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Hepatitis C Curriculum

Introduction1 Item

Hepatitis C Core Curriculum Introduction

The Hepatitis C Core Curriculum provides an outline to IDSA members of the foundational knowledge points for treating hepatitis C virus (HCV). The core curriculum provides self-guided, structured learning by directing users to publicly available educational resources. Upon completion of the Hepatitis C Core Curriculum, a clinician should be able to understand the pathogenesis of HCV, identify patients susceptible to HCV infection, perform critical pre-treatment evaluations to determine the most viable treatment option, and manage the complexities of patients undergoing treatment.

The Hepatitis C Curriculum was developed by the IDSA HCV Core Curriculum Work Group that consisted of Infectious Diseases Fellowship Program Directors from medical schools across the nation.

IDSA HCV Core Curriculum Work Group Members:

Susanna Naggie, MD, Duke University School of Medicine
Michael Melia, MD, Johns Hopkins University
Lisa Dever, MD, Rutgers New Jersey Medical School
Stacey Rizza, MD, Mayo Clinic College of Medicine
Dawd Siraj, MD, Brody School of Medicine at East Carolina University

 

To report broken links and suggest resources, please contact Danielle Heiny at dheiny@idsociety.org.

I. Pathogenesis: Virology5 Items

Virology

Vanderbilt University: The Flexner Discovery Lecture Series 4/30/2009

Dr. Charles Rice - “HCV:20  years Later”

This video lecture provides information on topics that include, but are not limited, to the following:
• HCV genotypes
• Progression of HCV
• Treatment of HCV
• HCV life cycle
• HCV entry – a multistep process
• RNA genome structure and organization
• HCV RNA replication
• Targets for antiviral drug development

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Virology

University of Washington

Dr. Stephen Polyak - “Molecular Virology of Hepatitis C Virus”

This video provides information on topics that include, but are not limited, to the following:
• HCV Genome
• Composition of hepatitis c virus
• HCV receptors/entry factors
• HCV life cycle key features
• HCV genotypes and quasispecies
• Drugs to fight HCV infection
• Targeting host cell functions required for HCV replication
• Complementary and alternative medicine

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Virology

Center for the Study of Hepatitis C

Hepatitis C Life-Cycle

The Center for the Study of Hepatitis C provides an interactive presentation on the sequence of biological events explaining how HCV enters a liver cell, makes copies of itself, and then exits to infect other cells. This process and the ensuing host immune response lead to cell damage that is the hallmark of liver disease.

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Virology

Published: ; 2007 ; 25 : 71 -99

Annual Review of Immunology

Flying Under the Radar: The Immunobiology of Hepatitis C

The hepatitis C virus (HCV) is a remarkably successful pathogen, establishing persistent infection in more than two-thirds of those who contract it. Its success is related to its abilities to blunt innate antiviral pathways and to evade adaptive immune responses. These two themes may be related. We propose that HCV takes advantage of the impaired innate response to delay the organization of an effective adaptive immune attack. The tolerogenic liver environment may provide cover, prolonging this delay. HCV's error-prone replication strategy permits rapid evolution under immune pressure. Persistent high levels of viral antigens may contribute to immune exhaustion. Finally, the virus may benefit from the efficient enlistment of memory T and B cells in the pursuit of a moving target.

Virology

Department of Veterans Affairs

Hepatitis C Genotypes and Quasispecies

The Department of Veterans Affairs’ topic review of Hepatitis C Genotypes and Quasispecies provides information on HCV genotypes, the clinical significance of hepatitis C genotypes, quasispecies and viral mutation, and clinical significance of quasispecies.  

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I. Pathogenesis: Immunology5 Items

Immunology

University of Washington Lecture Series 2009

Dr. Stanley Lemon – “Hepatitis C Virus and Hepatocellular Carcinoma”

This video provides information on topics that include, but are not limited, to the following:
• HCV pathogenesis
• Emergence of HCV-related liver cancer
• How HCV causes liver cancer
• Role of c-Myc responsive genes in malignant conversion
• Host factors in HCV replication and pathogenesis
• NS5B regulation of pRb
• HCV interactions with tumor suppressors and HCC

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Immunology

University of Washington Lecture Series 2009

Dr. Michael Gale – “Hepatitis C Virus Infection and Immunity”

This video provides information on topics that include, but are not limited, to the following:
• Spontaneous resolution of acute HCV
• Differential host response gene expression in HCV infection
• HCV: multiple interactions to antagonize interferon
• Acute HCV and progression to chronic infection
• HCV envelope proteins
• Hepatic interactions of immune cells in HCV liver
• CD4+ T cells determining outcome
• HCV persistence associate with evolution of CTL epitopes

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Immunology

Published: ; 2007 ; 4 : 622 -634

Nature Review Gastroenterology and Hepatology

Mechanisms of Disease: HCV-induced liver injury

HCV persistently infects the majority of patients exposed to it and can cause irreversible fibrosis, leading to the onerous clinical sequelae of cirrhosis. In this Review, we discuss the direct effects of HCV on hepatocytes and the role of the immune system in liver damage. HCV, like many viruses, has developed methods by which to subvert host innate and adaptive immune responses to infection. HCV proteins seem to modulate apoptosis and steatosis, ultimately leading to hepatic stellate cell activation, fibrosis and hepatocellular carcinoma. In addition, HCV manipulates the immune system, disrupting both innate and adaptive immunity to establish persistent infection. The immune system initially attempts to eradicate the virus, but, in the setting of chronic infection, probably promotes hepatocyte damage and fibrosis through direct cellular toxicity and the release of inflammatory cytokines. Multiple types of cytotoxic lymphocytes, comprising the unique immune hepatic microenvironment, are likely to be important in the pathogenesis of HCV-induced liver damage. The net liver damage from HCV infection depends on the balance between the host's antiviral mechanisms and the virus' ability to subvert them.

Immunology

Published: ; 2005 ; 436 : 946 -952

Nature

Adaptive immune responses in acute and chronic hepatitis C virus infection

The hepatitis C virus (HCV) persists in the majority of infected individuals and is a significant cause of human illness and death globally. Recent studies have yielded important insights into immunity to HCV, in particular revealing the central role of T cells in viral control and clearance. Other key features of adaptive immune responses remain obscure, including mechanisms by which T cells control HCV replication, the role of antibodies in conferring protection and how cellular and humoral immunity are subverted in persistent infection.

Immunology

Published: ; 2009 ; 119 : 1745 -1754

The Journal of Clinical Investigation

Hepatitis C virus versus innate and adaptive immune responses: a tale of
coevolution and coexistence

Since the identification of the hepatitis C virus (HCV) 20 years ago, much progress has been made in our understanding of its life cycle and interaction with the host immune system. Much has been learned from HCV itself, which, via decades of coevolution, gained an intricate knowledge of host innate and adaptive immune responses and developed sophisticated ways to preempt, subvert, and antagonize them. This review discusses the clinical, virological, and immunological features of acute and chronic hepatitis C and the role of the immune response in spontaneous and treatment-induced HCV clearance.

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I. Pathogenesis: Genetic Markers for Treatment Response3 Items

Genetic Markers of Treatment Response

American Gastroenterological Association

Hepatic Cell-Type Specific Gene Expression is a Better Predictor of HCV
Treatment Outcome than IL28B Genotype

Cell-type specific expression patterns of hepatic interferon-stimulated genes (ISGs) and single nucleotide polymorphisms (SNPs) near the IL28B gene are associated with response to interferon-based therapy in patients with chronic hepatitis C virus (HCV) infection. A study in the May issue of Gastroenterology finds that cell-type–specific expression pattern of ISGs varies among patients with different IL28B genotypes and is a strong predictor of response to interferon-based treatment. Dr. Kuemmerle discusses these findings with author Dr. Jordan Feld of the University of Toronto; Plus, a rundown of top stories from this month's issue of GI and Hepatology News.

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Genetic Markers of Treatment Response

Published: ; 2012 ; 9 : 406 -417

Nature Reviews Gastroenterology and Hepatology

Genetics of IL28B and HCV – response to infection and treatment

The IL28B locus attracted the attention of HCV researchers after a series of genome-wide association studies independently identified a strong association between common IL28B polymorphisms and the outcome of PEG-IFN-α plus ribavirin combination therapy in patients chronically infected with HCV genotype 1. This association was subsequently replicated for other HCV genotypes and has been linked to spontaneous eradication of HCV, development of steatosis and biochemical changes (such as altered levels of γ-glutamyl transpeptidase and LDL). Despite the introduction of direct-acting antiviral drugs, IL28B genetics are likely to play a part in patient selection and treatment decisions—moving towards a personalized approach to therapy. In HCV-infected patients with the so-called favourable IL28B genotype (rs12979860 CC; associated with better treatment response), hepatic expression levels of IL28B and interferon-stimulated genes seem to be reduced at baseline, but are induced more strongly after IFN-α administration, perhaps resulting in more effective elimination of the virus. Clarification of the mechanisms underlying these biological phenomena will lead to improved understanding of the antiviral effects of IFN-λ and, ideally, to the development of better therapies against HCV infection. This Review summarizes current understanding of the role of IL28B in HCV infection and response to therapy.

Genetic Markers of Treatment Response

Published: ; 2009 ; 461 : 399 -401

Nature

Genetic variation in IL28B predicts hepatitis C treatment-induced viral
clearance

Chronic infection with hepatitis C virus (HCV) affects 170 million people worldwide and is the leading cause of cirrhosis in North America1. Although the recommended treatment for chronic infection involves a 48-week course of peginterferon-α-2b (PegIFN-α-2b) or -α-2a (PegIFN-α-2a) combined with ribavirin (RBV), it is well known that many patients will not be cured by treatment, and that patients of European ancestry have a significantly higher probability of being cured than patients of African ancestry. In addition to limited efficacy, treatment is often poorly tolerated because of side effects that prevent some patients from completing therapy. For these reasons, identification of the determinants of response to treatment is a high priority. Here we report that a genetic polymorphism near the IL28B gene, encoding interferon-λ-3 (IFN-λ-3), is associated with an approximately twofold change in response to treatment, both among patients of European ancestry (P = 1.06 × 10-25) and African-Americans (P = 2.06 × 10-3). Because the genotype leading to better response is in substantially greater frequency in European than African populations, this genetic polymorphism also explains approximately half of the difference in response rates between African-Americans and patients of European ancestry.

