (Inception-v2) and an inexpensive (~US $10) USB endoscope integrated with a Dense Convolutional Network (DenseNet) classifier for self-examination [<xref ref-type="bibr" rid="ref15">15</xref>,<xref ref-type="bibr" rid="ref16">16</xref>]. A consumer Android-tethered otoendoscope, coupled with a rule-based model, demonstrated performance comparable to that of clinicians in diverse otology settings [<xref ref-type="bibr" rid="ref47">47</xref>]. Community programs frequently used Medtronic&#x2019;s ENTraview integrated with ClickMedix, and 1 program used the Mebird T5 SO (Black Bee Intelligent Manufacturing [Shenzhen] Technology Co., Ltd.) for asynchronous case discussion [<xref ref-type="bibr" rid="ref35">35</xref>,<xref ref-type="bibr" rid="ref46">46</xref>,<xref ref-type="bibr" rid="ref56">56</xref>,<xref ref-type="bibr" rid="ref57">57</xref>]. A multisensor kit (TytoPro) enabled remote pediatric interconsultation [<xref ref-type="bibr" rid="ref13">13</xref>]. The school-based hybrid audiology program integrated Madsen A450 audiometry (Otometrics Natus Medical), Natus Aurical Otocam 300 video-otoscopy, and Interacoustics MT10 tympanometry with videoconferencing [<xref ref-type="bibr" rid="ref64">64</xref>]. For training, Otosim2 (OtoSim Inc.) via AudioProConnect and a low-cost KZYEE USB otoscope improved teaching and landmark recognition [<xref ref-type="bibr" rid="ref38">38</xref>,<xref ref-type="bibr" rid="ref44">44</xref>]. Teslong pen endoscopes and the Mimi Hearing Test app (Mimi Hearing Technologies) were piloted for supervised home capture and hearing checks [<xref ref-type="bibr" rid="ref49">49</xref>,<xref ref-type="bibr" rid="ref63">63</xref>]. A structured &#x201C;Ear Portal&#x201D; pathway combined hearX HearScope video-otoscopy, HearScreen audiometry, Interacoustics Titan wideband tympanometry, and distortion product otoacoustic emissions into a scheduled multidisciplinary review [<xref ref-type="bibr" rid="ref14">14</xref>,<xref ref-type="bibr" rid="ref65">65</xref>].</p></sec><sec id="s3-3-3"><title>Technology Category &#x00D7; Care Model</title><p><xref ref-type="fig" rid="figure2">Figure 2</xref> maps technology categories against care models. Most studies used asynchronous store-and-forward workflows, primarily tele-otoscopy imaging alone or tele-otoscopy combined with adjunct testing (<xref ref-type="fig" rid="figure2">Figure 2</xref>). Hybrid models were less common and tended to involve multisensor kits or tele-otoscopy plus adjunct testing. Notable gaps included limited evidence for integrated pathway models beyond a small number of programs and sparse evaluation of outcomes beyond diagnostic performance, including long-term child outcomes and cost-effectiveness.</p><fig position="float" id="figure2"><label>Figure 2.</label><caption><p>Evidence gap map of technology category by care model in pediatric otitis media telemedicine. mHealth: mobile health.</p></caption><graphic alt-version="no" mimetype="image" position="float" xlink:type="simple" xlink:href="jmir_v28i1e85416_fig02.png"/></fig></sec><sec id="s3-3-4"><title>Operators and Workflow Roles</title><p><xref ref-type="fig" rid="figure3">Figure 3</xref> summarizes who captured otoscopic media (clinicians, nurses/community facilitators, caregivers/parents) and who interpreted it. Studies consistently indicated that diagnostic yield depended strongly on operator training and workflow support, which includes checklists, feedback loops, and cerumen management. Evidence gaps included limited direct comparisons of training intensity and limited reporting of minimum image quality thresholds.</p><fig position="float" id="figure3"><label>Figure 3.</label><caption><p>Operator workflow map showing who captures otoscopic media and who interprets it in pediatric otitis media tele-otoscopy. CHW: community health worker, ENT: ear, nose, and throat.</p></caption><graphic alt-version="no" mimetype="image" position="float" xlink:type="simple" xlink:href="jmir_v28i1e85416_fig03.png"/></fig></sec></sec><sec id="s3-4"><title>Diagnostic Performance</title><p>Across diagnostic accuracy studies, the reported &#x03BA;, sensitivity, and specificity varied by key sources of clinical and methodological heterogeneity, including pediatric age strata, OM phenotype definitions (AOM vs OME vs mixed), reference standards, operator training and experience, and device and workflow-specific image quality constraints (<xref ref-type="table" rid="table4">Table 4</xref>). To improve interpretability, we summarized diagnostic performance by capture-interpretation model and reference standard.</p><table-wrap id="t4" position="float"><label>Table 4.</label><caption><p>Key sources of clinical and methodological heterogeneity across diagnostic accuracy studies in pediatric otitis media tele-otoscopy.</p></caption><table id="table4" frame="hsides" rules="groups"><thead><tr><td align="left" valign="bottom">Study and category</td><td align="left" valign="bottom" colspan="6">Key heterogeneity</td><td align="left" valign="bottom">Performance (&#x03BA;<sup><xref ref-type="table-fn" rid="table4fn1">a</xref></sup>/Se<sup><xref ref-type="table-fn" rid="table4fn2">b</xref></sup>/Sp<sup><xref ref-type="table-fn" rid="table4fn3">c</xref></sup>/AUC<sup><xref ref-type="table-fn" rid="table4fn4">d</xref></sup>)</td></tr><tr><td align="left" valign="bottom"/><td align="left" valign="bottom">Age</td><td align="left" valign="bottom">Spectrum</td><td align="left" valign="bottom">Operator/training</td><td align="left" valign="bottom">Reference standard</td><td align="left" valign="bottom">Device</td><td align="left" valign="bottom">Quality</td><td align="left" valign="bottom"/></tr></thead><tbody><tr><td align="left" valign="top">(A) Trained operator/expert interpretation</td><td align="left" valign="top"/><td align="left" valign="top"/><td align="left" valign="top"/><td align="left" valign="top"/><td align="left" valign="top"/><td align="left" valign="top"/><td align="left" valign="top"/></tr><tr><td align="left" valign="top"><named-content content-type="indent">&#x00A0;&#x00A0;&#x00A0;&#x00A0;</named-content>Biagio et al (2014) [<xref ref-type="bibr" rid="ref29">29</xref>]</td><td align="left" valign="top">2-16 y</td><td align="left" valign="top">Normal/abnormal OM</td><td align="left" valign="top">Trained capture &#x2192; clinician read (2 sessions)</td><td align="left" valign="top">Otomicroscopy</td><td align="left" valign="top">Asynchronous video-otoscopy</td><td align="left" valign="top">Acceptable/excellent ratings (NR criteria)</td><td align="left" valign="top">&#x03BA; 0.68&#x2010;0.75; Se 72.4%&#x2010;79.3%; Sp 93.2%&#x2010;98%</td></tr><tr><td align="left" valign="top"><named-content content-type="indent">&#x00A0;&#x00A0;&#x00A0;&#x00A0;</named-content>Lundberg et al (2017) [<xref ref-type="bibr" rid="ref34">34</xref>]</td><td align="left" valign="top">Pediatrics (NR)<sup><xref ref-type="table-fn" rid="table4fn5">e</xref></sup></td><td align="left" valign="top">Normal/OME<sup><xref ref-type="table-fn" rid="table4fn6">f</xref></sup>/AOM<sup><xref ref-type="table-fn" rid="table4fn7">g</xref></sup>/CSOM<sup><xref ref-type="table-fn" rid="table4fn8">h</xref></sup> (abnormal pooled)</td><td align="left" valign="top">Facilitator capture &#x2192; GP<sup><xref ref-type="table-fn" rid="table4fn9">i</xref></sup> read (repeat)</td><td