Pub Date : 2025-08-19eCollection Date: 2025-01-01DOI: 10.1055/a-2663-6533
Anais Darnaude, Maxime Thobois, Philippe Onana Ndong, Cécile Gomercic, James Boulant, Geoffroy Vanbiervliet
Background and study aims: Migration remains a frequent and challenging situation following esophageal stent placement. The aims of this study were to evaluate efficiency and safety of a new anchorage technique using through-the-scope (TTS) clips to prevent esophageal stent migration.
Patients and methods: This was a retrospective case-control analysis of a prospective, monocentric database. Patients with a fully-covered esophageal stent, fixed or not for benign or malignant indications, were included. Fixation of the stent at the oral flange was achieved with TTS clips, placed for a bite in submucosal space after injection with saline and mucosal incision using the tip of a snare.
Results: A total of 52 patients were included, 24 stents with anchorage (fixed group) and 28 without (control group). Fixation was more frequently performed for benign disease (75.0% fixed group vs. 39.29% for control, P = 0.021). Median length of stent dwell time was 41.5 days in the fixed group and 30.5 days for controls ( P = 0.263). The overall migration rate was comparable (45.83% in the fixed group vs. 35.71% for controls, P = 0.647). A higher rate of early migration was observed in the control group (60.0% vs 18.18%, P = 0.080). A prior history of radio-chemotherapy was predictive of migration. There was no increased complication rate at placement or at removal in the treated group.
Conclusions: The new esophageal stent fixation technique appears to be simple, inexpensive, feasible, and safe. Although there is no impact on overall migration, there does seem to be a reduction in early migration.
背景和研究目的:食管支架置入术后迁移仍然是一个常见且具有挑战性的情况。本研究的目的是评估一种新的通过范围(TTS)夹子来防止食管支架移动的锚固技术的有效性和安全性。患者和方法:这是一项前瞻性单中心数据库的回顾性病例对照分析。患者全覆盖食管支架,固定或不为良性或恶性指征,包括。使用TTS夹子将支架固定在口腔法兰处,在注射生理盐水和使用圈套尖端的粘膜切口后放置在粘膜下间隙咬合。结果:共纳入52例患者,有支抗组24例(固定组),无支抗组28例(对照组)。良性疾病的固定更频繁(固定组75.0% vs对照组39.29%,P = 0.021)。固定组支架放置时间中位数为41.5天,对照组为30.5天(P = 0.263)。总体迁移率具有可比性(固定组为45.83%,对照组为35.71%,P = 0.647)。对照组早期迁移率较高(60.0% vs 18.18%, P = 0.080)。既往放化疗史可预测迁移。治疗组在放置或取出时并发症发生率均未增加。结论:新型食管支架固定技术简单、经济、可行、安全。尽管对总体迁移没有影响,但早期迁移似乎确实有所减少。
{"title":"Evaluation of the clip anchorage technique using mucosal elevation and incision in prevention of esophageal stent migration.","authors":"Anais Darnaude, Maxime Thobois, Philippe Onana Ndong, Cécile Gomercic, James Boulant, Geoffroy Vanbiervliet","doi":"10.1055/a-2663-6533","DOIUrl":"10.1055/a-2663-6533","url":null,"abstract":"<p><strong>Background and study aims: </strong>Migration remains a frequent and challenging situation following esophageal stent placement. The aims of this study were to evaluate efficiency and safety of a new anchorage technique using through-the-scope (TTS) clips to prevent esophageal stent migration.</p><p><strong>Patients and methods: </strong>This was a retrospective case-control analysis of a prospective, monocentric database. Patients with a fully-covered esophageal stent, fixed or not for benign or malignant indications, were included. Fixation of the stent at the oral flange was achieved with TTS clips, placed for a bite in submucosal space after injection with saline and mucosal incision using the tip of a snare.</p><p><strong>Results: </strong>A total of 52 patients were included, 24 stents with anchorage (fixed group) and 28 without (control group). Fixation was more frequently performed for benign disease (75.0% fixed group vs. 39.29% for control, <i>P</i> = 0.021). Median length of stent dwell time was 41.5 days in the fixed group and 30.5 days for controls ( <i>P</i> = 0.263). The overall migration rate was comparable (45.83% in the fixed group vs. 35.71% for controls, <i>P</i> = 0.647). A higher rate of early migration was observed in the control group (60.0% vs 18.18%, <i>P</i> = 0.080). A prior history of radio-chemotherapy was predictive of migration. There was no increased complication rate at placement or at removal in the treated group.</p><p><strong>Conclusions: </strong>The new esophageal stent fixation technique appears to be simple, inexpensive, feasible, and safe. Although there is no impact on overall migration, there does seem to be a reduction in early migration.</p>","PeriodicalId":11671,"journal":{"name":"Endoscopy International Open","volume":"13 ","pages":"a26636533"},"PeriodicalIF":2.3,"publicationDate":"2025-08-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12371653/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144947224","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 : 2025-08-19eCollection Date: 2025-01-01DOI: 10.1055/a-2685-7125
Michel Kahaleh, Vera Hapshy, Juan A Alcívar, Jorge Baquerizo-Burgos, Hannah Lukashok, Monica R Gaidhane, Iman Andalib, Amy Tyberg, Avik Sarkar, Haroon Shahid, Abid Allehibi, Resheed Alkhiari, Magda L Rodriguez, Carmen Bautista-Altamirano, Sarbelio Rodriguez, Maria G Porfilio, Mine Carames, Juan Carlos Carames, Amol Bapaye, Carlos Robles-Medranda
[This corrects the article DOI: 10.1055/a-2655-6550.].
