Summary of findings 3. Alirocumab compared with ezetimibe and statins.
Alirocumab compared with ezetimibe and statins | |||||||
Patient or population: people at high risk of CVD (history of CVD or high LDL‐C despite treatment) Setting: outpatient care settings Intervention: alirocumab PCSK9 monoclonal antibodies Comparison: ezetimibe and statins | |||||||
Outcomes | Illustrative comparative risk (95% CI) | Relative effect (95% CI) | RD (95% CI) | Number of participants (studies) | Certainty of the evidence (GRADE) | Comments | |
Assumed risk | Corresponding risk with PCSK9 inhibition | ||||||
CVD Follow‐up: 6–12 months |
CVD risk was 28 per 1000 participants | CVD risk in the intervention group was 37 (20 to 50 higher) per 1000 participants | OR 1.37 (0.65 to 2.87) | 0.01 (–0.01 to 0.03) | 1379 (3 RCTs) | ⊕⊕⊝⊝ Lowa |
< 1 is beneficial |
All‐cause mortality Follow‐up: 6–12 months |
All‐cause mortality risk was 9 per 1000 participants | All‐cause mortality risk in the intervention group was 3 (0 to 12) per 1000 participants |
OR 0.51 (0.18 to 1.40) | –0.01 (–0.02 to 0.00) | 1733 (5 RCTs) | ⊕⊕⊝⊝ Lowa | < 1 is beneficial |
Myocardial infarction Follow‐up: 6–12 months |
Myocardial infarction risk was 28 per 1000 participants | Myocardial infarction risk in the intervention group was 35 (22 to 48) per 1000 participants | OR 1.45 (0.64 to 3.28) | 0.01 (–0.01 to 0.02) | 1734 (5 RCTs) | ⊕⊕⊝⊝ Lowa |
< 1 is beneficial |
Any stroke Follow‐up: 6–12 months |
Stroke risk was 27 per 1000 participants | Stroke risk in the intervention group was 23 (20 to 26) per 1000 participants | OR 0.85 (0.13 to 5.61) | 0.00 (–0.01 to 0.01) | 1734 (5 RCTs) | ⊕⊕⊝⊝ Lowa |
< 1 is beneficial |
CI: confidence interval; CVD: cardiovascular disease; LDL‐C: low‐density lipoprotein cholesterol; OR: odds ratio; RCT: randomised controlled trial; RD: risk difference. | |||||||
GRADE Working Group grades of evidence High certainty: we are very confident that the true effect lies close to the estimate of effect. Moderate certainty: we are moderately confident in the effect estimate: the true effect is likely to be close to the estimate of effect but may be substantially different. Low certainty: our confidence in the effect estimate is limited: the true effect may be substantially different from the estimate of effect. Very low certainty: we have very little confidence in the effect estimate: the true effect is likely to be substantially different from the estimate of effect. |
aLow event rates and confidence intervals crossed null effect included both appreciable harm and benefit. Downgraded two levels for imprecision.