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Clinical Liver Disease最新文献

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Epidemiology, natural history, and management of patients with CHB concurrent with MASLD. CHB并发MASLD患者的流行病学、自然病史和管理。
Pub Date : 2024-06-19 eCollection Date: 2024-01-01 DOI: 10.1097/CLD.0000000000000171
Wenjing Ni, Junping Shi, Jie Li
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引用次数: 0
Management of chronic hepatitis B infection in children. 儿童慢性乙型肝炎感染的管理。
Pub Date : 2024-06-14 eCollection Date: 2024-01-01 DOI: 10.1097/CLD.0000000000000156
Huey-Ling Chen
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引用次数: 0
Management of patients with CHB outside the guidelines: Insights from Egyptian cohort with long-term follow-up. 指南之外的慢性阻塞性肺病患者管理:埃及队列长期随访的启示。
Pub Date : 2024-06-14 eCollection Date: 2024-01-01 DOI: 10.1097/CLD.0000000000000183
Gamal Shiha, Riham Soliman, Ayman Hassan, Ahmed Farahat, Ahmed Salem, Amr Taha, Ramy Sabry, Ahmed Geith, Ahmed Elshawaf, Nabiel Mikhail

It is alarming that globally, only 2.2% (6.6 million) of patients with chronic hepatitis B (CHB) received treatment in 2019. One contributing factor to this low treatment rate is the complexity and restrictive nature of clinical practice guidelines. Since 1998, we have adopted a "treat-all" approach to patients with CHB. A retrospective study was conducted involving patients with CHB who received treatment from 1998 to 2020 at 2 institutions in Egypt. These patients underwent evaluation through various clinical and laboratory methods, which included testing for liver enzymes and HBV DNA. The study analyzed 1825 patients with HBV, finding that 27.4% had viremia levels under 2000 IU/mL. Most (88%) were HBeAg-negative, with 12% positive. A large portion (77.6%) had normal alanine aminotransferase levels, though 5.6% exceeded twice the upper limit of normal. About 14.2% were diagnosed with liver cirrhosis, and 9.6% with F3 stage fibrosis at enrollment. Notably, 2% (25 cases) lost HBsAg over a median of 52 months. Patients with HBV DNA <2000 IU/mL had a higher HBsAg loss rate (4.2%) compared to those with levels >2000 IU/mL (1.3%). During follow-up, 9.5% (117 patients) experienced decompensation, with a higher incidence in those with HBV DNA <2000 IU/mL (16.8%) than those >2000 IU/mL (7.1%). HCC developed in 5.2% of patients with lower HBV DNA and 2.6% with higher levels, showing significant differences. Liver-related deaths occurred in 2.8% of the cohort, with a slightly higher rate in those with lower initial HBV DNA levels (3.5% vs. 2.5%). The findings suggest a paradigm shift in CHB management toward early and broader eligibility for antiviral therapy. This could improve patient outcomes and address the global treatment gap in CHB management, especially in regions with high CHB prevalence.

令人震惊的是,2019 年全球仅有 2.2% (660 万)的慢性乙型肝炎(CHB)患者接受了治疗。导致治疗率如此之低的一个因素是临床实践指南的复杂性和限制性。自 1998 年以来,我们一直对慢性乙型肝炎患者采取 "全面治疗 "的方法。我们开展了一项回顾性研究,涉及 1998 年至 2020 年期间在埃及两家机构接受治疗的 CHB 患者。这些患者接受了各种临床和实验室方法的评估,包括肝酶和 HBV DNA 检测。研究分析了 1825 名 HBV 患者,发现 27.4% 的患者病毒血症水平低于 2000 IU/mL。大多数患者(88%)HBeAg阴性,12%阳性。大部分人(77.6%)的丙氨酸氨基转移酶水平正常,但有 5.6% 的人超过了正常值上限的两倍。约有 14.2% 的人被确诊为肝硬化,9.6% 的人在入组时处于 F3 阶段的肝纤维化。值得注意的是,有 2% 的患者(25 例)在中位 52 个月内失去了 HBsAg。HBV DNA 为 2000 IU/mL 的患者占 1.3%。在随访期间,9.5%(117 例)的患者出现了失代偿,其中 HBV DNA 为 2000 IU/mL 的患者发生率更高(7.1%)。在 HBV DNA 水平较低和较高的患者中,分别有 5.2% 和 2.6% 的患者发展为 HCC,差异显著。2.8%的患者死于肝脏相关疾病,其中初始 HBV DNA 水平较低的患者死亡率略高(3.5% 对 2.5%)。研究结果表明,慢性阻塞性肺病的管理模式应向早期和更广泛的抗病毒治疗资格转变。这可以改善患者的预后,解决全球 CHB 管理中的治疗差距,尤其是在 CHB 高发地区。
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引用次数: 0
A severe case of hypercalcemia in a patient with presumed cryptogenic cirrhosis. 一例推测为隐源性肝硬化患者的严重高钙血症病例。
Pub Date : 2024-06-14 eCollection Date: 2024-01-01 DOI: 10.1097/CLD.0000000000000230
Agnieszka Maniak, Nancy Reau
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引用次数: 0
Noncirrhotic portal hypertension-Historical perspectives bring clarity to the entity and its management. 非肝硬化性门脉高压症--历史的视角让这一疾病及其治疗更加清晰。
Pub Date : 2024-06-14 eCollection Date: 2024-01-01 DOI: 10.1097/CLD.0000000000000232
Cyriac Abby Philips, Shiv K Sarin
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引用次数: 0
The role of patient-reported outcomes in a patient-centered care model for managing chronic liver diseases. 患者报告结果在以患者为中心的慢性肝病管理模式中的作用。
Pub Date : 2024-06-14 eCollection Date: 2024-01-01 DOI: 10.1097/CLD.0000000000000222
Manisha Verma, Archita P Desai
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引用次数: 0
Review of immune therapy in HCC: Where are we now and what is the future? 回顾 HCC 的免疫疗法:现状与未来?
Pub Date : 2024-06-14 eCollection Date: 2024-01-01 DOI: 10.1097/CLD.0000000000000149
Valentina Zanuso, Angelo Pirozzi, Giulia Tesini, Lorenza Rimassa
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引用次数: 0
Hepatotoxicity in inflammatory bowel disease: Immunomodulators, biologics, and beyond. 炎症性肠病的肝毒性:免疫调节剂、生物制剂及其他。
Pub Date : 2024-06-14 eCollection Date: 2024-01-01 DOI: 10.1097/CLD.0000000000000199
Helgi K Björnsson, Einar S Björnsson
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引用次数: 0
(P)rehabilitation in advanced chronic liver disease (advCLD): From basic exercise concepts to implementation challenges. (晚期慢性肝病(advCLD)的(康复)治疗:从基本运动概念到实施挑战。
Pub Date : 2024-06-14 eCollection Date: 2024-01-01 DOI: 10.1097/CLD.0000000000000184
Andrew P Kassa, Jonathan G Stine
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引用次数: 0
Ethics in hepatology: A professional and very personal journey. 肝病学的伦理:专业和个人的旅程。
Pub Date : 2024-06-14 eCollection Date: 2024-01-01 DOI: 10.1097/CLD.0000000000000231
Dirk J van Leeuwen
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引用次数: 0
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Clinical Liver Disease
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