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CCO Annual Update

Hepatitis Annual Update 2006

Hepatitis B Virus Resistance for Clinicians

Module 1 of 10

Program Director: Emmet B. Keeffe, MD, MACP

Faculty:

Anna S. F. Lok, MD
  • Anna S. F. Lok, MD

CREDIT INFORMATION

Release Date: 08/04/06

Expiration Date: 08/03/07


Physicians: maximum of 1.0 AMA PRA Category 1 Credit

Registered Nurses: 1.3 Nursing contact hours

Pharmacists: 1.0 contact hour (0.1 CEUs)

Status: Please log in to view status

Begin the Module

Anna Lok, MD, discusses the development of HBV drug resistance associated with nucleos(t)ide analogue therapy.

Learning Objectives

Upon completion of this activity, participants should be able to:

  • Describe the methods used to detect antiviral-resistant forms of HBV
  • Review ways to prevent the development of antiviral-resistant HBV
  • Discuss the management of antiviral-resistant HBV

The Changing Face of Antiviral Therapy in Hepatitis B

Module 2 of 10

Program Director: Emmet B. Keeffe, MD, MACP

Faculty:

Robert P. Perrillo, MD
  • Robert P. Perrillo, MD

CREDIT INFORMATION

Release Date: 08/01/06

Expiration Date: 07/31/07


Physicians: maximum of 1.0 AMA PRA Category 1 Credit

Registered Nurses: 1.2 Nursing contact hours

Pharmacists: 1.0 contact hour (0.1 CEUs)

Status: Please log in to view status

Begin the Module

Robert Perrillo, MD, discusses current and emerging treatment approaches for HBV infection, highlighting the potential role of long-term antiviral suppression.

Learning Objectives

Upon completion of this activity, participants should be able to:

  • Review advances with currently licensed antivirals and those in late-stage development
  • State the findings of recent studies linking long-term disease complications to hepatitis B virus replication
  • Discuss the implications that long-term antiviral suppression could have on the management of hepatitis B virus

New Agents in Development for Hepatitis B

Module 3 of 10

Program Director: Emmet B. Keeffe, MD, MACP

Faculty:

Patrick Marcellin, MD
  • Patrick Marcellin, MD

CREDIT INFORMATION

Release Date: 08/02/06

Expiration Date: 08/01/07


Physicians: maximum of 1.25 AMA PRA Category 1 Credits

Registered Nurses: 1.4 Nursing contact hours

Pharmacists: 1.2 contact hours (0.12 CEUs)

Status: Please log in to view status

Begin the Module

Patrick Marcellin, MD, PhD, discusses novel therapies for hepatitis B currently in development, some of which have alternative targets in the HBV viral life cycle and may improve virologic response and resistance rates.

Learning Objectives

Upon completion of this activity, participants should be able to:

  • List the drugs in clinical development for the treatment of hepatitis B, and their potential role in treatment
  • Recount the latest clinical trial data on new agents for the treatment of chronic hepatitis B
  • Identify drugs in earlier stages of development
  • Define strategies for developing new classes of drugs

Update on the Management of HBV

Module 4 of 10

Program Director: Emmet B. Keeffe, MD, MACP

Faculty:

Marc G. Ghany, MD
  • Marc G. Ghany, MD

CREDIT INFORMATION

Release Date: 07/27/06

Expiration Date: 07/26/07


Physicians: maximum of 1.0 AMA PRA Category 1 Credit

Registered Nurses: 1.3 Nursing contact hours

Pharmacists: 1.1 contact hours (0.11 CEUs)

Status: Please log in to view status

Begin the Module

Marc Ghany, MD, discusses a recent National Institutes of Health (NIH) Workshop on the management of chronic hepatitis B; experts gathered to assess issues such as current advances in the fundamental comprehension of the hepatitis B virus (HBV) and chronic hepatitis B, optimal management strategies, and viable directions for future research.

