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A retrospective review of α-gal syndrome complicating the management of suspected pancreatic exocrine insufficiency in one gastroenterology clinic in central Virginia 弗吉尼亚州中部一家胃肠病诊所的α-gal综合征并发疑似胰腺外分泌功能不全的治疗回顾
Pub Date : 2023-07-26 DOI: 10.3389/fgstr.2023.1162109
Nathan E. Richards, Jeffrey M. Wilson, T. Platts-Mills, R. Richards
The galactose-α-1,3-galactose (α-gal) mammalian meat allergy, α-gal syndrome, often includes diarrhea, abdominal pain, and other gastrointestinal (GI) symptoms. Pancreatic exocrine insufficiency causes similar symptoms. The pancreatic replacement enzymes, referred to here as pancreatic enzymes, used to treat pancreatic insufficiency are porcine products and contain α-gal. Patients with pancreatic insufficiency who also have α-gal syndrome may be intolerant of mammalian products in their diet and of α-gal in pancreatic enzymes. In this article, we describe 40 patients from one GI clinic in central Virginia with suspected pancreatic insufficiency and increased α-gal immunoglobulin E (IgE) levels. Over 50% of these patients had some clinical improvement when mammalian products were removed from the diet. Most patients could tolerate pancreatic enzymes; 10% could not tolerate them due to suspected allergy symptoms, but none developed anaphylaxis. Understanding that α-gal syndrome can be superimposed on pancreatic exocrine insufficiency and exacerbate symptoms, and that treatment with pancreatic enzymes may increase GI and/or allergy symptoms in this group, will lead to improved medical management of this complex patient population.
半乳糖-α-1,3-半乳糖(α-gal)哺乳动物肉类过敏,α-gal综合征,通常包括腹泻、腹痛和其他胃肠道(GI)症状。胰腺外分泌功能不全也会引起类似的症状。用于治疗胰腺功能不全的胰腺替代酶,在这里被称为胰腺酶,是猪的产品,含有α-gal。同时患有α-gal综合征的胰腺功能不全患者可能对饮食中的哺乳动物产品和胰腺酶中的α-gal不耐受。在这篇文章中,我们描述了来自弗吉尼亚州中部一家胃肠道诊所的40名疑似胰腺功能不全和α-gal免疫球蛋白E(IgE)水平升高的患者。当从饮食中去除哺乳动物产品时,超过50%的患者有一些临床改善。大多数患者可以耐受胰腺酶;10%的患者因疑似过敏症状而不能耐受,但没有一人出现过敏反应。了解α-gal综合征可能与胰腺外分泌功能不全叠加并加剧症状,以及胰腺酶治疗可能会增加这一群体的胃肠道和/或过敏症状,将有助于改善这一复杂患者群体的医疗管理。
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引用次数: 0
Severe respiratory distress secondary to pharyngeal perforation during endoscopic gastrostomy tube removal: a clinical case report 内镜下胃造口术中咽穿孔致严重呼吸窘迫1例临床报告
Pub Date : 2023-06-05 DOI: 10.3389/fgstr.2023.1191199
Dima Siblani, Laure Stiel, Stéphanie Husson-Wetzel, P. Barsotti
We present the case of a 60-year-old patient with advanced chronic obstructive pulmonary disease (COPD), who presented for planned endoscopic removal of her gastrostomy feeding tube, which was inserted for nutritional status optimization prior to lung transplantation. The procedure was complicated by accidental blockage of the device at the pharyngeal level, causing a transmural laceration. Rapid respiratory distress developed with subcutaneous emphysema that led to the intubation of the patient. A new endoscopic retrieval was attempted but failed, and the patient was sent to the operating room after a cervical and thoracic CT scan that showed the blocked piece in the cervical wall, in addition to diffuse subcutaneous emphysema, a large pneumomediastinum, and a left pneumothorax. The surgery consisted of a left cervicotomy, a pharyngeal incision, and retrieval of the trapped parts. The patient was sent to the intensive care unit (ICU) where she could be weaned and extubated 1 week later.
