Pub Date : 2024-05-23eCollection Date: 2024-01-01DOI: 10.1177/26317745241251708
Vasileios Oikonomou, Andrew Macpherson, Reiner Wiest, Ioannis Kapoglou
After failed biliary cannulation via standard endoscopic retrograde cholangiography approach, endoscopic-ultrasound-based rendezvous-endoscopic retrograde cholangiography (EUS-RV-ERC) is a valid alternative. One of the challenging factors in this setting is the management of the guidewire. Here, we propose a method, where a slim endoscope is used to stabilize the guidewire and optimize wire manipulation in a patient who underwent EUS-RV-ERC via a transgastric approach. This was executed in a patient suffering from severe alcoholic pancreatitis presented with a severely narrowed duodenum due to extrinsic compression and inflammation in the setting of cholangitis Tokyo Grade III.
通过标准内镜逆行胆管造影方法进行胆道插管失败后,基于内镜超声的会合内镜逆行胆管造影(EUS-RV-ERC)是一种有效的替代方法。在这种情况下,具有挑战性的因素之一是导丝的管理。在这里,我们提出了一种方法,即使用纤细的内窥镜来稳定导丝,并优化通过经腹途径进行 EUS-RV-ERC 患者的导丝操作。该方法是在一名患有严重酒精性胰腺炎的患者身上实施的,该患者的十二指肠因外源性压迫和炎症而严重狭窄,并伴有东京 III 级胆管炎。
{"title":"Slim-endoscope-stabilized rendezvous endoscopic retrograde cholangiography <i>via</i> endoscopic ultrasound transgastric bile duct access: utilization for severe pancreatitis with consecutive obstructive jaundice with cholangitis and inaccessible major papilla.","authors":"Vasileios Oikonomou, Andrew Macpherson, Reiner Wiest, Ioannis Kapoglou","doi":"10.1177/26317745241251708","DOIUrl":"10.1177/26317745241251708","url":null,"abstract":"<p><p>After failed biliary cannulation <i>via</i> standard endoscopic retrograde cholangiography approach, endoscopic-ultrasound-based rendezvous-endoscopic retrograde cholangiography (EUS-RV-ERC) is a valid alternative. One of the challenging factors in this setting is the management of the guidewire. Here, we propose a method, where a slim endoscope is used to stabilize the guidewire and optimize wire manipulation in a patient who underwent EUS-RV-ERC <i>via</i> a transgastric approach. This was executed in a patient suffering from severe alcoholic pancreatitis presented with a severely narrowed duodenum due to extrinsic compression and inflammation in the setting of cholangitis Tokyo Grade III.</p>","PeriodicalId":40947,"journal":{"name":"Therapeutic Advances in Gastrointestinal Endoscopy","volume":"17 ","pages":"26317745241251708"},"PeriodicalIF":2.6,"publicationDate":"2024-05-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11119345/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141155335","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-05-13eCollection Date: 2024-01-01DOI: 10.1177/26317745241251713
Tran Thi Anh Tuyet, Nguyen Van Thai, Nguyen Tien Thinh, Mai Thanh Binh
Objective: Endoscopic retrograde cholangiopancreatography (ERCP) in patients who have undergone Billroth II gastroenterostomy (B-II GE) has been challenging, requiring flexibility in technical approaches during execution. The study aims to assess the effectiveness of enhanced techniques in performing ERCP on this patient group in Vietnam.
Method: A total of 42 Vietnamese patients with B-II GE performed an ERCP using a duodenoscope or a modification of ERCP equipment (a cap-fitted regular forward-viewing endoscope) if the former failed. The effectiveness and safety of the ERCP technique were assessed, particularly in patients who underwent the forward-viewing endoscope method.
Result: A total of 39 out of 42 patients had the Vater's papilla identified, among whom 12 patients (30.8%) achieved successful cannulation into the bile duct using a side-viewing endoscope, significantly lower than the success rate using a forward-viewing endoscope (25/27, counted 92.6%, with p < 0.001). After successful cannulation, the rate of stone clearance, the procedural time, and the hospitalization duration of the patients were equivalent between the two methods and were not dependent on the number or size of the stones. On the other hand, post-ERCP complications in patients utilizing forward-viewing endoscopy included acute pancreatitis (22.2%), post-sphincterotomy bleeding (3.7%), septicemia (4.8%), and perforation (0%). These complications were mild and amenable to conservative endoscopic and medical management, and no mortality was observed. The rates of complications and adverse events after ERCP are comparable between the two treatment methods, even though the end-viewing endoscope is used after the failure of the side-viewing endoscope.
Conclusion: Alter ERCP utilizing a cap-fitted forward-viewing endoscope can be a primary choice for treating common bile duct stones in patients with a Billroth II gastric resection history because of high efficacy and acceptable complications. It requires a high level of procedural expertise that requires multiple training sessions.
