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Determining factors for dexmedetomidine sedation in endoscopic submucosal dissection for early-stage gastric cancer 在早期胃癌内镜黏膜下剥离术中使用右美托咪定镇静剂的决定因素
IF 1.7 Q3 GASTROENTEROLOGY & HEPATOLOGY Pub Date : 2024-05-10 DOI: 10.1002/jgh3.13065
Erika Yoshida, Yorimasa Yamamoto, Misako Tohata, Kuniyo Gomi, Tadashi Okayasu, Masatsugu Nagahama

Background and Aim

Although no specific sedation recommendations exist in early-stage gastric cancer (ESGC) for endoscopic submucosal dissection (ESD), dexmedetomidine (DEX) is useful along with benzodiazepines and analgesics. Furthermore, DEX is used for endoscopic treatment requiring lengthy sedation. However, it is unclear which patients should be administered DEX. We examined the factors that determine when DEX should be added for sedation during ESD for ESGC.

Methods

Of 316 patients undergoing ESD for ESGC at our hospital between January 2017 and December 2020, we examined 310 receiving intravenous anesthesia. Preoperative patient factors and treatment outcomes were retrospectively examined according to the sedation method.

Results

Among patients with ESGC undergoing ESD at our hospital, DEX was more frequently used alongside sedation in men, those undergoing gastrectomy, those with a lesion diameter ≥20 mm, and those with preoperative ulcers. In the standard group, patients whose treatment duration exceeded 120 min typically had a lesion diameter ≥20 mm, preoperative ulcers, lesions located outside the L region, and were treated by junior physicians.

Conclusion

It is important to evaluate specific preoperative factors (lesion diameter ≥20 mm, preoperative ulcers, lesion located outside the L region, and having a junior physician as the treating physician) in patients undergoing ESD for ESGC to determine whether the combined use of DEX in sedation is necessary.

背景和目的 虽然目前还没有针对早期胃癌(ESGC)内镜黏膜下剥离术(ESD)的特定镇静建议,但右美托咪定(DEX)与苯二氮卓类药物和镇痛剂一起使用还是很有用的。此外,右美托咪定还可用于需要长时间镇静的内窥镜治疗。然而,目前还不清楚哪些患者应该使用右美托咪定。我们研究了决定在ESGC的ESD治疗过程中添加DEX镇静的因素。 方法 在 2017 年 1 月至 2020 年 12 月期间,在我院接受 ESD 治疗 ESGC 的 316 例患者中,我们对 310 例接受静脉麻醉的患者进行了研究。根据镇静方法对患者的术前因素和治疗结果进行了回顾性研究。 结果 在我院接受ESD治疗的ESGC患者中,男性、接受胃切除术者、病变直径≥20毫米者以及术前有溃疡者在使用镇静剂的同时更多使用DEX。在标准组中,治疗时间超过 120 分钟的患者通常病变直径≥20 毫米、术前有溃疡、病变位于 L 区以外、由初级医师治疗。 结论 对接受ESD治疗的ESGC患者进行特定术前因素(病变直径≥20毫米、术前溃疡、病变位于L区以外、由低年资医生治疗)评估,以确定是否有必要在镇静中联合使用DEX,这一点非常重要。
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引用次数: 0
Implementing narrow banding imaging with dual focus magnification for histological prediction of small rectosigmoid polyps in Vietnamese setting 在越南采用双聚焦放大窄带成像技术,对直肠乙状结肠小息肉进行组织学预测
IF 1.7 Q3 GASTROENTEROLOGY & HEPATOLOGY Pub Date : 2024-05-10 DOI: 10.1002/jgh3.13058
Tien Manh Huynh, Quang Dinh Le, Nhan Quang Le, Huy Minh Le, Duc Trong Quach

Background and Aim

Small rectosigmoid colorectal polyps (<10 mm) are prevalent, with a low prevalence of advanced neoplastic lesions. The “diagnose-and-leave” strategy, employing narrow band imaging (NBI), is gaining popularity for its safety and cost-effectiveness by reducing polypectomy complications and minimizing histopathology expenses. This study assessed the diagnostic efficacy of NBI with dual focus (DF) magnification for real-time neoplastic prediction of rectosigmoid polyps and explored the feasibility of implementing this strategy in Vietnam.

Methods

In a prospective single-center study, 307 rectosigmoid polyps from 245 patients were analyzed using three consecutive endoscopic modes: white light endoscopy (WLE), NBI, and NBI-DF. Endoscopists assessed polyps for size, location, macroscopic shape, optical diagnosis, and confidence levels before histopathological evaluation. High confidence was assigned when the polyp exhibited all features of a single histology type. Predictions were compared with final histopathology results.

Results

Of the total, 237 (77.2%) were diminutive (≤5 mm) polyps, and 18 (5.8%) were advanced neoplastic lesions. WLE + NBI and WLE + NBI + NBI-DF exhibited significantly higher accuracy compared to WLE (88.6% and 90.2% vs 74.2%, P < 0.01). For diminutive polyps, the DF mode significantly increased the rate of high-confidence optical diagnoses (89.1% vs 94.9%, P < 0.001). WLE + NBI + NBI-DF demonstrated high sensitivity (90.1%), specificity (95.5%), and negative predictive value (93.4%) in high-confidence predictions, enabling the implementation of the “diagnose-and-leave” strategy. This approach would have reduced 58.2% of unnecessary polypectomies without missing any advanced neoplastic lesions.

Conclusion

NBI and DF modes provide accurate neoplastic predictions for rectosigmoid polyps. For diminutive polyps, DF magnification improves the confidence level of the optical diagnosis, allowing the safe implementation of the “diagnose-and-leave” strategy.

