Pub Date : 2026-02-01Epub Date: 2025-12-08DOI: 10.1002/ueg2.70015
Zlata Chkolnaia, Benedicte Lebrun-Vignes, Aurelien Amiot, Mathieu Uzzan, Nicolas Richard, Maeva Charkaoui, Guillaume Le Cosquer, Carmen Stefanescu, Melanie Serrero, Laurianne Plastaras, Sophie Vieujean, David Laharie, Philippe Seksik
Background: While tumor necrosis factor (TNF) inhibitors can induce paradoxical reactions, sarcoidosis-like disease has hardly been reported so far. This study aimed to describe the epidemiological, diagnostic and therapeutic features of TNF inhibitor-induced sarcoidosis-like lesions in patients with inflammatory bowel disease.
Methods: We conducted a case series across 59 institutions affiliated with the Groupe d'Etude Therapeutique des Affections Inflammatoires du Tube Digestif. Diagnosis of TNF inhibitor-induced sarcoidosis was based on typical clinical and radiological signs, histological evidence of non-necrotizing granuloma, exclusion of alternative diagnoses, and a timeline consistent with drug exposure. A pharmacovigilance expert reviewed each case to confirm drug causality.
Results: We identified 14 cases of sarcoidosis-like lesions, including 9 patients with Crohn's disease, 4 ulcerative colitis, and 1 with unclassified inflammatory bowel disease. The implicated medications were infliximab (8), adalimumab (5), and golimumab (1), predominantly in first-time biotherapy users (71%). The median time from treatment initiation to sarcoidosis diagnosis was 27.5 months (range 3-91). Common clinical manifestations included dyspnea (71%), coughing (50%) and fever (50%). Ten patients discontinued TNF inhibitor therapy and started oral steroids, leading to complete symptom resolution in seven cases and improvement in two. Median time from steroid initiation to clinical remission of sarcoidosis was 84 days (range 11-134). After a median follow-up of 40 months, while no relapses occurred in 13 patients, one showed persistent sarcoidosis activity.
Conclusions: TNF inhibitor-induced sarcoidosis should be considered in inflammatory bowel disease patients with chronic respiratory symptoms or fever after exclusion of mycobacterial infection. Management involves discontinuation of TNF inhibitors and a course of steroids.
{"title":"TNF Inhibitor-Induced Sarcoidosis-Like Lesions in Inflammatory Bowel Disease.","authors":"Zlata Chkolnaia, Benedicte Lebrun-Vignes, Aurelien Amiot, Mathieu Uzzan, Nicolas Richard, Maeva Charkaoui, Guillaume Le Cosquer, Carmen Stefanescu, Melanie Serrero, Laurianne Plastaras, Sophie Vieujean, David Laharie, Philippe Seksik","doi":"10.1002/ueg2.70015","DOIUrl":"10.1002/ueg2.70015","url":null,"abstract":"<p><strong>Background: </strong>While tumor necrosis factor (TNF) inhibitors can induce paradoxical reactions, sarcoidosis-like disease has hardly been reported so far. This study aimed to describe the epidemiological, diagnostic and therapeutic features of TNF inhibitor-induced sarcoidosis-like lesions in patients with inflammatory bowel disease.</p><p><strong>Methods: </strong>We conducted a case series across 59 institutions affiliated with the Groupe d'Etude Therapeutique des Affections Inflammatoires du Tube Digestif. Diagnosis of TNF inhibitor-induced sarcoidosis was based on typical clinical and radiological signs, histological evidence of non-necrotizing granuloma, exclusion of alternative diagnoses, and a timeline consistent with drug exposure. A pharmacovigilance expert reviewed each case to confirm drug causality.</p><p><strong>Results: </strong>We identified 14 cases of sarcoidosis-like lesions, including 9 patients with Crohn's disease, 4 ulcerative colitis, and 1 with unclassified inflammatory bowel disease. The implicated medications were infliximab (8), adalimumab (5), and golimumab (1), predominantly in first-time biotherapy users (71%). The median time from treatment initiation to sarcoidosis diagnosis was 27.5 months (range 3-91). Common clinical manifestations included dyspnea (71%), coughing (50%) and fever (50%). Ten patients discontinued TNF inhibitor therapy and started oral steroids, leading to complete symptom resolution in seven cases and improvement in two. Median time from steroid initiation to clinical remission of sarcoidosis was 84 days (range 11-134). After a median follow-up of 40 months, while no relapses occurred in 13 patients, one showed persistent sarcoidosis activity.