II. Appropriate Testing/Screening for HCV: Screening2 Items

Screening

Centers for Disease Control and Prevention, Morbidity and Mortality Weekly Report

Recommendations for the Identification of Chronic Hepatitis C Virus Infection
Among Persons During 1945-1965

Developed by a collection of experts from the CDC and other federal agencies, professional associations, community-based organizations, and medical associations, MMWR recommends the one-time screening of persons born during 1945-1965.

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Screening

University of Washington, International Antiviral Society-USA

Module 1. Screening and Diagnosis of Hepatitis C Infection

This module is intended for any clinician who may encounter persons with hepatitis C virus (HCV) infection who would like to establish core competence in screening, testing, and counseling patients regarding their initial testing results. Medical providers intended for this module include Primary care physicians, Advanced Registered Nurse Practitioners, Physician Assistants, Hospitalists, Infectious Diseases Specials, Gastroenterologists, and Hepatologists.

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II. Appropriate Testing/Screening for HCV: Testing8 Items

Testing

American Association for the Study of Liver Diseases Practice Guidelines

Diagnosis, Management, and Treatment of Hepatitis C: An Update

The AASLD Practice Guidelines provides recommendations for preferred approaches to the diagnostic, therapeutic, and preventive aspects of care. Sections of interest are Testing and Counseling, and Laboratory Testing.

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Testing

Centers for Disease Control and Prevention Morbidity and Mortality Weekly Report

Guidelines for Laboratory Testing and Result Reporting of Antibody to Hepatitis
C Virus

Testing for anti-HCV should include use of an antibody screening assay, and for screening test-positive results, a more specific supplemental assay. Verifying the presence of anti-HCV minimizes unnecessary medical visits and psychological harm for persons who test falsely positive by screening assays and ensures that counseling, medical referral, and evaluation are targeted for patients serologically confirmed as having been infected with HCV. However, substantial variation in reflex supplemental testing practices exists among laboratories, and an anti-HCV--positive laboratory report does not uniformly represent a confirmed positive result. These guidelines expand recommendations for anti-HCV testing to include an option for reflex supplemental testing based on screening-test--positive signal-to-cut--off (s/co) ratios. Use of s/co ratios minimizes the amount of supplemental testing that needs to be performed while improving the reliability of reported test results. These guidelines were developed on the basis of available knowledge of CDC staff in consultation with representatives from the Food and Drug Administration and public health, hospital, and independent laboratories. Adoption of these guidelines by all public and private laboratories that perform in vitro diagnostic anti-HCV testing will improve the accuracy and utility of reported anti-HCV test results for counseling and medical evaluation of patients by health-care professionals and for surveillance by public health departments.

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Testing

Department of Veterans Affairs

Laboratory Tests and Hepatitis C

The Department of Veterans Affairs provides information on serologic assays, assessment of HCV viremia, notes on methods of standardization for quantitative HCV RNA assays, genotype assays, and references.

 

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Testing

California Department of Public Health Office of AIDS

Hepatitis C Testing in Non-Health Care Settings

This manual is intended to provide guidelines to human immunodeficiency virus (HIV) testing sites in non-health care settings such as community-based organizations (CBOs), and to HIV test counselors performing the OraQuick1 hepatitis C virus (HCV) rapid test. The manual outlines recommendations for conducting OraQuick HCV rapid testing, including provision of HCV testing services and referrals.

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Testing

Published: ; 2012 ; 142 : 1303 -1313

Gastroenterology

New Virologic Tools for Management of Chronic Hepatitis B and C

Molecular biology techniques are routinely used to diagnose and monitor treatment of patients with chronic hepatitis B virus (HBV) and hepatitis C virus (HCV) infections. These tools can detect and quantify viral genomes and analyze their sequence to determine their genotype or subtype and to identify nucleotide or amino acid substitutions associated with resistance to antiviral drugs. They include real-time target amplification methods, which have been standardized and are widely used in clinical practice to diagnose and monitor HBV and HCV infections, and next-generation sequencing techniques, which are still restricted to research laboratories. In addition, new enzyme immunoassays can quantify hepatitis B surface and hepatitis C core antigens, and point-of-care tests and alternatives to biologic tests that require whole blood samples obtained by venipuncture have been developed. We review these new virologic methods and their clinical and research applications to HBV and HCV infections.

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Testing

Published: ; 2013 ; 56 : 853 -860

Clinical Infectious Diseases

Evaluation of the Hepatitis C Virus–Infected Patient: The Initial Encounter

Deaths from hepatitis C virus (HCV)–related disease are increasing, now exceeding those from human immunodeficiency virus. Up to 7 million Americans (2.3%) may be infected with HCV, and more than half are undiagnosed. Proposed expansion of hepatitis C screening to include all persons born between 1945 and 1965 will lead to many new diagnoses, and infectious diseases physicians have a unique opportunity to be part of managing these patients. Apart from a liver-focused history and examination, the initial evaluation includes determination of the liver function via serum tests and assessment of liver fibrosis and necroinflammation through biopsy or noninvasive means. Patients with cirrhosis require screening for esophageal varices and for liver cancer. Nonimmune patients need vaccinations against hepatitis A and B, and alcohol abstinence is critical. Initial counseling on therapy emphasizes viral cure rates of currently 70%–80% as well as expected side effects. New treatments with fewer side effects and potentially higher cure rates are currently in development.

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Testing

Centers for Disease Control and Prevention, Medscape

Medscape CDC Expert Commentary - Testing for Hepatitis C: New Guidance

Dr. Chong-Gee Teo, Laboratory Branch Chief in the Division of Viral Hepatitis at CDC, discusses CDC’s updated guidance for clinicians and laboratorians for testing for hepatitis C virus (HCV) infection. Testing for hepatitis C should be initiated with a test for antibody to HCV, and all reactive results should be followed by a test for HCV RNA. The bottom line - HCV testing must ensure the identification of persons with current HCV infection.

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Testing

Department of Veterans Affairs

Liver Biopsy

The Department of Veterans Affairs’ topic review of Liver Biopsy provides information on risks, the procedure, histopathology, references, and suggested readings.

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III. Medical Management: Risk Reduction16 Items

Risk Reduction

HCVinfo.org

Basics of Hepatitis C

Dr. Andrew Muir provides a complete overview of Hepatitis C that includes the topics of epidemiology, natural history, diagnosis, and treatment.

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Risk Reduction

Department of Veterans Affairs

Natural History of Hepatitis C

The Department of Veterans Affairs provides information on symptoms and clinical manifestations, extrahepatic manifestations, factors associated with liver disease progression, and cirrhosis associated with HCV.

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Risk Reduction

HCVinfo.org

Management of patients co-infected with HCV and HIV

Dr. Susanna Naggie provides information concerning HBV vaccination in co-infected persons as well as the role of biopsy, medication interactions, and side effects.

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Risk Reduction

Centers for Disease Control and Prevention - Morbidity and Mortality Weekly Report

Advisory Committee on Immunization Practices Recommended Immunization
Schedule for Adults Aged 19 Years and Older – United States, 2013

The Advisory Committee on Immunization Practices (ACIP) develops recommendations on how to use vaccines to control diseases in the United States.  The 2013 ACIP recommendations include updated vaccine practices regarding Hepatitis A and B.
  

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Risk Reduction

Department of Veterans Affairs

Vaccination against Hepatitis A and B

The Department of Veterans Affairs has developed a pocketcard and poster intended to educate health care providers on how to vaccinate against hepatitis A and/or B.

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Risk Reduction

HCVinfo.org

Non-invasive Assessment of Liver Fibrosis

Dr. Keyur Patel discusses reasons for liver biopsy, limitations of liver biopsy, serum markers, diagnostic imaging methods, non-invasive algorithm, and additional information concerning assessment of liver fibrosis.

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Risk Reduction

Department of Veterans Affairs

Hepatitis C and Alcohol

The Department of Veterans Affairs’ topic review of Hepatitis C and Alcohol provides information on Alcohol and Liver Disease in Patients with HCV, Alcohol and HCV Therapy, Alcohol and Hepatocellular Cancer in Patients with HCV, and References.  

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Risk Reduction

Department of Veterans Affairs

Hepatitis C and Alcohol: A Clinician’s Perspective

The Department of Veterans Affairs’ topic review of Hepatitis C and Alcohol: A Clinician’s Perspective provides answers for the following questions: Should I tell my patient with chronic hepatitis C that he/she shouldn’t drink alcohol? What should I advise my patient who only drinks alcohol once per week or less? and Should I wait until my actively drinking patient has been abstinent for 6 months or more before performing a liver biopsy or initiating anti-HCV therapies?

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Risk Reduction

Department of Veterans Affairs

Reducing Alcohol Use with Brief Intervention

The Department of Veterans Affairs provides a toolkit of materials to help providers discuss the reduction of alcohol consumption with patients infected with hepatitis C. A teaching guide for health care providers, audit-c score cards, OARS/FLO card, and interactive resources are available.

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Medical Management Additional Resources

HIVandHepatitis.com
Subcategories relevant to medical management
http://www.hivandhepatitis.com/hcv-disease-progression

Department of Veterans Affairs
Journal Articles concerning clinical management of HCV
http://www.hepatitis.va.gov/provider/journal-articles-index.asp#S4X

Hepatitis C Management and Treatment Algorithm
http://hivinsite.ucsf.edu/algorithm/HCV-treatment/intro.html

National Institute of Health
Management of Hepatitis C: 2002
http://consensus.nih.gov/2002/2002HepatitisC2002116html.htm

Centers for Disease Control and Prevention
Hepatitis C Information for Health Professionals
http://www.cdc.gov/hepatitis/HCV/index.htm

Recommendations for Prevention and Control of Hepatitis C Virus Infection and HCV-Related Chronic Disease
http://www.cdc.gov/hepatitis/HCV/Management.htm

Hepatitis C Information for Health Professionals
http://www.cdc.gov/hepatitis/HCV/ProfResourcesC.htm

Health Resources and Services Administration
Hepatitis C Infection
http://hab.hrsa.gov/deliverhivaidscare/clinicalguide11/

World Health Organization
Hepatitis C
http://www.who.int/csr/disease/hepatitis/whocdscsrlyo2003/en/index3.html
 

Risk Reduction

Published: ; 2013 ; : -

Nature Reviews Gastroenterology and Hepatology

Epidemiology and natural history of HCV infection.