我们报告一个60岁晚期慢性阻塞性肺疾病(COPD)患者的病例,她提出了计划的内镜切除胃造口饲管,这是为了在肺移植前优化营养状况而插入的。该程序是复杂的意外堵塞装置在咽水平,造成跨壁撕裂。快速呼吸窘迫并发皮下肺气肿,导致患者插管。尝试进行新的内镜检查,但失败,患者在进行颈椎和胸椎CT扫描后被送往手术室,CT扫描显示颈壁内有阻塞块,此外还有弥漫性皮下肺气肿、纵隔大气胸和左侧气胸。手术包括左颈切开术、咽切口和取出被困部分。患者被送往重症监护室(ICU), 1周后她可以断奶并拔管。
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引用次数: 0
Transoral incisionless fundoplication and open hiatal hernia repair: A case report 经口无切口胃底折叠术和开放性裂孔疝修补术1例
Pub Date : 2023-05-31 DOI: 10.3389/fgstr.2023.1207659
Anjani Turaga, Y. Salem
Introduction Transoral incisionless fundoplication is a new procedure that has recently emerged as a potential alternative to traditional anti-reflux surgeries. It is a less invasive option with fewer complications and reduced recovery time. Hiatal hernia repair is also commonly performed in conjunction with transoral incisionless fundoplication to improve outcomes. In this case, it details a successful transoral incisionless fundoplication and hiatal hernia repair procedure in a patient with long standing gastroesophageal reflux disease (GERD). The case is unique as it involved a patient with an uncharacteristically large hiatal hernia measuring above 5cm, which is a size that is generally not considered suitable for transoral incisionless fundoplication. The hiatal hernia was repaired with a gastrectomy instead of laparoscopically due to the size and adhesions present. Case details This case report presents an 86 year old female patient with a history of long-standing GERD symptoms from the past 10 years who had failed to respond to medical therapy. Endoscopic imaging revealed a hernia of more than 5cm in size, which was confirmed by a bravo study. A DeMeester score of 446 was reported. The patient was referred for surgery and underwent transoral incisionless fundoplication with hiatal hernia repair. Despite the large size of the hiatal hernia, it was decided to proceed with a transoral incisionless fundoplication (TIF) procedure combined with hiatal hernia repair. The gastrectomy was chosen due to significant adhesions and anatomical distortion, making it difficult to continue laparoscopically. The esophagus was fibrosed to the pericardium, and the stomach was stuck in a retrocardiac position. Laparoscopic removal of the adhesions proved difficult since the patient had friable tissues, and there was a high risk of injury to surrounding organs. The surgery was therefore converted to an open approach, and the hernia was repaired with a gastrectomy. The TIF procedure was performed successfully, and the patient had no complications postoperatively. Conclusion This case details a successful transoral incisionless fundoplication procedure for GERD in a patient with an uncharacteristically large hiatal hernia. Despite the challenges posed by the hernia’s size and anatomical distortion, the TIF procedure combined with hiatal hernia repair was successful in providing relief from GERD symptoms, with no postoperative complications. The case highlights the potential suitability of TIF as an alternative to laparoscopic fundoplication in patients with large hiatal hernias, although gastrectomy may be necessary in cases with significant adhesions or anatomical distortion.
