Guest guest Posted January 21, 2008 Report Share Posted January 21, 2008 Alimentary Pharmacology & Therapeutics (OnlineAccepted Articles). doi:10.1111/j.1365-2036.2008.03620.x Abstract Histologic benefits of virologic response to peginterferon alfa-2a monotherapy in patients with hepatitis C and advanced fibrosis or compensated cirrhosis G. T. EVERSON11Section of Hepatology, University of Colorado School of Medicine, University of Colorado Health Sciences Center, Denver, Colorado, L. BALART22FACG Section of Gastroenterology, Louisiana State University Health Sciences Center, New Orleans, Louisiana, S. S. LEE33Faculty of Medicine, University of Calgary, Calgary, Alberta, Canada, R. W. REINDOLLAR44Carolinas Center for Liver Disease, Charlotte, North Carolina, M. L. SHIFFMAN55Hepatology Section, Virginia Commonwealth University Medical Center, Richmond, Virginia, G. Y. MINUK66Section of Hepatology, Department of Medicine, University of Manitoba, Winnipeg, Manitoba, Canada, P. J. POCKROS77Division of Gastroenterology/Hepatology, The Scripps Clinic, La Jolla, California, S. GOVINDARAJAN88Department of Pathology, Keck School of Medicine, University of Southern California, Los Angeles, California, E. LENTZ99Roche Laboratories, Nutley, New Jersey & E. J. HEATHCOTE1010Department of Medicine, University Health Network, Toronto Western Hospital, Toronto, Ontario, Canada1Section of Hepatology, University of Colorado School of Medicine, University of Colorado Health Sciences Center, Denver, Colorado 2FACG Section of Gastroenterology, Louisiana State University Health Sciences Center, New Orleans, Louisiana 3Faculty of Medicine, University of Calgary, Calgary, Alberta, Canada 4Carolinas Center for Liver Disease, Charlotte, North Carolina 5Hepatology Section, Virginia Commonwealth University Medical Center, Richmond, Virginia 6Section of Hepatology, Department of Medicine, University of Manitoba, Winnipeg, Manitoba, Canada 7Division of Gastroenterology/Hepatology, The Scripps Clinic, La Jolla, California 8Department of Pathology, Keck School of Medicine, University of Southern California, Los Angeles, California 9Roche Laboratories, Nutley, New Jersey 10Department of Medicine, University Health Network, Toronto Western Hospital, Toronto, Ontario, Canada Correspondence and/or reprint requests to: T. Everson, MD, FACP Section of Hepatology University of Colorado School of Medicine University of Colorado Health Sciences Center UCH AOP, Hepatology Section 1635 N Ursula, B-154 PO Box 6510 Aurora, CO 80045 USA Telephone: 720-848-2291 Fax: 720-848-2246 Email: greg.everson@... Summary Background: Patients with chronic hepatitis C virus (HCV) and advanced fibrosis or cirrhosis are at risk for disease progression and hepatic decompensation. Aim: To determine the effects on hepatic histology of treatment with peginterferon alfa-2a (90 or 180 ìg/wk) or interferon alfa-2a (3 million units 3 times weekly) for 48 weeks in patients with paired biopsies. Methods: Liver biopsies were obtained at baseline and 6 months after end of treatment. Histologic and virologic responses were compared. Results: Patients attaining sustained virologic response (SVR; n=40) demonstrated the greatest improvements in fibrosis (-1.0, P _________________________________________________________________ Need to know the score, the latest news, or you need your HotmailR-get your " fix " . http://www.msnmobilefix.com/Default.aspx Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 21, 2008 Report Share Posted January 21, 2008 Alimentary Pharmacology & Therapeutics (OnlineAccepted Articles). doi:10.1111/j.1365-2036.2008.03620.x Abstract Histologic benefits of virologic response to peginterferon alfa-2a monotherapy in patients with hepatitis C and advanced fibrosis or compensated cirrhosis G. T. EVERSON11Section of Hepatology, University of Colorado School of Medicine, University of Colorado Health Sciences Center, Denver, Colorado, L. BALART22FACG Section of Gastroenterology, Louisiana State University Health Sciences Center, New Orleans, Louisiana, S. S. LEE33Faculty of Medicine, University of Calgary, Calgary, Alberta, Canada, R. W. REINDOLLAR44Carolinas Center for Liver Disease, Charlotte, North Carolina, M. L. SHIFFMAN55Hepatology Section, Virginia Commonwealth University Medical Center, Richmond, Virginia, G. Y. MINUK66Section of Hepatology, Department of Medicine, University of Manitoba, Winnipeg, Manitoba, Canada, P. J. POCKROS77Division of Gastroenterology/Hepatology, The Scripps Clinic, La Jolla, California, S. GOVINDARAJAN88Department of Pathology, Keck School of Medicine, University of Southern California, Los