Pub Date : 2026-03-12DOI: 10.1007/s00464-026-12652-5
Pattharasai Kachornvitaya, Mélissa V Wills, Juan S Barajas-Gamboa, Xinlei Zhu, Yung Lee, Suthep Udomsawaengsup, Salvador Navarrete, Ricard Corcelles, Andrew Strong, Matthew Kroh, Jerry Dang, Valentin Mocanu
Background: Bariatric surgery patients with body mass index (BMI) ≥ 60 kg/m2 present unique technical and perioperative challenges. While robotic-assisted bariatric surgery is thought to offer potential technical advantages, direct comparisons between robotic and laparoscopic approaches (R-BS and L-BS) in this population remains limited.
Methods: An analysis of the 2020-2023 MBSAQIP database was conducted and all patients with BMI ≥ 60 kg/m2 who underwent primary laparoscopic or robotic sleeve gastrectomy (SG) and Roux-en-Y gastric bypass (RYGB) were included. Baseline demographics, operative characteristics, and 30-day postoperative outcomes were compared. Multivariable logistic regression identified independent predictors of serious complications.
Results: Of 32,295 patients, 22,211 (68.8%) were L-BS and 10,084 (31.2%) were R-BS. Significant baseline differences existed between groups, including higher rates of gastroesophageal reflux disease (28.6% vs. 26.1%, p < 0.001), and hypertension (54.7% vs. 52.8%, p = 0.001) in the R-BS group. From 2020 to 2023, the proportion of R-BS doubled from 20.4% to 41.3%, whereas the proportion of L-BS declined slightly from 79.6% to 58.7%. There was no significant difference in robotic versus laparoscopic utilization for RYGB. (27.4% vs 26.4%, p = 0.059) and operative time was significantly longer in R-BS (106.5 ± 51.4 min vs. 83.5 ± 47.0 min, p < 0.001). Rates of individual 30-day complications, including leaks, bleeding, reoperation, and readmission, were low with no significant difference between cohorts. Independent predictors of serious complications included older age, hypertension, gastroesophageal reflux disease, prior myocardial infarction, therapeutic anticoagulation, longer operative time and RYGB. The robotic approach was neither independently associated with nor protective against serious complications.
Conclusions: In patients with a BMI ≥ 60 kg/m2 undergoing elective bariatric surgery, there were no significant differences in 30-day postoperative outcomes between laparoscopic and robotic approaches despite baseline patient differences between groups. Although operative times were 27% longer for the robotic approach, its utilization increased substantially over the study period. These findings suggest that perioperative outcomes in this high-risk population are primarily determined by patient comorbidities and procedural factors rather than surgical approach, and that neither approach demonstrates superior short-term safety.
{"title":"Evaluating trends and outcomes between robotic and laparoscopic bariatric surgery in patients with BMI ≥ 60 kg/m<sup>2</sup>: an MBSAQIP analysis of 32,295 cases.","authors":"Pattharasai Kachornvitaya, Mélissa V Wills, Juan S Barajas-Gamboa, Xinlei Zhu, Yung Lee, Suthep Udomsawaengsup, Salvador Navarrete, Ricard Corcelles, Andrew Strong, Matthew Kroh, Jerry Dang, Valentin Mocanu","doi":"10.1007/s00464-026-12652-5","DOIUrl":"https://doi.org/10.1007/s00464-026-12652-5","url":null,"abstract":"<p><strong>Background: </strong>Bariatric surgery patients with body mass index (BMI) ≥ 60 kg/m2 present unique technical and perioperative challenges. While robotic-assisted bariatric surgery is thought to offer potential technical advantages, direct comparisons between robotic and laparoscopic approaches (R-BS and L-BS) in this population remains limited.</p><p><strong>Methods: </strong>An analysis of the 2020-2023 MBSAQIP database was conducted and all patients with BMI ≥ 60 kg/m2 who underwent primary laparoscopic or robotic sleeve gastrectomy (SG) and Roux-en-Y gastric bypass (RYGB) were included. Baseline demographics, operative characteristics, and 30-day postoperative outcomes were compared. Multivariable logistic regression identified independent predictors of serious complications.</p><p><strong>Results: </strong>Of 32,295 patients, 22,211 (68.8%) were L-BS and 10,084 (31.2%) were R-BS. Significant baseline differences existed between groups, including higher rates of gastroesophageal reflux disease (28.6% vs. 26.1%, p < 0.001), and hypertension (54.7% vs. 52.8%, p = 0.001) in the R-BS group. From 2020 to 2023, the proportion of R-BS doubled from 20.4% to 41.3%, whereas the proportion of L-BS declined slightly from 79.6% to 58.7%. There was no significant difference in robotic versus laparoscopic utilization for RYGB. (27.4% vs 26.4%, p = 0.059) and operative time was significantly longer in R-BS (106.5 ± 51.4 min vs. 83.5 ± 47.0 min, p < 0.001). Rates of individual 30-day complications, including leaks, bleeding, reoperation, and readmission, were low with no significant difference between cohorts. Independent predictors of serious complications included older age, hypertension, gastroesophageal reflux disease, prior myocardial infarction, therapeutic anticoagulation, longer operative time and RYGB. The robotic approach was neither independently associated with nor protective against serious complications.</p><p><strong>Conclusions: </strong>In patients with a BMI ≥ 60 kg/m2 undergoing elective bariatric surgery, there were no significant differences in 30-day postoperative outcomes between laparoscopic and robotic approaches despite baseline patient differences between groups. Although operative times were 27% longer for the robotic approach, its utilization increased substantially over the study period. These findings suggest that perioperative outcomes in this high-risk population are primarily determined by patient comorbidities and procedural factors rather than surgical approach, and that neither approach demonstrates superior short-term safety.</p>","PeriodicalId":22174,"journal":{"name":"Surgical Endoscopy And Other Interventional Techniques","volume":" ","pages":""},"PeriodicalIF":2.7,"publicationDate":"2026-03-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147445167","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-03-12DOI: 10.1007/s00464-026-12704-w
Sofia Liljegard, Per-Anders Larsson, Erik Haraldsson
Background: Laparoscopy-assisted transgastric rendezvous ERCP (LAERCP) is a perioperative treatment option for common bile duct stones (CBDS) in Roux-en-Y gastric bypass (RYGB) patients. Although rendezvous ERCP (RV-ERCP) is a safe treatment for CBDS, comparative data with LAERCP in larger cohorts are lacking. This study compares outcomes of laparoscopic cholecystectomy (LC) and LAERCP in RYGB patients with LC and rendezvous ERCP (RV-ERCP) in patients with unaltered anatomy, using an extensive validated national registry.
Methods: A retrospective study on prospectively collected nationwide cohort data from the Swedish Registry of Gallstone Surgery and ERCP (GallRiks), including all patients from September 2016 to June 2021 who underwent LC with same-day rendezvous ERCP. Patients with prior RYGB (RYGB group) were compared to those without previous upper abdominal surgery (non-RYGB group). Outcome measures was therapeutic success, peri- and postoperative adverse events, procedural time and readmissions.
