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Hypersecretory villous adenoma as the primary cause of an intestinal intussusception and McKittrick-Wheelock syndrome. 高分泌性绒毛腺瘤是肠套叠和McKittrick-Wheelock综合征的主要原因。
IF 2.7 4区 医学 Q2 Medicine Pub Date : 2013-11-01 DOI: 10.1155/2013/252156
Susana Sanchez Garcia, Pedro Villarejo Campos, Maria Del Carmen Manzanares Campillo, Aurora Gil Rendo, Virginia Muñoz Atienza, Esther Pilar García Santos, Francisco Javier Ruescas García, Jose Luis Bertelli Puche
Intestinal invagination or intussusception is the most common cause of intestinal obstruction in children and represent 5% of adult cases. This intestinal obstruction is due to a lesion in the intestinal mucosa that initiates intussusception or intestinal invagination (90% of adult cases are malignant). Moreover, villous adenomas, which represent malignant potential, are found within these lesions of intestinal mucosa. There are variants of villous adenomas known as hypersecretory adenomas, which are described as intestinal lesions located more frequently in the rectum and distal colon. In addition, these variant adenomas can cause hypersecretory diarrhea and an electrolyte disturbance known as McKittrick-Wheelock syndrome.
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引用次数: 10
Percutaneous liver biopsy practice patterns among Canadian hepatologists. 加拿大肝病学家的经皮肝活检实践模式。
IF 2.7 4区 医学 Q2 Medicine Pub Date : 2013-11-01 DOI: 10.1155/2013/429834
Mohammed Aljawad, Eric M Yoshida, Julia Uhanova, Paul Marotta, Natasha Chandok

Background: Percutaneous liver biopsy (PLB) is the standard procedure to obtain histological samples essential for the management of various liver diseases. While safe, many hepatologists no longer perform their own PLBs; the reasons for this practice shift are unknown.

Objective: To describe the attitudes, practice patterns and barriers to PLB among hepatologists in Canada.

Methods: A survey was distributed to all hepatologists in Canada.

Results: Thirty-two of 40 (80%) hepatologists completed the survey; the majority of respondents were male (72%) and had been in practice for >5 years in an academic setting. Fifty-six per cent of hepatologists referred all PLBs to radiology, and only 19% of hepatologists reported performing their own PLBs most or all of the time. There were no sex differences nor were there differences based on years in practice. Fifty per cent of respondents who performed PLB routinely used ultrasound, and PLBs are performed in equal frequency in an ambulatory procedure area (50%) versus the endoscopy suite (36%). For almost one-half of hepatologists (47%), their performance of PLBs decreased in the past five years. The majority of respondents at an academic centre (75%) reported access to FibroScan (Echosens, France), and most estimated a resultant 25% to 50% reduction in the need for PLBs. Lack of resources, patient preference and suboptimal reimbursement were the most common reasons cited for not performing PLBs.

Conclusion: Most hepatologists in Canada do not perform PLBs to the extent that they did in the past, but refer to radiology. The reasons for this shift in practice include lack of resources, improved perception of safety and patient preference. Where available, FibroScan resulted in a perceived 25% to 50% reduction in required liver biopsies.

背景:经皮肝活检(PLB)是获得各种肝脏疾病治疗所必需的组织学样本的标准程序。虽然安全,但许多肝病学家不再执行自己的PLBs;这种做法转变的原因尚不清楚。目的:描述加拿大肝病学家对PLB的态度、实践模式和障碍。方法:对加拿大所有肝病学家进行调查。结果:40名肝病学家中有32名(80%)完成了调查;大多数受访者为男性(72%),并且在学术环境中从事实践工作超过5年。56%的肝病学家将所有plb转到放射科,只有19%的肝病学家报告自己大部分或全部时间都在做plb。没有性别差异,也没有基于实践年限的差异。在接受PLB常规检查的受访者中,有50%的人使用超声波,而在门诊手术区(50%)和内窥镜组(36%)进行PLB的频率相同。近一半的肝病学家(47%)在过去五年中,他们的PLBs表现有所下降。在一个学术中心,大多数受访者(75%)报告使用了FibroScan (Echosens, France),大多数人估计由此减少了25%到50%的PLBs需求。缺乏资源、患者偏好和不理想的报销是不执行PLBs的最常见原因。结论:加拿大大多数肝病学家不像过去那样进行PLBs,而是参考放射学。实践中这种转变的原因包括缺乏资源,提高了对安全性的认识和患者的偏好。在可行的情况下,纤维扫描可减少25%至50%的肝脏活检。
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引用次数: 8
Gastric biopsies: the gap between evidence-based medicine and daily practice in the management of gastric Helicobacter pylori infection. 胃活检:循证医学与胃幽门螺杆菌感染管理的日常实践之间的差距。
IF 2.7 4区 医学 Q2 Medicine Pub Date : 2013-10-01 DOI: 10.1155/2013/897423
Hala El-Zimaity, Stefano Serra, Eva Szentgyorgyi, Rajkumar Vajpeyi, Amir Samani

