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Int J STD AIDS. 2019 Aug;30(9):834-842. doi: 10.1177/0956462419832750. Epub 2019 Jun 3.
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HIV Coinfection Predicts Failure of Ledipasvir/Sofosbuvir in Treatment-Naïve Noncirrhotic Patients With HCV Genotype 1.HIV合并感染预示初治的非肝硬化丙型肝炎病毒1型患者使用来迪派韦/索磷布韦治疗失败。
Open Forum Infect Dis. 2019 May 7;6(5):ofz214. doi: 10.1093/ofid/ofz214. eCollection 2019 May.
3
Hepatitis C treatment uptake and response among human immunodeficiency virus/hepatitis C virus-coinfected patients in a large integrated healthcare system.大型综合医疗系统中人类免疫缺陷病毒/丙型肝炎病毒合并感染患者的丙型肝炎治疗接受情况及反应
Int J STD AIDS. 2019 Jun;30(7):689-695. doi: 10.1177/0956462419836520. Epub 2019 May 2.
4
HCV Screening and Treatment Uptake Among Patients in HIV Care During 2014-2015.2014-2015 年 HIV 护理患者中的 HCV 筛查和治疗接受情况。
J Acquir Immune Defic Syndr. 2019 Apr 15;80(5):559-567. doi: 10.1097/QAI.0000000000001949.
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Has Access to Hepatitis C Virus Therapy Changed for Patients With Mental Health or Substance Use Disorders in the Direct-Acting-Antiviral Period?在直接作用抗病毒治疗时期,精神健康或物质使用障碍患者获得丙型肝炎病毒治疗的机会是否发生了变化?
Hepatology. 2019 Jan;69(1):51-63. doi: 10.1002/hep.30171. Epub 2018 Dec 18.
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Real-World Clinical Efficacy and Tolerability of Direct-Acting Antivirals in Hepatitis C Monoinfection Compared to Hepatitis C/Human Immunodeficiency Virus Coinfection in a Community Care Setting.真实世界中直接作用抗病毒药物治疗丙型肝炎单感染与丙型肝炎/人类免疫缺陷病毒合并感染的临床疗效和耐受性比较:社区护理环境下的研究。
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Hepatitis C Virus Elimination in the Human Immunodeficiency Virus-Coinfected Population: Leveraging the Existing Human Immunodeficiency Virus Infrastructure.在人类免疫缺陷病毒合并感染人群中消除丙型肝炎病毒:利用现有的人类免疫缺陷病毒基础设施。
Infect Dis Clin North Am. 2018 Jun;32(2):407-423. doi: 10.1016/j.idc.2018.02.005.
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Disparities in Initiation of Direct-Acting Antiviral Agents for Hepatitis C Virus Infection in an Insured Population.保险人群中丙型肝炎病毒感染直接作用抗病毒药物起始治疗的差异。
Public Health Rep. 2018 Jul/Aug;133(4):452-460. doi: 10.1177/0033354918772059. Epub 2018 May 11.
9
Hepatitis C virus treatment as prevention in people who inject drugs.丙型肝炎病毒治疗作为对注射吸毒者的预防措施。
Lancet Infect Dis. 2018 Apr;18(4):379. doi: 10.1016/S1473-3099(18)30130-0. Epub 2018 Mar 21.
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Race/ethnicity and insurance status disparities in access to direct acting antivirals for hepatitis C virus treatment.种族/民族和保险状况差异对丙型肝炎病毒治疗直接作用抗病毒药物的获取的影响。
Am J Gastroenterol. 2018 Sep;113(9):1329-1338. doi: 10.1038/s41395-018-0033-8. Epub 2018 Mar 9.

HIV/丙型肝炎病毒合并感染人群中丙型肝炎直接作用抗病毒治疗的障碍。

Barriers to hepatitis C direct-acting antiviral therapy among HIV/hepatitis C virus-coinfected persons.

机构信息

David Geffen School of Medicine, UCLA, Los Angeles, California, USA.