Results: Seventy RYGB and 4342 non-RYGB patients were identified. CBDS were detected in 60 and 3067 patients, respectively. Therapeutic success was 100% in the RYGB group versus 91.4% in the non-RYGB group (p = 0.018). Perioperative adverse events occurred in 8.8% and 2.3% of cases (p < 0.001), but none in the RYGB group had postoperative consequences. Postoperative adverse events, antibiotic use and readmissions were similar. Median procedural time (180 vs. 131 min, p < 0.001) and hospital stay (2 vs. 1 days, p < 0.001) were longer for the RYGB group. No mortality occurred in either group.
Conclusions: Concomitant rendezvous LAERCP during LC is a safe and effective method for managing CBDS after RYGB. Despite a higher rate of perioperative events, outcomes were favorable relative to previously published data for non-concomitant LAERCP. These findings support LAERCP with rendezvous technique as the standard of care for RYGB patients in Sweden and provide registry-based evidence to inform future international guidelines.
{"title":"Laparoscopic cholecystectomy with laparoscopy-assisted transgastric rendezvous ERCP in gastric bypass patients.","authors":"Sofia Liljegard, Per-Anders Larsson, Erik Haraldsson","doi":"10.1007/s00464-026-12704-w","DOIUrl":"https://doi.org/10.1007/s00464-026-12704-w","url":null,"abstract":"<p><strong>Background: </strong>Laparoscopy-assisted transgastric rendezvous ERCP (LAERCP) is a perioperative treatment option for common bile duct stones (CBDS) in Roux-en-Y gastric bypass (RYGB) patients. Although rendezvous ERCP (RV-ERCP) is a safe treatment for CBDS, comparative data with LAERCP in larger cohorts are lacking. This study compares outcomes of laparoscopic cholecystectomy (LC) and LAERCP in RYGB patients with LC and rendezvous ERCP (RV-ERCP) in patients with unaltered anatomy, using an extensive validated national registry.</p><p><strong>Methods: </strong>A retrospective study on prospectively collected nationwide cohort data from the Swedish Registry of Gallstone Surgery and ERCP (GallRiks), including all patients from September 2016 to June 2021 who underwent LC with same-day rendezvous ERCP. Patients with prior RYGB (RYGB group) were compared to those without previous upper abdominal surgery (non-RYGB group). Outcome measures was therapeutic success, peri- and postoperative adverse events, procedural time and readmissions.</p><p><strong>Results: </strong>Seventy RYGB and 4342 non-RYGB patients were identified. CBDS were detected in 60 and 3067 patients, respectively. Therapeutic success was 100% in the RYGB group versus 91.4% in the non-RYGB group (p = 0.018). Perioperative adverse events occurred in 8.8% and 2.3% of cases (p < 0.001), but none in the RYGB group had postoperative consequences. Postoperative adverse events, antibiotic use and readmissions were similar. Median procedural time (180 vs. 131 min, p < 0.001) and hospital stay (2 vs. 1 days, p < 0.001) were longer for the RYGB group. No mortality occurred in either group.</p><p><strong>Conclusions: </strong>Concomitant rendezvous LAERCP during LC is a safe and effective method for managing CBDS after RYGB. Despite a higher rate of perioperative events, outcomes were favorable relative to previously published data for non-concomitant LAERCP. These findings support LAERCP with rendezvous technique as the standard of care for RYGB patients in Sweden and provide registry-based evidence to inform future international guidelines.</p>","PeriodicalId":22174,"journal":{"name":"Surgical Endoscopy And Other Interventional Techniques","volume":" ","pages":""},"PeriodicalIF":2.7,"publicationDate":"2026-03-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147445242","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-03-12DOI: 10.1007/s00464-026-12604-z
Andrea Balla, Pietro Mascagni, Milos Bjelovic, Marek Soltes, Dorin Eugen Popa, Salvador Morales-Conde
Background: The European Association for Endoscopic Surgery (EAES) three-month Fellowship Programme was established in 2014 to promote educational mobility, training, and international collaboration in minimally invasive surgery. A five-year analysis of the programme demonstrated educational and professional advantages. This study presents a ten-year update and an assessment of long-term outcomes, fellows' perspectives, and the implementation of previous recommendations.
Methods: A cross-sectional survey was conducted and is reported according to the Checklist for Reporting of Survey Studies (CROSS). A 54-item questionnaire (multiple-choice, five-point Likert scale, and short open-ended questions) was distributed by e-mail to all surgeons who participated in the Fellowship between 2014 and 2024. Questions explored participants' demographics; surgical and endoscopic activities; academic and educational activities; the perceived impact of the Fellowship on personal, surgical, and scientific growth; and the practical aspects and overall feedback on the Fellowship experience.
Results: Seventy-one of the 81 eligible Fellows completed the survey (87.7%). At the time of the Fellowship, the mean age was 36 ± 3.3 years, and 62 participants (87.3%) held a consultant position. Sixty-six Fellows (93%) completed the entire Fellowship period. During the Fellowship, 53 participants (74.6%) did not operate as first surgeons, whereas 58 Fellows (81.7%) assisted during surgical procedures. In collaboration with their Host Institutions, 21 Fellows (29.6%) presented oral communications, 16 (22.5%) presented posters, and 27 (38%) published articles. Participants strongly agreed that the Fellowship contributed to their personal (mean 4.7 ± 0.6) and surgical (mean 4.6 ± 0.8) growth. Forty-five Fellows (63.4%) continued research after the programme and 44 (62%) reported changes in their clinical practice. Fellowship was considered adequate in funding and duration (mean 4.1 ± 0.8 and 4 ± 1.1, respectively).
Conclusions: After ten years, the EAES Fellowship Programme continues to play a pivotal role in advancing minimally invasive surgical education, professional networking, and research, confirming and expanding the positive outcomes observed in the five-year evaluation.