Background: Many consider histology to be the gold standard for Helicobacter pylori detection. Because the number and distribution of H pylori organisms vary, particularly in patients taking proton pump inhibitors (PPIs), the American Gastroenterological Association recommends discontinuing PPIs two weeks before endoscopy, and taking biopsies from both the body and antrum.

Objective: To assess the influence of clinical practice on the histopathological detection of H pylori infection.

Methods: Electronic patient records were evaluated for the sites of gastric sampling and PPI use at endoscopy. One hundred fifty cases with biopsies taken from both antrum and body were randomly selected for pathological re-review with special stains. The gastric regions sampled, H pylori distribution and influence of clinical factors on pathological interpretation were assessed.

Results: Between 2005 and 2010, 10,268 biopsies were taken to detect H pylori. Only one region was sampled in 60% of patients (antrum 47%, body 13%). Re-review of biopsies taken from both antrum and body indicated that the correct regions were sampled in only 85 (57%) patients. Of these, 54 were H pylori positive and 96 were H pylori negative. H pylori was present in the antrum in only 15% of the patients and body only in 21%. Of 96 H pylori-negative patients, two were reinterpreted as positive. Forty-seven per cent of patients were taking PPIs at endoscopy, contributing to both false-negative and false-positive diagnoses.

Conclusion: Despite national and international guidelines for managing H pylori infection, the American Gastroenterological Association guidelines are infrequently adhered to, with PPIs frequently contributing to false diagnosis; sampling one region only increases the likelihood of missing active infection by at least 15%.

