TY - JOUR KW - Female KW - Humans KW - Male KW - Middle Aged KW - Risk Factors KW - Socioeconomic Factors KW - Cost-Benefit Analysis KW - Cardiovascular Diseases/economics/ epidemiology/prevention & control KW - Great Britain/epidemiology KW - Life Expectancy KW - Models, Cardiovascular KW - Morbidity/trends KW - Primary Prevention/ standards KW - Survival Rate/trends AU - Tunstall-Pedoe H. AU - Fox K. AU - Woodward Mark AU - Ford I. AU - Lewsey J. AU - Lawson K. AU - Ritchie L. AU - Watt G. AU - Kent S. AU - Neilson M. AU - Briggs A. AB -

OBJECTIVES: A policy model is a model that can evaluate the effectiveness and cost-effectiveness of interventions and inform policy decisions. In this study, we introduce a cardiovascular disease (CVD) policy model which can be used to model remaining life expectancy including a measure of socioeconomic deprivation as an independent risk factor for CVD. DESIGN: A state transition model was developed using the Scottish Heart Health Extended Cohort (SHHEC) linked to Scottish morbidity and death records. Individuals start in a CVD-free state and can transit to three CVD event states plus a non-CVD death state. Individuals who have a non-fatal first event are then followed up until death. Taking a competing risk approach, the cause-specific hazards of a first event are modelled using parametric survival analysis. Survival following a first non-fatal event is also modelled parametrically. We assessed discrimination, validation and calibration of our model. RESULTS: Our model achieved a good level of discrimination in each component (c-statistics for men (women)-non-fatal coronary heart disease (CHD): 0.70 (0.74), non-fatal cerebrovascular disease (CBVD): 0.73 (0.76), fatal CVD: 0.77 (0.80), fatal non-CVD: 0.74 (0.72), survival after non-fatal CHD: 0.68 (0.67) and survival after non-fatal CBVD: 0.65 (0.66)). In general, our model predictions were comparable with observed event rates for a Scottish randomised statin trial population which has an overlapping follow-up period with SHHEC. After applying a calibration factor, our predictions of life expectancy closely match those published in recent national life tables. CONCLUSIONS: Our model can be used to estimate the impact of primary prevention interventions on life expectancy and can assess the impact of interventions on inequalities.

AD - Health Economics and Health Technology Assessment, Institute of Health & Wellbeing, University of Glasgow, Glasgow, UK.
Robertson Centre for Biostatistics, Institute of Health & Wellbeing, University of Glasgow, Glasgow, UK.
BHF Centre for Research Excellence, University of Edinburgh, Edinburgh, UK.
Centre of Academic Primary Care, University of Aberdeen, University of Aberdeen, Aberdeen, UK.
Institute of Cardiovascular Research, University of Dundee, Ninewells Hospital, Dundee, UK.
General Practice & Primary Care, Institute of Health & Wellbeing, University of Glasgow, Glasgow, UK.
The George Institute for Global Health, The University of Sydney, Sydney, New South Wales, Australia. AN - 25324535 BT - Heart C2 - PMC4316925 DP - NLM ET - 2014/10/18 LA - eng LB - UK M1 - 3 N1 - Lewsey, J D
Lawson, K D
Ford, I
Fox, K A A
Ritchie, L D
Tunstall-Pedoe, H
Watt, G C M
Woodward, M
Kent, S
Neilson, M
Briggs, A H
CZH/4/557/Chief Scientist Office/United Kingdom
Research Support, Non-U.S. Gov't
England
Heart. 2015 Feb;101(3):201-8. doi: 10.1136/heartjnl-2014-305637. Epub 2014 Oct 16. N2 -

OBJECTIVES: A policy model is a model that can evaluate the effectiveness and cost-effectiveness of interventions and inform policy decisions. In this study, we introduce a cardiovascular disease (CVD) policy model which can be used to model remaining life expectancy including a measure of socioeconomic deprivation as an independent risk factor for CVD. DESIGN: A state transition model was developed using the Scottish Heart Health Extended Cohort (SHHEC) linked to Scottish morbidity and death records. Individuals start in a CVD-free state and can transit to three CVD event states plus a non-CVD death state. Individuals who have a non-fatal first event are then followed up until death. Taking a competing risk approach, the cause-specific hazards of a first event are modelled using parametric survival analysis. Survival following a first non-fatal event is also modelled parametrically. We assessed discrimination, validation and calibration of our model. RESULTS: Our model achieved a good level of discrimination in each component (c-statistics for men (women)-non-fatal coronary heart disease (CHD): 0.70 (0.74), non-fatal cerebrovascular disease (CBVD): 0.73 (0.76), fatal CVD: 0.77 (0.80), fatal non-CVD: 0.74 (0.72), survival after non-fatal CHD: 0.68 (0.67) and survival after non-fatal CBVD: 0.65 (0.66)). In general, our model predictions were comparable with observed event rates for a Scottish randomised statin trial population which has an overlapping follow-up period with SHHEC. After applying a calibration factor, our predictions of life expectancy closely match those published in recent national life tables. CONCLUSIONS: Our model can be used to estimate the impact of primary prevention interventions on life expectancy and can assess the impact of interventions on inequalities.

PY - 2015 SN - 1468-201X (Electronic)
1355-6037 (Linking) SP - 201 EP - 8 T2 - Heart TI - A cardiovascular disease policy model that predicts life expectancy taking into account socioeconomic deprivation VL - 101 ER -