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Limitations of the Location-Based and Polyp-Based Resect and Discard Strategies 基于位置和基于息肉的切除和丢弃策略的局限性
IF 1.2 Q4 GASTROENTEROLOGY & HEPATOLOGY Pub Date : 2024-01-01 DOI: 10.1016/j.tige.2024.05.002

BACKGROUND AND AIMS

Location-based resect and discard (LBRD) and polyp-based resect and discard (PBRD) are 2 recently proposed strategies to minimize the cost of colonoscopy screening and surveillance. Our study applied these strategies to our colonoscopy database retrospectively to determine the applicability of these strategies in our screening and surveillance colonoscopy population.

METHODS

In total, 6024 elective screening, surveillance, or diagnostic colonoscopies performed at the University of California, Irvine, were analyzed. We compared the LBRD and PBRD recommendations with longer and shorter 2020 United States Multi-Society Task Forces (USMSTF) surveillance interval recommendations. The primary outcome was the achievement of the 90% agreement threshold set by the American Society of Gastrointestinal Endoscopy Preservation and Incorporation of Valuable Endoscopic Innovations.

RESULTS

The LBRD strategy achieved 88.0% and 71.6% concordance with the longer and shorter 2020 USMSTF recommendation guidelines, respectively. The PBRD strategy only applied to 65.4% of procedures, with the remaining procedures still requiring pathologic evaluation. Among the applicable procedures, the PBRD strategy achieved 94.2% and 38.6% concordance with the longer and shorter USMSTF recommendation guidelines, respectively.

CONCLUSION

The PBRD strategy met the 90% preservation and incorporation of valuable endoscopic innovations threshold only when using the longer USMSTF recommendations, but concordance dropped to 38.6% when using the shorter surveillance intervals, which are commonly used in the United States. Although resect and discard may decrease reliance on pathology, these 2 strategies do not achieve the level of concordance required to replace the use of pathology for diminutive polyps in our population.

背景和目的基于位置的切除和丢弃(LBRD)和基于息肉的切除和丢弃(PBRD)是最近提出的将结肠镜筛查和监测成本降至最低的两种策略。我们的研究将这些策略应用于我们的结肠镜检查数据库,以确定这些策略在我们的筛查和监测结肠镜检查人群中的适用性。方法我们总共分析了 6024 例在加州大学欧文分校进行的选择性筛查、监测或诊断性结肠镜检查。我们将 LBRD 和 PBRD 建议与 2020 年美国多协会工作组 (USMSTF) 更长和更短的监测间隔建议进行了比较。主要结果是达到美国消化内镜学会设定的 90% 一致阈值。结果LBRD 策略与更长和更短的 2020 年 USMSTF 建议指南的一致性分别达到 88.0% 和 71.6%。PBRD策略仅适用于65.4%的手术,其余手术仍需进行病理评估。在适用的手术中,PBRD 策略与较长和较短的 USMSTF 建议指南的一致性分别达到 94.2% 和 38.6%。结论只有在使用较长的 USMSTF 建议时,PBRD 策略才能达到 90% 的保留率并纳入有价值的内镜创新阈值,但在使用较短的监测间隔时,一致性降至 38.6%,而这在美国是常用的。虽然切除和剔除可减少对病理的依赖,但这两种策略并不能达到在我们的人群中取代病理检查微小息肉所需的一致性水平。
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引用次数: 0
Endoscopic Ultrasound-Guided Liver Biopsy Is Safe and Effective in Post Liver Transplant Patients 肝移植术后患者在内镜超声引导下进行肝活检既安全又有效
IF 1.2 Q4 GASTROENTEROLOGY & HEPATOLOGY Pub Date : 2024-01-01 DOI: 10.1016/j.tige.2024.06.006
JOSHUA L. HUDSON , AMY BROWNLEE , NEIL D. SHAH , TODD H. BARON
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引用次数: 0
Endoscopy-Guided High-Pressure Spray “Power-Wash” for Detection of Gastric Intestinal Metaplasia and Dysplasia 内窥镜引导下的高压喷雾 "强力清洗 "检测胃肠化生和发育不良
IF 2.4 Q4 GASTROENTEROLOGY & HEPATOLOGY Pub Date : 2024-01-01 DOI: 10.1016/j.tige.2023.12.009
Charles J. Lightdale , Patricia Tiscornia-Wasserman , Amrita Sethi , Julian A. Abrams , Monika Laszkowska , Arshish Dua , Judith Kim , Ali Soroush , Haley M. Zylberberg , John T. Nathanson , Chin Hur
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引用次数: 0
Magnetic Compression Anastomosis for Esophageal Obstruction: Indications, Contraindications, Methodologies, and Technique Strategies 食道梗阻的磁压吻合术:适应症、禁忌症、方法和技术策略
IF 1.2 Q4 GASTROENTEROLOGY & HEPATOLOGY Pub Date : 2024-01-01 DOI: 10.1016/j.tige.2024.02.001

