Evidence

This page contains a snapshot of featured content which highlights evidence addressing key clinical questions including areas of uncertainty. Please see the main topic reference list for details of all sources underpinning this topic.

BMJ Best Practice evidence tables

Evidence table logo

Evidence tables provide easily navigated layers of evidence in the context of specific clinical questions, using GRADE and a BMJ Best Practice Effectiveness rating. Follow the links at the bottom of the table, which go to the related evidence score in the main topic text, providing additional context for the clinical question. Find out more about our evidence tables.

This table is a summary of the analysis reported in a guideline (underpinned by a systematic review) that focuses on the above important clinical question.


Confidence in the evidence is high or moderate to high where GRADE has been performed and there is no difference in effectiveness between the intervention and comparison for key outcomes.


Population: People with established CVD

Intervention: High-intensity statin ᵃ

Comparison: Medium-intensity statin ᵃ

OutcomeEffectiveness (BMJ rating)?Confidence in evidence (GRADE)?

All-cause mortality: all studies ᵇ

No statistically significant difference

High

CV mortality: all studies ᵇ

No statistically significant difference

High

Non-fatal myocardial infarction: all studies ᵇ

Favours intervention

High

Stroke: all studies ᵇ

No statistically significant difference

High

Myalgia: all studies ᵇ

Favours comparison

High

Rhabdomyolysis: all studies ᵇ

Favours comparison

High

Liver adverse events: all studies ᵇ

Occurs more commonly with high intensity statins compared with medium intensity statins (favours comparison)

Moderate

New-onset diabetes ᵇ

No statistically significant difference

High

Recommendations as stated in the source guideline

The National Institute of Health and Care Excellence (NICE) 2023 guideline on lipid modification recommends the following:

  • Start statin treatment in people with CVD with high-dose atorvastatin ᶜ. Use a lower dose of atorvastatin if any of the following apply:

    • potential drug interactions

    • high risk of adverse effects

    • patient preference.

Note

  • Due to the reduction in non-fatal myocardial infarction with high-intensity statin, the guideline group felt this to be the most cost effective option.

  • The guideline group noted a consistent higher rate of adverse events for high-intensity simvastatin compared with other higher-intensity statins.

ᵃ NICE defines statin intensities as follows:

Low intensity = LDL-cholesterol reduction of 20%–30%

Medium intensity = LDL-cholesterol reduction of 31%–40%

High intensity = greater than 40% LDL-cholesterol reduction

ᵇ The source material for this table (table 46 in the full text document) includes subgroup analyses which have not been listed here.

ᶜ See guideline for their recommendation on starting dose of atorvastatin.

This evidence table is related to the following section/s:

This table is a summary of the analysis reported in a guideline (underpinned by a systematic review) that focuses on the above important clinical question.


Confidence in the evidence is moderate or low to moderate where GRADE has been performed and there may be no difference in effectiveness between the intervention and comparison for key outcomes.


Population: People with established CVD

Intervention: High-intensity statin ᵃ

Comparison: Low-intensity statin ᵃ

OutcomeEffectiveness (BMJ rating)?Confidence in evidence (GRADE)?

All-cause mortality

Favours intervention

Low

CV mortality

No statistically significant difference

Moderate

Non-fatal myocardial infarction

No statistically significant difference

Moderate

Stroke

No statistically significant difference

Low

Myalgia

No statistically significant difference

Low

Rhabdomyolysis

No statistically significant difference

Very Low

Liver adverse events

Occurs more commonly with high-intensity statin compared with low-intensity statin (favours comparison)

Moderate

Recommendations as stated in the source guideline

The National Institute of Health and Care Excellence (NICE) 2023 guideline on lipid modification recommends the following:

Start statin treatment in people with CVD with high-dose atorvastatin.ᵇ Use a lower dose of atorvastatin if any of the following apply:

  • potential drug interactions

  • high risk of adverse effects

  • patient preference.

Note

  • The guideline development group notes that the evaluation of individual outcomes may underestimate the total clinical benefit of statins.

  • The guideline compares many different intensities of statin. Overall, the guideline development group felt the evidence (clinical and cost-effectiveness) for reduction in non-fatal myocardial infarction was best for high-intensity statins.

ᵃ NICE defines statin intensities as follows:

Low intensity = LDL-cholesterol reduction of 20%–30%

Medium intensity = LDL-cholesterol reduction of 31%–40%

High intensity = greater than 40% LDL-cholesterol reduction

ᵇ See guideline for their recommendation on starting dose of atorvastatin.

This evidence table is related to the following section/s:

Cochrane Clinical Answers

Cochrane library logo

Cochrane Clinical Answers (CCAs) provide a readable, digestible, clinically focused entry point to rigorous research from Cochrane systematic reviews. They are designed to be actionable and to inform decision making at the point of care and have been added to relevant sections of the main Best Practice text.

  • Is there randomized controlled trial evidence to support the use of statins for the primary prevention of cardiovascular disease?
    Show me the answer
  • How do fibrates compare with placebo for primary prevention of cardiovascular disease events?
    Show me the answer
  • What are the effects of PCSK9 monoclonal antibodies for preventing cardiovascular disease?
    Show me the answer
  • How do PCSK9 monoclonal antibodies compare with ezetimibe and/or statin for prevention of cardiovascular disease?
    Show me the answer

Use of this content is subject to our disclaimer