OTO Open最新文献

{"title":"Face and Neck Pilomatricoma Excision Using an Endoscope-Assisted Hairline Approach.","authors":"Ken Woo, Dong Kun Lee, Seung Hoon Woo","doi":"10.1002/oto2.70104","DOIUrl":"https://doi.org/10.1002/oto2.70104","url":null,"abstract":"<p><strong>Objective: </strong>Traditional transcutaneous approaches for pilomatricoma excision in the face and neck are effective but often leave conspicuous scars that compromise cosmetic outcomes. We aimed to evaluate a refined endoscope-assisted hairline approach that uses a concealed scalp incision and enhanced endoscopic visualization to improve esthetic results while maintaining surgical efficacy.</p><p><strong>Study design: </strong>Prospective observational study.</p><p><strong>Setting: </strong>Dankook University School of Medicine, Korea.</p><p><strong>Methods: </strong>Fifty patients with benign pilomatricomas of the face and neck were prospectively enrolled and allocated into two groups. Group A (n = 25) underwent the refined endoscope-assisted hairline approach, whereas Group B (n = 25) received the conventional transcutaneous approach. Clinical data including operative time and postoperative complications were recorded. Cosmetic outcomes were objectively evaluated using standardized photographic documentation and patient satisfaction scores collected at 3 and 12 months postoperatively.</p><p><strong>Results: </strong>The mean operative time was significantly longer in Group A compared to Group B (<i>P</i> < .001), reflecting the technical intricacies of the hairline approach. No significant differences were observed between the two groups in hospital stay or overall complication rates. Importantly, cosmetic satisfaction scores were significantly higher in Group A (<i>P</i> < .001), with objective assessments consistently demonstrating reduced scar visibility and superior preservation of skin integrity.</p><p><strong>Conclusion: </strong>The refined endoscope-assisted hairline approach is a safe and highly effective technique for pilomatricoma excision in cosmetically sensitive facial and neck regions. This innovative method offers significant improvements in esthetic outcomes without compromising safety, representing a distinct advance over conventional methods.</p>","PeriodicalId":19697,"journal":{"name":"OTO Open","volume":"9 2","pages":"e70104"},"PeriodicalIF":1.8,"publicationDate":"2025-05-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12080212/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144079393","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Office-Based Blue Laser Versus Coblation Therapy for Inferior Turbinate Hypertrophy: A Pilot Study.","authors":"Abdul-Latif Hamdan, Zeina Maria Semaan, Lana Ghzayel, Yara Yammine, Jonathan Abou Chaar, Jad Hosri, Patrick Abou Raji Feghali, Anne Marie Daou, Elie Alam","doi":"10.1002/oto2.70127","DOIUrl":"https://doi.org/10.1002/oto2.70127","url":null,"abstract":"<p><strong>Objective: </strong>The aim of this pilot study is to compare the effectiveness of office-based blue laser therapy with coblation therapy in patients with inferior turbinate hypertrophy (ITH).</p><p><strong>Study design: </strong>Retrospective chart review.</p><p><strong>Setting: </strong>Tertiary referral center.</p><p><strong>Methods: </strong>Patients presenting with nasal obstruction between November 2022 and November 2024, and underwent coblation or blue laser therapy for turbinate reduction were reviewed. Demographic data included age, gender, smoking, history of allergy, history of reflux disease, and history of prior nasal surgery. All patients had filled the nasal obstruction symptom evaluation (NOSE) questionnaire and the visual analog scale (VAS) before and on follow-up after treatment. Patient's level of comfort during the procedure was also rated using a 10-point Likert scale with a higher score indicating a greater level of comfort.