{"title":"Ten years of the European association of endoscopic surgery (EAES) fellowship programme: outcomes and future perspective.","authors":"Andrea Balla, Pietro Mascagni, Milos Bjelovic, Marek Soltes, Dorin Eugen Popa, Salvador Morales-Conde","doi":"10.1007/s00464-026-12604-z","DOIUrl":"https://doi.org/10.1007/s00464-026-12604-z","url":null,"abstract":"<p><strong>Background: </strong>The European Association for Endoscopic Surgery (EAES) three-month Fellowship Programme was established in 2014 to promote educational mobility, training, and international collaboration in minimally invasive surgery. A five-year analysis of the programme demonstrated educational and professional advantages. This study presents a ten-year update and an assessment of long-term outcomes, fellows' perspectives, and the implementation of previous recommendations.</p><p><strong>Methods: </strong>A cross-sectional survey was conducted and is reported according to the Checklist for Reporting of Survey Studies (CROSS). A 54-item questionnaire (multiple-choice, five-point Likert scale, and short open-ended questions) was distributed by e-mail to all surgeons who participated in the Fellowship between 2014 and 2024. Questions explored participants' demographics; surgical and endoscopic activities; academic and educational activities; the perceived impact of the Fellowship on personal, surgical, and scientific growth; and the practical aspects and overall feedback on the Fellowship experience.</p><p><strong>Results: </strong>Seventy-one of the 81 eligible Fellows completed the survey (87.7%). At the time of the Fellowship, the mean age was 36 ± 3.3 years, and 62 participants (87.3%) held a consultant position. Sixty-six Fellows (93%) completed the entire Fellowship period. During the Fellowship, 53 participants (74.6%) did not operate as first surgeons, whereas 58 Fellows (81.7%) assisted during surgical procedures. In collaboration with their Host Institutions, 21 Fellows (29.6%) presented oral communications, 16 (22.5%) presented posters, and 27 (38%) published articles. Participants strongly agreed that the Fellowship contributed to their personal (mean 4.7 ± 0.6) and surgical (mean 4.6 ± 0.8) growth. Forty-five Fellows (63.4%) continued research after the programme and 44 (62%) reported changes in their clinical practice. Fellowship was considered adequate in funding and duration (mean 4.1 ± 0.8 and 4 ± 1.1, respectively).</p><p><strong>Conclusions: </strong>After ten years, the EAES Fellowship Programme continues to play a pivotal role in advancing minimally invasive surgical education, professional networking, and research, confirming and expanding the positive outcomes observed in the five-year evaluation.</p>","PeriodicalId":22174,"journal":{"name":"Surgical Endoscopy And Other Interventional Techniques","volume":" ","pages":""},"PeriodicalIF":2.7,"publicationDate":"2026-03-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147445230","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-03-11DOI: 10.1007/s00464-026-12616-9
Yi Liu, Zhiping Ma, Pei Liu, Xiaowei Zhu, Long Zhao, Zhengjie Xu, Yuntao Ma, Jing Yang
Aim: To assess the clinical effectiveness, safety, technical feasibility, and challenges of remote robotic surgery in general surgery, gynecology, orthopedics, and urology, focusing on issues like communication technology, ethics, and cost.
Methods: Relevant reports on remote robotic surgery were retrieved from databases such as PubMed, EMbase, Web of Science, Cochrane Library, VIP, CNKI, and Wanfang (2001-2025). Literature quality was evaluated using tools from the Joanna Briggs Institute (JBI).
Results: A total of 26 articles were included (13 in Chinese, 13 in English) covering general surgery, gynecology, orthopedics, urology, and thyroid surgery. The results showed that the average operation time was slightly longer than that of traditional methods (about 10-30 min), but the safety was good. Most studies had communications backup plans, such as backup networks or local physician take-overs, to deal with the risk of disruption. Tele-robotic surgery has a high success rate and accuracy with controllable network latency, showing the potential to expand access to medical resources, especially in remote areas. However, it still faces challenges such as network stability, equipment cost, operation accuracy, data privacy, and ethical issues. Most of the included studies reported successful cases, and there was a lack of in-depth analysis of failure cases or adverse outcomes of patients, which may have publication bias.
Conclusion: Despite challenges, remote robotic surgery shows promise in overcoming geographical and resource limitations. The quality of current evidence is low, with serious methodological limitations and reporting bias. The establishment of international mandatory registration systems, standardized safety protocols, and transnational collaboration networks are urgent to promote this field from "proof of concept" to "clinical practice". But, with continuous technological advancements, it is expected to play an increasingly significant role in global healthcare.
目的:评估远程机器人手术在普外科、妇科、骨科和泌尿外科的临床效果、安全性、技术可行性和挑战,重点关注通信技术、伦理和成本等问题。方法:检索PubMed、EMbase、Web of Science、Cochrane Library、VIP、CNKI、万方等数据库2001-2025年远程机器人手术相关报道。使用乔安娜布里格斯研究所(JBI)的工具评估文献质量。结果:共纳入文献26篇(中文13篇,英文13篇),涵盖普外科、妇科、骨科、泌尿外科、甲状腺外科。结果表明,平均手术时间较传统方法略长(约10 ~ 30min),但安全性较好。大多数研究都有通信备份计划,如备用网络或当地医生接管,以应对中断的风险。远程机器人手术具有较高的成功率和准确性,且网络延迟可控,显示出扩大医疗资源获取的潜力,特别是在偏远地区。然而,它仍然面临着网络稳定性、设备成本、操作准确性、数据隐私和道德问题等挑战。纳入的研究大多报道了成功病例,缺乏对失败病例或患者不良结局的深入分析,可能存在发表偏倚。结论:尽管面临挑战,远程机器人手术在克服地理和资源限制方面显示出希望。现有证据的质量较低,存在严重的方法学局限性和报告偏倚。建立国际强制注册制度、标准化安全协议和跨国合作网络是推动该领域从“概念验证”到“临床实践”的迫切需要。但是,随着技术的不断进步,它有望在全球医疗保健中发挥越来越重要的作用。
{"title":"Remote robotic surgery: a systematic review.","authors":"Yi Liu, Zhiping Ma, Pei Liu, Xiaowei Zhu, Long Zhao, Zhengjie Xu, Yuntao Ma, Jing Yang","doi":"10.1007/s00464-026-12616-9","DOIUrl":"https://doi.org/10.1007/s00464-026-12616-9","url":null,"abstract":"<p><strong>Aim: </strong>To assess the clinical effectiveness, safety, technical feasibility, and challenges of remote robotic surgery in general surgery, gynecology, orthopedics, and urology, focusing on issues like communication technology, ethics, and cost.</p><p><strong>Methods: </strong>Relevant reports on remote robotic surgery were retrieved from databases such as PubMed, EMbase, Web of Science, Cochrane Library, VIP, CNKI, and Wanfang (2001-2025). Literature quality was evaluated using tools from the Joanna Briggs Institute (JBI).</p><p><strong>Results: </strong>A total of 26 articles were included (13 in Chinese, 13 in English) covering general surgery, gynecology, orthopedics, urology, and thyroid surgery. The results showed that the average operation time was slightly longer than that of traditional methods (about 10-30 min), but the safety was good. Most studies had communications backup plans, such as backup networks or local physician take-overs, to deal with the risk of disruption. Tele-robotic surgery has a high success rate and accuracy with controllable network latency, showing the potential to expand access to medical resources, especially in remote areas. However, it still faces challenges such as network stability, equipment cost, operation accuracy, data privacy, and ethical issues. Most of the included studies reported successful cases, and there was a lack of in-depth analysis of failure cases or adverse outcomes of patients, which may have publication bias.</p><p><strong>Conclusion: </strong>Despite challenges, remote robotic surgery shows promise in overcoming geographical and resource limitations. The quality of current evidence is low, with serious methodological limitations and reporting bias. The establishment of international mandatory registration systems, standardized safety protocols, and transnational collaboration networks are urgent to promote this field from \"proof of concept\" to \"clinical practice\". But, with continuous technological advancements, it is expected to play an increasingly significant role in global healthcare.</p>","PeriodicalId":22174,"journal":{"name":"Surgical Endoscopy And Other Interventional Techniques","volume":" ","pages":""},"PeriodicalIF":2.7,"publicationDate":"2026-03-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147434943","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-03-11DOI: 10.1007/s00464-026-12735-3
Wajahat Mirza, Mehak Ejaz Khan, Hania Iqbal, Alishbah Khan, Maaz Bin Badshah, Muhammad Bilal Moeen-Ud-Din, Hadi Mohammad Khan
Background: Iatrogenic colonic perforation is a rare but potentially catastrophic complication of colonoscopy (0.016-0.2% diagnostic; 0.15-5% therapeutic) with reported mortality of 15-25%. Rates may increase with expanding colonoscopy volume and advanced therapeutic interventions. Endoscopic closure is increasingly used, yet comparative outcomes remain uncertain.