[这更正了文章DOI: 10.1055/a-2655-6550]。
{"title":"Correction: Safety and efficacy of peroral endoscopic myotomy with endoscopic fundoplication compared with POEM alone: International multicenter cohort study.","authors":"Michel Kahaleh, Vera Hapshy, Juan A Alcívar, Jorge Baquerizo-Burgos, Hannah Lukashok, Monica R Gaidhane, Iman Andalib, Amy Tyberg, Avik Sarkar, Haroon Shahid, Abid Allehibi, Resheed Alkhiari, Magda L Rodriguez, Carmen Bautista-Altamirano, Sarbelio Rodriguez, Maria G Porfilio, Mine Carames, Juan Carlos Carames, Amol Bapaye, Carlos Robles-Medranda","doi":"10.1055/a-2685-7125","DOIUrl":"10.1055/a-2685-7125","url":null,"abstract":"<p><p>[This corrects the article DOI: 10.1055/a-2655-6550.].</p>","PeriodicalId":11671,"journal":{"name":"Endoscopy International Open","volume":"13 ","pages":"a26857125"},"PeriodicalIF":2.3,"publicationDate":"2025-08-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12371640/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144946991","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 : 2025-08-15eCollection Date: 2025-01-01DOI: 10.1055/a-2655-1083
Andrea C Armbrecht, Bojan Kovacevic, Maria Dyrehave Rasmussen, Michelle Katharina Bernth, Ann Merete Moeller, Peter Vilmann
Background and study aims: Remimazolam is a new ultra-short-acting benzodiazepine with a favorable safety-profile when used for sedation in endoscopy. The aim of this project was to investigate efficacy of remimazolam with fentanyl compared with midazolam with fentanyl for sedation in colonoscopy among fecal immunochemical test (FIT)-positive screening participants.
Patients and methods: The study was a prospective, single-blinded, randomized controlled trial. FIT-positive participants undergoing colonoscopy were randomized to intravenous remimazolam + fentanyl (RF) or midazolam + fentanyl (MF). Primary outcome was total time from start of medication until discharge. Secondary outcomes included time to reach cecum, need for post-procedure recovery, patient-reported pain and satisfaction, need for additional medication, and procedure completion.
Results: A total of 205 patients were included and randomized 1:1 (RF:103, MF:102). Mean age was 62.6 years, whereas female/male ratio was 97/108. Mean time from start of medication until discharge was 29.9 minutes (RF) versus 35.0 minutes (MF) (95% confidence interval 0.77-0.94, P = 0.012). Mean time to reach the cecum was 15.4 minutes (RF) compared with 20.2 minutes (MF) ( P = 0.001). Proportion of patients requiring postoperative observation was lower for RF 0.97% vs 9.8% for MF ( P = 0.022). Patients receiving remimazolam reported an average lower pain score (mean 2.25 (RF) vs 3.25 (MF) P = 0.012) and higher overall satisfaction score (4.65 vs 4.33, P = 0.012).
Conclusions: This study shows clear superiority of the combination of remimazolam with fentanyl over midazolam with fentanyl for conscious sedation in screening colonoscopy, obtaining shorter procedure time, less postoperative need for observation, lower patient pain scores, and higher patient satisfaction.