Background and Aims

There are several limitations to the application of conventional endoscopic therapy for refractory esophageal stenosis and even atresia, and the secondary option of surgery involving reanastomosis also has drawbacks. Magnetic compression anastomosis (MCA) is a novel technique that relies on magnetic attraction for recanalization and the repair of esophageal obstruction. We evaluate and discuss the clinical value and implementation strategies of the MCA technique as a promising countermeasure for esophageal obstruction.

Methods

In this study, we retrospectively enrolled 7 patients with esophageal stenosis or atresia who underwent MCA from December 2015 to June 2023. Gastroscopic combined with laparoscopic-assisted gastroesophageal MCA and jejunostomy were performed for patient 1; laparotomy and gastroscopic-assisted MCA and jejunostomy were performed for patient 2; laparoscopic gastrostomy combined with endoscopic-assisted MCA was performed for patients 3 and 4; thoracotomy combined with MCA and gastrostomy were performed for patient 5; and endoscopic-assisted MCA was performed for patients 6 and 7.

Results

Anastomosis and recanalization were successfully performed for all patients. A total of 42.86% (3/7) of the patients underwent subsequent conventional endoscopic treatment, including balloon dilatation and stent implantation. The incidences of postoperative pulmonary infection and anastomotic leakage were both 14.29% (1/7), and no other adverse events occurred. The magnetic complexes were removed at a median of postoperative day 18. All patients resumed oral feeding.

Conclusion

MCA appears to be a safe and effective therapy for the management of severe esophageal stenosis, refractory stenosis, and atresia of different etiologies, locations, lengths, and patterns, with the advantages of less trauma, high safety, and effectiveness. When making the operative proposal, diverse and individualized magnetic compression devices and methods should be flexibly adopted according to the patient's individual characteristics, history, obstruction distance, and obstruction patterns.

背景和目的应用传统内窥镜疗法治疗难治性食管狭窄甚至闭锁存在一些局限性,而二次手术(包括重新吻合)也存在缺陷。磁力压缩吻合术(MCA)是一种新技术,它依靠磁力吸引来重新闭塞并修复食道梗阻。我们评估并讨论了 MCA 技术的临床价值和实施策略,将其视为食道梗阻的一种有前途的对策。方法在这项研究中,我们回顾性地纳入了 2015 年 12 月至 2023 年 6 月期间接受 MCA 的 7 例食道狭窄或闭锁患者。1号患者行胃镜联合腹腔镜辅助胃食管MCA和空肠造口术;2号患者行开腹手术和胃镜辅助MCA和空肠造口术;3号和4号患者行腹腔镜胃造口术联合内镜辅助MCA;5号患者行开胸术联合MCA和胃造口术;6号和7号患者行内镜辅助MCA。结果 所有患者都成功进行了吻合和再通。42.86%的患者(3/7)随后接受了常规内镜治疗,包括球囊扩张和支架植入。术后肺部感染和吻合口漏的发生率均为14.29%(1/7),未发生其他不良事件。磁性复合体在术后第 18 天被移除。所有患者均恢复了口服喂养。结论:磁性复合器似乎是治疗不同病因、位置、长度和形态的重度食管狭窄、难治性狭窄和闭锁的一种安全有效的疗法,具有创伤小、安全性高、效果好等优点。在制定手术方案时,应根据患者的个体特征、病史、梗阻距离和梗阻形态,灵活采用多样化、个体化的磁加压装置和方法。
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引用次数: 0
Peroral Endoscopic Myotomy for the Management of Esophageal Diverticula: Tunneling Forward 用于治疗食管憩室的口周内窥镜肌切开术:隧道式前移
IF 2.4 Q4 GASTROENTEROLOGY & HEPATOLOGY Pub Date : 2024-01-01 DOI: 10.1016/j.tige.2023.12.003
Matt Pelton , Michel Kahaleh , Amy Tyberg