Methods: Registered in PROSPERO (CRD420251233077). We searched six databases from inception to November 2025 for adult observational cohorts comparing endoscopic closure versus surgery. Outcomes included treatment success, mortality, major morbidity, reoperation, length of stay, and fasting duration. Two reviewers independently screened studies, extracted data, and assessed bias using ROBINS-I. Random-effects models pooled risk ratios (RR) and mean differences (MD); GRADE rated certainty. Sensitivity and geographic subgroup analyses assessed robustness and effect modification.
Results: Four retrospective cohorts (n = 123; 52 endoscopic, 71 surgical) from Portugal, Korea, and Malaysia were included across care settings. Treatment success showed no clear difference (RR 1.00, 95% CI 0.94-1.06; I2 = 0%; low certainty). Mortality was rare and imprecise (8 events; RR 0.26, 95% CI 0.06-1.16; I2 = 0%; very low certainty). Hospital stay was shorter with endoscopic management (MD - 9.23 days, 95% CI - 13.74 to - 4.73; I2 = 43%; low certainty). Fasting duration did not differ significantly and was heterogeneous. No geographic subgroup effect was detected (P = 0.95). Sensitivity analysis supported robustness, except for hospital-stay heterogeneity driven by referred cases in one study.
Conclusions: In observational cohorts, endoscopic closure was typically used for immediately recognized, smaller perforations in favorable clinical conditions, whereas surgery was preferentially used for delayed diagnosis, larger defects, or suspected contamination, introducing substantial confounding by indication. Accordingly, the pooled estimates should not be interpreted as evidence of equivalence. In carefully selected patients (immediate recognition, < 2 cm, no generalized peritonitis/instability), endoscopic closure appears to be a viable first-line strategy and may reduce length of stay. Prospective multicenter studies with standardized definitions and rigorous confounder adjustment are needed.
背景:医源性结肠穿孔是结肠镜检查的一种罕见但潜在的灾难性并发症(诊断0.016-0.2%,治疗0.15-5%),据报道死亡率为15-25%。随着结肠镜检查容量的扩大和先进的治疗干预措施,发病率可能会增加。内窥镜闭合越来越多地被使用,但比较结果仍然不确定。方法:在PROSPERO注册(CRD420251233077)。我们检索了从成立到2025年11月的6个数据库,以比较内窥镜闭合与手术的成人观察队列。结果包括治疗成功、死亡率、主要发病率、再手术、住院时间和禁食时间。两位审稿人独立筛选研究,提取数据,并使用ROBINS-I评估偏倚。随机效应模型汇集了风险比(RR)和平均差异(MD);GRADE等级确定度。敏感性和地理亚组分析评估了稳健性和效果修正。结果:来自葡萄牙、韩国和马来西亚的四个回顾性队列(n = 123; 52个内窥镜组,71个手术组)纳入了各个护理机构。治疗成功率无明显差异(RR 1.00, 95% CI 0.94-1.06; I2 = 0%;低确定性)。死亡率罕见且不精确(8个事件;RR 0.26, 95% CI 0.06-1.16; I2 = 0%;非常低的确定性)。内镜治疗的住院时间较短(MD - 9.23天,95% CI - 13.74至- 4.73;I2 = 43%;低确定性)。禁食时间无显著差异,具有异质性。未发现地理亚群效应(P = 0.95)。敏感性分析支持稳健性,除了在一项研究中由转诊病例驱动的住院异质性。结论:在观察性队列中,内镜封闭通常用于临床条件良好的立即发现的较小穿孔,而手术优先用于延迟诊断,较大缺陷或疑似污染,这导致了大量的适应症混淆。因此,汇总的估计数不应被解释为等效的证据。在精心挑选的患者中(立即识别,
{"title":"Endoscopic versus surgical management for iatrogenic colonic perforations: a GRADE-assessed systematic review and meta-analysis of cohort studies.","authors":"Wajahat Mirza, Mehak Ejaz Khan, Hania Iqbal, Alishbah Khan, Maaz Bin Badshah, Muhammad Bilal Moeen-Ud-Din, Hadi Mohammad Khan","doi":"10.1007/s00464-026-12735-3","DOIUrl":"https://doi.org/10.1007/s00464-026-12735-3","url":null,"abstract":"<p><strong>Background: </strong>Iatrogenic colonic perforation is a rare but potentially catastrophic complication of colonoscopy (0.016-0.2% diagnostic; 0.15-5% therapeutic) with reported mortality of 15-25%. Rates may increase with expanding colonoscopy volume and advanced therapeutic interventions. Endoscopic closure is increasingly used, yet comparative outcomes remain uncertain.</p><p><strong>Methods: </strong>Registered in PROSPERO (CRD420251233077). We searched six databases from inception to November 2025 for adult observational cohorts comparing endoscopic closure versus surgery. Outcomes included treatment success, mortality, major morbidity, reoperation, length of stay, and fasting duration. Two reviewers independently screened studies, extracted data, and assessed bias using ROBINS-I. Random-effects models pooled risk ratios (RR) and mean differences (MD); GRADE rated certainty. Sensitivity and geographic subgroup analyses assessed robustness and effect modification.</p><p><strong>Results: </strong>Four retrospective cohorts (n = 123; 52 endoscopic, 71 surgical) from Portugal, Korea, and Malaysia were included across care settings. Treatment success showed no clear difference (RR 1.00, 95% CI 0.94-1.06; I<sup>2</sup> = 0%; low certainty). Mortality was rare and imprecise (8 events; RR 0.26, 95% CI 0.06-1.16; I<sup>2</sup> = 0%; very low certainty). Hospital stay was shorter with endoscopic management (MD - 9.23 days, 95% CI - 13.74 to - 4.73; I<sup>2</sup> = 43%; low certainty). Fasting duration did not differ significantly and was heterogeneous. No geographic subgroup effect was detected (P = 0.95). Sensitivity analysis supported robustness, except for hospital-stay heterogeneity driven by referred cases in one study.</p><p><strong>Conclusions: </strong>In observational cohorts, endoscopic closure was typically used for immediately recognized, smaller perforations in favorable clinical conditions, whereas surgery was preferentially used for delayed diagnosis, larger defects, or suspected contamination, introducing substantial confounding by indication. Accordingly, the pooled estimates should not be interpreted as evidence of equivalence. In carefully selected patients (immediate recognition, < 2 cm, no generalized peritonitis/instability), endoscopic closure appears to be a viable first-line strategy and may reduce length of stay. Prospective multicenter studies with standardized definitions and rigorous confounder adjustment are needed.</p>","PeriodicalId":22174,"journal":{"name":"Surgical Endoscopy And Other Interventional Techniques","volume":" ","pages":""},"PeriodicalIF":2.7,"publicationDate":"2026-03-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147435807","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-03-11DOI: 10.1007/s00464-026-12711-x
Nadeesha Samarasinghe, Wenjie Lin, Ahmer A Karimuddin, Carl J Brown, P Terry Phang, Manoj J Raval, Karen MacDonell, Amandeep Ghuman
Background: Anastomotic leaks in colorectal surgery increase mortality, local cancer recurrence, and hospital readmission rate. The Echelon Circular Powered Stapler (PCS) is marketed to reduce anastomotic leaks by minimizing operator errors through powered systems. We reviewed current evidence on the use of PCS in left-sided colorectal anastomoses to determine if there is a reduction in anastomotic leak rates versus manual circular staplers (MCS).