引言经口无切口胃底折叠术是一种新的手术方法,最近成为传统抗反流手术的潜在替代方案。这是一种微创的选择,并发症更少,恢复时间更短。疝修补术通常与经口无切口胃底折叠术结合使用,以改善疗效。在这种情况下,它详细介绍了一名患有长期胃食管反流病(GERD)的患者成功的经口无切口胃底折叠术和裂孔疝修补术。该病例是独特的,因为它涉及一名异常巨大的裂孔疝患者,其大小超过5厘米,通常不适合经口无切口胃底折叠术。由于食管裂孔疝的大小和粘连,用胃切除术而不是腹腔镜修复。病例详情本病例报告介绍了一名86岁的女性患者,她在过去10年中有长期GERD症状,但对药物治疗没有反应。内窥镜成像显示一个超过5厘米大小的疝,这一点得到了bravo研究的证实。据报道,德米斯特的得分为446。患者被转诊接受手术,并接受了经口无切口胃底折叠术和裂孔疝修补术。尽管裂孔疝体积较大,但仍决定采用经口无切口胃底折叠术(TIF)结合裂孔疝修补术。选择胃切除术是因为有明显的粘连和解剖扭曲,很难继续腹腔镜手术。食道被纤维包裹到心包,胃被卡在心后位置。腹腔镜切除粘连被证明是困难的,因为患者的组织易碎,并且周围器官损伤的风险很高。因此,手术改为开放式入路,并用胃切除术修复疝。TIF手术成功实施,患者术后无并发症。结论本病例详细介绍了一例经口无切口胃底折叠术成功治疗胃食管反流病的患者,该患者患有异常巨大的裂孔疝。尽管疝的大小和解剖结构扭曲带来了挑战,但TIF手术结合裂孔疝修补术成功地缓解了GERD症状,没有术后并发症。该病例强调了TIF作为腹腔镜胃底折叠术的替代方案在大裂孔疝患者中的潜在适用性,尽管在有严重粘连或解剖扭曲的情况下可能需要胃切除术。
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引用次数: 1
Monitoring of patients with active inflammatory bowel disease 活动性炎症性肠病患者的监测
Pub Date : 2023-05-25 DOI: 10.3389/fgstr.2023.1172318
T. Kucharzik, B. Verstockt, C. Maaser
In the current treat-to-target era, close and tight monitoring of patients with inflammatory bowel disease has become increasingly important. Although the importance of patient reported outcomes (PROMs) cannot be underestimated, its moderate association with biochemical and histo-endoscopic outcomes highlights the need for additional monitoring strategies. Endoscopic and histological remission are linked with improved long-term outcomes, but require more invasive assessments. Hence, non-invasive monitoring modalities are becoming increasingly relevant, with emerging evidence demonstrating the added clinical value of transmural assessment, both in Crohn’s disease and ulcerative colitis. The current review covers the multiple treatment targets present in IBD care, and focusses in particular on the increasing importance of intestinal ultrasound. Finally, we propose a potential algorithm to monitor patients with IBD in daily clinical practice and highlight gaps for future research in monitoring IBD strategies.
在当前的治疗目标时代,密切和严密监测炎症性肠病患者变得越来越重要。尽管患者报告结果(PROMs)的重要性不可低估,但其与生化和组织内窥镜结果的适度关联突出了需要额外的监测策略。内镜和组织学缓解与改善的长期预后有关,但需要更多的侵入性评估。因此,非侵入性监测模式正变得越来越重要,新出现的证据表明,在克罗恩病和溃疡性结肠炎中,跨壁评估具有附加的临床价值。目前的综述涵盖了IBD护理中存在的多种治疗目标,并特别关注肠道超声的重要性日益增加。最后,我们提出了一种在日常临床实践中监测IBD患者的潜在算法,并强调了未来IBD监测策略研究的空白。
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引用次数: 0
Molecular biomarkers of progression from Barrett’s esophagus to esophageal adenocarcinoma 巴雷特食管向食管腺癌进展的分子生物标志物
Pub Date : 2023-05-25 DOI: 10.3389/fgstr.2023.1007456
Luke Taylor, H. Alastal, A. Rasheed
Introduction Barrett’s esophagus (BO) is a pre-malignant condition for esophageal adenocarcinoma (OAC), the incidence rate of which has risen dramatically over the last four decades in the Western world. The 5-year survival rate of OAC is poor, and one of the ways to improve it would be by focusing on identifying high-risk Barrett’s patients through a surveillance program. Currently, histologic dysplasia is the only recognized marker of progression to OAC. Molecular biomarkers found in tissue samples that predict which patients have a higher risk of progression to OAC may act as a reliable tool for the stratification of patients with BO. Aim To determine whether molecular biomarkers have a potential use in predicting which patients with BO have a higher risk of progression to OAC. Methods