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Published on: November 10, 2017
Equitable lipid optimisation through a data-driven, pharmacist-led secondary prevention pathway
Joshua Xu1, Jasjit Syan2,3, Hussein Alhakem2
1James Cook University Hospital, Middlesbrough, UK joshua.xu2@nhs.net.
Insights
A pharmacist-led clinic significantly reduced low-density lipoprotein cholesterol (LDL-C) in high-risk patients. While target attainment was equitable across demographics, engagement was lower in the most deprived groups, indicating a need for improved reach.
Area of Science:
- Cardiology
- Public Health
- Pharmacology
Background:
- Atherosclerotic cardiovascular disease (ASCVD) is a major health concern in the UK, with suboptimal cholesterol management contributing to significant mortality.
- Disparities in cardiovascular risk exist based on ethnicity, sex, and socioeconomic status, necessitating targeted interventions.
- Pharmacist-led lipid clinics offer a structured approach to improve patient care and reduce variations in cholesterol management.
Purpose of the Study:
- To evaluate the effectiveness of an automated detection and referral system for a pharmacist-led lipid clinic.
- To assess the impact on low-density lipoprotein cholesterol (LDL-C) attainment in post-acute coronary syndrome patients.
- To determine if outcomes vary by sex, ethnicity, and socioeconomic deprivation.
Main Methods:
- Patients with established ASCVD and elevated lipids were identified via coding and referred to pharmacist-led reviews.
- Automated extraction of sex, ethnicity, age, and index of multiple deprivation (IMD) data was performed.
- A pre-post design assessed the primary outcome of LDL-C ≤2.0 mmol/L attainment following structured consultations and treatment intensification.
Main Results:
- The study included 204 patients, with 65% from diverse ethnic backgrounds and 71% male; mean baseline LDL-C was 3.39 mmol/L.
- Following the intervention, mean LDL-C decreased to 1.97 mmol/L, with 70.6% achieving target levels.
- LDL-C reductions were consistent across sex, ethnicity, and IMD quintiles, although engagement varied by deprivation level.
Conclusions:
- A data-driven, pharmacist-led pathway effectively reduced LDL-C levels in high-risk patients.
- While target attainment was equitable among engaged patients, low engagement from the most deprived group highlights challenges in achieving equitable reach.
- Further research is needed to address barriers to access and ensure the long-term sustainability of such interventions.
Background:
Atherosclerotic cardiovascular disease (ASCVD) is a leading cause of morbidity and mortality in the UK, with raised cholesterol contributing to 25%-28% of ASCVD deaths. Despite well-established guidelines, cholesterol levels remain suboptimally managed and can vary based on ethnicity, sex and socioeconomic deprivation, potentially leading to disproportionate cardiovascular risk for those living at these intersections. Pharmacist-led lipid clinics may reduce variation through structured review and continuity of care. This study evaluates whether automating the detection and referral of high-risk patients to a pharmacist-led clinic is associated with improved attainment of low-density lipoprotein cholesterol (LDL-C) among post-acute coronary syndrome patients in a West London borough, and whether outcomes vary by sex, ethnicity and socioeconomic deprivation.
Methods:
Patients with established ASCVD and residual elevated lipid levels were identified using the International Classification of Diseases, 10th revision and Systematised Nomenclature of Medicine coding and referred to a pharmacist-led review. Sex, ethnicity, age and index of multiple deprivation (IMD) were automatically extracted. The review involved a structured consultation, treatment intensification where required, and follow-up at agreed intervals. The primary outcome was attainment of LDL-C ≤2.0 mmol/L in line with National Institute for Health and Care Excellence recommendations assessed using a pre-post design.
Results:
Among 204 secondary prevention patients, 65% were from ethnically diverse backgrounds and 71% were male. Mean baseline LDL-C was 3.39 mmol/L and 13% were not actively receiving lipid-lowering therapy. Attendance by IMD quintile was 7.4% (most deprived), 34%, 33%, 13% and 12% (least deprived). Following the intervention, mean LDL-C reduced to 1.97 mmol/L with 70.6% achieving targets. Reductions were similar across sex, ethnicity and IMD quintile.
Conclusions:
A data-driven, pharmacist-led pathway was associated with significant LDL-C reduction. Among those who engaged, target attainment was similar across sex, ethnicity and IMD quintile, although low engagement from the most deprived quintile highlights that equitable reach has not yet been achieved. Further work is required to address upstream barriers and evaluate long-term sustainability.
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