Methods: This study followed PRISMA guidelines. MEDLINE, EMBASE, CINAHL, and OVID review databases were searched to January 2024. A broad search strategy for PCS versus MCS in colorectal surgery was used. Abstracts were reviewed for the primary outcome of anastomotic leaks, and data were extracted from full-text review. Statistical analysis was performed using RevMan 5.4 software.
Results: 109 articles were screened, 9 studies with 3110 patients were included. No randomized control trials (RCTs) were found. In pooled and sensitivity analysis excluding studies that used historic comparators, there was no significant difference in the rates of anastomotic leak (pooled RR 0.56, 95% CI [0.27-1.18], p = 0.13; sensitivity analysis RR 0.75, 95% CI [0.32-1.77], p = 0.52). Similarly, there was no significant difference in morbidity between PCS and MCS on pooled analysis (RR 0.84, 95% [CI 0.65-1.08], p = 0.17). However, on pooled analysis, there was a significantly lower rate of post-operative bleeding with the use of PCS (RR 0.2, 95% CI [0.08-0.51], p < 0.001).
Conclusion: The current systematic review and meta-analysis is unable to support the claim of lower leak rate with the use of PCS; however, there is preliminary evidence to indicate that powered staplers may decrease the rate of post-operative bleeding. Further evidence from RCTs investigating anastomotic leaks and bleeding rate with PCS and assessments of environmental impact should be conducted prior to the widespread use of powered staplers.
背景:结直肠手术吻合口瘘增加死亡率、局部肿瘤复发率和再入院率。Echelon圆形动力吻合器(PCS)的销售目的是通过动力系统减少操作人员的失误,从而减少吻合口泄漏。我们回顾了目前在左侧结肠吻合器中使用PCS的证据,以确定与手动圆形吻合器(MCS)相比,是否可以减少吻合口漏率。方法:本研究遵循PRISMA指南。检索MEDLINE、EMBASE、CINAHL和OVID综述数据库至2024年1月。对结肠直肠手术中的PCS与MCS进行了广泛的搜索策略。摘要回顾吻合口瘘的主要结局,并从全文综述中提取数据。采用RevMan 5.4软件进行统计分析。结果:109篇文章被筛选,9项研究共纳入3110例患者。未发现随机对照试验(rct)。在合并和敏感性分析中,排除使用历史比较物的研究,两组吻合口漏发生率无显著差异(合并RR 0.56, 95% CI [0.27-1.18], p = 0.13;敏感性分析RR 0.75, 95% CI [0.32-1.77], p = 0.52)。同样,合并分析中PCS和MCS的发病率无显著差异(RR 0.84, 95% [CI 0.65-1.08], p = 0.17)。然而,在汇总分析中,使用PCS的术后出血发生率明显降低(RR为0.2,95% CI [0.08-0.51], p)。结论:目前的系统评价和荟萃分析无法支持使用PCS的术后出血发生率较低的说法,但有初步证据表明,动力订书机可能会降低术后出血发生率。在广泛使用电动吻合器之前,应进行随机对照试验调查吻合口泄漏和出血率,并评估环境影响。
{"title":"Circular powered staplers versus manual staplers in left-sided colorectal anastomoses: a systematic review and meta-analysis.","authors":"Nadeesha Samarasinghe, Wenjie Lin, Ahmer A Karimuddin, Carl J Brown, P Terry Phang, Manoj J Raval, Karen MacDonell, Amandeep Ghuman","doi":"10.1007/s00464-026-12711-x","DOIUrl":"https://doi.org/10.1007/s00464-026-12711-x","url":null,"abstract":"<p><strong>Background: </strong>Anastomotic leaks in colorectal surgery increase mortality, local cancer recurrence, and hospital readmission rate. The Echelon Circular Powered Stapler (PCS) is marketed to reduce anastomotic leaks by minimizing operator errors through powered systems. We reviewed current evidence on the use of PCS in left-sided colorectal anastomoses to determine if there is a reduction in anastomotic leak rates versus manual circular staplers (MCS).</p><p><strong>Methods: </strong>This study followed PRISMA guidelines. MEDLINE, EMBASE, CINAHL, and OVID review databases were searched to January 2024. A broad search strategy for PCS versus MCS in colorectal surgery was used. Abstracts were reviewed for the primary outcome of anastomotic leaks, and data were extracted from full-text review. Statistical analysis was performed using RevMan 5.4 software.</p><p><strong>Results: </strong>109 articles were screened, 9 studies with 3110 patients were included. No randomized control trials (RCTs) were found. In pooled and sensitivity analysis excluding studies that used historic comparators, there was no significant difference in the rates of anastomotic leak (pooled RR 0.56, 95% CI [0.27-1.18], p = 0.13; sensitivity analysis RR 0.75, 95% CI [0.32-1.77], p = 0.52). Similarly, there was no significant difference in morbidity between PCS and MCS on pooled analysis (RR 0.84, 95% [CI 0.65-1.08], p = 0.17). However, on pooled analysis, there was a significantly lower rate of post-operative bleeding with the use of PCS (RR 0.2, 95% CI [0.08-0.51], p < 0.001).</p><p><strong>Conclusion: </strong>The current systematic review and meta-analysis is unable to support the claim of lower leak rate with the use of PCS; however, there is preliminary evidence to indicate that powered staplers may decrease the rate of post-operative bleeding. Further evidence from RCTs investigating anastomotic leaks and bleeding rate with PCS and assessments of environmental impact should be conducted prior to the widespread use of powered staplers.</p>","PeriodicalId":22174,"journal":{"name":"Surgical Endoscopy And Other Interventional Techniques","volume":" ","pages":""},"PeriodicalIF":2.7,"publicationDate":"2026-03-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147435767","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-03-10DOI: 10.1007/s00464-026-12618-7
Yuxin Chen, Yifei Chen, Bin Lv
Background: Peroral Endoscopic Myotomy (POEM) has become the first-line minimally invasive treatment for achalasia. Its short-term and mid-term (1-5 years) efficacy has been consistently demonstrated, but long-term follow-up data (≥ 5 years) remain limited. This systematic review and meta-analysis aims to comprehensively evaluate the long-term (median follow-up ≥ 5 years) clinical efficacy and safety of POEM.
