Pub Date : 2025-09-09eCollection Date: 2025-01-01DOI: 10.1055/a-2685-7610
Kotryna Truskaite, Laura Vossen Engblom, Greger Lindberg, Aldona Dlugosz
Background and study aims: Magnifying endoscopy with narrow-band imaging (ME-NBI) is regularly used in neoplasia diagnostics although its use in assessment of esophageal inflammatory changes is uncommon. The aim of this study was to evaluate the efficacy of eosinophilic esophagitis reference score and ME-NBI signs in predicting inflammation using gastroscopy with dual focus in patients with dysphagia.
Patients and methods: We conducted a prospective cohort study in adults undergoing gastroscopy with esophageal biopsies because of dysphagia/food bolus impaction. Number of eosinophiles and lymphocytes were calculated per high-power field. We used logistic regression with forward stepwise selection to determine the most relevant predictors (endoscopic signs) of inflammation. To assess the predictive value of endoscopic signs for eosinophilic or lymphocytic infiltration, we calculated sensitivity, specificity, and predictive values.
Results: In total 219 patients (71.2% male) were enrolled to the study. Most frequent endoscopic findings were furrows (121/219, 55%), positive NBI signs (106/219, 48%), and edema (102/219, 47%). Logistic regression analysis showed that furrows and NBI signs were the most significant predictors of eosinophilic infiltration. Edema was the only significant predictor of lymphocyte infiltration.
Conclusions: Positive NBI signs and furrows were the best predictors of eosinophile infiltration, whereas lymphocytic infiltration was predicted by edema. Given that NBI is already widely available, we encourage use of both white light and NBI in patients with suspected esophageal inflammation.
{"title":"Narrow band imaging complements eosinophilic esophagitis reference score in predicting inflammatory infiltration in patients with dysphagia.","authors":"Kotryna Truskaite, Laura Vossen Engblom, Greger Lindberg, Aldona Dlugosz","doi":"10.1055/a-2685-7610","DOIUrl":"10.1055/a-2685-7610","url":null,"abstract":"<p><strong>Background and study aims: </strong>Magnifying endoscopy with narrow-band imaging (ME-NBI) is regularly used in neoplasia diagnostics although its use in assessment of esophageal inflammatory changes is uncommon. The aim of this study was to evaluate the efficacy of eosinophilic esophagitis reference score and ME-NBI signs in predicting inflammation using gastroscopy with dual focus in patients with dysphagia.</p><p><strong>Patients and methods: </strong>We conducted a prospective cohort study in adults undergoing gastroscopy with esophageal biopsies because of dysphagia/food bolus impaction. Number of eosinophiles and lymphocytes were calculated per high-power field. We used logistic regression with forward stepwise selection to determine the most relevant predictors (endoscopic signs) of inflammation. To assess the predictive value of endoscopic signs for eosinophilic or lymphocytic infiltration, we calculated sensitivity, specificity, and predictive values.</p><p><strong>Results: </strong>In total 219 patients (71.2% male) were enrolled to the study. Most frequent endoscopic findings were furrows (121/219, 55%), positive NBI signs (106/219, 48%), and edema (102/219, 47%). Logistic regression analysis showed that furrows and NBI signs were the most significant predictors of eosinophilic infiltration. Edema was the only significant predictor of lymphocyte infiltration.</p><p><strong>Conclusions: </strong>Positive NBI signs and furrows were the best predictors of eosinophile infiltration, whereas lymphocytic infiltration was predicted by edema. Given that NBI is already widely available, we encourage use of both white light and NBI in patients with suspected esophageal inflammation.</p>","PeriodicalId":11671,"journal":{"name":"Endoscopy International Open","volume":"13 ","pages":"a26857610"},"PeriodicalIF":2.3,"publicationDate":"2025-09-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12445250/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145112309","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}
Pub Date : 2025-09-05eCollection Date: 2025-01-01DOI: 10.1055/a-2687-3552
Tina L N Meijering, David M de Jong, Swip Draijer, Marco J Bruno, Hendrikus J Dubbink, Jeroen de Jonge, Marie-Louise F van Velthuysen, Lydi M J W van Driel
Background and study aims: This study addressed the need for improved diagnostic tools to identify malignancy in suspicious biliary strictures. Traditional cytological morphology is often indecisive, prompting exploration of next-generation sequencing (NGS) for enhanced sensitivity. Our aim was to evaluate NGS's additional value in classifying biliary brushes and biopsies and its impact on clinical decision making (CDM).
Patients and methods: In this retrospective single-center cohort study, patients were included from 2019 to 2022 in whom morphologic interpretation and NGS were performed on cytological or histological material from suspicious biliary strictures. Sensitivity and specificity of NGS were calculated for benign or atypical vs. suspicious for malignancy or malignant morphology in biliary brushes and biopsies. In addition, changes in CDM after NGS outcome were evaluated.
Results: In total 109 samples from 106 patients were included in the study. NGS correctly identified 42 of 75 malignancies (56%). Sensitivity and specificity of morphology for brushes were 56% (95% confidence interval [CI] 43%-68%) and 94% (95% CI 79%-99%), respectively. Adding NGS resulted in sensitivity and specificity of 78% (95% CI 66%-87%) and 94% (95% CI 79%-99%). For biopsies, sensitivity and specificity of morphology were 67% (95% CI 35%-90%) and 67% (95% CI 9%-99%) and adding NGS did not alter these results. The outcome of NGS resulted in a change of classification of morphology in 36% and a change in CDM in 8%.
Conclusions: NGS in brushes contributed to more accurate/sensitive diagnoses of malignancy than morphology alone. There was a limited impact on CDM change, but in the future, NGS will undoubtedly play a bigger role when targeted therapy is incorporated in standard treatment and more sensitive NGS panels for cholangiocarcinoma are developed.