目的:对接受过比尔罗斯 II 型胃肠造口术(B-II GE)的患者进行内镜逆行胰胆管造影术(ERCP)一直是一项挑战,需要在实施过程中灵活运用技术方法。本研究旨在评估在越南对这一患者群体实施ERCP时增强技术的有效性:方法:共为 42 名越南 B-II GE 患者进行了 ERCP,如果前者失败,则使用十二指肠镜或 ERCP 设备的改良版(带帽普通前视内镜)。对ERCP技术的有效性和安全性进行了评估,尤其是对采用前视内窥镜方法的患者:结果:42 名患者中共有 39 名患者确定了 Vater 乳头,其中有 12 名患者(30.8%)使用侧视内窥镜成功插入胆管,明显低于使用前视内窥镜的成功率(25/27,占 92.6%,P 结论:ERCP 技术应改变使用帽状内窥镜的方法:使用带帽前视内镜的 Alter ERCP 可作为治疗有比洛斯 II 型胃切除术史患者胆总管结石的首选方法,因为其疗效高且并发症可接受。它对手术的专业性要求很高,需要多次培训。
{"title":"Practical application of the modification in endoscopic retrograde cholangiopancreatography treated common bile duct stones in patients with Billroth II gastroenterostomy in Vietnam.","authors":"Tran Thi Anh Tuyet, Nguyen Van Thai, Nguyen Tien Thinh, Mai Thanh Binh","doi":"10.1177/26317745241251713","DOIUrl":"10.1177/26317745241251713","url":null,"abstract":"<p><strong>Objective: </strong>Endoscopic retrograde cholangiopancreatography (ERCP) in patients who have undergone Billroth II gastroenterostomy (B-II GE) has been challenging, requiring flexibility in technical approaches during execution. The study aims to assess the effectiveness of enhanced techniques in performing ERCP on this patient group in Vietnam.</p><p><strong>Method: </strong>A total of 42 Vietnamese patients with B-II GE performed an ERCP using a duodenoscope or a modification of ERCP equipment (a cap-fitted regular forward-viewing endoscope) if the former failed. The effectiveness and safety of the ERCP technique were assessed, particularly in patients who underwent the forward-viewing endoscope method.</p><p><strong>Result: </strong>A total of 39 out of 42 patients had the Vater's papilla identified, among whom 12 patients (30.8%) achieved successful cannulation into the bile duct using a side-viewing endoscope, significantly lower than the success rate using a forward-viewing endoscope (25/27, counted 92.6%, with <i>p</i> < 0.001). After successful cannulation, the rate of stone clearance, the procedural time, and the hospitalization duration of the patients were equivalent between the two methods and were not dependent on the number or size of the stones. On the other hand, post-ERCP complications in patients utilizing forward-viewing endoscopy included acute pancreatitis (22.2%), post-sphincterotomy bleeding (3.7%), septicemia (4.8%), and perforation (0%). These complications were mild and amenable to conservative endoscopic and medical management, and no mortality was observed. The rates of complications and adverse events after ERCP are comparable between the two treatment methods, even though the end-viewing endoscope is used after the failure of the side-viewing endoscope.</p><p><strong>Conclusion: </strong>Alter ERCP utilizing a cap-fitted forward-viewing endoscope can be a primary choice for treating common bile duct stones in patients with a Billroth II gastric resection history because of high efficacy and acceptable complications. It requires a high level of procedural expertise that requires multiple training sessions.</p>","PeriodicalId":40947,"journal":{"name":"Therapeutic Advances in Gastrointestinal Endoscopy","volume":"17 ","pages":"26317745241251713"},"PeriodicalIF":2.6,"publicationDate":"2024-05-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11092305/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140923624","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-05-05eCollection Date: 2024-01-01DOI: 10.1177/26317745241246899
Scarlet Nazarian, Frank Po Wen Lo, Jianing Qiu, Nisha Patel, Benny Lo, Lakshmana Ayaru
Background: Acute upper gastrointestinal bleeding (AUGIB) is a major cause of morbidity and mortality. This presentation however is not universally high risk as only 20-30% of bleeds require urgent haemostatic therapy. Nevertheless, the current standard of care is for all patients admitted to an inpatient bed to undergo endoscopy within 24 h for risk stratification which is invasive, costly and difficult to achieve in routine clinical practice.
Objectives: To develop novel non-endoscopic machine learning models for AUGIB to predict the need for haemostatic therapy by endoscopic, radiological or surgical intervention.
Design: A retrospective cohort study.
Method: We analysed data from patients admitted with AUGIB to hospitals from 2015 to 2020 (n = 970). Machine learning models were internally validated to predict the need for haemostatic therapy. The performance of the models was compared to the Glasgow-Blatchford score (GBS) using the area under receiver operating characteristic (AUROC) curves.
Results: The random forest classifier [AUROC 0.84 (0.80-0.87)] had the best performance and was superior to the GBS [AUROC 0.75 (0.72-0.78), p < 0.001] in predicting the need for haemostatic therapy in patients with AUGIB. A GBS cut-off of ⩾12 was associated with an accuracy, sensitivity, specificity, positive predictive value (PPV) and negative predictive value (NPV) of 0.74, 0.49, 0.81, 0.41 and 0.85, respectively. The Random Forrest model performed better with an accuracy, sensitivity, specificity, PPV and NPV of 0.82, 0.54, 0.90, 0.60 and 0.88, respectively.
Conclusion: We developed and validated a machine learning algorithm with high accuracy and specificity in predicting the need for haemostatic therapy in AUGIB. This could be used to risk stratify high-risk patients to urgent endoscopy.