align="left" valign="top">Otologist otomicroscopy</td><td align="left" valign="top">Video-otoscopy vs otoscopy</td><td align="left" valign="top">NPD<sup><xref ref-type="table-fn" rid="table4fn10">j</xref></sup> due to wax/degree of cooperation/low quality</td><td align="left" valign="top">w&#x03BA;<sup><xref ref-type="table-fn" rid="table4fn11">k</xref></sup> 0.76&#x2192;0.82 (video) vs 0.69 (otoscopy); Se 0.77&#x2010;0.81; Sp 0.94&#x2010;0.98</td></tr><tr><td align="left" valign="top"><named-content content-type="indent">&#x00A0;&#x00A0;&#x00A0;&#x00A0;</named-content>Mandavia et al (2018) [<xref ref-type="bibr" rid="ref36">36</xref>]</td><td align="left" valign="top">Pediatrics (NR)</td><td align="left" valign="top">Screening (NR)</td><td align="left" valign="top">Trainees capture &#x2192; remote consultant read</td><td align="left" valign="top">On-site specialist otoscopy/referral</td><td align="left" valign="top">Smartphone otoscopy (Cupris TYM)</td><td align="left" valign="top">NR</td><td align="left" valign="top">Concordance 95% (&#x03BA;=0.89); Se 0.94; Sp 0.96; referral concordance 100%</td></tr><tr><td align="left" valign="top">(B) Parent/nonspecialist capture (training dependent)</td><td align="left" valign="top"/><td align="left" valign="top"/><td align="left" valign="top"/><td align="left" valign="top"/><td align="left" valign="top"/><td align="left" valign="top"/><td align="left" valign="top"/></tr><tr><td align="left" valign="top"><named-content content-type="indent">&#x00A0;&#x00A0;&#x00A0;&#x00A0;</named-content>Erkkola-Anttinen et al (2019) [<xref ref-type="bibr" rid="ref12">12</xref>]</td><td align="char" char="hyphen" valign="top">6-35 mo</td><td align="left" valign="top">AOM-focused</td><td align="left" valign="top">Parent capture (hands-on teaching) &#x2192; remote raters</td><td align="left" valign="top">Clinician assessment (NR)</td><td align="left" valign="top">Device: smartphone video-otoscopy</td><td align="left" valign="top">Sufficient quality 62%&#x2010;64% during intervention; diagnostic quality 40%</td><td align="left" valign="top">Detect/exclude AOM &#x03BA;=0.69 (87% possible)</td></tr><tr><td align="left" valign="top"><named-content content-type="indent">&#x00A0;&#x00A0;&#x00A0;&#x00A0;</named-content>Shah et al (2018) [<xref ref-type="bibr" rid="ref39">39</xref>]</td><td align="char" char="." valign="top">3 mo to 17 y</td><td align="left" valign="top">Mixed pathology</td><td align="left" valign="top">Parent or physician capture &#x2192; physician read (brief tutorial)</td><td align="left" valign="top">Pneumatic otoscopy (&#x00B1; tympanometry subset)</td><td align="left" valign="top">iPhone/CellScope</td><td align="left" valign="top">Wax common; wax-alert &#x03BA;&#x2248;0.01</td><td align="left" valign="top">Parent &#x03BA;=0.42; physician &#x03BA;=0.74 (vs pneumatic otoscopy)</td></tr><tr><td align="left" valign="top"><named-content content-type="indent">&#x00A0;&#x00A0;&#x00A0;&#x00A0;</named-content>Demant et al (2019) [<xref ref-type="bibr" rid="ref43">43</xref>]</td><td align="char" char="hyphen" valign="top">6-72 mo</td><td align="left" valign="top">Usefulness outcome</td><td align="left" valign="top">Nonspecialist HW capture (written instructions only) &#x2192; ENT<sup><xref ref-type="table-fn" rid="table4fn12">l</xref></sup> raters</td><td align="left" valign="top">NR</td><td align="left" valign="top">Smartphone otoscopy (Cupris TYM)</td><td align="left" valign="top">Useful videos 6.6% (&#x003C;24 mo), 22.7% (24-48 mo), 30.7% (&#x003E;48 mo)</td><td align="left" valign="top">Modified Fleiss &#x03BA; 0.73 (&#x003C;24 mo), 0.48 (24-48 mo), 0.60 (&#x003E;48 mo)</td></tr><tr><td align="left" valign="top">(C) Different outcomes/surrogate standards/different modalities</td><td align="left" valign="top"/><td align="left" valign="top"/><td align="left" valign="top"/><td align="left" valign="top"/><td align="left" valign="top"/><td align="left" valign="top"/><td align="left" valign="top"/></tr><tr><td align="left" valign="top"><named-content content-type="indent">&#x00A0;&#x00A0;&#x00A0;&#x00A0;</named-content>Kleinman et al (2021) [<xref ref-type="bibr" rid="ref53">53</xref>]</td><td align="left" valign="top">Pediatrics (NR)</td><td align="left" valign="top">Education/clinical trial</td><td align="left" valign="top">Trainees</td><td align="left" valign="top">Education/supervisor (NR gold standard)</td><td align="left" valign="top">Digital vs traditional otoscope</td><td align="left" valign="top">NR</td><td align="left" valign="top">Accuracy +11.2%; Fleiss &#x03BA; 0.40&#x2192;0.69; repeat confirmatory examinations 97.9%&#x2192;27.2%</td></tr><tr><td align="left" valign="top"><named-content content-type="indent">&#x00A0;&#x00A0;&#x00A0;&#x00A0;</named-content>Rappaport et al (2016) [<xref ref-type="bibr" rid="ref66">66</xref>]</td><td align="char" char="." valign="top">6 mo to 18 y</td><td align="left" valign="top">AOM via ED<sup><xref ref-type="table-fn" rid="table4fn13">m</xref></sup> diagnosis (ICD-9<sup><xref ref-type="table-fn" rid="table4fn14">n</xref></sup> surrogate)</td><td align="left" valign="top">ED capture &#x2192; blinded physician reviewers</td><td align="left" valign="top">ED diagnosis</td><td align="left" valign="top">Smartphone vs digital otoscope</td><td align="left" valign="top">NR</td><td align="left" valign="top">Overall &#x03BA;=0.375; smartphone &#x03BA;=0.368; digital &#x03BA;=0.381</td></tr><tr><td align="left" valign="top"><named-content content-type="indent">&#x00A0;&#x00A0;&#x00A0;&#x00A0;</named-content>Chan et al (2019) [<xref ref-type="bibr" rid="ref42">42</xref>]</td><td align="left" valign="top">18 mo to 17 y (median 5 y)</td><td align="left" valign="top">Chronic OME/recurrent AOM vs controls</td><td align="left" valign="top">Clinician testing;parental use tested after brief demo</td><td align="left" valign="top">Surgical fluid (myringotomy) and/or ENT pneumatic otoscopy</td><td align="left" valign="top">Smartphone acoustic method (paper funnel; ML)<sup><xref ref-type="table-fn" rid="table4fn15">o</xref></sup></td><td align="left" valign="top">Phone model calibration</td><td align="left" valign="top">AUC 0.898; Se 84.6%; Sp 81.9%; parents matched clinician 24/25 ears</td></tr><tr><td align="left" valign="top"><named-content content-type="indent">&#x00A0;&#x00A0;&#x00A0;&#x00A0;</named-content>Durgut et al (2020) [<xref ref-type="bibr" rid="ref48">48</xref>]</td><td align="char" char="hyphen" valign="top">5-15 y</td><td align="left" valign="top">OME (50 children; 88 ears with OME + 12 controls)</td><td align="left" valign="top">In-clinic testing</td><td align="left" valign="top">Booth pure-tone audiometry</td><td align="left" valign="top">Android Hearing Test app</td><td align="left" valign="top">Environmental noise limitation</td><td align="left" valign="top">Very poor agreement: &#x03BA;=0.059 (100 ears); no significant correlation 500&#x2010;4000 Hz</td></tr></tbody></table><table-wrap-foot><fn id="table4fn1"><p><sup>a</sup>&#x03BA;: Cohen kappa.</p></fn><fn id="table4fn2"><p><sup>b</sup>Se: sensitivity.</p></fn><fn id="table4fn3"><p><sup>c</sup>Sp: specificity.</p></fn><fn id="table4fn4"><p><sup>d</sup>AUC: area under the receiver operating characteristic curve.</p></fn><fn id="table4fn5"><p><sup>e</sup>NR: not reported.</p></fn><fn id="table4fn6"><p><sup>f</sup>OME: otitis media with effusion.