Immunohistochemistry was performed on 25 tissue samples obtained from the endoscopic biopsies of 19 patients with confirmed BO. Hematoxylin and eosin (H&E) staining was used to confirm the presence of BO and dysplasia. Staining was performed in an external independent laboratory. Statistical analysis using the Mann–Whitney U test was performed using R Studio® statistical software. Results Of the 19 patients sampled, three had low-grade dysplasia (LGD), and all had confirmed metaplasia diagnostic of BO. Expression of cyclin D1 was noted to be elevated in patients with LGD compared with those with metaplasia only (p = 0.042). Expression of Sox2 was elevated in metaplastic BO cells compared with normal squamous cells within the same stain (p = 0.046). Of all eight biomarkers tested, β-catenin had the greatest overall expression (p < 0.004). Conclusions Isolating elevated cyclin D1 in patients with LGD highlights its potential use as a biomarker in identifying BO patients at risk of developing dysplasia, and, in turn, their possible progression to OAC. Elevated levels of both Sox2 and β-catenin may also serve as markers for disease progression when overexpressed in BO patients. Both conclusions, however, would need long-term follow-up to fully establish their prognostic usefulness, as at the time of writing no patients in this study had gone on to develop OAC. Although only a small sample size was present for this study, and follow-up was limited, it serves as a strong pilot for further research into the use of novel biomarkers in predicting which BO patients are at high risk of developing dysplasia and progressing to OAC.
引言Barrett食管(BO)是食管腺癌(OAC)的一种恶性前期疾病,其发病率在过去四十年中在西方世界急剧上升。OAC的5年生存率很低,改善它的方法之一是通过监测计划重点识别高危巴雷特患者。目前,组织学发育不良是唯一公认的OAC进展标志。在组织样本中发现的分子生物标志物可以预测哪些患者进展为OAC的风险更高,这可能是对BO患者进行分层的可靠工具。方法对19例确诊BO患者的25份组织标本进行免疫组织化学染色,苏木精-伊红(H&E)染色证实BO和异型增生的存在。染色在外部独立实验室进行。使用R Studio®统计软件进行Mann–Whitney U检验的统计分析。结果19例患者中,3例为低度异型增生(LGD),均确诊为BO化生。与仅化生患者相比,LGD患者的细胞周期蛋白D1表达升高(p=0.042)。与同一染色中的正常鳞状细胞相比,化生BO细胞中Sox2的表达升高(p=0.046)。在所有八种测试的生物标志物中,β-连环蛋白的总体表达最高(p<0.004)。结论在LGD患者中分离出升高的细胞周期蛋白D1,突出了其作为生物标志物的潜在用途,可以识别有发育不良风险的BO患者,进而识别他们可能进展为OAC。当在BO患者中过表达时,Sox2和β-catenin水平的升高也可能作为疾病进展的标志物。然而,这两个结论都需要长期随访,以完全确定其预后有用性,因为在撰写本文时,本研究中没有患者发展为OAC。尽管这项研究的样本量很小,随访也很有限,但它为进一步研究使用新的生物标志物预测哪些BO患者发展为发育不良和进展为OAC的高风险提供了有力的先导。
{"title":"Molecular biomarkers of progression from Barrett’s esophagus to esophageal adenocarcinoma","authors":"Luke Taylor, H. Alastal, A. Rasheed","doi":"10.3389/fgstr.2023.1007456","DOIUrl":"https://doi.org/10.3389/fgstr.2023.1007456","url":null,"abstract":"Introduction Barrett’s esophagus (BO) is a pre-malignant condition for esophageal adenocarcinoma (OAC), the incidence rate of which has risen dramatically over the last four decades in the Western world. The 5-year survival rate of OAC is poor, and one of the ways to improve it would be by focusing on identifying high-risk Barrett’s patients through a surveillance program. Currently, histologic dysplasia is the only recognized marker of progression to OAC. Molecular biomarkers found in tissue samples that predict which patients have a higher risk of progression to OAC may act as a reliable tool for the stratification of patients with BO. Aim To determine whether molecular biomarkers have