</p><p><strong>Results: </strong>A total of 10 patients underwent office-based blue laser therapy for turbinate reduction, and 10 patients underwent office-based coblation of the inferior turbinates. In the subgroup of patients who underwent office-based blue laser therapy, the mean NOSE score and VAS score decreased significantly (<i>P</i> = .005). In the subgroup of patients who underwent coblation, the mean NOSE score and VAS score decreased significantly (<i>P</i> = .005). When comparing the two subgroups, the difference in the drop of the NOSE score was not statistically significant (<i>P</i> = .198). Similarly, the difference in the drop of VAS score was not statistically significant (<i>P</i> = .280).</p><p><strong>Conclusion: </strong>The results of this investigation indicate that both coblation therapy and blue laser therapy are effective office-based treatment modalities in patients with ITH with comparable results.</p>","PeriodicalId":19697,"journal":{"name":"OTO Open","volume":"9 2","pages":"e70127"},"PeriodicalIF":1.8,"publicationDate":"2025-05-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12076342/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144079395","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Feasibility of a Novel Autoinflation Device to Treat Pediatric Otitis Media With Effusion At-Home.","authors":"Maria-Jose Soto, Nanki Hura, Intan Oldakowska, Matthew Oldakowski, Paul Bumbak, Peter Luke Santa Maria","doi":"10.1002/oto2.70128","DOIUrl":"https://doi.org/10.1002/oto2.70128","url":null,"abstract":"<p><strong>Objective: </strong>Otitis media with effusion (OME) affects 90% of children before school age, with current guidelines recommending tympanostomy tubes for persistent OME and hearing loss after 3 months of \"Watchful Waiting,\" due to the risk of complications including long-term conductive hearing loss. Current nonsurgical treatment options are limited. This study evaluates the feasibility of at-home use of a novel prototype autoinflation device for children with OME or eustachian tube dysfunction.</p><p><strong>Study design: </strong>Single-arm cohort study.</p><p><strong>Setting: </strong>Pediatric otolaryngology private clinic.</p><p><strong>Methods: </strong>Children aged 1 to 12 years with OME were recruited from a pediatric otolaryngology clinic and asked to use the device twice daily for 4 weeks. Baseline audiometry and tympanometry were performed at recruitment, with subsequent tympanometry testing after first use and at 2, 4, 8, and 12 weeks. Audiometry testing was repeated at week 4. Compliance was tracked using an App.</p><p><strong>Results: </strong>Twenty-one patients were included (average age: 5.1 years, range: 2-12 years). After a single session, 86% of patients had middle ear pressure improvement in at least one ear, which maintained stable at 83% at week 4. Additionally, 86% of patients with hearing loss exhibited improvement at 4 weeks, where the average pure tone average in ears with baseline hearing loss improved from 26.8 to 18.9 dB HL.</p><p><strong>Conclusion: </strong>These results demonstrate significant improvement in both tympanometry and audiometry after 4 weeks of device use. This indicates a strong potential benefit in regular ventilation of the middle ear for pediatric patients with OME undergoing \"Watchful Waiting.\"</p>","PeriodicalId":19697,"journal":{"name":"OTO Open","volume":"9 2","pages":"e70128"},"PeriodicalIF":1.8,"publicationDate":"2025-05-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12076345/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144079394","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Ropivacaine Local Infiltration for Pain Control After Thyroidectomy: A Systematic Review and Meta-Analysis.","authors":"Ebraheem Albazee, Fahad Allafi, Abdulwahab Alsalem, Deemah AlShaya, Hayfaa Alhazami, Danah Alfalah","doi":"10.1002/oto2.70124","DOIUrl":"https://doi.org/10.1002/oto2.70124","url":null,"abstract":"<p><strong>Objective: </strong>To evaluate the analgesic role of ropivacaine local infiltration in patients undergoing thyroidectomy.</p><p><strong>Data sources: </strong>PubMed, Google Scholar, CENTRAL, Scopus, and Web of Science.