</p></fn><fn id="table4fn7"><p><sup>g</sup>AOM: acute otitis media.</p></fn><fn id="table4fn8"><p><sup>h</sup>CSOM: chronic suppurative otitis media.</p></fn><fn id="table4fn9"><p><sup>i</sup>GP: general practitioner.</p></fn><fn id="table4fn10"><p><sup>j</sup>NPD: not possible to diagnose.</p></fn><fn id="table4fn11"><p><sup>k</sup>w&#x03BA;: weighted kappa.</p></fn><fn id="table4fn12"><p><sup>l</sup>ENT: ear, nose, and throat.</p></fn><fn id="table4fn13"><p><sup>m</sup>ED: emergency department.</p></fn><fn id="table4fn14"><p><sup>n</sup>ICD-9: International Classification of Diseases, 9th Revision.</p></fn><fn id="table4fn15"><p><sup>o</sup>ML: machine learning.</p></fn></table-wrap-foot></table-wrap><sec id="s3-4-1"><title>Trained Operator Capture with Expert Interpretation Against Clinical Reference Standards</title><p>When images were captured by trained operators and interpreted by experienced clinicians, store-and-forward tele-otoscopy showed substantial agreement with in-person otomicroscopy. In a primary care cohort, asynchronous video-otoscopy yielded Cohen &#x03BA; values of 0.68&#x2010;0.75 across raters and 2 review sessions, 72.4%&#x2010;79.3% and specificities of 93.2%&#x2010;98% [<xref ref-type="bibr" rid="ref29">29</xref>]. In another clinic, repeated readings improved weighted &#x03BA; from 0.69 to 0.82, with specificity up to 0.98 [<xref ref-type="bibr" rid="ref34">34</xref>]. Smartphone otoscopy used by trainees, with remote consultant review, achieved 95% ear-level concordance with on-site specialist otoscopy (&#x03BA;=0.89; sensitivity 0.94; specificity 0.96) and 100% concordance with referral decisions [<xref ref-type="bibr" rid="ref36">36</xref>]. For training, pediatric emergency department residents demonstrated similar diagnostic accuracy when using a smartphone device compared with a traditional otoscope (0.74 vs 0.69; nonsignificant). However, novice users tended to favor the conventional tools, as they felt confident with them [<xref ref-type="bibr" rid="ref37">37</xref>]. A separate academic comparison showed that digital otoscopy improved trainee accuracy by 11.2%, increased interrater agreement (from Fleiss &#x03BA;of 0.40 to 0.69), and reduced repeat confirmatory examinations from 97.9% to 27.2% [<xref ref-type="bibr" rid="ref53">53</xref>].</p></sec><sec id="s3-4-2"><title>Parent and Nonspecialist Capture (Training- and Cooperation-Dependent Performance)</title><p>Parent and nonspecialist performance was highly dependent on training and cooperation. After structured teaching, parents produced videos of sufficient quality in 62%&#x2010;64% of submissions during the intervention periods, and the evaluators showed substantial agreement for detecting or excluding AOM (&#x03BA;=0.69) [<xref ref-type="bibr" rid="ref12">12</xref>]. In contrast, a brief tutorial yielded lower agreement with pneumatic otoscopy (parent &#x03BA;=0.42 vs physician &#x03BA;=0.74), while automated cerumen alerts showed negligible agreement (&#x03BA;=0.01), highlighting the advantage of structured teaching [<xref ref-type="bibr" rid="ref39">39</xref>]. Without hands-on training, local health care workers produced diagnostically useful videos in only 18% of cases, with insertion errors and cerumen as major barriers; usefulness increased proportionally with child age [<xref ref-type="bibr" rid="ref43">43</xref>]. Educational approaches also included a smartphone-adaptable video-otoscopy quiz developed to support otoscopic image interpretation skills, reflecting ongoing efforts to standardize competency development for tele-otoscopy workflows [<xref ref-type="bibr" rid="ref67">67</xref>].</p></sec><sec id="s3-4-3"><title>Alternative Modalities and/or Surrogate Outcomes (Interpret with Caution)</title><p>Beyond optical otoscopy workflows, a smartphone-based acoustic method to detect MEE achieved an area under the receiver operating characteristic curve (AUC) of 0.898, with approximately 85% sensitivity and 82% specificity under surgical and/or specialist reference standards, and caregiver performance approximated clinician performance in a subset [<xref ref-type="bibr" rid="ref42">42</xref>]. A smartphone tympanometer also demonstrated approximately 86% classification agreement with commercial devices, with only minor bias in peak admittance and pressure, supporting the feasibility of adjunct middle ear assessments beyond optical imaging [<xref ref-type="bibr" rid="ref60">60</xref>]. In contrast, a pediatric hearing test app demonstrated very poor agreement with booth audiometry (&#x03BA;&#x2248;0.06) [<xref ref-type="bibr" rid="ref48">48</xref>,<xref ref-type="bibr" rid="ref55">55</xref>]. These findings underscore that performance estimates are not directly comparable across studies when index test modality, outcome definition, and reference standards differ. Artificial intelligence&#x2013;supported classifiers have shown high performance on curated datasets but lower sensitivity for OM and limited external validation across devices and sites [<xref ref-type="bibr" rid="ref15">15</xref>,<xref ref-type="bibr" rid="ref16">16</xref>,<xref ref-type="bibr" rid="ref47">47</xref>].</p></sec></sec><sec id="s3-5"><title>Clinical and Implementation Outcomes</title><sec id="s3-5-1"><title>Comparison With Traditional Approaches</title><p>Tele-enabled programs have broadened access and accelerated clinical decision-making. A school or community program completed 2111 assessments in 1053 children, demonstrating 85% coverage. In another evaluation, it reduced waiting times and tertiary referrals as the program expanded [<xref ref-type="bibr" rid="ref28">28</xref>,<xref ref-type="bibr" rid="ref31">31</xref>]. A general practitioner-to-ear, nose, and throat (ENT) specialist smartphone endoscopy pathway was able to manage 83% of the 53 referrals remotely, with a median specialist response time of 48 (IQR 22-148) minutes [<xref ref-type="bibr" rid="ref50">50</xref>]. In a pediatric emergency department, a smartphone otoscope showed substantial within-physician agreement versus a traditional otoscope and changed the reported tympanic membrane view in 12%&#x2010;16% of examinations, including clinically relevant diagnostic changes to or from AOM in 6%&#x2010;7% of examinations [<xref ref-type="bibr" rid="ref71">71</xref>]. Community screening of 3000 individuals generated 54% of referrals, but only 13% were ultimately presented for hospital evaluation; nearly half of those evaluated required surgery, underscoring the barriers of pathway follow-through [<xref ref-type="bibr" rid="ref46">46</xref>]. A telehealth-supported surgical model achieved 80% clinical resolution, 88% hearing improvement, and reduced travel costs for postoperative review [<xref ref-type="bibr" rid="ref32">32</xref>]. Home tympanostomy tube surveillance demonstrated high interrater and intrarater agreement, rapid clinician review (1&#x2010;3 min), and high family satisfaction with reported time and cost savings [<xref ref-type="bibr" rid="ref54">54</xref>]. The Ear Portal pathway substantially shortened time to diagnosis and care plan (median 28 [IQR 19.8] days), and an economic analysis showed that it lowered per-visit costs, reached a break-even point after ~223 appointments, and increased specialist throughput [<xref ref-type="bibr" rid="ref14">14</xref>,<xref