背景与研究目的:雷马唑仑是一种新型超短效苯二氮卓类药物,在内镜下镇静时具有良好的安全性。本项目的目的是在粪便免疫化学试验(FIT)阳性筛查参与者中,比较雷马唑仑与芬太尼联合使用咪达唑仑与芬太尼在结肠镜检查中的镇静效果。患者和方法:本研究为前瞻性、单盲、随机对照试验。接受结肠镜检查的fit阳性参与者随机分为静脉注射雷马唑仑+芬太尼(RF)或咪达唑仑+芬太尼(MF)组。主要结局是从开始用药到出院的总时间。次要结局包括到达盲肠的时间、术后恢复的需要、患者报告的疼痛和满意度、需要额外的药物治疗和手术完成情况。结果:共纳入205例患者,按1:1随机分组(RF:103, MF:102)。平均年龄62.6岁,男女比例为97/108。从开始用药到出院的平均时间为29.9分钟(RF),而35.0分钟(MF)(95%置信区间0.77 ~ 0.94,P = 0.012)。到达盲肠的平均时间为15.4分钟(RF),而20.2分钟(MF) (P = 0.001)。RF组术后需要观察的患者比例为0.97%,MF组为9.8% (P = 0.022)。接受雷马唑仑治疗的患者报告的平均疼痛评分较低(平均2.25 (RF) vs 3.25 (MF) P = 0.012),总体满意度评分较高(4.65 vs 4.33, P = 0.012)。结论:本研究显示雷马唑仑联合芬太尼在结肠镜筛查中明显优于咪达唑仑联合芬太尼进行意识镇静,手术时间更短,术后观察需要更少,患者疼痛评分更低,患者满意度更高。
{"title":"Efficacy of remimazolam with fentanyl vs midazolam with fentanyl for sedation in screening colonoscopy: Randomized controlled study.","authors":"Andrea C Armbrecht, Bojan Kovacevic, Maria Dyrehave Rasmussen, Michelle Katharina Bernth, Ann Merete Moeller, Peter Vilmann","doi":"10.1055/a-2655-1083","DOIUrl":"10.1055/a-2655-1083","url":null,"abstract":"<p><strong>Background and study aims: </strong>Remimazolam is a new ultra-short-acting benzodiazepine with a favorable safety-profile when used for sedation in endoscopy. The aim of this project was to investigate efficacy of remimazolam with fentanyl compared with midazolam with fentanyl for sedation in colonoscopy among fecal immunochemical test (FIT)-positive screening participants.</p><p><strong>Patients and methods: </strong>The study was a prospective, single-blinded, randomized controlled trial. FIT-positive participants undergoing colonoscopy were randomized to intravenous remimazolam + fentanyl (RF) or midazolam + fentanyl (MF). Primary outcome was total time from start of medication until discharge. Secondary outcomes included time to reach cecum, need for post-procedure recovery, patient-reported pain and satisfaction, need for additional medication, and procedure completion.</p><p><strong>Results: </strong>A total of 205 patients were included and randomized 1:1 (RF:103, MF:102). Mean age was 62.6 years, whereas female/male ratio was 97/108. Mean time from start of medication until discharge was 29.9 minutes (RF) versus 35.0 minutes (MF) (95% confidence interval 0.77-0.94, <i>P</i> = 0.012). Mean time to reach the cecum was 15.4 minutes (RF) compared with 20.2 minutes (MF) ( <i>P</i> = 0.001). Proportion of patients requiring postoperative observation was lower for RF 0.97% vs 9.8% for MF ( <i>P</i> = 0.022). Patients receiving remimazolam reported an average lower pain score (mean 2.25 (RF) vs 3.25 (MF) <i>P</i> = 0.012) and higher overall satisfaction score (4.65 vs 4.33, <i>P</i> = 0.012).</p><p><strong>Conclusions: </strong>This study shows clear superiority of the combination of remimazolam with fentanyl over midazolam with fentanyl for conscious sedation in screening colonoscopy, obtaining shorter procedure time, less postoperative need for observation, lower patient pain scores, and higher patient satisfaction.</p>","PeriodicalId":11671,"journal":{"name":"Endoscopy International Open","volume":"13 ","pages":"a26551083"},"PeriodicalIF":2.3,"publicationDate":"2025-08-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12371649/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144947118","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}
Background and study aims: Advanced endoscopic resection methods are recommended for removing rectal neuroendocrine tumors (NETs) < 10 mm, but there is no consensus on optimal endoscopic technique. This study aimed to determine whether endoscopic mucosal resection with ligation (EMR-L) is superior to endoscopic submucosal dissection (ESD) in terms of efficacy and safety, focusing on achieving adequate vertical margin distance.
Patients and methods: This dual-center cohort study included consecutive patients with rectal NETs ≤ 10 mm. Adequate vertical margins were exploratively defined as a margin distance exceeding 115 μm, the 25th percentile threshold. Propensity score matching (PSM) was applied to compare outcomes between EMR-L and ESD.
Results: The study included 204 rectal NETs from 186 patients, with 61 lesions in each group after PSM. Compared with ESD, the EMR-L group demonstrated a higher R0 resection rate (98.4% vs. 83.6%, P = 0.021), a greater proportion of adequate vertical margins (80.3% vs. 62.3%, P = 0.030), and a lower rate of positive vertical margins (1.6% vs. 13.1%, P = 0.041). Subgroup analysis indicated that lesions ≤ 5 mm without prior biopsy or central depression derived greater benefit from EMR-L. Furthermore, EMR-L was associated with significantly shorter procedure times (median 5.0 vs. 19 minutes) and a markedly lower overall complication rate (8.2% vs. 29.5%, P = 0.005), particularly perforation (3.3% vs. 16.4%, P = 0.028).
Conclusions: EMR-L outperforms ESD for small rectal NETs by achieving higher R0 and better vertical margins in shorter times, while minimizing risk of perforation.
