Probabilistic cost-effectiveness analysis of cascade screening for familial hypercholesterolaemia using alternative diagnostic and identification strategies
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M Thorogood | S E Humphries | S. Humphries | M. Thorogood | D Marks | R Minhas | L Nherera | D. Marks | L. Nherera | R. Minhas | Nherera L | Minhas R | Humphries Se | Cardiovascular Genetics
[1] C. Boileau,et al. Genetic heterogeneity of autosomal dominant hypercholesterolemia , 2007, Clinical genetics.
[2] S. Humphries,et al. Development of sensitive and specific age- and gender-specific low-density lipoprotein cholesterol cutoffs for diagnosis of first-degree relatives with familial hypercholesterolaemia in cascade testing , 2008, Clinical chemistry and laboratory medicine.
[3] S. G. Hadfield,et al. Family tracing to identify patients with Familial Hypercholesterolaemia: the second Audit of the Department of Health Familial Hypercholesterolaemia Cascade Testing Project , 2009, Annals of clinical biochemistry.
[4] R. Levy,et al. Familial hypercholesterolemia (one form of familial type II hyperlipoproteinemia). A study of its biochemical, genetic and clinical presentation in childhood. , 1974, The Journal of clinical investigation.
[5] J. Robson,et al. Lipid modification: cardiovascular risk assessment and the modification of blood lipids for the primary and secondary prevention of cardiovascular disease , 2007, Heart.
[6] Risk of fatal coronary heart disease in familial hypercholesterolaemia. Scientific Steering Committee on behalf of the Simon Broome Register Group. , 1991, BMJ.
[7] Carolyn M Hutter,et al. Genetic causes of monogenic heterozygous familial hypercholesterolemia: a HuGE prevalence review. , 2004, American journal of epidemiology.
[8] S. Humphries,et al. Reductions in all-cause, cancer, and coronary mortality in statin-treated patients with heterozygous familial hypercholesterolaemia: a prospective registry study , 2008, European heart journal.
[9] S. Humphries,et al. Cost-effectiveness analysis of the use of a high-intensity statin compared to a low-intensity statin in the management of patients with familial hypercholesterolaemia , 2010, Current medical research and opinion.
[10] S. Humphries,et al. Comparing costs and benefits over a 10 year period of strategies for familial hypercholesterolaemia screening. , 2003, Journal of public health medicine.
[11] Andrew Briggs,et al. Cost-effectiveness acceptability curves--facts, fallacies and frequently asked questions. , 2004, Health economics.
[12] I. Young,et al. Genetic screening protocol for familial hypercholesterolemia which includes splicing defects gives an improved mutation detection rate. , 2005, Atherosclerosis.
[13] R. H. Dalaqua. University College, London , 1910, Nature.
[14] Carol Coupland,et al. Unintended effects of statins in men and women in England and Wales: population based cohort study using the QResearch database , 2010, BMJ : British Medical Journal.
[15] Carol Coupland,et al. Individualising the risks of statins in men and women in England and Wales: population-based cohort study , 2010, Heart.
[16] S. Humphries,et al. Genetic causes of familial hypercholesterolaemia in patients in the UK: relation to plasma lipid levels and coronary heart disease risk , 2006, Journal of Medical Genetics.
[17] S. Humphries,et al. Familial hypercholesterolaemia: summary of NICE guidance , 2008, BMJ : British Medical Journal.
[18] S. Humphries,et al. A review on the diagnosis, natural history, and treatment of familial hypercholesterolaemia. , 2003, Atherosclerosis.
[19] M. Pfeffer,et al. Early intensive vs a delayed conservative simvastatin strategy in patients with acute coronary syndromes: phase Z of the A to Z trial. , 2004, JAMA.
[20] O. Faergeman,et al. High-dose atorvastatin vs usual-dose simvastatin for secondary prevention after myocardial infarction: the IDEAL study: a randomized controlled trial. , 2005, JAMA.
[21] L. Curtis,et al. Unit Costs of Health and Social Care 2016 , 2015 .
[22] S. G. Hadfield,et al. Mutation detection rate and spectrum in familial hypercholesterolaemia patients in the UK pilot cascade project , 2010, Clinical genetics.
[23] A. Dhar,et al. National Institute for Health and Clinical Excellence , 2005 .
[24] Disciplinary Committee,et al. Royal Pharmaceutical Society of Great Britain , 2002 .
[25] S. Humphries,et al. Census of clinics providing specialist lipid services in the United Kingdom. , 2004, Journal of public health.
[26] Mortality in treated heterozygous familial hypercholesterolaemia: implications for clinical management. Scientific Steering Committee on behalf of the Simon Broome Register Group. , 1999, Atherosclerosis.
[27] Margaret Thorogood,et al. Cost effectiveness analysis of different approaches of screening for familial hypercholesterolaemia , 2002, BMJ : British Medical Journal.
[28] Intensive lipid lowering with atorvastatin in patients with stable coronary disease. , 2005, The New England journal of medicine.
[29] S. Humphries,et al. Risk of Fatal Stroke in Patients With Treated Familial Hypercholesterolemia: A Prospective Registry Study , 2003, Stroke.
[30] J. Kastelein,et al. Cost-effectiveness analysis of the genetic screening program for familial hypercholesterolemia in The Netherlands. , 2004, Seminars in vascular medicine.
[31] References , 1971 .
[32] A. Whitelaw,et al. Diagnosing familial hypercholesterolaemia in childhood by measuring serum cholesterol. , 1977, British medical journal.
[33] Thomas Weber,et al. Intensive versus moderate lipid lowering with statins after acute coronary syndromes. , 2004, The New England journal of medicine.
[34] S. Humphries,et al. Mutation screening in patients for familial hypercholesterolaemia (ADH) , 2010, Clinical genetics.