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Inflammatory leg nodules following acute pancreatitis. 急性胰腺炎后的炎性腿部结节。
IF 35.7 Pub Date : 2022-09-01 DOI: 10.1016/S2468-1253(22)00176-5
Margot Lehericey, Aurélie Baldolli, Renaud Verdon
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引用次数: 0
The prevalence and incidence of NAFLD worldwide: a systematic review and meta-analysis. 全球NAFLD的患病率和发病率:一项系统回顾和荟萃分析。
IF 35.7 Pub Date : 2022-09-01 Epub Date: 2022-07-05 DOI: 10.1016/S2468-1253(22)00165-0
Kiarash Riazi, Hassan Azhari, Jacob H Charette, Fox E Underwood, James A King, Elnaz Ehteshami Afshar, Mark G Swain, Stephen E Congly, Gilaad G Kaplan, Abdel-Aziz Shaheen

Background: Non-alcoholic fatty liver disease (NAFLD) is the most common liver disease worldwide and the leading cause of liver-related morbidity and mortality. We aimed to predict the burden of NAFLD by examining and estimating the temporal trends of its worldwide prevalence and incidence.

Methods: In this systematic review and meta-analysis, we searched MEDLINE, EMBASE, Scopus, and Web of Science without language restrictions for reports published between date of database inception and May 25, 2021. We included observational cross-sectional or longitudinal studies done in study populations representative of the general adult population, in whom NAFLD was diagnosed using an imaging method in the absence of excessive alcohol consumption and viral hepatitis. Studies were excluded if conducted in paediatric populations (aged <18 years) or subgroups of the general population. Summary estimates were extracted from included reports by KR and independently verified by HA using the population, intervention, comparison, and outcomes framework. Primary outcomes were the prevalence and incidence of NAFLD. A random-effects meta-analysis was used to calculate overall and sex-specific pooled effect estimates and 95% CIs.

Findings: The search identified 28 557 records, of which 13 577 records were screened; 299 records were also identified via other methods. In total, 72 publications with a sample population of 1 030 160 individuals from 17 countries were included in the prevalence analysis, and 16 publications with a sample population of 381 765 individuals from five countries were included in the incidence analysis. The overall prevalence of NAFLD worldwide was estimated to be 32·4% (95% CI 29·9-34·9). Prevalence increased significantly over time, from 25·5% (20·1-31·0) in or before 2005 to 37·8% (32·4-43·3) in 2016 or later (p=0·013). Overall prevalence of NAFLD was significantly higher in men than in women (39·7% [36·6-42·8] vs 25·6% [22·3-28·8]; p<0·0001). The overall incidence of NAFLD was estimated to be 46·9 cases per 1000 person-years (36·4-57·5); 70·8 cases per 1000 person-years (48·7-92·8) in men and 29·6 cases per 1000 person-years (20·2-38·9) in women (p<0·0001). There was considerable heterogeneity between studies of both NAFLD prevalence (I2=99·9%) and NAFLD incidence (I2=99·9%).

Interpretation: Worldwide prevalence of NAFLD is considerably higher than previously estimated and is continuing to increase at an alarming rate. Incidence and prevalence of NAFLD are significantly higher among men than among women. Greater awareness of NAFLD and the development of cost-effective risk stratification strategies are warranted to address the growing burden of NAFLD.

Funding: Canadian Institutes of Health.