背景与研究目的:对于< 10 mm的直肠神经内分泌肿瘤(NETs),建议采用先进的内镜切除方法,但对最佳内镜技术尚无共识。本研究旨在确定内镜下粘膜结扎切除术(EMR-L)是否优于内镜下粘膜剥离术(ESD)的有效性和安全性,重点关注是否能获得足够的垂直切缘距离。患者和方法:这项双中心队列研究包括直肠NETs≤10 mm的连续患者。适当的垂直边缘被探索性地定义为边缘距离超过115 μm,即第25个百分位阈值。倾向评分匹配(PSM)用于比较EMR-L和ESD的结果。结果:本研究纳入186例204例直肠NETs,每组经PSM后病变61个。与ESD组相比,EMR-L组的R0切除率更高(98.4%比83.6%,P = 0.021),垂直切缘充足的比例更高(80.3%比62.3%,P = 0.030),垂直切缘阳性的比例更低(1.6%比13.1%,P = 0.041)。亚组分析表明,病变≤5mm且没有事先活检或中枢性凹陷的患者从EMR-L中获益更大。此外,EMR-L显著缩短了手术时间(中位数5.0 vs 19分钟),显著降低了总并发症发生率(8.2% vs 29.5%, P = 0.005),尤其是穿孔(3.3% vs 16.4%, P = 0.028)。结论:EMR-L优于ESD,在更短的时间内获得更高的R0和更好的垂直切缘,同时最大限度地降低了穿孔的风险。
{"title":"Optimal endoscopic resection method based on vertical margin distance for small rectal neuroendocrine tumors: Propensity score-matched study.","authors":"Jianning Liu, Weihua Yu, Peng Liu, Hao Tian, Lihong Gan, Kaige Zhang, Hui Chen, Nian Fang","doi":"10.1055/a-2655-1320","DOIUrl":"10.1055/a-2655-1320","url":null,"abstract":"<p><strong>Background and study aims: </strong>Advanced endoscopic resection methods are recommended for removing rectal neuroendocrine tumors (NETs) < 10 mm, but there is no consensus on optimal endoscopic technique. This study aimed to determine whether endoscopic mucosal resection with ligation (EMR-L) is superior to endoscopic submucosal dissection (ESD) in terms of efficacy and safety, focusing on achieving adequate vertical margin distance.</p><p><strong>Patients and methods: </strong>This dual-center cohort study included consecutive patients with rectal NETs ≤ 10 mm. Adequate vertical margins were exploratively defined as a margin distance exceeding 115 μm, the 25th percentile threshold. Propensity score matching (PSM) was applied to compare outcomes between EMR-L and ESD.</p><p><strong>Results: </strong>The study included 204 rectal NETs from 186 patients, with 61 lesions in each group after PSM. Compared with ESD, the EMR-L group demonstrated a higher R0 resection rate (98.4% vs. 83.6%, <i>P</i> = 0.021), a greater proportion of adequate vertical margins (80.3% vs. 62.3%, <i>P</i> = 0.030), and a lower rate of positive vertical margins (1.6% vs. 13.1%, <i>P</i> = 0.041). Subgroup analysis indicated that lesions ≤ 5 mm without prior biopsy or central depression derived greater benefit from EMR-L. Furthermore, EMR-L was associated with significantly shorter procedure times (median 5.0 vs. 19 minutes) and a markedly lower overall complication rate (8.2% vs. 29.5%, <i>P</i> = 0.005), particularly perforation (3.3% vs. 16.4%, <i>P</i> = 0.028).</p><p><strong>Conclusions: </strong>EMR-L outperforms ESD for small rectal NETs by achieving higher R0 and better vertical margins in shorter times, while minimizing risk of perforation.</p>","PeriodicalId":11671,"journal":{"name":"Endoscopy International Open","volume":"13 ","pages":"a26551320"},"PeriodicalIF":2.3,"publicationDate":"2025-08-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12371650/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144947364","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 : 2025-08-14eCollection Date: 2025-01-01DOI: 10.1055/a-2663-6291
Gaurav Suryawanshi, Mohamed Abdallah, Guru Trikudanathan, Stuart K Amateau, Shawn Mallery, Martin Freeman, Nabeel Azeem
Background and study aims: Endoscopic papillectomy (EP) is an effective endoscopic modality for managing ampullary lesions. This study aimed to evaluate predictors for recurrence and adverse events (AEs) in patients who underwent EP for major papilla lesions.
Patients and methods: This was a retrospective analysis of all patients who underwent endoscopic snare papillectomy for a major papilla lesion between January 2006 and December 2021. We assessed multiple patient- and procedure-related variables to identify risk factors related to post-EP AEs and lesion recurrence using both univariate and multivariate analysis. In addition, we compared baseline characteristics and outcomes in patients with familial adenomatous polyposis (FAP) vs. sporadic ampullary lesions (SALs).
