BackgroundNon-alcoholic fatty liver disease (NAFLD) is a major healthcare burden. Real-world outcomes in dedicated tertiary care settings in Australia remain unknown. AimTo evaluate the initial outcomes of patients referred to a dedicated multidisciplinary tertiary care NAFLD clinic. MethodsRetrospective review of all adult patients with NAFLD who attended a dedicated tertiary care NAFLD clinic between January 2018 and February 2020 and who had two clinic visits and FibroScans at least 12 months apart. Demographic and health-related clinical and laboratory data were extracted from electronic medical records. Key outcome measures were serum liver chemistries, liver stiffness measurement (LSM) and weight control at 12 months. ResultsA total of 137 patients with NAFLD were included. Median (interquartile range (IQR)) follow-up time was 392 days (343-497 days). One hundred and eleven patients (81%) achieved weight control (i.e. weight loss or stability). Markers of liver disease activity were significantly improved, including median (IQR) serum alanine aminotransferase (48 (33-76) vs 41 (26-60) U/L, P = 0.009) and aspartate aminotransferase (35 (26-54) vs 32 (25-53) U/L, P = 0.020). Median (IQR) LSM across the whole cohort was significantly improved (8.4 (5.3-11.8) vs 7.0 (4.9-10.1) kPa, P = 0.001). No significant reduction was observed in mean body weight or the frequency of metabolic risk factors. ConclusionsThis study highlights a new model of care for patients with NAFLD and demonstrates promising initial outcomes in relation to significant reductions in markers of liver disease severity. Although most patients achieved weight control, further refinements are needed to achieve significant weight reduction including more frequent and structured dietetic and/or pharmacotherapeutic interventions.
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Univ Western Australia, Sir Charles Gairdner Hosp Unit, Sch Med & Pharmacol, Nedlands, WA 6009, AustraliaUniv Western Australia, Sir Charles Gairdner Hosp Unit, Sch Med & Pharmacol, Nedlands, WA 6009, Australia
Smith, Briohny W.
Adams, Leon A.
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Univ Western Australia, Sir Charles Gairdner Hosp Unit, Sch Med & Pharmacol, Nedlands, WA 6009, AustraliaUniv Western Australia, Sir Charles Gairdner Hosp Unit, Sch Med & Pharmacol, Nedlands, WA 6009, Australia
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Univ Paris Est Creteil Val de Marne, Grp Hosp Henri Mondor, F-94010 Creteil, FranceUniv Paris Est Creteil Val de Marne, Grp Hosp Henri Mondor, F-94010 Creteil, France
Calderaro, Julien
Zafrani, Elie Serge
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Univ Paris Est Creteil Val de Marne, Grp Hosp Henri Mondor, F-94010 Creteil, FranceUniv Paris Est Creteil Val de Marne, Grp Hosp Henri Mondor, F-94010 Creteil, France
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Canberra Hosp, Gastroenteorl & Hepatol Unit, Canberra, ACT, Australia
Australian Natl Univ, Med Sch, Canberra, ACT, AustraliaCanberra Hosp, Gastroenteorl & Hepatol Unit, Canberra, ACT, Australia
Farrell, Geoffrey C.
Wardell, Rebecca
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Canberra Hosp, Gastroenteorl & Hepatol Unit, Canberra, ACT, Australia
Australian Natl Univ, Med Sch, Canberra, ACT, AustraliaCanberra Hosp, Gastroenteorl & Hepatol Unit, Canberra, ACT, Australia
Wardell, Rebecca
Teoh, Narci
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Canberra Hosp, Gastroenteorl & Hepatol Unit, Canberra, ACT, Australia
Australian Natl Univ, Med Sch, Canberra, ACT, AustraliaCanberra Hosp, Gastroenteorl & Hepatol Unit, Canberra, ACT, Australia
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Gazi Univ, Dept Gen Surg, Fac Med, Ankara, Turkey
Mustafa Kemal Mah 2137 Sok 8-14, TR-06520 Ankara, TurkeyGazi Univ, Dept Gen Surg, Fac Med, Ankara, Turkey
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Mayo Clin & Mayo Fdn, Div Gastroenterol & Hepatol, Rochester, MN 55905 USAMayo Clin & Mayo Fdn, Div Gastroenterol & Hepatol, Rochester, MN 55905 USA
Alba, LM
Lindor, K
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Mayo Clin & Mayo Fdn, Div Gastroenterol & Hepatol, Rochester, MN 55905 USAMayo Clin & Mayo Fdn, Div Gastroenterol & Hepatol, Rochester, MN 55905 USA