Worldwide, an estimated 130-170 million people have HCV infection. HCV prevalence is highest in Egypt at >10% of the general population and China has the most people with HCV (29.8 million). Differences in past HCV incidence and current HCV prevalence, together with the generally protracted nature of HCV disease progression, has led to considerable diversity in the burden of advanced liver disease in different countries. Countries with a high incidence of HCV or peak incidence in the recent past will have further escalations in HCV-related cirrhosis and hepatocellular carcinoma (HCC) over the next two decades. Acute HCV infection is difficult to detect because of the generally asymptomatic nature of the disease and the marginalization of at-risk populations. Around 25% of patients with acute HCV infection undergo spontaneous clearance, with increased rates among those with favourable IL28B genotypes, acute symptoms and in women. The remaining 75% of patients progress to chronic HCV infection and are subsequently at risk of progression to hepatic fibrosis, cirrhosis and HCC. Chronic hepatitis C generally progresses slowly in the initial two decades, but can be accelerated during this time as a result of advancing age and co-factors such as heavy alcohol intake and HIV co-infection.

Risk Reduction: Education

Department of Veterans Affairs

Patient Education Brochures

The Department of Veterans Affairs makes available 27 patient brochures designed to educate persons infected with hepatitis C in addition to prevention information to those at risk for contracting the disease. Patient brochure topics include HAV, HBV, diet and nutrition, co-infection, treatment side effects, liver biopsy, and more.

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Risk Reduction: Education

Department of Veterans Affairs

Prevention and Transmission: Patient Education

The Department of Veterans Affairs makes available multiple patient education resources offered in different formats such as videos, posters, wallet cards, and handouts.

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Risk Reduction

Centers for Disease Control and Prevention

Module 2: Evaluation, Staging, and Monitoring of Chronic Hepatitis C
Lesson 4: Evaluation and Staging of Liver Disease

• MELD and Child-Turcotte-Pugh
• Compensated versus Decompensated Cirrhosis
• Non-Invasive Measures of Liver Fibrosis (includes lab studies and imaging)
• Performing and Interpreting Liver Biopsy 

Risk Reduction

Centers for Disease Control and Prevention

Module 2: Evaluation, Staging, and Monitoring of Chronic Hepatitis C
Lesson 3: Counseling Patients with Chronic Hepatitis C

• OTC and Prescription Medications
• Alcohol and Cannabis
• Diet and Modifying Obesity
• Complementary and Alternative Medicines

Risk Reduction

University of Washington, International Antiviral Society-USA

Module 2. Evaluation, Staging, and Monitoring of Chronic Hepatitis C

This module is intended for clinicians who play a substantial role in the long-term management of patients with chronic hepatitis C virus (HCV) infection, including Primary Care Physicians, Advanced Registered Nurse Practitioners, Physician Assistants, Infectious Diseases Specialists, Gastroenterologists, and Hepatologists. This module emphasizes the initial evaluation of a patient diagnosed with hepatitis C virus infection, understanding the natural history of hepatitis C, assessment for the degree of liver fibrosis, counseling patients on how to prevent further insults to their liver, evaluation of patients with cirrhosis, surveillance for hepatocellular carcinoma, and recognition of  HCV-related extrahepatic manifestations.

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III. Medical Management: Liver Disease5 Items

Liver Disease: Extrahepatic Manifestations

Published: ; 2007 ; 39 : 2 -17

Digestive and Liver Disease

Extrahepatic manifestations of Hepatitis C Virus infection: a general overview
and guidelines for a clinical approach.

Hepatitis C Virus is associated with a wide series of extrahepatic manifestations. Based on available data the link between the virus and some of these extrahepatic diseases is only suggested and needs further confirmation. Hepatitis C Virus-related lymphoproliferative disorders, whose prototype is mixed cryoglobulinaemia, represent the most closely related extrahepatic manifestations of Hepatitis C Virus. Other Hepatitis C Virus-associated disorders include nephropathies, thyreopathies, sicca syndrome, idiopathic pulmonary fibrosis, porphyria cutanea tarda, lichen planus, diabetes, chronic polyarthritis, cardiopathy and atherosclerosis. A pathogenetic link between Hepatitis C Virus and some extrahepatic manifestations was confirmed by their responsiveness to antiviral therapy, which is now deemed the first therapeutic option to consider. By contrast, there are diseases where treatment with interferon was ineffective or dangerous. The aim of the present paper is to outline the most recent evidence concerning extrahepatic disorders that are possibly associated with Hepatitis C Virus infection. Special emphasis will be given to discussion of the most appropriate clinical approaches to be adopted in order to diagnose, treat (possibly prevent) and follow-up extrahepathic diseases in patients with Hepatitis C Virus infection.

Liver Disease: Extrahepatic Manifestations

Published: ; 2008 ; 12 : 611 -636

Clinics in Liver Disease

Extrahepatic manifestations of hepatitis C virus infection.

Hepatitis C virus may cause hepatic and extrahepatic diseases. Extrahepatic manifestations range from disorders for which a significant association with viral infection is supported by epidemiologic and pathogenetic data, to anecdotal observations without clear proof of causality. This article describes the diagnosis and treatment of these diseases.

Liver Disease: Extrahepatic Manifestation

Published: ; 2012 ; : -

HCV Advocate, Alan Franciscus

An Overview of Extrahepatic Manifestations of Hepatitis C

The hepatitis C virus mainly affects the liver, but there are many other conditions that are associated with hepatitis C. Extrahepatic manifestation means diseases or conditions that affect organs other than the liver. Extrahepatic manifestations of hepatitis C can be found in the skin, eyes, joints, immune system, nervous system and kidneys. Some of these conditions – cryoglobulinemia, for example – are somewhat more common and well-documented, while others are infrequent or their association with hepatitis C has not yet been proven.

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Liver Disease

Published: ; 2010 ; : 307 -328

American Associate for the Study of Liver Diseases

Alcoholic Liver Disease

The Alcoholic Live Disease practice guidelines include information regarding the prevalence and natural history of alcoholic liver disease, the disease spectrum, risk factors, diagnosis, prognostic factors, therapy, long term management, and liver transplantation.

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Liver Disease

Published: ; 2011 ; : -

American Association for the Study of Liver Diseases

AASLD Position Paper: The Management of Acute Liver  Failure: Update 2011

The Management of Acute Liver Failure position paper provides guidelines for clinical practice of diagnosing, treating, and managing a patient affected by acute liver failure.

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III. Medical Management: Cirrhotic14 Items

Cirrhosis: Overview

International Antiviral Society-USA - Alexander Kuo, MD

Hepatology 101: Natural History of HCV and Complications of Cirrhosis

Dr. Alexander Kuo discusses the following topics:
• Burden of HCV disease
• Fibrosis progression and models for scoring
• Differences of compensated and decompensated cirrhosis
• Main complications of cirrhosis
• Role and timing of liver transplantation

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Cirrhosis

Published: ; 2011 ; 19 : 121 -125

Topics of Antiviral Medicine - International Antiviral Society-USA

Advanced Liver Disease: What Every Hepatitis C Virus Treater Should Know

Identification and treatment of advanced hepatitis C virus (HCV) infection is often challenging. Accurate fibrosis staging can be performed only by liver biopsy. For patients with advanced fibrosis (Metavir score, F3 or F4), progression to decompensated liver disease occurs at a rate of approximately 5% per year and progression to hepatocellular carcinoma occurs at a rate of 1% to 2% per year. Liver decompensation primarily results from altered hepatic blood flow caused by liver scarring and is characterized by ascites and its complications (hepatorenal syndrome, hepatic hydrothorax, and spontaneous bacterial peritonitis), hepatic encephalopathy, bleeding varices, and coagulopathy. Patients with advanced fibrosis need to be regularly monitored for evidence of decompensated disease, and complications need to be aggressively managed. This article summarizes a presentation by Kenneth E. Sherman, MD, at the IAS–USA live continuing medical education course, Management of Hepatitis C Virus in the New Era, held in New York City in April 2011.

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Cirrhosis

Department of Veterans Affairs

Hepatitis C and Hepatocellular Carcinoma

The Department of Veterans Affairs’ topic review of Hepatitis C and Hepatocellular Carcinoma provides information on risk factors, screening modalities, diagnosis, prognosis, treatment modalities, prevention of HCC, secondary prevention, and references.

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Cirrhosis

Department of Veterans Affairs

Management of Hepatocellular Carcinoma (HCC)

The Management of Hepatocellular Carcinoma practice guidelines provide information on the key points, surveillance, diagnosis, staging, treatment, and references relating to HCC.

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Cirrhosis: Quicknotes

Department of Veterans Affairs

Cirrhosis Quicknotes

The Hepatocellular Carcinoma Quicknotes provide bottom-line current recommendations regarding the workup of liver masses uncovered during screening as well as guidelines regarding the diagnosis and management of HCC, including guidance regarding referral for liver transplantation.

The Hepatocellular Carcinoma Quicknotes provide bottom-line current recommendations regarding the workup of liver masses uncovered during screening as well as guidelines regarding the diagnosis and management of HCC, including guidance regarding referral for liver transplantation. - See more at: http://www.idsociety.org/HCV_Curriculum/#III.%20Medical%20Management:%20Cirrhotic

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Cirrhosis

Department of Veterans Affairs

Hepatocellular Carcinoma Diagnostic & Treatment Algorithm

The Department of Veterans Affairs’ has developed an interactive treatment algorithm for the diagnosis and treatment of hepatocellular carcinoma. The recommendations are based on a critical review of the available data and expert consensus.

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Cirrhosis

Department of Veterans Affairs

Management and Treatment of Patients with Cirrhosis and Portal Hypertension

Provides practice guidelines on the management of compensated and decompensated cirrhosis and the screenign, diagnosis, and management of hepatocellular carcinoma.  A hypertext version that provides hyperlinks to quicknotes, CPT calculator etc is at http://www.hepatitis.va.gov/provider/guidelines/2009cirrhosis.asp

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Cirrhosis

Department of Veterans Affairs

Cirrhosis Quicknotes

Succinct summary of the management of compensated and decompensated cirrhosis, including guidelines for screening and management of varices and hepatocellular carcinoma (HCC) and guidelines for the management of ascites, encephalopathy, variceal hemorrhage, and spontaneous bacterial peritonitis. They also provide guidance regarding referral for liver transplantation.

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Cirrhosis

Published: ; 2010 ; 138 : 159 -164

Gastroenterology

MELD Score Is an Important Predictor of Pretransplantation Mortality in HIV-Infected Liver Transplant Candidates

Human immunodeficiency virus (HIV) infection accelerates liver disease progression in patients with hepatitis C virus (HCV) and could shorten survival of those awaiting liver transplants. The Model for End-Stage Liver Disease (MELD) score predicts mortality in HIV-negative transplant candidates, but its reliability has not been established in HIV-positive candidates.