ref-type="bibr" rid="ref65">65</xref>]. A community service integrating smartphone otoscopy with tablet audiometry discharged most patients at their first visit at a lower cost than other services using conventional methods, with specialist review rarely leading to changed decisions [<xref ref-type="bibr" rid="ref62">62</xref>]. However, televisits, which were performed predominantly without ear imaging, produced similar rates of tube recommendations but substantially lower documentation of effusion at surgery compared with encounters that incorporated ear imaging, indicating a potential risk of suboptimal decision-making when otoscopy is omitted [<xref ref-type="bibr" rid="ref52">52</xref>]. During the COVID-19 pandemic, telehealth encounters were overall less likely to end with tube recommendations, underscoring the limitations imposed by restricted physical examination [<xref ref-type="bibr" rid="ref58">58</xref>]. A multisensor interconsultation device demonstrated high agreement for several systems but lower sensitivity for ear canal and tympanic membrane findings than conventional methods, reinforcing the necessity of dedicated otoscopy using generalist kits [<xref ref-type="bibr" rid="ref13">13</xref>]. In pediatric telehealth, live video-otoscopy provided superior image quality and landmark visualization compared to still images, supporting synchronous visualization when feasible [<xref ref-type="bibr" rid="ref22">22</xref>]. A school-entry hybrid model demonstrated close agreement with face-to-face audiometry and tympanometry, with acceptable agreement for otoscopy [<xref ref-type="bibr" rid="ref64">64</xref>].</p></sec><sec id="s3-5-2"><title>Outcome Domains Reported</title><p><xref ref-type="table" rid="table5">Table 5</xref> summarizes the distribution of outcome domains reported across included studies (N=52). Diagnostic performance was the most frequently reported domain (38/52, 73.1%), followed by implementation and usability outcomes (29/52, 55.8%). Clinical and management impact (22/52, 42.3%) and audiology and tympanometry outcomes (19/52, 36.5%) were reported less often, while image or capture quality was reported in 15 of 52 studies (28.8%). Training and education and economic outcomes were each reported in 8 of 52 studies (15.4%), and artificial intelligence or automation was reported in 4 studies (7.7%; <xref ref-type="table" rid="table5">Table 5</xref>). Reports of longer-term patient outcomes and adverse events were uncommon, indicating priorities for future research.</p><table-wrap id="t5" position="float"><label>Table 5.</label><caption><p>Outcome domains reported across included studies (N=52).</p></caption><table id="table5" frame="hsides" rules="groups"><thead><tr><td align="left" valign="bottom">Outcome domain</td><td align="left" valign="bottom">Studies reporting domain, n (%)<sup><xref ref-type="table-fn" rid="table5fn1">a</xref></sup></td></tr></thead><tbody><tr><td align="left" valign="top">Diagnostic performance</td><td align="left" valign="top">38 (73.1%)</td></tr><tr><td align="left" valign="top">Implementation/usability</td><td align="left" valign="top">29 (55.8%)</td></tr><tr><td align="left" valign="top">Clinical/management impact</td><td align="left" valign="top">22 (42.3%)</td></tr><tr><td align="left" valign="top">Audiology/tympanometry outcomes</td><td align="left" valign="top">19 (36.5%)</td></tr><tr><td align="left" valign="top">Image/capture quality</td><td align="left" valign="top">15 (28.8%)</td></tr><tr><td align="left" valign="top">Training/education</td><td align="left" valign="top">8 (15.4%)</td></tr><tr><td align="left" valign="top">Economic outcomes</td><td align="left" valign="top">8 (15.4%)</td></tr><tr><td align="left" valign="top">Artificial intelligence/automation</td><td align="left" valign="top">4 (7.7%)</td></tr></tbody></table><table-wrap-foot><fn id="table5fn1"><p><sup>a</sup>Studies may contribute to multiple domains; therefore, percentages do not sum to 100%.</p></fn></table-wrap-foot></table-wrap></sec><sec id="s3-5-3"><title>Applications and Implementation Feasibility</title><p>Tele-enabled tools were applied in 4 management scenarios for pediatric ear diseases. For AOM diagnosis, asynchronous video-otoscopy demonstrated substantial agreement with otomicroscopy when images were captured by trained operators, as reported in South Africa using a laptop-tethered Dino-Lite Pro Earscope and specialist review [<xref ref-type="bibr" rid="ref29">29</xref>] and in a primary care study in which repeated readings of stored video sequences closely tracked the microscopic reference [<xref ref-type="bibr" rid="ref34">34</xref>]. At the bedside, smartphone-based digital otoscopy (CellScope Oto) demonstrated accuracy comparable to, or modestly better than, that of trainees using a conventional otoscope in a pediatric ED [<xref ref-type="bibr" rid="ref37">37</xref>]. With structured instructions, parents successfully captured diagnostically useful otoscopy videos at home, supporting remote triage for suspected AOM [<xref ref-type="bibr" rid="ref12">12</xref>]. For posttympanostomy tube surveillance and postoperative follow-up, home digital otoscopy with CellScope Oto enabled asynchronous specialist review and was rated highly acceptable by families. In remote Australian communities, a telehealth-supported surgical pathway cut travel and costs for postoperative care [<xref ref-type="bibr" rid="ref32">32</xref>,<xref ref-type="bibr" rid="ref54">54</xref>]. For screening and triage in underserved settings, school- and community-based programs&#x2014;ranging from mobile ear-screening services in Queensland to large-scale campaigns using the ENTraview smartphone otoscope integrated with the ClickMedix platform&#x2014;efficiently detected pathology, shortened time to specialist input, and improved surgical case prioritization, although barriers such as transport and out-of-pocket costs limited follow-through [<xref ref-type="bibr" rid="ref28">28</xref>,<xref ref-type="bibr" rid="ref46">46</xref>]. Additionally, a recent parent-led home ear health check pilot targeting children with complex needs highlighted feasibility and potential access benefits for populations facing barriers to clinic-based otoscopy [<xref ref-type="bibr" rid="ref68">68</xref>].</p><p>Although feasibility was consistently high across settings and devices, the diagnostic yield depended on operator training, child cooperation, and cerumen management. Parents performed better after structured teaching, but accuracy declined with only brief instructions or when wax removal was not addressed [<xref ref-type="bibr" rid="ref39">39</xref>]. Hands-on practice with a live tele-otoscopy simulation using Otosim2 with the AudioProConnect platform preserved accuracy and shortened task time, whereas written-only instructions under field conditions produced a low proportion of diagnostically useful videos [<xref ref-type="bibr" rid="ref43">43</xref>]. Clinicians generally rated smartphone otoscopy imagery as adequate and highlighted supervisory advantages of shared visualization, including fewer repeat confirmatory examinations during training encounters [<xref ref-type="bibr" rid="ref41">41</xref>,<xref ref-type="bibr" rid="ref53">53</xref>]. Conversely, environmental noise and calibration issues materially influenced app-based hearing tools, which demonstrated poor agreement with booth-based audiometry in children with OME, and a smartphone screening app demonstrated high sensitivity but low specificity when ambient noise was not well controlled [<xref ref-type="bibr" rid="ref48">48</xref>,<xref ref-type="bibr" rid="ref55">55</xref>].