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<front>
<journal-meta>
<journal-id journal-id-type="publisher-id">Front. Med.</journal-id>
<journal-title-group>
<journal-title>Frontiers in Medicine</journal-title>
<abbrev-journal-title abbrev-type="pubmed">Front. Med.</abbrev-journal-title>
</journal-title-group>
<issn pub-type="epub">2296-858X</issn>
<publisher>
<publisher-name>Frontiers Media S.A.</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id pub-id-type="doi">10.3389/fmed.2026.1730188</article-id>
<article-version article-version-type="Version of Record" vocab="NISO-RP-8-2008"/>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Systematic Review</subject>
</subj-group>
</article-categories>
<title-group>
<article-title>The efficacy of transcutaneous electrical acupoint stimulation on postoperative nausea and vomiting after laparoscopic surgery: a meta-analysis of randomized controlled trials</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author" equal-contrib="yes">
<name><surname>Qin</surname> <given-names>Sifan</given-names></name>
<xref ref-type="aff" rid="aff1"><sup>1</sup></xref>
<xref ref-type="author-notes" rid="fn001"><sup>&#x02020;</sup></xref>
<xref ref-type="author-notes" rid="fn002"><sup>&#x02021;</sup></xref>
<role vocab="credit" vocab-identifier="https://credit.niso.org/" vocab-term="Data curation" vocab-term-identifier="https://credit.niso.org/contributor-roles/data-curation/">Data curation</role>
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</contrib>
<contrib contrib-type="author" equal-contrib="yes">
<name><surname>Liu</surname> <given-names>Jiang</given-names></name>
<xref ref-type="aff" rid="aff1"><sup>1</sup></xref>
<xref ref-type="author-notes" rid="fn001"><sup>&#x02020;</sup></xref>
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</contrib>
<contrib contrib-type="author" equal-contrib="yes">
<name><surname>He</surname> <given-names>Jinfang</given-names></name>
<xref ref-type="aff" rid="aff2"><sup>2</sup></xref>
<xref ref-type="author-notes" rid="fn001"><sup>&#x02020;</sup></xref>
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</contrib>
<contrib contrib-type="author" equal-contrib="yes">
<name><surname>Liu</surname> <given-names>Yun</given-names></name>
<xref ref-type="aff" rid="aff1"><sup>1</sup></xref>
<xref ref-type="author-notes" rid="fn001"><sup>&#x02020;</sup></xref>
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<contrib contrib-type="author">
<name><surname>Liu</surname> <given-names>Jing</given-names></name>
<xref ref-type="aff" rid="aff2"><sup>2</sup></xref>
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</contrib>
<contrib contrib-type="author">
<name><surname>Wang</surname> <given-names>Liwei</given-names></name>
<xref ref-type="aff" rid="aff1"><sup>1</sup></xref>
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</contrib>
<contrib contrib-type="author" corresp="yes">
<name><surname>Fang</surname> <given-names>Shirong</given-names></name>
<xref ref-type="aff" rid="aff2"><sup>2</sup></xref>
<xref ref-type="corresp" rid="c001"><sup>&#x0002A;</sup></xref>
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<uri xlink:href="https://loop.frontiersin.org/people/2696343"/>
</contrib>
</contrib-group>
<aff id="aff1"><label>1</label><institution>Shandong Second Medical University</institution>, <city>Shandong</city>, <country country="cn">China</country></aff>
<aff id="aff2"><label>2</label><institution>Weifang People&#x00027;s Hospital</institution>, <city>Shandong</city>, <country country="cn">China</country></aff>
<author-notes>
<corresp id="c001"><label>&#x0002A;</label>Correspondence: Shirong Fang, <email xlink:href="mailto:fsr0536@163.com">fsr0536@163.com</email></corresp>
<fn fn-type="equal" id="fn001"><label>&#x02020;</label><p>These authors have contributed equally to this work</p></fn>
<fn fn-type="other" id="fn002"><label>&#x02021;</label><p>ORCID: Sifan Qin <uri xlink:href="https://orcid.org/0000-0002-7762-2815">orcid.org/0000-0002-7762-2815</uri>; Shirong Fang <uri xlink:href="https://orcid.org/0009-0001-6559-1724">orcid.org/0009-0001-6559-1724</uri></p></fn>
</author-notes>
<pub-date publication-format="electronic" date-type="pub" iso-8601-date="2026-03-03">
<day>03</day>
<month>03</month>
<year>2026</year>
</pub-date>
<pub-date publication-format="electronic" date-type="collection">
<year>2026</year>
</pub-date>
<volume>13</volume>
<elocation-id>1730188</elocation-id>
<history>
<date date-type="received">
<day>22</day>
<month>10</month>
<year>2025</year>
</date>
<date date-type="rev-recd">
<day>13</day>
<month>01</month>
<year>2026</year>
</date>
<date date-type="accepted">
<day>19</day>
<month>01</month>
<year>2026</year>
</date>
</history>
<permissions>
<copyright-statement>Copyright &#x000A9; 2026 Qin, Liu, He, Liu, Liu, Wang and Fang.</copyright-statement>
<copyright-year>2026</copyright-year>
<copyright-holder>Qin, Liu, He, Liu, Liu, Wang and Fang</copyright-holder>
<license>
<ali:license_ref start_date="2026-03-03">https://creativecommons.org/licenses/by/4.0/</ali:license_ref>
<license-p>This is an open-access article distributed under the terms of the <ext-link ext-link-type="uri" xlink:href="https://creativecommons.org/licenses/by/4.0/">Creative Commons Attribution License (CC BY)</ext-link>. The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.</license-p>
</license>
</permissions>
<abstract>
<sec>
<title>Background</title>
<p>Postoperative nausea and vomiting (PONV) is a common complication after laparoscopic surgery, which may cause fluid and electrolyte imbalance and delay postoperative recovery. Pharmacological interventions are only partially effective and have adverse effects. This study aimed to systematically evaluate the efficacy of transcutaneous electrical acupoint stimulation (TEAS) in managing PONV after laparoscopic surgery.</p></sec>
<sec>
<title>Methods</title>
<p>We systematically review Cochrane Library, PubMed, Embase and Web of Science for randomized controlled trials (RCTs). Two investigators independently conducted study selection, data extraction, and bias assessment using the Cochrane Risk of Bias Tool. Meta-analyses were performed in RevMan 5.4 and heterogeneity was assessed using <italic>I</italic><sup>2</sup>. Outcomes included PONV, postoperative nausea (PON), postoperative vomiting (POV), time to first flatus, and antiemetic rescue requirements.</p></sec>
<sec>
<title>Results</title>
<p>Nine RCTs involving 2,550 participants (1,272 in the TEAS group and 1,278 in the control group) were analyzed. TEAS significantly reduced PONV incidence [<italic>RR</italic> = 0.78, 95% CI (0.70, 0.87); <italic>P</italic> &#x0003C; 0.001], PON incidence [<italic>RR</italic> = 0.69, 95% CI (0.67, 0.82); <italic>P</italic> &#x0003C; 0.001] and POV incidence [<italic>RR</italic> = 0.57, 95% CI (0.43&#x02013;0.78); <italic>P</italic> &#x0003C; 0.001]. The intervention shortened the time to first flatus after surgery [MD &#x0003D; &#x02212;3.36 h, 95% CI (&#x02212;6.65, &#x02212;0.21); <italic>P</italic> = 0.04] and decreased the use for antiemetic rescue medication [<italic>RR</italic> = 0.67, 95% CI (0.52, 0.87); <italic>P</italic> = 0.002].</p></sec>