Results: Fifty-one patients (11 FAP) were included in the final analysis. Recurrence was seen in 17 patients (37.0%) among those who followed up after technical success. Complete histological (R0) resection was the only factor associated with no recurrence following EP (odds ratio [OR] 5.4, 95% confidence interval [CI] 1.4-20.8, P = 0.014). PEP was associated with delayed bleeding (OR 7.5, 95% CI 1.2-46.1, P = 0.03). In FAP vs. SAL, lesion size was smaller in FAP: 10 mm (interquartile range 6-15 mm) vs. 15 mm (12-21 mm, P = 0.03) and the en-bloc resection rate was higher (100 vs. 67.5%, P = 0.01). Although the recurrence rate was higher in FAP vs. SAL (55.6 vs. 32.4%, P = 0.2), this was not statistically significant. Rates of AEs were similar.
Conclusions: R0 resection was associated with reduced risk of recurrence whereas delayed bleeding after EP is associated with an increased risk of developing PEP. EP is safe and effective for removing ampullary lesions irrespective of lesion type.
背景和研究目的:内镜下乳头切除术(EP)是治疗壶腹部病变的有效内镜方式。本研究旨在评估因大乳头病变接受EP治疗的患者复发和不良事件(ae)的预测因素。患者和方法:这是对2006年1月至2021年12月期间因主要乳头病变接受内窥镜陷阱乳头切除术的所有患者的回顾性分析。我们评估了多个与患者和手术相关的变量,通过单变量和多变量分析来确定与ep后ae和病变复发相关的危险因素。此外,我们比较了家族性腺瘤性息肉病(FAP)和散发壶腹病变(SALs)患者的基线特征和结果。结果:51例患者(11例FAP)纳入最终分析。技术成功后随访的患者中有17例(37.0%)出现复发。完全组织学(R0)切除是EP术后无复发的唯一相关因素(优势比[OR] 5.4, 95%可信区间[CI] 1.4-20.8, P = 0.014)。PEP与迟发性出血相关(OR 7.5, 95% CI 1.2-46.1, P = 0.03)。FAP与SAL相比,FAP的病变大小更小:10 mm(四分位间距6-15 mm)比15 mm (12-21 mm, P = 0.03),整体切除率更高(100比67.5%,P = 0.01)。虽然FAP的复发率高于SAL(55.6%比32.4%,P = 0.2),但差异无统计学意义。ae的发生率相似。结论:R0切除与降低复发风险相关,而EP后延迟出血与发生PEP的风险增加相关。无论病变类型如何,EP均可安全有效地切除壶腹部病变。
{"title":"Endoscopic papillectomy of major papilla lesions: Single tertiary care center experience.","authors":"Gaurav Suryawanshi, Mohamed Abdallah, Guru Trikudanathan, Stuart K Amateau, Shawn Mallery, Martin Freeman, Nabeel Azeem","doi":"10.1055/a-2663-6291","DOIUrl":"10.1055/a-2663-6291","url":null,"abstract":"<p><strong>Background and study aims: </strong>Endoscopic papillectomy (EP) is an effective endoscopic modality for managing ampullary lesions. This study aimed to evaluate predictors for recurrence and adverse events (AEs) in patients who underwent EP for major papilla lesions.</p><p><strong>Patients and methods: </strong>This was a retrospective analysis of all patients who underwent endoscopic snare papillectomy for a major papilla lesion between January 2006 and December 2021. We assessed multiple patient- and procedure-related variables to identify risk factors related to post-EP AEs and lesion recurrence using both univariate and multivariate analysis. In addition, we compared baseline characteristics and outcomes in patients with familial adenomatous polyposis (FAP) vs. sporadic ampullary lesions (SALs).</p><p><strong>Results: </strong>Fifty-one patients (11 FAP) were included in the final analysis. Recurrence was seen in 17 patients (37.0%) among those who followed up after technical success. Complete histological (R0) resection was the only factor associated with no recurrence following EP (odds ratio [OR] 5.4, 95% confidence interval [CI] 1.4-20.8, <i>P</i> = 0.014). PEP was associated with delayed bleeding (OR 7.5, 95% CI 1.2-46.1, <i>P</i> = 0.03). In FAP vs. SAL, lesion size was smaller in FAP: 10 mm (interquartile range 6-15 mm) vs. 15 mm (12-21 mm, <i>P</i> = 0.03) and the en-bloc resection rate was higher (100 vs. 67.5%, <i>P</i> = 0.01). Although the recurrence rate was higher in FAP vs. SAL (55.6 vs. 32.4%, <i>P</i> = 0.2), this was not statistically significant. Rates of AEs were similar.</p><p><strong>Conclusions: </strong>R0 resection was associated with reduced risk of recurrence whereas delayed bleeding after EP is associated with an increased risk of developing PEP. EP is safe and effective for removing ampullary lesions irrespective of lesion type.</p>","PeriodicalId":11671,"journal":{"name":"Endoscopy International Open","volume":"13 ","pages":"a26636291"},"PeriodicalIF":2.3,"publicationDate":"2025-08-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12371659/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144947249","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 : 2025-08-14eCollection Date: 2025-01-01DOI: 10.1055/a-2677-0505
Jinyu Wu, Wen Wang, Kuncheng Yang
{"title":"Beyond the ruler: Measuring what truly matters in endoscopic ultrasound-guided pancreatic cancer genomics.","authors":"Jinyu Wu, Wen Wang, Kuncheng Yang","doi":"10.1055/a-2677-0505","DOIUrl":"10.1055/a-2677-0505","url":null,"abstract":"","PeriodicalId":11671,"journal":{"name":"Endoscopy International Open","volume":"13 ","pages":"a26770505"},"PeriodicalIF":2.3,"publicationDate":"2025-08-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12371656/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144946715","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}
Background and study aims: Endoscopic resection for duodenal gastrointestinal stromal tumors (GISTs) is still considered a great challenge with a high risk of complications. This study aimed to evaluate effectiveness and safety of endoscopic resection for duodenal GIST.
