Law Matthew G, Dore Gregory J, Bath Nicky, Thompson Sandra, Crofts Nick, Dolan Kate, Giles Wendy, Gow Paul, Kaldor John, Loveday Stuart, Powell Elizabeth, Spencer Jenean, Wodak Alex
National Centre in HIV Epidemiology and Clinical Research, The University of New South Wales, 376 Victoria Street, Darlinghurst, Sydney, NSW 2010, Australia.
Int J Epidemiol. 2003 Oct;32(5):717-24. doi: 10.1093/ije/dyg101.
To plan an appropriate public health response to the hepatitis C virus (HCV) epidemic requires that estimates of HCV incidence and prevalence, and projections of the long-term sequelae of infection, are as accurate as possible. In this paper, mathematical models are used to synthesize data on the epidemiology and natural history of HCV in Australia to estimate HCV incidence and prevalence in Australia to end 2001, and project future trends in the long-term sequelae of HCV infection.
Mathematical models of the HCV epidemic in Australia were developed based on estimates of the pattern of injecting drug use. Estimates of HCV infections due to injecting drug use were then adjusted to allow for HCV infections resulting from other transmission routes. Projections of the long-term sequelae of HCV infection were obtained by combining modelled HCV incidence with estimates of the progression rates to these outcomes.
It was estimated that there were 210 000 (lower and upper limits of 157 000 and 252 000) people in Australia living with HCV antibodies at the end of 2001, with HCV incidence in 2001 estimated to be 16 000 (11 000-19 000). It was estimated that 6500 (5000-8000) people were living with HCV-related cirrhosis in 2001, that 175 (130-210) people developed HCV-associated liver failure, and that there were 50 (40-60) incident cases of HCV-related hepatocellular carcinoma (HCC). It was estimated that in 2001 22 500 quality adjusted life years were lost to chronic HCV infection, the majority (77%) in people with early (stage 0/1) liver disease.
Model-based estimates were broadly consistent with other sources of information on the HCV epidemic in Australia. These models suggest that the prevalence of HCV-related cirrhosis and the incidence of HCV-related liver failure and HCC will more than triple in Australia by 2020.
要针对丙型肝炎病毒(HCV)流行制定适当的公共卫生应对措施,就需要尽可能准确地估计HCV发病率和患病率,以及对感染的长期后遗症进行预测。在本文中,运用数学模型综合澳大利亚HCV流行病学和自然史的数据,以估计截至2001年底澳大利亚的HCV发病率和患病率,并预测HCV感染长期后遗症的未来趋势。
基于对注射吸毒模式的估计,建立了澳大利亚HCV流行的数学模型。然后对因注射吸毒导致的HCV感染估计值进行调整,以纳入其他传播途径导致的HCV感染。通过将模拟的HCV发病率与这些结局的进展率估计值相结合,得出HCV感染长期后遗症的预测结果。
估计2001年底澳大利亚有210000人(下限和上限分别为157000人和252000人)感染HCV抗体,2001年HCV发病率估计为16000例(11000 - 19000例)。估计2001年有6500人(5000 - 8000人)患有HCV相关肝硬化,175人(130 - 210人)发生HCV相关肝衰竭,有50例(40 - 60例)HCV相关肝细胞癌(HCC)新发病例。估计2001年慢性HCV感染导致损失22500个质量调整生命年,其中大多数(77%)为早期(0/1期)肝病患者。
基于模型的估计与澳大利亚HCV流行的其他信息来源大致一致。这些模型表明,到2020年,澳大利亚HCV相关肝硬化的患病率以及HCV相关肝衰竭和HCC的发病率将增加两倍多。