Network
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Publication
Featured researches published by Shu Qin Li.
Australian and New Zealand Journal of Public Health | 2003
Shu Qin Li; Alan Cass; Joan Cunningham
Objectives:To assess concordance in reporting, in two Australian national datasets, of cause of death of patients with end‐stage renal disease (ESRD).
The Medical Journal of Australia | 2014
Shu Qin Li; Steven Guthridge; Padmasiri Eswara Aratchige; Michael Lowe; Zhiqiang Wang; Yuejen Zhao; Vicki Krause
Objective: To estimate the prevalence and incidence of dementia in Northern Territory Indigenous and non‐Indigenous populations.
Australian and New Zealand Journal of Public Health | 2014
Ramakrishna Chondur; Shu Qin Li; Steven Guthridge; Paul D. Lawton
Objective: To examine the variation of chronic disease mortality by remoteness areas of Australia, including states and territories.
Internal Medicine Journal | 2004
Shu Qin Li; Joan Cunningham; Alan Cass
Abstract
Australian and New Zealand Journal of Public Health | 2009
Emily Fearnley; Shu Qin Li; Steven Guthridge
Objective: To assess trends in chronic disease mortality in the Aboriginal population of the Northern Territory (NT), using both underlying and multiple causes of death.
Vaccine | 2012
Bette Liu; Steven Guthridge; Shu Qin Li; Peter Markey; Krause; Peter McIntyre; Elizabeth A. Sullivan; James Ward; Nicholas Wood; John M. Kaldor
BACKGROUND A universal newborn hepatitis B (HBV) vaccination program was introduced in the Northern Territory of Australia in 1990, followed by a school-based catch-up program. We evaluated the prevalence of hepatitis B infection in birthing women up to 20 years after vaccination and compared this to women born before the programs commenced. METHODS A cohort of birthing mothers was defined from Northern Territory public hospital birth records between 2005 and 2010 and linked to laboratory confirmed notifications of chronic HBV, based principally on a record of hepatitis B surface antigen detection. Prevalence of HBV was compared between women born before or after implementation of the newborn and catch-up vaccination programs. FINDINGS Among 10797 birthing mothers, 138 (1.3%) linked to a chronic HBV record. HBV prevalence was substantially higher in Aboriginal women compared to non-Indigenous women (2.4% versus 0.04%; p<0.001). Among 5678 Aboriginal women, those eligible for catch-up and newborn HBV vaccination programs had a significantly lower HBV prevalence than older women born prior to the programs: HBV prevalence respectively 2.2% versus 3.5%, (OR 0.61, 95%CI 0.43-0.88) and 0.8% versus 3.5% (OR 0.21, 95%CI 0.11-0.43). This represents a risk reduction of respectively 40% and 80% compared to unvaccinated women. INTERPRETATION The progressively greater reduction in the prevalence of chronic HBV in adult Aboriginal women co-inciding with eligibility for catch-up and newborn vaccination programs is consistent with a significant impact from both programs. The use of data derived from antenatal screening to track ongoing vaccine impact is applicable to a range of settings globally.
Australian and New Zealand Journal of Public Health | 2009
Shu Qin Li; Natalie Gray; Steven Guthridge; Sabine Pircher; Zhiqiang Wang; Yuejen Zhao
Objectives: To analyse rates of avoidable mortality in Aboriginal and non‐Aboriginal residents of the Northern Territory (NT) from 1985 to 2004, in order to assess the contribution of health care to life expectancy improvements.
Journal of Paediatrics and Child Health | 2015
Steven Guthridge; Lin Li; Sven Silburn; Shu Qin Li; John McKenzie; John Lynch
This study investigated the association between early‐life risk factors and school education outcomes.
PLOS ONE | 2017
Jane Davies; Shu Qin Li; Steven Y. C. Tong; Rob Baird; Miles H. Beaman; Geoff Higgins; Benjamin C. Cowie; John R. Condon; Joshua S. Davis
Background Indigenous populations globally are disproportionately affected by chronic hepatitis B virus (HBV) infection however contemporary sero-prevalence data are often absent. In the Indigenous population of the Northern Territory (NT) of Australia the unique C4 sub-genotype of HBV universally circulates. There are no studies of the sero-prevalence, nor the impact of the vaccination program (which has a serotype mismatch compared to C4), at a population-wide level. Methods We examined all available HBV serology results obtained from the three main laboratories serving NT residents between 1991 and 2011. Data were linked with a NT government database to determine Indigenous status and the most recent test results for each individual were extracted as a cross-sectional database including 88,112 unique individuals. The primary aim was to obtain a contemporary estimate of HBsAg positivity for the NT by Indigenous status. Results Based on all tests from 2007–2011 (35,633 individuals), hepatitis B surface antigen (HBsAg) positivity was 3·40% (95%CI 3·19–3·61), being higher in Indigenous (6·08%[5·65%-6·53%]) than non-Indigenous (1·56%[1·38%-1·76%]) Australians, p<0·0001. Birth cohort analysis showed HBsAg positivity fell over time for Indigenous people, with this decrease commencing prior to universal infant vaccination (which commenced in 1990), with an ongoing but slower rate of decline since 1990, (0·23% decrease per year versus 0·17%). Conclusions HBsAg positivity is high in the NT, particularly in the Indigenous population. HBsAg positivity has fallen over time but a substantial part of this decrease is due to factors other than the universal vaccination program.
Diabetic Medicine | 2017
Elizabeth L.M. Barr; J M Cunningham; Shaun Tatipata; Terry Dunbar; Nadarajan Kangaharan; Steve Guthridge; Shu Qin Li; John R. Condon; Jonathan E. Shaw; Kerin O'Dea; Louise J. Maple-Brown
To assess the relationships of diabetes and albuminuria with all‐cause mortality and cardiovascular disease outcomes in a population without prior cardiovascular disease using data from the Darwin Region Urban Indigenous Diabetes (DRUID) study.