Cirrhosis

Published: ; 2013 ; : -

American Association for the Study of Liver Diseases

Management of Adult Patients with Ascites Due to Cirrhosis: Update 2012

AASLD practice guidelines; includes information regarding evaluation and diagnosis, ascitic fluid analysis, differential diagnosis, treatment of ascites, refractory ascites, spontaneous bacterial peritonitis, prevention of spontaneous bacterial peritonitis, hepatorenal syndrome, additional considerations, and hepatic hydrothorax.

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Cirrhosis

Published: ; 2007 ; 46 : 922 -938

American Association for the Study of Liver Diseases

Prevention and Management of Gastroesophageal Varices and Variceal Hemorrhage in Cirrhosis

AASLD practice guidelines; includes information regarding the pathophysiology of portal hypertension in cirrhosis, evaluation of portal hypertension, natural history of varices, gastric varices, diagnosis of varices and variceal hemorrhage, and management recommendations.

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Cirrhosis

Published: ; 2010 ; 51 : 1 -16

American Association for the Study of Liver Diseases

The Role of Transjugular Intrahepatic PortosystemicShunt (TIPS) in the Management of PortalHypertension: Update 2009

AASLD practice guidelines; includes information regarding the procedure, pre-tips evaluation and contraindications, mortality, complications, indications, primary prevention of variceal bleeding, acutely bleeding varices, cirrhotic ascites, refractory hepatic hydrothorax, hepatorenal syndrome, veno-occlusive disease, and hepatopulmonary syndrome.

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Cirrhosis

Centers for Disease Control and Prevention

Module 3: Management of Cirrhosis-related Complications

Lesson 1: Diagnosis and Management of Ascites

• Diagnostic Paracentesis
• Analysis of Ascitic Fluid
• Basic Management of Ascites
• Management of Refractory Ascites

Lesson 2: Recognition and Management of Spontaneous Bacterial Peritonitis

• Indications for Spontaneous Bacterial Peritonitis Prophylaxis
• Regimens for Spontaneous Bacterial Peritonitis Prophylaxis
• Diagnosis of Spontaneous Bacterial Peritonitis
• Management of Spontaneous Bacterial Peritonitis

Lesson 3: Screening for Varices and Prevention of Bleeding

• Pathophysiology and Portal Dynamics
• Indications and Methods for Variceal Screening
• Pre-primary Prophylaxis of Variceal Bleeding
• Primary Prophylaxis of Variceal Bleeding

Lesson 4: Diagnosis and Management of Hepatic Encephalopathy

• Clinical Features
• Laboratory Abnormalities
• Correction of Precipitating Causes
• Medical Therapy

Cirrhosis Overview

International Antiviral Society-USA, Kenneth E. Sherman, MD, PhD

HCV is a LIVER Disease

Streaming video presentation of the following topics: 

  • Relationship between hepatic anatomy and liver disease
  • Hepatic decompensation and how to measure it
  • Key management issues in advanced liver disease
  • When a patient needs to be eferred to a hepatologist

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III. Medical Management: Liver Transplant4 Items

Liver Transplant

Published: ; 2012 ; 18 : 70 -81

Liver Transplantation

Epidemiology and outcome of infections in human immunodeficiency virus/hepatitis c virus–coinfected liver transplant recipients: A FIPSE/GESIDA Prospective Cohort Study

Information about infections unrelated to acquired immunodeficiency syndrome (AIDS) in human immunodeficiency virus (HIV)–infected liver recipients is scarce. The aims of this study were to describe the prevalence, clinical characteristics, time of onset, and outcomes of bacterial, viral, and fungal infections in HIV/hepatitis C virus (HCV)–coinfected orthotopic liver transplant recipients and to identify risk factors for developing severe infections. We studied 84 consecutive HIV/HCV-coinfected patients who underwent liver transplantation at 17 sites in Spain between 2002 and 2006 and were followed until December 2009. In conclusion, the rates of severe and opportunistic infections are high in HIV/HCV-coinfected liver recipients and especially in those with a history of AIDS, a high MELD score, or non–tacrolimus-based immunosuppression.

Liver Transplant

Published: ; 2013 ; 19 : 3 -26

American Association for the Study of Liver Diseases

Long-Term Management of the Successful Adult Liver Transplant: 2012 Practice
Guideline by the American Association for the Study of Liver Diseases and the American Society of Transplantation

Intended for use by physicians and health care providers working with adult recipients of liver transplantation (LT), these recommendations suggest preferred approaches to the diagnostic, therapeutic, and preventiveaspects of care. They are intended to be flexible, in contrast to standards of care, which are inflexible policies to be followed in every case.

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Liver Transplant

Health Services and Resources Administration

MELD Calculator

HRSA makes available a MELD Calculator that utilizes a formula approved by the Organ Procurement and Transplantation Network (OPTN) Board of Directors. The MELD score is on based on a patient's risk of dying while waiting for a liver transplant, and are based on objective and verifiable medical data.

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Liver Transplant

Published: ; 2013 ; : -

Current HIV/AIDS Reports

Solid Organ Transplants in HIV-Infected Patients

There is a growing need for kidney and liver transplants in persons living with HIV. Fortunately, with the significant advances in antiretroviral therapy and management of opportunistic infections, HIV infection is no longer an absolute contraindication for solid organ transplantation. Data from several large prospective multi-center cohort studies have shown that solid organ transplantation in carefully selected HIV-infected individuals is safe. However, significant challenges have been identified including prevention of acute rejection, management of drug-drug interactions and treatment of recurrent viral hepatitis. This article reviews the selection criteria, outcomes, and special management considerations for HIV-infected patients undergoing liver or kidney transplantation.

IV. Treatment Decision Making: The HCV Treatment Landscape – Setting the Stage5 Items

The HCV Treatment Landscape – Setting the stage

Hepatitis C Online - University of Washington

Module 4. Evaluation and Preparation for Hepatitis C Treatment
Lesson 1. Goals for Treatment and Predicting Response

Objectives
1. Discuss the goals and rationale for hepatitis C therapy with patients considering treatment.
2. Predict a patient's response to treatment for chronic hepatitis C infection based on specific host and viral factors.

The HCV Treatment Landscape – Setting the Stage

Published: ; 2013 ; 56 : 853 -860

Clinical Infectious Diseases

Evaluation of the Hepatitis C Virus–Infected Patient: The Initial Encounter

Deaths from hepatitis C virus (HCV)–related disease are increasing, now exceeding those from human immunodeficiency virus. Up to 7 million Americans (2.3%) may be infected with HCV, and more than half are undiagnosed. Proposed expansion of hepatitis C screening to include all persons born between 1945 and 1965 will lead to many new diagnoses, and infectious diseases physicians have a unique opportunity to be part of managing these patients. Apart from a liver-focused history and examination, the initial evaluation includes determination of the liver function via serum tests and assessment of liver fibrosis and necroinflammation through biopsy or noninvasive means. Patients with cirrhosis require screening for esophageal varices and for liver cancer. Nonimmune patients need vaccinations against hepatitis A and B, and alcohol abstinence is critical. Initial counseling on therapy emphasizes viral cure rates of currently 70%–80% as well as expected side effects. New treatments with fewer side effects and potentially higher cure rates are currently in development.

The HCV Treatment Landscape – Setting the Stage

Published: ; 2014 ; 146 - 5 : 1176 -1192

Jean–Michel Pawlotsky

New HCV Therapies: The Toolbox, Strategies, and Challenges

Therapy for hepatitis C is undergoing a revolution. Several new drugs against the hepatitis C virus (HCV) have reached the market and many others, including direct-acting antivirals and host-targeted agents, are in phase II or III clinical development. All-oral, interferon-free combinations of drugs are expected to cure more than 90% of infections. A vast amount of data from clinical trials are presented regularly at international conferences or released to the press before peer-review, creating confusion in the viral hepatitis field. The goal of this review is to clarify the current stage of HCV therapy and drug development. This review describes the different classes of drugs and their mechanisms and properties, as well as treatment strategies in development, including those that are interferon-based and interferon-free. HCV treatment options that will be available in 2014–2015 are presented for each genotype. A number of unanswered questions and challenges remain, such as how to treat special populations, the role of ribavirin in interferon-free regimens, the role of HCV resistance in treatment failures, and how to best re-treat patients who failed on treatment. Strategic choices, cost issues, HCV screening, and improving access to care in resource-constrained areas also are discussed.

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The HCV Treatment Landscape – Setting the Stage

BMJ

Antiviral treatment of HCV

Hepatitis C virus (HCV) infection is a substantial health problem worldwide. Most patients infected with HCV remain chronically infected, with an increased risk of cirrhosis and hepatocellular carcinoma. Although they are associated with toxicities and low sustained viral response rates, interferon alfa and ribavirin have been the mainstay of treatment until recently. New direct acting antivirals, specifically designed to inhibit three viral proteins (the NS3/4A protease, the NS5A protein, and the NS5B RNA dependent RNA polymerase) are now becoming available. The NS3/4A inhibitor simeprevir and NS5B inhibitor sofosbuvir have recently been licensed and can reduce the length of antiviral treatment, improve response rates, and allow for interferon-free regimens for some HCV genotypes. Several other newer direct acting antivirals have shown promise in clinical studies and are likely to be licensed soon. These agents seem to facilitate the use of shortened courses of combination interferon-free therapy, which are associated with high (>95%) sustained response rates and relatively few toxicities. These regimens have also been successful in patients who were previously difficult to treat, including those with cirrhosis, HIV coinfection, and those who have undergone liver transplantation. The high cost of these agents may be the biggest challenge to their implementation worldwide.

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The HCV Treatment Landscape – Setting the Stage

Published: ; 2014 ; 109 : 628 -635

Andrew J. Muir , MD, MHS

The Rapid Evolution of Treatment Strategies for Hepatitis C

The revolution in HCV treatment is being realized at a rapid pace, and most patients with HCV monoinfection and HCV / HIV-1 coinfection have excellent options in 2014. Genotypes 2 and 3 have a highly eff ective interferon-free regimen of sofosbuvir and ribavirin. Genotypes 1, 4, 5, and 6 have a 12-week regimen with sofosbuvir, peginterferon- α , and ribavirin, and the genotype 1 patients have an alternative with simeprevir, peginterferon- α, and ribavirin for 24 or 48 weeks. Given the predominance of genotype 1 infection in the United States, our ability to affect HCV disease on a large scale requires interferon-free regimens. The simeprevir and sofosbuvir combination is available, but not FDA approved and currently recommended for interferon-ineligible and prior nonresponders patients. FDA-approved interferon-free regimens are expected in late 2014 or early 2015. In 2014, clinicians will need to guide patients about their treatment options according to eligibility for peginterferon- α and fibrosis stage. We find ourselves in the gratifying position to offer almost all patients a future without HCV infection. Our challenges continue to be identifying patients through screening so we can offer these curative therapies. These exciting potent therapies are important tools for the public health campaign to eradicate HCV.