背景和研究目的:本研究探讨了改进诊断工具以识别可疑胆道狭窄中恶性肿瘤的必要性。传统的细胞学形态学往往是不确定的,促使探索下一代测序(NGS)提高灵敏度。我们的目的是评估NGS在胆道刷和活检分类中的附加价值及其对临床决策(CDM)的影响。患者和方法:在这项回顾性单中心队列研究中,纳入2019年至2022年的患者,对可疑胆道狭窄的细胞学或组织学材料进行形态学解释和NGS。计算了NGS在胆道刷和活检中对良性或非典型形态、对恶性或恶性形态可疑的敏感性和特异性。此外,评估NGS结果后CDM的变化。结果:106例患者共109份样本纳入研究。NGS正确识别了75例恶性肿瘤中的42例(56%)。毛刷形态的敏感性和特异性分别为56%(95%置信区间[CI] 43%-68%)和94% (95% CI 79%-99%)。添加NGS的敏感性和特异性分别为78% (95% CI 66%-87%)和94% (95% CI 79%-99%)。对于活组织检查,形态学的敏感性和特异性分别为67% (95% CI 35%-90%)和67% (95% CI 9%-99%),添加NGS并没有改变这些结果。NGS结果导致36%的形态学分类改变,8%的CDM改变。结论:刷子的NGS比单独的形态学诊断更准确/敏感。目前对CDM变化的影响有限,但在未来,当靶向治疗纳入标准治疗,开发出更敏感的胆管癌NGS筛查组时,NGS无疑将发挥更大的作用。
{"title":"Yield of next-generation sequencing in diagnostic work up of suspicious biliary strictures.","authors":"Tina L N Meijering, David M de Jong, Swip Draijer, Marco J Bruno, Hendrikus J Dubbink, Jeroen de Jonge, Marie-Louise F van Velthuysen, Lydi M J W van Driel","doi":"10.1055/a-2687-3552","DOIUrl":"10.1055/a-2687-3552","url":null,"abstract":"<p><strong>Background and study aims: </strong>This study addressed the need for improved diagnostic tools to identify malignancy in suspicious biliary strictures. Traditional cytological morphology is often indecisive, prompting exploration of next-generation sequencing (NGS) for enhanced sensitivity. Our aim was to evaluate NGS's additional value in classifying biliary brushes and biopsies and its impact on clinical decision making (CDM).</p><p><strong>Patients and methods: </strong>In this retrospective single-center cohort study, patients were included from 2019 to 2022 in whom morphologic interpretation and NGS were performed on cytological or histological material from suspicious biliary strictures. Sensitivity and specificity of NGS were calculated for benign or atypical vs. suspicious for malignancy or malignant morphology in biliary brushes and biopsies. In addition, changes in CDM after NGS outcome were evaluated.</p><p><strong>Results: </strong>In total 109 samples from 106 patients were included in the study. NGS correctly identified 42 of 75 malignancies (56%). Sensitivity and specificity of morphology for brushes were 56% (95% confidence interval [CI] 43%-68%) and 94% (95% CI 79%-99%), respectively. Adding NGS resulted in sensitivity and specificity of 78% (95% CI 66%-87%) and 94% (95% CI 79%-99%). For biopsies, sensitivity and specificity of morphology were 67% (95% CI 35%-90%) and 67% (95% CI 9%-99%) and adding NGS did not alter these results. The outcome of NGS resulted in a change of classification of morphology in 36% and a change in CDM in 8%.</p><p><strong>Conclusions: </strong>NGS in brushes contributed to more accurate/sensitive diagnoses of malignancy than morphology alone. There was a limited impact on CDM change, but in the future, NGS will undoubtedly play a bigger role when targeted therapy is incorporated in standard treatment and more sensitive NGS panels for cholangiocarcinoma are developed.</p>","PeriodicalId":11671,"journal":{"name":"Endoscopy International Open","volume":"13 ","pages":"a26873552"},"PeriodicalIF":2.3,"publicationDate":"2025-09-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12417792/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145039362","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}
Pub Date : 2025-09-05eCollection Date: 2025-01-01DOI: 10.1055/a-2669-5801
Nicolò de Pretis, Lorenzo Santaera, Luigi Martinelli, Maria Cristina Conti Bellocchi, Laura Bernardoni, Viola Fino, Adrian Miguel Pezua Sanjinez, Enrico Gasparini, Armando Gabbrielli, Luca Frulloni, Stefano Francesco Crinó
Background and study aims: Fully-covered-self-expandable-metal-stents (FC-SEMS) are commonly used for non-malignant biliary stricture treatment. Removal failure related to hyperplastic tissue development over the distal margin of the stent has been described but few data are available. FC-SEMS-in-FC-SEMS technique has been described in case reports to overcome FC-SEMS removal failure. Aims of this study were investigating technical success, clinical success, and safety of the FC-SEMS-in-FC-SEMS technique and identification of risk factors for FC-SEMS removal failure in patients with non-malignant distal biliary stricture.
Patients and methods: Endoscopic retrograde cholangiopancreatography (ERCP) procedures performed between January 1, 2020 and May 31, 2023 for FC-SEMS removal in non-malignant distal biliary strictures were retrospectively identified and analyzed. Cases of FC-SEMS-in-FC-SEMS technique were evaluated.
Results: FC-SEMS-in-FC-SEMS technique was used in 15 patients. FC-SEMS removal was achieved after a single treatment in 13 patients (86.7%). In the remaining two patients (13.3%), it was necessary to repeat treatment to achieve FC-SEMS removal, with an overall technical and clinical success of 100%. No significant adverse events were recorded. Among the 50 patients undergoing ERCP for FC-SEMS removal during the study period (median dwell stenting period of 306.5 days; Q1-Q3:160-392), failure was observed in 15 cases (30%). Previous biliary stenting and dwell stenting period > 300 days were identified as risk factors for FC-SEMS removal failure.
Conclusions: FC-SMES-in-FC-SEMS technique appears to be safe and effective to overcome FC-SEMS removal failure in patients with non-malignant distal biliary strictures. Reducing dwell stenting period, especially in patients with personal history of previous biliary stenting, may reduce risk of FC-SEMS removal failure.