背景:许多人认为组织学是检测幽门螺杆菌的金标准。由于幽门螺杆菌的数量和分布各不相同,特别是在服用质子泵抑制剂(PPIs)的患者中,美国胃肠病学协会建议在内窥镜检查前两周停止使用PPIs,并从身体和胃窦进行活检。目的:探讨临床实践对幽门螺杆菌感染组织病理学检测的影响。方法:对电子病历中胃取样部位和胃镜检查中PPI使用情况进行评估。随机选取150例同时行上腔和全身活检的患者进行特殊染色病理复查。评估胃区取样、幽门螺杆菌分布及临床因素对病理解释的影响。结果:2005年至2010年间,10268例活检检出幽门螺杆菌。60%的患者只对一个区域进行采样(上颌窦47%,身体13%)。重新检查从上腔和身体取的活检表明,只有85例(57%)患者取样正确。其中54例幽门螺杆菌阳性,96例幽门螺杆菌阴性。幽门螺杆菌仅在15%的患者中存在于胃窦,在21%的患者中存在于体内。在96例幽门螺杆菌阴性患者中,2例被重新解释为阳性。47%的患者在内窥镜检查时服用PPIs,导致假阴性和假阳性诊断。结论:尽管有管理幽门螺杆菌感染的国家和国际指南,但美国胃肠病学协会的指南很少得到遵守,ppi经常导致错误诊断;对一个地区进行抽样只会使漏掉活动性感染的可能性增加至少15%。
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引用次数: 29
Esophagitis dissecans superficialis: a case report and literature review. 浅表性食管炎1例报告并文献复习。
IF 2.7 4区 医学 Q2 Medicine Pub Date : 2013-10-01 DOI: 10.1155/2013/923073
Shumona De, Geoffrey S Williams
Esophagitis dissecans superficialis (EDS) is a rare condition characterized classically by sloughing of the esophageal mucosa, followed by vomiting or regurgitation of the esophageal cast (1). Since the advent of endoscopy, less dramatic cases of EDS have been diagnosed, characterized by stripped, whitish mucosa with or without bleeding, vertical fissures and circumferential cracks, in addition to long, linear mucosal breaks. EDS can be associated with medications such as bisphosphonates or nonsteroidal anti-inflammatory drugs, chemical irritants, celiac disease, hot beverages, autoimmune bullous dermatoses or idiopathy (2). EDS is known to be a benign condition that usually resolves without lasting pathological changes. Although biopsies from the esophageal mucosa of patients with EDS are sometimes associated with fungal or bacterial colonies (3), we report a case in which the appearance of EDS mimicked candidal esophagitis, and highlight the need to consider EDS in a differential diagnosis.
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引用次数: 22
Subsequent entry biologics - opportunities and challenges. 后续进入生物制剂——机遇与挑战。
IF 2.7 4区 医学 Q2 Medicine Pub Date : 2013-10-01 DOI: 10.1155/2013/634176
Subrata Ghosh
Currently, infliximab and adalimumab are the two antitumour necrosis factor (TNF) agents available in Canada for the treatment of Crohn disease and ulcerative colitis (adalimumab is not yet licensed for use in ulcerative colitis). At least one more anti-TNF monoclonal antibody (golimumab) is awaiting approval. Furthermore, the gut-specific antiadhesion antibody vedolizumab is also on the horizon for inflammatory bowel disease (IBD). Subsequent entry biologics (SEBs), also known as biosimilars, are monoclonal antibodies that are similar but not identical to the reference biologic drug (RBD). With the patents for anti-TNF antibodies, such as infliximab, coming to an end, anti-TNF SEBs have been manufactured and an important overview of this has been provided by Devlin et al (1) (pages 567–571) in the current issue of the Journal. Given the cost of biological drugs, the potential for SEBs to lower cost, both by virtue of lower cost of SEBs and competitive lowering of cost of RBDs, will be welcome. SEBs are already on the market in some geographical jurisdictions, such as South Korea, and are well on the way to approval in Europe. There are, however, certain considerations that may be of clinical relevance to practising gastroenterologists in Canada, which include the following: Are the molecular structures of SEBs and RBDs comparable?: Subtle differences in structure, such as fucosylated forms, may affect antibody-dependent cell-mediated cytotoxicity and binding to FcγR, which may affect drug clearance and serum drug levels. Therefore, SEBs cannot be viewed as a generic RBD (2). It is also not clear whether the ‘molecular drift’ between SEBs and RBDs may widen over time as part of the manufacturing process. Are the pharmacokinetics of SEBs and RBDs comparable?: RBDs are used in combination with methotrexate in rheumatoid arthritis, as monotherapy in ankylosing spondylitis, and often in psoriasis and in combination with azathioprine in IBD. The doses are different for different indications in the case of RBDs. Therefore, comprehensive pharmacokinetic studies at low and high dose levels, as well as single and multiple doses, may be required to ensure the comparability of SEBs and RBDs. Serum drug levels are critical for the efficacy of monoclonal antibodies in immune-mediated inflammatory diseases (3). Are trial designs sufficiently robust to test efficacy comparability of SEBs and RBDs?: Equivalency studies with sufficiently narrow comparability margins to establish efficacy may require very large studies, which are difficult to conduct, and would compete for the same patients who may otherwise enter studies for the development of novel compounds for the treatment of IBD. For logistical reasons, such very large equivalence studies may not be performed. Are the immunogenicities of SEBs and RBDs comparable?: Immunogenicity of biological drugs is an important consideration and depends on the molecular structure of the monoclonal
{"title":"Subsequent entry biologics - opportunities and challenges.","authors":"Subrata Ghosh","doi":"10.1155/2013/634176","DOIUrl":"https://doi.org/10.1155/2013/634176","url":null,"abstract":"Currently, infliximab and adalimumab are the two antitumour necrosis factor (TNF) agents available in Canada for the treatment of Crohn disease and ulcerative colitis (adalimumab is not yet licensed for use in ulcerative colitis). At least one more anti-TNF monoclonal antibody (golimumab) is awaiting approval. Furthermore, the gut-specific antiadhesion antibody vedolizumab is also on the horizon for inflammatory bowel disease (IBD). \u0000 \u0000 \u0000Subsequent entry biologics (SEBs), also known as biosimilars, are monoclonal antibodies that are similar but not identical to the reference biologic drug (RBD). With the patents for anti-TNF antibodies, such as infliximab, coming to an end, anti-TNF SEBs have been manufactured and an important overview of this has been provided by Devlin et al (1) (pages 567–571) in the current issue of the Journal. Given the cost of biological drugs, the potential for SEBs to lower cost, both by virtue of lower cost of SEBs and competitive lowering of cost of RBDs, will be welcome. SEBs are already on the market in some geographical jurisdictions, such as South Korea, and are well on the way to approval in Europe. There are, however, certain considerations that may be of clinical relevance to practising gastroenterologists in Canada, which include the following: \u0000 \u0000 \u0000Are the molecular structures of SEBs and RBDs comparable?: Subtle differences in structure, such as fucosylated forms, may affect antibody-dependent cell-mediated cytotoxicity and binding to FcγR, which may affect drug clearance and serum drug levels. Therefore, SEBs cannot be viewed as a generic RBD (2). It is also not clear whether the ‘molecular drift’ between SEBs and RBDs may widen over time as part of the manufacturing process. \u0000 \u0000 \u0000Are the pharmacokinetics of SEBs and RBDs comparable?: RBDs are used in combination with methotrexate in rheumatoid arthritis, as monotherapy in ankylosing spondylitis, and often in psoriasis and in combination with azathioprine in IBD. The doses are different for different indications in the case of RBDs. Therefore, comprehensive pharmacokinetic studies at low and high dose levels, as well as single and multiple doses, may be required to ensure the comparability of SEBs and RBDs. Serum drug levels are critical for the efficacy of monoclonal antibodies in immune-mediated inflammatory diseases (3). \u0000 \u0000 \u0000Are trial designs sufficiently robust to test efficacy comparability of SEBs and RBDs?: Equivalency studies with sufficiently narrow comparability margins to establish efficacy may require very large studies, which are difficult to conduct, and would compete for the same patients who may otherwise enter studies for the development of novel compounds for the treatment of IBD. For logistical reasons, such very large equivalence studies may not be performed. \u0000 \u0000 \u0000Are the immunogenicities of SEBs and RBDs comparable?: Immunogenicity of biological drugs is an important consideration and depends on the molecular structure of the monoclonal","PeriodicalId":55285,"journal":{"name":"Canadian Journal of Gastroenterology","volume":null,"pages":null},"PeriodicalIF":2.7,"publicationDate":"2013-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1155/2013/634176","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"31792722","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 3
Capnography improves detection of apnea during procedural sedation for percutaneous transhepatic cholangiodrainage. 经皮经肝胆管引流术中镇静术中呼吸暂停的检测。
IF 2.7 4区 医学 Q2 Medicine Pub Date : 2013-10-01 DOI: 10.1155/2013/852454
Christoph Schlag, Alexandra Wörner, Stefan Wagenpfeil, Eberhard F Kochs, Roland M Schmid, Stefan von Delius