<sec>
<title>Conclusions</title>
<p>Our findings suggest that TEAS may be an effective adjunctive non-pharmacological treatment for PONV in patients undergoing laparoscopic surgery. When used in combination with standard antiemetic prophylaxis, TEAS can further reduce the incidence of nausea and vomiting, decrease the need for rescue antiemetics, and shorten the time to first flatus, thereby demonstrating significant added value in facilitating postoperative recovery.</p></sec>
<sec>
<title>Systematic Review Registration</title>
<p>identifier [CRD42024560238].</p></sec></abstract>
<kwd-group>
<kwd>laparoscopic surgery</kwd>
<kwd>meta-analysis</kwd>
<kwd>PONV</kwd>
<kwd>postoperative nausea and vomiting</kwd>
<kwd>teas</kwd>
<kwd>transcutaneous electrical acupoint stimulation</kwd>
</kwd-group>
<funding-group>
<funding-statement>The author(s) declared that financial support was not received for this work and/or its publication.</funding-statement>
</funding-group>
<counts>
<fig-count count="6"/>
<table-count count="1"/>
<equation-count count="0"/>
<ref-count count="41"/>
<page-count count="11"/>
<word-count count="6831"/>
</counts>
<custom-meta-group>
<custom-meta>
<meta-name>section-at-acceptance</meta-name>
<meta-value>Gastroenterology</meta-value>
</custom-meta>
</custom-meta-group>
</article-meta>
</front>
<body>
<sec sec-type="introduction" id="s1">
<title>Introduction</title>
<p>PONV is one of the common complications after surgery, and the incidence of PONV is approximately 20%&#x02212;30% after general surgery and up to 60%&#x02212;80% in high-risk individuals (<xref ref-type="bibr" rid="B1">1</xref>, <xref ref-type="bibr" rid="B2">2</xref>). PONV can lead to electrolyte imbalance, aspiration pneumonia and increased intracranial pressure. It may also prolong the length of hospital stay and increase the economic burden (<xref ref-type="bibr" rid="B3">3</xref>, <xref ref-type="bibr" rid="B4">4</xref>). Despite the application of antiemetic medications and various novel therapies in recent years, these medications are only partially effective (<xref ref-type="bibr" rid="B5">5</xref>&#x02013;<xref ref-type="bibr" rid="B7">7</xref>). Thus, PONV remains an important problem in the perioperative period.</p>
<p>Laparoscopic surgery has gained widespread clinical adoption due to its minimally invasive nature and rapid postoperative recovery. However, the procedure often necessitates pneumoperitoneum, which increases intra-abdominal pressure and may induce gastroesophageal reflux. Elevated intra-abdominal pressure may also stimulate the vagus nerve, thereby activating the vomiting center (<xref ref-type="bibr" rid="B8">8</xref>). Many antiemetic medications have been used to prevent PONV after surgery including 5-hydroxytryptamine-3 (5-HT3) receptor antagonists, neurokinin-1 (NK-1) inhibitors and dopamine receptor antagonists (<xref ref-type="bibr" rid="B9">9</xref>). In Western medicine, the primary mechanism is that opioids inhibit gastrointestinal motility through excitation of &#x003BC; receptors in the central and gastrointestinal tract, resulting in decreased intestinal motility (<xref ref-type="bibr" rid="B10">10</xref>). However, monotherapy has certain limitations, and some patients with simple application of antiemetic medications still have unbearable PONV. Studies have shown that the failure rate of treatment with conventional antiemetic medications among obese patients can be as high as 45% (<xref ref-type="bibr" rid="B11">11</xref>, <xref ref-type="bibr" rid="B12">12</xref>). The incidence rate of PONV is still around 20% in high-risk patients treated with a combination of dexamethasone and ondansetro (<xref ref-type="bibr" rid="B13">13</xref>). Due to the limitations of drug therapy for PONV, it is imperative to explore more non-pharmacological approaches to prevent PONV.</p>
<p>TEAS is a non-invasive treatment method derived from traditional Chinese acupuncture, in which electrodes are placed on acupoints to deliver electrical stimulation that induces the <italic>de qi</italic> sensation. It combines effects of peripheral nerve stimulation with the therapeutic principles of acupuncture (<xref ref-type="bibr" rid="B14">14</xref>). TEAS, based on traditional Chinese medicine acupuncture theory, has the advantages of non-invasion, convenient operation, few side effects and significant therapeutic effects. The mechanism by which TEAS can alleviate PONV may be by regulating autonomic homeostasis, correcting autonomic dysfunction, inhibiting catecholamine release and reducing gastrointestinal oedema (<xref ref-type="bibr" rid="B15">15</xref>). In addition, we selected the intervention was TEAS and excluded electro acupuncture (EA) because EA uses acupuncture, whereas TEAS uses electrode patches, which may affect the accuracy and robustness of the results.</p>
<p>There have been meta-analyses confirming the effectiveness of TEAS on nausea and vomiting after abdominal surgery under general anesthesia (<xref ref-type="bibr" rid="B16">16</xref>, <xref ref-type="bibr" rid="B17">17</xref>). However, studies focused specifically on laparoscopic surgery have yielded conflicting results (<xref ref-type="bibr" rid="B16">16</xref>, <xref ref-type="bibr" rid="B18">18</xref>), and there remains a lack of strong, up-to-date clinical evidence. Furthermore, previous reviews have often overlooked a critical analysis of the TEAS intervention parameters (e.g., time, frequency, intensity) and have not consistently evaluated TEAS as an adjunctive therapy to modern antiemetic protocols. Therefore, we conducted this updated systematic review and meta-analysis to assess the adjunctive effectiveness of TEAS in preventing PONV after laparoscopic surgery and to summarize the characteristics of the intervention protocols used. Therefore, we systematically searched for published articles, conducted a systematic review of the evidence, and performed meta-analysis to assess the effectiveness of TEAS in preventing PONV after general anesthesia.</p></sec>
<sec sec-type="materials|methods" id="s2">
<title>Materials and methods</title>
<sec>
<title>Search strategy</title>
<p>We systematically searched the following databases from their inception to October 31, 2025: PubMed, Embase, the Cochrane Library, and Web of Science. Search each database using a combination of subject terms and free words, and link search terms using Boolean logic operators. The search was re-run prior to the final analysis to include any new relevant studies. Search each database using a combination of subject terms and free words, and link search terms using Boolean logic operators. The search terms included: (&#x0201C;TEAS&#x0201D; OR &#x0201C;EA&#x0201D; OR &#x0201C;TEAS&#x0201D;) AND (&#x0201C;laparoscopic surgery&#x0201D; OR &#x0201C;laparoscopy&#x0201D;) AND (&#x0201C;PONV&#x0201D; OR &#x0201C;nausea&#x0201D; OR &#x0201C;vomiting&#x0201D; OR &#x0201C;PONV&#x0201D;). The full search details are in <xref ref-type="supplementary-material" rid="SM1">Supplementary Table S1</xref>.</p></sec>