背景和目的 直肠乙状结肠小息肉(<10 mm)很常见,但晚期肿瘤病变的发病率很低。采用窄带成像(NBI)的 "诊断即切除 "策略因其安全性和成本效益而越来越受欢迎,因为它能减少息肉切除术的并发症,最大限度地降低组织病理学费用。本研究评估了采用双聚焦(DF)放大技术的 NBI 对直肠乙状结肠息肉进行实时肿瘤预测的诊断效果,并探讨了在越南实施这一策略的可行性。 方法 在一项前瞻性单中心研究中,使用三种连续的内窥镜模式:白光内窥镜(WLE)、NBI 和 NBI-DF,对 245 名患者的 307 个直肠乙状结肠息肉进行了分析。内镜医师在组织病理学评估前对息肉的大小、位置、宏观形状、光学诊断和置信度进行评估。当息肉表现出单一组织学类型的所有特征时,可信度高。预测结果与最终组织病理学结果进行了比较。 结果 237 例(77.2%)为小息肉(≤5 毫米),18 例(5.8%)为晚期肿瘤病变。与 WLE 相比,WLE + NBI 和 WLE + NBI + NBI-DF 的准确率明显更高(88.6% 和 90.2% vs 74.2%,P < 0.01)。对于微小息肉,DF 模式显著提高了高置信度光学诊断率(89.1% vs 94.9%,P < 0.001)。WLE + NBI + NBI-DF 在高置信度预测方面表现出较高的灵敏度(90.1%)、特异性(95.5%)和阴性预测值(93.4%),从而使 "诊断后即离开 "策略得以实施。这种方法可减少 58.2% 的不必要息肉切除术,同时不会漏掉任何晚期肿瘤病变。 结论 NBI 和 DF 模式能准确预测直肠乙状结肠息肉的肿瘤性。对于小息肉,DF 放大镜可提高光学诊断的置信度,从而安全地实施 "诊断后即离开 "策略。
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引用次数: 0
Integrated neural network and evolutionary algorithm approach for liver fibrosis staging: Can artificial intelligence reduce patient costs? 肝纤维化分期的综合神经网络和进化算法方法:人工智能能否降低患者成本?
IF 1.7 Q3 GASTROENTEROLOGY & HEPATOLOGY Pub Date : 2024-05-09 DOI: 10.1002/jgh3.13075
Ali Nazarizadeh, Touraj Banirostam, Taraneh Biglari, Mohammadreza Kalantarhormozi, Fatemeh Chichagi, Amir H Behnoush, Mohammad A Habibi, Ramin Shahidi

Background and Aim

Staging liver fibrosis is important, and liver biopsy is the gold standard diagnostic tool. We aim to design and evaluate an artificial neural network (ANN) method by taking advantage of the Teaching Learning-Based Optimization (TLBO) algorithm for the prediction of liver fibrosis stage in blood donors and hepatitis C patients.

Methods

We propose a method based on a selection of machine learning classification methods including multilayer perceptron (MLP) neural network, Naive Bayesian (NB), decision tree, and deep learning. Initially, the synthetic minority oversampling technique (SMOTE) is performed to address the imbalance in the dataset. Afterward, the integration of MLP and TLBO is implemented.

Results

We propose a novel algorithm that reduces the number of required patient features to seven inputs. The accuracy of MLP using 12 features is 0.903, while that of the proposed MLP with TLBO is 0.891. Besides, the diagnostic accuracy of all methods, except the model designed with the Bayesian network, increases when the SMOTE balancer is applied.

Conclusion

The decision tree-based deep learning methods show the highest levels of accuracy with 12 features. Interestingly, with the use of TLBO and seven features, MLP reached an accuracy rate of 0.891, which is quite satisfactory when compared with those of similar studies. The proposed model provides high diagnostic accuracy, while reducing the required number of properties from the samples. The results of our study show that the recruited algorithm of our study is more straightforward, with a smaller number of required properties and similar accuracy.

背景和目的 肝纤维化分期非常重要,而肝活检是金标准诊断工具。我们旨在利用基于教学的优化算法(TLBO)设计和评估一种人工神经网络(ANN)方法,用于预测献血者和丙型肝炎患者的肝纤维化分期。 方法 我们提出了一种基于机器学习分类方法的方法,包括多层感知器(MLP)神经网络、奈夫贝叶斯(NB)、决策树和深度学习。首先,采用合成少数超采样技术(SMOTE)来解决数据集中的不平衡问题。然后,实现 MLP 和 TLBO 的整合。 结果 我们提出了一种新颖的算法,将所需的患者特征数量减少到 7 个输入。使用 12 个特征的 MLP 的准确率为 0.903,而使用 TLBO 的拟议 MLP 的准确率为 0.891。此外,除了使用贝叶斯网络设计的模型外,所有方法的诊断准确率在使用 SMOTE 平衡器后都有所提高。 结论 基于决策树的深度学习方法在使用 12 个特征时显示出最高的准确率。有趣的是,在使用 TLBO 和 7 个特征的情况下,MLP 的准确率达到了 0.891,与同类研究相比,准确率相当令人满意。所提出的模型既能提供较高的诊断准确率,又能减少所需的样本属性数量。我们的研究结果表明,我们的研究中的招募算法更简单,所需的属性数量更少,准确率相似。
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引用次数: 0
Endoscopic mucosal phenotypes and endoscopic Sydney system gastritis assessment in relation to Helicobacter pylori infection and upper digestive clinical signs: A 2-year study among patients with gastroduodenal disorders in Cameroon 与幽门螺杆菌感染和上消化道临床症状相关的内镜粘膜表型和内镜悉尼系统胃炎评估:对喀麦隆胃十二指肠疾病患者进行的一项为期两年的研究
IF 1.7 Q3 GASTROENTEROLOGY & HEPATOLOGY Pub Date : 2024-05-08 DOI: 10.1002/jgh3.13060
Lionel Danny Tali Nguefak, Ghislaine Florice Faujo Nintewoue, Ngimgoh Ngemeshe Stanley, Paul Talla, Ghislaine Ngatcha, Sartre Michele Tagni, Nzoume Nsope Mengang Jude-Marcel, Dzoyem Jean Paul, Laure Brigitte Kouitcheu Mabeku

Background and Aim

Helicobacter pylori represents the major pathogen in the pathophysiology of diverse gastrointestinal conditions. This study sought to determine the endoscopic aspect of the gastric mucosa in relation to H. pylori infection in Cameroon.