</p><p><strong>Conclusions: </strong>TNF inhibitor-induced sarcoidosis should be considered in inflammatory bowel disease patients with chronic respiratory symptoms or fever after exclusion of mycobacterial infection. Management involves discontinuation of TNF inhibitors and a course of steroids.</p>","PeriodicalId":23444,"journal":{"name":"United European Gastroenterology Journal","volume":" ","pages":"e70015"},"PeriodicalIF":6.7,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12802563/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145701648","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Iuliana Nenu, Sara Nikolic, Eduardo Valdivielso, Giovanni Marasco
{"title":"Best of United European Gastroenterology Week 2025.","authors":"Iuliana Nenu, Sara Nikolic, Eduardo Valdivielso, Giovanni Marasco","doi":"10.1002/ueg2.70171","DOIUrl":"10.1002/ueg2.70171","url":null,"abstract":"","PeriodicalId":23444,"journal":{"name":"United European Gastroenterology Journal","volume":"14 1","pages":"e70171"},"PeriodicalIF":6.7,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12849201/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146067159","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-02-01Epub Date: 2025-12-06DOI: 10.1002/ueg2.70150
Míriam Mañosa, Margalida Calafat, Elena Ricart, Pilar Nos, Eva Iglesias, Sabino Riestra, Francisco Mesonero, Marta Calvo, Jordi Guardiola, Vicent Hernández, Montserrat Rivero, Daniel Carpio, Miguel Mínguez, Cristina Alba, Maria Dolores Martín-Arranz, Milagros Vela, Fernando Gomollón, Santiago García-López, Ana Gutiérrez Casbas, Xavier Calvet, Carlos González-Muñoza, Jesús Barrio, Javier P Gisbert, Beatriz Sicilia, José Lázaro Pérez-Calle, Luis Bujanda, Maria Esteve, Laura Ramos, Pilar Varela, Mónica Sierra, Olga Merino, Fernando Bermejo, Manuel Barreiro-de Acosta, Antonio Rodríguez Perez, Lucía Márquez-Mosquera, Orlando García-Bosch, Iago Rodríguez-Lago, Rufo H Lorente Poyatos, Mariana Fe García Sepulcre, Nuria Maroto, Pablo Vega, David Monfort, Lucía Zabalsa San Martín, David Busquets, Pilar Martinez-Montiel, Joan Riera, Guillermo Alcain, Jordina Llaó, Nacho Marin, Ignacio Marin-Jimenez, Eva Sesé, Manuel Van Domselaar, José M Huguet, Daniel Ginard, Francesc Bas-Cutrina, Yolanda Ber, Oscar Roncero, Alfredo J Lucendo, Alicia López-García, Margarita Menacho, Pedro Almela, Ángel Ponferrada, Ana Fuentes Coronel, Sergio Maestro, Teresa de Jesús Martínez-Pérez, Carmen Muñoz Vilafranca, Federico Argüelles, Jesús Legido, Pau Gilabert, Mara Charro, Ana M Trapero, Hipólito Fernández, Santiago Frago, Luis Hernández Villalba, Esther Muñoz, Eugeni Domènech
Background: Limited data are available on the management and outcomes of postoperative Crohn's disease (CD) in older patients. We aimed to describe the management of CD in the postoperative setting and assess surgical postoperative recurrence (POR) in this population.
Methods: This was a case-control study including all adult patients with CD from the ENEIDA registry who had undergone a first intestinal resection with ileo-colonic anastomosis. Patients were grouped according to their age at the time of the first surgery in older (over 60 years) subjects and controls (between 18 and 60 years of age).
Results: A total of 3982 (535 older subjects and 3454 controls) underwent a first intestinal resection for CD with an ileo-colonic anastomosis. Time from CD diagnosis to surgery was significantly longer in older patients (114 ± 128 vs. 93 ± 97 months; p < 0.001). Older patients also had a lower proportion of penetrating CD (25% vs. 39%; p < 0.0001) and perianal disease (14% vs. 25%; p < 0.0001). A significantly lower proportion of older patients started preventive therapies for POR (32% vs. 51%; p < 0.0001). The cumulative risk of surgical POR was 3.2%, 5.3% and 10.1% in the older group and 3.6%, 6.6% and 14.2% in the control group at three, five and 10 years, respectively (p = 0.093). In the multivariate logistic regression analysis, only prevention with thiopurines was associated with a lower risk of surgical POR.
Conclusions: Although postoperative preventive therapy with immunomodulators or biologicals is prescribed less often in older patients after a first intestinal resection, they develop surgical POR as often as younger adult patients.