Background: Capnography provides noninvasive monitoring of ventilation and can enable early recognition of altered respiration patterns and apnea.

Objective: To compare the detection of apnea and the prediction of oxygen desaturation and hypoxemia using capnography versus clinical surveillance during procedural sedation for percutaneous transhepatic cholangiodrainage (PTCD).

Methods: Twenty consecutive patients scheduled for PTCD were included in the study. All patients were sedated during the procedure using midazolam and propofol. Aside from standard monitoring, additional capnographic monitoring was used and analyzed by an independent observer.

Results: The mean (± SD) cumulative duration of apnea demonstrated by capnography was significantly longer than the mean cumulative duration of clinically detected apnea (207.5 ± 348.8 s versus 8.2 ± 17.9 s; P=0.015). The overall number of detected episodes of apnea was also significantly different (113 versus seven; P=0.012). There were 15 events of oxygen desaturation (decrease in oxygen saturation [SaO2] ≥ 5%), which were predicted in eight of 15 cases by capnography and in one of 15 cases by clinical observation. There were three events of hypoxemia (SaO2 <90%) that were predicted in three of three cases by capnography and in one of three cases by clinical observation.

Conclusion: Capnographic monitoring was superior to clinical surveillance in the detection of apnea and in the prediction of oxygen desaturation during procedural sedation for PTCD.