Methods

This study was conducted in three reference health facilities in Cameroon from October 2020 to October 2022. The study enrolled 494 consecutive volunteer dyspeptic patients attending to the gastroenterology department of the selected health facilities. A description of the aspect of gastric mucosa of all participants was performed during endoscopy examination, and biopsies were collected for H. pylori detection using rapid urease tests.

Results

Gastritis, ulcerated lesions, duodenitis, esophagitis, normal mucosa aspect, bulbitis, and gastric neoplastic lesions were found in 40.1, 22.3, 10.9, 10.3, 9.7, 6.3, and 0.40% of biopsy samples, respectively. Erythematous/exudative (45.9%) and enterogastric reflux (12.2%) were the main gastritis types recorded. H. pylori was present in 58.1, 46.3, 87.1, 66.7, and 61.8% in gastritis, duodenitis, bulbitis, esophagitis, and ulcerated lesions, respectively. A positive relationship was noticed between the presence of H. pylori and gastritis (1.037 [0.720–1.493]; P = 0.845), bulbitis (4.237 [1.602–11.235]; P = 0.004), esophagitis (1.515 [0.822–2.793]; P = 0.183), ulcerated lesions (1.233 [0.798–1.904]; P = 0.345), erythematous/exudative gastritis (1.354 [0.768–2.389]; P = 0.295), and enterogastric reflux gastritis (1.159 [0.492–2.733]; P = 0.736).

Conclusion

Gastritis and erythematous/exudative gastritis are the most frequent gastrointestinal pathophysiology conditions in dyspeptic patient in our milieu. H. pylori infection is responsible for 94.8% of the gastrointestinal pathophysiology conditions with bulbitis as the condition is significantly associated with this bacterium infection.

背景和目的 幽门螺杆菌是多种胃肠道疾病病理生理学中的主要病原体。本研究旨在确定喀麦隆与幽门螺杆菌感染有关的胃黏膜内窥镜方面的情况。 方法 本研究于 2020 年 10 月至 2022 年 10 月在喀麦隆的三家参考医疗机构进行。研究共招募了 494 名连续就诊于所选医疗机构消化科的消化不良患者。在内镜检查中对所有参与者的胃黏膜进行了描述,并采集活检样本,使用快速尿素酶测试法检测幽门螺杆菌。 结果 40.1%、22.3%、10.9%、10.3%、9.7%、6.3% 和 0.40%的活检样本中发现了胃炎、溃疡病变、十二指肠炎、食管炎、粘膜正常、球部炎和胃肿瘤病变。红斑/渗出性(45.9%)和肠胃反流(12.2%)是记录的主要胃炎类型。幽门螺杆菌在胃炎、十二指肠炎、球部炎、食管炎和溃疡性病变中的感染率分别为58.1%、46.3%、87.1%、66.7%和61.8%。幽门螺杆菌与胃炎(1.037 [0.720-1.493]; P = 0.845)、十二指肠炎(4.237 [1.602-11.235]; P = 0.004)、食管炎(1.515 [0.822-2.793]; P = 0.183)、溃疡病变(1.233 [0.798-1.904];P = 0.345)、红斑/渗出性胃炎(1.354 [0.768-2.389];P = 0.295)和肠胃反流性胃炎(1.159 [0.492-2.733];P = 0.736)。 结论 胃炎和红斑/渗出性胃炎是消化不良患者最常见的胃肠道病理生理状况。94.8%的胃肠道病理生理学症状与幽门螺杆菌感染有关,其中球茎炎与幽门螺杆菌感染密切相关。
{"title":"Endoscopic mucosal phenotypes and endoscopic Sydney system gastritis assessment in relation to Helicobacter pylori infection and upper digestive clinical signs: A 2-year study among patients with gastroduodenal disorders in Cameroon","authors":"Lionel Danny Tali Nguefak,&nbsp;Ghislaine Florice Faujo Nintewoue,&nbsp;Ngimgoh Ngemeshe Stanley,&nbsp;Paul Talla,&nbsp;Ghislaine Ngatcha,&nbsp;Sartre Michele Tagni,&nbsp;Nzoume Nsope Mengang Jude-Marcel,&nbsp;Dzoyem Jean Paul,&nbsp;Laure Brigitte Kouitcheu Mabeku","doi":"10.1002/jgh3.13060","DOIUrl":"https://doi.org/10.1002/jgh3.13060","url":null,"abstract":"<div>\u0000 \u0000 \u0000 <section>\u0000 \u0000 <h3> Background and Aim</h3>\u0000 \u0000 <p><i>Helicobacter pylori</i> represents the major pathogen in the pathophysiology of diverse gastrointestinal conditions. This study sought to determine the endoscopic aspect of the gastric mucosa in relation to <i>H. pylori</i> infection in Cameroon.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Methods</h3>\u0000 \u0000 <p>This study was conducted in three reference health facilities in Cameroon from October 2020 to October 2022. The study enrolled 494 consecutive volunteer dyspeptic patients attending to the gastroenterology department of the selected health facilities. A description of the aspect of gastric mucosa of all participants was performed during endoscopy examination, and biopsies were collected for <i>H. pylori</i> detection using rapid urease tests.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Results</h3>\u0000 \u0000 <p>Gastritis, ulcerated lesions, duodenitis, esophagitis, normal mucosa aspect, bulbitis, and gastric neoplastic lesions were found in 40.1, 22.3, 10.9, 10.3, 9.7, 6.3, and 0.40% of biopsy samples, respectively. Erythematous/exudative (45.9%) and enterogastric reflux (12.2%) were the main gastritis types recorded. <i>H. pylori</i> was present in 58.1, 46.3, 87.1, 66.7, and 61.8% in gastritis, duodenitis, bulbitis, esophagitis, and ulcerated lesions, respectively. A positive relationship was noticed between the presence of <i>H. pylori</i> and gastritis (1.037 [0.720–1.493]; <i>P</i> = 0.845), bulbitis (4.237 [1.602–11.235]; <i>P</i> = 0.004), esophagitis (1.515 [0.822–2.793]; <i>P</i> = 0.183), ulcerated lesions (1.233 [0.798–1.904]; <i>P</i> = 0.345), erythematous/exudative gastritis (1.354 [0.768–2.389]; <i>P</i> = 0.295), and enterogastric reflux gastritis (1.159 [0.492–2.733]; <i>P</i> = 0.736).</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Conclusion</h3>\u0000 \u0000 <p>Gastritis and erythematous/exudative gastritis are the most frequent gastrointestinal pathophysiology conditions in dyspeptic patient in our milieu. <i>H. pylori</i> infection is responsible for 94.8% of the gastrointestinal pathophysiology conditions with bulbitis as the condition is significantly associated with this bacterium infection.</p>\u0000 </section>\u0000 </div>","PeriodicalId":45861,"journal":{"name":"JGH Open","volume":"8 5","pages":""},"PeriodicalIF":1.7,"publicationDate":"2024-05-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/jgh3.13060","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140895280","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Safety of DOACs in patients with Child-Pugh Class C cirrhosis and trial fibrillation DOACs 在 Child-Pugh C 级肝硬化和试验性心颤患者中的安全性
IF 1.7 Q3 GASTROENTEROLOGY & HEPATOLOGY Pub Date : 2024-05-02 DOI: 10.1002/jgh3.13074
Mark Ayoub, Carol Faris, Julton Tomanguillo Chumbe, Ebubekir Daglilar, Nadeem Anwar, Vishnu Naravadi