{"title":"Comparative Study on the Management and Outcomes of Postoperative Crohn's Disease in Older Patients: Data From the ENEIDA Registry.","authors":"Míriam Mañosa, Margalida Calafat, Elena Ricart, Pilar Nos, Eva Iglesias, Sabino Riestra, Francisco Mesonero, Marta Calvo, Jordi Guardiola, Vicent Hernández, Montserrat Rivero, Daniel Carpio, Miguel Mínguez, Cristina Alba, Maria Dolores Martín-Arranz, Milagros Vela, Fernando Gomollón, Santiago García-López, Ana Gutiérrez Casbas, Xavier Calvet, Carlos González-Muñoza, Jesús Barrio, Javier P Gisbert, Beatriz Sicilia, José Lázaro Pérez-Calle, Luis Bujanda, Maria Esteve, Laura Ramos, Pilar Varela, Mónica Sierra, Olga Merino, Fernando Bermejo, Manuel Barreiro-de Acosta, Antonio Rodríguez Perez, Lucía Márquez-Mosquera, Orlando García-Bosch, Iago Rodríguez-Lago, Rufo H Lorente Poyatos, Mariana Fe García Sepulcre, Nuria Maroto, Pablo Vega, David Monfort, Lucía Zabalsa San Martín, David Busquets, Pilar Martinez-Montiel, Joan Riera, Guillermo Alcain, Jordina Llaó, Nacho Marin, Ignacio Marin-Jimenez, Eva Sesé, Manuel Van Domselaar, José M Huguet, Daniel Ginard, Francesc Bas-Cutrina, Yolanda Ber, Oscar Roncero, Alfredo J Lucendo, Alicia López-García, Margarita Menacho, Pedro Almela, Ángel Ponferrada, Ana Fuentes Coronel, Sergio Maestro, Teresa de Jesús Martínez-Pérez, Carmen Muñoz Vilafranca, Federico Argüelles, Jesús Legido, Pau Gilabert, Mara Charro, Ana M Trapero, Hipólito Fernández, Santiago Frago, Luis Hernández Villalba, Esther Muñoz, Eugeni Domènech","doi":"10.1002/ueg2.70150","DOIUrl":"10.1002/ueg2.70150","url":null,"abstract":"<p><strong>Background: </strong>Limited data are available on the management and outcomes of postoperative Crohn's disease (CD) in older patients. We aimed to describe the management of CD in the postoperative setting and assess surgical postoperative recurrence (POR) in this population.</p><p><strong>Methods: </strong>This was a case-control study including all adult patients with CD from the ENEIDA registry who had undergone a first intestinal resection with ileo-colonic anastomosis. Patients were grouped according to their age at the time of the first surgery in older (over 60 years) subjects and controls (between 18 and 60 years of age).</p><p><strong>Results: </strong>A total of 3982 (535 older subjects and 3454 controls) underwent a first intestinal resection for CD with an ileo-colonic anastomosis. Time from CD diagnosis to surgery was significantly longer in older patients (114 ± 128 vs. 93 ± 97 months; p < 0.001). Older patients also had a lower proportion of penetrating CD (25% vs. 39%; p < 0.0001) and perianal disease (14% vs. 25%; p < 0.0001). A significantly lower proportion of older patients started preventive therapies for POR (32% vs. 51%; p < 0.0001). The cumulative risk of surgical POR was 3.2%, 5.3% and 10.1% in the older group and 3.6%, 6.6% and 14.2% in the control group at three, five and 10 years, respectively (p = 0.093). In the multivariate logistic regression analysis, only prevention with thiopurines was associated with a lower risk of surgical POR.</p><p><strong>Conclusions: </strong>Although postoperative preventive therapy with immunomodulators or biologicals is prescribed less often in older patients after a first intestinal resection, they develop surgical POR as often as younger adult patients.</p>","PeriodicalId":23444,"journal":{"name":"United European Gastroenterology Journal","volume":" ","pages":""},"PeriodicalIF":6.7,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12781282/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145688476","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-02-01Epub Date: 2025-11-29DOI: 10.1002/ueg2.70153
Cihan Yurdaydin, Julia Kahlhöfer, Florin Alexandru Caruntu, Kendal Yalcin, Selim Gürel, Ulus S Akarca, Kathrin Sprinzl, Hans H Bock, Jan-Hendrik Bockmann, George V Papatheodoridis, Uta Merle, Münevver Demir, Svenja Hardtke, Onur Keskin, Ramazan Idilman, Markus Cornberg, Heiner Wedemeyer, Anika Wranke
Background: Chronic delta hepatitis represents a major health burden. Until recently, pegylated interferon-alfa-2a (PEG-IFNα) therapy was the only treatment option for patients infected with hepatitis D virus (HDV). The aim of this study was to evaluate 10-year long-term clinical and virological outcomes after 96 weeks of treatment with PEG-IFNα with or without tenofovir disoproxil fumarate (TDF).
Methods: We conducted a retrospective follow-up study of the Hep-Net-International-Delta-Hepatitis-Intervention-Study 2 (HIDIT-II trial). Patients had received 96 weeks of treatment with either PEG-IFNα-2a plus TDF or PEG-IFNα-2a alone. Patients were included if they had completed the 96-week treatment period and had at least one follow-up visit (PEG-IFNα-2a + TDF; n = 51, PEG-IFNα-2a alone; n = 56).
Results: Patients who received PEG-IFNα-2a + TDF were younger (37 vs. 42 years) and no significant differences were observed in other baseline characteristics between the two treatment arms. A total of 26 patients (24%) developed one or more liver-related endpoints after a mean time of 8.4 years. The incidence of endpoints was significantly lower in the combination group (14% vs. 34%, p = 0.02). The development of liver-related endpoints was also associated with non-response to therapy (HDV RNA and HBsAg), elevated HBV DNA at week 72, and baseline age, cirrhosis, platelets, INR, AST, GGT, bilirubin and albumin according to the Cox regression model.
