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Gastroenterologists, hepatologists, nurse practitioners, physician assistants, and other health care professionals involved in the treatment of patients with HCV.
HCV; drug-drug interactions; interferon-free regimens; HIV/HCV coinfection
Andrew J. Muir, MD, MHS, FACP, received his medical and master of health sciences degree from Duke University in Durham, North Carolina. He completed his residency in the department of medicine, where he served as chief resident. Dr. Muir also completed fellowships in gastroenterology and health services research at Duke and at the Durham Veterans Administration Medical Center, respectively. He joined the faculty of Duke in the division of gastroenterology.
Nancy Reau, MD, is associate professor of medicine at the University of Chicago School of Medicine. She received her Bachelor of Science degree from Oberlin College in Oberlin, OH, and her medical degree from Ohio State University College of Medicine in Columbus. She completed her internship, residency, and a fellowship in gastroenterology/hepatology at Ohio State and a fellowship in advanced transplant hepatology at Johns Hopkins Hospital in Baltimore, MD. Dr. Reau is board certified in internal medicine, gastroenterology, and transplant hepatology.
| 1. | Discuss the importance of HCV treatment and achievement of sustained viral response for improvement of hepatic and extrahepatic manifestations in mild as well as severe disease. | 2. | Apply the clinical evidence to optimize treatment duration, monitoring strategies, and drug-drug interactions for newly approved and emerging interferon-free regimens. |
| 3. | Appraise the clinical evidence to determine how to optimize the use of newly approved and emerging interferon-free regimens in special populations of patients including those with decompensated cirrhosis, HIV/HCV coinfection, transplant/post-transplant of liver, renal impairment, and HCV genotype 3. |
| 1. | Discuss the importance of HCV treatment and achievement of sustained viral response for improvement of hepatic and extrahepatic manifestations in mild as well as severe disease. |
| 2. | Apply the clinical evidence to optimize treatment duration, monitoring strategies, and drug-drug interactions for newly approved and emerging interferon-free regimens. |
| 3. | Appraise the clinical evidence to determine how to optimize the use of newly approved and emerging interferon-free regimens in special populations of patients including those with decompensated cirrhosis, HIV/HCV coinfection, transplant/post-transplant of liver, renal impairment, and HCV genotype 3. |

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