Diverticular peroral endoscopic myotomy (D-POEM) has emerged as a minimally invasive, safe, and effective option for Zenker's diverticula (ZDs) and several other types of esophageal diverticula. D-POEM involves submucosal dissection to create tunnels on the luminal and diverticular aspects of the diverticular septum, allowing for precise visualization of the septum. The operator then performs a myotomy, releasing the diverticula and reconnecting the diverticular and esophageal lumens. Approaches for D-POEM vary on the basis of the location of the initial incision for the submucosal dissection; in the long D-POEM approach, operators begin submucosal dissection 1-2 cm above the septum, whereas in the ultra-short D-POEM approach, operators begin submucosal dissection directly on the septum. Observational studies and systematic reviews demonstrate consistent technical success (93.4%-100%), high clinical success (87.1%-94.1%), few adverse events (4.6%-16.9%), and low recurrence rates (0.9%-4.4%). Meta-analyses of observational studies comparing D-POEM with surgical approaches (flexible endoscopic septotomy and rigid endoscopic septotomy) have found that D-POEM may have higher rates of clinical success (RR 1.13, CI 1.05-1.22 and RR 1.11, CI 1.03-1.18) with comparable technical success, adverse event, and recurrence rates. However, further rigorous prospective and randomized trials are warranted. Early comparisons of the ultra-short and long approaches to D-POEM have not found significant differences in efficacy. Outside of ZD, D-POEM should be further investigated for Killian-Jamieson, epiphrenic, and Rokitansky diverticula

憩室口周内镜下肌切开术(D-POEM)已成为一种微创、安全、有效的治疗 Zenker 食管憩室(ZDs)和其他几种食管憩室的方法。D-POEM 包括粘膜下剥离,在憩室隔膜的管腔和憩室方面创建隧道,以便精确观察憩室隔膜。然后,操作者进行肌层切开术,释放憩室并重新连接憩室和食管管腔。D-POEM 方法因粘膜下剥离初始切口的位置不同而各异;在长 D-POEM 方法中,操作者在隔膜上方 1-2 厘米处开始粘膜下剥离,而在超短 D-POEM 方法中,操作者直接在隔膜上开始粘膜下剥离。观察性研究和系统性综述显示了一致的技术成功率(93.4%-100%)、较高的临床成功率(87.1%-94.1%)、较少的不良事件(4.6%-16.9%)和较低的复发率(0.9%-4.4%)。将 D-POEM 与外科手术方法(柔性内窥镜隔膜切除术和刚性内窥镜隔膜切除术)进行比较的观察性研究的 Meta 分析发现,D-POEM 的临床成功率可能更高(RR 1.13,CI 1.05-1.22 和 RR 1.11,CI 1.03-1.18),而技术成功率、不良事件和复发率相当。不过,还需要进一步进行严格的前瞻性随机试验。早期对 D-POEM 的超短和超长方法进行的比较并未发现疗效上的显著差异。除 ZD 外,应进一步研究 D-POEM 对 Killian-Jamieson、虹吸管憩室和 Rokitansky 憩室的治疗效果。
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引用次数: 0
Development of an Automated Endoscopic Retrograde Cholangiopancreatography Quality Report Card Using an Integrated Analytics Suite 利用综合分析套件开发自动内镜逆行胰胆管造影质量报告单
IF 1.2 Q4 GASTROENTEROLOGY & HEPATOLOGY Pub Date : 2024-01-01 DOI: 10.1016/j.tige.2024.03.007