Conclusions: The long-term follow-up of this large randomised clinical trial demonstrates that combination therapy with TDF and virological response to PEG-IFNα-2a (undetectable HDV RNA and HBsAg loss) were associated with better clinical outcomes.
背景:慢性丁型肝炎是一种主要的健康负担。直到最近,聚乙二醇化干扰素- α -2a (PEG-IFNα)治疗是感染丁型肝炎病毒(HDV)患者的唯一治疗选择。本研究的目的是评估PEG-IFNα联合或不联合富马酸替诺福韦二氧吡酯(TDF)治疗96周后的10年长期临床和病毒学结果。方法:我们对Hep-Net-International-Delta-Hepatitis-Intervention-Study 2 (HIDIT-II试验)进行了回顾性随访研究。患者接受了96周的PEG-IFNα-2a联合TDF或PEG-IFNα-2a单独治疗。如果患者完成96周的治疗期,并且至少进行了一次随访(PEG-IFNα-2a + TDF, n = 51,单独使用PEG-IFNα-2a, n = 56),则纳入研究。结果:接受PEG-IFNα-2a + TDF治疗的患者更年轻(37岁vs 42岁),两个治疗组的其他基线特征无显著差异。共有26名患者(24%)在平均8.4年的时间后出现了一个或多个肝脏相关终点。联合治疗组终点发生率显著降低(14% vs. 34%, p = 0.02)。根据Cox回归模型,肝脏相关终点的发展也与治疗无反应(HDV RNA和HBsAg)、第72周HBV DNA升高、基线年龄、肝硬化、血小板、INR、AST、GGT、胆红素和白蛋白相关。结论:这项大型随机临床试验的长期随访表明,TDF联合治疗和PEG-IFNα-2a的病毒学反应(无法检测到HDV RNA和HBsAg丢失)与更好的临床结果相关。试验注册:NCT00932971, edract 2008-005560-13。
{"title":"Ten-Year Follow-Up After 96 Weeks Treatment With Peginterferon Plus Tenofovir in Hepatitis D (HIDIT-II): Improved Clinical Outcome After Combination Therapy.","authors":"Cihan Yurdaydin, Julia Kahlhöfer, Florin Alexandru Caruntu, Kendal Yalcin, Selim Gürel, Ulus S Akarca, Kathrin Sprinzl, Hans H Bock, Jan-Hendrik Bockmann, George V Papatheodoridis, Uta Merle, Münevver Demir, Svenja Hardtke, Onur Keskin, Ramazan Idilman, Markus Cornberg, Heiner Wedemeyer, Anika Wranke","doi":"10.1002/ueg2.70153","DOIUrl":"10.1002/ueg2.70153","url":null,"abstract":"<p><strong>Background: </strong>Chronic delta hepatitis represents a major health burden. Until recently, pegylated interferon-alfa-2a (PEG-IFNα) therapy was the only treatment option for patients infected with hepatitis D virus (HDV). The aim of this study was to evaluate 10-year long-term clinical and virological outcomes after 96 weeks of treatment with PEG-IFNα with or without tenofovir disoproxil fumarate (TDF).</p><p><strong>Methods: </strong>We conducted a retrospective follow-up study of the Hep-Net-International-Delta-Hepatitis-Intervention-Study 2 (HIDIT-II trial). Patients had received 96 weeks of treatment with either PEG-IFNα-2a plus TDF or PEG-IFNα-2a alone. Patients were included if they had completed the 96-week treatment period and had at least one follow-up visit (PEG-IFNα-2a + TDF; n = 51, PEG-IFNα-2a alone; n = 56).</p><p><strong>Results: </strong>Patients who received PEG-IFNα-2a + TDF were younger (37 vs. 42 years) and no significant differences were observed in other baseline characteristics between the two treatment arms. A total of 26 patients (24%) developed one or more liver-related endpoints after a mean time of 8.4 years. The incidence of endpoints was significantly lower in the combination group (14% vs. 34%, p = 0.02). The development of liver-related endpoints was also associated with non-response to therapy (HDV RNA and HBsAg), elevated HBV DNA at week 72, and baseline age, cirrhosis, platelets, INR, AST, GGT, bilirubin and albumin according to the Cox regression model.</p><p><strong>Conclusions: </strong>The long-term follow-up of this large randomised clinical trial demonstrates that combination therapy with TDF and virological response to PEG-IFNα-2a (undetectable HDV RNA and HBsAg loss) were associated with better clinical outcomes.</p><p><strong>Trial registration: </strong>NCT00932971, EudraCT 2008-005560-13.</p>","PeriodicalId":23444,"journal":{"name":"United European Gastroenterology Journal","volume":" ","pages":"e70153"},"PeriodicalIF":6.7,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12799903/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145640128","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-02-01Epub Date: 2025-12-05DOI: 10.1002/ueg2.70149
Katharina Zimmermann, Iago Rodríguez-Lago, Reena Sidhu, Henriette Heinrich, Paula Sousa, Egle Dieninyte, Marjolijn Duijvestein, Alexander Hann, Manik Gemilyan, Helge Knüttel, Andrea Nowak, Paolo Montalto, Mohamed G Shiha, Petra Krčálová, Petr Vanek, Vita Skuja, Martin Duricek, Francesca Manza, John Ong, Dina Tiniakos, Neeraj Bhala, Martina Müller
United European Gastroenterology (UEG) has launched an initiative to promote physician well-being and prevent burnout. This current concept article is based on a survey of the National Societies Forum and National Societies Committee, a meta-analysis by Shiha et al., and a scoping review of evidence-based interventions. It identifies key systemic and individual drivers of burnout, outlines its consequences, and presents strategies for intervention-recognising that physician burnout threatens individual health, patient safety, and the sustainability of health care systems. Burnout in gastroenterology is driven by demanding workloads, complex procedures, and increasing administrative tasks. Addressing physician well-being must be viewed as a systemic challenge requiring coordinated efforts from individuals, hospitals, and scientific societies. National and specialist GI societies are pivotal. They must implement initiatives and advocate for systemic change through education, policy advocacy, and sustainable work design. Acknowledgement of burnout is a start. Progress requires commitment to well-being and continuing research.