Patients and methods: Between June 2013 and August 2024, we performed a retrospective study of patients with duodenal GISTs who underwent endoscopic resection at Zhongshan Hospital. Data on patient characteristics, clinical outcome, and follow-up were collected.
Results: A total of 73 patients with duodenal GISTs were enrolled, including 31 patients who underwent endoscopic submucosal dissection (ESD) and 42 who underwent endoscopic full-thickness resection (EFTR). Mean lesion size was 1.2 ± 0.5 cm and 1.9 ± 0.9 cm, respectively. En bloc resection rates were 96.8% and 95.2%, respectively. Rates of R0 resection were 45.2% and 42.9%, respectively. Rates of R1 resection were 54.8% and 57.1%, respectively. No patient transferred to open surgery. Postoperative adverse events included delayed bleeding (1 case), delayed perforation (1 case), delayed wall edema (2 cases), hydrothorax (1 case), and retroperitoneal infection (1 case). Mean hospital stays were 4.1 ± 2.8 days and 6.2 ± 4.9 days, respectively. No metastasis or duodenal stenosis were detected during the follow-up period (64.8 ± 43.6 months and 61.3 ± 40.2 months, respectively). Local recurrence occurred in one patient with high recurrence risk at 56 months after EFTR.
Conclusions: ESD and EFTR are safe, minimally invasive treatments for duodenal GISTs. Moreover, the EFTR technique may have advantages of completely resecting lesions originating from the deep muscularis propria layer, particularly lesions with extraluminal growth.
{"title":"Feasibility and safety of endoscopic resection for duodenal gastrointestinal stromal tumors.","authors":"Shao-Bin Luo, Zu-Qiang Liu, Li Wang, Yi-Qun Zhang, Ming-Yan Cai, Quan-Lin Li, Ping-Hong Zhou","doi":"10.1055/a-2655-1439","DOIUrl":"10.1055/a-2655-1439","url":null,"abstract":"<p><strong>Background and study aims: </strong>Endoscopic resection for duodenal gastrointestinal stromal tumors (GISTs) is still considered a great challenge with a high risk of complications. This study aimed to evaluate effectiveness and safety of endoscopic resection for duodenal GIST.</p><p><strong>Patients and methods: </strong>Between June 2013 and August 2024, we performed a retrospective study of patients with duodenal GISTs who underwent endoscopic resection at Zhongshan Hospital. Data on patient characteristics, clinical outcome, and follow-up were collected.</p><p><strong>Results: </strong>A total of 73 patients with duodenal GISTs were enrolled, including 31 patients who underwent endoscopic submucosal dissection (ESD) and 42 who underwent endoscopic full-thickness resection (EFTR). Mean lesion size was 1.2 ± 0.5 cm and 1.9 ± 0.9 cm, respectively. En bloc resection rates were 96.8% and 95.2%, respectively. Rates of R0 resection were 45.2% and 42.9%, respectively. Rates of R1 resection were 54.8% and 57.1%, respectively. No patient transferred to open surgery. Postoperative adverse events included delayed bleeding (1 case), delayed perforation (1 case), delayed wall edema (2 cases), hydrothorax (1 case), and retroperitoneal infection (1 case). Mean hospital stays were 4.1 ± 2.8 days and 6.2 ± 4.9 days, respectively. No metastasis or duodenal stenosis were detected during the follow-up period (64.8 ± 43.6 months and 61.3 ± 40.2 months, respectively). Local recurrence occurred in one patient with high recurrence risk at 56 months after EFTR.</p><p><strong>Conclusions: </strong>ESD and EFTR are safe, minimally invasive treatments for duodenal GISTs. Moreover, the EFTR technique may have advantages of completely resecting lesions originating from the deep muscularis propria layer, particularly lesions with extraluminal growth.</p>","PeriodicalId":11671,"journal":{"name":"Endoscopy International Open","volume":"13 ","pages":"a26551439"},"PeriodicalIF":2.3,"publicationDate":"2025-08-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12371658/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144947272","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 : 2025-08-07eCollection Date: 2025-01-01DOI: 10.1055/a-2655-6550
Michel Kahaleh, Vera Hapshy, Juan A Alcívar, Jorge Baquerizo-Burgos, Hannah Lukashok, Monica R Gaidhane, Iman Andalib, Amy Tyberg, Avik Sarkar, Haroon Shahid, Abid Allehibi, Resheed Alkhiari, Magda L Rodriguez, Carmen Bautista-Altamirano, Sarbelio Rodriguez, Maria G Porfilio, Mine Carames, Juan Carlos Carames, Amol Bapaye, Carlos Robles-Medranda
Background and study aims: Gastroesophageal reflux (GERD) can occur in a significant number of achalasia patients undergoing post-peroral endoscopic myotomy (POEM). POEM with endoscopic fundoplication (POEM-F) is a new endoscopic technique to treat post- POEM GERD. We conducted a multicenter cohort study to compare outcomes between POEM and POEM-F.