</p></sec><sec id="s3-5-4"><title>Risk of Bias and Study Limitations</title><p>Limitations include small, single-site samples; convenience sampling; mixed adult and pediatric cohorts in some studies; lack of blinded reference standards; heterogeneous operator training; device or discontinuation issues; and industrial involvement in some implementations. Parent and nonspecialist performance was sensitive to training and cerumen management, while omitting otoscopy in televisits risked misclassification of MEE [<xref ref-type="bibr" rid="ref52">52</xref>].</p></sec><sec id="s3-5-5"><title>Key Practical Takeaways</title><p>Across the included studies, the following points were notably identified as key practical takeaways:</p><p>1. Diagnostic performance depended strongly on who captured the otoscopic media and on the training and quality protocol rather than on the device alone.</p><p>2. Predefined image quality thresholds, multiview capture, and repeat capture when needed materially affected interpretability and downstream clinical decisions.</p><p>3. Telehealth encounters conducted without otoscopic imaging risk underdetecting middle ear pathology, including effusion, and may therefore alter management decisions when objective findings are required.</p><p>4. Hub-based or hybrid workflows&#x2014;such as facilitated capture with remote review&#x2014;appear to support access and feasibility while maintaining diagnostic reliability in many settings.</p><p>5. Evidence remains limited regarding scale-up outcomes (including sustainability/maintenance), formal economic evaluations (particularly in lower-middle-income countries), and external validation of artificial intelligence&#x2013;enabled tools across devices and sites.</p></sec></sec></sec><sec id="s4" sec-type="discussion"><title>Discussion</title><sec id="s4-1"><title>Principal Findings</title><p>This scoping review mapped a rapidly evolving evidence base for telehealth in pediatric OM. Three consistent signals were observed. First, when images were captured using standardized techniques by trained operators and interpreted by experienced clinicians, store-and-forward tele-otoscopy demonstrated diagnostic performance similar to in-person examination. In primary care and community clinics, agreement with otomicroscopy was frequently in the substantial range, with high specificity for excluding the disease [<xref ref-type="bibr" rid="ref29">29</xref>,<xref ref-type="bibr" rid="ref34">34</xref>,<xref ref-type="bibr" rid="ref36">36</xref>]. Second, operator training proved pivotal: performance declined markedly with brief, unsupervised capture by parents or lay workers; agreement with pneumatic otoscopy was low; and fewer than 20% of videos were diagnostically useful [<xref ref-type="bibr" rid="ref43">43</xref>]. However, structured instruction or simulation improved the performance of workers without hands-on training [<xref ref-type="bibr" rid="ref38">38</xref>,<xref ref-type="bibr" rid="ref39">39</xref>,<xref ref-type="bibr" rid="ref43">43</xref>]. Example of practical structured training can remain minimal, such as a 5- to 10-minute tutorial, a 1-page capture checklist, and brief hands-on coaching including cerumen management. Embedding a simple feedback loop on image quality further improves yield without adding substantial workload. Third, adjunct digital tools are promising: a smartphone-only acoustic method that infers tympanic membrane mobility detected MEE with the AUC approaching 0.90, whereas digital otoscopy platforms improved trainee-supervisor agreement and reduced duplicate examinations [<xref ref-type="bibr" rid="ref42">42</xref>,<xref ref-type="bibr" rid="ref53">53</xref>]. The contribution of this review is an implementation-facing synthesis that links &#x201C;which tool,&#x201D; &#x201C;which care model,&#x201D; and &#x201C;under what conditions&#x201D; to observed diagnostic performance, thereby informing scalable hybrid workflows.</p></sec><sec id="s4-2"><title>Interpretation and Implications</title><sec id="s4-2-1"><title>Diagnostic Performance and Care Models</title><p>When image acquisition was standardized and performed by trained facilitators, remote specialists and generalists demonstrated diagnostic agreement with in-person reference standards that are clinically feasible for triage and management in many settings [<xref ref-type="bibr" rid="ref29">29</xref>,<xref ref-type="bibr" rid="ref34">34</xref>,<xref ref-type="bibr" rid="ref36">36</xref>,<xref ref-type="bibr" rid="ref50">50</xref>]. Programs embedding store-and-forward video-otoscopy, tympanometry, and audiometry in school- and community-based screening have demonstrated high coverage, efficient specialist sorting, reduced wait times, and identified surgical candidates [<xref ref-type="bibr" rid="ref28">28</xref>,<xref ref-type="bibr" rid="ref31">31</xref>,<xref ref-type="bibr" rid="ref64">64</xref>]. In primary care, asynchronous tele-referral pathways allowed most cases to be managed without face-to-face review while offering timely specialist input and educational feedback to referrers [<xref ref-type="bibr" rid="ref50">50</xref>].</p><p>Simultaneously, telehealth visits performed without otoscopic visualization carry a risk of misclassification. In a pandemic-era cohort, children evaluated for RAOM via video-only visits were less likely to have effusion confirmed at the time of tympanostomy tube placement than office-based comparators (39% vs 79%), highlighting that history alone is insufficient for surgical decision-making [<xref ref-type="bibr" rid="ref52">52</xref>]. These findings support hybrid models&#x2014;telehistory plus rapid access to digital otoscopy (clinic kiosk, drive-through nurse station, and community facilitators) or validated home solutions&#x2014;especially when management depends on objective middle ear findings [<xref ref-type="bibr" rid="ref52">52</xref>,<xref ref-type="bibr" rid="ref54">54</xref>,<xref ref-type="bibr" rid="ref68">68</xref>].</p></sec><sec id="s4-2-2"><title>Operators, Training, and Human Factors</title><p>Evidence has consistently demonstrated that the person capturing the image is as critical as the device used. Across included studies, capture quality and diagnostic yield varied substantially by operator type, training intensity, child cooperation, and cerumen burden [<xref ref-type="bibr" rid="ref12">12</xref>,<xref ref-type="bibr" rid="ref39">39</xref>,<xref ref-type="bibr" rid="ref43">43</xref>]. Hands-on coaching and structured capture approaches were associated with higher proportions of interpretable recordings in parents and nonspecialists, whereas written-only or brief instruction yielded lower rates of diagnostically useful media in field settings [<xref ref-type="bibr" rid="ref12">12</xref>,<xref ref-type="bibr" rid="ref39">39</xref>,<xref ref-type="bibr" rid="ref43">43</xref>]. In simulation settings, trained facilitators using Otosim2 with the AudioProConnect platform maintained expert accuracy without time penalties [<xref ref-type="bibr" rid="ref38">38</xref>]. In clinical supervision settings, digital otoscopy improved trainee accuracy by approximately 11 percentage points and increased trainee-supervisor agreement from kappa 0.40 to 0.69, while reducing confirmatory reexaminations from ~98% to ~27% [<xref ref-type="bibr" rid="ref53">53</xref>]. A randomized comparison in pediatric emergency department demonstrated similar accuracy for smartphones versus conventional otoscopy (0.74 vs 0.69) but revealed lower confidence among inexperienced users, emphasizing the value of familiarization [<xref ref-type="bibr" rid="ref37">37</xref>]. Smartphone otoscopy may meaningfully affect clinical impressions. In a pediatric emergency department study, CellScope Oto altered the reported view in 12% to 16% of exams, with clinically relevant diagnostic changes in approximately 6%; notably, it was rated by clinicians as easy to use and valuable for teaching [<xref ref-type="bibr" rid="ref71">71</xref>].