BACKGROUND AND AIMS

Quality indicators (QIs) are essential for evaluating the safety and effectiveness of endoscopy but are difficult to measure accurately for endoscopic retrograde cholangiopancreatography (ERCP). We developed a fully automated, real-time endoscopy analytics tool using Health Level-7 standards that collects ERCP QIs from an endoscopy reporting system to generate an ERCP quality report card in a third-party analytics suite.

METHODS

ERCP report data were collected between June 2021 and December 2022 from 4 referral centers. Discrete data elements from endoscopy reports generated in the EndoPro reporting platform were imported into the Qlik analytics suite, and QI data were aggregated into a report card. The collected data were manually validated to confirm accuracy.

RESULTS

Pooled data were successfully used to generate a comprehensive institutional ERCP quality report card comprising a total of 2146 ERCPs performed by 12 endoscopists. Manual review confirmed high accuracy (96.5%-100%) of automatic extraction of ERCP QIs from endoscopy reports. Multiple procedural data elements were successfully extracted, including cannulation difficulty, success rate, and administration of post-ERCP pancreatitis prophylaxis for procedures with biliary and pancreatic indication. Generation of the report card required minimal additional work on the part of the performing endoscopist and was updated in real time.

CONCLUSION

We developed an automated ERCP analytics tool that accurately and automatically extracts QI data into a succinct ERCP quality report card without the need for manual data extraction or natural language processing. The use of the Health Level-7 standard provides a framework for the creation of similar tools in other electronic health records. This tool allows for accurate ERCP quality and performance data evaluation at individual and institutional levels.