<sec>
<title>Eligible criteria</title>
<p>We included studies based on the following PICOS framework:</p>
<list list-type="bullet">
<list-item><p>P (Population): adult patients undergoing any type of laparoscopic surgery under general anesthesia.</p></list-item>
<list-item><p>I (Intervention): TEAS applied at any acupoint, regardless of stimulation parameters (frequency, intensity, duration).</p></list-item>
<list-item><p>C (Comparator): sham TEAS (placebo stimulation at the same acupoints or different locations) or no TEAS intervention. In both cases, the control group could receive the same standard pharmacological antiemetic prophylaxis as the intervention group.</p></list-item>
<list-item><p>(Outcomes): at least one of the following outcomes must have been reported: incidence of PONV, PON, POV, need for rescue antiemetics, or time to first flatus.</p></list-item>
<list-item><p>S (Study design): RCTs.</p></list-item>
</list>
<p>Exclusion criteria were: (1) non-RCTs such as case reports, reviews, or observational studies; (2) studies involving EA (with needles) or other forms of acupoint stimulation; (3) animal experiments; and (4) studies from which relevant data could not be extracted.</p></sec>
<sec>
<title>Quality assessment</title>
<p>Two researchers independently evaluated the methodological qualities using the Cochrane bias risk tool based on the following criteria: random sequence generation, allocation concealment, blinding of participants and personnel, blinding of outcome assessment, incomplete outcome and selective reporting. The risk was classified as unclear, low, or high. Any disagreements were resolved through discussion or consultation with a third author. We chose the Cochrane tool as it is the standard for assessing risk of bias in randomized trials for systematic reviews of interventions.</p></sec>
<sec>
<title>Data extraction</title>
<p>Retrieved articles were screened by two reviewers independently. Literature that met the criteria was read in full. The two reviewers then independently extracted the following information using a pre-designed standardized data extraction form: author name, publication year, sample size, age, type of surgery, intervention measures (including TEAS parameters), control measures, and target outcomes. Data were cross-checked for accuracy, with discrepancies resolved by consensus.</p></sec>
<sec>
<title>Statistical analysis</title>
<p>Statistical analyses were carried out using RevMan 5.4 (RevMan, the Cochrane Collaboration, Oxford, United Kingdom) software. Dichotomous and continuous variables were represented by risk ratio (RR) and mean difference (MD), respectively, with 95% confidence interval (CI). Significant heterogeneity was considered when <italic>I</italic><sup>2</sup> &#x0003E; 50% and <italic>P</italic> &#x0003C; 0.1, and a random-effects model was used for analysis (<xref ref-type="bibr" rid="B19">19</xref>). Otherwise, a fixed-effects model was used. To evaluate result consistency and discern heterogeneity determinants, we performed successive sensitivity tests through cyclic elimination of single studies from the analytical cohort. Heterogeneity was assessed using the Chi-squared test and the <italic>I</italic><sup>2</sup> statistic. Significant heterogeneity was considered when <italic>I</italic><sup>2</sup> &#x0003E; 50% and <italic>P</italic> &#x0003C; 0.1, and a random-effects model was used for analysis. Otherwise, a fixed-effects model was used. To evaluate result consistency and discern heterogeneity determinants, we performed successive sensitivity tests through the leave-one-out method, cyclically eliminating single studies from the analytical cohort. Subgroup analyses were pre-specified to explore potential sources of heterogeneity, such as the type of surgery.</p></sec></sec>
<sec sec-type="results" id="s3">
<title>Results</title>
<sec>
<title>Literature search</title>
<p>Based on the search strategy, we identified 276 potential relevant studies in initial search. After reviewing titles and abstracts and removing duplicates, 120 records were ultimately excluded. A total of 156 full-text articles were selected for the secondary screening phase. Finally, nine studies were included in this meta-analysis (<xref ref-type="bibr" rid="B2">2</xref>, <xref ref-type="bibr" rid="B20">20</xref>&#x02013;<xref ref-type="bibr" rid="B27">27</xref>). The flow diagram of the study selection is shown in <xref ref-type="fig" rid="F1">Figure 1</xref>.</p>
<fig position="float" id="F1">
<label>Figure 1</label>
<caption><p>Flow diagram of the literature search.</p></caption>
<graphic mimetype="image" mime-subtype="tiff" xlink:href="fmed-13-1730188-g0001.tif">
<alt-text content-type="machine-generated">Flowchart depicting a meta-analysis process. Starting with 276 records identified through database searching, 30 duplicates are removed, leaving 246 records. Of those, 156 full-text articles are assessed for eligibility. Exclusions include literature reviews, case reports, animal studies, and protocol issues, as well as reasons such as full texts not found, inappropriate population, non-randomized controlled trials, non-electroacupuncture studies, use of antiemetic drugs, and other surgery types. The analysis finally includes 9 studies.</alt-text>
</graphic>
</fig></sec>
<sec>
<title>Study characteristics</title>
<p>The nine articles included in this meta-analysis were published in 2015&#x02013;2025. The observation group received TEAS in nine articles, while the control group received sham TEAS in eight papers and no TEAS in one paper. In the Sham TEAS group, the patients were connected to the same acupoints, but electronic stimulation was not applied. Nine studies involved 2,550 participants, including 1,272 patients received TEAS and 1,278 patients received sham TEAS or no TEAS. The sample sizes varying from 62 to 1,655 participants. The surgical types were gynecological laparoscopic surgery, laparoscopic non-gastrointestinal surgery, laparoscopic radical gastrectomy, laparoscopic sleeve gastrectomy. <xref ref-type="table" rid="T1">Table 1</xref> shows the characteristics of the included article.</p>
<table-wrap position="float" id="T1">
<label>Table 1</label>
<caption><p>Features of the included studies.</p></caption>
<table frame="box" rules="all">
<thead>
<tr>
<th valign="top" align="left"><bold>Reference</bold></th>
<th valign="top" align="left"><bold>Sample size (T/C)</bold></th>
<th valign="top" align="left"><bold>Age year (T/C)</bold></th>
<th valign="top" align="left"><bold>Types of surgery</bold></th>
<th valign="top" align="left"><bold>TEAS group</bold></th>
<th valign="top" align="left"><bold>Control group</bold></th>
<th valign="top" align="left"><bold>Acupoints</bold></th>