Background

Anticoagulation (AC) is used for stroke prevention in atrial fibrillation (AF). Direct Oral Anticoagulants (DOACs) are safe in patients with AF without cirrhosis, they are hardly studied in patients with advanced cirrhosis. Our study evaluates the safety and outcomes of DOACs in patients with Child-Pugh class C cirrhosis (CPC).

Methods

We queried TriNetX Database. Patients with CPC and AF were divided into three cohorts: patients on DOACs, no AC, and warfarin. Three study arms were created using a 1:1 propensity score matching system (PSM).

Results

Totally 16 029 patients met the inclusion criteria. Of those, 20.2% (n = 3235) were on DOACs, 47.1% (n = 7552) were not on AC, and 32.7% (n = 5242) were on warfarin. First arm comparing AC versus no AC, a statistically significant benefit was identified in 3-year mortality risk (47% vs 71%, P < 0.0001) and transplant status (17% vs 5%, p < 0.0001) with AC. However, no significant difference was identified regarding intracranial hemorrhage and GI bleeding risk. Second arm comparing patients on DOACs versus no AC, we identified mortality benefit (40% vs 72%, P < 0.0001) and a higher transplant rate (9% vs 3.2%, P < 0.0001) with DOACs. Intracranial hemorrhage rates (6% vs 4%, P = 0.03) were higher in patients on DOACs. Third arm comparing patients on DOACs versus Warfarin, a statistically significant lower risk of intracranial hemorrhage (6.6% vs 8.7%, P = 0.004) and GI bleed (2% vs 2.4%, P < 0.0001) were identified in patients on DOACs.

Conclusion

Anticoagulation is safe in patients with CPC with AF and may provide a mortality benefit. DOACs are a safer alternative to warfarin.