背景:非酒精性脂肪性肝病(NAFLD)是世界范围内最常见的肝脏疾病,也是肝脏相关发病率和死亡率的主要原因。我们的目的是通过检查和估计其全球患病率和发病率的时间趋势来预测NAFLD的负担。方法:在本系统评价和荟萃分析中,我们检索了MEDLINE、EMBASE、Scopus和Web of Science,检索了数据库建立日期至2021年5月25日之间发表的无语言限制的报告。我们纳入了在具有代表性的普通成人人群中进行的观察性横断面或纵向研究,在没有过度饮酒和病毒性肝炎的情况下,使用影像学方法诊断NAFLD。如果在儿科人群中进行研究,则排除研究。结果:检索确定了28557份记录,其中筛选了13577份记录;299条记录也通过其他方法进行了识别。患病率分析共纳入了来自17个国家的72份出版物,样本人口为1 030 160人;发病率分析共纳入了来自5个国家的16份出版物,样本人口为381 765人。全球NAFLD的总体患病率估计为32.4% (95% CI 29.9 - 34.9)。随着时间的推移,患病率明显增加,从2005年或之前的25.5%(20.1 ~ 31.0)增加到2016年或之后的37.8% (32.4 ~ 43.3)(p= 0.013)。男性NAFLD总体患病率明显高于女性(39.7% [36.6 - 42.8]vs 25.6% [22.3 - 28.8]);p2= 99.9%)和NAFLD发生率(I2= 99.9%)。解释:全球NAFLD患病率远高于先前的估计,并继续以惊人的速度增长。男性NAFLD的发病率和流行率明显高于女性。有必要提高对NAFLD的认识,并制定具有成本效益的风险分层策略,以解决NAFLD日益增加的负担。资助:加拿大卫生研究院。
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引用次数: 336
Management of pouch neoplasia: consensus guidelines from the International Ileal Pouch Consortium. 眼袋瘤变的处理:来自国际回肠眼袋协会的共识指南。
IF 35.7 Pub Date : 2022-09-01 Epub Date: 2022-07-05 DOI: 10.1016/S2468-1253(22)00039-5
Ravi P Kiran, Gursimran S Kochhar, Revital Kariv, Douglas K Rex, Akira Sugita, David T Rubin, Udayakumar Navaneethan, Tracy L Hull, Huaibin Mabel Ko, Xiuli Liu, Lisa A Kachnic, Scott Strong, Marietta Iacucci, Willem Bemelman, Philip Fleshner, Rachael A Safyan, Paulo G Kotze, André D'Hoore, Omar Faiz, Simon Lo, Jean H Ashburn, Antonino Spinelli, Charles N Bernstein, Sunanda V Kane, Raymond K Cross, Jason Schairer, James T McCormick, Francis A Farraye, Shannon Chang, Ellen J Scherl, David A Schwartz, David H Bruining, Jessica Philpott, Stuart Bentley-Hibbert, Dino Tarabar, Sandra El-Hachem, William J Sandborn, Mark S Silverberg, Darrell S Pardi, James M Church, Bo Shen

Surveillance pouchoscopy is recommended for patients with restorative proctocolectomy with ileal pouch-anal anastomosis in ulcerative colitis or familial adenomatous polyposis, with the surveillance interval depending on the risk of neoplasia. Neoplasia in patients with ileal pouches mainly have a glandular source and less often are of squamous cell origin. Various grades of neoplasia can occur in the prepouch ileum, pouch body, rectal cuff, anal transition zone, anus, or perianal skin. The main treatment modalities are endoscopic polypectomy, endoscopic ablation, endoscopic mucosal resection, endoscopic submucosal dissection, surgical local excision, surgical circumferential resection and re-anastomosis, and pouch excision. The choice of the treatment modality is determined by the grade, location, size, and features of neoplastic lesions, along with patients' risk of neoplasia and comorbidities, and local endoscopic and surgical expertise.