Learning Objectives

Upon completion of this activity, participants should be able to:

  • Describe the purpose of the National Institutes of Health (NIH) workshop on management of Hepatitis B
  • Review the conclusions of the NIH workshop
  • Discuss the unresolved issues and challenges raised by the workshop

Interferon and Ribavirin: Mechanisms of Action, Resistance, and Why It Matters

Module 5 of 10

CME Program Director: Emmet B. Keeffe, MD, MACP

Faculty:

Raymond T. Chung, MD
  • Raymond T. Chung, MD

CREDIT INFORMATION

Release Date: 08/03/06

Expiration Date: 08/02/07


Physicians: maximum of 1.25 AMA PRA Category 1 Credits

Registered Nurses: 1.6 Nursing contact hours

Pharmacists: 1.3 contact hours (0.13 CEUs)

Status: Please log in to view status

Begin the Module

Raymond Chung, MD, describes the natural history, structure, and life cycle of HCV, and uses viral kinetic modeling as a framework for conceptualizing interferon’s various mechanisms of action as well as those of other antiviral agents acting through different mechanisms.

Learning Objectives

Upon completion of this activity, participants should be able to:

  • Describe the epidemiology, natural history, and life cycle of hepatitis C virus (HCV)
  • Review mechanisms of current approaches for the treatment of HCV
  • Recount the rationale and potential for novel agents in the treatment of HCV

New Therapies for Chronic Hepatitis C

Module 6 of 10

Program Director: Emmet B. Keeffe, MD, MACP

Faculty:

Gary L. Davis, MD
  • Gary L. Davis, MD

CREDIT INFORMATION

Release Date: 08/25/06

Expiration Date: 08/24/07


Physicians: maximum of 1.0 AMA PRA Category 1 Credit

Registered Nurses: 1.2 Nursing contact hours

Pharmacists: 1.0 contact hour (0.1 CEUs)

Status: Please log in to view status

Begin the Module

Gary Davis, MD, discusses novel agents currently in development for hepatitis C treatment; in contrast to interferon and ribavirin, these new drugs target critical processes in the HCV life cycle.

Learning Objectives

Upon completion of this activity, participants should be able to:

  • Discuss prospective therapeutic targets inherent in the mechanism of hepatitis C virus (HCV) viral replication
  • Explain the rationale for and potential utility of novel agents under development for the treatment of HCV
  • Summarize recent data from clinical trials of investigational new anti-HCV drugs

Customizing HCV Therapy With Current Agents: Optimizing Patient Outcomes

Module 7 of 10

Program Director: Emmet B. Keeffe, MD, MACP

Faculty:

Mark S. Sulkowski, MD
  • Mark S. Sulkowski, MD

CREDIT INFORMATION

Release Date: 08/01/06

Expiration Date: 07/31/07


Physicians: maximum of 1.25 AMA PRA Category 1 Credits

Registered Nurses: 1.5 Nursing contact hours

Pharmacists: 1.2 contact hours (0.12 CEUs)

Status: Please log in to view status

Begin the Module

Mark S. Sulkowski, MD, reviews emerging data supporting the use of viral kinetics to improve individual patient outcomes in the treatment of HCV with peginterferon plus ribavirin.

Learning Objectives

Upon completion of this activity, participants should be able to:

  • Describe general principles of individualizing therapy based on patient and viral characteristics
  • Recount factors or markers that are predictive of HCV treatment success
  • Discuss specific strategies for optimizing treatment, such as longer treatment for genotype 1 and shorter treatment for genotype 2/3

Debate: Are Noninvasive Tests Ready to Replace Liver Biopsy?

Module 8 of 10

Program Director: Emmet B. Keeffe, MD, MACP

Faculty:

Nezam H. Afdhal, MD, FRCPIMitchell L. Shiffman, MD
  • Nezam H. Afdhal, MD, FRCPI
  • Mitchell L. Shiffman, MD

CREDIT INFORMATION

Release Date: 06/30/06

Expiration Date: 06/29/07


Physicians: maximum of 1.5 AMA PRA Category 1 Credits

Registered Nurses: 1.7 Nursing contact hours

Pharmacists: 1.4 contact hours (0.14 CEUs)

Status: Please log in to view status

Begin the Module

Nezam Afdhal, MD, and Mitchell Shiffman, MD, debate the pros and cons of various direct and indirect biomarkers that have been developed for monitoring fibrosis vs liver biopsy, their implications for clinical practice, and the potential for their use in place of liver biopsies for assessing a patient’s type and grade of fibrosis.