{"title":"Promoting Well-Being Among Gastroenterologists - A Call for Systemic Action.","authors":"Katharina Zimmermann, Iago Rodríguez-Lago, Reena Sidhu, Henriette Heinrich, Paula Sousa, Egle Dieninyte, Marjolijn Duijvestein, Alexander Hann, Manik Gemilyan, Helge Knüttel, Andrea Nowak, Paolo Montalto, Mohamed G Shiha, Petra Krčálová, Petr Vanek, Vita Skuja, Martin Duricek, Francesca Manza, John Ong, Dina Tiniakos, Neeraj Bhala, Martina Müller","doi":"10.1002/ueg2.70149","DOIUrl":"10.1002/ueg2.70149","url":null,"abstract":"<p><p>United European Gastroenterology (UEG) has launched an initiative to promote physician well-being and prevent burnout. This current concept article is based on a survey of the National Societies Forum and National Societies Committee, a meta-analysis by Shiha et al., and a scoping review of evidence-based interventions. It identifies key systemic and individual drivers of burnout, outlines its consequences, and presents strategies for intervention-recognising that physician burnout threatens individual health, patient safety, and the sustainability of health care systems. Burnout in gastroenterology is driven by demanding workloads, complex procedures, and increasing administrative tasks. Addressing physician well-being must be viewed as a systemic challenge requiring coordinated efforts from individuals, hospitals, and scientific societies. National and specialist GI societies are pivotal. They must implement initiatives and advocate for systemic change through education, policy advocacy, and sustainable work design. Acknowledgement of burnout is a start. Progress requires commitment to well-being and continuing research.</p>","PeriodicalId":23444,"journal":{"name":"United European Gastroenterology Journal","volume":" ","pages":"e70149"},"PeriodicalIF":6.7,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12799596/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145678962","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-02-01Epub Date: 2025-12-09DOI: 10.1002/ueg2.70151
Benedikt Kaufmann, André Mihaljevic
{"title":"From Guideline to Clinical Practice: Towards an Era Without Surgical Site Infections.","authors":"Benedikt Kaufmann, André Mihaljevic","doi":"10.1002/ueg2.70151","DOIUrl":"10.1002/ueg2.70151","url":null,"abstract":"","PeriodicalId":23444,"journal":{"name":"United European Gastroenterology Journal","volume":" ","pages":"e70151"},"PeriodicalIF":6.7,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12799901/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145716065","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-02-01Epub Date: 2025-12-15DOI: 10.1002/ueg2.70146
Hayder Alqaisi, Anders Dige, Ole Thorlacius-Ussing, Lilli Lundby
Background: Ileal pouch-anal anastomosis (IPAA) is a standard surgical procedure for ulcerative colitis (UC) and familial adenomatous polyposis. However, pouch-related fistulae (PRF) are a significant complication. There is no consensus on the optimal treatment for PRF.
Objective: This study evaluated the effectiveness of autologous adipose tissue injection (AATI) as a treatment for PRF.
Methods: Twenty-one patients with IPAA and a total of 29 PRF were treated with AATI. Patients who did not achieve healing after the first treatment were offered repeated injections. Patients were followed for a median of 16 months after AATI. Outcomes including clinical healing, treatment complications, and recurrence of PRF were registered.
Results: After a single treatment with AATI, 48% of the fistulae were clinically healed. Repeated treatments increased the healing rate to 69%. An additional 14% responded to AATI by reduced secretion from PRF. The procedure was well tolerated with minimal complications.
Conclusion: AATI appears to be a safe, minimally invasive, and sphincter-saving treatment for PRF with promising healing rates. Further studies with larger cohorts are necessary to validate these findings.