a potential use in predicting which patients with BO have a higher risk of progression to OAC. Methods Immunohistochemistry was performed on 25 tissue samples obtained from the endoscopic biopsies of 19 patients with confirmed BO. Hematoxylin and eosin (H&E) staining was used to confirm the presence of BO and dysplasia. Staining was performed in an external independent laboratory. Statistical analysis using the Mann–Whitney U test was performed using R Studio® statistical software. Results Of the 19 patients sampled, three had low-grade dysplasia (LGD), and all had confirmed metaplasia diagnostic of BO. Expression of cyclin D1 was noted to be elevated in patients with LGD compared with those with metaplasia only (p = 0.042). Expression of Sox2 was elevated in metaplastic BO cells compared with normal squamous cells within the same stain (p = 0.046). Of all eight biomarkers tested, β-catenin had the greatest overall expression (p < 0.004). Conclusions Isolating elevated cyclin D1 in patients with LGD highlights its potential use as a biomarker in identifying BO patients at risk of developing dysplasia, and, in turn, their possible progression to OAC. Elevated levels of both Sox2 and β-catenin may also serve as markers for disease progression when overexpressed in BO patients. Both conclusions, however, would need long-term follow-up to fully establish their prognostic usefulness, as at the time of writing no patients in this study had gone on to develop OAC. Although only a small sample size was present for this study, and follow-up was limited, it serves as a strong pilot for further research into the use of novel biomarkers in predicting which BO patients are at high risk of developing dysplasia and progressing to OAC.","PeriodicalId":73085,"journal":{"name":"Frontiers in gastroenterology (Lausanne, Switzerland)","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2023-05-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"44865998","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
An exceptional finding in an explanted liver: a case report of cirrhotomimetic hepatocellular carcinoma 一个特殊的发现在一个外植肝:1例报告的模拟肝硬化肝细胞癌
Pub Date : 2023-05-24 DOI: 10.3389/fgstr.2023.1181037
E. Aby, Susan M. Lou, Khalid Amin, T. Leventhal
We present a case of cirrhotomimetic hepatocellular carcinoma (HCC) diagnosed on an explant following a liver transplantation (LT). The pre-LT computerized tomography (CT) scan demonstrated a nodular, cirrhotic-appearing liver; there was no evidence of lesions consistent with HCC. The level of serum alpha fetoprotein (AFP) 1 month pre LT was 4 ng/dL. Following LT, the patient underwent surveillance for HCC. Eight months post LT, he was noted to have lytic osseous lesions in his sternum and T10 vertebral body. Biopsies of these lesions demonstrated metastatic poorly differentiated carcinoma, which was concerning for progression to metastatic HCC. It is important to spread awareness of cirrhotomimetic HCC as it often evades detection by current screening methods, and if patients are inadvertently transplanted with a liver with cirrhotomimetic HCC, this can have significant consequences downstream. A multidisciplinary team approach is critical to ensure early detection of any recurrence and timely treatment.
