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Comparison of Adenoma Detection Rate Between Three-dimensional and Standard Colonoscopy: A Multicenter Randomized Controlled Trial.
IF 11.5 1区 医学 Q1 GASTROENTEROLOGY & HEPATOLOGY Pub Date : 2025-01-07 DOI: 10.1055/a-2510-8759
Wei-Yuan Chang, Li-Chun Chang, Hsuan-Ho Lin, Pin-Ya Wei, Hsing-Chien Wu, Wei-Chih Liao, Han-Mo Chiu, Ming-Shiang Wu

Background and study aim: Improvement of adenoma detection rate (ADR) effectively reduces the subsequent incidence of colorectal cancer (CRC). Three-dimensional (3D) colonoscopy provided more anatomical details than standard two-dimensional (2D) colonoscopy and improved ADR in a simulation study. We aimed to compare the ADR between 2D and 3D colonoscopy.

Patients and methods: In this multicenter randomized controlled trial, subjects aged ≥ 40 years who underwent colonoscopy for screening, surveillance, or symptoms were consecutively enrolled between February 2022 and June 2023 and randomized into 2D or 3D groups with a 1:1 ratio. The primary outcome was ADR. The secondary outcomes included the detection rates of flat adenoma, right-sided adenoma, proximal adenoma, sessile serrated lesion and advanced adenoma.

Results: Of the 348 participants recruited, 158 and 160 were allocated to 2D and 3D colonoscopy, respectively. The mucosa inspection time was comparable between the 3D (9.8±2.6 minutes) and 2D (9.4±3.1 minutes) groups (p=.21). The 3D group had significantly higher ADR (53.1% vs. 38.6%, difference (95% confidence interval, CI): 14.5% (3.7-25.4), p=.0094), as well as higher detection rates for flat adenoma (35.0% vs. 21.5%, difference: 13.5% (3.7-23.3), p=.0076), right-sided adenoma (26.3% vs. 15.2%, difference: 11.1% (2.2-19.9), p=.015), proximal adenoma (38.1% vs. 23.4%, difference: 14.7% (4.7-24.7), p=.0045) and adenoma sized 5-9mm (45.0% vs. 31.0%, difference: 14.0% (3.4-24.5), p=.010). However, there was no difference in the detection rate of sessile serrated lesion and advanced adenoma.

Conclusions: 3D colonoscopy improved the detection of adenomas without significantly increasing the mucosa inspection time. (ClinicalTrials.gov: NCT05153746).

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引用次数: 0
Adenoma detection rate by colonoscopy in real-world population-based studies: a systematic review and meta-analysis. 基于真实世界人群研究的结肠镜检查腺瘤检出率:系统回顾和荟萃分析。
IF 11.5 1区 医学 Q1 GASTROENTEROLOGY & HEPATOLOGY Pub Date : 2025-01-01 Epub Date: 2024-09-03 DOI: 10.1055/a-2382-5795
Carlos Fernandes, Manuela Estevinho, Manuel Marques Cruz, Leonardo Frazzoni, Pedro Pereira Rodrigues, Lorenzo Fuccio, Mário Dinis-Ribeiro

Background: Adenoma detection rate (ADR) is a quality indicator set at a minimum of 25% in unselected populations by the European Society of Gastrointestinal Endoscopy (ESGE). Nevertheless, a lack of pooled observational data resembling real-world practice limits support for this threshold. We aimed to perform a systematic review with meta-analysis to evaluate the pooled rates for conventional adenoma detection, polyp detection (PDR), cecal intubation, bowel preparation, and complications in population-based studies.

Methods: The PubMed, Scopus, and Web of Science databases were searched until May 2023 for populational-based studies reporting overall ADR in unselected individuals. A random-effects model was used for meta-analysis.