背景 抗凝(AC)用于预防房颤(AF)患者中风。直接口服抗凝药(DOACs)对未患肝硬化的房颤患者是安全的,但对晚期肝硬化患者几乎没有研究。我们的研究评估了 DOACs 在 Child-Pugh C 级肝硬化 (CPC) 患者中的安全性和疗效。 方法 我们查询了 TriNetX 数据库。CPC 和房颤患者被分为三个队列:使用 DOACs 的患者、不使用 AC 的患者和使用华法林的患者。使用 1:1 倾向评分匹配系统 (PSM) 创建了三个研究臂。 结果 共有 16 029 名患者符合纳入标准。其中,20.2%(n = 3235)使用 DOACs,47.1%(n = 7552)未使用 AC,32.7%(n = 5242)使用华法林。第一臂比较了使用 AC 与不使用 AC,发现使用 AC 在 3 年死亡风险(47% vs 71%,P < 0.0001)和移植状态(17% vs 5%,P < 0.0001)方面有显著统计学获益。但是,在颅内出血和消化道出血风险方面没有发现明显差异。第二组比较了使用 DOACs 和不使用 AC 的患者,我们发现使用 DOACs 有死亡率优势(40% vs 72%,P < 0.0001)和更高的移植率(9% vs 3.2%,P < 0.0001)。使用 DOACs 的患者颅内出血率更高(6% vs 4%,P = 0.03)。第三组将使用 DOACs 的患者与使用华法林的患者进行比较,发现使用 DOACs 的患者发生颅内出血(6.6% vs 8.7%,P = 0.004)和消化道出血(2% vs 2.4%,P < 0.0001)的风险显著低于使用华法林的患者。 结论 抗凝治疗对合并房颤的 CPC 患者是安全的,并可降低死亡率。DOACs 是一种比华法林更安全的替代药物。
{"title":"Safety of DOACs in patients with Child-Pugh Class C cirrhosis and trial fibrillation","authors":"Mark Ayoub,&nbsp;Carol Faris,&nbsp;Julton Tomanguillo Chumbe,&nbsp;Ebubekir Daglilar,&nbsp;Nadeem Anwar,&nbsp;Vishnu Naravadi","doi":"10.1002/jgh3.13074","DOIUrl":"https://doi.org/10.1002/jgh3.13074","url":null,"abstract":"<div>\u0000 \u0000 \u0000 <section>\u0000 \u0000 <h3> Background</h3>\u0000 \u0000 <p>Anticoagulation (AC) is used for stroke prevention in atrial fibrillation (AF). Direct Oral Anticoagulants (DOACs) are safe in patients with AF without cirrhosis, they are hardly studied in patients with advanced cirrhosis. Our study evaluates the safety and outcomes of DOACs in patients with Child-Pugh class C cirrhosis (CPC).</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Methods</h3>\u0000 \u0000 <p>We queried TriNetX Database. Patients with CPC and AF were divided into three cohorts: patients on DOACs, no AC, and warfarin. Three study arms were created using a 1:1 propensity score matching system (PSM).</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Results</h3>\u0000 \u0000 <p>Totally 16 029 patients met the inclusion criteria. Of those, 20.2% (<i>n</i> = 3235) were on DOACs, 47.1% (<i>n</i> = 7552) were not on AC, and 32.7% (<i>n</i> = 5242) were on warfarin. First arm comparing AC <i>versus</i> no AC, a statistically significant benefit was identified in 3-year mortality risk (47% <i>vs</i> 71%, <i>P</i> &lt; 0.0001) and transplant status (17% <i>vs</i> 5%, p &lt; 0.0001) with AC. However, no significant difference was identified regarding intracranial hemorrhage and GI bleeding risk. Second arm comparing patients on DOACs <i>versus</i> no AC, we identified mortality benefit (40% <i>vs</i> 72%, <i>P</i> &lt; 0.0001) and a higher transplant rate (9% <i>vs</i> 3.2%, <i>P</i> &lt; 0.0001) with DOACs. Intracranial hemorrhage rates (6% <i>vs</i> 4%, <i>P</i> = 0.03) were higher in patients on DOACs. Third arm comparing patients on DOACs <i>versus</i> Warfarin, a statistically significant lower risk of intracranial hemorrhage (6.6% <i>vs</i> 8.7%, <i>P</i> = 0.004) and GI bleed (2% <i>vs</i> 2.4%, <i>P</i> &lt; 0.0001) were identified in patients on DOACs.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Conclusion</h3>\u0000 \u0000 <p>Anticoagulation is safe in patients with CPC with AF and may provide a mortality benefit. DOACs are a safer alternative to warfarin.</p>\u0000 </section>\u0000 </div>","PeriodicalId":45861,"journal":{"name":"JGH Open","volume":"8 5","pages":""},"PeriodicalIF":1.7,"publicationDate":"2024-05-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/jgh3.13074","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140819019","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
A rare case of schwannoma of the small intestine discovered during intussusception 肠套叠时发现的罕见小肠裂孔瘤病例
IF 1.7 Q3 GASTROENTEROLOGY & HEPATOLOGY Pub Date : 2024-05-02 DOI: 10.1002/jgh3.13078
Sachiyo Onishi, Takashi Ibuka, Yukari Uno, Kentaro Kojima, Jun Takada, Masaya Kubota, Masahito Shimizu

A woman in her 60s with anemia was diagnosed with a small intestinal intussusception on computed tomography. She underwent a double-balloon endoscopy, which revealed submucosal tumor in the ileum. Suspected to be the cause of anemia and intussusception, surgical intervention was carried out, revealing it to be a schwannoma. Schwannomas of the small intestine are very rare, and because exophytic growths are common, intussusception due to luminal side development is even rarer.

一名 60 多岁的妇女患有贫血症,经计算机断层扫描确诊为小肠肠套叠。她接受了双气囊内窥镜检查,发现回肠黏膜下肿瘤。怀疑这是贫血和肠套叠的原因,于是进行了手术治疗,结果发现这是一个裂孔瘤。小肠的许旺瘤非常罕见,由于外生性生长很常见,因管腔侧发育而导致的肠套叠就更加罕见了。
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引用次数: 0
Double-blind, randomized, 8-week multicenter study of the efficacy and safety of STW 5-II versus placebo in functional dyspepsia STW 5-II 与安慰剂对功能性消化不良的疗效和安全性的双盲、随机、为期 8 周的多中心研究
IF 1.7 Q3 GASTROENTEROLOGY & HEPATOLOGY Pub Date : 2024-05-02 DOI: 10.1002/jgh3.13054
Bettina Vinson, Careen Fink, Manfred Wargenau, Nicholas J Talley, Gerald Holtmann

Background and Aim

Herbal products are widely used to treat patients with disorders of gut brain interaction but clinical efficacy and safety data for treatments lasting >4 weeks are widely lacking. We evaluated the efficacy and safety of 8 weeks of treatment with the herbal combination product STW 5-II for patients with functional dyspepsia (FD) meeting Rome II criteria. We also conducted a post hoc analysis including patients meeting Rome IV criteria for FD and evaluated the effect of the G-protein beta 3 (GNB3) subunit polymorphism (C825T) on therapeutic response.

Methods

This multicenter, placebo-controlled, double-blind study included 272 FD patients meeting Rome II criteria in the intention-to-treat cohort and 266 meeting Rome IV criteria. We used the validated Gastrointestinal Symptom Score (GIS) to assess GI symptoms, defining response rate as the proportion of patients with ≥50% GIS improvement in at least three of four assessments.