背景与研究目的:全覆盖自扩展金属支架(FC-SEMS)是一种常用的非恶性胆道狭窄治疗方法。与支架远端边缘增生组织发育相关的移除失败已被描述,但很少有数据可用。FC-SEMS中的FC-SEMS技术已在案例报告中描述,以克服FC-SEMS去除失败。本研究的目的是调查FC-SEMS-in-FC-SEMS技术的技术成功、临床成功和安全性,并确定非恶性胆道远端狭窄患者FC-SEMS切除失败的危险因素。患者和方法:回顾性分析2020年1月1日至2023年5月31日期间为FC-SEMS切除非恶性胆道远端狭窄而进行的内镜逆行胆管造影(ERCP)手术。对FC-SEMS-in-FC-SEMS技术的病例进行了评价。结果:15例患者采用FC-SEMS-in-FC-SEMS技术。13例患者(86.7%)在单次治疗后实现了FC-SEMS去除。其余2例患者(13.3%)需要重复治疗以实现FC-SEMS去除,总体技术和临床成功率为100%。无明显不良事件记录。在研究期间,50例接受ERCP进行FC-SEMS移除的患者(中位支架置入时间为306.5天;q1 - q2:160-392)中,15例(30%)失败。既往胆道支架置入术和留置支架置入术时间超过300天是FC-SEMS取出失败的危险因素。结论:fc - sme -in-FC-SEMS技术对于非恶性胆道远端狭窄患者FC-SEMS切除失败是安全有效的。减少留置支架时间,特别是有胆道支架置入术史的患者,可以降低FC-SEMS取出失败的风险。
{"title":"Fully-covered metal stent removal failure in case of non-malignant biliary strictures: Risk factors and resolution technique.","authors":"Nicolò de Pretis, Lorenzo Santaera, Luigi Martinelli, Maria Cristina Conti Bellocchi, Laura Bernardoni, Viola Fino, Adrian Miguel Pezua Sanjinez, Enrico Gasparini, Armando Gabbrielli, Luca Frulloni, Stefano Francesco Crinó","doi":"10.1055/a-2669-5801","DOIUrl":"10.1055/a-2669-5801","url":null,"abstract":"<p><strong>Background and study aims: </strong>Fully-covered-self-expandable-metal-stents (FC-SEMS) are commonly used for non-malignant biliary stricture treatment. Removal failure related to hyperplastic tissue development over the distal margin of the stent has been described but few data are available. FC-SEMS-in-FC-SEMS technique has been described in case reports to overcome FC-SEMS removal failure. Aims of this study were investigating technical success, clinical success, and safety of the FC-SEMS-in-FC-SEMS technique and identification of risk factors for FC-SEMS removal failure in patients with non-malignant distal biliary stricture.</p><p><strong>Patients and methods: </strong>Endoscopic retrograde cholangiopancreatography (ERCP) procedures performed between January 1, 2020 and May 31, 2023 for FC-SEMS removal in non-malignant distal biliary strictures were retrospectively identified and analyzed. Cases of FC-SEMS-in-FC-SEMS technique were evaluated.</p><p><strong>Results: </strong>FC-SEMS-in-FC-SEMS technique was used in 15 patients. FC-SEMS removal was achieved after a single treatment in 13 patients (86.7%). In the remaining two patients (13.3%), it was necessary to repeat treatment to achieve FC-SEMS removal, with an overall technical and clinical success of 100%. No significant adverse events were recorded. Among the 50 patients undergoing ERCP for FC-SEMS removal during the study period (median dwell stenting period of 306.5 days; Q1-Q3:160-392), failure was observed in 15 cases (30%). Previous biliary stenting and dwell stenting period > 300 days were identified as risk factors for FC-SEMS removal failure.</p><p><strong>Conclusions: </strong>FC-SMES-in-FC-SEMS technique appears to be safe and effective to overcome FC-SEMS removal failure in patients with non-malignant distal biliary strictures. Reducing dwell stenting period, especially in patients with personal history of previous biliary stenting, may reduce risk of FC-SEMS removal failure.</p>","PeriodicalId":11671,"journal":{"name":"Endoscopy International Open","volume":"13 ","pages":"a26695801"},"PeriodicalIF":2.3,"publicationDate":"2025-09-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12417772/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145039407","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}
Pub Date : 2025-09-04eCollection Date: 2025-01-01DOI: 10.1055/a-2687-3086
Qiao Yun Liao, Yi Meng Tang, Li Sha Zhan, Yao Fan
Background and study aims: Submucosal tunneling endoscopic resection (STER) has emerged as an innovative approach for the treatment of giant submucosal tumors (SMTs) in the esophagus. However, complications such as esophageal fistula or submucosal infection remain a concern. This article explores how preventive wound drainage can play a significant role in reducing these complications.
Patients and methods: We devised an innovative and straightforward method for negative pressure drainage. This approach involves positioning the drainage device with metal clips before closing the esophageal mucosa wound. A retrospective analysis was conducted on 46 patients with giant SMTs who underwent the STER procedure, among whom 28 had drainage and 18 had no drainage. Patient characteristics, adverse events, and risk factors were comprehensively evaluated.
Results: In 46 patients, the transverse diameter of the tumor exceeded 5 cm. No significant difference was observed in age, gender, tumor size, surgical scope, or mucosal injury between the two groups studied ( P > 0.05). Esophageal fistula or submucosal infection rates in the drainage group were lower than those in the no drainage group (2/28 vs 14/18, P < 0.05). Subgroup analyses revealed that multiple injuries in the esophageal mucosa combined with full-thickness resection of the esophageal muscle layer were the immediate causes of esophageal fistula or submucosal infection following STER surgery.
Conclusions: In the context of STER for giant esophageal submucosal tumors with muscular layer full-thickness resection and mucosal injury, preventive drainage is an effective strategy for minimizing postoperative esophageal fistula and submucosal infection complications.