Angeles, California, E. LENTZ99Roche Laboratories, Nutley, New Jersey & E. J. HEATHCOTE1010Department of Medicine, University Health Network, Toronto Western Hospital, Toronto, Ontario, Canada1Section of Hepatology, University of Colorado School of Medicine, University of Colorado Health Sciences Center, Denver, Colorado 2FACG Section of Gastroenterology, Louisiana State University Health Sciences Center, New Orleans, Louisiana 3Faculty of Medicine, University of Calgary, Calgary, Alberta, Canada 4Carolinas Center for Liver Disease, Charlotte, North Carolina 5Hepatology Section, Virginia Commonwealth University Medical Center, Richmond, Virginia 6Section of Hepatology, Department of Medicine, University of Manitoba, Winnipeg, Manitoba, Canada 7Division of Gastroenterology/Hepatology, The Scripps Clinic, La Jolla, California 8Department of Pathology, Keck School of Medicine, University of Southern California, Los Angeles, California 9Roche Laboratories, Nutley, New Jersey 10Department of Medicine, University Health Network, Toronto Western Hospital, Toronto, Ontario, Canada Correspondence and/or reprint requests to: T. Everson, MD, FACP Section of Hepatology University of Colorado School of Medicine University of Colorado Health Sciences Center UCH AOP, Hepatology Section 1635 N Ursula, B-154 PO Box 6510 Aurora, CO 80045 USA Telephone: 720-848-2291 Fax: 720-848-2246 Email: greg.everson@... Summary Background: Patients with chronic hepatitis C virus (HCV) and advanced fibrosis or cirrhosis are at risk for disease progression and hepatic decompensation. Aim: To determine the effects on hepatic histology of treatment with peginterferon alfa-2a (90 or 180 ìg/wk) or interferon alfa-2a (3 million units 3 times weekly) for 48 weeks in patients with paired biopsies. Methods: Liver biopsies were obtained at baseline and 6 months after end of treatment. Histologic and virologic responses were compared. Results: Patients attaining sustained virologic response (SVR; n=40) demonstrated the greatest improvements in fibrosis (-1.0, P _________________________________________________________________ Need to know the score, the latest news, or you need your HotmailR-get your " fix " . http://www.msnmobilefix.com/Default.aspx Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 21, 2008 Report Share Posted January 21, 2008 Alimentary Pharmacology & Therapeutics (OnlineAccepted Articles). doi:10.1111/j.1365-2036.2008.03620.x Abstract Histologic benefits of virologic response to peginterferon alfa-2a monotherapy in patients with hepatitis C and advanced fibrosis or compensated cirrhosis G. T. EVERSON11Section of Hepatology, University of Colorado School of Medicine, University of Colorado Health Sciences Center, Denver, Colorado, L. BALART22FACG Section of Gastroenterology, Louisiana State University Health Sciences Center, New Orleans, Louisiana, S. S. LEE33Faculty of Medicine, University of Calgary, Calgary, Alberta, Canada, R. W. REINDOLLAR44Carolinas Center for Liver Disease, Charlotte, North Carolina, M. L. SHIFFMAN55Hepatology Section, Virginia Commonwealth University Medical Center, Richmond, Virginia, G. Y. MINUK66Section of Hepatology, Department of Medicine, University of Manitoba, Winnipeg, Manitoba, Canada, P. J. POCKROS77Division of Gastroenterology/Hepatology, The Scripps Clinic, La Jolla, California, S. GOVINDARAJAN88Department of Pathology, Keck School of Medicine, University of Southern California, Los Angeles, California, E. LENTZ99Roche Laboratories, Nutley, New Jersey & E. J. HEATHCOTE1010Department of Medicine, University Health Network, Toronto Western Hospital, Toronto, Ontario, Canada1Section of Hepatology, University of Colorado School of Medicine, University of Colorado Health Sciences Center, Denver, Colorado 2FACG Section of Gastroenterology, Louisiana State University Health Sciences Center, New Orleans, Louisiana 3Faculty of Medicine, University of Calgary, Calgary, Alberta, Canada 4Carolinas Center for Liver Disease, Charlotte, North Carolina 5Hepatology Section, Virginia Commonwealth University Medical Center, Richmond, Virginia 6Section of Hepatology, Department of Medicine, University of Manitoba, Winnipeg, Manitoba, Canada 7Division of Gastroenterology/Hepatology, The Scripps Clinic, La Jolla, California 8Department of Pathology, Keck School of Medicine, University of Southern California, Los Angeles, California 9Roche Laboratories, Nutley, New Jersey 10Department of Medicine, University Health Network, Toronto Western Hospital, Toronto, Ontario, Canada Correspondence and/or reprint requests to: T. Everson, MD, FACP Section of Hepatology University