Results

After 8 weeks, the response rate was significantly higher in the STW 5-II group versus placebo (61.2% vs 45.1%, P = 0.008). Mean GIS non-significantly improved with STW 5-II treatment (7.9 ± 4.41 vs 6.7 ± 4.91 with placebo; P = 0.07). In the Rome IV subgroup analysis, STW 5-II yielded a better response rate (P = 0.01) versus placebo and greater postprandial distress symptom improvement (P = 0.04) versus placebo. Safety parameters did not differ between groups, and GNB3 status was not linked with therapeutic response.

Conclusion

STW 5-II is efficacious, with no observed safety signals at up to 8 weeks of treatment in patients with FD meeting Rome II or IV criteria.

背景和目的 草药产品被广泛用于治疗肠脑相互作用紊乱的患者,但目前普遍缺乏持续4周治疗的临床疗效和安全性数据。我们对符合罗马II标准的功能性消化不良(FD)患者使用草药复方产品STW 5-II治疗8周的疗效和安全性进行了评估。我们还对符合罗马IV标准的功能性消化不良患者进行了事后分析,并评估了G蛋白β3(GNB3)亚基多态性(C825T)对治疗反应的影响。 方法 这项多中心、安慰剂对照、双盲研究纳入了 272 名符合罗马 II 标准的 FD 患者和 266 名符合罗马 IV 标准的患者。我们使用有效的胃肠道症状评分(GIS)来评估胃肠道症状,将反应率定义为在四次评估中至少有三次GIS改善≥50%的患者比例。 结果 8周后,STW 5-II 组的应答率明显高于安慰剂组(61.2% vs 45.1%,P = 0.008)。STW 5-II 治疗后,平均 GIS 无显著改善(7.9 ± 4.41 vs 6.7 ± 4.91;P = 0.07)。在罗马 IV 亚组分析中,STW 5-II 的应答率(P = 0.01)高于安慰剂,餐后窘迫症状的改善程度(P = 0.04)高于安慰剂。各组之间的安全性参数没有差异,GNB3 状态与治疗反应无关。 结论 STW 5-II 疗效显著,对于符合罗马 II 或 IV 标准的 FD 患者,在长达 8 周的治疗中未观察到安全信号。
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引用次数: 0
Efficacy and safety of bismuth quadruple regimens containing minocycline and vonoprazan for eradication of Helicobacter pylori: Real-world evidence 含有米诺环素和沃诺普拉赞的铋剂四联疗法根除幽门螺旋杆菌的有效性和安全性:真实世界的证据
IF 1.7 Q3 GASTROENTEROLOGY & HEPATOLOGY Pub Date : 2024-05-01 DOI: 10.1002/jgh3.13070
Qiyunna He, Yan Ou, Huili Zhu, Zhiqian Chen, Dailan Yang, Qian Cheng, Xia Yin, Lina Xiao, Lin Cai, Yan Ye, Xin Xu, Juan Liao

Background and Aim

To evaluate the efficacy and safety of minocycline, vonoprazan, amoxicillin, and bismuth quadruple therapy for Helicobacter pylori (H. pylori) treatment.

Methods

From August 2022 to May 2023, clinical data were collected from patients who received H. pylori eradication treatment at West China Fourth Hospital, Sichuan University. One group received the MVAB regimen (amoxicillin, minocycline, vonoprazan, and colloidal bismuth pectin), while another group received the FOAB regimen (amoxicillin, furazolidone, omeprazole, and colloidal bismuth pectin), both administered for 14 days. Follow-up assessments of safety and compliance were conducted within 1 week after treatment completion. One and a half months after treatment, the success of eradication was evaluated using the urea breath test.

Results

For the MVAB regimen as a first-line treatment, the eradication rate was 90.1% (127/141, 95% CI: 85.1–95.1%) in the ITT analysis and 93.4% (127/136, 95% CI: 89.2–97.6%) in the PP analysis as a first-line treatment. As a second-line treatment, the eradication rate was 91.3% (21/23, 95% CI: 78.8–103.8%) in both analyses. For the FOAB regimen as a first-line treatment, the eradication rate was 98.0% (50/51, 95% CI: 94.1–101.2%) in the ITT analysis and 100% (50/50, 95% CI: 100%) in the PP analysis. As a second-line treatment, the eradication rate was 100% (6/6, 95% CI: 100%) in both analyses. Moreover, there was no significant difference in the incidence of adverse events between the two groups (MVAB regimen: 5.5% and FOAB regimen: 8.8%; P > 0.05).

Conclusions

The MVAB regimen could indeed be a viable alternative treatment option to conventional therapies.