背景和目的质量指标(QIs)对于评估内镜检查的安全性和有效性至关重要,但内镜逆行胰胆管造影术(ERCP)却很难精确测量。我们采用 Health Level-7 标准开发了一款全自动实时内镜分析工具,该工具可从内镜报告系统中收集 ERCP QIs,并在第三方分析套件中生成 ERCP 质量报告卡。将 EndoPro 报告平台生成的内镜报告中的离散数据元素导入 Qlik 分析套件,并将 QI 数据汇总到报告卡中。结果汇集的数据被成功用于生成一份全面的机构ERCP质量报告单,其中包括由12名内镜医师实施的共计2146例ERCP。人工审核证实,从内镜检查报告中自动提取ERCP QIs的准确率很高(96.5%-100%)。成功提取了多个手术数据元素,包括插管难度、成功率,以及对有胆道和胰腺适应症的手术实施ERCP术后胰腺炎预防。结论我们开发了一种自动化 ERCP 分析工具,它能准确、自动地将 QI 数据提取到简洁的 ERCP 质量报告单中,而无需手动提取数据或进行自然语言处理。健康水平-7 标准的使用为在其他电子病历中创建类似工具提供了框架。该工具可在个人和机构层面进行准确的 ERCP 质量和绩效数据评估。
{"title":"Development of an Automated Endoscopic Retrograde Cholangiopancreatography Quality Report Card Using an Integrated Analytics Suite","authors":"","doi":"10.1016/j.tige.2024.03.007","DOIUrl":"10.1016/j.tige.2024.03.007","url":null,"abstract":"<div><h3>BACKGROUND AND AIMS</h3><p>Quality indicators (QIs) are essential for evaluating the safety and effectiveness of endoscopy but are difficult to measure accurately for endoscopic retrograde cholangiopancreatography (ERCP). We developed a fully automated, real-time endoscopy analytics tool using Health Level-7 standards that collects ERCP QIs from an endoscopy reporting system to generate an ERCP quality report card in a third-party analytics suite.</p></div><div><h3>METHODS</h3><p>ERCP report data were collected between June 2021 and December 2022 from 4 referral centers. Discrete data elements from endoscopy reports generated in the EndoPro reporting platform were imported into the Qlik analytics suite, and QI data were aggregated into a report card. The collected data were manually validated to confirm accuracy.</p></div><div><h3>RESULTS</h3><p>Pooled data were successfully used to generate a comprehensive institutional ERCP quality report card comprising a total of 2146 ERCPs performed by 12 endoscopists. Manual review confirmed high accuracy (96.5%-100%) of automatic extraction of ERCP QIs from endoscopy reports. Multiple procedural data elements were successfully extracted, including cannulation difficulty, success rate, and administration of post-ERCP pancreatitis prophylaxis for procedures with biliary and pancreatic indication. Generation of the report card required minimal additional work on the part of the performing endoscopist and was updated in real time.</p></div><div><h3>CONCLUSION</h3><p>We developed an automated ERCP analytics tool that accurately and automatically extracts QI data into a succinct ERCP quality report card without the need for manual data extraction or natural language processing. The use of the Health Level-7 standard provides a framework for the creation of similar tools in other electronic health records. This tool allows for accurate ERCP quality and performance data evaluation at individual and institutional levels.</p></div>","PeriodicalId":36169,"journal":{"name":"Techniques and Innovations in Gastrointestinal Endoscopy","volume":"26 3","pages":"Pages 230-236"},"PeriodicalIF":1.2,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2590030724000217/pdfft?md5=d5468471c598744e8a9f817bc39b143e&pid=1-s2.0-S2590030724000217-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140404952","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}
引用次数: 0
Patient Perception of Endoscopic and Medical Therapies for Weight Loss 患者对内窥镜和药物减肥疗法的看法
IF 2.4 Q4 GASTROENTEROLOGY & HEPATOLOGY Pub Date : 2024-01-01 DOI: 10.1016/j.tige.2023.11.001
MONICA SAUMOY , YINGLIN GAO , KELLY ALLISON , PETER F. CRONHOLM , OCTAVIA PICKETT-BLAKELY , MICHAEL L. KOCHMAN , NIKHIL R. THIRUVENGADAM
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引用次数: 0
Cost-Effectiveness Analysis of Endoscopic Sleeve Gastroplasty 内镜袖状胃成形术的成本效益分析
IF 1.2 Q4 GASTROENTEROLOGY & HEPATOLOGY Pub Date : 2024-01-01 DOI: 10.1016/j.tige.2024.06.001
Michael Daniel , Cassandra Fritz , Tsehay Abebe , Ahmad N. Bazarbashi , Shelby Sullivan , Su-Hsin Chang , Vladimir Kushnir

BACKGROUND AND AIMS

Obesity is prevalent in the United States. Endoscopic sleeve gastroplasty (ESG) has been shown to produce effective weight loss and improvement in obesity-related disease. The cost effectiveness of ESG is currently unclear in patients with obesity with and without type 2 diabetes (T2DM).

METHODS

A decision analytic model with time horizon of 5 years and lifetime, from a health system's perspective was constructed to compare ESG to no weight loss intervention (no ESG) in patients with obesity aged 35-45 years with a body mass index of ≥30 kg/m2 with or without T2DM. Parameters were obtained based on peer-reviewed data. One-way and 2-way sensitivity analyses were performed for variations in T2DM resolution and ESG costs.