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IV. Treatment Decision Making: Who/When to Treat?7 Items

Treatment Candidacy Considerations

Centers for Disease Control and Prevention

Module 4: Evaluation and Preparation for Hepatitis C Treatment
Lesson 5: Addressing Anticipated Adherence Problems Prior to Treatment

• Adherence and the Risk of Viral Resistance and Treatment Failure
• Factors Negatively Influencing Adherence
• Methods to Enhance Adherence

Treatment Candidacy Considerations

Department of Veterans Affairs

Clinical Management

The Department of Veterans Affairs provides guidelines, topic reviews, provider education material, clinician tools, case studies, and journal articles relating to the clinical management of HCV.

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Treatment Candidacy Considerations

Department of Veterans Affairs

The Alcohol Use Disorders Identification Test

The Department of Veterans Affairs provides an Audit-C Test and Scoring Cards to help identify patients who are hazardous drinkers or have active alcohol use disorders.

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Treatment Candidacy Considerations

Department of Veterans Affairs

Hepatitis C and Alcohol

The Department of Veterans Affairs’ topic review of Hepatitis C and Alcohol provides information on alcohol and liver disease in patients with HCV, alcohol and HCV therapy, alcohol and hepatocellular cancer in patients with HCV, and references.

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Treatment Candidacy Considerations

Published: ; 2013 ; 33 Suppl 1 : 105 -110

Liver International

Patients with HCV and F1 and F2 fibrosis stage: treat now or wait?

The current standard of care (SOC) for patients with chronic HCV genotype 1 is a combination of either boceprevir or telaprevir with peginterferon (PEG-IFN) and ribavirin (RBV). Although it is effective in a high percentage of patients, this treatment is associated with significant adverse events (AEs). The next generation of protease inhibitors, simeprevir and faldaprevir, will also be used with PEG-IFN/RBV. Interferon-free therapy with sofosbuvir appears promising and on the horizon for patients with genotypes 2 and 3, but may still be many years away for patients with HCV genotype 1. The factors which should be considered when deciding whether to treat a patient with HCV and mild fibrosis with the current SOC now, or to delay treatment until less toxic and/or more effective therapy is available is discussed.

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Treatment Candidacy Considerations

Published: ; 2012 ; 57 : 1439 -1444

Digestive Diseases & Sciences

Tangible resources for preparing patients for antiviral therapy for chronic hepatitis C.

Chronic hepatitis C (HCV) infected patients with coexisting mental health and/or substance abuse issues face significant barriers to treatment and are often deferred. This paper sought to highlight critical pre-treatment strategies and provide tangible resources for HCV clinicians to facilitate preparation and successful treatment of these patients.

IV. Treatment Decision Making: Liver Disease Staging7 Items

Liver Disease Staging - Non-invasive

Centers for Disease Control and Prevention

Module 2: Evaluation, Staging, and Monitoring of Chronic Hepatitis C
Lesson 4: Evaluation and Staging of Liver Disease

• MELD and Child-Turcotte-Pugh
• Compensated versus Decompensated Cirrhosis
• Non-invasive Measures of Liver Fibrosis (includes lab studies and imaging)
• Performing and Interpreting Liver Biopsy

Liver Disease Staging - Non-invasive

HCVinfo.org

Non-invasive Assessment of Liver Fibrosis

Dr. Keyur Patel discusses reasons for liver biopsy, limitations of liver biopsy, serum markers, diagnostic imaging methods, non-invasive algorithm, and additional information concerning assessment of liver fibrosis.

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Liver Disease Staging - Non-invasive

American Association for the Study of Liver Diseases

Diagnosis, Management, and Treatment of Hepatitis C: An Update - Utility of the
Liver Biopsy and Noninvasive Tests of Fibrosis

(Pages 1339-1340)

The AASLD diagnosis, management, and treatment practice guidelines provide information to clinicians with evidence-based approaches to the prevention, diagnosis, and management of HCV infection.

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Liver Disease Staging - Non-invasive

Published: ; 2012 ; 142 : 1293 -1302

Gastroenterology

Noninvasive methods to assess liver disease in patients with hepatitis B or C.

The prognosis and management of patients with chronic viral hepatitis B and C depend on the amount and progression of liver fibrosis and the risk for cirrhosis. Liver biopsy, traditionally considered to be the reference standard for staging of fibrosis, has been challenged over the past decade by the development of noninvasive methodologies. These methods rely on distinct but complementary approaches: a biologic approach, which quantifies serum levels of biomarkers of fibrosis, and a physical approach, which measures liver stiffness by ultrasound or magnetic resonance elastography. Noninvasive methods were initially studied and validated in patients with chronic hepatitis C but are now used increasingly for patients with hepatitis B, reducing the need for liver biopsy analysis. We review the advantages and limitations of the noninvasive methods used to manage patients with chronic viral hepatitis B or C infection.

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Liver Disease Staging - Non-invasive

Published: ; 2007 ; 102 : 2589 -2600

The American Journal of Gastroenterology

FibroTest and FibroScan for the prediction of hepatitis C-related fibrosis: a
systematic review of diagnostic test accuracy.

The accurate diagnosis of hepatitis C virus (HCV)-related fibrosis is crucial for prognostication and treatment decisions. Due to the limitations of biopsy, noninvasive alternatives including FibroTest and FibroScan have been developed. Our objective was to systematically review studies describing the accuracy of these tests for predicting HCV-related fibrosis.

Liver Disease Staging - Non-invasive

Published: ; 2008 ; 9 : 43 -51

HIV Clinical Trials

Systematic review and meta-analysis of the diagnostic accuracy of fibrosis
marker panels in patients with HIV/hepatitis C coinfection.

Accurately staging hepatitis C virus (HCV)-related fibrosis is crucial for treatment decisions and prognostication. Our objective was to systematically review studies describing the accuracy of serum marker panels for predicting fibrosis in HIV/HCV-coinfected patients.

Liver Disease Staging - Non-invasive

Published: ; 2011 ; 53 : 726 -736

Hepatology

Performance of the aspartate aminotransferase-to-platelet ratio index for the
staging of hepatitis C-related fibrosis: an updated meta-analysis.

The aspartate aminotransferase-to-platelet ratio index (APRI), a tool with limited expense and widespread availability, is a promising noninvasive alternative to liver biopsy for detecting hepatic fibrosis. The objective of this study was to update the 2007 meta-analysis to systematically assess the accuracy of APRI in predicting significant fibrosis, severe fibrosis, and cirrhosis stage in hepatitis C virus (HCV) monoinfected and HCV / human immunodeficiency virus (HIV) coinfected individuals. Studies comparing APRI versus biopsy in HCV patients were identified via a thorough literature search. Areas under summary receiver operating characteristic curves (AUROC), sensitivity, specificity, positive predictive value (PPV), and negative predictive value (NPV) were used to examine the APRI accuracy for the diagnosis of significant fibrosis, severe fibrosis, and cirrhosis. Heterogeneity was explored using meta-regression. Twenty-one additional studies were eligible for the update and, in total, 40 studies were included in this review (n = 8,739). The summary AUROC of the APRI for the diagnosis of significant fibrosis, severe fibrosis, and cirrhosis were 0.77, 0.80, and 0.83, respectively. For significant fibrosis, an APRI threshold of 0.7 was 77% sensitive and 72% specific. For severe fibrosis, a threshold of 1.0 was 61% sensitive and 64% specific. For cirrhosis, a threshold of 1.0 was 76% sensitive and 72% specific. Moreover, we found that the APRI was less accurate for the identification of significant fibrosis, severe fibrosis, and cirrhosis in HIV/HCV coinfected patients. CONCLUSION: Our large meta-analysis suggests that APRI can identify hepatitis C-related fibrosis with a moderate degree of accuracy. Application of this index may decrease the need for staging liver biopsy specimens among chronic hepatitis C patients.

V. Treatment: Current Standard of Care/Overview for Genotype 1 Infection1 Item

Current Standard of Care/Overview for Genotype 1 Infection

International Antiviral Society-USA

Overview of the Basics of Hepatitis C Virus (HCV) Infection Management

Dr. Susanna Naggie provides information on topics that include, but are not limited, to the following:
• HCV Epidemiology
• HCV Genome and Drug Targets
• Viral Kinetics
• Prior Standard of Care
• Pharmacogenomic discoveries
• What SVR really means?

V. Treatment: Viral Kinetics/Decision Rules/On Treatment Testing/Definition of Response for Genotype2 Items

Viral Kinetics/Decision Rules/On Treatment Testing

Department of Veterans Affairs

Definitions of Response

The Department of Veterans Affairs provides information on the definitions of response associated with HCV treatment and the patterns of virologic response related to treatment.

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Viral Kinetics/Decision Rules/On Treatment Testing

Published: ; 2012 ; 142 : 1303 -1313

Gastroenterology

New virologic tools for management of chronic hepatitis B and C

Molecular biology techniques are routinely used to diagnose and monitor treatment of patients with chronic hepatitis B virus (HBV) and hepatitis C virus (HCV) infections. These tools can detect and quantify viral genomes, and analyze their sequence, in order to determine their genotype or subtype and to identify nucleotide or amino acid substitutions associated with resistance to antiviral drugs. They include real-time target amplification methods, which have been standardized and are widely used in clinical practice to diagnose and monitor HBV and HCV infections, and next-generation sequencing techniques, which are still restricted to research laboratories. In addition, new enzyme immunoassays can quantify hepatitis B surface and hepatitis C core antigens, and point-of-care tests and alternatives to biologic tests that require whole-blood samples obtained by venipuncture have been developed. We review these new virologic methods and their clinical and research applications to HBV and HCV infections.

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V. Treatment: Treatment Naïve with Standard of Care for Genotype 1 Infection16 Items

Treatment Naïve with SOC for Genotype 1 Infection

Centers for Disease Control and Prevention

Module 5: Treatment of Hepatitis C Infection
Lesson 4: Recommendations for Treatment-Naïve Patients

• Treatment for genotype 1, 2, 3, 4, 5, 6
• Treatment for acute hepatitis C
• Treatment for Patients with compensated cirrhosis

Treatment Naïve with SOC for Genotype 1 Infection

International Antiviral Society-USA

Approaches to Managing Treatment-Naive Hepatitis C Virus-Infected Patients: A Case-Based Discussion

Dr. Susanna Naggie discusses the characteristics of the Boceprevir and Telaprevir trials and how the data can be applied on the patient level.