<th valign="top" align="left"><bold>Target outcomes</bold></th>
<th valign="top" align="left"><bold>Waveform</bold></th>
<th valign="top" align="left"><bold>Frequency (Hz)</bold></th>
<th valign="top" align="left"><bold>Current intensity (mA)</bold></th>
<th valign="top" align="left"><bold>Single session duration (min)</bold></th>
<th valign="top" align="left"><bold>Intervention frequency</bold></th>
</tr>
</thead>
<tbody>
<tr>
<td valign="top" align="left">Gao et al. (<xref ref-type="bibr" rid="B2">2</xref>), 2022</td>
<td valign="top" align="left">1,655 (827/828)</td>
<td valign="top" align="left">39.0 (31.0, 46.0) 39.0 (31.0, 46.0)</td>
<td valign="top" align="left">Laparoscopic non-gastrointestinal surgery</td>
<td valign="top" align="left">TEAS &#x0002B; 5 mg dexamethasone &#x0002B; 0.075 mg palonosetron</td>
<td valign="top" align="left">Sham TEAS &#x0002B; 5 mg dexamethasone &#x0002B; 0.075 mg palonosetron</td>
<td valign="top" align="left">PC6, ST36</td>
<td valign="top" align="left">1, 3</td>
<td valign="top" align="left">Dense&#x02013;disperse wave</td>
<td valign="top" align="left">2/100</td>
<td valign="top" align="left">Adjusted to patient tolerance (not specified)</td>
<td valign="top" align="left">30</td>
<td valign="top" align="left">Once before anesthesia induction</td>
</tr>
<tr>
<td valign="top" align="left">Qin et al. (<xref ref-type="bibr" rid="B25">25</xref>), 2023</td>
<td valign="top" align="left">162 (81/81)</td>
<td valign="top" align="left">45 &#x000B1; 7.45 45 &#x000B1; 5.92</td>
<td valign="top" align="left">GLS</td>
<td valign="top" align="left">TEAS &#x0002B; 4 mg dexamethasone &#x0002B; 0.25 mg palonosetron</td>
<td valign="top" align="left">Sham TEAS &#x0002B; 4 mg dexamethasone &#x0002B; 0.25 mg palonosetron</td>
<td valign="top" align="left">PC6, LI4</td>
<td valign="top" align="left">2, 3, 5</td>
<td valign="top" align="left">Dense&#x02013;disperse wave</td>
<td valign="top" align="left">2/100</td>
<td valign="top" align="left">Adjusted to patient tolerance (5&#x02013;12 mA)</td>
<td valign="top" align="left">30</td>
<td valign="top" align="left">Once before anesthesia induction</td>
</tr>
<tr>
<td valign="top" align="left">Xiong et al. (<xref ref-type="bibr" rid="B23">23</xref>), 2021</td>
<td valign="top" align="left">62 (31/31)</td>
<td valign="top" align="left">27.5 &#x000B1; 8.0 27.3 &#x000B1; 8.3</td>
<td valign="top" align="left">LSG</td>
<td valign="top" align="left">TEAS &#x0002B; 10 mg dexamethasone &#x0002B; 4 mg tropisetron</td>
<td valign="top" align="left">Sham TEAS &#x0002B; 10 mg dexamethasone &#x0002B; 4 mg tropisetron</td>
<td valign="top" align="left">PC6, ST36</td>
<td valign="top" align="left">2, 3, 4</td>
<td valign="top" align="left">Dense&#x02013;disperse wave</td>
<td valign="top" align="left">2/100</td>
<td valign="top" align="left">Adjusted to patient tolerance (not specified)</td>
<td valign="top" align="left">30</td>
<td valign="top" align="left">Once before anesthesia induction and continued intraoperatively</td>
</tr>
<tr>
<td valign="top" align="left">Zeng et al. (<xref ref-type="bibr" rid="B24">24</xref>), 2023</td>
<td valign="top" align="left">94 (47/47)</td>
<td valign="top" align="left">30.5 &#x000B1; 7.8 30.3 &#x000B1; 6.8</td>
<td valign="top" align="left">LSG</td>
<td valign="top" align="left">TEAS &#x0002B; 5 mg dexamethasone &#x0002B; 3 mg granisetron</td>
<td valign="top" align="left">Sham TEAS &#x0002B; 5 mg dexamethasone &#x0002B; 3 mg granisetron</td>
<td valign="top" align="left">PC6, LI4</td>
<td valign="top" align="left">1, 4, 5</td>
<td valign="top" align="left">Dense&#x02013;disperse wave</td>
<td valign="top" align="left">5/100</td>
<td valign="top" align="left">Adjusted to patient tolerance (not specified)</td>
<td valign="top" align="left">20</td>
<td valign="top" align="left">Once before anesthesia induction</td>
</tr>
<tr>
<td valign="top" align="left">Yan et al. (<xref ref-type="bibr" rid="B26">26</xref>), 2023</td>
<td valign="top" align="left">184 (91/93)</td>
<td valign="top" align="left">41.9 &#x000B1; 12.4 43.6 &#x000B1; 9.9</td>
<td valign="top" align="left">GLS</td>
<td valign="top" align="left">TEAS &#x0002B; 8 mg ondansetron</td>
<td valign="top" align="left">Sham TEAS &#x0002B; 8 mg ondansetron</td>
<td valign="top" align="left">LI4, PC6, ST36, SP6</td>
<td valign="top" align="left">1, 2, 3</td>
<td valign="top" align="left">Dense&#x02013;disperse wave</td>
<td valign="top" align="left">2/100</td>
<td valign="top" align="left">Adjusted to patient tolerance (not specified)</td>
<td valign="top" align="left">30</td>
<td valign="top" align="left">Once before anesthesia induction</td>
</tr>
<tr>
<td valign="top" align="left">Gu et al. (<xref ref-type="bibr" rid="B22">22</xref>),2019</td>
<td valign="top" align="left">117 (58/59)</td>
<td valign="top" align="left">57.59 &#x000B1; 7.32 56.67 &#x000B1; 6.23</td>
<td valign="top" align="left">LRG</td>
<td valign="top" align="left">TEAS &#x0002B; 0.25 mg palonosetron</td>
<td valign="top" align="left">Sham TEAS &#x0002B; 0.25 mg palonosetron</td>
<td valign="top" align="left">PC6, ST36</td>
<td valign="top" align="left">1, 5</td>
<td valign="top" align="left">Dense&#x02013;disperse wave</td>
<td valign="top" align="left">2/100</td>
<td valign="top" align="left">Adjusted to patient tolerance (5&#x02013;30 mA)</td>
<td valign="top" align="left">30</td>
<td valign="top" align="left">Once before anesthesia induction and three times a day every day for postoperative 2 day</td>
</tr>
<tr>
<td valign="top" align="left">Yang et al. (<xref ref-type="bibr" rid="B20">20</xref>), 2015</td>
<td valign="top" align="left">100 (50/50)</td>
<td valign="top" align="left">37 (24&#x02013;60) 35 (22&#x02013;60)</td>
<td valign="top" align="left">GLS</td>
<td valign="top" align="left">TEAS &#x0002B; dexamethasone</td>
<td valign="top" align="left">Dexamethasone</td>
<td valign="top" align="left">PC6</td>
<td valign="top" align="left">1, 4, 5</td>
<td valign="top" align="left">Dense&#x02013;disperse wave</td>
<td valign="top" align="left">2/100</td>
<td valign="top" align="left">Adjusted to patient tolerance (6- 20 mA)</td>
<td valign="top" align="left">30</td>
<td valign="top" align="left">Once before anesthesia induction and continued intraoperatively</td>
</tr>
<tr>
<td valign="top" align="left">Yao et al. (<xref ref-type="bibr" rid="B21">21</xref>), 2015</td>
<td valign="top" align="left">71 (35/36)</td>
<td valign="top" align="left">34.2 &#x000B1; 7.2 35.6 &#x000B1; 8.7</td>
<td valign="top" align="left">GLS</td>
<td valign="top" align="left">TEAS &#x0002B; 5mg tropisetron</td>
<td valign="top" align="left">Sham TEAS &#x0002B; 5mg tropisetron</td>
<td valign="top" align="left">LI4, PC6, ST36, SP6</td>
<td valign="top" align="left">2, 3</td>
<td valign="top" align="left">Dense&#x02013;disperse wave</td>
<td valign="top" align="left">2/100</td>
<td valign="top" align="left">Adjusted to patient tolerance (6&#x02013;9 mA)</td>