</p><p><strong>Review methods: </strong>A systematic review and meta-analysis synthesizing evidence from randomized controlled trials (RCTs). Our specific endpoints include pain severity, total opioid analgesia consumption, patient satisfaction, length of hospital stay, postanesthesia care unit (PACU) length of stay, surgery duration, and the incidence of postoperative nausea and vomiting (PONV). Using Stata, we pooled dichotomous outcomes and continuous outcomes using risk ratio (RR) and standardized mean difference (SMD) or mean difference (MD), respectively, with a 95% confidence interval (CI).</p><p><strong>Results: </strong>Eight RCTs and 633 patients were included. Ropivacaine significantly decreased pain after 1 to 2 hours postoperatively (SMD: -1.40, 95% CI [-2.30, -0.51]). However, there was no difference between both groups after 4 hours (<i>P</i> = .11), 6 to 8 hours (<i>P</i> = .05), 16 to 18 hours (<i>P</i> = .10), and 24 hours (<i>P</i> = .37). Also, ropivacaine significantly decreased analgesia consumption (SMD: -0.75, 95% CI [-1.30, -0.20]), with no effect on surgery duration (<i>P</i> = .59), length of hospital stays (<i>P</i> = .32), patient satisfaction score (<i>P</i> = .25), and PACU length of stay (<i>P</i> = .25). Finally, there was no difference between both groups regarding the incidence of PONV (RR: 1.01, 95% CI [0.70, 1.45]).</p><p><strong>Conclusion: </strong>Ropivacaine local infiltration after thyroidectomy significantly decreased pain for up to 1 to 2 hours and analgesia consumption compared to control, but with uncertain evidence. However, ropivacaine had no effect on pain from 4 to 24 hours, surgery duration, length of PACU stay, length of hospital stay, and patient satisfaction.</p>","PeriodicalId":19697,"journal":{"name":"OTO Open","volume":"9 2","pages":"e70124"},"PeriodicalIF":1.8,"publicationDate":"2025-05-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12051372/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144034869","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Domain-Specific Customization for Language Models in Otolaryngology: The ENT GPT Assistant.","authors":"Brenton T Bicknell, Nicholas J Rivers, Adam Skelton, Delaney Sheehan, Charis Hodges, Stevan C Fairburn, Benjamin J Greene, Bharat Panuganti","doi":"10.1002/oto2.70125","DOIUrl":"https://doi.org/10.1002/oto2.70125","url":null,"abstract":"<p><strong>Objective: </strong>To develop and evaluate the effectiveness of domain-specific customization in large language models (LLMs) by assessing the performance of the ENT GPT Assistant (E-GPT-A), a model specifically tailored for otolaryngology.</p><p><strong>Study design: </strong>Comparative analysis using multiple-choice questions (MCQs) from established otolaryngology resources.</p><p><strong>Setting: </strong>Tertiary care academic hospital.</p><p><strong>Methods: </strong>Two hundred forty clinical-vignette style MCQs were sourced from BoardVitals Otolaryngology and OTOQuest, covering a range of otolaryngology subspecialties (n = 40 for each). The E-GPT-A was developed using targeted instructions and customized to otolaryngology. The performance of E-GPT-A was compared against top-performing and widely used artificial intelligence (AI) LLMs, including GPT-3.5, GPT-4, Claude 2.0, and Claude 2.1. Accuracy was assessed across subspecialties, varying question difficulty tiers, and in diagnostics and management.</p><p><strong>Results: </strong>E-GPT-A achieved an overall accuracy of 74.6%, outperforming GPT-3.5 (60.4%), Claude 2.0 (61.7%), Claude 2.1 (60.8%), and GPT-4 (68.3%). The model performed best in allergy and rhinology (85.0%) and laryngology (82.5%), whereas showing lower accuracy in pediatrics (62.5%) and facial plastics/reconstructive surgery (67.5%). Accuracy also declined as question difficulty increased. The average correct response percentage among otolaryngologists and otolaryngology trainees was 71.1% in the question set.</p><p><strong>Conclusion: </strong>This pilot study using the E-GPT-A demonstrates the potential benefits of domain-specific customizations of language models for otolaryngology. However, further development, continuous updates, and continued real-world validation are needed to fully assess the capabilities of LLMs in otolaryngology.