背景与研究目的:粘膜下隧道内镜切除术(STER)已成为治疗食管巨大粘膜下肿瘤(SMTs)的一种创新方法。然而,并发症如食管瘘或粘膜下感染仍然是一个问题。本文探讨了预防性伤口引流如何在减少这些并发症中发挥重要作用。患者和方法:我们设计了一种创新的、直接的负压引流方法。该方法包括在关闭食管粘膜伤口前用金属夹定位引流装置。回顾性分析46例行STER手术的巨大smt患者,其中28例引流,18例未引流。对患者特征、不良事件和危险因素进行综合评价。结果:46例患者肿瘤横径超过5cm。两组患者在年龄、性别、肿瘤大小、手术范围、粘膜损伤等方面均无统计学差异(P < 0.05)。引流组食管瘘及粘膜下感染发生率低于未引流组(2/28 vs 14/18, P < 0.05)。亚组分析显示,食管黏膜多发损伤联合食管肌层全层切除是STER手术后食管瘘或粘膜下感染的直接原因。结论:在STER手术治疗巨大食管粘膜下肿瘤合并肌肉层全层切除及粘膜损伤的情况下,预防性引流是减少术后食管瘘及粘膜下感染并发症的有效策略。
{"title":"Preventive wound drainage reduces esophageal fistula or infection after endoscopic resection of giant submucosal tumors in the esophagus.","authors":"Qiao Yun Liao, Yi Meng Tang, Li Sha Zhan, Yao Fan","doi":"10.1055/a-2687-3086","DOIUrl":"10.1055/a-2687-3086","url":null,"abstract":"<p><strong>Background and study aims: </strong>Submucosal tunneling endoscopic resection (STER) has emerged as an innovative approach for the treatment of giant submucosal tumors (SMTs) in the esophagus. However, complications such as esophageal fistula or submucosal infection remain a concern. This article explores how preventive wound drainage can play a significant role in reducing these complications.</p><p><strong>Patients and methods: </strong>We devised an innovative and straightforward method for negative pressure drainage. This approach involves positioning the drainage device with metal clips before closing the esophageal mucosa wound. A retrospective analysis was conducted on 46 patients with giant SMTs who underwent the STER procedure, among whom 28 had drainage and 18 had no drainage. Patient characteristics, adverse events, and risk factors were comprehensively evaluated.</p><p><strong>Results: </strong>In 46 patients, the transverse diameter of the tumor exceeded 5 cm. No significant difference was observed in age, gender, tumor size, surgical scope, or mucosal injury between the two groups studied ( <i>P</i> > 0.05). Esophageal fistula or submucosal infection rates in the drainage group were lower than those in the no drainage group (2/28 vs 14/18, <i>P</i> < 0.05). Subgroup analyses revealed that multiple injuries in the esophageal mucosa combined with full-thickness resection of the esophageal muscle layer were the immediate causes of esophageal fistula or submucosal infection following STER surgery.</p><p><strong>Conclusions: </strong>In the context of STER for giant esophageal submucosal tumors with muscular layer full-thickness resection and mucosal injury, preventive drainage is an effective strategy for minimizing postoperative esophageal fistula and submucosal infection complications.</p>","PeriodicalId":11671,"journal":{"name":"Endoscopy International Open","volume":"13 ","pages":"a26873086"},"PeriodicalIF":2.3,"publicationDate":"2025-09-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12417784/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145039510","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}
Pub Date : 2025-09-03eCollection Date: 2025-01-01DOI: 10.1055/a-2681-2859
Gabriel de Oliveira Amaral, João Pedro Schmitt, Lucas Monteiro Delgado, Gilmara Coelho Meine
Background and study aims: Intragastric balloon (IGB) is a minimally invasive and reversible endoscopic option for treating obesity. This systematic review and meta-analysis compared the effectiveness of IGB versus standard medical therapy (SMT) for obesity management, including studies with a minimum treatment duration of 6 months. Subgroup analyses were performed based on IGB type, baseline mean body mass index (BMI), and use of pharmacological therapy in the SMT group.
Methods: We searched for randomized controlled trials (RCTs) in MEDLINE, EMBASE, and Cochrane Library databases. Outcomes were evaluated at 6, 9, and 12 months after initiation of treatment. A random-effects model was used to calculate the pooled mean difference (MD) with 95% confidence interval (CI) for continuous outcomes.
Results: We included 15 RCTs (1961 patients). Compared with SMT, IGB significantly improved the percentage of excess weight loss at 6 months (MD 16.80; 95% CI 9.22-24.38), 9 months (MD 14.36; 95% CI 7.67-21.04), and 12 months (MD 13.10; 95% CI 10.43-15.77). IGB also showed superior results in percentage of total weight loss, absolute weight loss, and BMI reduction at all time points compared with SMT. There were significant subgroup differences for some outcomes according to IGB type and baseline mean BMI.
Conclusions: In obese adults, IGB is more effective than SMT for weight loss at 6, 9, and 12 months.