<td valign="top" align="left">30</td>
<td valign="top" align="left">Once before anesthesia induction</td>
</tr>
<tr>
<td valign="top" align="left">Pan et al. (<xref ref-type="bibr" rid="B27">27</xref>), 2023</td>
<td valign="top" align="left">105 (52/53)</td>
<td valign="top" align="left">42.2 &#x000B1; 5.5 43.2 &#x000B1; 6.3</td>
<td valign="top" align="left">GLS</td>
<td valign="top" align="left">TEAS &#x0002B; 5mg tropisetron</td>
<td valign="top" align="left">Sham TEAS &#x0002B; 5mg tropisetron</td>
<td valign="top" align="left">LI4, PC6, ST36, SP6</td>
<td valign="top" align="left">3, 4</td>
<td valign="top" align="left">Dense&#x02013;disperse wave</td>
<td valign="top" align="left">2/100</td>
<td valign="top" align="left">Adjusted to patient tolerance (not specified)</td>
<td valign="top" align="left">30</td>
<td valign="top" align="left">Once before anesthesia induction and continued intraoperatively</td>
</tr></tbody>
</table>
<table-wrap-foot>
<p>GLS, gynecological laparoscopic surgery; LSG: Laparoscopic sleeve gastrectomy; LRG: laparoscopic radical gastrectomy.</p>
<p>1: postoperative nausea and vomiting; 2: postoperative nausea; 3: postoperative vomiting; 4: the incidence of requiring antiemetic rescue; 5: time to first flatus; acupoint: Neiguan PC6, Zusanli ST36, Hegu LI4, Sanyinjiao SP6.</p>
</table-wrap-foot>
</table-wrap></sec>
<sec>
<title>Risk of bias assessment</title>
<p>We assessed the quality of the literature using the Cochrane bias risk tool. Among the included studies, six studies (<xref ref-type="bibr" rid="B22">22</xref>, <xref ref-type="bibr" rid="B23">23</xref>, <xref ref-type="bibr" rid="B25">25</xref>&#x02013;<xref ref-type="bibr" rid="B27">27</xref>) reported appropriate randomization and allocation concealment methods, two studies (<xref ref-type="bibr" rid="B2">2</xref>, <xref ref-type="bibr" rid="B20">20</xref>) did not reported randomization methods and one studies (<xref ref-type="bibr" rid="B21">21</xref>) did not mention allocation concealment, leading to an assessment of some selection bias. One study (<xref ref-type="bibr" rid="B20">20</xref>) did not include a sham group. Two studies (<xref ref-type="bibr" rid="B20">20</xref>, <xref ref-type="bibr" rid="B27">27</xref>) employed randomized designs but did not specify detailed data collection methods. No studies have incomplete outcome data. One study (<xref ref-type="bibr" rid="B20">20</xref>) may have selective reporting bias (<xref ref-type="fig" rid="F2">Figures 2</xref>, <xref ref-type="fig" rid="F3">3</xref>).</p>
<fig position="float" id="F2">
<label>Figure 2</label>
<caption><p>Risk of bias graph from the Cochrane risk of bias tool. Red indicates a high risk of bias, yellow indicates an unclear risk of bias, and green indicates a low risk of bias.</p></caption>
<graphic mimetype="image" mime-subtype="tiff" xlink:href="fmed-13-1730188-g0002.tif">
<alt-text content-type="machine-generated">A table assessing risk of bias across several studies, with columns for different types of biases: random sequence generation, allocation concealment, blinding of participants and personnel, blinding of outcome assessment, incomplete outcome data, selective reporting, and other bias. Each cell contains a green circle with a plus or a yellow circle with a question mark, indicating low or unclear risk, respectively. Study references are listed on the left.</alt-text>
</graphic>
</fig>
<fig position="float" id="F3">
<label>Figure 3</label>
<caption><p>Risk of bias summary: review authors&#x00027; judgments about each methodological quality item presented as percentages across all included studies. Red represents a high risk of bias, yellow represents an unclear risk of bias, and green represents a low risk of bias.</p></caption>
<graphic mimetype="image" mime-subtype="tiff" xlink:href="fmed-13-1730188-g0003.tif">
<alt-text content-type="machine-generated">Bar chart depicting different types of biases in a study. Categories include random sequence generation, allocation concealment, blinding of participants and personnel, blinding of outcome assessment, incomplete outcome data, selective reporting, and other bias. Risks of bias are color-coded: low risk in green, unclear risk in yellow, and high risk in red. Most categories show predominantly low risk.</alt-text>
</graphic>
</fig></sec>
<sec>
<title>Incidences of PONV, PON, and POV</title>
<p>Six studies included 2,212 participants (control group 1,104 and intervention group 1,108) and measured the results of the incidence of PONV within postoperative 24 h. A fixed-effects model was used (<italic>P</italic> = 0.09; <italic>I</italic><sup>2</sup>= 47%). The results indicated that participants who received TEAS exhibited a significantly lower incidence of PONV than those in the control group [<italic>RR</italic> = 0.78; 95% CI (0.70, 0.87); <italic>P</italic> <bold>&#x0003C;</bold> 0.001; <xref ref-type="fig" rid="F4">Figure 4A</xref>].</p>
<fig position="float" id="F4">
<label>Figure 4</label>
<caption><p><bold>(A)</bold> Forest plots comparing the incidence of PONV between TEAS and Control group. <bold>(B)</bold> Forest plots comparing the incidence of PON between TEAS and Control group. <bold>(C)</bold> Forest plots comparing the incidence of POV between TEAS and Control group.</p></caption>
<graphic mimetype="image" mime-subtype="tiff" xlink:href="fmed-13-1730188-g0004.tif">
<alt-text content-type="machine-generated">Forest plots labeled A, B, and C show meta-analysis results. Each plot includes different studies with columns for experimental and control events, total, weight, and risk ratio with 95% confidence intervals. Forest plots visually display risk ratios with diamond symbols representing overall effect estimates. Plot A shows a risk ratio of 0.78, plot B shows 0.69, and plot C shows 0.57. Axes indicate favoring experimental or control groups. Each plot includes heterogeneity statistics and overall effect tests.</alt-text>
</graphic>
</fig>
<p>Five RCTs reported the incidence of PON. There was no evidence of heterogeneity among the studies and a fixed-effects model was performed to analyze the outcome (<italic>P</italic> = 0.63, <italic>I</italic><sup>2</sup> = 0%). The meta-analysis found participants in TEAS group had lower incidence of PON [RR=0.69; 95% CI (0.57, 0.82), <italic>P</italic> <bold>&#x0003C;</bold> 0.001] than control group (<xref ref-type="fig" rid="F4">Figure 4B</xref>).</p>
<p>Seven RCTs reported the incidence of POV. A random-effects model was used (<italic>P</italic> = 0.05, <italic>I</italic><sup>2</sup> = 52%). The meta-analysis also found that TEAS group has lower incidence of POV [<italic>RR</italic> = 0.57; 95% CI (0.43, 0.78), <italic>P</italic> <bold>&#x0003C;</bold> 0.001] than the control group (<xref ref-type="fig" rid="F4">Figure 4C</xref>).</p></sec>
<sec>
<title>Time to first flatus after surgery</title>
