共 50 条
Trends in decompensated cirrhosis and hepatocellular carcinoma among people with a hepatitis B notification in New South Wales
被引:4
|作者:
Shah, Syed Hassan Bin Usman
[1
,6
]
Alavi, Maryam
[1
]
Hajarizadeh, Behzad
[1
]
Matthews, Gail V.
[1
,2
]
Martinello, Marianne
[1
]
Danta, Mark
[2
]
Amin, Janaki
[3
]
Law, Matthew G.
[1
]
George, Jacob
[4
,5
]
Valerio, Heather
[1
]
Dore, Gregory J.
[1
]
机构:
[1] Univ New South Wales UNSW Sydney, Kirby Inst, Sydney, NSW, Australia
[2] St Vincents Hosp, Sydney, Australia
[3] Macquarie Univ, Dept Hlth Syst & Populat, Sydney, NSW, Australia
[4] Univ Sydney, Storr Liver Ctr, Westmead Millennium Inst, Westmead, Australia
[5] Westmead Hosp, Westmead, Australia
[6] UNSW Sydney, Kirby Inst, Wallace Wurth Bldg, Sydney, NSW 2052, Australia
来源:
基金:
澳大利亚国家健康与医学研究理事会;
关键词:
DC;
HCC;
hepatitis B;
late HBV notification;
liver disease;
liver mortality;
population-level;
record linkage;
risk factors;
cause of death;
FIBROSIS PROGRESSION;
ANTIVIRAL TREATMENT;
HCV NOTIFICATION;
DIAGNOSIS;
RISK;
INFECTION;
AUSTRALIA;
THERAPY;
BURDEN;
IMPACT;
D O I:
10.1016/j.jhepr.2022.100552
中图分类号:
R57 [消化系及腹部疾病];
学科分类号:
摘要:
Background & Aims: Population-level trends and factors associated with HBV-related decompensated cirrhosis (DC), he-patocellular carcinoma (HCC), and liver-related mortality are crucial to evaluate the impacts of therapeutic interventions.Methods: Trends in HBV-DC and-HCC diagnoses and liver-related mortality in New South Wales, Australia, were determined through linkage of HBV notifications (1993-2017) to hospital admissions (2001-2018), mortality (1993-2018), and cancer registry (1994-2014) databases. Late HBV notification was defined as notification at or within 2 years of a DC or HCC diagnosis. Cox proportional-hazards regression and multivariable logistic regression analyses were performed to evaluate associated factors.Results: Among 60,660 people with a HBV notification, 1,276 (2.0%) DC and 1,087 (1.8%) HCC diagnoses, and 1,219 (2.0%) liver -related deaths were documented. Since the early 2000s, the number of DC and HCC diagnoses increased; however, age -standardised incidence decreased from 2.64 and 1.95 in 2003 to 1.14 and 1.09 per 1,000 person-years in 2017, respectively. Similarly, age-standardised liver mortality decreased from 2.60 in 2003 to 1.14 per 1,000 person-years in 2017. Among people with DC and HCC diagnoses, late HBV notification declined from 41% and 40% between 2001-2009 to 29% and 25% in 2010-2018, respectively. Predictors of DC diagnosis included older age (birth <1944, adjusted hazard ratio [aHR] 2.06, 95% CI 1.57-2.69), alcohol use disorder (aHR 4.82, 95% CI 3.96-5.87) and HCV co-infection (aHR 1.88, 95% CI 1.53-2.31). Predictors of HCC diagnosis included older age (birth <1944, aHR 3.94, 95% CI 2.91-5.32) and male sex (aHR 3.79, 95% CI 3.05-4.71).Conclusion: In an era of improved antiviral therapies, the risk of HBV-related liver morbidity and mortality has declined. HCV co-infection and alcohol use disorder are key modifiable risk factors associated with the burden of HBV.Lay summary: Rising hepatitis B-related morbidity and mortality is a major public health concern. However, the development of highly effective medicines against hepatitis B virus (HBV) has brought renewed optimism for its elimination by 2030. This study shows a steady decline in HBV-related liver morbidity and mortality in New South Wales, Australia. Moreover, late hepatitis notification has also declined, allowing individuals with HBV to have access to timely antiviral treatment. Despite this, hepatitis C co-infection and alcohol use disorder are key modifiable risk factors associated with HBV disease burden. To attain the desired benefits from highly effective antiviral treatment, managing comorbidities, including hepatitis C and high alcohol use, must improve among individuals with hepatitis B.(c) 2022 The Author(s). Published by Elsevier B.V. on behalf of European Association for the Study of the Liver (EASL). This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
引用
收藏
页数:12
相关论文