{"title":"Autologous Adipose Tissue Injection as Treatment for Ileoanal Pouch-Related Fistulae.","authors":"Hayder Alqaisi, Anders Dige, Ole Thorlacius-Ussing, Lilli Lundby","doi":"10.1002/ueg2.70146","DOIUrl":"10.1002/ueg2.70146","url":null,"abstract":"<p><strong>Background: </strong>Ileal pouch-anal anastomosis (IPAA) is a standard surgical procedure for ulcerative colitis (UC) and familial adenomatous polyposis. However, pouch-related fistulae (PRF) are a significant complication. There is no consensus on the optimal treatment for PRF.</p><p><strong>Objective: </strong>This study evaluated the effectiveness of autologous adipose tissue injection (AATI) as a treatment for PRF.</p><p><strong>Methods: </strong>Twenty-one patients with IPAA and a total of 29 PRF were treated with AATI. Patients who did not achieve healing after the first treatment were offered repeated injections. Patients were followed for a median of 16 months after AATI. Outcomes including clinical healing, treatment complications, and recurrence of PRF were registered.</p><p><strong>Results: </strong>After a single treatment with AATI, 48% of the fistulae were clinically healed. Repeated treatments increased the healing rate to 69%. An additional 14% responded to AATI by reduced secretion from PRF. The procedure was well tolerated with minimal complications.</p><p><strong>Conclusion: </strong>AATI appears to be a safe, minimally invasive, and sphincter-saving treatment for PRF with promising healing rates. Further studies with larger cohorts are necessary to validate these findings.</p>","PeriodicalId":23444,"journal":{"name":"United European Gastroenterology Journal","volume":" ","pages":"e70146"},"PeriodicalIF":6.7,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12803014/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145764309","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Tom van Gils, Ryo Katsumata, Jóhann P Hreinsson, Douglas A Drossman, Jan Tack, Hans Törnblom, Boris Le Nevé, Laurent Quinquis, Rim Hassouna, Max J Schmulson, Shrikant I Bangdiwala, Olafur S Palsson, Magnus Simrén
Background: Bloating refers to the sensation of tension in the abdomen, reported in the presence or absence of visible abdominal distension. These and other gas-related symptoms are often reported by patients with irritable bowel syndrome (IBS) and functional dyspepsia (FD). However, the prevalence of bloating and visible abdominal distension as separate symptoms in these disorders is not well known. The aim of this study was to investigate the link between bloating, distension, and intestinal gas-related symptoms with IBS and FD, and their overall impact.
Methods: Data from a population-based internet survey of adults from the US, UK, and Mexico were used. This survey included Rome IV diagnostic questions for IBS and FD, questions to distinguish between ≥ weekly bloating and/or distension, and the Intestinal Gas Questionnaire (IGQ) to assess the impact of six gas-related symptoms.
Results: The analyses included 131 individuals with only IBS, 360 with only FD, 217 with IBS + FD and 4740 without IBS and FD (reference group). Individuals with IBS (64.9%), FD (50.6%), and especially IBS + FD (88.5%) reported bloating and/or distension more frequently than the reference group (13.7%). Bloating and distension as distinct and combined symptoms were strongly linked to IBS and FD even after correcting for confounding factors. Also, other gas-related symptoms had a higher impact on individuals with IBS and/or FD compared with the reference group.
Discussion: Bloating and visible abdominal distension can occur as concomitant or distinct impactful symptoms and are, together with other gas-related symptoms, strongly linked to IBS and FD. These findings may provide arguments to include bloating and distension as supportive criteria for IBS and FD diagnoses.