{"title":"Development and validation of machine learning models to predict the need for haemostatic therapy in acute upper gastrointestinal bleeding.","authors":"Scarlet Nazarian, Frank Po Wen Lo, Jianing Qiu, Nisha Patel, Benny Lo, Lakshmana Ayaru","doi":"10.1177/26317745241246899","DOIUrl":"10.1177/26317745241246899","url":null,"abstract":"<p><strong>Background: </strong>Acute upper gastrointestinal bleeding (AUGIB) is a major cause of morbidity and mortality. This presentation however is not universally high risk as only 20-30% of bleeds require urgent haemostatic therapy. Nevertheless, the current standard of care is for all patients admitted to an inpatient bed to undergo endoscopy within 24 h for risk stratification which is invasive, costly and difficult to achieve in routine clinical practice.</p><p><strong>Objectives: </strong>To develop novel non-endoscopic machine learning models for AUGIB to predict the need for haemostatic therapy by endoscopic, radiological or surgical intervention.</p><p><strong>Design: </strong>A retrospective cohort study.</p><p><strong>Method: </strong>We analysed data from patients admitted with AUGIB to hospitals from 2015 to 2020 (<i>n</i> = 970). Machine learning models were internally validated to predict the need for haemostatic therapy. The performance of the models was compared to the Glasgow-Blatchford score (GBS) using the area under receiver operating characteristic (AUROC) curves.</p><p><strong>Results: </strong>The random forest classifier [AUROC 0.84 (0.80-0.87)] had the best performance and was superior to the GBS [AUROC 0.75 (0.72-0.78), <i>p</i> < 0.001] in predicting the need for haemostatic therapy in patients with AUGIB. A GBS cut-off of ⩾12 was associated with an accuracy, sensitivity, specificity, positive predictive value (PPV) and negative predictive value (NPV) of 0.74, 0.49, 0.81, 0.41 and 0.85, respectively. The Random Forrest model performed better with an accuracy, sensitivity, specificity, PPV and NPV of 0.82, 0.54, 0.90, 0.60 and 0.88, respectively.</p><p><strong>Conclusion: </strong>We developed and validated a machine learning algorithm with high accuracy and specificity in predicting the need for haemostatic therapy in AUGIB. This could be used to risk stratify high-risk patients to urgent endoscopy.</p>","PeriodicalId":40947,"journal":{"name":"Therapeutic Advances in Gastrointestinal Endoscopy","volume":"17 ","pages":"26317745241246899"},"PeriodicalIF":2.6,"publicationDate":"2024-05-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11071626/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140855445","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-04-25eCollection Date: 2024-01-01DOI: 10.1177/26317745241247175
Khushboo Gala, Wissam Ghusn, Vitor Brunaldi, Eric J Vargas, Andrew C Storm, Andres Acosta, Barham K Abu Dayyeh
Background: Endoscopic sleeve gastroplasty (ESG) is a safe and effective obesity treatment. The individualized metabolic score (IMS) is a validated score that uses preoperative variables predicting T2D remission (DR) in bariatric surgery.
Objectives: We evaluated the applicability of using the IMS score to predict DR in patients after ESG.
Design/methods: We performed a retrospective review of patients with obesity and T2D who underwent ESG. We calculated DR, IMS score, and severity, and divided patients based on IMS category.
Results: The cohort comprised 20 patients: 25% (5) mild, 55% (11) moderate, and 20% (4) severe IMS stages. DR was achieved in 60%, 45.5%, and 0% of patients with mild, moderate, and severe IMS scores (p = 0.08), respectively. IMS score was significantly associated with DR (p = 0.03), with the area under the curve of the receiver operating characteristic for predicting DR 0.85.
Conclusion: These pilot data demonstrate that the IMS score appears to be useful in predicting DR after ESG.
{"title":"Applicability of individualized metabolic surgery score for prediction of diabetes remission after endoscopic sleeve gastroplasty.","authors":"Khushboo Gala, Wissam Ghusn, Vitor Brunaldi, Eric J Vargas, Andrew C Storm, Andres Acosta, Barham K Abu Dayyeh","doi":"10.1177/26317745241247175","DOIUrl":"https://doi.org/10.1177/26317745241247175","url":null,"abstract":"<p><strong>Background: </strong>Endoscopic sleeve gastroplasty (ESG) is a safe and effective obesity treatment. The individualized metabolic score (IMS) is a validated score that uses preoperative variables predicting T2D remission (DR) in bariatric surgery.</p><p><strong>Objectives: </strong>We evaluated the applicability of using the IMS score to predict DR in patients after ESG.</p><p><strong>Design/methods: </strong>We performed a retrospective review of patients with obesity and T2D who underwent ESG. We calculated DR, IMS score, and severity, and divided patients based on IMS category.</p><p><strong>Results: </strong>The cohort comprised 20 patients: 25% (5) mild, 55% (11) moderate, and 20% (4) severe IMS stages. DR was achieved in 60%, 45.5%, and 0% of patients with mild, moderate, and severe IMS scores (<i>p</i> = 0.08), respectively. IMS score was significantly associated with DR (<i>p</i> = 0.03), with the area under the curve of the receiver operating characteristic for predicting DR 0.85.</p><p><strong>Conclusion: </strong>These pilot data demonstrate that the IMS score appears to be useful in predicting DR after ESG.</p>","PeriodicalId":40947,"journal":{"name":"Therapeutic Advances in Gastrointestinal Endoscopy","volume":"17 ","pages":"26317745241247175"},"PeriodicalIF":2.6,"publicationDate":"2024-04-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11047249/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140868966","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-03-10eCollection Date: 2024-01-01DOI: 10.1177/26317745241233083
Hasan Tankut Köseoğlu, Kerem Kenarli, Ahmet Akbay, Çağdaṣ Erdoğan, Alper Macif, Meryem Didem Göktaṣ, Mevlüt Hamamci, Çağdaṣ Kalkan, Firathan Sarialtin, Mahmut Yüksel
Background: In recent years, various novel surgical and non-surgical therapeutic options have been developed for treating obesity. Due to its disputed success, intragastric botulinum toxin A (BTX-A) injection is still being debated.
