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Secondary Prevention of Cardiovascular Disease

 

The link to RCHT lipid teams flow chart summarising national guidelines (NICE/ACC) on lipid management can be found here.
 

The key messages in secondary prevention are below:
 

Lipid Targets

  • Aim for LDLc ≤ 2.0 mmol/L or non-HDLc ≤ 2.6 mmol/L (consistent with NICE/QOF targets)
  • If baseline LDLc ≥ 4.0 mmol/L OR Familial Hypercholesterolaemia, aim for at least a 50% reduction from baseline
  • Targets should be individualised using clinical judgement and shared decision-making, taking into account cardiovascular risk, comorbidities, treatment tolerability, and patient preference
  • Some patients reviewed in secondary care may have been given a lower LDL-C target (e.g. < 1.8 mmol/L, < 1.4 mmol/L or < 1.0 mmol/L), in line with specialist recommendations.

 

Lifestyle & Risk Factor Management

  • Smoking cessation, weight reduction (if required), alcohol reduction, healthy diet, and regular exercise.
  • Direct patients to HEART UK for self-assessment tools and educational resources.
  • Manage secondary causes* and address other risk factors for CVD
  • Consider familial hypercholesterolaemia and Lpa if meets criteria (see lipid home page)

 

*e.g. diabetes mellitus, excessive alcohol intake, poor diet, obesity, profound hypothyroidism, medications (e.g. thiazide diuretics, ciclosporin), nephrotic syndrome



Lipid Lowering Therapy

Statins

  • High intensity statin therapy remains first line treatment in secondary prevention e.g.

    • atorvastatin 80mg
      Use lower initial dose of Atorvastatin and slowly increased if tolerated if: eGFR <60ml/min, high risk of adverse effects (see statin intolerance), or patient preference

  • See statin intolerance page if unable to tolerate statins

  • Recheck lipids and liver function tests as per monitoring guidelines (below)

  • If despite maximum tolerated statin therapy:

    •  LDLc remains above target but ≤ 2.5 mmol/L then consider:

      • Ezetimibe

      • If target is still not achieved then consider adding Bempedoic Acid (combination tablets available)
        Prescribe bempedoic acid with caution if history of gout (raises uric acid)

  • Both ezetimibe and bempedoic acid can be used in combination with any other lipid therapy

  • Recheck lipids and liver function tests as per monitoring guidelines below

  • If despite maximum tolerated statin therapy:

    •  LDLc ≥2.6 - 4 mmol/L OR

    • LDLc 2.6 - 3.5 in very high-risk patients*

      Then consider:

      • Inclisiran (if not already taking a PCSK9i monoclonal antibody)

    • Recheck lipids and liver function tests as per monitoring guidelines below


Inclisiran Prescribing and Administration

The status of inclisiran prescribing and administration within the GMS/PMS contract remains unclear. The Kernow LMC and BMA position is that practices should wait for an appropriately commissioned LES before starting. However, some practices have already chosen to prescribe inclisiran. Clinicians should refer to their own practice or PCN policy when deciding how to proceed.


  • If after maximum tolerated statin therapy:
    • LDLc remains >4  OR >3.5  in very high risk patients* consider referral to lipid clinic for:
      • PCSK9i monoclonal antibodies (e.g. Evolocumab or Alirocumab)
      • These are self injected by patient and are initiated by the lipid clinic.

* e.g. ≥2 CVD episode or CVD in >1 vascular bed e.g. peripheral arterial disease and coronary artery disease

 

Monitoring

  • Recheck lipid profile 8–12 weeks after each initiation or dose adjustment
  • Once at target recheck as part of annual CVD review
  • Check liver function alongside lipids at each review point
  • Reaffirm lifestyle advice

 

Advice & Guidance

There is a Lipid Advice & Guidance service available for complex or unclear cases

 

Referral

Refer to the lipid clinic for consideration of monoclonal antibody PCSK9i in the context of secondary prevention if:

  • LDLc >4 despite maximal tolerated statin* OR
  • if LDLc >3.5 despite maximal tolerated statin in very high risk patients**

AND

  • Initiation is considered clinically appropriate, taking into account patient preference, comorbidities, frailty, and overall clinical context.

 

Review referral criteria for referral for familial hypercholesterolaemia and or Lipoprotein (a) [Lp(a)] and refer if appropriate

 

* *e.g. ≥2 CVD episode or CVD in >1 vascular bed e.g. peripheral arterial disease and coronary artery disease

 

Information Required with Referral

  • Current and previously tried lipid lower medications
  • CVD history
  • Most recent lipid profile and LFTs

 

Patient information

·       HEART UK - The Cholesterol Charity

·       British Heart Foundation - What are statins, how do they work and their side effects?

 

References

·       NHS England. Statin Intolerance Pathway (v2, April 2020). https://www.england.nhs.uk/aac/wp-content/uploads/sites/50/2020/04/statin-intolerance-pathway-v2.pdf.

·       England, NHS. Summary of national guidance for lipid management for primary and secondary prevention of CVD (lipid-management-pathway v6, Apr 2020).

·       National Institute for Health and Care Excellence (NICE). Lipid modification – CVD prevention. Clinical Knowledge Summaries (CKS). Updated September 2024. Available at: https://cks.nice.org.uk/topics/lipid-modification-cvd-prevention/

 

Page Review Information

Review date:           01 May 2026
Next review date:    01 May 2028
Clinical editors:       Dr Jack Munro Berry – RMS GP
Contributors:           Dr Rachel Cooper – Consultant Clinical Biochemist