Please use this identifier to cite or link to this item: http://repository.kln.ac.lk/handle/123456789/25822
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dc.contributor.authorMaiwall, R.
dc.contributor.authorPasupuleti, S.S.R.
dc.contributor.authorChoudhury, A.
dc.contributor.authorKim, D.J.
dc.contributor.authorSood, A.
dc.contributor.authorGoyal, O.
dc.contributor.authorMidha, V.
dc.contributor.authorDevarbhavi, H.
dc.contributor.authorArora, A.
dc.contributor.authorKumar, A.
dc.contributor.authorSahu, M.K.
dc.contributor.authorMaharshi, S.
dc.contributor.authorDuseja, A.K.
dc.contributor.authorSingh, V.
dc.contributor.authorTaneja, S.
dc.contributor.authorRao, P.N.
dc.contributor.authorKulkarni, A.
dc.contributor.authorGhazinian, H.
dc.contributor.authorHamid, S.
dc.contributor.authorEapen, C.E.
dc.contributor.authorGoel, A.
dc.contributor.authorShreshtha, A.
dc.contributor.authorShah, S.
dc.contributor.authorHu, J.
dc.contributor.authorPrasad, V.G.M.
dc.contributor.authorYuemin, N.
dc.contributor.authorShaojie, X.
dc.contributor.authorDhiman, R.K.
dc.contributor.authorChen, T.
dc.contributor.authorNing, Q.
dc.contributor.authorPanackel, C.
dc.contributor.authorNiriella, M.A.
dc.contributor.authorLama, T.K.
dc.contributor.authorTan, S.S.
dc.contributor.authorDokmeci, A.K.
dc.contributor.authorShukla, A.
dc.contributor.authorSharma, M.K.
dc.contributor.authorSarin, S.K.
dc.date.accessioned2023-01-19T06:24:02Z
dc.date.available2023-01-19T06:24:02Z
dc.date.issued2023
dc.identifier.citationHepatology International.2023:17(3):662-675. [Epub 2022 Dec 26.]en_US
dc.identifier.issn1936-0533
dc.identifier.urihttp://repository.kln.ac.lk/handle/123456789/25822
dc.descriptionIndexed in MEDLINE.en_US
dc.description.abstractBACKGROUND AND AIM: Acute-on-chronic liver failure (ACLF) is a severe form of alcoholic hepatitis (SAH). We aimed to study the natural course, response to corticosteroids (CS), and the role of the Asian Pacific Association for the Study of Liver (APASL) research consortium (AARC) score in determining clinical outcomes in AH patients. METHODS: Prospectively collected data from the AARC database were analyzed. RESULTS: Of the 1249 AH patients, (aged 43.8 ± 10.6 years, 96.9% male, AARC score 9.2 ± 1.9), 38.8% died on a 90 day follow-up. Of these, 150 (12.0%) had mild-moderate AH (MAH), 65 (5.2%) had SAH and 1034 (82.8%) had ACLF. Two hundred and eleven (16.9%) patients received CS, of which 101 (47.87%) were steroid responders by day 7 of Lille's model, which was associated with improved survival [Hazard ratio (HR) 0.15, 95% CI 0.12-0.19]. AARC-ACLF grade 3 [OR 0.28, 0.14-0.55] was an independent predictor of steroid non-response and mortality [HR 3.29, 2.63-4.11]. Complications increased with degree of liver failure [AARC grade III vs. II vs I], bacterial infections [48.6% vs. 37% vs. 34.7%; p < 0.001); extrahepatic organ failure [66.9% vs. 41.8% vs. 35.4%; p < 0.001] respectively. The AARC score better discriminated 90-day mortality. Harrell's C-index was 0.72 compared to other scores. CONCLUSION: Nearly 4 of 5 patients with AH present with ACLF. Such patients have a higher risk of infections, organ failures, lower response to CS, and higher mortality. Patients with AH and ACLF with AARC grade 3 should be considered for an early liver transplant.en_US
dc.language.isoenen_US
dc.publisherSpringeren_US
dc.subjectA.K.Ien_US
dc.subjectAcute-On-Chronic Liver Failureen_US
dc.subjectHepatitis, Alcoholicen_US
dc.subjectHepatitis, Alcoholic-complicationsen_US
dc.subjectLiver Transplantationen_US
dc.subjectLiver Transplantation-adverse effectsen
dc.titleAARC score determines outcomes in patients with alcohol-associated hepatitis: a multinational studyen_US
dc.typeArticleen_US
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