RESULTS

For the 5-year time horizon in patients with T2DM, ESG produced 4.28 quality-adjusted life years (QALYs) and cost $77,874, compared with 3.99 QALYs and a cost of $73,738 for no ESG, resulting in an incremental cost-effectiveness ratio (ICER) of $13,922 per QALY. For the lifetime horizon, ESG produced 29.57 QALYs and a lifetime cost of $451,261, compared with 26.69 QALYs and a lifetime cost of $493,806 for no ESG, resulting in a negative ICER (ie, cost saving). The 5-year time horizon in patients without T2DM demonstrated that ESG produced 4.42 QALYs, compared with 4.08 QALYs with no ESG, resulting in an ICER of $39,116 per QALY gained. For the lifetime horizon ESG produced 34.21 QALYs, compared with 31.60 QALYs for no ESG, resulting ICER of $4752.

CONCLUSION

This cost-effectiveness analysis suggests that ESG is cost effective in 5 years and cost saving over a lifetime for patients with obesity and type 2 diabetes. ESG remains cost effective at 5 years and over a lifetime in patients without T2DM.

背景和目的肥胖症在美国十分普遍。内镜袖带胃成形术(ESG)已被证明能有效减轻体重并改善肥胖相关疾病。方法从医疗系统的角度出发,构建了一个时间跨度为 5 年和终生的决策分析模型,对年龄在 35-45 岁、体重指数≥30 kg/m2 且伴有或不伴有 T2DM 的肥胖患者进行 ESG 与无减肥干预(无 ESG)的比较。参数根据同行评议数据得出。结果在 T2DM 患者的 5 年时间跨度内,ESG 可产生 4.28 个质量调整生命年 (QALY),成本为 77,874 美元,而不使用 ESG 可产生 3.99 个质量调整生命年,成本为 73,738 美元,因此每 QALY 的增量成本效益比 (ICER) 为 13,922 美元。在终生范围内,ESG 产生了 29.57 QALYs 和 451,261 美元的终生成本,而没有 ESG 产生了 26.69 QALYs 和 493,806 美元的终生成本,因此 ICER 为负值(即节省成本)。对未患 T2DM 的患者进行的 5 年时间跨度研究表明,ESG 可产生 4.42 QALYs,而不使用 ESG 可产生 4.08 QALYs,因此每 QALY 收益的 ICER 为 39,116 美元。结论这项成本效益分析表明,ESG 在 5 年内具有成本效益,在肥胖症和 2 型糖尿病患者的整个生命周期内都能节约成本。对于没有 T2DM 的患者而言,ESG 在 5 年内和终生都具有成本效益。
{"title":"Cost-Effectiveness Analysis of Endoscopic Sleeve Gastroplasty","authors":"Michael Daniel ,&nbsp;Cassandra Fritz ,&nbsp;Tsehay Abebe ,&nbsp;Ahmad N. Bazarbashi ,&nbsp;Shelby Sullivan ,&nbsp;Su-Hsin Chang ,&nbsp;Vladimir Kushnir","doi":"10.1016/j.tige.2024.06.001","DOIUrl":"10.1016/j.tige.2024.06.001","url":null,"abstract":"<div><h3>BACKGROUND AND AIMS</h3><p>Obesity is prevalent in the United States. Endoscopic sleeve gastroplasty (ESG) has been shown to produce effective weight loss and improvement in obesity-related disease. The cost effectiveness of ESG is currently unclear in patients with obesity with and without type 2 diabetes (T2DM).</p></div><div><h3>METHODS</h3><p>A decision analytic model with time horizon of 5 years and lifetime, from a health system's perspective was constructed to compare ESG to no weight loss intervention (no ESG) in patients with obesity aged 35-45 years with a body mass index of ≥30 kg/m<sup>2</sup> with or without T2DM. Parameters were obtained based on peer-reviewed data. One-way and 2-way sensitivity analyses were performed for variations in T2DM resolution and ESG costs.</p></div><div><h3>RESULTS</h3><p>For the 5-year time horizon in patients with T2DM, ESG produced 4.28 quality-adjusted life years (QALYs) and cost $77,874, compared with 3.99 QALYs and a cost of $73,738 for no ESG, resulting in an incremental cost-effectiveness ratio (ICER) of $13,922 per QALY. For the lifetime horizon, ESG produced 29.57 QALYs and a lifetime cost of $451,261, compared with 26.69 QALYs and a lifetime cost of $493,806 for no ESG, resulting in a negative ICER (ie, cost saving). The 5-year time horizon in patients without T2DM demonstrated that ESG produced 4.42 QALYs, compared with 4.08 QALYs with no ESG, resulting in an ICER of $39,116 per QALY gained. For the lifetime horizon ESG produced 34.21 QALYs, compared with 31.60 QALYs for no ESG, resulting ICER of $4752.</p></div><div><h3>CONCLUSION</h3><p>This cost-effectiveness analysis suggests that ESG is cost effective in 5 years and cost saving over a lifetime for patients with obesity and type 2 diabetes. ESG remains cost effective at 5 years and over a lifetime in patients without T2DM.</p></div>","PeriodicalId":36169,"journal":{"name":"Techniques and Innovations in Gastrointestinal Endoscopy","volume":"26 3","pages":"Pages 244-251"},"PeriodicalIF":1.2,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2590030724000357/pdfft?md5=7a35690a07a3ad25989ed8724c19fd4f&pid=1-s2.0-S2590030724000357-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141961110","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}
引用次数: 0
Colonoscopy Quality, Innovation, and the Assessment of New Technology 结肠镜检查质量、创新和新技术评估
IF 2.4 Q4 GASTROENTEROLOGY & HEPATOLOGY Pub Date : 2024-01-01 DOI: 10.1016/j.tige.2024.03.001
Sanjay R.V. Gadi , Sriya S. Muralidharan , Jeremy R. Glissen Brown