背景:二氧化碳造影提供无创通气监测,可以早期识别呼吸模式改变和呼吸暂停。目的:比较经皮经肝胆管引流术(PTCD)镇静过程中应用血管造影检测呼吸暂停、预测氧不饱和和低氧血症与临床监测的差异。方法:连续20例计划PTCD患者纳入研究。所有患者在手术过程中使用咪达唑仑和异丙酚镇静。除了标准监测外,还使用了额外的二氧化碳监测,并由独立观察者进行了分析。结果:造影显示的呼吸暂停平均累积时间(±SD)明显长于临床检测到的呼吸暂停平均累积时间(207.5±348.8 s vs 8.2±17.9 s);P = 0.015)。检测到的呼吸暂停发作的总次数也有显著差异(113次vs 7次;P = 0.012)。15例患者中有8例血氧饱和度[SaO2]降低≥5%,15例患者中有1例临床观察可预测血氧饱和度降低。结论:在PTCD手术镇静过程中,血糖监测在检测呼吸暂停和预测氧饱和度方面优于临床监测。
{"title":"Capnography improves detection of apnea during procedural sedation for percutaneous transhepatic cholangiodrainage.","authors":"Christoph Schlag,&nbsp;Alexandra Wörner,&nbsp;Stefan Wagenpfeil,&nbsp;Eberhard F Kochs,&nbsp;Roland M Schmid,&nbsp;Stefan von Delius","doi":"10.1155/2013/852454","DOIUrl":"https://doi.org/10.1155/2013/852454","url":null,"abstract":"<p><strong>Background: </strong>Capnography provides noninvasive monitoring of ventilation and can enable early recognition of altered respiration patterns and apnea.</p><p><strong>Objective: </strong>To compare the detection of apnea and the prediction of oxygen desaturation and hypoxemia using capnography versus clinical surveillance during procedural sedation for percutaneous transhepatic cholangiodrainage (PTCD).</p><p><strong>Methods: </strong>Twenty consecutive patients scheduled for PTCD were included in the study. All patients were sedated during the procedure using midazolam and propofol. Aside from standard monitoring, additional capnographic monitoring was used and analyzed by an independent observer.</p><p><strong>Results: </strong>The mean (± SD) cumulative duration of apnea demonstrated by capnography was significantly longer than the mean cumulative duration of clinically detected apnea (207.5 ± 348.8 s versus 8.2 ± 17.9 s; P=0.015). The overall number of detected episodes of apnea was also significantly different (113 versus seven; P=0.012). There were 15 events of oxygen desaturation (decrease in oxygen saturation [SaO2] ≥ 5%), which were predicted in eight of 15 cases by capnography and in one of 15 cases by clinical observation. There were three events of hypoxemia (SaO2 <90%) that were predicted in three of three cases by capnography and in one of three cases by clinical observation.</p><p><strong>Conclusion: </strong>Capnographic monitoring was superior to clinical surveillance in the detection of apnea and in the prediction of oxygen desaturation during procedural sedation for PTCD.</p>","PeriodicalId":55285,"journal":{"name":"Canadian Journal of Gastroenterology","volume":null,"pages":null},"PeriodicalIF":2.7,"publicationDate":"2013-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1155/2013/852454","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"31792726","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 14
Canadian Association of Gastroenterology position statement: hip fracture and proton pump inhibitor therapy-a 2013 update. 加拿大胃肠病学协会立场声明:髋部骨折和质子泵抑制剂治疗- 2013年更新。
IF 2.7 4区 医学 Q2 Medicine Pub Date : 2013-10-01 DOI: 10.1155/2013/321379
Paul Moayyedi, Yuhong Yuan, Grigorios Leontiadis
Health Canada recently provided an information update on proton pump inhibitor (PPI) therapy and risk of fracture in April 2013 (1) stating “Several scientific studies suggest that PPI therapy may be associated with a small increased risk for fractures of the hip, wrist, or spine related to osteoporosis, a disease resulting in the weakening of bones. The risk of fracture was higher in patients who received multiple daily doses of PPIs and therapy for a year or longer. Additional risk factors for osteoporosis, such as age, gender and the presence of other health conditions, may also contribute to the increased risk of fractures. At Health Canada’s request, manufacturers of all PPIs marketed in Canada have updated the drug labels for their products to include information on this risk.”
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引用次数: 16
A pilot study examining the relationship among Crohn disease activity, glucagon-like peptide-2 signalling and intestinal function in pediatric patients. 一项试点研究,探讨克罗恩病活动、胰高血糖素样肽-2 信号和儿科患者肠道功能之间的关系。
IF 2.7 4区 医学 Q2 Medicine Pub Date : 2013-10-01 DOI: 10.1155/2013/460958
David L Sigalet, Dragan Kravarusic, Decker Butzner, Bolette Hartmann, Jens J Holst, Jon Meddings

Unlabelled: BACKGROUND⁄

Objectives: The relationship between the enteroendocrine hormone glucagon-like peptide 2 (GLP-2) and intestinal inflammation is unclear. GLP-2 promotes mucosal growth, decreases permeability and reduces inflammation in the intestine; physiological stimulation of GLP-2 release is triggered by nutrient contact. The authors hypothesized that ileal Crohn disease (CD) affects GLP-2 release.