Patients and methods: We included patients who underwent POEM or POEM-F from six tertiary centers. Primary outcomes were: 1) clinical success, defined as post-procedure cessation or reduction of proton-pump inhibitors; 2) post procedure percent time pH < 4 and DeMeester score; and 3) post-procedure Eckardt scores. Secondary outcomes included adverse events, procedure time, and hospital stay duration.
Results: Sixty-four patients were included: 31 patients underwent POEM-F (mean age 51, 48% male), whereas 33 patients POEM (mean age 56, 58% male). Technical success was 100% in both groups. POEM-F patients achieved reduction/cessation in proton pump inhibitor use in 25 of 31 patients (80%); POEM patients in eight of 33 (24%) ( P ≤ 0.00001). Percent time with pH < 4 was significantly lower in the POEM-F group (2.75 +/- 2.53 vs 9.3 +/- 3.6 min, P ≤ 0.0001). Post-procedure DeMeester scores were lower (< 14.7) in POEM-F (mean 9.6) than POEM (mean 15.8) ( P ≤ 0.0011). There were three mucosal injuries in the POEM-F group and four in the POEM group. Hospital stay duration and procedure time did not differ between groups. In the POEM group, four patients required Dor fundoplication. No repeat interventions were recommended for the POEM- F group at 6-month follow-up.
Conclusions: POEM-F achieves statistically significant improvement in post- POEM GERD compared with POEM alone.
{"title":"Safety and efficacy of peroral endoscopic myotomy with endoscopic fundoplication compared with POEM alone: International multicenter cohort study.","authors":"Michel Kahaleh, Vera Hapshy, Juan A Alcívar, Jorge Baquerizo-Burgos, Hannah Lukashok, Monica R Gaidhane, Iman Andalib, Amy Tyberg, Avik Sarkar, Haroon Shahid, Abid Allehibi, Resheed Alkhiari, Magda L Rodriguez, Carmen Bautista-Altamirano, Sarbelio Rodriguez, Maria G Porfilio, Mine Carames, Juan Carlos Carames, Amol Bapaye, Carlos Robles-Medranda","doi":"10.1055/a-2655-6550","DOIUrl":"10.1055/a-2655-6550","url":null,"abstract":"<p><strong>Background and study aims: </strong>Gastroesophageal reflux (GERD) can occur in a significant number of achalasia patients undergoing post-peroral endoscopic myotomy (POEM). POEM with endoscopic fundoplication (POEM-F) is a new endoscopic technique to treat post- POEM GERD. We conducted a multicenter cohort study to compare outcomes between POEM and POEM-F.</p><p><strong>Patients and methods: </strong>We included patients who underwent POEM or POEM-F from six tertiary centers. Primary outcomes were: 1) clinical success, defined as post-procedure cessation or reduction of proton-pump inhibitors; 2) post procedure percent time pH < 4 and DeMeester score; and 3) post-procedure Eckardt scores. Secondary outcomes included adverse events, procedure time, and hospital stay duration.</p><p><strong>Results: </strong>Sixty-four patients were included: 31 patients underwent POEM-F (mean age 51, 48% male), whereas 33 patients POEM (mean age 56, 58% male). Technical success was 100% in both groups. POEM-F patients achieved reduction/cessation in proton pump inhibitor use in 25 of 31 patients (80%); POEM patients in eight of 33 (24%) ( <i>P</i> ≤ 0.00001). Percent time with pH < 4 was significantly lower in the POEM-F group (2.75 +/- 2.53 vs 9.3 +/- 3.6 min, <i>P</i> ≤ 0.0001). Post-procedure DeMeester scores were lower (< 14.7) in POEM-F (mean 9.6) than POEM (mean 15.8) ( <i>P</i> ≤ 0.0011). There were three mucosal injuries in the POEM-F group and four in the POEM group. Hospital stay duration and procedure time did not differ between groups. In the POEM group, four patients required Dor fundoplication. No repeat interventions were recommended for the POEM- F group at 6-month follow-up.</p><p><strong>Conclusions: </strong>POEM-F achieves statistically significant improvement in post- POEM GERD compared with POEM alone.</p>","PeriodicalId":11671,"journal":{"name":"Endoscopy International Open","volume":"13 ","pages":"a26556550"},"PeriodicalIF":2.3,"publicationDate":"2025-08-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12371642/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144947327","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 : 2025-08-07eCollection Date: 2025-01-01DOI: 10.1055/a-2638-6177
Jun-Yu Pan, Hui-Xin Zhi, Jie-Li Chen, Hao-Xin Chen, De-Feng Li, Jun Yao, Li-Sheng Wang
Background and study aims: Direct visualization endoscopic retrograde appendicitis therapy (ERAT), an advanced technique building upon conventional ERAT, represents a novel endoscopic approach for managing acute uncomplicated appendicitis. This study aimed to assess clinical efficacy and safety of employing cholangioscope-guided endoscopic intervention as a therapeutic approach.