Objectives: We aim to contribute to this controversial issue in the literature by sharing our center's findings regarding intragastric BTX-A injections in the treatment of obesity.
Design: Patients with a body mass index (BMI) of greater than 25 kg/m2 and at least one obesity-related complication, or a BMI of greater than 30 kg/m2 without complications, were eligible for the study if they were between the ages of 18 and 65.
Methods: Following the same procedure, two endoscopists administered BTX-A to all patients. All patients were evaluated for obesity by measuring their lipid profile, hormone profile, and insulin resistance level before treatment.
Results: In our study on 82 patients, we saw a significant mean weight loss (-9.2 kg, p < 0.001) in the second month, and there was no additional mean weight loss in the sixth month of follow-up. In addition, this result seems to be independent of the patient's insulin resistance. We did not see any serious side effects in any of the patients.
Conclusion: Although the use of intragastric injection of BTX-A in the treatment of obesity is a controversial issue, we showed in our study that it causes significant weight loss. Further studies are needed on this subject, as it can be a safe method when the ideal dose and application site are combined with appropriate patient selection.
{"title":"Intragastric injection of botulinum toxin in the treatment of obesity: a single-center study.","authors":"Hasan Tankut Köseoğlu, Kerem Kenarli, Ahmet Akbay, Çağdaṣ Erdoğan, Alper Macif, Meryem Didem Göktaṣ, Mevlüt Hamamci, Çağdaṣ Kalkan, Firathan Sarialtin, Mahmut Yüksel","doi":"10.1177/26317745241233083","DOIUrl":"10.1177/26317745241233083","url":null,"abstract":"<p><strong>Background: </strong>In recent years, various novel surgical and non-surgical therapeutic options have been developed for treating obesity. Due to its disputed success, intragastric botulinum toxin A (BTX-A) injection is still being debated.</p><p><strong>Objectives: </strong>We aim to contribute to this controversial issue in the literature by sharing our center's findings regarding intragastric BTX-A injections in the treatment of obesity.</p><p><strong>Design: </strong>Patients with a body mass index (BMI) of greater than 25 kg/m<sup>2</sup> and at least one obesity-related complication, or a BMI of greater than 30 kg/m<sup>2</sup> without complications, were eligible for the study if they were between the ages of 18 and 65.</p><p><strong>Methods: </strong>Following the same procedure, two endoscopists administered BTX-A to all patients. All patients were evaluated for obesity by measuring their lipid profile, hormone profile, and insulin resistance level before treatment.</p><p><strong>Results: </strong>In our study on 82 patients, we saw a significant mean weight loss (-9.2 kg, <i>p</i> < 0.001) in the second month, and there was no additional mean weight loss in the sixth month of follow-up. In addition, this result seems to be independent of the patient's insulin resistance. We did not see any serious side effects in any of the patients.</p><p><strong>Conclusion: </strong>Although the use of intragastric injection of BTX-A in the treatment of obesity is a controversial issue, we showed in our study that it causes significant weight loss. Further studies are needed on this subject, as it can be a safe method when the ideal dose and application site are combined with appropriate patient selection.</p>","PeriodicalId":40947,"journal":{"name":"Therapeutic Advances in Gastrointestinal Endoscopy","volume":"17 ","pages":"26317745241233083"},"PeriodicalIF":2.6,"publicationDate":"2024-03-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10929057/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140111750","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-02-21eCollection Date: 2024-01-01DOI: 10.1177/26317745241231102
Andrea C Buitrago-Tamayo, Carlos E Lombo-Moreno, Valentina Ursida, Ana M Leguizamo-Naranjo, Oscar M Muñoz-Velandia, Rómulo D Vargas-Rubio
Background: Narrow-Band imaging International Colorectal Endoscopic (NICE) could reduce histopathology study requirements in colorectal polyp evaluation. Local and regional studies are required to validate its utility.
Objectives: To evaluate concordance between NICE classification and histopathology.
Design: Prospective analytic study performed in the Hospital Universitario San Ignacio, Bogotá (Colombia) between 2021 and 2022.
Methods: Concordance between NICE I, II and III classification and histopathology [Hyperplastic Polyp (HP), adenoma and deep submucosal invasive cancer (DSIC)] was evaluated using weighted kappa. Diagnostic performance was evaluated for NICE I-II versus NICE III for DSIC versus adenoma/HP. A subgroup analysis was performed for polyps ⩾10 mm and those located in the rectum, sigmoid, and left colon.