对于溃疡性结肠炎或家族性腺瘤性息肉病患者行恢复性直结肠切除术并回肠袋-肛门吻合术的患者,建议进行监测袋镜检查,监测间隔取决于肿瘤的发生风险。回肠小袋患者的肿瘤主要是腺源性的,很少是鳞状细胞性的。不同级别的肿瘤可发生在回肠前、袋体、直肠袖、肛门过渡区、肛门或肛周皮肤。主要治疗方式有内镜下息肉切除、内镜下消融、内镜下粘膜切除、内镜下粘膜下剥离、手术局部切除、手术环切再吻合、眼袋切除。治疗方式的选择取决于肿瘤病变的级别、位置、大小和特征,以及患者发生肿瘤的风险和合并症,以及当地的内窥镜和外科专业知识。
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引用次数: 4
Clinical trial designs for artificial intelligence in gastrointestinal endoscopy. 胃肠道内窥镜人工智能临床试验设计。
IF 35.7 Pub Date : 2022-09-01 DOI: 10.1016/S2468-1253(22)00232-1
Yuichi Mori, Michal F Kaminski, Cesare Hassan, Michael Bretthauer
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引用次数: 4
The International Liver Congress 2022. 2022年国际肝脏大会。
Pub Date : 2022-09-01 DOI: 10.1016/s2468-1253(22)00244-8
R. Brierley, Hugh Thomas
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引用次数: 0
Odevixibat treatment in progressive familial intrahepatic cholestasis: a randomised, placebo-controlled, phase 3 trial. 奥维西巴治疗进行性家族性肝内胆汁淤积症:一项随机、安慰剂对照的3期试验。
IF 35.7 Pub Date : 2022-09-01 Epub Date: 2022-07-01 DOI: 10.1016/S2468-1253(22)00093-0
Richard J Thompson, Henrik Arnell, Reha Artan, Ulrich Baumann, Pier Luigi Calvo, Piotr Czubkowski, Buket Dalgic, Lorenzo D'Antiga, Özlem Durmaz, Björn Fischler, Emmanuel Gonzalès, Tassos Grammatikopoulos, Girish Gupte, Winita Hardikar, Roderick H J Houwen, Binita M Kamath, Saul J Karpen, Lise Kjems, Florence Lacaille, Alain Lachaux, Elke Lainka, Cara L Mack, Jan P Mattsson, Patrick McKiernan, Hasan Özen, Sanjay R Rajwal, Bertrand Roquelaure, Mohammad Shagrani, Eyal Shteyer, Nisreen Soufi, Ekkehard Sturm, Mary Elizabeth Tessier, Henkjan J Verkade, Patrick Horn
<p><strong>Background: </strong>Progressive familial intrahepatic cholestasis (PFIC) is a group of inherited paediatric liver diseases resulting from mutations in genes that impact bile secretion. We aimed to evaluate the effects of odevixibat, an ileal bile acid transporter inhibitor, versus placebo in children with PFIC.</p><p><strong>Methods: </strong>Patients eligible for this 24-week, randomised, double-blind, completed, phase 3 study were paediatric outpatients diagnosed with PFIC1 or PFIC2 who had pruritus and elevated serum bile acids at screening. Patients were randomly assigned (1:1:1) using an interactive web-based system to once a day oral placebo, odevixibat 40 μg/kg, or odevixibat 120 μg/kg. Randomisation was done in a block size of six and stratified by PFIC type and patient age; patients, clinicians, and study staff were blinded to treatment allocation. Patients were enrolled at one of 33 global sites. Two primary endpoints were evaluated: proportion of positive pruritus assessments (PPAs; ie, scratching score of ≤1 or ≥1-point decrease as assessed by caregivers using the Albireo observer-reported outcome [ObsRO] PRUCISION instrument) over 24 weeks, and proportion of patients with serum bile acid response (ie, serum bile acids reduced by ≥70% from baseline or concentrations of ≤70 μmol/L) at week 24. Efficacy and safety were analysed in randomly allocated patients who received one or more doses of study drug. This study is registered with ClinicalTrials.gov, NCT03566238.</p><p><strong>Findings: </strong>Between June 21, 2018, and Feb 10, 2020, 62 patients (median age 3·2 [range 0·5-15·9] years) were randomly allocated to placebo (n=20), odevixibat 40 μg/kg per day (n=23), or odevixibat 120 μg/kg per day (n=19). Model-adjusted (least squares) mean proportion of PPAs was significantly higher with odevixibat versus placebo (55% [SE 8] in the combined odevixibat group [58% in the 40 μg/kg per day group and 52% in the 120 μg/kg per day group] vs 30% [SE 9] in the placebo group; model-adjusted mean difference 25·0% [95% CI 8·5-41·5]; p=0·0038). The percentage of patients with serum bile acid response was