背景和研究目的:胃内球囊(IGB)是一种微创、可逆的内窥镜治疗肥胖的方法。本系统综述和荟萃分析比较了IGB与标准药物治疗(SMT)在肥胖管理方面的有效性,包括最低治疗持续时间为6个月的研究。根据IGB类型、基线平均体重指数(BMI)和SMT组的药物治疗使用情况进行亚组分析。方法:我们在MEDLINE、EMBASE和Cochrane图书馆数据库中检索随机对照试验(RCTs)。在开始治疗后6、9和12个月评估结果。采用随机效应模型计算连续结果的合并平均差(MD), 95%置信区间(CI)。结果:我们纳入15项随机对照试验(1961例)。与SMT相比,IGB在6个月(MD 16.80; 95% CI 9.22-24.38)、9个月(MD 14.36; 95% CI 7.67-21.04)和12个月(MD 13.10; 95% CI 10.43-15.77)时显著提高了超重减重的百分比。与SMT相比,IGB在所有时间点的总体重减轻百分比、绝对体重减轻百分比和BMI降低方面也显示出更好的结果。根据IGB类型和基线平均BMI,某些结果存在显著的亚组差异。结论:在肥胖成人中,IGB在6、9和12个月时比SMT更有效。
{"title":"Intragastric balloon for obesity treatment: Systematic review and meta-analysis of randomized controlled trials.","authors":"Gabriel de Oliveira Amaral, João Pedro Schmitt, Lucas Monteiro Delgado, Gilmara Coelho Meine","doi":"10.1055/a-2681-2859","DOIUrl":"10.1055/a-2681-2859","url":null,"abstract":"<p><strong>Background and study aims: </strong>Intragastric balloon (IGB) is a minimally invasive and reversible endoscopic option for treating obesity. This systematic review and meta-analysis compared the effectiveness of IGB versus standard medical therapy (SMT) for obesity management, including studies with a minimum treatment duration of 6 months. Subgroup analyses were performed based on IGB type, baseline mean body mass index (BMI), and use of pharmacological therapy in the SMT group.</p><p><strong>Methods: </strong>We searched for randomized controlled trials (RCTs) in MEDLINE, EMBASE, and Cochrane Library databases. Outcomes were evaluated at 6, 9, and 12 months after initiation of treatment. A random-effects model was used to calculate the pooled mean difference (MD) with 95% confidence interval (CI) for continuous outcomes.</p><p><strong>Results: </strong>We included 15 RCTs (1961 patients). Compared with SMT, IGB significantly improved the percentage of excess weight loss at 6 months (MD 16.80; 95% CI 9.22-24.38), 9 months (MD 14.36; 95% CI 7.67-21.04), and 12 months (MD 13.10; 95% CI 10.43-15.77). IGB also showed superior results in percentage of total weight loss, absolute weight loss, and BMI reduction at all time points compared with SMT. There were significant subgroup differences for some outcomes according to IGB type and baseline mean BMI.</p><p><strong>Conclusions: </strong>In obese adults, IGB is more effective than SMT for weight loss at 6, 9, and 12 months.</p>","PeriodicalId":11671,"journal":{"name":"Endoscopy International Open","volume":"13 ","pages":"a26812859"},"PeriodicalIF":2.3,"publicationDate":"2025-09-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12417771/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145039375","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}
Pub Date : 2025-09-01eCollection Date: 2025-01-01DOI: 10.1055/a-2637-2047
Ivana Radosavljevic, Aamir Dam, Anjuli K Luthra, Luis Pena, Saraswathi Cappelle, Jennifer B Permuth, Seth Felder, Julian Sanchez, Amalia Stefanou, Mark Friedman, Shaffer R Mok
Background and study aims: The current standard of care for patients who are found to have malignancy within a resected colorectal polyp segment is surgical resection. Our study aimed to illustrate the efficacy and safety of using endoscopic full thickness resection (EFTR) to achieve histologically complete (R0) resection and formal staging in malignant polypectomy scars.
Patients and methods: This was a prospective case series of 14 patients who underwent scar consolidation via EFTR following piecemeal polypectomy or endoscopic mucosal resection (EMR) of a malignant colorectal polyp. Variables collected assessed R0 resection, technical success of the procedure, residual disease within the scar, recurrence during follow up, and adverse events (AEs).
Results: Of the 14 patient cases reviewed, there was 100% technical success and residual malignancy (RM) found in 14%. Of the two patients with residual disease, one achieved R0 resection with EFTR whereas the other did not and subsequently underwent surgery with no histopathological evidence of malignancy in the resected tissue. There was one AE of rectal bleeding that did not require any surgical intervention or blood transfusions.
Conclusions: EFTR could offer endoscopists a safe, efficacious, and minimally invasive mechanism for formal tumor (T) staging of malignancies found within polypectomy segments. Further studies with larger sample sizes are needed to assess outcomes in patients with residual neoplastic disease.
{"title":"Assessing outcomes of full-thickness resection in piecemeal polypectomy scar consolidation of colon adenomas containing cancer.","authors":"Ivana Radosavljevic, Aamir Dam, Anjuli K Luthra, Luis Pena, Saraswathi Cappelle, Jennifer B Permuth, Seth Felder, Julian Sanchez, Amalia Stefanou, Mark Friedman, Shaffer R Mok","doi":"10.1055/a-2637-2047","DOIUrl":"10.1055/a-2637-2047","url":null,"abstract":"<p><strong>Background and study aims: </strong>The current standard of care for patients who are found to have malignancy within a resected colorectal polyp segment is surgical resection. Our study aimed to illustrate the efficacy and safety of using endoscopic full thickness resection (EFTR) to achieve histologically complete (R0) resection and formal staging in malignant polypectomy scars.</p><p><strong>Patients and methods: </strong>This was a prospective case series of 14 patients who underwent scar consolidation via EFTR following piecemeal polypectomy or endoscopic mucosal resection (EMR) of a malignant colorectal polyp. Variables collected assessed R0 resection, technical success of the procedure, residual disease within the scar, recurrence during follow up, and adverse events (AEs).</p><p><strong>Results: </strong>Of the 14 patient cases reviewed, there was 100% technical success and residual malignancy (RM) found in 14%. Of the two patients with residual disease, one achieved R0 resection with EFTR whereas the other did not and subsequently underwent surgery with no histopathological evidence of malignancy in the resected tissue. There was one AE of rectal bleeding that did not require any surgical intervention or blood transfusions.</p><p><strong>Conclusions: </strong>EFTR could offer endoscopists a safe, efficacious, and minimally invasive mechanism for formal tumor (T) staging of malignancies found within polypectomy segments. Further studies with larger sample sizes are needed to assess outcomes in patients with residual neoplastic disease.</p>","PeriodicalId":11671,"journal":{"name":"Endoscopy International Open","volume":"13 ","pages":"a26372047"},"PeriodicalIF":2.3,"publicationDate":"2025-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12417760/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145039348","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}
Pub Date : 2025-09-01eCollection Date: 2025-01-01DOI: 10.1055/a-2681-2538
Eduardo Guimarães Hourneaux de Moura, Matheus Ferreira de Carvalho, Victor Lira de Oliveira, Mateus Bond Boghossian, Antonio Afonso Miranda Neto, Eduardo Turiani Hourneaux de Moura, André Orsini Ardengh, Ary Nasi, Kenneth Chang, Mateus Pereira Funari
Background and study aims: Achalasia is a condition related to failure of relaxation of the lower esophageal sphincter (LES). Treatment is based on reducing LES pressure. Although treatment is traditionally surgical, poor candidates for this modality may be treated with peroral endoscopic myotomy (POEM). However, POEM is associated with a relatively high incidence of gastroesophageal reflux disease (GERD). For cases refractory to proton pump inhibitors (PPIs), transoral incisionless fundoplication (TIF) is one of the endoscopic therapies proposed.