Colonoscopy serves a vital role in screening and surveillance for colorectal cancer and has seen incredible innovations in the past several decades. Amidst a growing landscape of emerging technologies, it has become increasingly critical to develop a process for the evaluation and adoption of new technology into the endoscopy suite. In this paper, we propose a framework for assessing a new colonoscopy technology utilizing quality improvement principles applied in procedural and integration assessments. After defining key quality indicators in colonoscopy, we follow the arc of innovation across preprocedural, intraprocedural, and postprocedural advancements in colonoscopy to highlight the process and outcome measures that constitute the procedural assessment. This discussion is followed by case studies in key structure and balance measures that serve to assess the feasibility of integrating novel technology into the endoscopy suite. At both assessment levels, we explore the advent of artificial intelligence in colonoscopy, citing relevant examples in computer-aided detection and computer-aided diagnosis. We highlight innovations that have been successfully adopted into clinical practice alongside technologies that had limited uptake or were otherwise retired from standard of care. In doing so, we illustrate the iterative nature of this process of innovation and technological development.

结肠镜检查在筛查和监测结直肠癌方面发挥着重要作用,在过去的几十年里,结肠镜检查经历了令人难以置信的创新。在新兴技术不断发展的背景下,为内窥镜检查室制定评估和采用新技术的流程变得越来越重要。在本文中,我们提出了一个评估结肠镜检查新技术的框架,该框架利用了程序和集成评估中应用的质量改进原则。在定义了结肠镜检查的关键质量指标后,我们沿着结肠镜检查术前、术中和术后进步的创新弧线,强调了构成程序评估的过程和结果测量。讨论结束后,我们将对关键结构和平衡措施进行案例研究,以评估将新技术整合到内窥镜检查室的可行性。在这两个评估层面,我们探讨了人工智能在结肠镜检查中的应用,并列举了计算机辅助检测和计算机辅助诊断中的相关实例。我们重点介绍了已成功应用于临床实践的创新技术,以及使用率有限或已退出标准护理的技术。在此过程中,我们说明了这一创新和技术发展过程的反复性。
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引用次数: 0
Immediate Direct Endoscopic Necrosectomy Versus Delayed Direct Endoscopic Necrosectomy 即刻直接内镜坏死组织切除术与延迟直接内镜坏死组织切除术的比较
IF 1.2 Q4 GASTROENTEROLOGY & HEPATOLOGY Pub Date : 2024-01-01 DOI: 10.1016/j.tige.2024.06.008
Abdullah A. Al-Shahrani , Benjamin W. Warren , Samuel Han , Steven A. Edmundowicz , Mihir S. Wagh , Sachin B. Wani , Hazem T. Hammad , Augustin R. Attwell , Raj J. Shah