我们报告了一例肝移植(LT)后在外植体上诊断为肝硬化样肝细胞癌(HCC)的病例。肝移植前计算机断层扫描(CT)显示肝结节,肝硬化;没有证据表明病变与HCC一致。LT前1个月血清甲胎蛋白(AFP)水平为4ng/dL。LT后,患者接受了HCC监测。LT后8个月,他发现胸骨和T10椎体有溶骨性病变。这些病变的活检显示转移性低分化癌,这与向转移性HCC的进展有关。传播对肝硬化样HCC的认识是很重要的,因为目前的筛查方法往往无法检测到它,如果患者无意中移植了肝硬化型HCC的肝脏,这可能会对下游产生重大影响。多学科团队方法对于确保早期发现任何复发并及时治疗至关重要。
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引用次数: 0
Gaps in obesity management in the UAE and the role of bariatric endoscopy 阿联酋肥胖管理的差距和减肥内窥镜检查的作用
Pub Date : 2023-05-05 DOI: 10.3389/fgstr.2023.1174640
Maryam Alkhatry
The definitions of overweight and obesity include increased fat storage that might compromise one’s health. According to the World Health Organization (WHO), an adult is considered overweight if their Body Mass Index (BMI) is greater than or equal to 25, and obese if their BMI is greater than or equal to 30. Age must be taken into account when defining overweight and obesity in children. The prevalence of obesity and overweight was reported to be at 21% and 33%, respectively, in the Middle East region. As obesity incidence rises with ageing, those over 40 were found to have the highest prevalence of obesity and overweight. According to the Central Intelligence Agency’s World Factbook, the UAE has a prevalence rate of obesity of 31.7%, making it one of the top 20 nations in the world for high obesity rates in 2016. The prevalence of overweight and obesity in the UAE is estimated to have increased between 1989 and 2017 threefold.
超重和肥胖的定义包括可能危害健康的脂肪储存增加。根据世界卫生组织(世界卫生组织)的说法,如果成年人的体重指数(BMI)大于或等于25,则被视为超重;如果他们的BMI大于或等于30,则被认为肥胖。在定义儿童超重和肥胖时,必须考虑年龄。据报道,中东地区的肥胖和超重患病率分别为21%和33%。随着年龄的增长,肥胖发病率也在上升,40岁以上的人肥胖和超重的患病率最高。根据中央情报局的《世界概况》,阿联酋的肥胖率为31.7%,是2016年世界上肥胖率最高的20个国家之一。据估计,1989年至2017年间,阿联酋超重和肥胖的患病率增加了三倍。
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引用次数: 0
Preventing acute diverticulitis. any roles for non-absorbable antibiotics? in search of evidence: a systematic review, meta-analysis, and trial sequential analysis 预防急性憩室炎。非吸收性抗生素有什么作用?寻找证据:系统综述、荟萃分析和试验序列分析
Pub Date : 2023-05-01 DOI: 10.3389/fgstr.2023.1170271
M. Koch, A. Maraolo, G. Natoli, S. Corrao
Background Hospital admissions for diverticulitis, a complication of diverticular disease, are very much on the increase. Prevention of diverticulitis could cut costs and save lives. Aims To identify whether the risk of the first episode of diverticulitis (primary prevention) or recurrence of diverticulitis (secondary prevention) can be reduced in patients with diverticular disease using non-absorbable antibiotics (mainly rifaximin). Methods The studies were identified by searching PubMed and CENTRAL from 1990 to May 2022. The methodological quality of each study was also evaluated. The outcome of the meta-analysis was the occurrence of a first or subsequent episode of diverticulitis. In addition, a trial sequential analysis was performed to evaluate whether the results would be subject to type I or type II errors. Results Primary prevention: the risk difference was statistically significant in favor of rifaximin (-0,019, or -1.9%, CI -0,6 to -3,3%). There was no evidence of heterogeneity (I2 0%). At one year, two years, and eight years of age, the NNT was 62, 52, and 42, respectively. The level of evidence had a moderate degree of certainty. Secondary prevention: the risk difference was statistically significant in favor of rifaximin (- 0,24, or -24%, CI -47 to -2%). There was evidence of heterogeneity (I2 92%); NNT resulted in 5. The grade level was low. Conclusions Rifaximin can lower the risk of a first episode of diverticulitis. However, the cost-benefit ratio currently appears too high. Rifaximin could also reduce the risk of a second episode, but the quality of the evidence is low. Systematic review registration https://www.crd.york.ac.uk/prospero/, identifier CRD42022379258.