</p>","PeriodicalId":19697,"journal":{"name":"OTO Open","volume":"9 2","pages":"e70125"},"PeriodicalIF":1.8,"publicationDate":"2025-05-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12051367/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144004508","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Predictors of Donor-Site Wound Complications Following Fibula Free Flap Reconstruction.","authors":"Soroush Ershadifar, Angela Colback, Ugur Nur Basmaci, Machelle Wilson, Andrew C Birkeland, Dustin A Silverman","doi":"10.1002/oto2.70126","DOIUrl":"https://doi.org/10.1002/oto2.70126","url":null,"abstract":"<p><strong>Objective: </strong>The fibula free flap (FFF) remains the workhorse flap for head and neck defects necessitating osteocutaneous reconstruction. Although lower extremity angiography, ultrasound (US), and other vascular studies are routinely used for fibula assessment and patient selection, predictors of donor-site morbidity following harvest remain poorly understood. We sought to investigate the factors associated with FFF donor-site complications.</p><p><strong>Study design: </strong>Retrospective analysis of patients at a tertiary care center.</p><p><strong>Setting: </strong>Tertiary care center.</p><p><strong>Methods: </strong>In total, 119 patients undergoing FFF reconstruction during the years 2012 to 2022 were included. Multivariable logistic regression was used to identify independent predictors of soft-tissue donor-site wound complications.</p><p><strong>Results: </strong>A total of 48 (40.3%) patients developed a donor-site wound complication with an average time to diagnosis of 24 days (±16) following surgery. In multivariable regression, history of alcohol use disorder (<i>P</i> = .0083) and method of donor-site closure (<i>P</i> = .0368) were independent predictors of donor-site wound complications. Split-thickness skin graft closure was associated with a 146% increased odds of wound complications (odds ratio [OR] = 2.46, 1.11-5.43, 95% confidence interval). Patient age, body mass index, Charlson comorbidity index, skin paddle size, and Doppler US characteristics were not predictive of postoperative donor-site morbidity.</p><p><strong>Conclusion: </strong>Predictors of FFF donor-site wound complications included history of alcohol abuse and method of donor-site closure. This study highlights unique lower extremity Doppler US findings in patients undergoing FFF reconstruction in addition to modifiable risk factors associated with fibula donor-site morbidity and soft-tissue complications. Our findings underscore the need to critically evaluate wound closure techniques in this population.</p>","PeriodicalId":19697,"journal":{"name":"OTO Open","volume":"9 2","pages":"e70126"},"PeriodicalIF":1.8,"publicationDate":"2025-05-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12053048/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144006787","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"The Impact of Bioabsorbable Nasal Implants, Nasal Radiofrequency Remodeling, and Anesthesia Type on Patient Selection for Nasal Valve Surgery.","authors":"F Jeffrey Lorenz, Cheng Ma, Scott G Walen","doi":"10.1002/oto2.70123","DOIUrl":"https://doi.org/10.1002/oto2.70123","url":null,"abstract":"<p><strong>Objective: </strong>To compare patient demographics, comorbidities, anesthesia type, and trends in nasal valve implantation (NVI) and nasal radiofrequency remodeling (NRR) techniques versus traditional nasal valve repair (NVR).</p><p><strong>Study design: </strong>Retrospective case-control.</p><p><strong>Setting: </strong>In total, 58 health care organizations (HCOs) across the United States.</p><p><strong>Methods: </strong>The TriNetX Research Network was queried from 2021 through 2023, forming three cohorts of patients who underwent (1) NVR, (2) NVI, or (3) NRR. Demographics, comorbidities, and anesthesia type were compared across groups at the time of intervention.