Methods: With ethics board approval, pediatric patients hospitalized with CD were studied; controls were recruited from local schools. Inclusion criteria were endoscopy-confirmed CD (primarily of the small intestine) with a disease activity index >150. Fasting and postprandial GLP-2 levels and quantitative urinary recovery of orally administered 3-O-methyl-glucose (active transport) and lactulose⁄mannitol (passive) were quantified during the acute and remission phases.

Results: Seven patients (mean [± SD] age 15.3 ± 1.3 years) and 10 controls (10.3 ± 1.6 years) were studied. In patients with active disease, fasting levels of GLP-2 remained stable but postprandial levels were reduced. Patients with active disease exhibited reduced glucose absorption and increased lactulose⁄mannitol recovery; all normalized with disease remission. The change in the lactulose⁄mannitol ratio was due to both reduced lactulose and increased mannitol absorption.

Conclusions: These findings suggest that pediatric patients with acute ileal CD have decreased postprandial GLP-2 release, reduced glucose absorption and increased intestinal permeability. Healing of CD resulted in normalization of postprandial GLP-2 release and mucosal functioning (nutrient absorption and permeability), the latter due to an increase in mucosal surface area. These findings have implications for the use of GLP-2 and feeding strategies as a therapy in CD patients; further studies of the effects of inflammation and the GLP-2 axis are recommended.