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Treatment Naïve with SOC for Genotype 1 Infection

ProjectECHO™

New Insights for the Management of the Treatment Naïve Patient

This presentation provides information on topics that include, but are not limited, to the following:
• Target of Direct Antiviral Agents
• HCV Treatment Decisions for Protease Inhibitors
• Candidates for DAA Triple Therapy
• Treatment Initiation and Patient Education
• Stopping Rules
• Telaprevir and boceprevir adverse events
• Treatment Adherence Strategies

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Treatment Naïve with SOC for Genotype 1 Infection

Department of Veterans Affairs

Update on the Management and Treatment of Hepatitis C Virus Infection:

Therapy against Hepatitis C in Patients with Genotype 1

The Update on the Management and Treatment of Hepatitis C Virus Infection practice guideline provides the current best practice in the management of hepatitis C that include the use of peginterferon, ribavirin, boceprevir, and telaprevir containing therapy regimens.

Treatment Naïve with SOC for Genotype 1 Infection

American Association for the Study of Liver Disease

An Update on Treatment of Genotype 1 Chronic Hepatitis C Virus Infection

(Pages 1434-1437)

The updated AASLD practice uidelines include information regarding the changes for the optimal treatment regimen of genotype 1 chronic HCV patients, the development of direct-acting antiviral agents, and the identification of several single-nucleotide polymorphisms associated with spontaneous and treatment-induced clearance of HCV infection.

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Treatment Naïve with SOC for Genotype 1 Infection

New England Journal of Medicine

Telaprevir for Previously Untreated Chronic Hepatitis C Virus Infection

In phase 2 trials, telaprevir, a hepatitis C virus (HCV) genotype 1 protease inhibitor, in combination with peginterferon–ribavirin, as compared with peginterferon–ribavirin alone, has shown improved efficacy, with potential for shortening the duration of treatment in a majority of patients.

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Treatment Naïve with SOC for Genotype 1 Infection

Published: ; 2009 ; 360 : 1839 -1850

New England Journal of Medicine

Telaprevir and Peginterferon with or without Ribavirin for Chronic HCV Infection

In patients with chronic infection with hepatitis C virus (HCV) genotype 1, treatment with peginterferon alfa and ribavirin for 48 weeks results in rates of sustained virologic response of 40 to 50%. Telaprevir is a specific inhibitor of the HCV serine protease and could be of value in HCV treatment.

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Treatment Naïve with SOC for Genotype 1 Infection

New England Journal of Medicine

Boceprevir for Untreated Chronic HCV Genotype 1 Infection

Peginterferon–ribavirin therapy is the current standard of care for chronic infection with hepatitis C virus (HCV). The rate of sustained virologic response has been below 50% in cases of HCV genotype 1 infection. Boceprevir, a potent oral HCV-protease inhibitor, has been evaluated as an additional treatment in phase 1 and phase 2 studies.

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Treatment Naïve with SOC for Genotype 1 Infection

The Lancet

Efficacy of boceprevir, an NS3 protease inhibitor, in combination with peginterferon alfa-2b and ribavirin in treatment-naive patients with genotype 1 hepatitis C infection (SPRINT-1): an open-label, randomised, multicentre phase 2 trial.

Peginterferon plus ribavirin achieves sustained virological response (SVR) in fewer than half of patients with genotype 1 chronic hepatitis C virus infection treated for 48 weeks. We tested the efficacy of boceprevir, an NS3 hepatitis C virus oral protease inhibitor, when added to peginterferon alfa-2b and ribavirin.

Treatment Naïve with SOC for Genotype 1 Infection

Published: ; 2012 ; 142 : 1314 -1323

Gastroenterology

Maximizing opportunities and avoiding mistakes in triple therapy for hepatitis C virus.

Recently developed drugs and innovative strategies for the treatment of chronic infection with genotype 1 hepatitis C virus (HCV) have become the standard of care. The protease inhibitors telaprevir (Incivek) and boceprevir (Victrelis) are the first direct-acting antiviral (DAA) agents approved, and many more are being developed. These drugs substantially increased rates of sustained virologic response in treatment-naïve and -experienced patients, in conjunction with peginterferon and ribavirin (triple therapy), in phase 3 trials. The efficacy of triple therapy depends on appropriate selection of patients, although the population of patients that receive triple therapy could be expanded as the risk/benefit ratio improves. Attention to details that reflect the standard of care, such as appropriate dosing, anticipation of adverse effects, and strict adherence to stopping rules, will insure the success of these drugs and lead the way for new combination therapies.

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Treatment Naïve with SOC for Genotype 1 Infection

Published: ; 2013 ; 368 : 1878 -1887

New England Journal of Medicine

Sofosbuvir for previously untreated chronic hepatitis C infection.

In a single-group study of sofosbuvir combined with peginterferon-ribavirin, patients with predominantly genotype 1 or 4 HCV infection had a rate of sustained virologic response of 90% at 12 weeks. In a noninferiority trial, patients with genotype 2 or 3 infection who received either sofosbuvir or peginterferon with ribavirin had nearly identical rates of response (67%). Adverse events were less frequent with sofosbuvir than with peginterferon.

Key Reference

Published: ; 2014 ; 370(20) : 1889 -1898

Afdhal N, et al

Ledipasvir and Sofosbuvir for Untreated HCV Genotype 1 Infection

Article provides the results of a phase 3 trial in which previously patients with HCV genotype 1 infection were randomized to receive ledipasvir and sofosbuvir in a fixed-dose combination tablet once daily for 12 weeks, ledipasvir-sofosbuvir plus ribavirin for 12 weeks, ledipasvir-sofosbuvir for 24 weeks, or ledipasvir-sofosbuvir plus ribavirin for 24 weeks. Of enrolled patients, 16% had cirrhosis. The rates of sustained virologic response were 99% (95% confidence interval [CI], 96 to 100) in the group that received 12 weeks of ledipasvir-sofosbuvir; 97% (95% CI, 94 to 99) in the group that received 12 weeks of ledipasvir-sofosbuvir plus ribavirin; 98% (95% CI, 95 to 99) in the group that received 24 weeks of ledipasvir-sofosbuvir; and 99% (95% CI, 97 to 100) in the group that received 24 weeks of ledipasvir-sofosbuvir plus ribavirin.

Key Reference

Published: ; 2014 ; 370(20) : 1878 -1887

Lawitz E, et al

Ledipasvir and Sofosbuvir for 8 or 12 Weeks for Chronic HCV without Cirrhosis

Article provides the results of a phase 3 trial in which previously untreated non-cirrhotic, patients with HCV genotype 1 infection without cirrhosis were randomized to receive ledipasvir and sofosbuvir (ledipasvir-sofosbuvir) for 8 weeks, ledipasvir-sofosbuvir plus ribavirin for 8 weeks, or ledipasvir-sofosbuvir for 12 weeks. The rate of sustained virologic response was 94% (95% confidence interval [CI], 90 to 97) with 8 weeks of ledipasvir-sofosbuvir, 93% (95% CI, 89 to 96) with 8 weeks of ledipasvir-sofosbuvir plus ribavirin, and 95% (95% CI, 92 to 98) with 12 weeks of ledipasvir-sofosbuvir.

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Key Reference

Published: ; 2013 ; 368(20) : 1878 -1887

Lawtiz, E. et al

Sofosbuvir for Previously Untreated Chronic Hepatitis C Infection

Article provides the results of two phase 3 trials. The NEURTINO study was a single arm evaluation of the assessment of the effectiveness of sofosbuvir combined with peginterferon-ribavirin in patients with HCV genotype 1, 4, 5, or 6 (of whom 98% had genotype 1 or 4). In the FISSION trials was a patients with HCV genotype 2 or 3 infection were randomly assigned to receive sofosbuvir plus ribavirin for 12 weeks or peginterferon alfa-2a plus ribavirin for 24 weeks. In the two studies, the primary end point was a sustained virologic response at 12 weeks after the end of therapy.

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Key Reference

Published: ; 2014 ; 370(21) : 1983 -1992

Ferenci P, et al.

ABT-450/r-ombitasvir and dasabuvir with or without ribavirin for HCV

Article provides the results of a two phase 3 trials in which previously untreated patients with HCV genotype 1b infection (PEARL-III study, n = 419) or HCV 1a infection (PEARL-IV study, n 305) were randomized to receive 12 weeks of ABT-450/r-ombitasvir (at a once-daily dose of 150 mg of ABT-450, 100 mg of ritonavir, and 25 mg of ombitasvir), dasabuvir (250 mg twice daily), and ribavirin administered according to body weight or to matching placebo for ribavirin. The study regimen resulted in high rates of sustained virologic response among patients with HCV genotype 1b infection (99.5% with ribavirin and 99.0% without ribavirin) and among those with genotype 1a infection (97.0% and 90.2%, respectively).

Key Reference

Published: ; 2014 ; 370(17) : 1594 -1603

Field JJ, et al

Treatment of HCV with ABT-450/r-ombitasvir and dasabuvir with ribavirin

Article provides the results of a phase 3 trial in which previously patients with HCV genotype 1 infection were randomized to receive twelve weeks of a single-tablet coformulation of ABT-450/r-ombitasvir (at a once-daily dose of 150 mg of ABT-450, 100 mg of ritonavir, and 25 mg of ombitasvir), and dasabuvir (250 mg twice daily) with ribavirin (in doses determined according to body weight) (group A) or matching placebos (group B). The rate of sustained virologic response in group A was 96.2% (95.3% among patients with HCV genotype 1a infection and 98.0% among those with HCV genotype 1b infection).

 

V. Treatment: Treatment Experience with Standard of Care for Genotype 1 Infection2 Items

Treatment Experience with SOC for Genotype 1 Infection

Treatment Experience with Standard of Care

Module 5: Treatment of Hepatitis C Infection
Lesson 5: Recommendations for Treatment-Experienced Patients

• Characterizing prior treatment failure
• Retreatment of genotype 1 with prior partial response or relapse
• Retreatment of genotype 1 with prior nonresponse
• Retreatment of genotype 2 or 3
• Retreatment of genotype 4, 5, or 6

Treatment Experience with SOC for Genotype 1 Infection

American Association for the Study of Liver Diseases

An Update on Treatment of Genotype 1 Chronic Hepatitis C Virus Infection

(Pages 1437-1439)

The updated AASLD practice guidelines include information regarding the changes for the optimal treatment regimen of genotype 1 chronic HCV patients, the development of direct-acting antiviral agents, and the identification of several single-nucleotide polymorphisms associated with spontaneous and treatment-induced clearance of HCV infection.