also significantly higher with odevixibat versus placebo (14 [33%] of 42 patients in the combined odevixibat group [10 in the 40 μg/kg per day group and four in the 120 μg/kg per day group] vs none of 20 in the placebo group; adjusting for stratification factor [PFIC type], the proportion difference was 30·7% [95% CI 12·6-48·8; p=0·0030]). The most common treatment-emergent adverse events (TEAEs) were diarrhoea or frequent bowel movements (13 [31%] of 42 for odevixibat vs two [10%] of 20 for placebo) and fever (12 [29%] of 42 vs five [25%] of 20); serious TEAEs occurred in three (7%) of 42 odevixibat-treated patients and in five (25%) of 20 placebo-treated patients.</p><p><strong>Interpretation: </strong>In children with PFIC, odevixibat effectively reduced pruritus and serum bile acids versus placebo and was generally well tolerated. O
背景:进行性家族性肝内胆汁淤积症(PFIC)是一组由影响胆汁分泌的基因突变引起的遗传性儿科肝病。我们的目的是评估odevixibat(一种回肠胆汁酸转运蛋白抑制剂)与安慰剂在PFIC儿童中的作用。方法:符合这项为期24周、随机、双盲、完成的3期研究的患者是诊断为PFIC1或PFIC2的儿科门诊患者,他们在筛查时有瘙痒和血清胆汁酸升高。使用交互式网络系统随机分配患者(1:1:1),每天一次口服安慰剂,odevixibat 40 μg/kg或odevixibat 120 μg/kg。随机分组大小为6个,按PFIC类型和患者年龄分层;患者、临床医生和研究人员对治疗分配不知情。患者在全球33个地点之一入组。评估了两个主要终点:瘙痒评估阳性的比例(PPAs);即,护理人员使用Albireo观察者报告的结果[ObsRO] PRUCISION仪器评估的抓痕评分在24周内下降≤1或≥1分,以及血清胆汁酸反应(即血清胆汁酸较基线降低≥70%或浓度≤70 μmol/L)的患者比例。对随机分配的接受一剂或多剂研究药物的患者进行疗效和安全性分析。本研究已在ClinicalTrials.gov注册,编号NCT03566238。研究结果:在2018年6月21日至2020年2月10日期间,62例患者(中位年龄为6.2岁[范围0.5 - 15.9]岁)被随机分配到安慰剂组(n=20)、奥维西巴40 μg/kg / d组(n=23)和奥维西巴120 μg/kg / d组(n=19)。经模型校正(最小二乘)的平均PPAs比例,奥维西巴组显著高于安慰剂组(联合奥维西巴组为55% [SE 8] [40 μg/kg /天组为58%,120 μg/kg /天组为52%],安慰剂组为30% [SE 9];模型校正平均差25.0% [95% CI 8.5 - 41.5];p = 0·0038)。奥维西巴与安慰剂相比,血清胆汁酸应答的患者比例也显著更高(42例患者中,联合奥维西巴组有14例(33%)[40 μg/kg /天组有10例,120 μg/kg /天组有4例],而安慰剂组20例患者中无一例;调整分层因素[PFIC类型]后,比例差异为30.7% [95% CI 12.6 - 48.8;p = 0·0030)。最常见的治疗不良事件(teae)是腹泻或频繁排便(odevixibat组42例中的13例[31%]vs安慰剂组20例中的2例[10%])和发烧(42例中的12例[29%]vs 20例中的5例[25%]);42例odevixibat组患者中有3例(7%)发生严重teae, 20例安慰剂组患者中有5例(25%)发生严重teae。结论:在PFIC患儿中,与安慰剂相比,odevixibat有效地减少了瘙痒和血清胆汁酸,并且通常耐受性良好。Odevixibat口服胶囊,每天一次,是PFIC患者中断肠肝循环的非手术药物选择。资助:Albireo Pharma。
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引用次数: 34
Standardising early liver transplantation for severe alcohol-related hepatitis. 规范重度酒精性肝炎早期肝移植。
IF 35.7 Pub Date : 2022-08-01 DOI: 10.1016/S2468-1253(22)00171-6
Gene Y Im
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引用次数: 1
Correction to Lancet Gastroenterol Hepatol 2022; 7: 736-46. 《柳叶刀Gastroenterol Hepatol 2022》修正;7: 736 - 46。
IF 35.7 Pub Date : 2022-08-01 DOI: 10.1016/S2468-1253(22)00211-4
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引用次数: 0
Bridging the gap to achieve viral hepatitis mortality targets. 弥合差距,实现病毒性肝炎死亡率目标。
IF 35.7 Pub Date : 2022-08-01 DOI: 10.1016/S2468-1253(22)00163-7
Ericka Flores, Jessica Howell
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引用次数: 0
Standardising early liver transplantation for severe alcohol-related hepatitis - Authors' reply. 规范重度酒精性肝炎早期肝移植——作者的答复。
IF 35.7 Pub Date : 2022-08-01 DOI: 10.1016/S2468-1253(22)00195-9
Philippe Mathurin, Sebastien Dharancy, Alexandre Louvet
{"title":"Standardising early liver transplantation for severe alcohol-related hepatitis - Authors' reply.","authors":"Philippe Mathurin,&nbsp;Sebastien Dharancy,&nbsp;Alexandre Louvet","doi":"10.1016/S2468-1253(22)00195-9","DOIUrl":"https://doi.org/10.1016/S2468-1253(22)00195-9","url":null,"abstract":"","PeriodicalId":114609,"journal":{"name":"The lancet. Gastroenterology & hepatology","volume":" ","pages":"698-699"},"PeriodicalIF":35.7,"publicationDate":"2022-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"40487845","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
期刊
The lancet. Gastroenterology & hepatology
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