Hepatitis C: Treatment of difficult to treat patients

被引:1
|
作者
Eric G Hilgenfeldt [1 ]
Alex Schlachterman [2 ]
Roberto J Firpi [2 ,3 ]
机构
[1] Department of Internal Medicine, University of Florida College of Medicine
[2] Department of Gastroen-terology, Hepatology and Nutrition, University of Florida College of Medicine
[3] Section of Hepatobiliary Diseases and Trans-plantation, University of Florida
关键词
Hepatitis C virus; Direct acting antiviral; Human immunodeficiency virus; Cirrhosis; Treatment experienced;
D O I
暂无
中图分类号
R512.63 [];
学科分类号
100401 ;
摘要
Over the past several years, more so recently, treatment options for hepatitis C virus(HCV) have seemed to exponentially grow. Up until recently, the regimen of pegylated interferon(peg-IFN) and ribavirin(RBV) stood as the standard of care. Direct acting antivirals, which target nonstructural proteins involved in replication and infection of HCV were first approved in 2011 as an addition to the peg-IFN and RBV regimen and with them have come increased sustained virological response rates(SVR). The previously reported 50%-70% SVR rates using the combination of peg-IFN and RBV are no longer the standard of care with direct acting antiviral(DAA) based regimens now achieving SVR of 70%-90%. PegIFN free as well as "all oral" regimens are also available. The current randomized controlled trials available show favorable SVRs in patients who are naive to treatment, non-cirrhotic, and not human immunodeficiency virus(HIV)-co-infected. What about patients who do not fit into these categories? In this review, we aim to discuss the currently approved and soon to be approved DAAs while focusing on their roles in patients that are treatment experienced, cirrhotic, or co-infected with HIV. In this discussion, review of the clinical trials leading to recent consensus guidelines as well as discussion of barriers to treatment will occur. A case will attempt will be made that social services, including financial support and drug/alcohol treatment, should be provided to all HCV infected patients to improve chances of cure and thus prevention of late stage sequela.
引用
收藏
页码:1953 / 1963
页数:11
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