BACKGROUND AND AIMS

Lumen-apposing metal stents (LAMSs) are effective in resolving walled-off necrosis (WON) of the pancreas and enable direct endoscopic necrosectomy (DEN). However, optimal DEN timing is controversial. We aimed to study if early DEN shortens WON resolution time.

METHODS

We retrospectively reviewed patients who underwent LAMS placement for WON at a tertiary center. We collected patient demographics, WON characteristics, DEN sessions, and outcomes. We compared those who underwent immediate DEN (iDEN; index DEN at LAMS placement) and delayed DEN (dDEN; index DEN on a separate day from LAMS placement). We identified predictors for resolution time via linear regression, and constructed Nelson-Aalen cumulative hazards curves showing resolution time stratified by index DEN timing.

RESULTS

Between January 2011 and June 2019, 175 patients underwent LAMS placement for peripancreatic fluid collections, 155 (88.6%) of which were WON. Of these, 50 (32.3%) required DEN. The majority were male (80%) with an average age of 52.5 years. WON size and double-pigtail stent use through LAMS were similar. Overall, the mean time to WON resolution was 90.6 days, 44.5 (iDEN) versus 100.7 (dDEN), P = 0.02, with similar DEN sessions (P = 0.64). The average length of stay was 0.9 in iDEN versus 14.7 days in dDEN (P = 0.03). All had WON resolution with a similar adverse event rate (18.5% iDEN vs 25.1% dDEN, P = 0.45). In multivariate analysis, double-pigtail stent use suggested greater complexity and longer WON resolution time (P = 0.005).

CONCLUSION

Despite similar DEN sessions, LAMS with iDEN significantly reduced resolution time compared with dDEN. Only one-third of WON patients treated with LAMS placement required DEN.
背景和目的腔内金属支架(LAMS)能有效解决胰腺贴壁坏死(WON),并能直接进行内镜下坏死切除术(DEN)。然而,最佳的内镜下坏死切除术时机尚存争议。我们的目的是研究早期 DEN 是否能缩短 WON 的解决时间。方法 我们回顾性分析了在一家三级中心接受 LAMS 置入术治疗 WON 的患者。我们收集了患者的人口统计学特征、WON特征、DEN疗程和结果。我们比较了立即进行 DEN(iDEN;在 LAMS 置入时进行指数 DEN)和延迟进行 DEN(dDEN;在 LAMS 置入后的另一天进行指数 DEN)的患者。结果2011年1月至2019年6月期间,175名患者因胰周积液接受了LAMS置管,其中155人(88.6%)为WON。其中 50 人(32.3%)需要进行 DEN。大多数患者为男性(80%),平均年龄为 52.5 岁。WON 大小和通过 LAMS 使用双辫支架的情况相似。总体而言,WON解决的平均时间为90.6天,44.5天(iDEN)对100.7天(dDEN),P = 0.02,DEN疗程相似(P = 0.64)。iDEN的平均住院时间为0.9天,而dDEN为14.7天(P = 0.03)。所有患者都解决了 WON 问题,不良事件发生率相似(iDEN 为 18.5% 对 dDEN 为 25.1%,P = 0.45)。在多变量分析中,使用双辫支架表明手术更复杂,WON解决时间更长(P = 0.005)。结论尽管DEN疗程相似,但与dDEN相比,使用iDEN的LAMS显著缩短了解决时间。只有三分之一接受 LAMS 置入治疗的 WON 患者需要 DEN。
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引用次数: 0
期刊
Techniques and Innovations in Gastrointestinal Endoscopy
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