Results: 31 studies were included, comprising 3 644 561 subjects. A high quality of procedures was noticeable, with a high cecal intubation rate and low complication rate. The overall pooled ADR, PDR, and rate of cancer detection were 26.5% (95%CI 23.3% to 29.7%), 38.3% (95%CI 32.5% to 44.1%), and 2.7% (95%CI 1.5% to 3.9%), respectively. ADR varied according to indication: screening 33.3% (95%CI 24.5% to 42.2%), surveillance 42.9% (95%CI 36.9% to 49.0%), and diagnostic 24.7% (95%CI 19.5% to 29.9%), with subgroup analysis revealing rates of 34.4% (95%CI 22.0% to 40.5%) for post-fecal occult blood test and 26.6% (95%CI 22.6% to 30.5%) for primary colonoscopy screening. Diminutive conventional adenomas yielded a pooled rate of 59.9% (95%CI 43.4% to 76.3%). The pooled rate for overall serrated lesion detection was 12.4% (95%CI 8.8% to 16.0%). Male sex and higher age were significantly associated with an ADR above the benchmark.

Conclusion: This first meta-analysis relying on real-world observational studies supports the ESGE benchmark for ADR, while suggesting that different benchmarks might be used according to indication, sex, and age.

背景:腺瘤检出率(ADR)是欧洲消化内镜学会(ESGE)设定的一项质量指标,在非选择人群中的检出率至少为 25%。然而,由于缺乏与真实世界实践相似的综合观察数据,限制了对这一阈值的支持。我们旨在通过荟萃分析进行系统性回顾,评估基于人群的研究中常规腺瘤检测、息肉检测 (PDR)、盲肠插管、肠道准备和并发症的汇总率:方法:在 PubMed、Scopus 和 Web of Science 数据库中检索了截至 2023 年 5 月报告未入选者总体 ADR 的基于人群的研究。采用随机效应模型进行荟萃分析:结果:共纳入 31 项研究,包括 3 644 561 名受试者。结果:31 项研究共纳入了 3 644 561 名受试者,研究过程质量较高,盲肠插管率较高,并发症发生率较低。总体汇总的ADR、PDR和癌症检出率分别为26.5%(95%CI为23.3%至29.7%)、38.3%(95%CI为32.5%至44.1%)和2.7%(95%CI为1.5%至3.9%)。ADR因适应症而异:筛查33.3%(95%CI为24.5%至42.2%),监测42.9%(95%CI为36.9%至49.0%),诊断24.7%(95%CI为19.5%至29.9%),亚组分析显示粪便隐血试验后的ADR率为34.4%(95%CI为22.0%至40.5%),初筛结肠镜检查的ADR率为26.6%(95%CI为22.6%至30.5%)。微小常规腺瘤的汇总率为 59.9%(95%CI 为 43.4% 至 76.3%)。锯齿状病变的总检出率为 12.4%(95%CI 8.8% 至 16.0%)。男性和较高的年龄与高于基准的 ADR 显著相关:这项首次基于真实世界观察研究的荟萃分析支持 ESGE 的 ADR 基准,同时建议可根据适应症、性别和年龄采用不同的基准。
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引用次数: 0
The variation in post-endoscopy upper gastrointestinal cancer rates among endoscopy providers in England and associated factors: a population-based study. 英格兰内镜检查机构内镜检查后上消化道癌症发病率的变化及相关因素:一项基于人群的研究。
IF 11.5 1区 医学 Q1 GASTROENTEROLOGY & HEPATOLOGY Pub Date : 2025-01-01 Epub Date: 2024-08-29 DOI: 10.1055/a-2378-1464
Umair Kamran, Felicity Evison, Eva Judith Ann Morris, Matthew J Brookes, Matthew David Rutter, Mimi McCord, Nicola J Adderley, Nigel Trudgill

Background: Post-endoscopy upper gastrointestinal cancer (PEUGIC) is an important key performance indicator for endoscopy quality. We examined variation in PEUGIC rates among endoscopy providers in England and explored associated factors.

Methods: The was a population-based, retrospective, case-control study, examining data from National Cancer Registration and Analysis Service and Hospital Episode Statistics databases for esophageal and gastric cancers diagnosed between 2009 and 2018 in England. PEUGIC were cancers diagnosed 6 to 36 months after an endoscopy that did not diagnose cancer. Associated factors were identified using multivariable logistic regression analyses.

