Please use this identifier to cite or link to this item: https://swslhd.intersearch.com.au/swslhdjspui/handle/1/12891
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dc.contributor.authorClark, P. J.-
dc.contributor.authorValery, P. C.-
dc.contributor.authorStrasser, S. I.-
dc.contributor.authorWeltman, M.-
dc.contributor.authorThompson, A.-
dc.contributor.authorLevy, M. T.-
dc.contributor.authorLeggett, B.-
dc.contributor.authorZekry, A.-
dc.contributor.authorRong, J.-
dc.contributor.authorSinclair, M.-
dc.contributor.authorGeorge, J.-
dc.contributor.authorSievert, W.-
dc.contributor.authorMacQuillan, G.-
dc.contributor.authorTse, E.-
dc.contributor.authorNicoll, A.-
dc.contributor.authorWade, A.-
dc.contributor.authorCheng, W.-
dc.contributor.authorRoberts, S. K.-
dc.date.accessioned2024-09-02T05:56:30Z-
dc.date.available2024-09-02T05:56:30Z-
dc.date.issued2024-
dc.identifier.issn09595236 (ISSN)-
dc.identifier.urihttps://swslhd.intersearch.com.au/swslhdjspui/handle/1/12891-
dc.description.abstractIntroduction: Alcohol use is common in patients with chronic hepatitis C virus (HCV) infection. We examined the impact of alcohol use on direct-acting antiviral (DAA) therapy outcome and the clinical course of liver disease and 2-year survival for patients receiving HCV DAA therapy. Methods: Adults (n = 2624) recruited from 26 Australian hospital liver clinics during 2016?2021 were followed up for 2 years. Risky alcohol use was defined by a combination of self-report (?40 g/day of ethanol), physician-reported history of problematic alcohol use, and anti-craving medication prescription via population-based database linkage. We examined factors associated with advanced liver fibrosis and survival using multivariable logistic and Cox regression. Results: Among 1634 patients (62.3%) with risky alcohol use, 24.6% reported consuming ?40 g/day of alcohol, 98.3% physician-reported problematic alcohol use; only 4.1% were dispensed naltrexone/acamprosate. One hundred and forty-three patients with cirrhosis reported ?40 g/day of alcohol, 6 (4.3%) were prescribed naltrexone/acamprosate. Risky alcohol use was associated with advanced fibrosis (adjusted-odds ratio 1.69, 95% confidence interval 1.32?2.17) and patients were over-represented for cirrhosis (45.1% vs. 25.6% in no-risky alcohol use [p < 0.001]) and hepatocellular carcinoma (5.7% vs. 2.5% [p < 0.001]). Sustained viral response (p = 0.319) and 2-year survival (adjusted-hazard ratio 1.98, 95% confidence interval 0.84?4.63) after DAA therapy were not associated with risky alcohol use. Discussion and Conclusions: Risky alcohol use in HCV patients was prevalent, but did not reduce HCV cure. Treatment for alcohol dependence was low. Risky alcohol use may be under-recognised in liver clinics. Better integration of addiction medicine into liver services and increased resourcing and addiction medicine training opportunities for hepatologists may help address this. � 2024 The Author(s). Drug and Alcohol Review published by John Wiley & Sons Australia, Ltd on behalf of Australasian Professional Society on Alcohol and other Drugs.-
dc.publisherJohn Wiley and Sons Inc-
dc.subjectalcohol dependence alcohol-use disorder cirrhosis liver fibrosis mortality-
dc.titleAlcohol does not impact chronic hepatitis C treatment outcomes but increases risk for progressive liver disease: Findings from a prospective multicentre Australian study (OPERA-C)-
dc.typeJournal Article-
dc.contributor.swslhdauthorLevy, Miriam T.-
dc.description.affiliatesDepartment of Gastroenterology, Alcohol and Drug Assessment Unit, Princess Alexandra and Mater Hospitals, Brisbane, Australia Faculty of Medicine, The University of Queensland, Brisbane, Australia QIMR Berghofer Medical Research Institute, Brisbane, Australia AW Morrow Gastroenterology and Liver Centre, Royal Prince Alfred Hospital, Sydney, Australia Hepatology Services, Nepean Hospital, Sydney, Australia Department of Gastroenterology, St Vincent's Hospital, Melbourne, Australia Department of Gastroenterology and Liver, Liverpool Hospital, Sydney, Australia Department of Gastroenterology and Hepatology, Royal Brisbane and Women's Hospital, Brisbane, Australia Department of Gastroenterology and Hepatology, St George Hospital, Sydney, Australia Gippsland Gastroenterology, Latrobe Regional Hospital, Traralgon, Australia Department of Gastroenterology and Hepatology, Austin Hospital, Melbourne, Australia Faculty of Medicine, The University of Sydney, Sydney, Australia Storr Liver Centre, Westmead Hospital, Sydney, Australia Gastrointestinal and Liver Unit, Monash Health and Monash University, Melbourne, Australia Department of Hepatology and Liver Transplant Unit, Sir Charles Gairdner Hospital, Perth, Australia Hepatology, Royal Adelaide Hospital, Adelaide, Australia Eastern Health, Melbourne, Australia Burnet Institute, Melbourne, Australia Barwon Health Liver Clinic University Hospital, Geelong, Australia Department of Gastroenterology & Hepatology, Royal Perth Hospital, Perth, Australia The Alfred Hospital and Monash University CCS, Melbourne, Australia-
dc.identifier.doi10.1111/dar.13914-
dc.identifier.departmentLiverpool Hospital, Department of Gastroenterology and Hepatology-
dc.type.studyortrialArticle-
dc.identifier.journaltitleDrug and Alcohol Review-
Appears in Collections:Liverpool Hospital

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