Patients and methods: This was a pilot single-center prospective cohort study including 10 patients with post-POEM GERD refractory to clinical management who underwent endoscopic treatment with the TIF procedure between February and November 2021. We included patients ≥ 18 years old who developed GERD after POEM.
Results: Technical success was achieved in all 10 cases treated with TIF. In 6- and 12-month follow-up, seven patients (70%) reduced PPI use. Two patients (20%) had no esophagitis initially, increasing to five (55%) at 6 months and four (44%) at 12 months. Symptom evaluation and GERD-HRQL questionnaire showed a significant score reduction at 6 months and a downward trend at 12 months. Mean Eckardt score showed a decreasing trend, although mean dysphagia score showed a slight tendency to increase in 1 year. The procedure was considered safe, with no adverse events.
Conclusions: Use of TIF seems to be a feasible alternative for treating GERD after POEM, improving both clinical and endoscopic parameters and pHmetry in a considerable percentage of cases.
{"title":"Transoral incisionless fundoplication for patients with gastroesophageal reflux disease after peroral endoscopic myotomy: Prospective cohort.","authors":"Eduardo Guimarães Hourneaux de Moura, Matheus Ferreira de Carvalho, Victor Lira de Oliveira, Mateus Bond Boghossian, Antonio Afonso Miranda Neto, Eduardo Turiani Hourneaux de Moura, André Orsini Ardengh, Ary Nasi, Kenneth Chang, Mateus Pereira Funari","doi":"10.1055/a-2681-2538","DOIUrl":"10.1055/a-2681-2538","url":null,"abstract":"<p><strong>Background and study aims: </strong>Achalasia is a condition related to failure of relaxation of the lower esophageal sphincter (LES). Treatment is based on reducing LES pressure. Although treatment is traditionally surgical, poor candidates for this modality may be treated with peroral endoscopic myotomy (POEM). However, POEM is associated with a relatively high incidence of gastroesophageal reflux disease (GERD). For cases refractory to proton pump inhibitors (PPIs), transoral incisionless fundoplication (TIF) is one of the endoscopic therapies proposed.</p><p><strong>Patients and methods: </strong>This was a pilot single-center prospective cohort study including 10 patients with post-POEM GERD refractory to clinical management who underwent endoscopic treatment with the TIF procedure between February and November 2021. We included patients ≥ 18 years old who developed GERD after POEM.</p><p><strong>Results: </strong>Technical success was achieved in all 10 cases treated with TIF. In 6- and 12-month follow-up, seven patients (70%) reduced PPI use. Two patients (20%) had no esophagitis initially, increasing to five (55%) at 6 months and four (44%) at 12 months. Symptom evaluation and GERD-HRQL questionnaire showed a significant score reduction at 6 months and a downward trend at 12 months. Mean Eckardt score showed a decreasing trend, although mean dysphagia score showed a slight tendency to increase in 1 year. The procedure was considered safe, with no adverse events.</p><p><strong>Conclusions: </strong>Use of TIF seems to be a feasible alternative for treating GERD after POEM, improving both clinical and endoscopic parameters and pHmetry in a considerable percentage of cases.</p>","PeriodicalId":11671,"journal":{"name":"Endoscopy International Open","volume":"13 ","pages":"a26812538"},"PeriodicalIF":2.3,"publicationDate":"2025-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12417786/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145039317","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}
Pub Date : 2025-09-01eCollection Date: 2025-01-01DOI: 10.1055/a-2681-2659
Juanjuan Huang, Tingsheng Ling, Junlin Zhang, Lianzhen Wei, Lei Chen, Huiwen Cao, Lei Wang, Yitong Liu, Dongkun Wen, Danrui Ren, Yang Li
Background and study aims: Simethicone has been extensively utilized in endoscopy examinations and therapies; however, consensus regarding its impact on endoscopy cleaning is still lacking. The aim of this study was to assess impact of simethicone use during endoscopic examination on efficacy of endoscope cleaning.
Methods: This was a prospective real-world study that involved use of varying concentrations of simethicone in the endoscope biopsy channel and auxiliary water channel.
Results: All simethicone residual amounts and adenosine triphosphate (ATP) values were analyzed every month for 1 year. Use of 1% and 2% concentrations of simethicone generally resulted in variations in residual simethicone levels between the two channels. There was no significant alteration in ATP values in any concentration between the two channels. However, there was a significant difference in ATP values between the two channels at the concentration of 1% simethicone. After 1 year of usage, suspected adherent was observed in the 2% simethicone group, whereas no crystals were detected adhering to the biopsy channel walls in the 1% group or the control group. Sensitivity analysis suggested that the study results did not differ between the gastroscopy and colonoscopy subgroups.
Conclusions: Simethicone may remain in the biopsy and water infusion channels, regardless of whether it is used or not. It is recommended to utilize a simethicone concentration of 1% or less when administering it through the biopsy or auxiliary water channels of the endoscope.