<p>Four articles including 277 patients in the TEAS group and 280 patients in the control group reported the effect of TEAS on the time of first flatus after operation. Our results showed heterogeneity among the outcome indicators (<italic>P</italic> = 0.006, <italic>I</italic><sup>2</sup> = 76%). A randomized effect model was used to analyze the outcome. Our results revealed that TEAS could significantly shorten the time to first flatus compared with the control group [MD &#x0003D; &#x02212;3.36; 95% CI (-6.5,&#x02212;0.21), <italic>P</italic>=0.04; <xref ref-type="fig" rid="F5">Figure 5</xref>].</p>
<fig position="float" id="F5">
<label>Figure 5</label>
<caption><p>Forest plot comparing the risk ratios of the time to first flatus after surgery between the TEAS group and the control group.</p></caption>
<graphic mimetype="image" mime-subtype="tiff" xlink:href="fmed-13-1730188-g0005.tif">
<alt-text content-type="machine-generated">Forest plot depicting mean differences between experimental and control groups across four studies. Each study lists its mean, standard deviation, and total for both groups. The mean differences and 95% confidence intervals (CI) are shown on the right, with a diamond representing the overall effect size. Heterogeneity statistics include Tau-squared, Chi-squared, and I-squared, with a test for overall effect indicating Z = 2.09 and P = 0.04. The plot suggests an overall mean difference favoring the experimental group.</alt-text>
</graphic>
</fig>
<p>To explore the source of this high heterogeneity, we performed a subgroup analysis based on the type of surgery (gynecological vs. non-gynecological laparoscopic surgery). The analysis showed that the effect of TEAS was more pronounced and consistent in the non-gynecological surgery subgroup [Two studies; MD &#x0003D; &#x02212;5.50; 95% CI (&#x02212;7.15, &#x02212;3.85); I<sup>2</sup> = 0%] compared to the gynecological surgery subgroup [2 studies; MD &#x0003D; &#x02212;1.20; 95% CI (-4.55, 2.15); <italic>I</italic><sup>2</sup> = 65%]. This suggests that the type of surgery is a significant source of heterogeneity for this outcome.</p></sec>
<sec>
<title>Incidence of patients needing antiemetic rescue</title>
<p>Five studies reported the patients who required antiemetic rescue. We analyzed the results using a fixed-effects mode (<italic>P</italic> = 0.22; <italic>I</italic><sup>2</sup> = 31%). The results showed the use of rescue antiemetics was significantly lower in the TEAS group than in the control groups [RR = 0.67; 95% CI (0.52, 0.87); <italic>P</italic> = 0.002; <xref ref-type="fig" rid="F6">Figure 6</xref>].</p>
<fig position="float" id="F6">
<label>Figure 6</label>
<caption><p>Forest plot comparing the risk ratios of the incidence of patients needing antiemetic rescue between the TEAS group and the control group.</p></caption>
<graphic mimetype="image" mime-subtype="tiff" xlink:href="fmed-13-1730188-g0006.tif">
<alt-text content-type="machine-generated">Forest plot showing risk ratios from five studies comparing experimental and control groups. Each study is represented by a blue square with a horizontal line indicating the confidence interval. A diamond at the bottom represents the overall effect estimate with a risk ratio of 0.67, favoring the experimental group. Statistical details include heterogeneity (Chi&#x000B2; = 5.76, P = 0.22) and overall effect significance (Z = 3.04, P = 0.002).</alt-text>
</graphic>
</fig></sec>
<sec>
<title>Safety evaluation</title>
<p>None of the nine included studies reported any serious adverse events related to TEAS, such as skin infections, electrical burns, or significant pain intolerance. Some studies mentioned minor, transient skin redness at the electrode site, which resolved spontaneously. However, it is important to note that the systematic monitoring and reporting of minor adverse effects were not consistently detailed across all trials. Therefore, the absence of reported adverse events in the literature should be interpreted with caution, as it does not definitively confirm the complete absence of any potential side effects.</p></sec></sec>
<sec sec-type="discussion" id="s4">
<title>Discussion</title>
<p>The results of data synthesis demonstrated that the application of TEAS reduced the incidences of PONV, PON, and POV, reduce the use of postoperative antiemetic drugs and shorten the time to first flatus after surgery. This suggests that TEAS confers multiple benefits during the recovery period and helps to facilitate postoperative recovery. The most commonly used acupoints across the nine trials were PC6 (nine studies), ST36 (six), LI4 (five), and SP6 (three).</p>
<p>Our analysis of the time to first flatus revealed high heterogeneity (<italic>I</italic><sup>2</sup> = 76%). To investigate this, we conducted a subgroup analysis based on the type of surgery. The results suggest that TEAS has a more consistent and significant effect in accelerating gastrointestinal recovery in patients undergoing non-gynecological laparoscopic surgery compared to those undergoing gynecological procedures. A possible explanation is that patients undergoing gynecological surgery, who are predominantly female, already have a higher baseline risk for postoperative gastrointestinal dysfunction due to hormonal influences and the specific nature of pelvic surgery. This higher baseline impairment might make the additional benefit of TEAS less pronounced or harder to detect compared to a more general surgical population. This finding highlights the importance of considering patient populations and surgical types when evaluating the efficacy of TEAS.</p>
<p>The precise mechanism by which TEAS alleviates PONV after laparoscopic surgery is multifactorial, but can be understood in the context of the procedure&#x00027;s specific physiological challenges. Laparoscopic surgery necessitates pneumoperitoneum, which increases intra-abdominal pressure and can cause significant vagal nerve stimulation, a primary trigger for PONV (<xref ref-type="bibr" rid="B8">8</xref>). TEAS, particularly at acupoints like PC6 and ST36, is thought to modulate autonomic nervous system activity, specifically by enhancing vagal tone in a regulatory manner (<xref ref-type="bibr" rid="B28">28</xref>). This may counteract the disruptive vagal stimulation from pneumoperitoneum and help restore normal gastrointestinal motility. Furthermore, the surgical stress inherent in laparoscopy triggers a neuroendocrine response, including activation of the hypothalamic-pituitary-adrenal (HPA) axis, which is linked to PONV (<xref ref-type="bibr" rid="B29">29</xref>). TEAS has been shown to attenuate HPA axis hyperactivity, thereby mitigating the stress response. This may be particularly relevant for the gynecological surgery patients included in our review, who are considered a high-risk population for PONV. Lastly, by stimulating A&#x003B2; and A&#x003B4; fibers, TEAS can trigger the release of endogenous opioids like endorphins in the central nervous system (<xref ref-type="bibr" rid="B30">30</xref>, <xref ref-type="bibr" rid="B31">31</xref>), which not only contributes to analgesia but also modulates the chemoreceptor trigger zone and vomiting center. Clinical studies suggest broader perioperative benefits, including analgesia, immunomodulation, and complication reduction (<xref ref-type="bibr" rid="B31">31</xref>&#x02013;<xref ref-type="bibr" rid="B33">33</xref>). In addition, the inflammatory response triggered by laparoscopic surgery may exacerbate PONV. TEAS exerts anti-inflammatory effects and may indirectly alleviate symptoms by down-regulating pro-inflammatory mediators such as IL-6 and TNF-&#x003B1; (<xref ref-type="bibr" rid="B34">34</xref>, <xref ref-type="bibr" rid="B35">35</xref>).</p>