Learning Objectives

Upon completion of this activity, participants should be able to:

  • Describe the role of liver biopsy and the noninvasive tests available (and in development) for the diagnosis of liver fibrosis and inflammation
  • Review the latest data supporting the use of liver biopsy or noninvasive tests, including data on risk, sensitivity, and specificity
  • Discuss the limitations of liver biopsy and noninvasive tests

Liver Transplantation: The Past Quarter Century and the Future

Module 9 of 10

Program Director: Emmet B. Keeffe, MD, MACP

Faculty:

Emmet B. Keeffe, MD, MACP
  • Emmet B. Keeffe, MD, MACP

CREDIT INFORMATION

Release Date: 06/28/06

Expiration Date: 06/27/07


Physicians: maximum of 1.0 AMA PRA Category 1 Credit

Registered Nurses: 1.1 Nursing contact hours

Pharmacists: 1.0 contact hour (0.1 CEUs)

Status: Please log in to view status

Begin the Module

Emmet Keeffe, MD, MACP, traces progress in human liver transplantation over the past 25 years, provides a brief summary of the current use of liver transplantation, and speculates on the future directions of liver transplantation.

Learning Objectives

Upon completion of this activity, participants should be able to:

  • Review the changes in liver transplantation over the past 25 years
  • Discuss the impact of different systems for assigning scarce liver to patients with end-stage liver disease or hepatocellular carcinoma
  • Describe what the trends in liver disease and transplantation suggest for the future

The Paradox of Treating Liver Disease With Potentially Hepatotoxic Drugs

Module 10 of 10

Program Director: Emmet B. Keeffe, MD, MACP

Faculty:

Eugene R. Schiff, MD, MACP, FRCP, MACGRonald Concha, MD
  • Eugene R. Schiff, MD, MACP, FRCP, MACG
  • Ronald Concha, MD

CREDIT INFORMATION

Release Date: 07/03/06

Expiration Date: 07/02/07


Physicians: maximum of 1.0 AMA PRA Category 1 Credit

Registered Nurses: 1.1 Nursing contact hours

Pharmacists: 1.0 contact hour (0.1 CEUs)

Status: Please log in to view status

Begin the Module

Ronald Concha, MD, and Eugene Schiff, MD, review common examples of potentially hepatotoxic drugs used to treat disorders associated with liver disease.

Learning Objectives

Upon completion of this activity, participants should be able to:

  • Review the impact of hepatotoxic drugs on the liver
  • Discuss the effect of statins, thiazolidinediones, and other lipid-lowering and antiglycemic agents on liver disease
  • Describe the impact of acetaminophen on liver disease

Animations

Life Cycle of Hepatitis C Virus


Presents the steps by which the hepatitis C virus infects and replicates in the cell.


This animation and others are available for use offline from the Download Library.


To download to your own computer and use for personal or teaching purposes, click here


Format: Adobe Flash (.swf) | File size: 4.31 MB

Drug Targets in the Hepatitis C Virus Life Cycle


Dr. Gary Davis discusses potential targets for new therapeutic agents in the hepatitis C virus life cycle. This animation and others are available for use offline from the Download Library.


This animation and others are available for use offline from the Download Library.


To download to your own computer and use for personal or teaching purposes, click here


Format: Adobe Flash (.swf) | File size: 18.14 MB

CCO Slidesets

4th Annual Clinical Care Options for Hepatitis Symposium: HBV Highlights

Download the Slideset


Format: Microsoft PowerPoint (.ppt) | File size: 1.26 MB | Date posted: 8/9/2006


4th Annual Clinical Care Options for Hepatitis Symposium: HCV Highlights

Download the Slideset


Format: Microsoft PowerPoint (.ppt) | File size: 2.66 MB | Date posted: 8/7/2006


4th Annual Clinical Care Options for Hepatitis Symposium: Hot Topics

Download the Slideset


Format: Microsoft PowerPoint (.ppt) | File size: 1.00 MB | Date posted: 8/11/2006


Disclaimer: The materials published on the Clinical Care Options Web site reflect the views of the reviewers or authors of the CCO material, not those of Clinical Care Options, LLC, the CME provider, or the companies providing educational grants. The materials may discuss uses and dosages for therapeutic products that have not been approved by the United States Food and Drug Administration. A qualified healthcare professional should be consulted before using any therapeutic product discussed. Readers should verify all information and data before treating patients or using any therapies described in these materials.

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