无标签:背景⁄目的:肠内分泌激素胰高血糖素样肽2(GLP-2)与肠道炎症之间的关系尚不清楚。GLP-2能促进肠道黏膜生长、降低渗透性并减轻炎症;营养接触会触发GLP-2的生理性释放刺激。作者假设回肠克罗恩病(CD)会影响 GLP-2 的释放:方法:经伦理委员会批准,研究对象为住院治疗的儿童克罗恩病患者;对照组从当地学校招募。纳入标准为内镜检查确诊为 CD(主要是小肠),疾病活动指数大于 150。研究人员对急性期和缓解期患者的空腹和餐后GLP-2水平以及口服3-O-甲基葡萄糖(主动转运)和乳糖⁄甘露醇(被动转运)的定量尿回收率进行了量化:研究对象包括 7 名患者(平均 [± SD] 年龄为 15.3 ± 1.3 岁)和 10 名对照组患者(10.3 ± 1.6 岁)。在活动期患者中,空腹 GLP-2 水平保持稳定,但餐后水平降低。活动性疾病患者的葡萄糖吸收减少,乳糖⁄甘露醇恢复增加;随着病情的缓解,这些变化都趋于正常。乳糖⁄甘露醇比率的变化是由于乳糖吸收减少和甘露醇吸收增加所致:这些研究结果表明,患有急性回肠 CD 的儿童患者餐后 GLP-2 释放减少,葡萄糖吸收减少,肠道通透性增加。CD 愈合后,餐后 GLP-2 释放和粘膜功能(营养吸收和渗透性)恢复正常,后者是由于粘膜表面积增加所致。这些发现对使用 GLP-2 和喂养策略作为 CD 患者的疗法具有重要意义;建议进一步研究炎症和 GLP-2 轴的影响。
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引用次数: 0
Overview of subsequent entry biologics for the management of inflammatory bowel disease and Canadian Association of Gastroenterology position statement on subsequent entry biologics. 治疗炎症性肠病的后续入境生物制剂概述和加拿大胃肠病学协会对后续入境生物制剂的立场声明。
IF 2.7 4区 医学 Q2 Medicine Pub Date : 2013-10-01 DOI: 10.1155/2013/327120
Shane M Devlin, Brian Bressler, Charles N Bernstein, Richard N Fedorak, Alain Bitton, Harminder Singh, Brian G Feagan
The advent of biologic molecules is one of the most important therapeutic advances to have occurred in the medical management of inflammatory bowel disease (IBD). From a Canadian perspective, the monoclonal antibodies directed against tumour necrosis factor-alpha (TNF-α), namely infliximab (Remicade, Johnson & Johnson, USA) and adalimumab (Humira, AbbVie Corporation, USA), are the only approved and commercially available biologics for the treatment of either Crohn disease (CD) or ulcerative colitis (UC) in Canada. These molecules have a large and complex structure and are generated with the aid of DNA recombination technology. This complexity makes the development of biologically similar substitutes – as is common with smaller, less complex molecules – a challenge. However, following the expiry of the patent on Remicade, a biosimilar infliximab has been developed (CT-P13, Remsima [Celltrion, South Korea], Inflectra [Hospira Inc, USA]). In addition, another biosimilar infliximab has been developed by an Indian pharmaceutical company, Reliance Life Sciences. Standard, small-molecule pharmaceuticals are significantly different from their complex biological counterparts (Figure 1). Most synthesized pharmaceuticals have a molecular size of only a few hundred Daltons (Da) (eg, omeprazole is 345 Da). In comparison, infliximab is 149,000 Da. Moreover, monoclonal antibodies have a complex structure that is influenced by the vector and post-translational modification, among other factors (1–3). In addition, although the overall structure of a monoclonal antibody may be known, the manufacturing platform used by the manufacturer of the reference biologic drug (RBD) is not, due to the proprietary nature of the information. As such, a different biological system that is used to produce a biosimilar agent will likely translate into subtle differences that could be difficult to characterize. Such differences have the potential to translate into clinically relevant differences in efficacy, safety and immunogenicity. Therefore, it will be extremely challenging to ensure that a subsequent entry biologic (SEB) is, in fact, ‘equivalent’ to the RBD. Clinical equivalence can only be proven in clinical trials. Figure 1) Comparison between a biologic monoclonal antibody and an acetylsalicylic acid molecule. From Kozlowski S, Woodcock J, Midthun K, Behrman Sherman R. Developing the Nation’s Biosimilars Program. N Engl J Med 2011;365:385–8. Reprinted with ... It is important for the Canadian gastroenterology community to gain a full understanding of the important issues in the context of the development and entry into the marketplace of such biologic agents. The objectives of the present document are to: Provide a brief primer on the terminology germane to this issue. Describe the current state of SEBs and the existing guidelines from Health Canada and other jurisdictions. Provide perspective on the potential opportunity in the Ca
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引用次数: 32
Minimal hepatic encephalopathy. 轻度肝性脑病。
IF 2.7 4区 医学 Q2 Medicine Pub Date : 2013-10-01 DOI: 10.1155/2013/547670
Laura M Stinton, Saumya Jayakumar

Minimal hepatic encephalopathy (MHE) is the earliest form of hepatic encephalopathy and can affect up to 80% of cirrhotic patients. By definition, it has no obvious clinical manifestation and is characterized by neurocognitive impairment in attention, vigilance and integrative function. Although often not considered to be clinically relevant and, therefore, not diagnosed or treated, MHE has been shown to affect daily functioning, quality of life, driving and overall mortality. The diagnosis of MHE has traditionally been achieved through neuropsychological examination, psychometric tests or the newer critical flicker frequency test. A new smartphone application (EncephalApp Stroop Test) may serve to function as a screening tool for patients requiring further testing. In addition to physician reporting and driving restrictions, medical treatment for MHE includes non-absorbable disaccharides (eg, lactulose), probiotics or rifaximin. Liver transplantation may not result in reversal of the cognitive deficits associated with MHE.

轻度肝性脑病(MHE)是肝性脑病的最早形式,可影响高达80%的肝硬化患者。从定义上看,它没有明显的临床表现,以注意、警觉性和综合功能的神经认知障碍为特征。虽然通常不被认为与临床相关,因此没有得到诊断或治疗,但MHE已被证明会影响日常功能、生活质量、驾驶和总体死亡率。MHE的诊断传统上是通过神经心理学检查、心理测量测试或较新的临界闪烁频率测试来实现的。一款新的智能手机应用程序(EncephalApp Stroop Test)可能会成为需要进一步检测的患者的筛查工具。除了医生报告和驾驶限制外,MHE的治疗还包括不可吸收的双糖(如乳果糖)、益生菌或利福昔明。肝移植可能无法逆转与MHE相关的认知缺陷。
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引用次数: 22
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Canadian Journal of Gastroenterology
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