<p>It is also important to consider the heterogeneity within the control groups of the included studies. Eight of the nine trials employed a &#x0201C;sham TEAS&#x0201D; group, where patients were connected to a non-functional device, while one study used a &#x0201C;no TEAS&#x0201D; control. Studies using a sham TEAS control are methodologically stronger for assessing the specific physiological effects of the electrical stimulation itself, as they control for the powerful placebo effect associated with the ritual of applying electrodes and receiving attention. The inclusion of one study with a no-intervention control might slightly inflate the overall effect size. This distinction is crucial for interpreting the magnitude of the benefit attributed to TEAS and underscores the need for rigorous sham controls in future trials.</p>
<p>Meta-analys has demonstrated that TEAS is significantly effective in preventing PONV following general anesthesia (<xref ref-type="bibr" rid="B13">13</xref>). Our research indicates that TEAS effectively prevents PONV following laparoscopic surgery, consistent with previous studies. However, it is noteworthy that the study by Yan et al. (<xref ref-type="bibr" rid="B26">26</xref>), despite its significant weight in our analysis, did not show a statistically significant benefit of TEAS for the primary PONV outcome. Several factors might contribute to this discrepancy. Firstly, as the authors noted, the study population consisted exclusively of high-risk patients (Apfel score &#x02265; 3), where the baseline PONV incidence is exceptionally high, making it more challenging to demonstrate a significant effect from any single intervention. Secondly, the study employed a four-acupoint combination (LI4, PC6, ST36, SP6), which differs from other positive studies that used two or three acupoints. The specific synergistic or antagonistic effects of this combination warrant further investigation. Finally, the control group received standard prophylactic ondansetron, setting a high therapeutic bar for TEAS to show an additional benefit. This highlights the importance of context when interpreting results, particularly when TEAS is evaluated as an adjunctive therapy rather than a standalone one. In addition to gynecological procedures, RCTs covering other types of laparoscopic abdominal surgery were included. Thus, our study provides a more comprehensive assessment than the 2020 TEAS meta-analysis (<xref ref-type="bibr" rid="B16">16</xref>).</p>
<p>PC6 (Neiguan), located on the pericardium meridian, is effective in relieving PONV (<xref ref-type="bibr" rid="B36">36</xref>). According to the theory of Chinese medicine theory, the acupoints ST36 (Zusanli), located on Foot Yangming Stomach Meridian, can restore gastrointestinal function and alleviate PONV. Stimulation of ST36 can promote the recovery of gastrointestinal function and alleviate PONV (<xref ref-type="bibr" rid="B37">37</xref>, <xref ref-type="bibr" rid="B38">38</xref>). LI4 (Hegu) is the original point of the large intestine channel of Hand Yangming Large Intestine Meridian. LI4 has been confirmed to be related to analgesic and sedative effects (<xref ref-type="bibr" rid="B39">39</xref>). In addition, a meta-analysis has shown that the use of LI4, PC6 and ST36 exerts a synergistic analgesic effect in laparoscopic surgery (<xref ref-type="bibr" rid="B40">40</xref>).</p>
<p>The Cochrane bias risk tool was used to assess the quality of the literature, and while most studies were rated as having a low risk of bias in key domains like randomization, we identified some articles with potential bias including selection bias, performance bias, detection bias and reporting bias, with a critical appraisal of performance bias being warranted. It is notoriously difficult to achieve effective participant and personnel blinding in TEAS trials; even when a sham device is used (i.e., identical electrode placement without electrical current), participants may discern the lack of sensation, potentially unblinding them to the intervention. This potential for unblinding constitutes a significant performance bias that could lead to an overestimation of the treatment effect due to placebo or expectation effects. Although we have reported the bias risk as assessed by the original study authors, readers should interpret the findings with caution, acknowledging that the true effect size of TEAS might be more modest than what is reported here, and this issue is a major challenge for the entire field of non-pharmacological stimulation research. The results of this meta-analysis demonstrated that the incidence of PONV and the need for remedial antiemesis within 24 h postoperatively were significantly lower in the TEAS group than in the control group. These findings align with those reported by Gao et al. (<xref ref-type="bibr" rid="B2">2</xref>) and Sun et al. (<xref ref-type="bibr" rid="B41">41</xref>), which suggest that TEAS enhances gastrointestinal function in patients undergoing general anesthesia, while notably differing from those of Zhang et al. (<xref ref-type="bibr" rid="B18">18</xref>), who found no significant effect of TEAS on PONV, and the discrepancy may be attributable to differences in surgical types and acupoint selection between the studies. In addition, no serious adverse events and treatment-related safety concerns related to TEAS were reported in the included studies, confirming its current safety and efficacy in clinical practice. Some patients may experience redness and itching on the skin where the surface electrode is applied, but this is not associated with any serious adverse events. Further studies are warranted to confirm the long-term safety of TEAS.</p>
<p>A key aspect that this meta-analysis aimed to address was the variability in TEAS intervention protocols. The most common stimulation frequency was a dense-disperse wave (2/100 Hz), utilized in the majority of trials. The intensity was typically adjusted to the patient&#x00027;s tolerance, usually described as a strong but non-painful sensation. The duration of stimulation also varied, with most studies applying TEAS for approximately 30 min before anesthesia induction and continuing it throughout the surgery. This lack of standardization makes it difficult to determine an optimal TEAS protocol. The heterogeneity in these parameters could contribute to the variability in treatment effects observed across studies. Future research should focus on head-to-head comparisons of different stimulation parameters to establish evidence-based guidelines for clinical practice.</p>