Results: The national PEUGIC rate was 8.5%, varying from 5% to 13% among endoscopy providers. Factors associated with PEUGIC included: female sex (odds ratio [OR] 1.29 [95%CI 1.23-1.36]); younger age (age >80 years, OR 0.52 [0.48-0.56], compared with ≤60 years); increasing comorbidity (Charlson score >4, OR 5.06 [4.45-5.76]); history of esophageal ulcer (OR 3.30 [3.11-3.50]), Barrett's esophagus (OR 3.21 [3.02-3.42]), esophageal stricture (OR 1.28 [1.20-1.37]), or gastric ulcer (OR 1.55 [1.44-1.66]); squamous cell carcinoma (OR 1.50 [1.39-1.61]); and UK national endoscopy accreditation status - providers requiring improvement (OR 1.10 [1.01-1.20]), providers never assessed (OR 1.24 [1.04-1.47]).

Conclusion: PEUGIC rates varied threefold among endoscopy providers, suggesting unwarranted differences in endoscopy quality. PEUGIC was associated with endoscopy findings known to be associated with upper gastrointestinal cancer and a lack of national endoscopy provider accreditation. PEUGIC variations suggest an opportunity to raise performance standards to detect upper gastrointestinal cancers earlier and improve outcomes.

背景:内镜检查后上消化道癌(PEUGIC)是内镜检查质量的一项重要关键绩效指标。我们研究了英格兰内镜提供商之间内镜检查后上消化道癌发生率的差异,并探讨了相关因素:这是一项基于人群的回顾性病例对照研究,研究数据来自国家癌症登记与分析服务和医院病例统计数据库,涉及 2009 年至 2018 年期间在英格兰确诊的食管癌和胃癌。PEUGIC是在内镜检查未诊断出癌症后6至36个月诊断出的癌症。通过多变量逻辑回归分析确定了相关因素:全国PEUGIC率为8.5%,不同内镜提供者的PEUGIC率从5%到13%不等。与 PEUGIC 相关的因素包括:女性(几率比 [OR] 1.29 [95%CI 1.23-1.36]);年轻(年龄大于 80 岁,OR 0.52 [0.48-0.56],小于 60 岁);合并症增加(Charlson 评分大于 4,OR 5.06 [4.45-5.76]);食管溃疡病史(OR 3.30 [3.11-3.50])、巴雷特食管(OR 3.21[3.02-3.42])、食管狭窄(OR 1.28 [1.20-1.37])或胃溃疡(OR 1.55 [1.44-1.66]);鳞状细胞癌(OR 1.50 [1.39-1.61]);英国国家内镜鉴定状态--需要改进的医疗机构(OR 1.10 [1.01-1.20]),从未接受过评估的医疗机构(OR 1.24 [1.04-1.47]):结论:不同内镜医疗机构的PEUGIC率相差三倍,表明内镜检查质量存在不必要的差异。PEUGIC与已知与上消化道癌症有关的内镜检查结果以及缺乏国家内镜检查机构认证有关。PEUGIC 的差异表明有机会提高绩效标准,以尽早发现上消化道癌症并改善预后。
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引用次数: 0
Overtubes: a bridge to successful colonoscopic resection? 套管:通向成功结肠镜切除术的桥梁?
IF 11.5 1区 医学 Q1 GASTROENTEROLOGY & HEPATOLOGY Pub Date : 2025-01-01 Epub Date: 2024-09-03 DOI: 10.1055/a-2386-9098
Adolfo Parra-Blanco
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引用次数: 0
Prospective feasibility study of a novel rigidizing stabilizing overtube in the resection of complex gastrointestinal polyps. 在复杂胃肠道息肉切除术中使用新型硬质稳定套管的前瞻性可行性研究。
IF 11.5 1区 医学 Q1 GASTROENTEROLOGY & HEPATOLOGY Pub Date : 2025-01-01 Epub Date: 2024-07-11 DOI: 10.1055/a-2350-4059
Salmaan Jawaid, Ahmed F Aboelezz, Gehad Daba, Mai Khalaf, Fares Ayoub, Noor Zabad, Michael Mercado, Tara Keihanian, Mohamed Othman

Background: A novel rigidizing overtube (ROT) was developed to facilitate endoscopic removal of complex gastrointestinal polyps. We aimed to prospectively evaluate the efficacy and safety of the device in the management of large gastrointestinal polyps.

