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乙型肝炎或丙型肝炎感染后死亡率的趋势:1992-2006 年。

Trends in mortality after diagnosis of hepatitis B or C infection: 1992-2006.

机构信息

National Centre in HIV Epidemiology and Clinical Research, The University of New South Wales, Sydney, Australia.

出版信息

J Hepatol. 2011 May;54(5):879-86. doi: 10.1016/j.jhep.2010.08.035. Epub 2010 Oct 23.

DOI:10.1016/j.jhep.2010.08.035
PMID:21145812
Abstract

BACKGROUND & AIMS: Chronic hepatitis B (HBV) or C (HCV) virus infection has been associated with increased risk of death, particularly from liver- and drug-related causes. We examined specific causes of death among a population-based cohort of people infected with HBV or HCV to identify areas of excess risk and examine trends in mortality.

METHODS

HBV and HCV cases notified to the New South Wales (NSW) Health Department between 1992 and 2006 were linked to cause of death data and HIV/AIDS notifications. Mortality rates and standardised mortality ratios (SMRs) were calculated using person time methodology, with NSW population rates used as a comparison.

RESULTS

The study cohort comprised 42,480 individuals with HBV mono-infection and 82,034 with HCV mono-infection. HIV co-infection increased the overall mortality rate three to 10-fold compared to mono-infected groups. Liver-related deaths were associated with high excess risk of mortality in both HBV and HCV groups (SMR 10.0, 95% CI 9.0-11.1; 15.8, 95% CI 14.8-16.8). Drug-related deaths among the HCV group also represented an elevated excess risk (SMR 15.4, 95% CI 14.5-16.3). Rates of hepatocellular carcinoma (HCC)-related death remained steady in both groups. A decrease in non-HCC liver-related deaths was seen in the HBV group between 1997 and 2006, but not in the HCV group. After a sharp decrease between 1999 and 2002, drug-related mortality rates in the HCV group have been stable.

CONCLUSIONS

Improvements in HBV treatment and uptake have most likely reduced non-HCC liver-related mortality. Encouragingly, HCV drug-related mortality remained low compared to pre-2002 levels, likely due to changes in opiate supply, and maintenance or improvement in harm reduction strategies.

摘要

背景与目的

慢性乙型肝炎(HBV)或丙型肝炎(HCV)病毒感染与死亡风险增加相关,尤其是与肝脏和药物相关的原因。我们检查了乙型肝炎或丙型肝炎感染者的基于人群队列的特定死因,以确定高风险区域并检查死亡率趋势。

方法

1992 年至 2006 年间,新南威尔士州(NSW)卫生部报告的 HBV 和 HCV 病例与死因数据和 HIV/AIDS 通知相关联。使用人员时间方法计算死亡率和标准化死亡率比(SMR),并使用新南威尔士州人口率作为比较。

结果

研究队列包括 42480 名 HBV 单一感染和 82034 名 HCV 单一感染的个体。与单一感染组相比,HIV 合并感染使总体死亡率增加了 3 到 10 倍。在 HBV 和 HCV 组中,肝脏相关死亡与高死亡率的超额风险相关(SMR 分别为 10.0,95%CI 9.0-11.1 和 15.8,95%CI 14.8-16.8)。HCV 组中与药物相关的死亡也代表了一个升高的超额风险(SMR 为 15.4,95%CI 为 14.5-16.3)。两组的肝细胞癌(HCC)相关死亡的比率保持稳定。HBV 组的非 HCC 肝脏相关死亡从 1997 年到 2006 年减少,但 HCV 组没有。在 1999 年至 2002 年之间急剧下降后,HCV 组的药物相关死亡率保持稳定。

结论

HBV 治疗和采用的改善很可能降低了非 HCC 肝脏相关的死亡率。令人鼓舞的是,与 2002 年之前的水平相比,HCV 药物相关死亡率仍然较低,这可能是由于阿片类药物供应的变化,以及减少伤害策略的维持或改善。

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