</p><p>Given the established effectiveness of video-otoscopy, careful consideration of the methods and timing of use may enable promising integration [<xref ref-type="bibr" rid="ref72">72</xref>]. Standardized training packages and minimum quality thresholds should be considered prerequisites for scaling, particularly for parents, community health workers, and very young children, in whom cooperation and ear canal size may complicate capture [<xref ref-type="bibr" rid="ref12">12</xref>,<xref ref-type="bibr" rid="ref39">39</xref>,<xref ref-type="bibr" rid="ref43">43</xref>].</p></sec><sec id="s4-2-3"><title>Adjunct Technologies and Artificial Intelligence&#x2013;Based Decision Support</title><p>Smartphone-only acoustic reflectometry with embedded machine learning demonstrated high accuracy for effusion detection and performed comparably across platforms and even in parents&#x2019; hands [<xref ref-type="bibr" rid="ref42">42</xref>]. This suggests a low-barrier screening pathway that does not depend on optical access, which is particularly valuable in toddlers with narrow ear canals or when video quality is suboptimal [<xref ref-type="bibr" rid="ref42">42</xref>,<xref ref-type="bibr" rid="ref43">43</xref>]. Early studies of automated image classification demonstrated throughput advantages, but clinical readiness remains limited due to scarce external validation across devices, sites, and pediatric populations and incomplete reporting of training datasets and labeling methods, which constrains generalizability and risk-of-bias assessment [<xref ref-type="bibr" rid="ref15">15</xref>,<xref ref-type="bibr" rid="ref16">16</xref>,<xref ref-type="bibr" rid="ref47">47</xref>]. Although numerous models were developed using artificial intelligence to classify middle ear diseases on the basis of tympanic membrane findings or short-wave infrared imaging, there were few studies addressing its actual clinical implementation [<xref ref-type="bibr" rid="ref15">15</xref>,<xref ref-type="bibr" rid="ref16">16</xref>,<xref ref-type="bibr" rid="ref73">73</xref>-<xref ref-type="bibr" rid="ref76">76</xref>]. It is therefore necessary to consider not only the accuracy of these models but also the optimal point and method of integration within the clinical workflow [<xref ref-type="bibr" rid="ref15">15</xref>,<xref ref-type="bibr" rid="ref47">47</xref>]. Most studies also provide limited information on deployment pathways, including regulatory considerations, governance for performance monitoring, and safeguards when image quality is insufficient, and direct comparisons with human experts under identical capture conditions remain uncommon [<xref ref-type="bibr" rid="ref15">15</xref>,<xref ref-type="bibr" rid="ref47">47</xref>]. Accordingly, priority next steps include multisite, device-agnostic external validation using real-world pediatric data and prospective evaluations of workflow-level impact and safety rather than reliance on curated test-set metrics alone. In parallel, self-management apps for OME demonstrated high acceptability and reasonable correlation with clinic audiometry, supporting family engagement and between-visit monitoring rather than diagnosis [<xref ref-type="bibr" rid="ref45">45</xref>].</p></sec><sec id="s4-2-4"><title>Safety, Stewardship, and Workflow</title><p>Across randomized and comparative studies, smartphone otoscopy did not increase AOM diagnosis or antibiotic prescription in emergency settings compared to conventional otoscopy, and in some trainee contexts, it was associated with fewer prescriptions, likely due to better shared visualization and supervision [<xref ref-type="bibr" rid="ref41">41</xref>,<xref ref-type="bibr" rid="ref53">53</xref>]. Programs that integrate remote reviews into perioperative pathways have demonstrated high postoperative success rates and measurable cost savings for families in remote regions [<xref ref-type="bibr" rid="ref32">32</xref>,<xref ref-type="bibr" rid="ref54">54</xref>]. Collectively, these findings support protocolized tele-otoscopy within antibiotic stewardship approaches and access pathways that do not rely exclusively on family-owned smartphones, such as facilitated capture in schools, community programs, and clinics [<xref ref-type="bibr" rid="ref28">28</xref>,<xref ref-type="bibr" rid="ref29">29</xref>,<xref ref-type="bibr" rid="ref34">34</xref>,<xref ref-type="bibr" rid="ref61">61</xref>,<xref ref-type="bibr" rid="ref64">64</xref>]. Additionally, remote hearing screening initiatives, when paired with follow-up during rehabilitation, may integrate synergistically with OM care, ultimately contributing to comprehensive pediatric ear health services [<xref ref-type="bibr" rid="ref64">64</xref>,<xref ref-type="bibr" rid="ref77">77</xref>-<xref ref-type="bibr" rid="ref79">79</xref>]. In this review, reporting on governance and medicolegal arrangements was uncommon, representing a gap in implementation evidence. Implementation should include explicit consent, minimum image quality thresholds with default to in-person examination when unmet, and red-flag escalation [<xref ref-type="bibr" rid="ref52">52</xref>,<xref ref-type="bibr" rid="ref58">58</xref>,<xref ref-type="bibr" rid="ref72">72</xref>]. Future studies should report on adverse events and medicolegal frameworks.