Methods: A prospective, single-center study, conducted between May 2021 and April 2023, enrolled patients undergoing endoscopic resection of colon/duodenal polyps ≥25 mm. Primary outcomes were safety, technical success, and clinical success defined as the ability of ROT to facilitate endoscopic polyp removal without changing the initial resection method.

Results: 97 patients (98 polyps), with a mean polyp size of 33.2 mm (median 31.1), were evaluated. Technical and clinical success rates were 100% and 84%, respectively. Ileocecal valve location was the only predictor of clinical failure (P = 0.02). The mean time to reach the lesion was 7.2 minutes (95%CI 5-8), with overall resection and procedure times of 53.6 minutes (95%CI 48-61) and 88.9 minutes (95%CI 79-95), respectively. No device-related adverse events occurred. Lower technical (67%) and clinical (67%) success rates were seen for duodenal polyps (n = 6).

Conclusion: The novel ROT was safe, with high technical and clinical success during resection of complex colon polyps. Future studies will determine timing of implementation during routine endoscopic resection.

背景:为了便于内镜下切除复杂的胃肠道息肉,我们开发了一种新型硬化剂套管(ROT)。我们旨在前瞻性地评估该设备在治疗大型胃肠息肉方面的有效性和安全性:一项前瞻性单中心研究于 2021 年 5 月至 2023 年 4 月间进行,招募了接受结肠/十二指肠息肉≥25 毫米内镜切除术的患者。主要结果是安全性、技术成功率和临床成功率,临床成功率是指 ROT 在不改变初始切除方法的情况下促进内镜下息肉切除的能力:共评估了 97 名患者(98 个息肉),息肉平均大小为 33.2 毫米(中位数为 31.1)。技术和临床成功率分别为 100%和 84%。回盲瓣位置是临床失败的唯一预测因素(P = 0.02)。到达病灶的平均时间为 7.2 分钟(95%CI 5-8),总体切除和手术时间分别为 53.6 分钟(95%CI 48-61)和 88.9 分钟(95%CI 79-95)。没有发生与设备相关的不良事件。十二指肠息肉(n = 6)的技术成功率(67%)和临床成功率(67%)较低:结论:新型 ROT 很安全,在切除复杂结肠息肉时技术和临床成功率都很高。未来的研究将确定在常规内镜切除术中实施的时机。
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引用次数: 0
Foreword Endoscopy - Issue 1.
IF 11.5 1区 医学 Q1 GASTROENTEROLOGY & HEPATOLOGY Pub Date : 2025-01-01 Epub Date: 2024-12-19 DOI: 10.1055/a-2419-2840
Peter D Siersema
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引用次数: 0
Author commentary on Paula Arruda do Espirito Santo et al.
IF 11.5 1区 医学 Q1 GASTROENTEROLOGY & HEPATOLOGY Pub Date : 2025-01-01 Epub Date: 2024-12-19 DOI: 10.1055/a-2368-2271
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引用次数: 0
Comparing recurrence rates between endoscopic mucosal resection and endoscopic submucosal dissection in Barrett's endoscopic therapy: timing and definitions matter! 比较巴雷特内镜疗法中内镜粘膜切除术和内镜粘膜下剥离术的复发率:时机和定义很重要!
IF 11.5 1区 医学 Q1 GASTROENTEROLOGY & HEPATOLOGY Pub Date : 2025-01-01 Epub Date: 2024-10-16 DOI: 10.1055/a-2427-7128
Kornpong Vantanasiri, Prasad G Iyer
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引用次数: 0
Use of an endoscopic virtual ruler based on the fiber laser principle and artificial intelligence technology.
IF 11.5 1区 医学 Q1 GASTROENTEROLOGY & HEPATOLOGY Pub Date : 2025-01-01 Epub Date: 2024-12-19 DOI: 10.1055/a-2438-0202
Yaxian Kuai, Shiwei Zhou, Bin Sun, Xu Wang, Youwei Xiao, Aijiu Wu, Derun Kong
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引用次数: 0
Endoscopic ultrasound-guided versus percutaneous liver biopsy: a systematic review and meta-analysis of randomized controlled trials. 内镜超声引导与经皮肝活检:随机对照试验的系统回顾和荟萃分析。
IF 11.5 1区 医学 Q1 GASTROENTEROLOGY & HEPATOLOGY Pub Date : 2025-01-01 Epub Date: 2024-08-28 DOI: 10.1055/a-2368-4608
Paula Arruda do Espirito Santo, Gilmara Coelho Meine, Angélica Luciana Nau, Eduardo Cerchi Barbosa, Stefano Baraldo, Luciano Lenz, Fauze Maluf-Filho