Results: A total of 238 polyps from 135 patients were evaluated. Median age 67 years (IQR 58.5-74.5), 54.4% males. 23 (17.1%) had ⩾3 polyps. Of polyps, 52.1% were located on rectum, sigmoid and left colon. A total of 182 (76.5%) were <10 mm. NICE and histopathology evidenced a fair-moderate concordance (quadratic weighted kappa 0.36, linear weighted kappa 0.43). NICE classification (NICE I-II versus III) compared to histopathology (DSIC versus adenoma/HP) evidenced a sensitivity of 90.9% and specificity of 99.1%. For DSIC diagnosis specificity was ⩾95% on polyps ⩾10 mm and those left sided located.
Conclusion: NICE and histopathology concordance is suboptimal. However, NICE III for DSIC diagnosis evidence good specificity. Therefore, NICE III polyps require a prompt histopathological evaluation and follow-up. Good operative characteristics stand in polyps ⩾10 mm and left sided located. NBI formal training is recommended in gastroenterology units in Latin America.
背景:窄带成像国际结直肠内窥镜(NICE)可减少结直肠息肉评估中对组织病理学研究的要求。需要进行地方和区域研究以验证其实用性:评估 NICE 分类与组织病理学之间的一致性:设计:2021 年至 2022 年在哥伦比亚波哥大圣伊格纳西奥大学医院进行的前瞻性分析研究:采用加权卡帕法评估 NICE I、II 和 III 分类与组织病理学[增生性息肉(HP)、腺瘤和深粘膜下浸润癌(DSIC)]之间的一致性。对 NICE I-II 与 NICE III 的诊断性能进行了评估,对 DSIC 与腺瘤/HP 的诊断性能进行了评估。对10毫米以下的息肉以及位于直肠、乙状结肠和左结肠的息肉进行了亚组分析:共评估了 135 名患者的 238 个息肉。中位年龄 67 岁(IQR 58.5-74.5),54.4% 为男性。23人(17.1%)有⩾3个息肉。息肉中,52.1%位于直肠、乙状结肠和左侧结肠。与组织病理学(DSIC 与腺瘤/HP)相比,共有 182 个息肉(76.5%)与 III 型息肉相比,敏感性为 90.9%,特异性为 99.1%。对于 10 毫米以下和位于左侧的息肉,DSIC 诊断的特异性为 95%:结论:NICE 和组织病理学的一致性并不理想。然而,NICE III 诊断 DSIC 的特异性良好。因此,NICE III 级息肉需要及时进行组织病理学评估和随访。10 毫米以下且位于左侧的息肉具有良好的手术特征。建议拉丁美洲的胃肠病学单位开展 NBI 正规培训。
{"title":"Concordance between nice classification and histopathology in colonic polyps: a tertiary center experience.","authors":"Andrea C Buitrago-Tamayo, Carlos E Lombo-Moreno, Valentina Ursida, Ana M Leguizamo-Naranjo, Oscar M Muñoz-Velandia, Rómulo D Vargas-Rubio","doi":"10.1177/26317745241231102","DOIUrl":"10.1177/26317745241231102","url":null,"abstract":"<p><strong>Background: </strong>Narrow-Band imaging International Colorectal Endoscopic (NICE) could reduce histopathology study requirements in colorectal polyp evaluation. Local and regional studies are required to validate its utility.</p><p><strong>Objectives: </strong>To evaluate concordance between NICE classification and histopathology.</p><p><strong>Design: </strong>Prospective analytic study performed in the Hospital Universitario San Ignacio, Bogotá (Colombia) between 2021 and 2022.</p><p><strong>Methods: </strong>Concordance between NICE I, II and III classification and histopathology [Hyperplastic Polyp (HP), adenoma and deep submucosal invasive cancer (DSIC)] was evaluated using weighted kappa. Diagnostic performance was evaluated for NICE I-II <i>versus</i> NICE III for DSIC <i>versus</i> adenoma/HP. A subgroup analysis was performed for polyps ⩾10 mm and those located in the rectum, sigmoid, and left colon.</p><p><strong>Results: </strong>A total of 238 polyps from 135 patients were evaluated. Median age 67 years (IQR 58.5-74.5), 54.4% males. 23 (17.1%) had ⩾3 polyps. Of polyps, 52.1% were located on rectum, sigmoid and left colon. A total of 182 (76.5%) were <10 mm. NICE and histopathology evidenced a fair-moderate concordance (quadratic weighted kappa 0.36, linear weighted kappa 0.43). NICE classification (NICE I-II <i>versus</i> III) compared to histopathology (DSIC <i>versus</i> adenoma/HP) evidenced a sensitivity of 90.9% and specificity of 99.1%. For DSIC diagnosis specificity was ⩾95% on polyps ⩾10 mm and those left sided located.</p><p><strong>Conclusion: </strong>NICE and histopathology concordance is suboptimal. However, NICE III for DSIC diagnosis evidence good specificity. Therefore, NICE III polyps require a prompt histopathological evaluation and follow-up. Good operative characteristics stand in polyps ⩾10 mm and left sided located. NBI formal training is recommended in gastroenterology units in Latin America.</p>","PeriodicalId":40947,"journal":{"name":"Therapeutic Advances in Gastrointestinal Endoscopy","volume":"17 ","pages":"26317745241231102"},"PeriodicalIF":2.6,"publicationDate":"2024-02-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10882955/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139933377","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-01-12eCollection Date: 2024-01-01DOI: 10.1177/26317745231223312
Dimitrios S Kourdakis, Savvas P Deftereos
Splenic injury is an extremely rare complication of endoscopic retrograde cholangiopancreatography (ERCP). There are only 34 cases reported in the literature up to now. Based on a case of a 72-year-old man, who after ERCP due to choledocholithiasis developed a large perisplenic and subcapsular hematoma, we carried out an extensive review of all cases of ERCP-induced splenic injury found in the literature. We searched PubMed/Medline and Google Scholar till 15 April 2023, for published case reports and series using the following terms: splenic injury after ERCP, ERCP-induced splenic injury, and post-ERCP splenic trauma. The case reports included were in English, Spanish, and German literature. We attempt to discuss the possible clinical image, the available diagnostic methods, the potential treatment alternatives, and predisposing factors related to this entity. Furthermore, a theory of a possible mechanism of this injury is discussed and supported schematically. The ERCP-induced splenic injury is rare and a high index of suspicion is needed for diagnosis. Therefore, we present two diagnostic algorithms, which according to our opinion may assist the evaluation of this complication and lead to early accurate diagnosis and appropriate management. Collectively, our findings support that although ERCP-induced splenic injury is an unexpected/unusual complication of ERCP, following the proper steps can be timely diagnosed and treated.