</p><p><strong>Results: </strong>A total of 10,568 NVR, 764 NVI, and 485 NRR cases were identified. Patients undergoing NVI or NRR compared to NVR were more likely to be older and exhibit a higher prevalence of medical comorbidities, including sleep apnea, hyperlipidemia, type 2 diabetes, gastroesophageal reflux disease, liver disease, hypertension, ischemic heart disease, other heart diseases, cerebrovascular disease, hearing loss, and kidney disease (all <i>P</i> < .05). Of all cases, 82.4% of NVR, 84.8% of NVI, and 55.2% of NRR were performed under general anesthesia. Patients who underwent NRR had the highest comorbidity burden of all cohorts and were most likely to receive local anesthesia. However, when analyzing anesthesia type by specific procedure (NVR, NVI, and NRR), most comorbidities were not significantly more common in those who underwent local anesthesia compared to general anesthesia.</p><p><strong>Conclusion: </strong>NVI and NRR have provided surgeons with alternative treatment options for nasal valve collapse, especially for patients who are older and with a higher burden of medical comorbidities.</p>","PeriodicalId":19697,"journal":{"name":"OTO Open","volume":"9 2","pages":"e70123"},"PeriodicalIF":1.8,"publicationDate":"2025-05-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12046381/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144018529","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Intracapsular Tonsillectomy With Monopolar Cautery-A Cost-Effective Surgical Technique.","authors":"Rebecca Sinard Arch, Sanjeet Rangarajan, Kris Jatana, Evan Tobin","doi":"10.1002/oto2.70119","DOIUrl":"https://doi.org/10.1002/oto2.70119","url":null,"abstract":"<p><strong>Objective: </strong>To illustrate improved posttonsillectomy hemorrhage rates with a novel cost-effective monopolar intracapsular tonsillectomy (ICT) technique.</p><p><strong>Study design: </strong>Retrospective cohort.</p><p><strong>Setting: </strong>Single physician's experience at a Midwest private practice.</p><p><strong>Methods: </strong>A single surgeon's chart review of 576 pediatric patients who underwent a tonsillectomy in the last 20 years was completed. In total, 331 cases were treated with ICT performed with a novel monopolar bovie electrocautery technique, as opposed to the more widely used microdebrider or coblator techniques. In total, 246 were treated with the traditional extracapsular tonsillectomy (ECT) technique using monopolar electrocautery.</p><p><strong>Results: </strong>Of the 331 ICTs performed, one postoperative hemorrhage requiring intervention was identified, resulting in an ICT postoperative bleed rate of 0.3%. Of the 246 ECTs performed, 9 postoperative bleeds requiring intervention were identified, resulting in an ECT postoperative bleed rate of 3.7%. In this cohort, the relative risk of developing a bleed with ECT was 12 times higher than the bleed risk with ICT (<i>P</i> = .018). Every 30 cases of ICT prevented one tonsil bleed (number needed to treat [NNT] = 29.8). Potential savings of ICT with monopolar cautery is $1.5 to $1.6 million for every 10,000 cases that transition to ICT with electrocautery from a microdebrider or coblator technique.</p><p><strong>Conclusion: </strong>ICT with monopolar electrocautery resulted in a significantly decreased bleed rate compared to the ECT technique in this single surgeon experience and at a much lower cost compared to the more widely used microdebrider or coblator techniques.</p>","PeriodicalId":19697,"journal":{"name":"OTO Open","volume":"9 2","pages":"e70119"},"PeriodicalIF":1.8,"publicationDate":"2025-05-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12046380/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144034118","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Robotic Revolution in Thyroid Surgery: An Umbrella Review of Clinical Outcomes.","authors":"Si-Yue Yin, Ping-Ting Zhou, Zi-Hui Xie, Chuan-Lu Shen, Fen-Fen Li, Bing-Yu Liang, Yi-Pin Yang, Zi-Yue Fu, Jian-Peng Wang, Yan-Xun Han, Shan-Wen Chen, Cong-Jun Zhang, Ye-Hai Liu, Yi Zhao, Yu-Chen Liu","doi":"10.1002/oto2.70120","DOIUrl":"https://doi.org/10.1002/oto2.70120","url":null,"abstract":"<p><strong>Objective: </strong>This umbrella review aims to evaluate the clinical outcomes of robotic-assisted thyroid surgery compared to traditional endoscopic and open surgical approaches.</p><p><strong>Data sources: </strong>We conducted a systematic search of PubMed, EMBASE, and Cochrane Database through August 2024.