{"title":"Bloating, Visible Abdominal Distension, and Other Intestinal Gas-Related Symptoms in Irritable Bowel Syndrome and Functional Dyspepsia.","authors":"Tom van Gils, Ryo Katsumata, Jóhann P Hreinsson, Douglas A Drossman, Jan Tack, Hans Törnblom, Boris Le Nevé, Laurent Quinquis, Rim Hassouna, Max J Schmulson, Shrikant I Bangdiwala, Olafur S Palsson, Magnus Simrén","doi":"10.1002/ueg2.70186","DOIUrl":"10.1002/ueg2.70186","url":null,"abstract":"<p><strong>Background: </strong>Bloating refers to the sensation of tension in the abdomen, reported in the presence or absence of visible abdominal distension. These and other gas-related symptoms are often reported by patients with irritable bowel syndrome (IBS) and functional dyspepsia (FD). However, the prevalence of bloating and visible abdominal distension as separate symptoms in these disorders is not well known. The aim of this study was to investigate the link between bloating, distension, and intestinal gas-related symptoms with IBS and FD, and their overall impact.</p><p><strong>Methods: </strong>Data from a population-based internet survey of adults from the US, UK, and Mexico were used. This survey included Rome IV diagnostic questions for IBS and FD, questions to distinguish between ≥ weekly bloating and/or distension, and the Intestinal Gas Questionnaire (IGQ) to assess the impact of six gas-related symptoms.</p><p><strong>Results: </strong>The analyses included 131 individuals with only IBS, 360 with only FD, 217 with IBS + FD and 4740 without IBS and FD (reference group). Individuals with IBS (64.9%), FD (50.6%), and especially IBS + FD (88.5%) reported bloating and/or distension more frequently than the reference group (13.7%). Bloating and distension as distinct and combined symptoms were strongly linked to IBS and FD even after correcting for confounding factors. Also, other gas-related symptoms had a higher impact on individuals with IBS and/or FD compared with the reference group.</p><p><strong>Discussion: </strong>Bloating and visible abdominal distension can occur as concomitant or distinct impactful symptoms and are, together with other gas-related symptoms, strongly linked to IBS and FD. These findings may provide arguments to include bloating and distension as supportive criteria for IBS and FD diagnoses.</p>","PeriodicalId":23444,"journal":{"name":"United European Gastroenterology Journal","volume":"14 1","pages":"e70186"},"PeriodicalIF":6.7,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12904287/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146195766","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-02-01Epub Date: 2025-12-17DOI: 10.1002/ueg2.70161
Marcello Maida, Alessandro Vitello, Fabio Salvatore Macaluso, Marco Daperno, Giammarco Mocci, Antonio Rispo, Giulio Calabrese, Nicola L Decarli, Lucrezia Laschi, Caterina Fattorini, Giorgia Locci, Rachele Del Sordo, Dario Ligresti, Matteo Tacelli, Manuele Furnari, Sandro Sferrazza, Giovanni Marasco, Antonio Facciorusso, Ambrogio Orlando, Vincenzo Villanacci
Background: Histopathological interpretation is crucial for diagnosing inflammatory bowel disease (IBD), distinguishing between Crohn's Disease (CD), Ulcerative Colitis (UC), IBD-Unclassified (IBD-U), and Non-IBD colitis (NIBDC). However, interobserver variability and limited expertise can reduce diagnostic accuracy. Large Language Models (LLMs) such as GPT-5 may offer clinical support in interpreting histology reports.
Methods: We analyzed 100 real-life histological reports from ileo-colonoscopies, equally representing CD, UC, IBD-U, and NIBDC, collected across five Italian healthcare centers, including both IBD-specialized and non-specialized hospitals. A reference standard was established by an expert pathologist. Independent classifications were generated by GPT-5, five gastrointestinal pathologists, five IBD-expert gastroenterologists (GIs), and five non-expert GIs. Diagnostic performance (accuracy, recall, precision, F1-score), agreement with the reference standard (Cohen's κ), and inter-rater reliability (Fleiss' κ) were assessed.
Results: GPT-5 achieved the highest agreement with the reference standard with the highest accuracy (76.0%), compared to pathologists (68.6%), IBD-experts (69.2%), and non-experts (63.2%). Agreement with the reference standard was substantial for GPT-5 (κ = 0.671) and moderate for human groups (κ = 0.508-0.588). GPT-5 showed perfect recall for CD and UC, high recall for NIBDC (96.0%), but poor performance for IBD-U (recall 8.0%, F1-score 14.3%). Fleiss' κ indicated moderate agreement among pathologists and IBD-experts, and fair agreement among non-experts.
Conclusion: GPT-5 demonstrated reliable performance in interpreting IBD histological reports, exhibiting high accuracy and strong agreement with the reference standard. While unreliable for IBD-U, GPT-5 may serve as a supportive tool in histopathological interpretation of IBD, particularly in centers with limited access to expert pathologists or IBD-specialists.
{"title":"Performance of GPT-5 in the Interpretation of IBD Histopathology Reports.","authors":"Marcello Maida, Alessandro Vitello, Fabio Salvatore Macaluso, Marco Daperno, Giammarco Mocci, Antonio Rispo, Giulio Calabrese, Nicola L Decarli, Lucrezia Laschi, Caterina Fattorini, Giorgia Locci, Rachele Del Sordo, Dario Ligresti, Matteo Tacelli, Manuele Furnari, Sandro Sferrazza, Giovanni Marasco, Antonio Facciorusso, Ambrogio Orlando, Vincenzo Villanacci","doi":"10.1002/ueg2.70161","DOIUrl":"10.1002/ueg2.70161","url":null,"abstract":"<p><strong>Background: </strong>Histopathological interpretation is crucial for diagnosing inflammatory bowel disease (IBD), distinguishing between Crohn's Disease (CD), Ulcerative Colitis (UC), IBD-Unclassified (IBD-U), and Non-IBD colitis (NIBDC). However, interobserver variability and limited expertise can reduce diagnostic accuracy. Large Language Models (LLMs) such as GPT-5 may offer clinical support in interpreting histology reports.