{"title":"Endoscopic retrograde cholangiopancreatography induced splenic injury: comprehensive analysis and new perspectives based on a case report.","authors":"Dimitrios S Kourdakis, Savvas P Deftereos","doi":"10.1177/26317745231223312","DOIUrl":"10.1177/26317745231223312","url":null,"abstract":"<p><p>Splenic injury is an extremely rare complication of endoscopic retrograde cholangiopancreatography (ERCP). There are only 34 cases reported in the literature up to now. Based on a case of a 72-year-old man, who after ERCP due to choledocholithiasis developed a large perisplenic and subcapsular hematoma, we carried out an extensive review of all cases of ERCP-induced splenic injury found in the literature. We searched PubMed/Medline and Google Scholar till 15 April 2023, for published case reports and series using the following terms: splenic injury after ERCP, ERCP-induced splenic injury, and post-ERCP splenic trauma. The case reports included were in English, Spanish, and German literature. We attempt to discuss the possible clinical image, the available diagnostic methods, the potential treatment alternatives, and predisposing factors related to this entity. Furthermore, a theory of a possible mechanism of this injury is discussed and supported schematically. The ERCP-induced splenic injury is rare and a high index of suspicion is needed for diagnosis. Therefore, we present two diagnostic algorithms, which according to our opinion may assist the evaluation of this complication and lead to early accurate diagnosis and appropriate management. Collectively, our findings support that although ERCP-induced splenic injury is an unexpected/unusual complication of ERCP, following the proper steps can be timely diagnosed and treated.</p>","PeriodicalId":40947,"journal":{"name":"Therapeutic Advances in Gastrointestinal Endoscopy","volume":"17 ","pages":"26317745231223312"},"PeriodicalIF":2.6,"publicationDate":"2024-01-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10787536/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139467216","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2023-12-25eCollection Date: 2023-01-01DOI: 10.1177/26317745231220477
Lakshman Ramu, Soo Kian-Tak, Gerald Ci-An Tay
A 72-year-old patient presented with malaena secondary to two antral ulcers which were discovered in oesophagogastroduodenoscopy (OGD) after admission. One of the ulcers with a visible vessel was injected with adrenaline and clipped with an OVESCO clip. The patient continued to have coffee ground vomitus on the following day with a drop in haemoglobin level. Repeat OGD showed a large intra-mural haematoma with the clip still in situ and no bleeding from the surface of the ulcer. Patient underwent a coil embolization of the distal gastroduodenal artery (GDA), right gastroepiploic artery and a medial branch of the GDA. Repeat OGD showed that the submucosal haematoma had evacuated, leaving a large, clean-based mucosal defect.
{"title":"An unusual complication after endoscopic clipping of a gastric ulcer.","authors":"Lakshman Ramu, Soo Kian-Tak, Gerald Ci-An Tay","doi":"10.1177/26317745231220477","DOIUrl":"10.1177/26317745231220477","url":null,"abstract":"<p><p>A 72-year-old patient presented with malaena secondary to two antral ulcers which were discovered in oesophagogastroduodenoscopy (OGD) after admission. One of the ulcers with a visible vessel was injected with adrenaline and clipped with an OVESCO clip. The patient continued to have coffee ground vomitus on the following day with a drop in haemoglobin level. Repeat OGD showed a large intra-mural haematoma with the clip still <i>in situ</i> and no bleeding from the surface of the ulcer. Patient underwent a coil embolization of the distal gastroduodenal artery (GDA), right gastroepiploic artery and a medial branch of the GDA. Repeat OGD showed that the submucosal haematoma had evacuated, leaving a large, clean-based mucosal defect.</p>","PeriodicalId":40947,"journal":{"name":"Therapeutic Advances in Gastrointestinal Endoscopy","volume":"16 ","pages":"26317745231220477"},"PeriodicalIF":2.6,"publicationDate":"2023-12-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10752134/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139049513","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2023-12-23eCollection Date: 2023-01-01DOI: 10.1177/26317745231219597
Maryam Hasanzarrini, Samira Nirumandi Jahromi, Amir Mohammad Salehi, Sara Ataei, Zohreh Seyfi, Jalal Poorolajal
Background: Digestive endoscopy (DE) is uncomfortable for most patients. Lorazepam is a potent benzodiazepine with anxiolytic and sedative effects.