Methods: Using medical literature databases, we retrieved randomized controlled trials (RCTs) and non-randomized comparative studies from the inception of the databases through September 2025. Data were extracted using the Cochrane Risk of Bias 2.0 tool and the Newcastle-Ottawa Scale to assess risk of bias for RCTs and cohort studies, respectively. Meta-analyses were conducted using either fixed-effect or random-effects models.
Results: A total of 16 studies involving 2421 patients (50.4% male) were included, with a median follow-up duration of 72 months (range, 60-144 months). The pooled clinical success rate was 87.1% (95% CI 82.4-91.8%; I2 = 84.2%). The pooled incidence of endoscopically detectable reflux esophagitis was 24.2% (95% CI 11.6-36.8%; I2 = 85.4%), whereas symptomatic reflux was inconsistently reported, with a pooled incidence of 27.2% (95% CI 19.2-35.3%; I2 = 83.6%). Long-term follow-up reported 2 cases of Barrett's esophagus and isolated cases of esophageal cancer.
Conclusion: POEM has demonstrated consistent long-term efficacy and safety. Postoperative symptomatic reflux is the most common long-term complication, while the risks of Barrett's esophagus and peptic stricture remain low. POEM represents a reliable first-line treatment option; however, further multicenter prospective studies are needed to validate its long-term efficacy and safety.
背景:经口内窥镜下肌切开术(POEM)已成为贲门失弛缓症的一线微创治疗方法。其短期和中期(1-5年)疗效已得到一致证明,但长期随访数据(≥5年)仍然有限。本系统综述和荟萃分析旨在全面评价POEM的长期(中位随访≥5年)临床疗效和安全性。方法:使用医学文献数据库,检索从数据库建立到2025年9月的随机对照试验(rct)和非随机对照研究。分别使用Cochrane风险偏倚2.0工具和Newcastle-Ottawa量表提取数据,以评估随机对照试验和队列研究的偏倚风险。采用固定效应或随机效应模型进行meta分析。结果:共纳入16项研究,涉及2421例患者(50.4%为男性),中位随访时间72个月(范围60-144个月)。合并临床成功率为87.1% (95% CI 82.4 ~ 91.8%; I2 = 84.2%)。内镜下可检测到的反流性食管炎的总发生率为24.2% (95% CI 11.6-36.8%; I2 = 85.4%),而症状性反流的总发生率不一致,为27.2% (95% CI 19.2-35.3%; I2 = 83.6%)。长期随访报告2例Barrett食管及孤立食管癌。结论:POEM具有一致的长期疗效和安全性。术后症状性反流是最常见的长期并发症,而Barrett食管和消化性狭窄的风险仍然很低。POEM是一种可靠的一线治疗方案;然而,需要进一步的多中心前瞻性研究来验证其长期有效性和安全性。
{"title":"Long-term outcomes of peroral endoscopic myotomy for achalasia: a systematic review and meta-analysis with median follow-up ≥ 5 years.","authors":"Yuxin Chen, Yifei Chen, Bin Lv","doi":"10.1007/s00464-026-12618-7","DOIUrl":"https://doi.org/10.1007/s00464-026-12618-7","url":null,"abstract":"<p><strong>Background: </strong>Peroral Endoscopic Myotomy (POEM) has become the first-line minimally invasive treatment for achalasia. Its short-term and mid-term (1-5 years) efficacy has been consistently demonstrated, but long-term follow-up data (≥ 5 years) remain limited. This systematic review and meta-analysis aims to comprehensively evaluate the long-term (median follow-up ≥ 5 years) clinical efficacy and safety of POEM.</p><p><strong>Methods: </strong>Using medical literature databases, we retrieved randomized controlled trials (RCTs) and non-randomized comparative studies from the inception of the databases through September 2025. Data were extracted using the Cochrane Risk of Bias 2.0 tool and the Newcastle-Ottawa Scale to assess risk of bias for RCTs and cohort studies, respectively. Meta-analyses were conducted using either fixed-effect or random-effects models.</p><p><strong>Results: </strong>A total of 16 studies involving 2421 patients (50.4% male) were included, with a median follow-up duration of 72 months (range, 60-144 months). The pooled clinical success rate was 87.1% (95% CI 82.4-91.8%; I<sup>2</sup> = 84.2%). The pooled incidence of endoscopically detectable reflux esophagitis was 24.2% (95% CI 11.6-36.8%; I<sup>2</sup> = 85.4%), whereas symptomatic reflux was inconsistently reported, with a pooled incidence of 27.2% (95% CI 19.2-35.3%; I<sup>2</sup> = 83.6%). Long-term follow-up reported 2 cases of Barrett's esophagus and isolated cases of esophageal cancer.</p><p><strong>Conclusion: </strong>POEM has demonstrated consistent long-term efficacy and safety. Postoperative symptomatic reflux is the most common long-term complication, while the risks of Barrett's esophagus and peptic stricture remain low. POEM represents a reliable first-line treatment option; however, further multicenter prospective studies are needed to validate its long-term efficacy and safety.</p>","PeriodicalId":22174,"journal":{"name":"Surgical Endoscopy And Other Interventional Techniques","volume":" ","pages":""},"PeriodicalIF":2.7,"publicationDate":"2026-03-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147435744","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-03-10DOI: 10.1007/s00464-026-12718-4
Manik Aggarwal, Jad P AbiMansour, Reem Matar, Manus Rugivarodom, Yara Salameh, Hadi Abou Zeid, Shunsuke Kamba, Naomi M Gades, Elizabeth Rajan, Andrew C Storm
Background: Flexible endoscopic suturing tools are complex and may have a long learning curve. This porcine study evaluated the safety and performance of a simplified suturing system compared with a commercially available device for the repair of gastrointestinal mucosal defects.
Methods: This IACUC-approved study included four healthy swine. A total of ten defects (six in the stomach and four in the rectosigmoid colon) were created in each animal. Defects were randomly assigned to closure with either the novel or the commercially available system using a therapeutic gastroscope. Technical success was defined as mucosal closure of the defect with the inability to visualize any significant portion of the resection bed. Additional performance metrics included procedure time and device ease of use (assessed using the NASA Task Load Index [TLI]) and adverse events.