of Colorado School of Medicine University of Colorado Health Sciences Center UCH AOP, Hepatology Section 1635 N Ursula, B-154 PO Box 6510 Aurora, CO 80045 USA Telephone: 720-848-2291 Fax: 720-848-2246 Email: greg.everson@... Summary Background: Patients with chronic hepatitis C virus (HCV) and advanced fibrosis or cirrhosis are at risk for disease progression and hepatic decompensation. Aim: To determine the effects on hepatic histology of treatment with peginterferon alfa-2a (90 or 180 ìg/wk) or interferon alfa-2a (3 million units 3 times weekly) for 48 weeks in patients with paired biopsies. Methods: Liver biopsies were obtained at baseline and 6 months after end of treatment. Histologic and virologic responses were compared. Results: Patients attaining sustained virologic response (SVR; n=40) demonstrated the greatest improvements in fibrosis (-1.0, P _________________________________________________________________ Need to know the score, the latest news, or you need your HotmailR-get your " fix " . http://www.msnmobilefix.com/Default.aspx Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 21, 2008 Report Share Posted January 21, 2008 Alimentary Pharmacology & Therapeutics (OnlineAccepted Articles). doi:10.1111/j.1365-2036.2008.03620.x Abstract Histologic benefits of virologic response to peginterferon alfa-2a monotherapy in patients with hepatitis C and advanced fibrosis or compensated cirrhosis G. T. EVERSON11Section of Hepatology, University of Colorado School of Medicine, University of Colorado Health Sciences Center, Denver, Colorado, L. BALART22FACG Section of Gastroenterology, Louisiana State University Health Sciences Center, New Orleans, Louisiana, S. S. LEE33Faculty of Medicine, University of Calgary, Calgary, Alberta, Canada, R. W. REINDOLLAR44Carolinas Center for Liver Disease, Charlotte, North Carolina, M. L. SHIFFMAN55Hepatology Section, Virginia Commonwealth University Medical Center, Richmond, Virginia, G. Y. MINUK66Section of Hepatology, Department of Medicine, University of Manitoba, Winnipeg, Manitoba, Canada, P. J. POCKROS77Division of Gastroenterology/Hepatology, The Scripps Clinic, La Jolla, California, S. GOVINDARAJAN88Department of Pathology, Keck School of Medicine, University of Southern California, Los Angeles, California, E. LENTZ99Roche Laboratories, Nutley, New Jersey & E. J. HEATHCOTE1010Department of Medicine, University Health Network, Toronto Western Hospital, Toronto, Ontario, Canada1Section of Hepatology, University of Colorado School of Medicine, University of Colorado Health Sciences Center, Denver, Colorado 2FACG Section of Gastroenterology, Louisiana State University Health Sciences Center, New Orleans, Louisiana 3Faculty of Medicine, University of Calgary, Calgary, Alberta, Canada 4Carolinas Center for Liver Disease, Charlotte, North Carolina 5Hepatology Section, Virginia Commonwealth University Medical Center, Richmond, Virginia 6Section of Hepatology, Department of Medicine, University of Manitoba, Winnipeg, Manitoba, Canada 7Division of Gastroenterology/Hepatology, The Scripps Clinic, La Jolla, California 8Department of Pathology, Keck School of Medicine, University of Southern California, Los Angeles, California 9Roche Laboratories, Nutley, New Jersey 10Department of Medicine, University Health Network, Toronto Western Hospital, Toronto, Ontario, Canada Correspondence and/or reprint requests to: T. Everson, MD, FACP Section of Hepatology University of Colorado School of Medicine University of Colorado Health Sciences Center UCH AOP, Hepatology Section 1635 N Ursula, B-154 PO Box 6510 Aurora, CO 80045 USA Telephone: 720-848-2291 Fax: 720-848-2246 Email: greg.everson@... Summary Background: Patients with chronic hepatitis C virus (HCV) and advanced fibrosis or cirrhosis are at risk for disease progression and hepatic decompensation. Aim: To determine the effects on hepatic histology of treatment with peginterferon alfa-2a (90 or 180 ìg/wk) or interferon alfa-2a (3 million units 3 times weekly) for 48 weeks in patients with paired biopsies. Methods: Liver biopsies were obtained at baseline and 6 months after end of treatment. Histologic and virologic responses were compared. Results: Patients attaining sustained virologic response (SVR; n=40) demonstrated the greatest improvements in fibrosis (-1.0, P _________________________________________________________________ Need to know the score, the latest news, or you need your HotmailR-get your " fix " . http://www.msnmobilefix.com/Default.aspx Quote Link to comment Share on other sites More sharing options...
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