Objective: This study aims to determine the sedative effect of sublingual lorazepam versus placebo as a premedication in patients who underwent DE.
Design: This is a mono-center, double-blind, and randomized controlled trial.
Methods: A lorazepam sublingual tablet was made by researchers and physical tests were done on it, then the double-blind placebo-controlled trial was done to investigate the efficacy of 2 mg sublingually administered lorazepam as a premedication for endoscopy. Lorazepam or a placebo tablet was administered sublingually 30 min before the endoscopy. The patients, nurses, and physicians were blinded to the patient group. The depth of sedation was evaluated according to the American Society of Anesthesiology.
Results: In all, 116 patients were randomly assigned to take either lorazepam (n = 58) or a placebo (n = 58). The results of physical properties tests were acceptable according to United States Pharmacopeia. There were no statistical differences between groups regarding age and gender. In the lorazepam group, 75.8% of patients showed mild sedation, and 24.2% of patients showed no sedation. All of the patients in the placebo had no sedation (p = 0.001). Time of procedure (p < 0.001), intraoperative O2 saturation (p < 0.001), intraoperative heart rate (p < 0.001), and intraoperative blood pressure (p < 0.001) were significantly lower in the lorazepam group. No significant or dangerous side effects were observed except a bit of giddiness and dizziness.
Conclusion: The results of this study showed that prescription of sublingual lorazepam 25-30 min before endoscopy provided mild sedation.
背景:消化内镜检查(DE)会让大多数患者感到不适。劳拉西泮是一种强效苯二氮卓类药物,具有抗焦虑和镇静作用:本研究旨在确定舌下含服劳拉西泮与安慰剂作为消化内镜检查前用药对患者的镇静效果:设计:这是一项单中心、双盲、随机对照试验:研究人员制作了一种劳拉西泮舌下含片,并对其进行了物理测试,然后进行了双盲安慰剂对照试验,以研究2毫克劳拉西泮舌下含片作为内窥镜检查前用药的疗效。内窥镜检查前 30 分钟,舌下含服劳拉西泮或安慰剂片剂。患者、护士和医生均为盲人。镇静深度根据美国麻醉学会的标准进行评估:共有 116 名患者被随机分配服用劳拉西泮(58 人)或安慰剂(58 人)。物理性质测试结果符合美国药典标准。各组在年龄和性别方面没有统计学差异。在劳拉西泮组中,75.8% 的患者表现出轻度镇静,24.2% 的患者没有镇静。安慰剂组的所有患者均无镇静作用(p = 0.001)。手术时间(p 2 饱和度(p p p 结论:本研究结果表明,在内窥镜检查前 25-30 分钟舌下含服氯羟安定可提供轻度镇静:IRCT201611039014N130 (05/11/2016); https://en.irct.ir/trial/9568.
{"title":"Evaluation of the sedative effect of sublingual lorazepam <i>versus</i> placebo in patients underwent endoscopy: a double-blind, randomized controlled clinical trial.","authors":"Maryam Hasanzarrini, Samira Nirumandi Jahromi, Amir Mohammad Salehi, Sara Ataei, Zohreh Seyfi, Jalal Poorolajal","doi":"10.1177/26317745231219597","DOIUrl":"https://doi.org/10.1177/26317745231219597","url":null,"abstract":"<p><strong>Background: </strong>Digestive endoscopy (DE) is uncomfortable for most patients. Lorazepam is a potent benzodiazepine with anxiolytic and sedative effects.</p><p><strong>Objective: </strong>This study aims to determine the sedative effect of sublingual lorazepam <i>versus</i> placebo as a premedication in patients who underwent DE.</p><p><strong>Design: </strong>This is a mono-center, double-blind, and randomized controlled trial.</p><p><strong>Methods: </strong>A lorazepam sublingual tablet was made by researchers and physical tests were done on it, then the double-blind placebo-controlled trial was done to investigate the efficacy of 2 mg sublingually administered lorazepam as a premedication for endoscopy. Lorazepam or a placebo tablet was administered sublingually 30 min before the endoscopy. The patients, nurses, and physicians were blinded to the patient group. The depth of sedation was evaluated according to the American Society of Anesthesiology.</p><p><strong>Results: </strong>In all, 116 patients were randomly assigned to take either lorazepam (<i>n</i> = 58) or a placebo (<i>n</i> = 58). The results of physical properties tests were acceptable according to United States Pharmacopeia. There were no statistical differences between groups regarding age and gender. In the lorazepam group, 75.8% of patients showed mild sedation, and 24.2% of patients showed no sedation. All of the patients in the placebo had no sedation (<i>p</i> = 0.001). Time of procedure (<i>p</i> < 0.001), intraoperative O<sub>2</sub> saturation (<i>p</i> < 0.001), intraoperative heart rate (<i>p</i> < 0.001), and intraoperative blood pressure (<i>p</i> < 0.001) were significantly lower in the lorazepam group. No significant or dangerous side effects were observed except a bit of giddiness and dizziness.</p><p><strong>Conclusion: </strong>The results of this study showed that prescription of sublingual lorazepam 25-30 min before endoscopy provided mild sedation.</p><p><strong>Registration: </strong>IRCT201611039014N130 (05/11/2016); https://en.irct.ir/trial/9568.</p>","PeriodicalId":40947,"journal":{"name":"Therapeutic Advances in Gastrointestinal Endoscopy","volume":"16 ","pages":"26317745231219597"},"PeriodicalIF":2.6,"publicationDate":"2023-12-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10748895/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139032679","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2023-11-21eCollection Date: 2023-01-01DOI: 10.1177/26317745231210120