</p><p><strong>Review methods: </strong>We conducted a comprehensive analysis of systematic reviews and meta-analyses that compare robotic-assisted thyroid surgery with endoscopic or open methods. The primary outcomes assessed include surgical efficiency indicators, general postoperative complications, specific complications (nerve and endocrine), postoperative recovery and patient experience, and recurrence and long-term prognosis. The methodological quality of the included reviews was assessed using the AMSTAR2 tool.</p><p><strong>Results: </strong>Of the 1987 articles retrieved, 21 were eligible. Robotic surgery, though associated with longer operative times, offers distinct advantages in terms of precision. Although robotic surgery shows some variation in central lymph node dissection and an increase in postoperative drainage, its safety is comparable to both open and endoscopic techniques. Additionally, robotic surgery demonstrates superior cosmetic outcomes and shorter hospital stays from multiple approaches, though its high costs remain a significant factor. In terms of recurrence and survival rates, no significant differences were observed between robotic and open surgery.</p><p><strong>Conclusion: </strong>Robotic surgery choices should balance benefits, costs, and patient needs. As technology and skills improve, efficiency and cost-effectiveness may increase, expanding its clinical role.</p>","PeriodicalId":19697,"journal":{"name":"OTO Open","volume":"9 2","pages":"e70120"},"PeriodicalIF":1.8,"publicationDate":"2025-05-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12046382/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143993502","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"The Effect of Tongue Volume and Adipose Content on Obstructive Sleep Apnea: Meta-analysis & Systematic Review.","authors":"Emily Baker, Meghana Chanamolu, Chad Nieri, Stephen F White, Josiah Brandt, Marion Boyd Gillespie","doi":"10.1002/oto2.70067","DOIUrl":"https://doi.org/10.1002/oto2.70067","url":null,"abstract":"<p><strong>Objective: </strong>Macroglossia is a risk factor for obstructive sleep apnea (OSA) and has been linked to an elevated apnea-hypopnea index (AHI). Obesity may contribute to macroglossia, but its exact relationship is unknown and likely multifactorial, and the degree to which increased adiposity of the tongue affects the development of OSA is not understood. The primary objective of this study was to evaluate how tongue fat and volume relate to the presence and severity of OSA.</p><p><strong>Data sources: </strong>Studies reporting the impact of tongue fat or volume were identified using predefined inclusion criteria from September 2002 to 2022.</p><p><strong>Review methods: </strong>All studies underwent a 2-stage blinded screening, extraction, and evaluation process. Primary outcomes were the effect of tongue fat and volume on OSA severity and evaluation of study quality. Secondary outcomes included the impact of obesity on tongue fat distribution and OSA severity.</p><p><strong>Results: </strong>Out of 930 studies, 6 studies with 219 patients and 133 controls were included in meta-analysis. All 6 studies were case-control designs. Included studies showed low (4) and moderate (2) risks of bias. All studies compared tongue volume with an observed significant increase in tongue volume in OSA patients (<i>P</i> < .00001) with a weighted mean difference of 19.00 cm³ [15.53, 22.47]. Two studies compared tongue fat, and there was a significant increase in tongue fat in patients with OSA (<i>P</i> < .00001) with a weighted mean difference of 8.04 cm³ [4.25, 11.82].</p><p><strong>Conclusion: </strong>This meta-analysis supports increased tongue volume and tongue adipose as important risk factors associated with OSA. Larger studies investigating tongue fat distribution and the effect of weight changes on tongue fat and volume and OSA severity are needed to characterize this relationship better.</p>","PeriodicalId":19697,"journal":{"name":"OTO Open","volume":"9 2","pages":"e70067"},"PeriodicalIF":1.8,"publicationDate":"2025-04-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12023004/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143974607","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}