Proprotein Convertase Subtilisin/Kexin Type 9 Inhibitor Eligibility and Prescription Rates in Patients Presenting With Recurrent Acute Coronary Syndromes.

IF 2.2 4区 医学 Q2 CARDIAC & CARDIOVASCULAR SYSTEMS Heart, Lung and Circulation Pub Date : 2024-10-17 DOI:10.1016/j.hlc.2024.07.012
William B He, Dylan Jape, Shane Nanayakkara, James A Shaw
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Abstract

Background: Proprotein convertase subtilisin/kexin type 9 (PCSK9) inhibitors are novel medications for reducing low-density lipoprotein cholesterol (LDL-C) levels. In 2020, the Australian Pharmaceutical Benefits Scheme (PBS) began subsidising PCSK9 inhibitors for secondary prevention of cardiovascular disease in patients with LDL-C >2.6 mmol/L despite statin and ezetimibe therapy. This criterion was expanded to LDL-C >1.8 mmol/L in 2022.

Method: A retrospective analysis was conducted on patients admitted to a quaternary hospital with acute coronary syndrome (ACS) between 2020-2022. PCSK9 inhibitor eligibility and prescribing patterns were compared between recurrent ACS patients (≥2 events within 5 years) and first-presentation ACS patients. Australian PBS 2020 and 2022 criteria were applied to assess eligibility.

Results: Of 817 ACS patients with LDL-C >1.8 mmol/L, 118 (14.4%) were categorised as recurrent ACS (33.9% female, mean age 67 years, LDL-C 2.9 mmol/L). When compared with first-presentation ACS patients (n=699), recurrent ACS patients had significantly higher proportions already on statin therapy (49.2% vs 6.0%, p<0.001) and ezetimibe (20.3% vs 2.4%, p<0.001). Recurrent ACS patients had significantly higher proportions of 2020 PBS-eligible patients (11.0% vs 1.3%, p<0.001) and 2022 PBS-eligible patients (20.3% vs 2.2%, p<0.001). There were no significant differences in PCSK9 inhibitor prescription rates among eligible patients (four of 13, 30.8% vs four of nine, 44.4%, p=0.51). Univariate binary logistic regression demonstrated that statin intolerance was significantly associated with PCSK9 inhibitor prescription (odds ratio 10; 95% confidence interval 1.3-79.3; p=0.029).

Conclusions: Despite significantly higher eligibility rates, PCSK9 inhibitor uptake remains low in recurrent ACS patients, demonstrating the need to raise further awareness about eligibility criteria and encourage proactive prescription to prevent recurrent cardiovascular events.

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Proprotein Convertase Subtilisin/Kexin Type 9抑制剂在复发性急性冠状动脉综合征患者中的使用资格和处方率。
背景:Protein convertase subtilisin/kexin type 9 (PCSK9) 抑制剂是降低低密度脂蛋白胆固醇(LDL-C)水平的新型药物。2020 年,澳大利亚药品福利计划(PBS)开始补贴 PCSK9 抑制剂,用于他汀类药物和依折麦布治疗后 LDL-C 仍大于 2.6 mmol/L 的患者的心血管疾病二级预防。2022 年,这一标准扩大到 LDL-C >1.8 mmol/L:对一家四级医院 2020-2022 年间收治的急性冠状动脉综合征(ACS)患者进行了回顾性分析。比较了复发性 ACS 患者(5 年内≥2 次)和首次出现 ACS 患者使用 PCSK9 抑制剂的资格和处方模式。澳大利亚 PBS 2020 和 2022 标准用于评估资格:在 817 名 LDL-C >1.8 mmol/L 的 ACS 患者中,118 人(14.4%)被归类为复发性 ACS(33.9% 为女性,平均年龄 67 岁,LDL-C 2.9 mmol/L)。与首次就诊的 ACS 患者(n=699)相比,复发性 ACS 患者已接受他汀类药物治疗的比例明显更高(49.2% vs 6.0%,p结论:尽管符合条件的比例明显较高,但复发性 ACS 患者对 PCSK9 抑制剂的吸收率仍然很低,这表明有必要进一步提高对符合条件标准的认识,并鼓励积极处方以预防复发性心血管事件的发生。
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来源期刊
Heart, Lung and Circulation
Heart, Lung and Circulation CARDIAC & CARDIOVASCULAR SYSTEMS-
CiteScore
4.50
自引率
3.80%
发文量
912
审稿时长
11.9 weeks
期刊介绍: Heart, Lung and Circulation publishes articles integrating clinical and research activities in the fields of basic cardiovascular science, clinical cardiology and cardiac surgery, with a focus on emerging issues in cardiovascular disease. The journal promotes multidisciplinary dialogue between cardiologists, cardiothoracic surgeons, cardio-pulmonary physicians and cardiovascular scientists.
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