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Changes in quality of life and sexual health are associated with low-dose peginterferon therapy and disease progression in patients with chronic hepatitis C

dc.contributor.authorSnow, Kristin K.en_US
dc.contributor.authorBonkovsky, Herbert L.en_US
dc.contributor.authorFontana, Robert Johnen_US
dc.contributor.authorKim, H. -Y.en_US
dc.contributor.authorSterling, Richard K.en_US
dc.contributor.authorDi Bisceglie, Adrian M.en_US
dc.contributor.authorMorgan, Timothy R.en_US
dc.contributor.authorDienstag, Jules L.en_US
dc.contributor.authorGhany, Marc G.en_US
dc.date.accessioned2011-01-31T17:47:54Z
dc.date.available2011-06-09T15:09:40Zen_US
dc.date.issued2010-04en_US
dc.identifier.citationSnow, K. K.; Bonkovsky, H. L.; Fontana, R. J.; Kim, H.-Y.; Sterling, R. K.; Di Bisceglie, A. M.; Morgan, T. R.; Dienstag, J. L.; Ghany, M. G.; (2010). "Changes in quality of life and sexual health are associated with low-dose peginterferon therapy and disease progression in patients with chronic hepatitis C." Alimentary Pharmacology & Therapeutics 31(7): 719-734. <http://hdl.handle.net/2027.42/79272>en_US
dc.identifier.issn0269-2813en_US
dc.identifier.issn1365-2036en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/79272
dc.description.abstractAliment Pharmacol Ther   31 , 719–734Primary analysis of the Hepatitis C Antiviral Long-Term Treatment against Cirrhosis (HALT-C) Trial showed long-term peginterferon therapy did not reduce complications in patients with chronic hepatitis C and advanced fibrosis or cirrhosis.To assess the effects of long-term peginterferon therapy and disease progression on health-related quality of life (HRQOL), symptoms and sexual health in HALT-C patients.A total of 517 HALT-C patients received peginterferon alfa-2a (90 μg/week); 532 received no additional treatment for 3.5 years. Patients were followed up for outcomes of death, hepatocellular carcinoma and hepatic decompensation. Sexual health, SF-36 scores and symptoms were serially assessed by repeated-measures analyses of covariance.Patients with cirrhosis ( n  = 427) reported lower general well-being and more fatigue ( P  < 0.001) than patients with fibrosis ( n  = 622). Physical scores declined significantly over time, independent of treatment, and patients with cirrhosis reported lower scores. Vitality scores were lower in those with cirrhosis, and treated patients experienced a greater decline over time than untreated patients; HRQOL rebounded after treatment ended. Patients with a clinical outcome had significantly greater declines in all SF-36 and symptom scores. Among men, Sexual Health scores were significantly worse in treated patients and in those with a clinical outcome.Clinical progression of chronic hepatitis C and maintenance peginterferon therapy led to worsening of symptoms, HRQOL and, in men, sexual health in a large patient cohort followed up over 4 years (NCT00006164).en_US
dc.format.extent397808 bytes
dc.format.extent3106 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.publisherBlackwell Publishing Ltden_US
dc.titleChanges in quality of life and sexual health are associated with low-dose peginterferon therapy and disease progression in patients with chronic hepatitis Cen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelOtolaryngologyen_US
dc.subject.hlbsecondlevelPharmacy and Pharmacologyen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Internal Medicine, University of Michigan Medical Center, Ann Arbor, MI, USAen_US
dc.contributor.affiliationotherNew England Research Institutes, Watertown, MA, USAen_US
dc.contributor.affiliationotherDepartments of Medicine and Molecular & Structural Biology and The Liver-Biliary-Pancreatic Center, University of Connecticut Health Center, Farmington, CT, USAen_US
dc.contributor.affiliationotherHepatology Section, Virginia Commonwealth University Medical Center, Richmond, VA, USAen_US
dc.contributor.affiliationotherDivision of Gastroenterology and Hepatology, Saint Louis University School of Medicine, St Louis, MO, USAen_US
dc.contributor.affiliationotherDivision of Gastroenterology, University of California – Irvine, Irvine, CA and Gastroenterology Service, VA Long Beach Healthcare System, Long Beach, CA, USAen_US
dc.contributor.affiliationotherGastrointestinal Unit (Medical Services), Massachusetts General Hospital and the Department of Medicine, Harvard Medical School, Boston, MA, USAen_US
dc.contributor.affiliationotherLiver Diseases Branch, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Department of Health and Human Services, Bethesda, MD, USAen_US
dc.identifier.pmid20070284en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/79272/1/j.1365-2036.2010.04235.x.pdf
dc.identifier.doi10.1111/j.1365-2036.2010.04235.xen_US
dc.identifier.sourceAlimentary Pharmacology & Therapeuticsen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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