Nick Scott
Burnet Institute
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Publication
Featured researches published by Nick Scott.
Gut | 2017
Nick Scott; Emma S. McBryde; Alexander J. Thompson; Joseph S. Doyle; Margaret Hellard
Aims The WHOs draft HCV elimination targets propose an 80% reduction in incidence and a 65% reduction in HCV-related deaths by 2030. We estimate the treatment scale-up required and cost-effectiveness of reaching these targets among injecting drug use (IDU)-acquired infections using Australian disease estimates. Methods A mathematical model of HCV transmission, liver disease progression and treatment among current and former people who inject drugs (PWID). Treatment scale-up and the most efficient allocation to priority groups (PWID or patients with advanced liver disease) were determined; total healthcare and treatment costs, quality-adjusted life years (QALYs) and incremental cost-effectiveness ratios (ICERs) compared with inaction were calculated. Results 5662 (95% CI 5202 to 6901) courses per year (30/1000 IDU-acquired infections) were required, prioritised to patients with advanced liver disease, to reach the mortality target. 4725 (3278–8420) courses per year (59/1000 PWID) were required, prioritised to PWID, to reach the incidence target; this also achieved the mortality target, but to avoid clinically unacceptable HCV-related deaths an additional 5564 (1959–6917) treatments per year (30/1000 IDU-acquired infections) were required for 5 years for patients with advanced liver disease. Achieving both targets in this way cost
International Journal of Drug Policy | 2017
Nick Scott; Joseph S. Doyle; David Wilson; Amanda Wade; Jess Howell; Alisa Pedrana; Alexander J. Thompson; Margaret Hellard
A4.6 (
Journal of Gastroenterology and Hepatology | 2016
Nick Scott; David Iser; Alexander J. Thompson; Joseph S. Doyle; Margaret Hellard
A4.2–
arXiv: Algebraic Geometry | 2011
Paul Norbury; Nick Scott
A4.9) billion more than inaction, but gained 184 000 (119 000–417 000) QALYs, giving an ICER of
PLOS ONE | 2016
Jack Stone; Natasha K. Martin; Matthew Hickman; Margaret Hellard; Nick Scott; Emma S. McBryde; Heidi E. Drummer; Peter Vickerman
A25 121 (
Drug and Alcohol Dependence | 2016
Nick Scott; Elise R. Carrotte; Peter Higgs; Shelley Cogger; Mark Stoové; Campbell Aitken; Paul Dietze
A11 062–
Virulence | 2016
Nick Scott; Margaret Hellard; Emma S. McBryde
A39 036) per QALY gained. Conclusions Achieving WHO elimination targets with treatment scale-up is likely to be cost-effective, based on Australian HCV burden and demographics. Reducing incidence should be a priority to achieve both WHO elimination goals in the long-term.
Journal of Artificial Societies and Social Simulation | 2016
Nick Scott; Michael Livingston; Aaron Hart; James Wilson; David Moore; Paul Dietze
BACKGROUND Modelling suggests that achieving the World Health Organizations elimination targets for hepatitis C virus (HCV) is possible by scaling up use of direct-acting antiviral (DAA) therapy. However, poor linkage to health services and retention in care presents a major barrier, in particular among people who inject drugs (PWID). We identify and assess the cost-effectiveness of additional health system interventions required to achieve HCV elimination targets in Australia, a setting where all people living with HCV have access to DAA therapy. METHODS We used a dynamic HCV transmission and liver-disease progression mathematical model among current and former PWID, capturing testing, treatment and other features of the care cascade. Interventions tested were: availability of point-of-care RNA testing; increased testing of PWID; using biomarkers in place of liver stiffness measurement; and scaling up primary care treatment delivery. RESULTS The projected treatment uptake in Australia reduced the number of people living with HCV from approximately 230,000 in 2015 to approximately 24,000 by 2030 and reduced incidence by 45%. However, the majority (74%) of remaining infections were undiagnosed and among PWID. Scaling up primary care treatment delivery and using biomarkers in place of liver stiffness measurement only reduced incidence by a further 1% but saved AU
Australian and New Zealand Journal of Public Health | 2017
Kathryn Snow; Nick Scott; Hazel J Clothier; Jennifer H. MacLachlan; Benjamin C. Cowie
32 million by 2030, with no change to health outcomes. Additionally replacing HCV antibody testing with point-of-care RNA testing increased healthcare cost savings to AU
Geometry & Topology | 2014
Paul Norbury; Nick Scott
62 million, increased incidence reduction to 64% and gained 11,000 quality-adjusted life years, but critically, additional screening of PWID was required to achieve HCV elimination targets. CONCLUSION Even with unlimited and unrestricted access to HCV DAA treatment, interventions to improve the HCV cascade of care and target PWID will be required to achieve elimination targets.