Background: Percutaneous liver biopsy (PC-LB) has long been the usual method for acquisition of liver tissue. Recently, endoscopic ultrasound-guided liver biopsy (EUS-LB) has gained popularity as an alternative modality. We aimed to compare the efficacy and safety of EUS-LB versus PC-LB.

Methods: We systematically searched PubMed, Embase, and the Cochrane Library databases for randomized controlled trials (RCTs) comparing EUS-LB with PC-LB published until October 20, 2023. The primary outcome was diagnostic adequacy. Secondary outcomes were: the number of complete portal tracts (CPTs), longest sample length (LSL), total sample length (TSL), post-procedure pain scores, and adverse events (AEs), including overall AEs and AEs excluding minor post-procedure symptoms. We compared binary outcomes using risk ratios (RRs) and continuous outcomes using the mean difference (MD) or standardized mean difference (SMD), with 95%CIs.

Results: Four RCTs (258 patients) were included. The EUS-LB group presented lower post-procedure pain scores (SMD -0.58, 95%CI -0.95 to -0.22) than the PC-LB group. Both groups performed similarly in terms of diagnostic adequacy (RR 1.0, 95%CI 0.96 to 1.04), number of CPTs (MD 2.57, 95%CI -4.09 to 9.22), LSL (MD -2.91 mm, 95%CI -5.86 to 0.03), TSL (MD 4.16 mm, 95%CI -10.12 to 18.45), overall AEs (RR 0.54, 95%CI 0.20 to 1.46), and AEs excluding minor post-procedure symptoms (RR 1.65, 95%CI 0.21 to 13.02).

Conclusions: This meta-analysis suggests that EUS-LB is as safe and effective as PC-LB and is associated with lower post-procedure pain scores.Registration on PROSPERO: CRD42023469469.

背景:经皮肝活检(PC-LB)一直是获取肝组织的常用方法。近来,内镜超声引导肝活检(EUS-LB)作为一种替代方法越来越受欢迎。我们旨在比较 EUS-LB 与 PC-LB 的有效性和安全性:我们系统地检索了 PubMed、Embase 和 Cochrane Library 数据库中截至 2023 年 10 月 20 日发表的比较 EUS-LB 与 PC-LB 的随机对照试验 (RCT)。主要结果是诊断充分性。次要结果包括:完整门静脉道(CPT)数量、最长样本长度(LSL)、总样本长度(TSL)、术后疼痛评分和不良事件(AE),包括总体不良事件和不包括术后轻微症状的不良事件。我们使用风险比(RRs)对二元结果进行了比较,使用平均差(MD)或标准化平均差(SMD)对连续结果进行了比较,并得出了95%CIs:结果:共纳入四项研究(258 名患者)。EUS-LB 组的术后疼痛评分(SMD -0.58,95%CI -0.95--0.22)低于 PC-LB 组。两组在诊断充分性(RR 1.0,95%CI 0.96 至 1.04)、CPTs 数量(MD 2.57,95%CI -4.09 至 9.22)、LSL(MD -2.91 mm,95%CI -5.86 至 0.03)、TSL(MD 4.00 mm,95%CI -0.95 至 0.22)、TSL(MD 4.00 mm,95%CI -5.86 至 0.03)、CPTs 数量(MD 2.57,95%CI -4.09 至 9.22)方面表现相似。03)、TSL(MD 4.16 mm,95%CI -10.12至18.45)、总体AEs(RR 0.54,95%CI 0.20至1.46)和不包括术后轻微症状的AEs(RR 1.65,95%CI 0.21至13.02):这项荟萃分析表明,EUS-LB与PC-LB一样安全有效,而且术后疼痛评分较低。
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引用次数: 0
期刊
Endoscopy
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