Cultural advice

The Australian National University acknowledges, celebrates and pays our respects to the Ngunnawal and Ngambri people of the Canberra region and to all First Nations Australians on whose traditional lands we meet and work, and whose cultures are among the oldest continuing cultures in human history.

Aboriginal and Torres Strait Islander peoples are advised that ANU Library collections may include images, names, voices, and other representations of deceased persons.

Material in the collection may contain terms, language or views that reflect the period in which the item was created and may be considered inappropriate today.

Chronic hepatitis B surveillance in Victoria, 1998-2008: instituting a 21st century approach to an old disease

Loading...
Thumbnail Image

Date

Authors

Williams, Stephanie
Vally, Hassan
Fielding, James E
Cowie, Benjamin

Journal Title

Journal ISSN

Volume Title

Publisher

Public Health Association of Australia

Abstract

Objective: To describe the epidemiology and assess the quality of the Victorian chronic hepatitis B (CHB) surveillance data in light of revised recommendations for the management of people with CHB infection published by the Centers for Disease Control (CDC). Methods: Records of confirmed non-acute hepatitis B cases notified from 1998-2008 were extracted from the Victorian Notifiable Infectious Diseases Surveillance database. Age-standardised notification rates were calculated using population data from the Australian Bureau of Statistics. Descriptive epidemiological analyses were conducted on demographic fields and notifications were assessed for identity of notifier and completeness, especially for country of birth data as prioritised by the CDC. Results: There were 19,024 notifications of CHB from 1998-2008. The annual agestandardised notification rates ranged from 28-38 per 100,000 population, with an upward trend from 2006. Country of birth information reflected the heterogeneity of HBV prevalence worldwide. A decreasing trend of doctor notifications resulted in poor completeness of risk factor fields such as Indigenous status (37%) and country of birth (27%). Conclusion: This analysis highlighted the burden of CHB in Victorians born in high prevalence countries; however a true estimate of this burden was limited by the high proportion of incomplete notifications. Implications: Improving the information collected from notifications will improve surveillance for CHB and ability to target appropriate responses. We suggest a pilot of enhanced surveillance to meet revised standards from CDC.

Description

Citation

Source

Australian and New Zealand Journal of Public Health

Book Title

Entity type

Access Statement

Open Access

License Rights

Restricted until