</p></sec><sec id="s4-2-5"><title>Equity and Access</title><p>Tele-otoscopy is particularly valuable in indigenous and rural settings with few specialists, where school-based or outreach models led by local health workers can achieve over 80% screening coverage and facilitate timely surgical intervention [<xref ref-type="bibr" rid="ref28">28</xref>]. Jacups et al [<xref ref-type="bibr" rid="ref80">80</xref>] reported that the telehealth model was the most cost-effective method for providing ENT surgery to children living in remote regions, primarily by reducing patient travel. However, equity implications depend strongly on implementation design, including whether capture is facilitated and whether connectivity and device requirements are minimized [<xref ref-type="bibr" rid="ref28">28</xref>,<xref ref-type="bibr" rid="ref43">43</xref>,<xref ref-type="bibr" rid="ref50">50</xref>]. Not all low-burden mHealth interventions translate into short-term clinical improvements; for example, multimedia or text messaging alone did not increase clinic attendance or improve ear outcomes over 6 weeks in a high-risk remote population, despite good acceptability [<xref ref-type="bibr" rid="ref70">70</xref>]. Digital divide factors&#x2014;device availability, connectivity and bandwidth requirements, caregiver digital and health literacy, and accessibility beyond geography (including language support and cultural adaptation)&#x2014;were infrequently reported or measured systematically across included studies [<xref ref-type="bibr" rid="ref43">43</xref>,<xref ref-type="bibr" rid="ref50">50</xref>]. Age-related constraints are also salient in pediatrics, with lower capture quality reported in children under 24 months, which can shift burden onto caregivers when programs rely primarily on home capture [<xref ref-type="bibr" rid="ref43">43</xref>]. Care model choice has direct equity consequences. In lower-middle-income countries, implementation models pairing screening with video-otoscopy and electronic medical record capture can broaden the scope beyond hearing thresholds alone by identifying otologic pathology, even among children with normal hearing, while enabling structured follow-up workflows [<xref ref-type="bibr" rid="ref69">69</xref>]. Hub-based or facilitated capture workflows (community-hosted capture hubs or school programs) can reduce reliance on family-owned devices and high-bandwidth connections while enabling standardized training and explicit image quality thresholds [<xref ref-type="bibr" rid="ref28">28</xref>,<xref ref-type="bibr" rid="ref29">29</xref>,<xref ref-type="bibr" rid="ref34">34</xref>]. In contrast, home-based models can improve convenience but may disproportionately disadvantage families facing barriers in time, literacy, language, connectivity, or device access unless hardware and support are provisioned [<xref ref-type="bibr" rid="ref43">43</xref>,<xref ref-type="bibr" rid="ref68">68</xref>].</p><p>Therefore, equity-focused deployment should prioritize community-hosted capture hubs, offline-capable apps, and hardware provision [<xref ref-type="bibr" rid="ref28">28</xref>,<xref ref-type="bibr" rid="ref43">43</xref>,<xref ref-type="bibr" rid="ref50">50</xref>]. In pediatrics, careful consideration of caregivers&#x2019; role is essential, as their involvement can influence capture quality and follow-through [<xref ref-type="bibr" rid="ref12">12</xref>,<xref ref-type="bibr" rid="ref65">65</xref>]. Importantly, few included studies conducted formal health equity analyses or reported outcomes stratified by socioeconomic status, geography, or ethnicity, limiting conclusions on differential benefits across populations and underscoring the need for equity endpoints and subgroup reporting in future evaluations [<xref ref-type="bibr" rid="ref43">43</xref>,<xref ref-type="bibr" rid="ref50">50</xref>].</p></sec></sec><sec id="s4-3"><title>Limitations</title><p>This scoping review emphasized breadth rather than quantitative synthesis and therefore did not include a meta-analysis; however, we conducted a targeted QUADAS-2 appraisal for diagnostic accuracy studies. Limitations included the enrollment of mixed-age cohorts, lack of blinded reference standards, and the rapid evolution of device ecosystems, which may reduce the generalizability of device-specific findings. Additionally, language and publication restrictions may have led to the exclusion of relevant gray literature. Although we searched multiple bibliographic databases and used both controlled vocabulary and free-text terms, relevant studies may have been missed due to terminology variation across disciplines and incomplete indexing of emerging digital health tools. Future studies should prioritize large, multicenter evaluations that incorporate standardized blinded reference standards to strengthen diagnostic accuracy across diverse pediatric populations and care settings. External validation efforts must address varied device ecosystems and real-world image quality to ensure generalizability. Comparative research is warranted to establish the relative performance and cost-effectiveness of emerging digital otoscopy, acoustic, and decision support tools. This scoping review protocol was not prospectively registered. Core methodological decisions were defined a priori; minor refinements to screening guidance were made during pilot screening to improve consistency. Although scoping reviews do not always require registration, the absence of prospective registration may reduce transparency and should be considered when interpreting the findings. In addition, interpretation of diagnostic accuracy is constrained by substantial clinical and methodological heterogeneity across studies, which limits cross-setting comparability of &#x03BA;, sensitivity, and specificity. Equity-relevant reporting was uncommon, restricting conclusions on differential benefits across populations. Finally, while implementation outcomes were frequently described, most studies did not evaluate sustainability or scale-up using an explicit implementation framework, and evidence for long-term maintenance remains limited.</p></sec><sec id="s4-4"><title>Future Research Agenda</title><p>Based on mapped gaps across technologies, care models, and operators, priority research directions include (1) multisite pragmatic evaluations with standardized reporting of pediatric age strata, OM phenotype, reference standards, operator training content and competency, and explicit image quality thresholds; (2) comparative evaluation of hub-based facilitated capture versus home-based capture models, including equity-relevant endpoints and subgroup analyses; (3) workflow-focused outcomes beyond accuracy; (4) sustainability and scale-up studies using an implementation framework, including maintenance, governance, and medicolegal arrangements; and (5) for artificial intelligence&#x2013;enabled tools, external validation across devices or sites with real-world image quality, transparent dataset description, and prospective evaluation of clinical impact within the care pathway rather than standalone discrimination metrics.</p></sec><sec id="s4-5"><title>Conclusions</title><p>Telehealth for pediatric OM now spans mature technologies and care models. Store-and-forward tele-otoscopy is feasible and, with standardized image capture and brief structured training, can approach in-person diagnostic performance. Implementation quality requires predefined image quality thresholds and a default to in-person care when those thresholds are not met. It also requires integration into hybrid workflows and basic governance covering consent, documentation, and data protection. Programs should ensure equitable access, especially in resource-limited settings. Video-only encounters without otoscopic imaging are inadequate when decisions require objective middle ear findings. Key evidence gaps include multicenter child-level outcomes, economic evaluations&#x2014;particularly in low- and middle-income countries&#x2014;and external validation of artificial intelligence&#x2013;based diagnostic tools across devices and sites. These priorities should guide the next phase of research and scale-up.