背景和目的 评价米诺环素、冯诺普拉赞、阿莫西林和铋剂四联疗法治疗幽门螺杆菌(H. pylori)的疗效和安全性。 方法 从 2022 年 8 月至 2023 年 5 月,收集在四川大学华西第四医院接受幽门螺杆菌根除治疗的患者的临床数据。一组患者接受 MVAB 方案(阿莫西林、米诺环素、沃诺普拉赞和胶体果胶铋)治疗,另一组患者接受 FOAB 方案(阿莫西林、呋喃唑酮、奥美拉唑和胶体果胶铋)治疗,疗程均为 14 天。治疗结束后 1 周内对安全性和依从性进行随访评估。治疗一个半月后,使用尿素呼气试验评估根除效果。 结果 在 ITT 分析中,MVAB 方案作为一线治疗的根除率为 90.1%(127/141,95% CI:85.1-95.1%),在 PP 分析中,作为一线治疗的根除率为 93.4%(127/136,95% CI:89.2-97.6%)。作为二线治疗,两项分析的根除率均为 91.3%(21/23,95% CI:78.8-103.8%)。对于 FOAB 方案的一线治疗,ITT 分析中的根除率为 98.0%(50/51,95% CI:94.1-101.2%),PP 分析中的根除率为 100%(50/50,95% CI:100%)。作为二线治疗,两项分析的根除率均为 100%(6/6,95% CI:100%)。此外,两组的不良反应发生率无明显差异(MVAB 方案:5.5%;FOAB 方案:8.8%;P >;0.05)。 结论 MVAB疗法确实是传统疗法的一种可行的替代疗法。
{"title":"Efficacy and safety of bismuth quadruple regimens containing minocycline and vonoprazan for eradication of Helicobacter pylori: Real-world evidence","authors":"Qiyunna He,&nbsp;Yan Ou,&nbsp;Huili Zhu,&nbsp;Zhiqian Chen,&nbsp;Dailan Yang,&nbsp;Qian Cheng,&nbsp;Xia Yin,&nbsp;Lina Xiao,&nbsp;Lin Cai,&nbsp;Yan Ye,&nbsp;Xin Xu,&nbsp;Juan Liao","doi":"10.1002/jgh3.13070","DOIUrl":"https://doi.org/10.1002/jgh3.13070","url":null,"abstract":"<div>\u0000 \u0000 \u0000 <section>\u0000 \u0000 <h3> Background and Aim</h3>\u0000 \u0000 <p>To evaluate the efficacy and safety of minocycline, vonoprazan, amoxicillin, and bismuth quadruple therapy for <i>Helicobacter pylori</i> (<i>H. pylori</i>) treatment.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Methods</h3>\u0000 \u0000 <p>From August 2022 to May 2023, clinical data were collected from patients who received <i>H. pylori</i> eradication treatment at West China Fourth Hospital, Sichuan University. One group received the MVAB regimen (amoxicillin, minocycline, vonoprazan, and colloidal bismuth pectin), while another group received the FOAB regimen (amoxicillin, furazolidone, omeprazole, and colloidal bismuth pectin), both administered for 14 days. Follow-up assessments of safety and compliance were conducted within 1 week after treatment completion. One and a half months after treatment, the success of eradication was evaluated using the urea breath test.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Results</h3>\u0000 \u0000 <p>For the MVAB regimen as a first-line treatment, the eradication rate was 90.1% (127/141, 95% CI: 85.1–95.1%) in the ITT analysis and 93.4% (127/136, 95% CI: 89.2–97.6%) in the PP analysis as a first-line treatment. As a second-line treatment, the eradication rate was 91.3% (21/23, 95% CI: 78.8–103.8%) in both analyses. For the FOAB regimen as a first-line treatment, the eradication rate was 98.0% (50/51, 95% CI: 94.1–101.2%) in the ITT analysis and 100% (50/50, 95% CI: 100%) in the PP analysis. As a second-line treatment, the eradication rate was 100% (6/6, 95% CI: 100%) in both analyses. Moreover, there was no significant difference in the incidence of adverse events between the two groups (MVAB regimen: 5.5% and FOAB regimen: 8.8%; <i>P</i> &gt; 0.05).</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Conclusions</h3>\u0000 \u0000 <p>The MVAB regimen could indeed be a viable alternative treatment option to conventional therapies.</p>\u0000 </section>\u0000 </div>","PeriodicalId":45861,"journal":{"name":"JGH Open","volume":"8 5","pages":""},"PeriodicalIF":1.7,"publicationDate":"2024-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/jgh3.13070","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140819002","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Surveillance colonoscopy findings in asymptomatic participants over 75 years of age 75 岁以上无症状参与者的结肠镜监测结果
IF 1.7 Q3 GASTROENTEROLOGY & HEPATOLOGY Pub Date : 2024-05-01 DOI: 10.1002/jgh3.13071
Madelyn Agaciak, Molla M Wassie, Kalindra Simpson, Charles Cock, Peter Bampton, Robert Fraser, Erin L Symonds

Background and Aim

Surveillance colonoscopy for colorectal cancer (CRC) is generally not recommended beyond 75 years of age. The study determined incidence and predictors of advanced adenoma and CRC in older individuals undergoing surveillance colonoscopy.

Methods

This was a retrospective cohort study of asymptomatic older participants (≥75 years), enrolled in a South Australian CRC surveillance program who underwent colonoscopy (2015–2020). Clinical records were extracted for demographics, personal or family history of CRC, comorbidities, polypharmacy, and colonoscopy findings. The associations between clinical variables and advanced adenoma or CRC at surveillance were assessed with multivariable Poisson regression analysis.

Results

Totally 698 surveillance colonoscopies were analyzed from 574 participants aged 75–91 years (55.6% male). The incidence of CRC was 1.6% (11/698), while 37.9% (260/698) of procedures had advanced adenoma detected. Previous CRC (incidence rate ratio [IRR] 5.9, 95% CI 1.5–22.5), age ≥85 years (IRR 5.8, 95% CI 1.6–20.1) and active smoking (IRR 4.9, 95% CI 1.0–24.4) were independently associated with CRC diagnosis, while advanced adenoma at immediately preceding colonoscopy (IRR 1.6, 95% CI 1.3–2.0) and polypharmacy (IRR 1.2, 95% CI 1.0–1.5) were associated with advanced adenoma at surveillance colonoscopy in asymptomatic older participants (≥75 years).

Conclusion

Advanced neoplasia was found in more than one third of the surveillance procedures completed in this cohort. Continuation of surveillance beyond age 75 yeasrs may be considered in participants who have previous CRC or are active smokers (provided they are fit to undergo colonoscopy). In other cases, such as past advanced adenoma only, the need for ongoing surveillance should be considered alongside participant preference and health status.

