首个关于依洛尤单抗在西班牙心内科临床实践中的有效性和安全性的全国性登记研究。RETOSS-CARDIO 研究。

First national registry on the effectiveness and safety of evolocumab in clinical practice in patients attended in cardiology in Spain. The RETOSS-CARDIO study.

机构信息

Servicio de Cardiología, Hospital Universitario Ramón y Cajal, Universidad de Alcalá, Madrid, España.

Servicio de Cardiología, Hospital Universitario La Paz, Madrid, España.

出版信息

Clin Investig Arterioscler. 2020 Nov-Dec;32(6):231-241. doi: 10.1016/j.arteri.2020.05.002. Epub 2020 Jun 27.

Abstract

OBJECTIVE

To present the first registry used to analyse the clinical profile of patients treated with evolocumab in Spain, including the effectiveness on the lipid profile and safety in the «real world» setting.

METHODS

Multicentre, retrospective, and observational study of patients starting treatment with evolocumab from February 2016 to May 2017 in clinical practice in Spanish cardiology units.

RESULTS

A total of 186 patients (mean age 60.3 ± 9.8 years were included, 35.5% with familial hypercholesterolaemia, and 94.1% with a previous cardiovascular event) from 31 cardiology units. Baseline lipid profile: Total cholesterol 219.4 ± 52.2 mg/dL, LDL-cholesterol 144.0 ± 49.0mg/dL, HDL-cholesterol 47.7 ± 13.0mg/dL, and triglycerides 151.0 ± 76.2mg/dL. At the time of initiating evolocumab, 53.8% of patients were taking statins (50% had partial or total intolerance to statins), and 51.1% ezetimibe. In all cases, the dose of evolocumab used was 140 mg, mainly every 2 weeks (97.3%). Evolocumab compliance was high (92.3%). Treatment with evolocumab was interrupted in 6 patients (3.2%), with only 1 (0.5%) due to a probable side effect. Evolocumab significantly reduced total cholesterol (30.9% at week 2, and 39.3% at week 12; P<.001), LDL cholesterol (44.4% and 57.6%, respectively; P<.001), and triglycerides (14.8% and 5.2%, respectively; P<001), with no significant changes in HDL-cholesterol (6.7% and 2.0%; P=.14).

CONCLUSIONS

In clinical practice, evolocumab is associated with reductions in LDL cholesterol, with nearly 60% after 12 weeks of treatment, and with low rates of interruptions due to side effects and high medication compliance. These results are consistent with those reported in randomised clinical trials.

摘要

目的

介绍首个用于分析在西班牙接受依洛尤单抗治疗的患者临床特征的登记研究,包括在“真实世界”环境下对血脂谱的影响和安全性。

方法

这是一项多中心、回顾性、观察性研究,纳入了 2016 年 2 月至 2017 年 5 月在西班牙心脏病学中心接受依洛尤单抗治疗的患者。

结果

共纳入 186 例患者(平均年龄 60.3±9.8 岁,35.5%为家族性高胆固醇血症,94.1%有心血管病史),来自 31 个心脏病学中心。基线血脂谱:总胆固醇 219.4±52.2mg/dL,低密度脂蛋白胆固醇 144.0±49.0mg/dL,高密度脂蛋白胆固醇 47.7±13.0mg/dL,甘油三酯 151.0±76.2mg/dL。在开始使用依洛尤单抗时,53.8%的患者正在服用他汀类药物(50%有他汀类药物部分或完全不耐受),51.1%在服用依折麦布。所有患者均使用 140mg 依洛尤单抗,主要为每两周一次(97.3%)。依洛尤单抗的依从性很高(92.3%)。6 例(3.2%)患者中断了依洛尤单抗治疗,仅 1 例(0.5%)因可能的不良反应而中断。依洛尤单抗显著降低了总胆固醇(第 2 周时降低 30.9%,第 12 周时降低 39.3%;P<.001)、低密度脂蛋白胆固醇(分别降低 44.4%和 57.6%;P<.001)和甘油三酯(分别降低 14.8%和 5.2%;P<001),高密度脂蛋白胆固醇无显著变化(分别降低 6.7%和 2.0%;P=.14)。

结论

在临床实践中,依洛尤单抗可降低 LDL 胆固醇,治疗 12 周后 LDL 胆固醇降低近 60%,且因不良反应和高药物依从性导致中断治疗的发生率较低。这些结果与随机临床试验报告的结果一致。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索