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V. Treatment: Acute HCV1 Item

Acute HCV

Hepatitis C Online - University of Washington

 
Module 1. Screening and Diagnosis of Hepatitis Infection
Lesson 5. Diagnosis of Acute HCV Infection

  • Definition of Acute HCV
  • Clinical Features of Acute HCV
  • Laboratory Diagnosis of Acute HCV
  • CDC Case Definition for Acute HCV
  • V. Treatment: Management with Adverse Events8 Items

    Management with Adverse Events

    Centers for Disease Control and Prevention

    Module 5: Treatment of Hepatitis C Infection
    Lesson 6: Treatment-related Adverse Effects

    • Monitoring for side effects and treatment-related toxicity
    • Management of peginterferon and ribavirin-related toxicity
    • Management of boceprevir-related toxicity
    • Management of telaprevir-related toxicity

    Management with Adverse Events

    International Antiviral Society-USA

    A Practical Approach to the Management of Adverse Effects and Complications in the Treatment of HCV Infection: A Case-Based Discussion

    This case-study presentation provides information on topics that include, but are not limited, to the following:
    • Common HCV management techniques
    • Treatment discontinuation
    • Psychiatric issues
    • Depression
    • Telaprevir dose reduction
    • Thrombocytopenia
    • Dermatologic issues
    • Dermatologic management considerations
    • Weight loss

    Management with Adverse Events

    ProjectECHO™

    Additional Challenges in the Era of DAAs – Adverse Event Management and Drug
    Interactions Viral Resistance (Slides 1-22)

    This presentation provides information on topics that include, but are not limited, to the following:
    • The basics: telaprevir and boceprevir adverse events
    • Historical perspective on anemia in HCV
    • Boceprevir anemia summary
    • Telaprevir anemia summary
    • Occurrence of rash and management strategies
    • Managing drug-drug interactions

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    Management with Adverse Events

    Department of Veterans Affairs

    Interferon and Ribavirin Treatment Side Effects

    The Department of Veterans Affairs provide a topic review of the side effects of interferon and ribavirin treatment. The review contains sections on the management of side effects, constitutional, gastrointestinal, psychiatric side effects, dermatological, laboratory, other side effects, and references.

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    Management with Adverse Events

    Department of Veterans Affairs

    Update on the Management and Treatment of Hepatitis C Virus Infection

    (Pages 11-13)

    The Update on the Management and Treatment of Hepatitis C Virus Infection practice guideline provides the current best practice in the management of hepatitis C that include the use of peginterferon, ribavirin, boceprevir, and telaprevir containing therapy regimens.

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    Management with Adverse Events

    American Association for the Study of Liver Diseases

    An Update on Treatment of Genotype 1 Chronic Hepatitis C Virus Infection

    (Pages 1440-1441)

    The updated AASLD practice guidelines include information regarding the changes for the optimal treatment regimen of genotype 1 chronic HCV patients, the development of direct-acting antiviral agents, and the identification of several single-nucleotide polymorphisms associated with spontaneous and treatment-induced clearance of HCV infection.

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    Management with Adverse Events

    Published: ; 2010 ; 31 : 929 -937

    Alimentary Pharmacology and Therapeutics

    Review article: optimizing SVR and management of the haematological side effects of peginterferon/ribavirin antiviral therapy for HCV - the role of epoetin, G-CSF and novel agents.

    Chronic hepatitis C is one of the leading causes for chronic liver disease globally. The past two decades have seen many advances in hepatitis C treatment. Despite these advances, side effects of treatment are common. Haematological complications of treatment can result in treatment cessation and suboptimal results. Recent data have suggested a role for epoetin/granulocyte colony stimulating factor (G-CSF) in optimizing sustained virological response (SVR). This study investigates the nature, frequency and management of haematological side effects in the treatment of chronic hepatitis C infection.

    Management with Adverse Events

    Published: ; 2007 ; 102 : 880 -889

    The American Journal of Gastroenterology

    Strategies for managing anemia in hepatitis C patients undergoing antiviral therapy.

    Anemia is a common side effect that begins soon after the initiation of peginterferon/ribavirin in the treatment of hepatitis C virus (HCV) infection. It can cause symptoms that negatively impact quality of life (QOL) and is the most common reason for reducing the dose and temporarily or permanently discontinuing ribavirin. Such dose modifications have been shown to reduce the efficacy of treatment. Administering erythropoietin can improve anemia caused by peginterferon and ribavirin therapy and is more effective than dose reduction at improving QOL during treatment. However, erythropoietin, which is not approved by the U.S. Food and Drug Administration (FDA) for use in patients with HCV infection, adds another parenteral drug to the patient's treatment regimen, and is associated with additional costs, inconvenience, and potential side effects. A new ribavirin analog, viramidine, is expected to be associated with a lower incidence of anemia and, if proven effective, may eventually be substituted for ribavirin in combination with peginterferon to treat chronic hepatitis C. In the meantime, physicians must make the best possible use of the available options for managing anemia, especially in select patient groups who are most at risk for anemia and its complications.

    V. Treatment: Viral Resistance4 Items

    Viral Resistance

    International Antiviral Society-USA

    HCV Drug Resistance Mutations

    The International Antiviral Society-USA has developed a chart that presents mutations in hepatitis C virus that impact susceptibility to HCV drugs approved by the US FDA and to investigational drugs.

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    Viral Resistance

    Hepatitis C Online - University of Washington

    Slide Lecture: HCV Resistance to Protease Inhibitors

    • Resistance concepts and nomenclature
    • HCV virology as it relates to resistance
    • Overview of telaprevir and boceprevir resistance
    • Guidance on practical management of resistance
    • Drug resistance and the emergence of interferon alfa-free regimens

    Treatment: Viral Resistance

    Published: ; 2014 ; 108 : 181 -191

    Antiviral Research

    Update on hepatitis C virus resistance to direct-acting antiviral agents    

    Eva Poveda, David L. Wyles, Álvaro Mena, José D. Pedreira, Ángeles Castro-Iglesias, Edward Cachay

     

    • We review recent data on hepatitis C virus (HCV) resistance to direct-acting antiviral (DAA) agents.

    • An update on HCV resistance to DAA is provided for an optimized clinical management of resistance.

    • Polymorphisms conferring resistance might exist in some genotypes/subtypes at high rates.

    • Q80K, related to resistance to simeprevir, is found among 19–48% of genotype 1a sequences.

    • L31M and Y93H, key mutations to NS5A inhibitors, are found in 6–12% of NS5A genotype 1 sequences

     

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    V. Treatment: Drug-Drug Interaction7 Items

    Drug-Drug Interactions

    Centers for Disease Control and Prevention

    Module 5: Treatment of Hepatitis C Infection
    Lesson 7: Drug-Drug Interactions

    • Overview of inhibition and induction
    • Key drug-drug interactions

    Drug-Drug Interaction

    International Antiviral Society-USA

    Important Drug-Drug Interactions with Hepatitis C Virus Treatments

    This presentation provides information on the following topics:

    • Compare and contrast the clinical pharmacology of BOC and TVR
    • Identify therapeutic classes of drugs with the potential for drug interactions with BOC and TVR
    • Discuss management of interactions with BOC and TVR
    • Examine pharmacology and interaction potential of next "batch" of Hepatitis C agents

    Drug-Drug Interactions

    International Antiviral Soceity-USA

    HCV Drug Interactions: Trials, Tribulations, and Downright Confusion: A Case-Based Discussion

    This case-based presentation provides information on topics that include, but are not limited, to the following:
    • BOC, TVR and drug interactions
    • Effect of BOC and TVR on other CYP3A and/or Pgp substrates
    • Telaprevir effect on ortho-OH-atorvastatin
    • Impact of Ritonavir on TVR,BOC pharamcokinetics
    • HIV protease inhibitors interactions with TVR,BOC 

    Drug-Drug Interactions

    ProjectECHO™

    Additional Challenges in the Era of DAAs – Adverse Event Management and Drug Interactions Viral Resistance

    (Slides 23-32)

    This presentation provides information on topics that include, but are not limited, to the following:
    • The basics: telaprevir and boceprevir adverse events
    • Historical perspective on anemia in HCV
    • Boceprevir anemia summary
    • Telaprevir anemia summary
    • Occurrence of rash and management strategies
    • Managing drug-drug interactions

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    Drug-Drug Interactions

    www.hep-druginteractions.org

    www.hep-druginteractions.org

    Hep-druginteractions.org provides evidence-based drug-drug interaction resources available as HCV drug interaction charts, current articles, webcasts, video presentations, and links.

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    Drug-Drug Interactions

    International Antiviral Society-USA

    Drug Interactions With Medications for Treating Hepatitis C Virus Infection

    This Cases on the Web activity describes a case and presents various clinical decision points, each about a patient with hepatitis C virus (HCV) infection who may be experiencing complications resulting from an interaction between the drugs in his HCV regimen and other coadministered drugs.

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    Drug-Drug Interactions

    Published: ; 2012 ; 55 : 1620 -1628

    Hepatology

    Review and Management of Drug Interactions with Boceprevir and Telaprevir

    Boceprevir and telaprevir, when added to pegylated interferon and ribavirin for the treatment of chronic hepatitis C virus infection, increase the rates of sustained virologic response in treatment naïve persons to approximately 70%. While these agents represent an important advance in the treatment of chronic hepatitis C virus, they present new treatment challenges to the Hepatology community. Boceprevir and telaprevir are both substrates and inhibitors of the hepatic enzyme cytochrome P450 3A and the drug transporter, P-glycoprotein, which predisposes these agents to many drug interactions. Identification and appropriate management of potential drug interactions with telaprevir and boceprevir is critical for optimizing therapeutic outcomes during hepatitis C treatment. This review highlights the pharmacologic characteristics and drug interaction potential of boceprevir and telaprevir and provides guidance on the management of drug interactions with these agents.

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    V. Treatment: Investigational Agents3 Items

    Investigational Agents

    Published: ; 2013 ; : -

    Hepatology

    Faldaprevir combined with peginterferon alfa-2a and ribavirin in treatment-naïve
    patients with chronic genotype-1 HCV: SILEN-C1 trial.