</p><p><strong>Methods: </strong>We analyzed 100 real-life histological reports from ileo-colonoscopies, equally representing CD, UC, IBD-U, and NIBDC, collected across five Italian healthcare centers, including both IBD-specialized and non-specialized hospitals. A reference standard was established by an expert pathologist. Independent classifications were generated by GPT-5, five gastrointestinal pathologists, five IBD-expert gastroenterologists (GIs), and five non-expert GIs. Diagnostic performance (accuracy, recall, precision, F1-score), agreement with the reference standard (Cohen's κ), and inter-rater reliability (Fleiss' κ) were assessed.</p><p><strong>Results: </strong>GPT-5 achieved the highest agreement with the reference standard with the highest accuracy (76.0%), compared to pathologists (68.6%), IBD-experts (69.2%), and non-experts (63.2%). Agreement with the reference standard was substantial for GPT-5 (κ = 0.671) and moderate for human groups (κ = 0.508-0.588). GPT-5 showed perfect recall for CD and UC, high recall for NIBDC (96.0%), but poor performance for IBD-U (recall 8.0%, F1-score 14.3%). Fleiss' κ indicated moderate agreement among pathologists and IBD-experts, and fair agreement among non-experts.</p><p><strong>Conclusion: </strong>GPT-5 demonstrated reliable performance in interpreting IBD histological reports, exhibiting high accuracy and strong agreement with the reference standard. While unreliable for IBD-U, GPT-5 may serve as a supportive tool in histopathological interpretation of IBD, particularly in centers with limited access to expert pathologists or IBD-specialists.</p>","PeriodicalId":23444,"journal":{"name":"United European Gastroenterology Journal","volume":" ","pages":"e70161"},"PeriodicalIF":6.7,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12803013/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145769244","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-02-01Epub Date: 2025-11-28DOI: 10.1002/ueg2.70148
Laura Retzbach, Karl-Hermann Fuchs, Markus Brand, Thomas J Lux, Alexander Meining
Background: Data on patient-reported outcome measures (PROMs) of patients undergoing endoscopic resections have been sparse. The aim of our study was the prospective assessment of the Gastrointestinal Quality of Life Index (GIQLI) as a baseline and post-endoscopic resection (ER) measurement in patients with epithelial mucosal neoplasms, adenomas and superficial tumours in the upper and lower gastrointestinal tract.
Methods: The study was designed as a prospective single-centre clinical trial. The applied GIQLI consists of 36 items, which are questions assessing symptoms, emotional facts, and the physical and social status of the patient. A baseline assessment and subsequent follow-up after ER were conducted. The ER consisted of EMR, ESD and EFTR techniques following the guidelines.
Results: Of 347 enroled patients, 238 with an indication for ER were analysed. Prior to the procedure, the GIQLI was at 112.74 ± 20.6, which increased after 4-6 weeks to 115.70 ± 20.6 (p < 0.0001, paired t-test). The improvement of PROMs was due to a highly significant rise in the emotional dimension and to some extent by the improvement of the GI-symptom dimension.
Discussion: This prospective study on PROMs shows a significant improvement in quality of life following endoscopic resection. This appears to be related to a decrease in troublesome symptoms and emotional burden after ER. Further studies are necessary to determine whether the choice of specific endoscopic procedures can have a significant impact on the decision-making process in individual patients.
{"title":"Patient-Reported-Outcome-Measures (PROMs) After Gastrointestinal Endoscopic Resections.","authors":"Laura Retzbach, Karl-Hermann Fuchs, Markus Brand, Thomas J Lux, Alexander Meining","doi":"10.1002/ueg2.70148","DOIUrl":"10.1002/ueg2.70148","url":null,"abstract":"<p><strong>Background: </strong>Data on patient-reported outcome measures (PROMs) of patients undergoing endoscopic resections have been sparse. The aim of our study was the prospective assessment of the Gastrointestinal Quality of Life Index (GIQLI) as a baseline and post-endoscopic resection (ER) measurement in patients with epithelial mucosal neoplasms, adenomas and superficial tumours in the upper and lower gastrointestinal tract.</p><p><strong>Methods: </strong>The study was designed as a prospective single-centre clinical trial. The applied GIQLI consists of 36 items, which are questions assessing symptoms, emotional facts, and the physical and social status of the patient. A baseline assessment and subsequent follow-up after ER were conducted. The ER consisted of EMR, ESD and EFTR techniques following the guidelines.</p><p><strong>Results: </strong>Of 347 enroled patients, 238 with an indication for ER were analysed. Prior to the procedure, the GIQLI was at 112.74 ± 20.6, which increased after 4-6 weeks to 115.70 ± 20.6 (p < 0.0001, paired t-test). The improvement of PROMs was due to a highly significant rise in the emotional dimension and to some extent by the improvement of the GI-symptom dimension.</p><p><strong>Discussion: </strong>This prospective study on PROMs shows a significant improvement in quality of life following endoscopic resection. This appears to be related to a decrease in troublesome symptoms and emotional burden after ER. Further studies are necessary to determine whether the choice of specific endoscopic procedures can have a significant impact on the decision-making process in individual patients.</p>","PeriodicalId":23444,"journal":{"name":"United European Gastroenterology Journal","volume":" ","pages":""},"PeriodicalIF":6.7,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12781181/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145639908","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}