Kathryn Coyle
Brunel University London
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Featured researches published by Kathryn Coyle.
Value in Health | 2013
Doug Coyle; Kathryn Coyle; Chris Cameron; Karen Lee; Shannon Kelly; Sabine Steiner; George A. Wells
OBJECTIVES The primary objective was to assess the cost-effectiveness of new oral anticoagulants compared with warfarin in patients with nonvalvular atrial fibrillation. Secondary objectives related to assessing the cost-effectiveness of new oral anticoagulants stratified by center-specific time in therapeutic range, age, and CHADS2 score. METHODS Cost-effectiveness was assessed by the incremental cost per quality-adjusted life-year (QALY) gained. Analysis used a Markov cohort model that followed patients from initiation of pharmacotherapy to death. Transition probabilities were obtained from a concurrent network meta-analysis. Utility values and costs were obtained from published data. Numerous deterministic sensitivity analyses and probabilistic analysis were conducted. RESULTS The incremental cost per QALY gained for dabigatran 150 mg versus warfarin was
International Journal of Technology Assessment in Health Care | 2009
Julie Polisena; Doug Coyle; Kathryn Coyle; Sarah McGill
20,797. Apixaban produced equal QALYs at a higher cost. Dabigatran 110 mg and rivaroxaban were dominated by dabigatran 150 mg and apixaban. Results were sensitive to the drug costs of apixaban, the time horizon adopted, and the consequences from major and minor bleeds with dabigatran. Results varied by a centers average time in therapeutic range, a patients CHADS2 score, and patient age, with either dabigatran 150 mg or apixaban being optimal. CONCLUSIONS Results were highly sensitive to patient characteristics. Rivaroxaban and dabigatran 110 mg were unlikely to be cost-effective. For different characteristics, apixaban or dabigatran 150 mg were optimal. Thus, the choice between these two options may come down to the price of apixaban and further evidence on the impact of major and minor bleeds with dabigatran.
BMJ Open | 2014
Chris Cameron; Doug Coyle; Trevor Richter; Shannon Kelly; Kasandra Gauthier; Sabine Steiner; Marc Carrier; Kathryn Coyle; Annie Bai; Kristen Moulton; Tammy Clifford; George A. Wells
OBJECTIVES The research objectives were two-fold: first, to systematically review the literature on the cost-effectiveness of home telehealth for chronic diseases, and second to develop a framework for the conduct of economic evaluation of home telehealth projects for patients with chronic diseases. METHODS A comprehensive literature search identified twenty-two studies (n = 4,871 patients) on home telehealth for chronic diseases published between 1998 and 2008. Studies were reviewed in terms of their methodological quality and their conclusions. RESULTS Home telehealth was found to be cost saving from the healthcare system and insurance provider perspectives in all but two studies, but the quality of the studies was generally low. An evaluative framework was developed which provides a basis to improve the quality of future studies to facilitate improved healthcare decision making, and an application of the framework is illustrated using data from an existing program evaluation of a home telehealth program. CONCLUSIONS Current evidence suggests that home telehealth has the potential to reduce costs, but its impact from a societal perspective remains uncertain until higher quality studies become available.
Journal of Oncology Practice | 2014
Doug Coyle; Eva Grunfeld; Kathryn Coyle; Gregory R. Pond; Jim A. Julian; Mark N. Levine
Objective To examine the comparative efficacy and safety of antithrombotic treatments (apixaban, dabigatran, edoxaban, rivaroxaban and vitamin K antagonists (VKA) at a standard adjusted dose (target international normalised ratio 2.0–3.0), acetylsalicylic acid (ASA), ASA and clopidogrel) for non-valvular atrial fibrillation and among subpopulations. Design Systematic review and network meta-analysis. Data sources A systematic literature search strategy was designed and carried out using MEDLINE, EMBASE, the Cochrane Register of Controlled Trials and the grey literature including the websites of regulatory agencies and health technology assessment organisations for trials published in English from 1988 to January 2014. Eligibility criteria for selecting studies Randomised controlled trials were selected for inclusion if they were published in English, included at least one antithrombotic treatment and involved patients with non-valvular atrial fibrillation eligible to receive anticoagulant therapy. Results For stroke or systemic embolism, dabigatran 150 mg and apixaban twice daily were associated with reductions relative to standard adjusted dose VKA, whereas low-dose ASA and the combination of clopidogrel plus low-dose ASA were associated with increases. Absolute risk reductions ranged from 6 fewer events per 1000 patients treated for dabigatran 150 mg twice daily to 15 more events for clopidogrel plus ASA. For major bleeding, edoxaban 30 mg daily, apixaban, edoxaban 60 mg daily and dabigatran 110 mg twice daily were associated with reductions compared to standard adjusted dose VKA. Absolute risk reductions with these agents ranged from 18 fewer per 1000 patients treated each year for edoxaban 30 mg daily to 24 more for medium dose ASA. Conclusions Compared with standard adjusted dose VKA, new oral anticoagulants were associated with modest reductions in the absolute risk of stroke and major bleeding. People on antiplatelet drugs experienced more strokes compared with anticoagulant drugs without any reduction in bleeding risk. To fully elucidate the comparative benefits and harms of antithrombotic agents across the various subpopulations, rigorously conducted comparative studies or network meta-regression analyses of patient-level data are required. Systematic review registration number PROSPERO registry—CRD42012002721.
