Please use this identifier to cite or link to this item: https://swslhd.intersearch.com.au/swslhdjspui/handle/1/12992
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dc.contributor.authorPrince, D. S.-
dc.contributor.authorHoque, S.-
dc.contributor.authorKim, C.-
dc.contributor.authorMaher, S.-
dc.contributor.authorMiller, J.-
dc.contributor.authorChomley, P.-
dc.contributor.authorPritchard-Jones, J.-
dc.contributor.authorSpruce, S.-
dc.contributor.authorMcGarry, N.-
dc.contributor.authorBaker, D.-
dc.contributor.authorElix, P.-
dc.contributor.authorLiu, K.-
dc.contributor.authorStrasser, S. I.-
dc.contributor.authorGoodger, B.-
dc.contributor.authorZekry, A.-
dc.contributor.authorMcCaughan, G. W.-
dc.date.accessioned2024-09-02T05:57:09Z-
dc.date.available2024-09-02T05:57:09Z-
dc.date.issued2024-
dc.identifier.issn2471254X (ISSN)-
dc.identifier.urihttps://swslhd.intersearch.com.au/swslhdjspui/handle/1/12992-
dc.description.abstractBackground: Identifying patients with undiagnosed advanced chronic liver disease (ACLD) is a public health challenge. Patients with advanced fibrosis or compensated cirrhosis have much better outcomes than those with decompensated disease and may be eligible for interventions to prevent disease progression. Methods: A cloud-based software solution (?the Liver Toolkit?) was developed to access primary care practice software to identify patients at risk of ACLD. Clinical history and laboratory results were extracted to calculate aspartate aminotransferase-to-platelet ratio index and fibrosis 4 scores. Patients identified were recalled for assessment, including Liver Stiffness Measurement (LSM) via transient elastography. Those with an existing diagnosis of cirrhosis were excluded. Results: Existing laboratory results of more than 32,000 adults across nine general practices were assessed to identify 703 patients at increased risk of ACLD (2.2% of the cohort). One hundred seventy-nine patients (26%) were successfully recalled, and 23/179 (13%) were identified to have ACLD (LSM ? 10.0 kPa) (10% found at indeterminate risk [LSM 8.0?9.9 kPa] and 77% low risk of fibrosis [LSM <8.0 kPa]). In most cases, the diagnosis of liver disease was new, with the most common etiology being metabolic Copyright � 2024 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of the American Association for the Study of Liver Diseases.-
dc.publisherLippincott Williams and Wilkins-
dc.subjectalbumin creatinine adult alanine aminotransferase level alcohol consumption Article aspartate aminotransferase level aspartate aminotransferase to platelet ratio index body mass chronic liver disease disease severity dyslipidemia electronic medical record female follow up hepatitis C human hypertension liver disease liver fibrosis liver function test liver stiffness major clinical study male medical practice metabolic fatty liver middle aged nonalcoholic fatty liver obesity pilot study platelet count prevalence public health risk factor screening sensitivity and specificity transient elastography-
dc.titleScreening patients in general practice for advanced chronic liver disease using an innovative IT solution: The Liver Toolkit-
dc.typeJournal Article-
dc.contributor.swslhdauthorPrince, David S.-
dc.description.affiliatesAW Morrow Gastroenterology and Liver Centre, Royal Prince Alfred Hospital, Sydney, NSW, Australia Liver Injury and Cancer Program, Centenary Institute, Sydney, NSW, Australia Department of Gastroenterology and Liver, Liverpool Hospital, Liverpool, NSW, Australia Faculty of Medicine and Health, The University of New South Wales, Sydney, NSW, Australia Department of Gastroenterology and Hepatology, St George Hospital, Kogarah, NSW, Australia Central and Eastern Sydney Primary Health Network, Mascot, NSW, Australia East Sydney Doctors Darlinghurst, NSW, Australia Fountain Street General Practice, Alexandria, NSW, Australia Faculty of Medicine and Health, University of Sydney, Sydney, NSW, Australia-
dc.identifier.doi10.1097/HC9.0000000000000482-
dc.identifier.departmentLiverpool Hospital, Department of Gastroenterology and Hepatology-
dc.type.studyortrialArticle-
dc.identifier.journaltitleHepatology Communications-
Appears in Collections:Liverpool Hospital

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