Becerra, 2015, UK20
|
Cost-utility analysis third-party payer |
Secondary cardiovascular disease prevention |
Fixed-dose combination polypill (aspirin, atorvastatin and ramipril) vs. multiple monotherapy |
Markov, lifetime (3.5% costs and outcomes) |
Drugs Cardiovascular disease events and death Hospitalisations Surgical procedures |
Yes |
The polypill strategy appears to be cost-effective |
Yes |
No |
McConnachie, 2013, UK21
|
Cost-utility analysis third-party payer |
Primary cardiovascular disease prevention |
Pravastatin vs. placebo |
Cox proportional hazards, 15 years (3.5% costs and outcomes) |
Drugs Medical and nurse visits Monitoring and laboratory tests |
No |
Pravastatin treatment is cost saving and increases QALYs in middle-aged men |
Yes |
No |
Barrios, 2012, Spain22
|
Cost-utility analysis third-party payer |
Primary and secondary cardiovascular disease prevention |
Rosuvastatin vs. generic atorvastatin |
Markov, 20 years (3% costs and outcomes) |
Drugs Hospitalisation and follow-up |
No |
Rosuvastatin is more cost-effective than generic atorvastatin |
Yes |
No |
Liew, 2012, Belgium23
|
Cost-utility analysis third-party payer |
Primary cardiovascular disease prevention |
Remaining on atorvastatin vs. switching to simvastatin |
Markov, 20 years (3% costs, 1.5% outcomes) |
Drugs Hospitalisation and follow-up |
No |
Remaining on atorvastatin should be costeffective |
Yes |
No |
Ohsfeldt, 2012, Sweden24
|
Cost-utility analysis third-party payer |
Primary cardiovascular disease prevention |
Rosuvastatin vs. placebo |
Probabilistic Monte Carlo, lifetime (3% costs and outcomes) |
Drugs Medical visits Monitoring tests Hospitalisations |
Yes |
Rosuvastatin is cost-saving in patients with 10-year risk of cardiovascular disease events |
Yes |
No |
Michailov, 2012, Germany25
|
Cost-utility analysis third-party payer |
Secondary cardiovascular disease prevention |
Simvastatin plus niacin/laropiprant vs. simvastatin |
Markov, lifetime (3% costs and outcomes) |
Drugs Medical visits Laboratory tests cardiovascular disease events and deaths |
No |
Addition of niacin/laropiprant to simvastatin is cost-effective in patients not at low-density lipoprotein cholesterol goal |
Yes |
Yes |
Ara, 2012, UK26
|
Cost-utility analysis third-party payer |
Patient with acute coronary syndrome |
Atorvastatin 80 mg /rosuvastatin 40 mg vs. simvastatin 40 mg |
Markov, lifetime (3.5% costs and outcomes) |
Drugs Medical visits Laboratory tests Cardiovascular disease events and follow-up |
Yes |
Rosuvastatin 40 mg is estimated to be more cost-effective |
No |
No |
Greving, 2011, NL27
|
Cost-utility analysis third-party payer |
Primary cardiovascular disease prevention |
Low-dose statin vs. no treatment |
Markov, 10 years (4% costs, 1.5% outcomes) |
Drugs Medical visits Pharmacists’ fees Laboratory tests Cardiovascular disease events, follow-up and death |
Yes |
Statins seem not to be cost-effective for primary prevention in patients at low risk |
No |
No |
Plans-Rubió, 2010, Spain28
|
Cost-effectiveness analysis third-party payer |
Primary cardiovascular disease prevention |
Atorvastatin/fluvastatin/lovastatin/pravastatin/rosuvastatin/ simvastatin vs. no treatment Statin + cholestyramine/ezetimibe vs. no treatment |
Metanalysis for efficacy, 1 year |
Drugs Medical visits Laboratory tests Adverse effects |
No |
Rosuvastatin should be cost-effective for patients with high risk, but combination therapies for greater reductions in low-density lipoprotein cholesterol, and simvastatin for those with moderate or low CHD risk |
No |
Yes |
Reckless, 2010, UK29
|
