Nicholas G. Hirst
Griffith University
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Featured researches published by Nicholas G. Hirst.
Gastrointestinal Endoscopy | 2014
Louisa Gordon; George C. Mayne; Nicholas G. Hirst; Tim Bright; David C. Whiteman; David I. Watson
BACKGROUND Endoscopic surveillance for non-dysplastic Barretts esophagus (BE) is contentious and its cost effectiveness unclear. OBJECTIVE To perform an economic analysis of endoscopic surveillance strategies. DESIGN Cost-utility analysis by using a simulation Markov model to synthesize evidence from large epidemiologic studies and clinical data for surveillance, based on international guidelines, applied in a coordinator-managed surveillance program. SETTING Tertiary care hospital, South Australia. PATIENTS A total of 2040 patient-years of follow-up. INTERVENTION (1) No surveillance, (2) 2-yearly endoscopic surveillance of patients with non-dysplastic BE and 6-monthly surveillance of patients with low-grade dysplasia, (3) a hypothetical strategy of biomarker-modified surveillance. MAIN OUTCOME MEASUREMENTS U.S. cost per quality-adjusted life year (QALY) ratios. RESULTS Compared with no surveillance, surveillance produced an estimated incremental cost per QALY ratio of
Journal of Gastroenterology and Hepatology | 2011
Nicholas G. Hirst; Louisa Gordon; David C. Whiteman; David I. Watson; Jan J. Barendregt
60,858. This was reduced to
Value in Health | 2012
Nicholas G. Hirst; Louisa Gordon; Paul Anthony Scuffham; Adèle C. Green
38,307 when surveillance practice was modified by a hypothetical biomarker-based strategy. Sensitivity analyses indicated that the likelihood that surveillance alone was cost-effective compared with no surveillance was 16.0% and 60.6% if a hypothetical biomarker-based strategy was added to surveillance, at an acceptability threshold of
Health Policy | 2009
Nicholas G. Hirst; Louisa Gordon; Peter Gies; Adèle C. Green
100,000 per QALY gained. LIMITATIONS Treatment options for BE that overlap those for symptomatic GERD were omitted. CONCLUSION By using best available estimates of the malignant potential of BE, endoscopic surveillance of patients with non-dysplastic BE is unlikely to be cost-effective for the majority of patients and depends heavily on progression rates between dysplasia grades. However, strategies that modify surveillance according to cancer risk might be cost-effective, provided that high-risk individuals can be identified and prioritized for surveillance.
Journal of Health Psychology | 2012
Louisa Gordon; Nicholas G. Hirst; Adèle C. Green; Rachel E. Neale
Background and Aim: Several health economic evaluations have explored the cost‐effectiveness of endoscopic surveillance for patients with non‐dysplastic Barretts esophagus, with conflicting results. By comparing results across studies and highlighting key methodological and data limitations a platform for future, more rigorous analyses, can be developed.
Cost Effectiveness and Resource Allocation | 2010
Louisa Gordon; Nicholas G. Hirst; Robert P Young; Paul Brown
OBJECTIVES Health-care costs for the treatment of skin cancers are disproportionately high in many white populations, yet they can be reduced through the promotion of sun-protective behaviors. We investigated the lifetime health costs and benefits of sunscreen promotion in the primary prevention of skin cancers, including melanoma. METHODS A decision-analytic model with Markov chains was used to integrate data from a central community-based randomized controlled trial conducted in Australia and other epidemiological and published sources. Incremental cost per quality-adjusted life-year was the primary outcome. Extensive one-way and probabilistic sensitivity analyses were performed to test the uncertainty in the base findings with plausible variation to the model parameters. RESULTS Using a combined household and government perspective, the discounted incremental cost per quality-adjusted life-year gained from the sunscreen intervention was AU
Journal of Medical Economics | 2011
Nicholas G. Hirst; Jennifer A. Whitty; Robyn Synnott; Diann Eley; Paul Anthony Scuffham
40,890. Over the projected lifetime of the intervention cohort, this would prevent 33 melanomas, 168 cutaneous squamous-cell carcinomas, and 4 melanoma-deaths at a cost of approximately AU
Value in Health | 2009
Louisa Gordon; Nicholas G. Hirst; Rp Young; Paul Brown
808,000. The likelihood that the sunscreen intervention was cost-effective was 64% at a willingness-to-pay threshold of AU
The Medical Journal of Australia | 2008
Louisa Gordon; Nicholas G. Hirst; Peter Gies; Adèle C. Green
50,000 per quality-adjusted life-year gained. CONCLUSIONS Subject to the best-available evidence depicted in our model, the active promotion of routine sunscreen use to white populations residing in sunny settings is likely to be a cost-effective investment for governments and consumers over the long term.
Journal of Gastrointestinal Surgery | 2012
Louisa Gordon; Nicholas G. Hirst; George C. Mayne; David I. Watson; Timothy Bright; Wang Cai; Andrew P. Barbour; B. M. Smithers; David C. Whiteman; Simon Eckermann
OBJECTIVE In Australia there is growing concern about the expanding solarium industry, and the additive effect of persons seeking exposure to artificial ultraviolet radiation (UVR) against already intense background levels of solar UVR. We estimated the numbers of potential skin cancers prevented through regulation of solaria and the associated cost-savings to the Federal Government. METHODS A lifetime decision-analytic model was created using relative risk estimates based on a meta-analysis of the literature assessing the link between skin cancer risk and solarium use. The costs were limited to those incurred by Medicare Australia, for the medical care of individuals treated for skin cancer. RESULTS With stricter regulations, we estimated between 18 and 31 melanomas, 200-251 squamous cell carcinomas and associated costs of