背景:憩室炎是憩室疾病的一种并发症,因憩室炎住院的人数在不断增加。预防憩室炎可以降低成本,挽救生命。目的探讨使用非吸收性抗生素(主要是利福昔明)是否可以降低憩室疾病患者首次发作(一级预防)或复发(二级预防)的风险。方法通过PubMed和CENTRAL检索1990年至2022年5月的研究。对每项研究的方法学质量也进行了评估。荟萃分析的结果是首次或随后发生憩室炎。此外,进行了试验序列分析,以评估结果是否会受到I型或II型错误的影响。结果一级预防:利福昔明的风险差异有统计学意义(-0,019,或-1.9%,CI -0,6 ~ -3,3%)。没有证据表明存在异质性(i2%)。在1岁、2岁和8岁时,NNT分别为62、52和42。证据水平具有中等程度的确定性。二级预防:利福昔明的风险差异具有统计学意义(- 0,24或-24%,CI -47至-2%)。有证据表明存在异质性(I2 92%);NNT导致5人死亡。年级水平很低。结论利福昔明可降低憩室炎首次发作的风险。然而,成本效益比目前似乎过高。利福昔明也可以降低第二次发作的风险,但证据的质量很低。系统综述注册https://www.crd.york.ac.uk/prospero/,标识符CRD42022379258。
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引用次数: 0
Visual analysis of the research hotspots in neoadjuvant therapy for patients with gastric cancer 胃癌新辅助治疗研究热点可视化分析
Pub Date : 2023-04-28 DOI: 10.3389/fgstr.2023.1148787
Tian Chen, Yating Liu, Jing Gao, Dekui Zhang
Objective This study aimed to analyze the research hotspots and frontiers in the field of neoadjuvant therapy for patients with gastric cancer (GC) using bibliometric and identify its developmental trends. Methods The literature related to neoadjuvant therapy for GC systematically retrieved between 1991 and 2021. Bibliometric methods were used to analysis the research hotspots and trends by CiteSpace and VOS-viewer software. Results The number of studies related to neoadjuvant therapies for GC showed an upward trend. Moreover, the current research directions were mostly focused on the clinical trials and applications of neoadjuvant therapies for GC. The frontier research directions included microsatellite instability, peritoneal metastasis, randomized controlled trials, multicenter studies, and regression analysis. Conclusions The interest and attention of researchers in this field are still growing. In the past five years, the literature related to neoadjuvant therapy and immunotherapy for gastric cancer has exploded. It is still an important period and a key stage for the development of neoadjuvant therapy for gastric cancer.
目的应用文献计量学方法分析癌症新辅助治疗领域的研究热点和前沿,并确定其发展趋势。方法系统检索1991年至2021年间GC新辅助治疗的相关文献。通过CiteSpace和VOS查看器软件,采用文献计量方法分析研究热点和趋势。结果GC新辅助治疗的相关研究数量呈上升趋势。此外,目前的研究方向主要集中在GC新辅助治疗的临床试验和应用上。前沿研究方向包括微卫星不稳定性、腹膜转移、随机对照试验、多中心研究和回归分析。结论研究者对该领域的兴趣和关注仍在增长。在过去五年中,与癌症新辅助治疗和免疫疗法相关的文献呈爆炸式增长。目前仍是癌症新辅助治疗发展的重要时期和关键阶段。
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引用次数: 2
Editorial: Editors’ showcase: hepatology 社论:编辑的展示:肝病学
Pub Date : 2023-04-21 DOI: 10.3389/fgstr.2023.1198142
N. Verma, A. Singal
COPYRIGHT © 2023 Verma and Singal. This is an openaccess article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. TYPE Editorial PUBLISHED 21 April 2023 DOI 10.3389/fgstr.2023.1198142
版权所有©2023 Verma and Singal。这是一篇基于知识共享署名许可(CC BY)的开放获取文章。允许在其他论坛上使用、分发或复制,前提是要注明原作者和版权所有者,并根据公认的学术惯例引用本期刊的原始出版物。不遵守这些条款的使用、分发或复制是不被允许的。类型社论发表于2023年4月21日DOI 10.3389/fgstr.2023.1198142
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引用次数: 0
期刊
Frontiers in gastroenterology (Lausanne, Switzerland)
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