</p></sec></sec></body><back><ack><p>This work was undertaken as part of the activities of the Domestic Scientific Committee of the Japanese Society of Pediatric Otorhinolaryngology. We would like to thank Editage (www.editage.com) for English language editing. The authors are involved in a research project supported by the Japan Science and Technology Agency (JST) under the COI-NEXT (Collaborative Creation of New Social Systems) Program (Grant Number JPMJPF2403). However, this specific study did not receive direct financial support from that grant.</p><p>Disclosure of delegation to generative artificial intelligence (GenAI): The authors declare the use of GenAI in the research and writing process. According to the GAIDeT taxonomy (2025), the following tasks were delegated to GenAI tools under full human supervision: proofreading and editing and translation. The GenAI tool used was ChatGPT-5.2. Responsibility for the final manuscript lies entirely with the authors. GenAI tools are not listed as authors and do not bear responsibility for the final outcomes. Declaration submitted by Corresponding Author. In accordance with the GAIDeT taxonomy, GenAI tools were used solely for reformatting and limited language editing tasks under full human supervision.</p></ack><notes><sec><title>Funding</title><p>This study did not receive any specific grant from funding agencies in the public, commercial, or not-for-profit sectors.</p></sec><sec><title>Data Availability</title><p>All data underlying this scoping review were derived from published studies cited in the Reference list. The study-level data extraction table and the QUADAS-2 assessments for diagnostic accuracy studies are provided in the supplementary materials (<xref ref-type="supplementary-material" rid="app2">Multimedia Appendix 2</xref>, <xref ref-type="supplementary-material" rid="app3">Multimedia Appendix 3</xref>, and <xref ref-type="supplementary-material" rid="app4">Multimedia Appendix 4</xref>. Additional materials (the data charting form/codebook and analytic files used to generate summary tables/figures) are available from the corresponding author upon reasonable request.</p></sec></notes><fn-group><fn fn-type="con"><p>Conceptualization: MN, RA</p><p>Data curation: MN, RA</p><p>Formal analysis: MN, RA</p><p>Investigation: RA, MN, MH</p><p>Methodology: MN, RA, MH</p><p>Project administration: MN, RA</p><p>Supervision: HY, HF, YT, MI</p><p>Validation: RA, MN, MH</p><p>Visualization: MN, RA</p><p>Writing &#x2013; original draft: MN, RA</p><p>Writing &#x2013; review &#x0026; editing: MN, RA, MH, CS, RK, HY, YM, HF, YT, MI</p></fn><fn fn-type="conflict"><p>None declared.</p></fn></fn-group><glossary><title>Abbreviations</title><def-list><def-item><term id="abb1">AOM</term><def><p>acute otitis media</p></def></def-item><def-item><term id="abb2">AUC</term><def><p>area under the receiver operating characteristic curve</p></def></def-item><def-item><term id="abb3">CSOM</term><def><p>chronic suppurative otitis media</p></def></def-item><def-item><term id="abb4">DenseNet</term><def><p>Dense Convolutional Network</p></def></def-item><def-item><term id="abb5">ENT</term><def><p>ear, nose, and throat</p></def></def-item><def-item><term id="abb6">JBI</term><def><p>Joanna Briggs Institute</p></def></def-item><def-item><term id="abb7">MEE</term><def><p>middle ear effusion</p></def></def-item><def-item><term id="abb8">mHealth</term><def><p>mobile health</p></def></def-item><def-item><term id="abb9">OM</term><def><p>otitis media</p></def></def-item><def-item><term id="abb10">OME</term><def><p>otitis media with effusion</p></def></def-item><def-item><term id="abb11">PCC</term><def><p>population, concept, and context</p></def></def-item><def-item><term id="abb12">PRISMA-S</term><def><p>an extension to the PRISMA Statement for Reporting Literature Searches in Systematic Reviews</p></def></def-item><def-item><term id="abb13">PRISMA-ScR</term><def><p>Preferred Reporting Items for Systematic Reviews and Meta-Analyses extension for Scoping Reviews</p></def></def-item><def-item><term id="abb14">QUADAS-2</term><def><p>revised Quality Assessment of Diagnostic Accuracy Studies tool</p></def></def-item><def-item><term id="abb15">RAOM</term><def><p>recurrent acute otitis media</p></def></def-item><def-item><term id="abb16">RE-AIM</term><def><p>reach, effectiveness, adoption, implementation, and maintenance</p></def></def-item><def-item><term id="abb17">ROC</term><def><p>receiver operating characteristic</p></def></def-item></def-list></glossary><ref-list><title>References</title><ref id="ref1"><label>1</label><nlm-citation citation-type="journal"><person-group person-group-type="author"><name name-style="western"><surname>Bajwa</surname><given-names>NM</given-names> </name><name name-style="western"><surname>Perron</surname><given-names>NJ</given-names> </name><name name-style="western"><surname>Braillard</surname><given-names>O</given-names> </name><etal/></person-group><article-title>Has telemedicine come to fruition? 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pub-id-type="medline">30311714</pub-id></nlm-citation></ref></ref-list><app-group><supplementary-material id="app1"><label>Multimedia Appendix 1</label><p>Full search strategies for this scoping review.</p><media xlink:href="jmir_v28i1e85416_app1.docx" xlink:title="DOCX File, 18 KB"/></supplementary-material><supplementary-material id="app2"><label>Multimedia Appendix 2</label><p>Study-level characteristics and data charting for included studies (N=52). This appendix presents the data extraction (data charting) table for all included studies in this scoping review. Variables include study design and setting, country, participant characteristics (pediatric population), otitis media phenotype, telehealth care model (asynchronous/synchronous/hybrid), device or technology category, operator or capture and interpretation workflow, training and image quality considerations, outcome domains reported, and funding or conflict of interest statements where available.</p><media xlink:href="jmir_v28i1e85416_app2.xlsx" xlink:title="XLSX File, 50 KB"/></supplementary-material><supplementary-material id="app3"><label>Multimedia Appendix 3</label><p>RE-AIM mapping of implementation-related outcomes and reporting gaps. This appendix summarizes implementation-relevant constructs using the Reach, Effectiveness, Adoption, Implementation, and Maintenance (RE-AIM) framework across included studies. The table highlights commonly reported elements and underreported domains to inform future research and reporting in telehealth-supported pediatric otitis media care.</p><media xlink:href="jmir_v28i1e85416_app3.xlsx" xlink:title="XLSX File, 10 KB"/></supplementary-material><supplementary-material id="app4"><label>Multimedia Appendix 4</label><p>Revised Quality Assessment of Diagnostic Accuracy Studies (QUADAS-2). This appendix reports the QUADAS-2 risk of bias and applicability assessments for the subset of included studies that evaluated diagnostic accuracy. Judgments are provided across QUADAS-2 domains (patient selection, index test, reference standard, flow and timing) and applicability domains (patient selection, index test, reference standard), with signaling questions and domain-level ratings.</p><media xlink:href="jmir_v28i1e85416_app4.xlsx" xlink:title="XLSX File, 12 KB"/></supplementary-material><supplementary-material id="app5"><label>Checklist 1</label><p>PRISMA-ScR checklist.</p><media xlink:href="jmir_v28i1e85416_app5.pdf" xlink:title="PDF File, 134 KB"/></supplementary-material></app-group></back></article>