Daniel B Maselli, Anna C Hoff, Ashley Kucera, Areebah Waseem, Chase Wooley, Lauren L Donnangelo, Brian Coan, Christopher E McGowan
Weight recurrence after one-anastomosis gastric bypass (OAGB), the third most common metabolic and bariatric surgery performed worldwide, is observed in a subset of patients due to the chronic, progressive nature of obesity. Endoscopic revision of the OAGB (ER-OAGB) through full-thickness suturing to reduce the gastrojejunal anastomosis and gastric pouch is a potential alternative to surgical revision. Here, we present a case series of ER-OAGB and long-term nutritional support at two international centers with expertise in bariatric endoscopy. Data were retrospectively evaluated from a prospectively maintained database. The primary outcome was total body weight loss (TBWL) at 12 months. Secondary outcomes included TBWL at 3, 6, and 15 months; excess weight loss (EWL) at 3, 6, 12, and 15 months; frequency of new/worsening symptoms of gastroesophageal reflux disease (GERD); and the frequency of serious adverse events. In this series, 17 adults (70.6% female, mean age 46.8 years, mean BMI 39.1 kg/m2) successfully underwent ER-OAGB an average of 8 years (range 2-21 years) after OAGB for a mean weight recurrence of 43.2% (range 10.9-86.9%). TBWL from ER-OAGB was 9.7 ± 1.8% at 3 months, 13.4 ± 3.5% at 6 months, 18.5 ± 2.1% at 12 months, and 18.1 ± 2.2% at 15 months. EWL from ER-OAGB was 30.5 ± 14.7% at 3 months, 42.6 ± 16.2% at 6 months, 54.2 ± 11.3% at 12 months, and 54.2 ± 11.7% at 15 months. There were no instances of new/worsening GERD symptoms or serious adverse events. In this small series of adults who experienced weight recurrence after OAGB, ER-OAGB facilitated safe and clinically meaningful weight loss, without new or worsening GERD symptoms, when performed by experienced bariatric endoscopists in concert with longitudinal nutritional support.
{"title":"Endoscopic revision of one-anastomosis gastric bypass (ER-OAGB) for weight recurrence: a case series of 17 adults.","authors":"Daniel B Maselli, Anna C Hoff, Ashley Kucera, Areebah Waseem, Chase Wooley, Lauren L Donnangelo, Brian Coan, Christopher E McGowan","doi":"10.1177/26317745231210120","DOIUrl":"https://doi.org/10.1177/26317745231210120","url":null,"abstract":"<p><p>Weight recurrence after one-anastomosis gastric bypass (OAGB), the third most common metabolic and bariatric surgery performed worldwide, is observed in a subset of patients due to the chronic, progressive nature of obesity. Endoscopic revision of the OAGB (ER-OAGB) through full-thickness suturing to reduce the gastrojejunal anastomosis and gastric pouch is a potential alternative to surgical revision. Here, we present a case series of ER-OAGB and long-term nutritional support at two international centers with expertise in bariatric endoscopy. Data were retrospectively evaluated from a prospectively maintained database. The primary outcome was total body weight loss (TBWL) at 12 months. Secondary outcomes included TBWL at 3, 6, and 15 months; excess weight loss (EWL) at 3, 6, 12, and 15 months; frequency of new/worsening symptoms of gastroesophageal reflux disease (GERD); and the frequency of serious adverse events. In this series, 17 adults (70.6% female, mean age 46.8 years, mean BMI 39.1 kg/m<sup>2</sup>) successfully underwent ER-OAGB an average of 8 years (range 2-21 years) after OAGB for a mean weight recurrence of 43.2% (range 10.9-86.9%). TBWL from ER-OAGB was 9.7 ± 1.8% at 3 months, 13.4 ± 3.5% at 6 months, 18.5 ± 2.1% at 12 months, and 18.1 ± 2.2% at 15 months. EWL from ER-OAGB was 30.5 ± 14.7% at 3 months, 42.6 ± 16.2% at 6 months, 54.2 ± 11.3% at 12 months, and 54.2 ± 11.7% at 15 months. There were no instances of new/worsening GERD symptoms or serious adverse events. In this small series of adults who experienced weight recurrence after OAGB, ER-OAGB facilitated safe and clinically meaningful weight loss, without new or worsening GERD symptoms, when performed by experienced bariatric endoscopists in concert with longitudinal nutritional support.</p>","PeriodicalId":40947,"journal":{"name":"Therapeutic Advances in Gastrointestinal Endoscopy","volume":"16 ","pages":"26317745231210120"},"PeriodicalIF":2.6,"publicationDate":"2023-11-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10666552/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"138463288","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}