• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

[捷克共和国实际应用中艾尔巴韦/格拉瑞韦固定剂量组合的首次经验]

[First experience with elbasvir/grazoprevir fixed-dose combination in real-life practice in the Czech Republic].

作者信息

Husa Petr, Husová Libuše

机构信息

Department of Infectious Diseases University Hospital Brno, Czech Republic, e-mail:

出版信息

Klin Mikrobiol Infekc Lek. 2017 Dec;23(4):137-141.

PMID:29378382
Abstract

Hepatitis C virus infection (HCV) is one of the leading causes of chronic liver disease worldwide. The new fixed-dose combination of the highly potent second wave first generation NS5A inhibitor elbasvir (50 mg) and the second generation protease inhibitor grazoprevir (100 mg) is contained in the drug Zepatier. This combination is indicated for the treatment of patients chronically infected with HCV genotypes 1 or 4. Between June and August 2017, the treatment was initiated in 22 patients with chronic viral hepatitis C, with 17 patients being treated in the Department of Infectious Diseases University Hospital Brno and five patients in the Center of Cardiovascular and Transplant Surgery in Brno. All patients were infected with HCV subtype 1b. In all cases, the duration of Zepatier monotherapy (without simultaneous ribavirin administration) was 12 weeks. At the moment, only preliminary results are available. All 22 patients achieved end-of-treatment virologic response. In nine patients, it was already possible to evaluate the virologic response at four weeks after the end of treatment, with sustained virological response (SVR12) was observed in all these patients. The most common complaints were fatigue (3 patients, 14 %) and headache (2.9 %). These problems were not serious and did not interfere with normal daily activities of treated persons.

摘要

丙型肝炎病毒感染(HCV)是全球慢性肝病的主要病因之一。药物Zepatier含有高效第二代第一代NS5A抑制剂艾尔巴韦(50毫克)和第二代蛋白酶抑制剂格拉瑞韦(100毫克)的新型固定剂量组合。该组合适用于治疗HCV基因型1或4慢性感染的患者。2017年6月至8月期间,对22例慢性丙型病毒性肝炎患者开始进行治疗,其中17例在布尔诺大学医院传染病科接受治疗,5例在布尔诺心血管和移植外科中心接受治疗。所有患者均感染HCV 1b亚型。在所有病例中,Zepatier单药治疗(不同时给予利巴韦林)的疗程为12周。目前,仅有初步结果。所有22例患者均实现治疗结束时病毒学应答。在9例患者中,已能够在治疗结束后四周评估病毒学应答,所有这些患者均观察到持续病毒学应答(SVR12)。最常见的主诉是疲劳(3例患者,14%)和头痛(2.9%)。这些问题并不严重,未干扰接受治疗者的正常日常活动。

相似文献

1
[First experience with elbasvir/grazoprevir fixed-dose combination in real-life practice in the Czech Republic].[捷克共和国实际应用中艾尔巴韦/格拉瑞韦固定剂量组合的首次经验]
Klin Mikrobiol Infekc Lek. 2017 Dec;23(4):137-141.
2
Regulatory Analysis of Effects of Hepatitis C Virus NS5A Polymorphisms on Efficacy of Elbasvir and Grazoprevir.丙型肝炎病毒 NS5A 多态性对 Elbasvir 和 Grazoprevir 疗效影响的监管分析。
Gastroenterology. 2017 Feb;152(3):586-597. doi: 10.1053/j.gastro.2016.10.017. Epub 2016 Oct 20.
3
Safety and efficacy of elbasvir/grazoprevir in Asian participants with hepatitis C virus genotypes 1 and 4 infection.艾尔巴韦格拉瑞韦在亚洲 HCV 基因 1 型和 4 型感染患者中的安全性和疗效。
J Gastroenterol Hepatol. 2019 Sep;34(9):1597-1603. doi: 10.1111/jgh.14636. Epub 2019 Apr 17.
4
An Open-Label, Randomized, Active-Controlled Trial of 8 Versus 12 Weeks of Elbasvir/Grazoprevir for Treatment-Naive Patients With Chronic Hepatitis C Genotype 1b Infection and Mild Fibrosis (EGALITE Study): Impact of Baseline Viral Loads and NS5A Resistance-Associated Substitutions.一项评估替诺福韦艾拉酚胺(TAF)用于中国初治慢性乙型肝炎患者的有效性和安全性的随机、双盲、安慰剂对照、多中心 III 期临床研究
J Infect Dis. 2019 Jul 19;220(4):557-566. doi: 10.1093/infdis/jiz154.
5
Real-world use of elbasvir-grazoprevir in patients with chronic hepatitis C: retrospective analyses from the TRIO network.真实世界中使用 Elbasvir 和 Grazoprevir 治疗慢性丙型肝炎患者:TRIO 网络的回顾性分析。
Aliment Pharmacol Ther. 2018 Jun;47(11):1511-1522. doi: 10.1111/apt.14635. Epub 2018 Apr 17.
6
Elbasvir/Grazoprevir: A Review in Chronic HCV Genotypes 1 and 4.Elbasvir/Grazoprevir:治疗慢性 HCV 基因型 1 和 4 的综述。
Drugs. 2017 May;77(8):911-921. doi: 10.1007/s40265-017-0739-8.
7
Safety and efficacy of an 8-week regimen of grazoprevir plus ruzasvir plus uprifosbuvir compared with grazoprevir plus elbasvir plus uprifosbuvir in participants without cirrhosis infected with hepatitis C virus genotypes 1, 2, or 3 (C-CREST-1 and C-CREST-2, part A): two randomised, phase 2, open-label trials.在未患有肝硬化且感染 HCV 基因 1、2 或 3 型的参与者中,与格拉瑞韦/艾尔巴韦/奥比他韦相比,格拉瑞韦/鲁索那韦/乌帕司他韦 8 周疗程的安全性和疗效(C-CREST-1 和 C-CREST-2,A 部分):两项随机、2 期、开放性标签试验。
Lancet Gastroenterol Hepatol. 2017 Nov;2(11):805-813. doi: 10.1016/S2468-1253(17)30159-0. Epub 2017 Aug 10.
8
Grazoprevir and Elbasvir in Patients with Genotype 1 Hepatitis C Virus Infection: A Comprehensive Efficacy and Safety Analysis.格卡瑞韦联合 Elbasvir 治疗基因 1 型丙型肝炎病毒感染:全面的疗效和安全性分析。
Can J Gastroenterol Hepatol. 2017;2017:8186275. doi: 10.1155/2017/8186275. Epub 2017 Jan 9.
9
The efficacy and safety of elbasvir/grazoprevir treatment in HCV genotype 1 patients in Taiwan.在台湾地区,HCV 基因型 1 患者接受 Elbasvir/Grazoprevir 治疗的疗效和安全性。
J Med Virol. 2020 Feb;92(2):219-226. doi: 10.1002/jmv.25605. Epub 2019 Oct 22.
10
Grazoprevir plus elbasvir in HCV genotype-1 or -4 infected patients with stage 4/5 severe chronic kidney disease is safe and effective.格拉瑞韦联合艾尔巴韦格拉瑞韦治疗 4/5 期重度慢性肾脏病合并 HCV 基因型 1 或 4 感染患者是安全有效的。
Kidney Int. 2018 Jul;94(1):206-213. doi: 10.1016/j.kint.2018.02.019. Epub 2018 May 5.