Division of Infectious Diseases, Department of Medicine, David Geffen School of Medicine, UCLA, Los Angeles, California, USA.

出版信息

J Gastroenterol Hepatol. 2021 Apr;36(4):1095-1102. doi: 10.1111/jgh.15228. Epub 2020 Sep 8.

DOI:10.1111/jgh.15228
PMID:32840904
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7904967/
Abstract

BACKGROUND AND AIM

Direct-acting antivirals (DAAs) have increased hepatitis C virus (HCV) treatment opportunities for vulnerable HIV/HCV coinfected persons. The aim of this study was to identify the frequency of and potential barriers to DAA prescription in HIV/HCV patients during the first few years of DAA availability in the United States.

METHODS

The AIDS Healthcare Foundation electronic medical record system was queried to identify all HCV viremic HIV-infected patients in care at AIDS Healthcare Foundation Healthcare centers in January 2015-August 2017 and compare characteristics by receipt of a DAA prescription. Multivariate logistic regression analyses were conducted to examine factors associated with DAA prescription.

RESULTS

Of 826 eligible patients, 355 (43%) were prescribed a DAA; among those not prescribed a DAA, 301 (64%) had well-controlled HIV (HIV RNA ≤ 200 copies per mL). In multivariate logistic regression analysis, patients with a history of substance use (odds ratio [OR], 0.51 [95% confidence interval 0.35-0.73]) or on select HIV antiretroviral regimens were less likely to be prescribed a DAA. Those who had well-controlled HIV (OR, 5.03 [3.06-8.27]), CD4 + T cell count >200 cells per mm (OR, 1.85 [1.04-3.30]), estimated glomerular filtration rate >60 mL/min/1.73 m (OR, 3.32 [1.08-10.15]), or established care prior to January 2015 (OR, 1.57 [1.08-2.29] were more likely to be prescribed a DAA.

CONCLUSIONS

In addition to lack of HIV suppression, select antiretroviral regimens, substance use, and kidney disease appeared to limit DAA prescription in the early interferon-free DAA era. Many were not prescribed DAAs despite HIV suppression. Further research is needed to determine if the observed associations persist today.

摘要

背景和目的

直接作用抗病毒药物(DAAs)增加了易感染艾滋病毒/丙型肝炎病毒(HCV)的脆弱人群的 HCV 治疗机会。本研究的目的是确定在美国 DAA 上市的最初几年中,HIV/HCV 合并感染患者中 DAA 处方的频率和潜在障碍。

方法

通过查询艾滋病保健基金会电子病历系统,确定 2015 年 1 月至 2017 年 8 月在艾滋病保健基金会医疗中心接受治疗的所有 HCV 病毒血症 HIV 感染患者,并比较接受 DAA 处方的患者的特征。采用多变量 logistic 回归分析方法,分析与 DAA 处方相关的因素。

结果

在 826 名合格患者中,355 名(43%)被开具了 DAA 处方;在未开具 DAA 处方的患者中,301 名(64%)HIV 得到了很好的控制(HIV RNA≤200 拷贝/ml)。在多变量 logistic 回归分析中,有药物滥用史(比值比[OR],0.51[95%置信区间 0.35-0.73])或使用特定 HIV 抗逆转录病毒方案的患者开具 DAA 的可能性较低。HIV 得到很好控制(OR,5.03[3.06-8.27])、CD4+T 细胞计数>200 个/平方毫米(OR,1.85[1.04-3.30])、估计肾小球滤过率>60ml/min/1.73m(OR,3.32[1.08-10.15])或在 2015 年 1 月之前建立治疗关系的患者更有可能被开具 DAA 处方。

结论

除了 HIV 抑制不足外,选择的抗逆转录病毒方案、药物滥用和肾脏疾病似乎限制了早期无干扰素 DAA 时代 DAA 的处方。尽管 HIV 得到了抑制,但许多人没有被开具 DAA 处方。需要进一步研究以确定观察到的关联是否仍然存在。