<p>In our meta-analysis, we included a larger number of patients and RCTs. Compared with previous meta-analyses, we highlight that the RCTs included herein explicitly documented the peri-operative administration of antiemetics such as dexamethasone or metoclopramide. Although the mechanism underlying the combined use of TEAS and antiemetic drugs remains unclear at present. This further supports the effectiveness of TEAS as a complementary therapy for preventing PONV.</p>
<sec>
<title>Limitations</title>
<p>This systematic review and meta-analysis has several limitations that should be considered when interpreting the results. First, despite our efforts to explore heterogeneity through subgroup analysis, significant unexplained heterogeneity remained for some outcomes, such as the time to first flatus. This suggests that other variables, not fully captured in our analysis, may be influencing the results. Second, the methodological quality of the included RCTs was variable. As discussed, the inherent difficulty of blinding in TEAS studies led to an &#x0201C;unclear&#x0201D; risk of performance bias in several trials, which could potentially inflate the observed treatment effect. Third, a significant limitation is the geographic concentration of the included evidence. All nine RCTs were conducted in China. This may limit the generalizability of our findings to other ethnic populations and healthcare systems and raises the possibility of location bias. Therefore, a degree of caution is necessary when applying these conclusions to a global patient population. Finally, the substantial variability in TEAS protocols (e.g., acupoint selection, stimulation parameters) and control group interventions (sham vs. no TEAS) across studies complicates the formulation of a specific, evidence-based clinical recommendation. While our findings support the general use of TEAS as an adjunct, the optimal method of application remains unclear. Future large-scale, multicenter, and multinational RCTs with standardized protocols are needed to address these limitations. Even in the latest guidelines on acupoint stimulation in China, there is no relevant recommendations of frequency model choice.</p>
<p>Compared with previous meta-analyses, this study provides several key contributions. Firstly, it offers the most up-to-date evidence synthesis by including several recent, large-scale RCTs, thereby increasing the statistical power and precision of the findings. Secondly, our study explicitly reframes TEAS as an adjunctive therapy and evaluates its &#x0201C;added value&#x0201D; on top of standard pharmacological antiemetics, which reflects current clinical practice more accurately. Finally, we provide a systematic summary of the TEAS stimulation parameters used in the included trials, offering valuable information for designing future studies and guiding clinical application, a gap identified in prior reviews.</p></sec></sec>
<sec sec-type="conclusions" id="s5">
<title>Conclusion</title>
<p>In summary, our study suggests that TEAS, when used as an adjunctive therapy to standard pharmacological prophylaxis, can significantly decrease the incidence of PONV, PON, and POV, accelerate the return of postoperative bowel function, and reduce the use of rescue antiemetics. These findings indicate that TEAS is an effective and safe complementary intervention for managing PONV in the context of laparoscopic surgery. It may be promising to promote postoperative gastrointestinal recovery. Future studies of high quality and large samples are needed to support the clinical benefits of TEAS therapy on gastrointestinal function.</p></sec>
</body>
<back>
<sec sec-type="data-availability" id="s6">
<title>Data availability statement</title>
<p>The original contributions presented in the study are included in the article/<xref ref-type="sec" rid="s11">Supplementary material</xref>, further inquiries can be directed to the corresponding author.</p>
</sec>
<sec sec-type="author-contributions" id="s7">
<title>Author contributions</title>
<p>SQ: Data curation, Writing &#x02013; original draft, Writing &#x02013; review &#x00026; editing. JL: Methodology, Writing &#x02013; review &#x00026; editing. JH: Data curation, Writing &#x02013; review &#x00026; editing. YL: Software, Writing &#x02013; review &#x00026; editing. JL: Supervision, Writing &#x02013; review &#x00026; editing. LW: Methodology, Writing &#x02013; review &#x00026; editing. SF: Project administration, Writing &#x02013; original draft, Writing &#x02013; review &#x00026; editing.</p>
</sec>
<sec sec-type="COI-statement" id="conf1">
<title>Conflict of interest</title>
<p>The author(s) declared that this work was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.</p>
</sec>
<sec sec-type="ai-statement" id="s9">
<title>Generative AI statement</title>
<p>The author(s) declared that generative AI was not used in the creation of this manuscript.</p>
<p>Any alternative text (alt text) provided alongside figures in this article has been generated by Frontiers with the support of artificial intelligence and reasonable efforts have been made to ensure accuracy, including review by the authors wherever possible. If you identify any issues, please contact us.</p></sec>
<sec sec-type="disclaimer" id="s10">
<title>Publisher&#x00027;s note</title>
<p>All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.</p>
</sec><sec sec-type="supplementary-material" id="s11">
<title>Supplementary material</title>
<p>The Supplementary Material for this article can be found online at: <ext-link ext-link-type="uri" xlink:href="https://www.frontiersin.org/articles/10.3389/fmed.2026.1730188/full#supplementary-material">https://www.frontiersin.org/articles/10.3389/fmed.2026.1730188/full#supplementary-material</ext-link></p>
<supplementary-material xlink:href="Table_1.doc" id="SM1" mimetype="application/msword" xmlns:xlink="http://www.w3.org/1999/xlink"/></sec>
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<fn fn-type="custom" custom-type="edited-by" id="fn0001">
<p>Edited by: <ext-link ext-link-type="uri" xlink:href="https://loop.frontiersin.org/people/1358389/overview">Huan Tong</ext-link>, Sichuan University, China</p>
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<fn fn-type="custom" custom-type="reviewed-by" id="fn0002">
<p>Reviewed by: <ext-link ext-link-type="uri" xlink:href="https://loop.frontiersin.org/people/1878924/overview">Iain Brownlee</ext-link>, Northumbria University, United Kingdom</p>
<p><ext-link ext-link-type="uri" xlink:href="https://loop.frontiersin.org/people/2981574/overview">Yefan Cao</ext-link>, Fudan University, China</p>
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