statins for primary prevention of cardiovascular disease (Cochrane review 2013)
Last reviewed 05/2021
- included randomised controlled trials of statins versus placebo or usual care control with minimum treatment duration of one year and follow-up of six months, in adults with no restrictions on total, low density lipoprotein (LDL) or high density lipoprotein (HDL) cholesterol levels, and where 10% or less had a history of cardiovascular disease (CVD)
- outcomes included all-cause mortality, fatal and non-fatal CHD, CVD and
stroke events, combined endpoints (fatal and non-fatal CHD, CVD and stroke
events), revascularisation, change in total and LDL cholesterol concentrations,
adverse events, quality of life and costs. Odds ratios (OR) and risk ratios
(RR) were calculated for dichotomous data, and for continuous data, pooled
mean differences (MD) (with 95% confidence intervals (CI)) were calculated
- analysis and results
- eighteen randomised control trials (19 trial arms; 56,934 participants) were included. Fourteen trials recruited patients with specific conditions (raised lipids, diabetes, hypertension, microalbuminuria)
- all-cause mortality was reduced by statins (OR 0.86, 95% CI 0.79 to 0.94); as was combined fatal and non-fatal CVD RR 0.75 (95% CI 0.70 to 0.81), combined fatal and non-fatal CHD events RR 0.73 (95% CI 0.67 to 0.80) and combined fatal and non-fatal stroke (RR 0.78, 95% CI 0.68 to 0.89). Reduction of revascularisation rates (RR 0.62, 95% CI 0.54 to 0.72) was also seen
- total cholesterol and LDL cholesterol were reduced in all trials but there was evidence of heterogeneity of effects
- no evidence of any serious harm caused by statin prescription
- findings from the Cholesterol Treatment Trialists study using individual
patient data meta-analysis indicate that these benefits are similar
in people at lower (< 1% per year) risk of a major cardiovascular event
(i.e. Ten year CVD risk of <10%)
- conclusions
- reductions in all-cause mortality, major vascular events and revascularisations were found with no excess of adverse events among people without evidence of CVD treated with statin
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