Results: No adverse events were reported post-procedurally for any of the test animals. The proportion of target resection sites achieving technical success was 100% in both treatment groups. The mean SimpleStitch NASA-TLI score was lower compared to the OverStitch device. Closure times were similar between the two devices. Histological assessment scores indicated expected healing response without evidence of perforation, leakage, or abscess formation.
Conclusion: A novel full-thickness suturing system safely and effectively closed mucosal defects. Lower NASA-TLI scores suggest that the novel suturing device may offer simpler, less demanding use compared to the predicate device, potentially reducing the learning curve for endoscopic suturing procedures.
{"title":"Evaluation of the envision endoscopy SimpleStitch suturing system for closure of gastrointestinal defects in a porcine model.","authors":"Manik Aggarwal, Jad P AbiMansour, Reem Matar, Manus Rugivarodom, Yara Salameh, Hadi Abou Zeid, Shunsuke Kamba, Naomi M Gades, Elizabeth Rajan, Andrew C Storm","doi":"10.1007/s00464-026-12718-4","DOIUrl":"https://doi.org/10.1007/s00464-026-12718-4","url":null,"abstract":"<p><strong>Background: </strong>Flexible endoscopic suturing tools are complex and may have a long learning curve. This porcine study evaluated the safety and performance of a simplified suturing system compared with a commercially available device for the repair of gastrointestinal mucosal defects.</p><p><strong>Methods: </strong>This IACUC-approved study included four healthy swine. A total of ten defects (six in the stomach and four in the rectosigmoid colon) were created in each animal. Defects were randomly assigned to closure with either the novel or the commercially available system using a therapeutic gastroscope. Technical success was defined as mucosal closure of the defect with the inability to visualize any significant portion of the resection bed. Additional performance metrics included procedure time and device ease of use (assessed using the NASA Task Load Index [TLI]) and adverse events.</p><p><strong>Results: </strong>No adverse events were reported post-procedurally for any of the test animals. The proportion of target resection sites achieving technical success was 100% in both treatment groups. The mean SimpleStitch NASA-TLI score was lower compared to the OverStitch device. Closure times were similar between the two devices. Histological assessment scores indicated expected healing response without evidence of perforation, leakage, or abscess formation.</p><p><strong>Conclusion: </strong>A novel full-thickness suturing system safely and effectively closed mucosal defects. Lower NASA-TLI scores suggest that the novel suturing device may offer simpler, less demanding use compared to the predicate device, potentially reducing the learning curve for endoscopic suturing procedures.</p>","PeriodicalId":22174,"journal":{"name":"Surgical Endoscopy And Other Interventional Techniques","volume":" ","pages":""},"PeriodicalIF":2.7,"publicationDate":"2026-03-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147435747","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Background: Safe establishment of pneumoperitoneum is essential in laparoscopic surgery because most access-related injuries occur during peritoneal entry. In Veress needle procedures, this step is performed blindly, and conventional verification tests are subjective and often unreliable. The negative pressure-based visualization (NPV) technique enables real-time confirmation of peritoneal entry using a saline column. We therefore developed a manometric modification (NPMV) and a four-forceps technique (NPMV4) to improve practicality and applicability in obese patients.
Methods: This retrospective study included two cohorts: a standard-weight cohort of 475 patients undergoing laparoscopic groin hernia repair (243 NPMV, 232 NPV) and an obese cohort of 53 patients undergoing laparoscopic sleeve gastrectomy (33 four-forceps, 20 two-forceps). In the NPMV, the Veress needle was connected to an insufflator with a manometric display, and peritoneal entry was confirmed at a pressure of minus 2 mmHg or lower. Primary outcomes were pneumoperitoneum success and access-related complications; secondary outcomes included access time and puncture attempts.
Results: In the standard-weight cohort, pneumoperitoneum success was 99% in both groups, with no differences in complications or puncture attempts. The NPMV group achieved a significantly shorter time to insufflation (median 1.0 vs 2.0 min, p < 0.001). In the obese cohort, the four-forceps group showed fewer failed entries (3% vs 15%) and significantly fewer puncture attempts (median 1.0 vs 3.5, p = 0.019), without increased gas-related complications.
Conclusion: Replacing the saline column with a manometric display did not increase access-related complications and improved procedural efficiency. The NPMV4 technique further improved the reliability of laparoscopic access in obese patients. These stepwise modifications provide a simple, reproducible, and reliable approach to Veress needle access across diverse surgical populations.
背景:安全建立气腹在腹腔镜手术中是必不可少的,因为大多数与通道相关的损伤发生在腹膜进入期间。在Veress针程序中,这一步是盲目进行的,而传统的验证测试是主观的,往往不可靠。负压可视化(NPV)技术可以使用生理盐水柱实时确认腹膜进入。因此,我们开发了一种测压改良技术(NPMV)和一种四钳技术(NPMV4),以提高肥胖患者的实用性和适用性。方法:本回顾性研究包括两个队列:标准体重队列475例接受腹腔镜腹股沟疝修补术的患者(243例NPMV, 232例NPV)和肥胖队列53例接受腹腔镜袖式胃切除术的患者(33例四钳,20例二钳)。在NPMV中,将Veress针连接到带有测压显示的注入器,并在- 2mmhg或更低的压力下确认进入腹膜。主要结局是气腹手术成功和通路相关并发症;次要结果包括进入时间和穿刺次数。结果:在标准体重队列中,两组的气腹成功率均为99%,并发症和穿刺次数无差异。NPMV组的充气时间明显缩短(中位1.0 vs 2.0 min, p)。结论:用血压计显示代替生理盐水柱不会增加通路相关并发症,并提高了手术效率。NPMV4技术进一步提高了肥胖患者腹腔镜通路的可靠性。这些逐步修改提供了一种简单、可重复和可靠的方法,以在不同的手术人群中使用Veress针。
{"title":"Stepwise evolution and clinical applicability of negative pressure-based manometric visualization for reliable Veress needle access.","authors":"Masanori Sato, Kakeru Torii, Yoshihiro Hiramatsu, Yuki Sakai, Ryoma Haneda, Wataru Soneda, Tomohiro Murakami, Eisuke Booka, Tomohiro Matsumoto, Hirotoshi Kikuchi, Hiroya Takeuchi","doi":"10.1007/s00464-026-12693-w","DOIUrl":"https://doi.org/10.1007/s00464-026-12693-w","url":null,"abstract":"<p><strong>Background: </strong>Safe establishment of pneumoperitoneum is essential in laparoscopic surgery because most access-related injuries occur during peritoneal entry. In Veress needle procedures, this step is performed blindly, and conventional verification tests are subjective and often unreliable. The negative pressure-based visualization (NPV) technique enables real-time confirmation of peritoneal entry using a saline column. We therefore developed a manometric modification (NPMV) and a four-forceps technique (NPMV4) to improve practicality and applicability in obese patients.</p><p><strong>Methods: </strong>This retrospective study included two cohorts: a standard-weight cohort of 475 patients undergoing laparoscopic groin hernia repair (243 NPMV, 232 NPV) and an obese cohort of 53 patients undergoing laparoscopic sleeve gastrectomy (33 four-forceps, 20 two-forceps). In the NPMV, the Veress needle was connected to an insufflator with a manometric display, and peritoneal entry was confirmed at a pressure of minus 2 mmHg or lower. Primary outcomes were pneumoperitoneum success and access-related complications; secondary outcomes included access time and puncture attempts.</p><p><strong>Results: </strong>In the standard-weight cohort, pneumoperitoneum success was 99% in both groups, with no differences in complications or puncture attempts. The NPMV group achieved a significantly shorter time to insufflation (median 1.0 vs 2.0 min, p < 0.001). In the obese cohort, the four-forceps group showed fewer failed entries (3% vs 15%) and significantly fewer puncture attempts (median 1.0 vs 3.5, p = 0.019), without increased gas-related complications.</p><p><strong>Conclusion: </strong>Replacing the saline column with a manometric display did not increase access-related complications and improved procedural efficiency. The NPMV4 technique further improved the reliability of laparoscopic access in obese patients. These stepwise modifications provide a simple, reproducible, and reliable approach to Veress needle access across diverse surgical populations.</p>","PeriodicalId":22174,"journal":{"name":"Surgical Endoscopy And Other Interventional Techniques","volume":" ","pages":""},"PeriodicalIF":2.7,"publicationDate":"2026-03-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147435532","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Background: Few studies have compared the invasiveness and safety of pure single-incision robotic surgery using the da Vinci SP system (SP) without an assistant port with those using the da Vinci Xi system (Xi) for right-sided colon cancer. Surgical invasiveness was assessed using the C-reactive protein/albumin (CRP/Alb) ratio and postoperative pain using the Numerical Rating Scale (NRS).