{"title":"Influence of a defoaming agent - simethicone - on endoscope cleaning and disinfection: Prospective real-world study.","authors":"Juanjuan Huang, Tingsheng Ling, Junlin Zhang, Lianzhen Wei, Lei Chen, Huiwen Cao, Lei Wang, Yitong Liu, Dongkun Wen, Danrui Ren, Yang Li","doi":"10.1055/a-2681-2659","DOIUrl":"10.1055/a-2681-2659","url":null,"abstract":"<p><strong>Background and study aims: </strong>Simethicone has been extensively utilized in endoscopy examinations and therapies; however, consensus regarding its impact on endoscopy cleaning is still lacking. The aim of this study was to assess impact of simethicone use during endoscopic examination on efficacy of endoscope cleaning.</p><p><strong>Methods: </strong>This was a prospective real-world study that involved use of varying concentrations of simethicone in the endoscope biopsy channel and auxiliary water channel.</p><p><strong>Results: </strong>All simethicone residual amounts and adenosine triphosphate (ATP) values were analyzed every month for 1 year. Use of 1% and 2% concentrations of simethicone generally resulted in variations in residual simethicone levels between the two channels. There was no significant alteration in ATP values in any concentration between the two channels. However, there was a significant difference in ATP values between the two channels at the concentration of 1% simethicone. After 1 year of usage, suspected adherent was observed in the 2% simethicone group, whereas no crystals were detected adhering to the biopsy channel walls in the 1% group or the control group. Sensitivity analysis suggested that the study results did not differ between the gastroscopy and colonoscopy subgroups.</p><p><strong>Conclusions: </strong>Simethicone may remain in the biopsy and water infusion channels, regardless of whether it is used or not. It is recommended to utilize a simethicone concentration of 1% or less when administering it through the biopsy or auxiliary water channels of the endoscope.</p>","PeriodicalId":11671,"journal":{"name":"Endoscopy International Open","volume":"13 ","pages":"a26812659"},"PeriodicalIF":2.3,"publicationDate":"2025-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12417768/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145039378","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}
Pub Date : 2025-08-29eCollection Date: 2025-01-01DOI: 10.1055/a-2676-4144
Azizullah Beran, Tarek Nayfeh, Daryl Ramai, Almaza Albakri, Nasir Saleem, Marco Spadaccini, Cesare Hassan, Alessandro Repici, John J Guardiola, Douglas K Rex
Background and study aims: Artificial intelligence (AI) and mucosal exposure devices like Endocuff have independently improved the adenoma detection rate (ADR) during colonoscopy. This meta-analysis evaluated the combined effect of Endocuff and AI versus AI alone on colorectal neoplasia detection rates.
Methods: We searched PubMed, Embase, and Web of Science for randomized controlled trials (RCTs) comparing the impact of Endocuff+AI versus AI alone on colorectal neoplasia detection. Primary outcome was ADR; secondary outcomes included advanced adenoma detection rate (AADR), sessile serrated lesion detection rate (SSLDR), cecal intubation time, and withdrawal time. Pooled risk ratios (RRs) and mean differences (MDs) with 95% confidence intervals (CIs) were calculated using a random-effects model.
Results: Three RCTs with 2404 subjects were included (n = 1198 Endocuff+AI vs. n = 1206 AI alone). ADR was significantly higher in the Endocuff+AI group than in the AI alone group (54% vs. 48%, respectively) (RR 1.12, 95% CI 1.03-1.21, P = 0.01, I 2 = 0%). There was a trend toward higher AADR (12.3% vs. 10%, RR 1.23, 95% CI 0.96-1.59, P = 0.10, I 2 = 17%) and SSLDR (17.6% vs. 15.5%, RR 1.16, 95% CI 0.96-1.40, P = 0.13, I 2 = 0%) in the Endocuff+AI group compared with the AI alone group, but it did not reach statistical significance. Both cecal intubation time (MD -0.61 minutes; 95% CI -1.54-0.33; P = 0.20; I 2 = 87%) and withdrawal time (MD -0.42 minutes; 95% CI -1.01-0.17; P = 0.17, I 2 = 60%) were similar between the two groups.
Conclusions: Endocuff combined with AI was superior to AI alone in improving the adenoma detection rate without increasing intubation or withdrawal times.
背景与研究目的:人工智能(AI)和endocff等粘膜暴露设备各自提高了结肠镜检查时腺瘤的检出率(ADR)。本荟萃分析评估了恩多夫联合人工智能与单独使用人工智能对结直肠肿瘤检出率的影响。方法:我们检索了PubMed、Embase和Web of Science的随机对照试验(rct),比较endocff +AI与单独AI对结直肠肿瘤检测的影响。主要结局为不良反应;次要结局包括晚期腺瘤检出率(AADR)、无底锯齿状病变检出率(SSLDR)、盲肠插管时间和停药时间。采用随机效应模型计算合并风险比(rr)和95%置信区间(ci)的平均差异(md)。结果:纳入3个随机对照试验,共2404名受试者(n = 1198 endocff +AI vs n = 1206 AI单独)。endocff +AI组不良反应明显高于单独使用AI组(54% vs 48%) (RR 1.12, 95% CI 1.03 ~ 1.21, P = 0.01, i2 = 0%)。endocff +AI组的AADR (12.3% vs. 10%, RR 1.23, 95% CI 0.96 ~ 1.59, P = 0.10, i2 = 17%)和SSLDR (17.6% vs. 15.5%, RR 1.16, 95% CI 0.96 ~ 1.40, P = 0.13, i2 = 0%)均高于单纯AI组,但差异无统计学意义。两组间盲肠插管时间(MD -0.61 min; 95% CI -1.54 ~ 0.33; P = 0.20; i2 = 87%)和停药时间(MD -0.42 min; 95% CI -1.01 ~ 0.17; P = 0.17, i2 = 60%)相似。结论:恩多夫联合人工智能在提高腺瘤检出率方面优于单独人工智能,且不增加插管和停药次数。
{"title":"Artificial Intelligence-Assisted Colonoscopy With or Without Mucosal Exposure Device for Detection of Colorectal Adenomas: A Meta-Analysis.","authors":"Azizullah Beran, Tarek Nayfeh, Daryl Ramai, Almaza Albakri, Nasir Saleem, Marco Spadaccini, Cesare Hassan, Alessandro Repici, John J Guardiola, Douglas K Rex","doi":"10.1055/a-2676-4144","DOIUrl":"10.1055/a-2676-4144","url":null,"abstract":"<p><strong>Background and study aims: </strong>Artificial intelligence (AI) and mucosal exposure devices like Endocuff have independently improved the adenoma detection rate (ADR) during colonoscopy. This meta-analysis evaluated the combined effect of Endocuff and AI versus AI alone on colorectal neoplasia detection rates.</p><p><strong>Methods: </strong>We searched PubMed, Embase, and Web of Science for randomized controlled trials (RCTs) comparing the impact of Endocuff+AI versus AI alone on colorectal neoplasia detection. Primary outcome was ADR; secondary outcomes included advanced adenoma detection rate (AADR), sessile serrated lesion detection rate (SSLDR), cecal intubation time, and withdrawal time. Pooled risk ratios (RRs) and mean differences (MDs) with 95% confidence intervals (CIs) were calculated using a random-effects model.