Cost-utility analysis third-party payer |
Patients with acute coronary syndrome |
Switching to simvastatin + ezetimibe vs. doubling submaximal statin doses |
Markov, lifetime (3.5% costs and outcomes) |
Drugs Medical visits Cardiovascular disease events, follow-up and death |
No |
Switching to simvastatin + ezetimibe is cost-effective |
Yes |
No |
Lorgelly, 2010, UK30
|
Cost-effectiveness analysis third-party payer |
Systolic heart failure |
Rosuvastatin vs. placebo |
Within trial analysis, 3 years (3.5% costs and outcomes) |
Drugs Hospitalisations Surgical procedures |
Yes |
Rosuvastatin significantly reduces healthcare costs |
Yes |
No |
Nherera, 2010, UK31
|
Cost-utility analysis third-party payer |
Familial hypercholesterolaemia (FH) |
High-intensive statins vs. low-intensive statins |
Markov, lifetime (3.5% costs and outcomes) |
Drugs Cardiovascular disease events and follow-up Surgical procedures |
No |
High-intensive statins are cost-effective for younger FH patients |
No |
No |
Martikainen, 2010, Sweden32
|
Cost-effectiveness analysis third-party payer |
High-risk patients with hypercholes terolaemia |
Eight treatment strategies including high-intensive statins |
Probabilistic decision tree, 1 year |
Drugs Medical visits Laboratory tests Travelling |
No |
Rosuvastatin in high low-density lipoprotein cholesterol patients is cost-effective |
Yes |
Yes |
Soini, 2010, Finland33
|
Cost-utility analysis Society |
Secondary prevention of coronary heart disease |
Simvastatin 40 mg/ atorvastatin 20 mg/ rosuvastatin 10 mg + ezetimibe 10 mg vs. simvastatin 40mg |
Markov, lifetime (3% costs and outcomes) |
Drugs Medical visits Monitoring and laboratory tests Hospitalisations Travelling |
No |
Switching to simvastatin + ezetimibe is cost-effective in patients not at goal |
Yes |
Yes |
Taylor, 2009, UK, Spain, Germany34
|
Cost-utility analysis third-party payer |
Secondary cardiovascular disease prevention |
Atorvastatin 80 mg vs. atorvastatin 10 mg |
Markov, lifetime (3.5% costs and outcomes) |
Drugs Cardiovascular disease events Surgical procedures |
No |
Atorvastatin 80 mg is cost-effective |
Yes |
No |
Peura, 2008, Finland35
|
Cost-utility analysis third-party payer |
Primary and secondary coronary heart disease prevention |
Rosuvastatin/ vs. simvastatin |
Markov, lifetime (5% costs and outcomes) |
Drugs Medical visitsLaboratory tests Myocardial infarction events and death Travelling |
No |
Rosuvastatin can be considered potentially cost-effective |
Yes |
No |
Gouveia Pinto, 2008, Portugal36
|
Cost-effectiveness analysis third-party payer |
Hypercholesterolemia and prevention of ischemic heart disease |
Rosuvastatin vs. atorvastatin/pravastatin/simvastatin |
Markov, lifetime (5% costs and outcomes) |
Drugs Medical visits Laboratory tests Myocardial infarction events Examinations |
Np |
Rosuvastatin is a cost-effective alternative |
Yes |
No |
Lindgren, 2007, Scandinavian countries37
|
Cost-effectiveness analysis, Cost-utility analysis Society |
Secondary cardiovascular disease prevention |
High-dose atorvastatin vs. regular dose simvastatin |
Markov, lifetime (3% costs and outcomes) |
Drugs Hospitalisations Surgical procedures Productivity loss |
Np |
High-dose atorvastatin appears to be cost-effective |
Yes |
No |
Scuffham, 2006, Hungary38
|
Cost-effectiveness analysis, Cost-utility analysis third-party payer |
Treatment after percutaneous coronary intervention |
Fluvastatin vs. no treatment |
Markov, 10 years (5% costs and outcomes) |
Drugs Medical visits Cardiovascular disease deaths Hospitalisations |
Yes |
Fluvastatin is cost-effective |
Yes |
No |