Canadian Journal of Infectious Diseases & Medical Microbiology | 2012
Doug Coyle; Kathryn Coyle; Julie A. Bettinger; Scott A. Halperin; Wendy Vaudry; David W. Scheifele; Nicole Le Saux
PURPOSE Survivorship care plans (SCPs) are recommended for patients who have completed primary treatment and are transitioning to routine follow-up care. However, SCPs may be costly, and their effectiveness is unproven. The study objective was to assess the cost effectiveness of an SCP for breast cancer survivors transitioning to routine follow-up care with their own primary care physician (PCP) using data from a recent randomized controlled trial (RCT). METHODS Resource use and utility data for 408 patients with breast cancer enrolled in the RCT comparing an SCP with standard care (no SCP) were used. The intervention group received a 30-minute educational session with a nurse and their SCP, and their PCPs received the SCP plus a full guideline on follow-up. Analysis assessed the societal costs and quality-adjusted life years (QALYs) for the intervention group and the control group over the 2-year follow-up of the RCT. Uncertainty concerning cost effectiveness was assessed through nonparametric bootstrapping and deterministic sensitivity analysis. RESULTS The no-SCP group had better outcomes than the SCP group: total costs per patient were lower for standard care (Canadian
International Journal of Technology Assessment in Health Care | 2012
Doug Coyle; Kathryn Coyle; Glen P. Kenny; Normand G. Boulé; George A. Wells; Michelle Fortier; Robert D. Reid; Penny Phillips; Ronald J. Sigal
698 v
Addiction | 2018
Robert West; Kathryn Coyle; Lesley Owen; Doug Coyle; Subhash Pokhrel
765), and total QALYs were almost equivalent (1.42 for standard care v 1.41 for the SCP). The probability that the SCP was cost effective was 0.26 at a threshold value of a QALY of
Addiction | 2018
Kathryn Coyle; Doug Coyle; Adam Lester-George; Robert West; Bertalan Németh; Mickaël Hiligsmann; Marta Trapero-Bertran; Reiner Leidl; Subhash Pokhrel
50,000. A variety of sensitivity analyses did not change the conclusions of the analysis. CONCLUSION This SCP would be costly to introduce and would not be a cost effective use of scarce health care resources.
Thrombosis Research | 2017
Kathryn Coyle; Marc Carrier; Alejandro Lazo-Langner; Sudeep Shivakumar; Vicky Tagalakis; Susan Solymoss; Nathalie Routhier; James D. Douketis; Douglas Coyle
INTRODUCTION Rotavirus is the main cause of gastroenteritis in Canadian children younger than five years of age, resulting in significant morbidity and cost. The present study provides evidence on the cost effectiveness of two alternative rotavirus vaccinations (RotaTeq [Merck Frosst Canada Ltd, Canada] and Rotarix [GlaxoSmithKline, Canada]) available in Canada. METHODS Analysis was conducted through a Markov model that followed a cohort of children from birth to five years of age. Analysis used pertinent data on the natural history of rotavirus and the effects of vaccination. Estimates of heath care costs for children requiring hospitalizations and emergency department visits were derived from the Canadian Immunization Monitoring Program, Active (IMPACT) surveillance, emergency department studies, as well as other Canadian studies. The model estimated the effect of vaccination on costs and quality-adjusted life years (QALYs). RESULTS The incremental cost per QALY gained from the health care system perspective was
Journal of the American College of Cardiology | 2015
Doug Coyle; Kathryn Coyle; Vidal Essebag; David H. Birnie; Kamran Ahmad; Satish Toal; John L. Sapp; Jeff S. Healey; Atul Verma; George A. Wells; Andrew D. Krahn
122,000 for RotaTeq and