背景和目的 一般不建议 75 岁以上的老年人接受结肠直肠癌 (CRC) 监控结肠镜检查。本研究确定了接受监视结肠镜检查的老年人中晚期腺瘤和 CRC 的发病率和预测因素。 方法 这是一项回顾性队列研究,研究对象是参加南澳大利亚州 CRC 监测计划并接受结肠镜检查(2015-2020 年)的无症状老年参与者(≥75 岁)。研究人员提取了临床记录,包括人口统计学特征、个人或家族 CRC 病史、合并症、多种药物治疗以及结肠镜检查结果。通过多变量泊松回归分析评估了临床变量与监测中的晚期腺瘤或 CRC 之间的关系。 结果 共对 574 名 75-91 岁的参与者(55.6% 为男性)进行了 698 次结肠镜监测分析。结肠癌的发病率为 1.6%(11/698),37.9%(260/698)的手术中发现了晚期腺瘤。既往患过 CRC(发病率比 [IRR] 5.9,95% CI 1.5-22.5)、年龄≥85 岁(IRR 5.8,95% CI 1.6-20.1)和主动吸烟(IRR 4.9,95% CI 1.0-24.4)与 CRC 诊断独立相关,而紧接结肠镜检查之前的晚期腺瘤(IRR 1.6,95% CI 1.3-2.0)和多药(IRR 1.2,95% CI 1.0-1.5)与无症状老年参与者(≥75 岁)接受结肠镜监测时的晚期腺瘤相关。 结论 该队列中超过三分之一的监测过程中发现了晚期肿瘤。对于既往患过 CRC 或吸烟者(只要他们适合接受结肠镜检查),可考虑在 75 岁以后继续进行监测。在其他情况下,如仅有过晚期腺瘤,则应结合参与者的偏好和健康状况来考虑是否需要持续监控。
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引用次数: 0
Effect of treatment periods on efficacy of glecaprevir and pibrentasvir in chronic hepatitis C: A nationwide, prospective, multicenter study 治疗周期对格列卡韦和匹布伦达韦治疗慢性丙型肝炎疗效的影响:一项全国性、前瞻性、多中心研究
IF 1.7 Q3 GASTROENTEROLOGY & HEPATOLOGY Pub Date : 2024-04-25 DOI: 10.1002/jgh3.13068
Atsuhiro Morita, Nobuharu Tamaki, Haruhiko Kobashi, Nami Mori, Keiji Tsuji, Shintaro Takaki, Chitomi Hasebe, Takehiro Akahane, Hironori Ochi, Toshie Mashiba, Naohito Urawa, Hideki Fujii, Akeri Mitsuda, Masahiko Kondo, Chikara Ogawa, Yasushi Uchida, Ryoichi Narita, Hiroyuki Marusawa, Yoshihito Kubotsu, Tomomichi Matsushita, Masaya Shigeno, Hideo Yoshida, Katsuaki Tanaka, Eisuke Okamoto, Toyotaka Kasai, Toru Ishii, Kazuhiko Okada, Masayuki Kurosaki, Namiki Izumi

Background and aim

In patients with chronic hepatitis C, 8 weeks of glecaprevir and pibrentasvir (GLE/PIB) treatment for chronic hepatitis (non-cirrhosis) and 12 weeks for cirrhosis have been approved in Japan. However, whether 8 weeks of treatment for cirrhosis may reduce treatment efficacy has not been adequately investigated.

Methods

This prospective, nationwide, multicenter cohort study enrolled 1275 patients with chronic hepatitis C who received GLE/PIB therapy. The effect of liver fibrosis and treatment periods on the efficiency of GLE/PIB therapy was investigated. The primary endpoint was the sustained virological response (SVR) rate in patients with chronic hepatitis (non-cirrhosis) and cirrhosis. The association between treatment periods and liver fibrosis on the SVR after 12 weeks of treatment rate was investigated.

Results

The SVR rates in patients with chronic hepatitis with 8 weeks of treatment, chronic hepatitis with 12 weeks of treatment, cirrhosis with 8 weeks of treatment, and cirrhosis with 12 weeks of treatment were 98.9% (800/809), 100% (87/87), 100% (166/166), and 99.1% (211/213), respectively, and were was not different among these groups (P = 0.4).

Conclusion

GLE/PIB therapy for chronic hepatitis C had high efficacy regardless of liver fibrosis status and treatment periods. Periods of GLE/PIB therapy could be chosen with available modalities, and high SVR rates could be achieved regardless of the decision.

背景和目的 对于慢性丙型肝炎患者,日本已批准对慢性肝炎(非肝硬化)患者进行为期 8 周的格列卡韦和匹布恩达韦(GLE/PIB)治疗,对肝硬化患者进行为期 12 周的格列卡韦和匹布恩达韦(GLE/PIB)治疗。然而,对肝硬化治疗 8 周是否会降低疗效尚未进行充分研究。 方法 这项前瞻性、全国性、多中心队列研究纳入了 1275 名接受 GLE/PIB 治疗的慢性丙型肝炎患者。研究调查了肝纤维化和治疗时间对 GLE/PIB 治疗效率的影响。主要终点是慢性肝炎(非肝硬化)和肝硬化患者的持续病毒学应答(SVR)率。研究还探讨了治疗周期和肝纤维化对 12 周治疗后 SVR 率的影响。 结果 治疗 8 周的慢性肝炎患者、治疗 12 周的慢性肝炎患者、治疗 8 周的肝硬化患者和治疗 12 周的肝硬化患者的 SVR 率分别为 98.9%(800/809)、100%(87/87)、100%(166/166)和 99.1%(211/213),且各组间无差异(P = 0.4)。 结论 GLE/PIB 疗法治疗慢性丙型肝炎疗效显著,与肝纤维化状态和治疗周期无关。GLE/PIB治疗的疗程可根据现有模式进行选择,无论做出何种决定,都能获得较高的SVR率。
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引用次数: 0
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