The Kirby Institute, UNSW Sydney, Sydney, NSW, Australia.
The Kirby Institute, UNSW Sydney, Sydney, NSW, Australia.
J Hepatol. 2019 Aug;71(2):281-288. doi: 10.1016/j.jhep.2019.04.014. Epub 2019 May 10.
BACKGROUND & AIMS: Population-level evidence for the impact of direct-acting antiviral (DAA) therapy on hepatitis C virus (HCV)-related disease burden is lacking. We aimed to evaluate trends in HCV-related decompensated cirrhosis and hepatocellular carcinoma (HCC) hospitalisation, and liver-related and all-cause mortality in the pre-DAA (2001-2014) and DAA therapy (2015-2017) eras in New South Wales, Australia.
HCV notifications (1993-2016) were linked to hospital admissions (2001-2017) and mortality (1995-2017). Segmented Poisson regressions and Poisson regression were used to assess the impact of DAA era and factors associated with liver-related mortality, respectively.
Among 99,910 people with an HCV notification, 3.8% had a decompensated cirrhosis diagnosis and 1.8% had an HCC diagnosis, while 3.3% and 10.5% died of liver-related and all-cause mortality, respectively. In the pre-DAA era, the number of decompensated cirrhosis and HCC diagnoses, and liver-related and all-cause mortality consistently increased (incidence rate ratios 1.04 [95% CI 1.04-1.05], 1.08 [95% CI 1.07-1.08], 1.07 [95% CI 1.06-1.07], and 1.05 [95% CI 1.04-1.05], respectively) over each 6-monthly band. In the DAA era, decompensated cirrhosis diagnosis and liver-related mortality numbers declined (incidence rate ratios 0.97 [95% CI 0.95-0.99] and 0.96 [95% CI 0.94-0.98], respectively), and HCC diagnosis and all-cause mortality numbers plateaued (incidence rate ratio 1.00 [95% CI 0.97-1.03] and 1.01 [95% CI 1.00-1.02], respectively) over each 6-monthly band. In the DAA era, alcohol-use disorder (AUD) was common in patients diagnosed with decompensated cirrhosis and HCC (65% and 46% had a history of AUD, respectively). AUD was independently associated with liver-related mortality (incidence rate ratio 3.35; 95% CI 3.14-3.58).
In the DAA era, there has been a sharp decline in liver disease morbidity and mortality in New South Wales, Australia. AUD remains a major contributor to HCV-related liver disease burden, highlighting the need to address comorbidities.
Rising hepatitis C-related morbidity and mortality is a major public health issue. However, development of highly effective medicines against hepatitis C (called direct-acting antivirals or DAAs) means hepatitis C could be eliminated as a public health threat by 2030. This study shows a sharp decline in liver disease morbidity and mortality since the introduction of DAAs in New South Wales, Australia. Despite this, heavy alcohol use remains an important risk factor for liver disease among people with hepatitis C. To ensure that the benefits of new antiviral treatments are not compromised, management of major comorbidities, including heavy alcohol use must improve among people with hepatitis C.
缺乏直接作用抗病毒(DAA)治疗对丙型肝炎病毒(HCV)相关疾病负担影响的人群水平证据。本研究旨在评估澳大利亚新南威尔士州 DAA 治疗前(2001-2014 年)和 DAA 治疗后(2015-2017 年)时期与失代偿性肝硬化和肝细胞癌(HCC)住院、肝脏相关和全因死亡率相关的 HCV 相关失代偿性肝硬化和 HCC 住院的趋势。
将 HCV 通知(1993-2016 年)与医院入院(2001-2017 年)和死亡率(1995-2017 年)相关联。使用分段泊松回归和泊松回归分别评估 DAA 时代的影响和与肝脏相关死亡率相关的因素。
在 99910 名 HCV 感染者中,3.8%患有失代偿性肝硬化诊断,1.8%患有 HCC 诊断,而 3.3%和 10.5%分别死于肝脏相关和全因死亡率。在 DAA 治疗前时期,失代偿性肝硬化和 HCC 诊断数量以及肝脏相关和全因死亡率持续增加(发病率比 1.04 [95%CI 1.04-1.05]、1.08 [95%CI 1.07-1.08]、1.07 [95%CI 1.06-1.07]和 1.05 [95%CI 1.04-1.05],分别),每 6 个月为一个波段。在 DAA 治疗后时期,失代偿性肝硬化诊断和肝脏相关死亡率下降(发病率比 0.97 [95%CI 0.95-0.99]和 0.96 [95%CI 0.94-0.98],分别),而 HCC 诊断和全因死亡率趋于平稳(发病率比 1.00 [95%CI 0.97-1.03]和 1.01 [95%CI 1.00-1.02],分别),每 6 个月为一个波段。在 DAA 治疗后时期,酒精使用障碍(AUD)在患有失代偿性肝硬化和 HCC 的患者中很常见(分别有 65%和 46%有 AUD 病史)。AUD 与肝脏相关死亡率独立相关(发病率比 3.35;95%CI 3.14-3.58)。
在 DAA 治疗后时期,澳大利亚新南威尔士州的肝病发病率和死亡率急剧下降。AUD 仍然是 HCV 相关肝病负担的主要因素,这突出表明需要解决合并症。
丙型肝炎相关发病率和死亡率上升是一个主要的公共卫生问题。然而,开发针对丙型肝炎的高效药物(称为直接作用抗病毒药物或 DAA)意味着到 2030 年,丙型肝炎可能会被消除为公共卫生威胁。本研究显示,自 DAA 在澳大利亚新南威尔士州推出以来,肝脏疾病的发病率和死亡率急剧下降。尽管如此,在丙型肝炎患者中,大量饮酒仍然是肝脏疾病的一个重要危险因素。为了确保新抗病毒治疗的益处不受影响,必须改善丙型肝炎患者的主要合并症管理,包括大量饮酒。