Patients and methods: A retrospective analysis was conducted on 656 patients presenting with suspected acute appendicitis between February 2024 and November 2024. To minimize baseline differences, propensity score matching was applied, resulting in a final study population of 34 patients undergoing direct visualization ERAT and 68 patients treated with laparoscopic appendectomy (LA). Key outcome measures included technical and clinical success rates, operative time, time to postoperative pain resolution, length of hospital stay, recurrence rate, incidence of adverse events (AEs), and overall patient satisfaction.
Results: The technical success rate was 97.06% (33/34) in the ERAT group and 100% in the LA group ( P = 0.333), while clinical success was achieved in 94.12% (32/34) of ERAT cases compared with 100% in the LA cohort ( P = 0.109). Notably, ERAT was associated with a significantly shorter operative time (37 vs 50 minutes; P < 0.001) and more rapid postoperative pain relief ( P = 0.001), with a greater proportion of patients reporting complete symptom resolution within 2 days of the procedure. There were no significant differences between the two groups in terms of AEs, length of hospital stay, or patient satisfaction. During follow-up, a recurrence of appendicitis was observed in one ERAT patient (2.94%, 1/34).
Conclusions: Direct visualization ERAT demonstrated high feasibility and effectiveness as a diagnostic and therapeutic modality for acute uncomplicated appendicitis, offering a promising alternative to conventional approaches.
{"title":"Direct visualization endoscopic retrograde appendicitis therapy versus laparoscopic appendectomy for management of acute uncomplicated appendicitis.","authors":"Jun-Yu Pan, Hui-Xin Zhi, Jie-Li Chen, Hao-Xin Chen, De-Feng Li, Jun Yao, Li-Sheng Wang","doi":"10.1055/a-2638-6177","DOIUrl":"10.1055/a-2638-6177","url":null,"abstract":"<p><strong>Background and study aims: </strong>Direct visualization endoscopic retrograde appendicitis therapy (ERAT), an advanced technique building upon conventional ERAT, represents a novel endoscopic approach for managing acute uncomplicated appendicitis. This study aimed to assess clinical efficacy and safety of employing cholangioscope-guided endoscopic intervention as a therapeutic approach.</p><p><strong>Patients and methods: </strong>A retrospective analysis was conducted on 656 patients presenting with suspected acute appendicitis between February 2024 and November 2024. To minimize baseline differences, propensity score matching was applied, resulting in a final study population of 34 patients undergoing direct visualization ERAT and 68 patients treated with laparoscopic appendectomy (LA). Key outcome measures included technical and clinical success rates, operative time, time to postoperative pain resolution, length of hospital stay, recurrence rate, incidence of adverse events (AEs), and overall patient satisfaction.</p><p><strong>Results: </strong>The technical success rate was 97.06% (33/34) in the ERAT group and 100% in the LA group ( <i>P</i> = 0.333), while clinical success was achieved in 94.12% (32/34) of ERAT cases compared with 100% in the LA cohort ( <i>P</i> = 0.109). Notably, ERAT was associated with a significantly shorter operative time (37 vs 50 minutes; <i>P</i> < 0.001) and more rapid postoperative pain relief ( <i>P</i> = 0.001), with a greater proportion of patients reporting complete symptom resolution within 2 days of the procedure. There were no significant differences between the two groups in terms of AEs, length of hospital stay, or patient satisfaction. During follow-up, a recurrence of appendicitis was observed in one ERAT patient (2.94%, 1/34).</p><p><strong>Conclusions: </strong>Direct visualization ERAT demonstrated high feasibility and effectiveness as a diagnostic and therapeutic modality for acute uncomplicated appendicitis, offering a promising alternative to conventional approaches.</p>","PeriodicalId":11671,"journal":{"name":"Endoscopy International Open","volume":"13 ","pages":"a26386177"},"PeriodicalIF":2.3,"publicationDate":"2025-08-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12371657/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144947111","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}