     

    Investigational Agents

    Hepatology

    Faldaprevir combined with peginterferon Alfa-2a and ribavirin in chronic HCV genotype-1 patients with prior nonresponse: SILEN-C2 trial.

     

    Investigational Agents

    Published: ; 2012 ; 366 : 216 -224

    New England Journal of Medicine

    Preliminary Study of Two Antiviral Agents for Hepatitis C Genotype 1

    Daclatasvir is a first-in-class, highly selective HCV NS5A replication complex inhibitor with picomolar potency in vitro. Asunaprevir is a highly active HCV NS3 protease inhibitor. Both daclatasvir and asunaprevir produce robust declines in HCV RNA levels in patients with HCV genotype 1 infection, and administration of the two drugs in combination did not produce a clinically meaningful pharmacokinetic interaction. In this study, daclatasvir and asunaprevir were administered in combination, with or without peginterferon alfa-2a and ribavirin, for 24 weeks in patients with HCV genotype 1 infection who had not had a response to previous treatment with peginterferon and ribavirin. We report preliminary data from the exploratory cohort, including the percentages of patients with sustained virologic response at 12, 24, and 48 weeks after the end of the treatment period.

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    V. Treatment: Special Populations – HIV/HCV Co-infection, Non-genotype 1 Infection, Liver Transplant10 Items

    Special Populations

    Centers for Disease Control and Prevention

    Module 6: Treatment of Special Populations and Special Situations

    Lesson 3: Treatment of Patients with HIV Coinfection

    • High Burden of HCV Disease in Corrections
    • Timing of Treatment

    Lesson 4: Treatment of Patients with HBV Coinfection

    Lesson 5: Treatment of Patients with Renal Disease

    Lesson 6: Treatment of Patients with Extrahepatic Manifestations

    Lesson 7: Treatment of Patients with Decompensated Cirrhosis




    Special Populations

    Department of Veterans Affairs

    Update on the Management and Treatment of Hepatitis C Virus Infection:

    Groups with Special Considerations for Therapy

    The Update on the Management and Treatment of Hepatitis C Virus Infection practice guideline provides the current best practice in the management of hepatitis C that include the use of peginterferon, ribavirin, boceprevir, and telaprevir containing therapy regimens.

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    Special Populations

    Department of Veterans Affairs

    Update on the Management and Treatment of Hepatitis C Virus Infection:

    Supplement - Additional Groups with Special Considerations for Therapy

    The Update on the Management and Treatment of Hepatitis C Virus Infection practice guideline provides the current best practice in the management of hepatitis C that include the use of peginterferon, ribavirin, boceprevir, and telaprevir containing therapy regimens.

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    Special Populations

    International Antiviral Society-USA

    The Use of Heaptitis C Virus (HCV) Protease Inhibitors in HIV/HCV-Coinfected Patients

    This Cases on the Web activity describes 3 cases and presents various clinical decision points, each focusing on use of hepatitis C virus protease inhibitors (HCV PIs) in treating a patient who has HIV and HCV coinfection.

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    Special Populations

    International Antiviral Society-USA

    Issues in the Care of HIV and Hepatitis C Virus-Coinfected Patients:
    Antiretroviral Pharmacokinetics, Drug Interactions, and Liver Transplantation

    This Cases on the Web activity consists of 2 cases and various clinical decision points, each focusing on providing care for HIV-infected patients with ongoing liver disease.

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    Special Population

    Published: ; 2012 ; 142 : 1324 -1334

    Gastroenterology

    Management of Patients Coinfected With HCV and HIV: A Close Look at the Role for Direct-Acting Antivirals

    With the development of effective therapies against human immunodeficiency virus (HIV), hepatitis C virus (HCV) infection has become a major cause of morbidity and mortality among patients with both infections (coinfection). In addition to the high prevalence of chronic HCV, particularly among HIV-infected injection drug users, the rate of incident HIV infections is increasing among HIV-infected men who have sex with men, leading to recommendations for education and screening for HCV in this population. Liver disease is the second leading and, in some cases, a preventable cause of death among coinfected patients. Those at risk for liver disease progression are usually treated with a combination of interferon (IFN) and ribavirin (RBV), which is not highly effective; it has low rates of sustained virologic response (SVR), especially for coinfected patients with HCV genotype 1 and those of African descent. Direct-acting antivirals might overcome factors such as immunodeficiency that can reduce the efficacy of IFN. However, for now it remains challenging to treat coinfected patients due to interactions among drugs, additive drug toxicities, and the continued need for combination therapies that include pegylated IFN. Recently developed HCV protease inhibitors such as telaprevir and boceprevir, given in combination with pegylated IFN and RBV, could increase the rate of SVR with manageable toxicity and drug interactions. We review the latest developments and obstacles to treating coinfected patients.

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    Special Populations

    International Antiviral Society-USA

    Hepatitis C Virus Coinfection: New Drugs, New Strategies

    This presentation provides information on the following topics:

    • HCV standard of care treatment in HIV
    • Use of TVR and BOC - lessons from monoinfection
    • Genotype 1 treatment algorithms (monoinfected)
    • TVR and BOC HIV/HCV study data
    • Future treatment strategies
    • Individualized decision - treat vs. wait?

    Treatment of HIV/HCV Co-infected Patients – May 30, 2014

    Kristen Marks, MD, MS

    Kristen Marks, MD, MS
    Assistant Professor of Medicine
    Division of Infectious Diseases
    Weill Cornell Medical College

    Dr. Marks discusses the following topics during this webinar video:
    • Important Topics for the Coinfected
    • HCV versus HIV/HCV Geno 1 in Clinical Trials (Not head to head comparisons)
    • Risk of Liver Decompensation in HIV/HCV w/ Advanced Fibrosis
    • Minimum to Know Pre-treatment
    • HIV/HCV CoInfection, GT2 and GT3 guidelines
    • SOF + RBV in HIV/HCV (PHOTON)
    • Frequency of virologic failures
    • Sofosbuvir, Simeprevir, and HIV Medications
    • Drug interactions 

    Special Populations

    Department of Veterans Affairs

    Chronic Hepatitis C Virus (HCV) Infection: Treatment Considerations.  Groups with Special Considerations for Therapy

    This section of the VA treatment guidelines addresses current treatment strategies for the treatment of patients with renal insufficiency or hepatic impairment, in patients in the pre- or post-liver transplant period or who have received other solid organ transplants.

    Special Populations

    EASL guidelines: Treatment of patients with severe liver disease

    V. Treatment: Patient Resources2 Items

    Patient Resources

    HCVinfo.org

    HCVinfo.org

    The goal of hcvinfo.org is to provide resources to providers, patients, and patient supporters to help with the care of patients with hepatitis C. Through the clinics at Duke, HCVinfo.org content providers have gained tremendous experience in this field, and hope to share their resources and tools.

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    Patient Resources

    Department of Veterans Affairs

    Department of Veterans Affiars Hepatitis C Patient Resources

    The Department of Veterans Affairs makes available information concerning Hepatitis A, B, C, getting tested, diagnosis, treatment, liver complications, living with hepatitis C, and community resources.

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    VI. SVR and Post-SVR Management and Follow-up2 Items

    Follow-up and Screening for HCC

    Dr. Dawd Siraj

    Management After SVR

    Dr. Dawd Siraj discusses the benefits of sustained virologic response (SVR) longevity, the durability of SVR, SVR follow-up, and literature references for a better understanding of management after SVR is achieved.

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    SVR

    Published: ; 2011 ; 52 : 889 -900

    Clinical Infectious Diseases

    Sustained Virologic Response to Antiviral Therapy for Chronic Hepatitis C Virus Infection: A Cure and So Much More

    Sustained virologic response (SVR) is defined as aviremia 24 weeks after completion of antiviral therapy for chronic hepatitis C virus (HCV) infection. In analyses of SVR durability, the incidence of late relapse is extremely low (<1%). Histologic regression of both necroinflammation and fibrosis has been demonstrated in paired liver biopsy samples in SVR-achieving patients. More noteworthy is the sustained responder's favorable prognosis even with baseline cirrhosis; despite mostly retrospective analyses, relative to nonresponders or to those untreated, patients with SVR have significantly fewer liver-related complications, less hepatocellular carcinoma, and fewer liver-related deaths. Although HCV is associated with insulin resistance, successful eradication of HCV appears to reduce the risk of impaired fasting glucose and diabetes development. In summary, chronic HCV infection is curable with SVR attainment, and with cure comes improved liver histology and more favorable clinical outcomes, in comparison with patients who do not achieve the same therapeutic milestone.

    VII. Guidance on Developing/Managing a HCV Clinic1 Item

    Developing and Managing a HCV Clinic

    Brody School of Medicine, East Carolina University

    HCV Management Manual – Preparing the office prior to starting to treat HCV
    infected patients

    The Brody School of Medicine, East Carolina University HCV Management Manual provides information on staff education and roles, clinic hours of operation, procedures, resources, and clinic organization that is necessary to provide comprehensive care to HCV patients receiving treatment.

    The Brody School of Medicine, East Carolina University HCV Management Manual was developed from information referenced from Projects in Knowledge® eHandbook HCV & Guidance: Chapter 1: Getting Ready for Direct-Acting Antiviral (DAA) Therapy (Free Registration Required).

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    VIII. Additional Resources: Registration Required4 Items

    Additional References

    Clinical Care Options

    Clinical Care Options

    Clinical Care Options' interactive programs inform practitioners about hepatitis treatments, guidelines, and management strategies, and provides conference coverage.

    Download

    Additional Resources

    IDCareLive

    IDCareLive

    Offers free online sessions on management and treatment strategies of hepatitis C and HIV.

    Download

    Additional Resources

    Projects in Knowledge

    Projects in Knowledge

    Projects In Knowledge provides physicians and other clinical professionals ACCME accredited educational resources on a variety of topics.

    Download

    Additonal Resources

    American Association for the Study of Liver Disease

    ACT on HCV: A Practical Introduction to Treating HCV

    AASLD Curriculum & Training (ACT) is a initiative that will provide strategies and mentoring for managing HCV and is designed to increase the confidence and competence of healthcare professionals new to providing care for patients with HCV.

    ACT on HCV Curriculum includes the following components: five online interactive CME/CE-certified modules; an experiential component which includes logging direct clinical experiences, mentoring from "Expert Resources", and participation in case-based discussions via the ACT on HCV community teleconference/web-based programming; an online final examination, and a Certificate of Curriculum Completion for successful trainees.

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