Methods: This single-center retrospective study included 163 patients who underwent robot-assisted surgery for right-sided colon cancer between October 2022 and August 2025 (SP = 60, Xi = 103). Confounding factors were adjusted using propensity score matching and stabilized inverse probability of treatment weighting based on body mass index (BMI) ≥ 25 kg/m2, American Society of Anesthesiologists (ASA) ≥ III, tumor size ≥ 40 mm, surgical procedure, and preoperative CRP/Alb ratio ≥ 0.03; short-term outcomes were compared.
Results: After adjustment, baseline characteristics were well balanced. The SP approach was associated with a shorter incision length (3.0 vs 5.5 cm, p < 0.01) and lower postoperative pain on day 3 (NRS scores 2 vs. 3, p < 0.01). Operative time, postoperative inflammatory response assessed by CRP/Alb ratio, complications, and pathological outcomes were comparable between the groups.
Conclusions: Pure single-incision robotic surgery using the da Vinci SP system demonstrated comparable short-term safety and oncological adequacy to the Xi system, with modest advantages in incision length and postoperative pain. No clear benefit in systemic inflammatory response was observed, and further validation in larger, prospective, multicenter studies is warranted.
背景:很少有研究比较使用无辅助端口的达芬奇SP系统(SP)和使用达芬奇Xi系统(Xi)的纯单切口机器人手术治疗右侧结肠癌的侵入性和安全性。采用c反应蛋白/白蛋白(CRP/Alb)比率评估手术侵入性,采用数值评定量表(NRS)评估术后疼痛。方法:这项单中心回顾性研究纳入了163例在2022年10月至2025年8月期间接受机器人辅助手术的右侧结肠癌患者(SP = 60, Xi = 103)。根据体重指数(BMI)≥25 kg/m2、美国麻醉医师学会(ASA)≥III、肿瘤大小≥40 mm、手术方式和术前CRP/Alb比值≥0.03,采用倾向评分匹配法调整混杂因素,稳定治疗权重的逆概率;比较短期结果。结果:调整后基线特征平衡良好。SP入路切口长度较短(3.0 cm vs 5.5 cm), p结论:使用达芬奇SP系统的纯单切口机器人手术与Xi系统具有相当的短期安全性和肿瘤充分性,在切口长度和术后疼痛方面具有一定的优势。没有观察到系统性炎症反应的明显益处,需要在更大的、前瞻性的、多中心的研究中进一步验证。
{"title":"Assessing the minimal invasiveness of pure single-incision da Vinci SP surgery for right-sided colon cancer: comparative analysis with the da Vinci Xi system using PSM and IPTW.","authors":"Sohei Akuta, Yasumitsu Hirano, Yasuhiro Ishiyama, Yume Minagawa, Yusuke Nishi, Hisashi Hayashi, Akihito Nakanishi, Takatsugu Fujii, Hirofumi Sugita, Chikashi Hiranuma, Yusuke Kinugasa","doi":"10.1007/s00464-026-12712-w","DOIUrl":"https://doi.org/10.1007/s00464-026-12712-w","url":null,"abstract":"<p><strong>Background: </strong>Few studies have compared the invasiveness and safety of pure single-incision robotic surgery using the da Vinci SP system (SP) without an assistant port with those using the da Vinci Xi system (Xi) for right-sided colon cancer. Surgical invasiveness was assessed using the C-reactive protein/albumin (CRP/Alb) ratio and postoperative pain using the Numerical Rating Scale (NRS).</p><p><strong>Methods: </strong>This single-center retrospective study included 163 patients who underwent robot-assisted surgery for right-sided colon cancer between October 2022 and August 2025 (SP = 60, Xi = 103). Confounding factors were adjusted using propensity score matching and stabilized inverse probability of treatment weighting based on body mass index (BMI) ≥ 25 kg/m<sup>2</sup>, American Society of Anesthesiologists (ASA) ≥ III, tumor size ≥ 40 mm, surgical procedure, and preoperative CRP/Alb ratio ≥ 0.03; short-term outcomes were compared.</p><p><strong>Results: </strong>After adjustment, baseline characteristics were well balanced. The SP approach was associated with a shorter incision length (3.0 vs 5.5 cm, p < 0.01) and lower postoperative pain on day 3 (NRS scores 2 vs. 3, p < 0.01). Operative time, postoperative inflammatory response assessed by CRP/Alb ratio, complications, and pathological outcomes were comparable between the groups.</p><p><strong>Conclusions: </strong>Pure single-incision robotic surgery using the da Vinci SP system demonstrated comparable short-term safety and oncological adequacy to the Xi system, with modest advantages in incision length and postoperative pain. No clear benefit in systemic inflammatory response was observed, and further validation in larger, prospective, multicenter studies is warranted.</p>","PeriodicalId":22174,"journal":{"name":"Surgical Endoscopy And Other Interventional Techniques","volume":" ","pages":""},"PeriodicalIF":2.7,"publicationDate":"2026-03-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147435812","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}