Ramachandran Sudarshan, Maarouf Amro, Mitchell Karen, Avades Tony, Smith Peter, Boulton Lee, Kelly Jennifer, Vekaria Nitasha, Hughes Elizabeth
University Hospitals Birmingham NHS Foundation Trust, Birmingham, UK.
Calderdale and Huddersfield NHS Foundation Trust, Acre Street, Lindley, Huddersfield, UK.
Drugs Context. 2024 Aug 8;13. doi: 10.7573/dic.2024-2-4. eCollection 2024.
Bempedoic acid, an adenosine triphosphate citrate lyase inhibitor, was introduced to UK practice via a pre-reimbursement access scheme for adults with primary hypercholesterolaemia or mixed dyslipidaemia who are at high risk of cardiovascular disease, in whom statins are either not tolerated or contraindicated, who have not achieved target cholesterol, despite being on ezetimibe therapy, and do not qualify for PCSK9 inhibitor treatment. This retrospective multicentre audit aimed to evaluate the achievement of lipid-lowering targets with bempedoic acid in UK patients based on recommendations in the Joint British Societies (JBS) guidelines for the prevention of cardiovascular disease.
Pseudo-anonymized medical record data for 221 adults treated with bempedoic acid as part of the UK scheme were entered into a bespoke data collection tool at four UK hospitals. Patient demographics, clinical characteristics, treatment pathways and lipid assessment results (against JBS lipid-lowering targets) were collected against pre-specified criteria.
Overall, 54% (99/184) of patients achieved the JBS2 audit standard (total cholesterol (TC) <5 mmol/L and low-density lipoprotein cholesterol (LDL-C) <3 mmol/L or ≥25% reduction in TC and ≥30% reduction in LDL-C) at 12 weeks post-initiation. At week 12, the mean absolute change in LDL-C was -1.0 mmol/L; the mean percentage reduction from baseline was 22.0%. Additionally, 52% (96/185) of patients had an LDL-C of <3 mmol/L and 10% (18/185) an LDL-C of <1.8 mmol/L at 12 weeks (as per JBS3).
This audit highlights the role of bempedoic acid as part of combination therapy for a population with previously limited treatment options.
贝派地酸是一种三磷酸腺苷柠檬酸裂解酶抑制剂,通过预报销准入计划引入英国,用于患有原发性高胆固醇血症或混合性血脂异常且心血管疾病风险高的成年人,这些患者对他汀类药物不耐受或有禁忌,尽管接受依折麦布治疗但未达到胆固醇目标,且不符合前蛋白转化酶枯草溶菌素9(PCSK9)抑制剂治疗条件。这项回顾性多中心审计旨在根据英国联合学会(JBS)心血管疾病预防指南中的建议,评估英国患者使用贝派地酸实现降脂目标的情况。
在英国的四家医院,将作为英国该计划一部分接受贝派地酸治疗的221名成年人的伪匿名医疗记录数据录入定制的数据收集工具。根据预先指定的标准收集患者的人口统计学、临床特征、治疗途径和血脂评估结果(对照JBS降脂目标)。
总体而言,54%(99/184)的患者在开始治疗12周后达到了JBS2审计标准(总胆固醇(TC)<5 mmol/L且低密度脂蛋白胆固醇(LDL-C)<3 mmol/L或TC降低≥25%且LDL-C降低≥30%)。在第12周时,LDL-C的平均绝对变化为-1.0 mmol/L;从基线的平均百分比降低为22.0%。此外,52%(96/185)的患者在12周时LDL-C<3 mmol/L,10%(18/185)的患者LDL-C<1.8 mmol/L(根据JBS3)。
这项审计突出了贝派地酸作为联合治疗一部分对先前治疗选择有限人群的作用。