</p><p><strong>Results: </strong>Three RCTs with 2404 subjects were included (n = 1198 Endocuff+AI vs. n = 1206 AI alone). ADR was significantly higher in the Endocuff+AI group than in the AI alone group (54% vs. 48%, respectively) (RR 1.12, 95% CI 1.03-1.21, <i>P</i> = 0.01, I <sup>2</sup> = 0%). There was a trend toward higher AADR (12.3% vs. 10%, RR 1.23, 95% CI 0.96-1.59, <i>P</i> = 0.10, I <sup>2</sup> = 17%) and SSLDR (17.6% vs. 15.5%, RR 1.16, 95% CI 0.96-1.40, <i>P</i> = 0.13, I <sup>2</sup> = 0%) in the Endocuff+AI group compared with the AI alone group, but it did not reach statistical significance. Both cecal intubation time (MD -0.61 minutes; 95% CI -1.54-0.33; <i>P</i> = 0.20; I <sup>2</sup> = 87%) and withdrawal time (MD -0.42 minutes; 95% CI -1.01-0.17; <i>P</i> = 0.17, I <sup>2</sup> = 60%) were similar between the two groups.</p><p><strong>Conclusions: </strong>Endocuff combined with AI was superior to AI alone in improving the adenoma detection rate without increasing intubation or withdrawal times.</p>","PeriodicalId":11671,"journal":{"name":"Endoscopy International Open","volume":"13 ","pages":"a26764144"},"PeriodicalIF":2.3,"publicationDate":"2025-08-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12417794/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145039366","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}
Pub Date : 2025-08-28eCollection Date: 2025-01-01DOI: 10.1055/a-2663-6177
Su Luo, Feng Xiong, Sheng-Gang Zhan, Zhenglei Xu, Ding-Guo Zhang, Ting-Ting Liu, Ying-Xue Li, Cheng Wei, Ben-Hua Wu, Yi-Teng Meng, Rui-Yue Shi, Jun Yao, Li-Sheng Wang, De-Feng Li
Background and study aims: Endocut Q (effect 2, effect 3 and effect 4) commonly is used for endoscopic mucosal resection (EMR) when removing colorectal polyps. However, there is debate over the type of electrosurgical setting of Endocut Q being recommended in clinical practice. We performed a randomized controlled trial to assess effectiveness and safety of three effects with EMR for removal of non-pedunculated 10- to 20-mm colorectal polyps.
Patients and methods: Patients with non-pedunculate colorectal polyps undergoing EMR were randomly allocated into effect 2, effect 3, and effect 4 groups. The primary outcome was rates of intra-procedural bleeding. Secondary outcomes were rates of post-procedural bleeding, perforation, complete resection, en bloc resection, R0 resection, and residual polyps.
Results: A total of 2637 eligible patients were included in the study and randomly assigned into the effect 2, effect 3, or effect 4 group. There were no significant differences among the three groups in baseline characteristics ( P > 0.05). In addition, no significant differences were observed in rates of post-procedural bleeding, perforation, complete resection, en bloc resection, R0 resection, residual polyps, or post-polypectomy syndrome ( P > 0.05). However, the rate of intra-procedural bleeding was significantly lower in the effect 2 group than in the effect 3 and effect 4 groups (4.0% vs. 12.2% vs. 12.7%, P < 0.01).
Conclusions: Endocut Q (effect 2, effect 3 and effect 4) was effective and safe for removing 10- to 20-mm non-pedunculated colorectal polyps. However, effect 2 may be superior to effect 3 and effect 4 in reducing intra-procedural bleeding.
{"title":"Comparison of three electrosurgical modes for endoscopic mucosal resection of 10- to 20-mm colorectal polyps: Randomized controlled trial.","authors":"Su Luo, Feng Xiong, Sheng-Gang Zhan, Zhenglei Xu, Ding-Guo Zhang, Ting-Ting Liu, Ying-Xue Li, Cheng Wei, Ben-Hua Wu, Yi-Teng Meng, Rui-Yue Shi, Jun Yao, Li-Sheng Wang, De-Feng Li","doi":"10.1055/a-2663-6177","DOIUrl":"10.1055/a-2663-6177","url":null,"abstract":"<p><strong>Background and study aims: </strong>Endocut Q (effect 2, effect 3 and effect 4) commonly is used for endoscopic mucosal resection (EMR) when removing colorectal polyps. However, there is debate over the type of electrosurgical setting of Endocut Q being recommended in clinical practice. We performed a randomized controlled trial to assess effectiveness and safety of three effects with EMR for removal of non-pedunculated 10- to 20-mm colorectal polyps.</p><p><strong>Patients and methods: </strong>Patients with non-pedunculate colorectal polyps undergoing EMR were randomly allocated into effect 2, effect 3, and effect 4 groups. The primary outcome was rates of intra-procedural bleeding. Secondary outcomes were rates of post-procedural bleeding, perforation, complete resection, en bloc resection, R0 resection, and residual polyps.</p><p><strong>Results: </strong>A total of 2637 eligible patients were included in the study and randomly assigned into the effect 2, effect 3, or effect 4 group. There were no significant differences among the three groups in baseline characteristics ( <i>P</i> > 0.05). In addition, no significant differences were observed in rates of post-procedural bleeding, perforation, complete resection, en bloc resection, R0 resection, residual polyps, or post-polypectomy syndrome ( <i>P</i> > 0.05). However, the rate of intra-procedural bleeding was significantly lower in the effect 2 group than in the effect 3 and effect 4 groups (4.0% vs. 12.2% vs. 12.7%, <i>P</i> < 0.01).</p><p><strong>Conclusions: </strong>Endocut Q (effect 2, effect 3 and effect 4) was effective and safe for removing 10- to 20-mm non-pedunculated colorectal polyps. However, effect 2 may be superior to effect 3 and effect 4 in reducing intra-procedural bleeding.</p>","PeriodicalId":11671,"journal":{"name":"Endoscopy International Open","volume":"13 ","pages":"a26636177"},"PeriodicalIF":2.3,"publicationDate":"2025-08-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12418810/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145039334","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}